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Alexander Rauch - Publications

Affiliations: 
Physiology of Cognitive Processes Max Planck Institute for Biological Cybernetics, Tübingen, Baden-Württemberg, Germany 
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Year Citation  Score
2018 Zaldivar D, Rauch A, Logothetis NK, Goense J. Two distinct profiles of fMRI and neurophysiological activity elicited by acetylcholine in visual cortex. Proceedings of the National Academy of Sciences of the United States of America. PMID 30510000 DOI: 10.1073/Pnas.1808507115  0.558
2014 Zaldivar D, Rauch A, Whittingstall K, Logothetis NK, Goense J. Dopamine-induced dissociation of BOLD and neural activity in macaque visual cortex. Current Biology : Cb. 24: 2805-11. PMID 25456449 DOI: 10.1016/J.Cub.2014.10.006  0.538
2014 Musall S, von Pföstl V, Rauch A, Logothetis NK, Whittingstall K. Effects of neural synchrony on surface EEG. Cerebral Cortex (New York, N.Y. : 1991). 24: 1045-53. PMID 23236202 DOI: 10.1093/Cercor/Bhs389  0.516
2012 Sultan F, Augath M, Hamodeh S, Murayama Y, Oeltermann A, Rauch A, Thier P. Unravelling cerebellar pathways with high temporal precision targeting motor and extensive sensory and parietal networks. Nature Communications. 3: 924. PMID 22735452 DOI: 10.1038/Ncomms1912  0.35
2012 von Pföstl V, Li J, Zaldivar D, Goense J, Zhang X, Serr N, Logothetis NK, Rauch A. Effects of lactate on the early visual cortex of non-human primates, investigated by pharmaco-MRI and neurochemical analysis. Neuroimage. 61: 98-105. PMID 22426350 DOI: 10.1016/J.Neuroimage.2012.02.082  0.537
2012 Li J, von Pföstl V, Zaldivar D, Zhang X, Logothetis N, Rauch A. Measuring multiple neurochemicals and related metabolites in blood and brain of the rhesus monkey by using dual microdialysis sampling and capillary hydrophilic interaction chromatography-mass spectrometry. Analytical and Bioanalytical Chemistry. 402: 2545-54. PMID 21956265 DOI: 10.1007/S00216-011-5427-Z  0.48
2010 Logothetis NK, Augath M, Murayama Y, Rauch A, Sultan F, Goense J, Oeltermann A, Merkle H. The effects of electrical microstimulation on cortical signal propagation. Nature Neuroscience. 13: 1283-91. PMID 20818384 DOI: 10.1038/Nn.2631  0.523
2010 Biebmann F, Meinecke FC, Gretton A, Rauch A, Rainer G, Logothetis NK, Müller KR. Temporal kernel CCA and its application in multimodal neuronal data analysis Machine Learning. 79: 5-27. DOI: 10.1007/S10994-009-5153-3  0.52
2009 Bießmann F, Gretton A, Meinecke FC, Zhang X, Rainer G, Logothetis NK, Müller K, Rauch A. Investigating neurovascular coupling using canonical correlation analysis between pharmacological MRI and electrophysiology Bmc Neuroscience. 10. DOI: 10.1186/1471-2202-10-S1-P86  0.534
2008 Zhang X, Rauch A, Xiao H, Rainer G, Logothetis NK. Mass spectrometry-based neurochemical analysis: perspectives for primate research. Expert Review of Proteomics. 5: 641-52. PMID 18937555 DOI: 10.1586/14789450.5.5.641  0.468
2008 Rauch A, Rainer G, Logothetis NK. The effect of a serotonin-induced dissociation between spiking and perisynaptic activity on BOLD functional MRI. Proceedings of the National Academy of Sciences of the United States of America. 105: 6759-64. PMID 18456837 DOI: 10.1073/Pnas.0800312105  0.551
2008 Rauch A, Rainer G, Augath M, Oeltermann A, Logothetis NK. Pharmacological MRI combined with electrophysiology in non-human primates: effects of Lidocaine on primary visual cortex. Neuroimage. 40: 590-600. PMID 18215804 DOI: 10.1016/J.Neuroimage.2007.12.009  0.57
2008 Rauch A, F MFB, Müller K, Logothetis N, Rainer G. The effect of a serotonine agonist on neural activity and BOLD activity in monkey primary visual cortex, a pharmacological fMRI (PhMRI) study Frontiers in Computational Neuroscience. 2. DOI: 10.3389/Conf.Neuro.10.2008.01.013  0.533
2007 Zhang X, Rauch A, Lee H, Xiao H, Rainer G, Logothetis NK. Capillary hydrophilic interaction chromatography/mass spectrometry for simultaneous determination of multiple neurotransmitters in primate cerebral cortex. Rapid Communications in Mass Spectrometry : Rcm. 21: 3621-8. PMID 17939159 DOI: 10.1002/Rcm.3251  0.504
2006 La Camera G, Rauch A, Thurbon D, Lüscher HR, Senn W, Fusi S. Multiple time scales of temporal response in pyramidal and fast spiking cortical neurons. Journal of Neurophysiology. 96: 3448-64. PMID 16807345 DOI: 10.1152/Jn.00453.2006  0.317
Low-probability matches (unlikely to be authored by this person)
2006 Jolivet R, Rauch A, Lüscher HR, Gerstner W. Predicting spike timing of neocortical pyramidal neurons by simple threshold models. Journal of Computational Neuroscience. 21: 35-49. PMID 16633938 DOI: 10.1007/S10827-006-7074-5  0.285
2008 Jolivet R, Kobayashi R, Rauch A, Naud R, Shinomoto S, Gerstner W. A benchmark test for a quantitative assessment of simple neuron models. Journal of Neuroscience Methods. 169: 417-24. PMID 18160135 DOI: 10.1016/J.Jneumeth.2007.11.006  0.269
2007 Clopath C, Jolivet R, Rauch A, Lüscher HR, Gerstner W. Predicting neuronal activity with simple models of the threshold type: Adaptive Exponential Integrate-and-Fire model with two compartments Neurocomputing. 70: 1668-1673. DOI: 10.1016/J.Neucom.2006.10.047  0.264
2012 Paul VG, Rauch AV, Kugel H, Ter Horst L, Bauer J, Dannlowski U, Ohrmann P, Lindner C, Donges US, Kersting A, Egloff B, Suslow T. High responsivity to threat during the initial stage of perception in repression: a 3 T fMRI study. Social Cognitive and Affective Neuroscience. 7: 980-90. PMID 22133562 DOI: 10.1093/Scan/Nsr080  0.218
2014 Rauch AV, Ter Horst L, Paul VG, Bauer J, Dannlowski U, Konrad C, Ohrmann P, Kugel H, Egloff B, Arolt V, Suslow T. Influence of repressive coping style on cortical activation during encoding of angry faces. Plos One. 9: e112398. PMID 25502775 DOI: 10.1371/Journal.Pone.0112398  0.193
2003 Rauch A, La Camera G, Luscher HR, Senn W, Fusi S. Neocortical pyramidal cells respond as integrate-and-fire neurons to in vivo-like input currents. Journal of Neurophysiology. 90: 1598-612. PMID 12750422 DOI: 10.1152/jn.00293.2003  0.166
2009 Suslow T, Kugel H, Rauch AV, Dannlowski U, Bauer J, Konrad C, Arolt V, Heindel W, Ohrmann P. Attachment avoidance modulates neural response to masked facial emotion. Human Brain Mapping. 30: 3553-62. PMID 19347874 DOI: 10.1002/Hbm.20778  0.16
2004 La Camera G, Rauch A, Lüscher HR, Senn W, Fusi S. Minimal models of adapted neuronal response to in vivo-like input currents. Neural Computation. 16: 2101-24. PMID 15333209 DOI: 10.1162/0899766041732468  0.133
2010 Reker M, Ohrmann P, Rauch AV, Kugel H, Bauer J, Dannlowski U, Arolt V, Heindel W, Suslow T. Individual differences in alexithymia and brain response to masked emotion faces. Cortex; a Journal Devoted to the Study of the Nervous System and Behavior. 46: 658-67. PMID 19524887 DOI: 10.1016/J.Cortex.2009.05.008  0.131
2002 Giugliano M, La Camera G, Rauch A, Lüscher HR, Fusi S. Non-monotonic current-to-rate response function in a novel integrate-and-fire model neuron Lecture Notes in Computer Science (Including Subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics). 2415: 141-146.  0.126
2007 Rauch AV, Ohrmann P, Bauer J, Kugel H, Engelien A, Arolt V, Heindel W, Suslow T. Cognitive coping style modulates neural responses to emotional faces in healthy humans: a 3-T FMRI study. Cerebral Cortex (New York, N.Y. : 1991). 17: 2526-35. PMID 17218478 DOI: 10.1093/cercor/bhl158  0.123
2024 Hansen MS, Madsen K, Price M, Søe K, Omata Y, Zaiss MM, Gorvin CM, Frost M, Rauch A. Transcriptional reprogramming during human osteoclast differentiation identifies regulators of osteoclast activity. Bone Research. 12: 5. PMID 38263167 DOI: 10.1038/s41413-023-00312-6  0.122
2007 Ohrmann P, Rauch AV, Bauer J, Kugel H, Arolt V, Heindel W, Suslow T. Threat sensitivity as assessed by automatic amygdala response to fearful faces predicts speed of visual search for facial expression. Experimental Brain Research. 183: 51-9. PMID 17607567 DOI: 10.1007/s00221-007-1022-0  0.121
2015 Abela L, Simmons L, Steindl K, Schmitt B, Mastrangelo M, Joset P, Papuc M, Sticht H, Baumer A, Crowther LM, Mathis D, Rauch A, Plecko B. N(8)-acetylspermidine as a potential plasma biomarker for Snyder-Robinson syndrome identified by clinical metabolomics. Journal of Inherited Metabolic Disease. PMID 26174906 DOI: 10.1007/s10545-015-9876-y  0.12
2010 Griffin HR, Töpf A, Glen E, Zweier C, Stuart AG, Parsons J, Peart I, Deanfield J, O'Sullivan J, Rauch A, Scambler P, Burn J, Cordell HJ, Keavney B, Goodship JA. Systematic survey of variants in TBX1 in non-syndromic tetralogy of Fallot identifies a novel 57 base pair deletion that reduces transcriptional activity but finds no evidence for association with common variants. Heart (British Cardiac Society). 96: 1651-5. PMID 20937753 DOI: 10.1136/hrt.2010.200121  0.117
2015 Vulto-van Silfhout AT, Nakagawa T, Bahi-Buisson N, Haas SA, Hu H, Bienek M, Vissers LE, Gilissen C, Tzschach A, Busche A, Müsebeck J, Rump P, Mathijssen IB, Avela K, Somer M, ... ... Rauch A, et al. Variants in CUL4B are associated with cerebral malformations. Human Mutation. 36: 106-17. PMID 25385192 DOI: 10.1002/Humu.22718  0.115
2019 Wiwie C, Kuznetsova I, Mostafa A, Rauch A, Haakonsson A, Barrio-Hernandez I, Blagoev B, Mandrup S, Schmidt HHHW, Pleschka S, Röttger R, Baumbach J. Time-Resolved Systems Medicine Reveals Viral Infection-Modulating Host Targets. Systems Medicine (New Rochelle, N.Y.). 2: 1-9. PMID 31119214 DOI: 10.1089/sysm.2018.0013  0.115
2010 Ekici AB, Hilfinger D, Jatzwauk M, Thiel CT, Wenzel D, Lorenz I, Boltshauser E, Goecke TW, Staatz G, Morris-Rosendahl DJ, Sticht H, Hehr U, Reis A, Rauch A. Disturbed Wnt Signalling due to a Mutation in CCDC88C Causes an Autosomal Recessive Non-Syndromic Hydrocephalus with Medial Diverticulum. Molecular Syndromology. 1: 99-112. PMID 21031079 DOI: 10.1159/000319859  0.109
2020 Madsen JGS, Madsen MS, Rauch A, Traynor S, Van Hauwaert EL, Haakonsson AK, Javierre BM, Hyldahl M, Fraser P, Mandrup S. Highly interconnected enhancer communities control lineage-determining genes in human mesenchymal stem cells. Nature Genetics. PMID 33020665 DOI: 10.1038/s41588-020-0709-z  0.108
2017 Madsen JGS, Rauch A, Van Hauwaert EL, Schmidt SF, Winnefeld M, Mandrup S. Integrated analysis of motif activity and gene expression changes of transcription factors. Genome Research. PMID 29233921 DOI: 10.1101/gr.227231.117  0.106
2011 Thiel C, Kessler K, Giessl A, Dimmler A, Shalev SA, von der Haar S, Zenker M, Zahnleiter D, Stöss H, Beinder E, Abou Jamra R, Ekici AB, Schröder-Kress N, Aigner T, Kirchner T, ... ... Rauch A, et al. NEK1 mutations cause short-rib polydactyly syndrome type majewski. American Journal of Human Genetics. 88: 106-14. PMID 21211617 DOI: 10.1016/j.ajhg.2010.12.004  0.104
2006 Schubbert S, Zenker M, Rowe SL, Böll S, Klein C, Bollag G, van der Burgt I, Musante L, Kalscheuer V, Wehner LE, Nguyen H, West B, Zhang KY, Sistermans E, Rauch A, et al. Germline KRAS mutations cause Noonan syndrome. Nature Genetics. 38: 331-6. PMID 16474405 DOI: 10.1038/Ng1748  0.104
2018 Ahmad M, Kroll T, Jakob J, Rauch A, Ploubidou A, Tuckermann J. Cell-based RNAi screening and high-content analysis in primary calvarian osteoblasts applied to identification of osteoblast differentiation regulators. Scientific Reports. 8: 14045. PMID 30232406 DOI: 10.1038/s41598-018-32364-8  0.104
2011 Asada M, Rauch A, Shimizu H, Maruyama H, Miyaki S, Shibamori M, Kawasome H, Ishiyama H, Tuckermann J, Asahara H. DNA binding-dependent glucocorticoid receptor activity promotes adipogenesis via Krüppel-like factor 15 gene expression. Laboratory Investigation; a Journal of Technical Methods and Pathology. 91: 203-15. PMID 20956975 DOI: 10.1038/labinvest.2010.170  0.104
2009 Engels H, Wohlleber E, Zink A, Hoyer J, Ludwig KU, Brockschmidt FF, Wieczorek D, Moog U, Hellmann-Mersch B, Weber RG, Willatt L, Kreiss-Nachtsheim M, Firth HV, Rauch A. A novel microdeletion syndrome involving 5q14.3-q15: clinical and molecular cytogenetic characterization of three patients. European Journal of Human Genetics : Ejhg. 17: 1592-9. PMID 19471318 DOI: 10.1038/ejhg.2009.90  0.104
2013 Stuhrmann A, Dohm K, Kugel H, Zwanzger P, Redlich R, Grotegerd D, Rauch AV, Arolt V, Heindel W, Suslow T, Zwitserlood P, Dannlowski U. Mood-congruent amygdala responses to subliminally presented facial expressions in major depression: associations with anhedonia. Journal of Psychiatry & Neuroscience : Jpn. 38: 249-58. PMID 23171695 DOI: 10.1503/Jpn.120060  0.102
2011 Rotger M, Dalmau J, Rauch A, McLaren P, Bosinger SE, Martinez R, Sandler NG, Roque A, Liebner J, Battegay M, Bernasconi E, Descombes P, Erkizia I, Fellay J, Hirschel B, et al. Comparative transcriptomics of extreme phenotypes of human HIV-1 infection and SIV infection in sooty mangabey and rhesus macaque. The Journal of Clinical Investigation. 121: 2391-400. PMID 21555857 DOI: 10.1172/Jci45235  0.102
2012 Baune BT, Konrad C, Grotegerd D, Suslow T, Ohrmann P, Bauer J, Arolt V, Heindel W, Domschke K, Schöning S, Rauch AV, Sehlmeyer C, Kugel H, Dannlowski U. Tumor necrosis factor gene variation predicts hippocampus volume in healthy individuals. Biological Psychiatry. 72: 655-62. PMID 22554453 DOI: 10.1016/J.Biopsych.2012.04.002  0.101
2011 Kortüm F, Das S, Flindt M, Morris-Rosendahl DJ, Stefanova I, Goldstein A, Horn D, Klopocki E, Kluger G, Martin P, Rauch A, Roumer A, Saitta S, Walsh LE, Wieczorek D, et al. The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis. Journal of Medical Genetics. 48: 396-406. PMID 21441262 DOI: 10.1136/Jmg.2010.087528  0.101
2011 Nelson EK, Piehler B, Eckels J, Rauch A, Bellew M, Hussey P, Ramsay S, Nathe C, Lum K, Krouse K, Stearns D, Connolly B, Skillman T, Igra M. LabKey Server: an open source platform for scientific data integration, analysis and collaboration. Bmc Bioinformatics. 12: 71. PMID 21385461 DOI: 10.1186/1471-2105-12-71  0.101
2009 Chichelnitskiy E, Vegiopoulos A, Berriel Diaz M, Ziegler A, Kleiman A, Rauch A, Tuckermann J, Herzig S. In vivo phosphoenolpyruvate carboxykinase promoter mapping identifies disrupted hormonal synergism as a target of inflammation during sepsis in mice. Hepatology (Baltimore, Md.). 50: 1963-71. PMID 19821526 DOI: 10.1002/hep.23194  0.1
2007 Pasutto F, Sticht H, Hammersen G, Gillessen-Kaesbach G, Fitzpatrick DR, Nürnberg G, Brasch F, Schirmer-Zimmermann H, Tolmie JL, Chitayat D, Houge G, Fernández-Martínez L, Keating S, Mortier G, Hennekam RC, ... ... Rauch A, et al. Mutations in STRA6 cause a broad spectrum of malformations including anophthalmia, congenital heart defects, diaphragmatic hernia, alveolar capillary dysplasia, lung hypoplasia, and mental retardation. American Journal of Human Genetics. 80: 550-60. PMID 17273977 DOI: 10.1086/512203  0.099
2006 Rauch A, Bellew M, Eng J, Fitzgibbon M, Holzman T, Hussey P, Igra M, Maclean B, Lin CW, Detter A, Fang R, Faca V, Gafken P, Zhang H, Whiteaker J, et al. Computational Proteomics Analysis System (CPAS): an extensible, open-source analytic system for evaluating and publishing proteomic data and high throughput biological experiments. Journal of Proteome Research. 5: 112-21. PMID 16396501 DOI: 10.1021/Pr0503533  0.098
2011 Eckels J, Hussey P, Nelson EK, Myers T, Rauch A, Bellew M, Connolly B, Law W, Eng JK, Katz J, McIntosh M, Mallick P, Igra M. Installation and use of LabKey Server for proteomics. Current Protocols in Bioinformatics / Editoral Board, Andreas D. Baxevanis ... [Et Al.]. Unit 13.5.. PMID 22161569 DOI: 10.1002/0471250953.Bi1305S36  0.096
2013 Rauch A, Wohner N, Christophe OD, Denis CV, Susen S, Lenting PJ. On the versatility of von Willebrand factor. Mediterranean Journal of Hematology and Infectious Diseases. 5: e2013046. PMID 23936617 DOI: 10.4084/MJHID.2013.046  0.095
2015 Fauth C, Steindl K, Toutain A, Farrell S, Witsch-Baumgartner M, Karall D, Joset P, Böhm S, Baumer A, Maier O, Zschocke J, Weksberg R, Marshall CR, Rauch A. A recurrent germline mutation in the PIGA gene causes Simpson-Golabi-Behmel syndrome type 2. American Journal of Medical Genetics. Part A. PMID 26545172 DOI: 10.1002/Ajmg.A.37452  0.094
2013 Hofmann K, Zweier M, Sticht H, Zweier C, Wittmann W, Hoyer J, Uebe S, van Haeringen A, Thiel CT, Ekici AB, Reis A, Rauch A. Biallelic SEMA3A defects cause a novel type of syndromic short stature. American Journal of Medical Genetics. Part A. 161: 2880-9. PMID 24124006 DOI: 10.1002/ajmg.a.36250  0.092
2010 Renard M, Holm T, Veith R, Callewaert BL, Adès LC, Baspinar O, Pickart A, Dasouki M, Hoyer J, Rauch A, Trapane P, Earing MG, Coucke PJ, Sakai LY, Dietz HC, et al. Altered TGFbeta signaling and cardiovascular manifestations in patients with autosomal recessive cutis laxa type I caused by fibulin-4 deficiency. European Journal of Human Genetics : Ejhg. 18: 895-901. PMID 20389311 DOI: 10.1038/Ejhg.2010.45  0.092
2010 Endele S, Rosenberger G, Geider K, Popp B, Tamer C, Stefanova I, Milh M, Kortüm F, Fritsch A, Pientka FK, Hellenbroich Y, Kalscheuer VM, Kohlhase J, Moog U, Rappold G, ... Rauch A, et al. Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes. Nature Genetics. 42: 1021-6. PMID 20890276 DOI: 10.1038/Ng.677  0.09
2015 Maass PG, Aydin A, Luft FC, Schächterle C, Weise A, Stricker S, Lindschau C, Vaegler M, Qadri F, Toka HR, Schulz H, Krawitz PM, Parkhomchuk D, Hecht J, Hollfinger I, ... ... Rauch A, et al. PDE3A mutations cause autosomal dominant hypertension with brachydactyly. Nature Genetics. 47: 647-53. PMID 25961942 DOI: 10.1038/Ng.3302  0.089
2013 Nelson EK, Piehler B, Rauch A, Ramsay S, Holman D, Asare S, Asare A, Igra M. Ancillary study management systems: a review of needs. Bmc Medical Informatics and Decision Making. 13: 5. PMID 23294514 DOI: 10.1186/1472-6947-13-5  0.089
2008 Cisse B, Caton ML, Lehner M, Maeda T, Scheu S, Locksley R, Holmberg D, Zweier C, den Hollander NS, Kant SG, Holter W, Rauch A, Zhuang Y, Reizis B. Transcription factor E2-2 is an essential and specific regulator of plasmacytoid dendritic cell development. Cell. 135: 37-48. PMID 18854153 DOI: 10.1016/J.Cell.2008.09.016  0.089
2011 Kalay E, Yigit G, Aslan Y, Brown KE, Pohl E, Bicknell LS, Kayserili H, Li Y, Tüysüz B, Nürnberg G, Kiess W, Koegl M, Baessmann I, Buruk K, Toraman B, ... ... Rauch A, et al. CEP152 is a genome maintenance protein disrupted in Seckel syndrome. Nature Genetics. 43: 23-6. PMID 21131973 DOI: 10.1038/Ng.725  0.089
2015 Martinelli S, Stellacci E, Pannone L, D'Agostino D, Consoli F, Lissewski C, Silvano M, Cencelli G, Lepri F, Maitz S, Pauli S, Rauch A, Zampino G, Selicorni A, Melançon S, et al. Molecular Diversity and Associated Phenotypic Spectrum of Germline CBL Mutations. Human Mutation. 36: 787-96. PMID 25952305 DOI: 10.1002/Humu.22809  0.089
2013 Goubau C, Devriendt K, Van der Aa N, Crepel A, Wieczorek D, Kleefstra T, Willemsen MH, Rauch A, Tzschach A, de Ravel T, Leemans P, Van Geet C, Buyse G, Freson K. Platelet defects in congenital variant of Rett syndrome patients with FOXG1 mutations or reduced expression due to a position effect at 14q12. European Journal of Human Genetics : Ejhg. 21: 1349-55. PMID 23632790 DOI: 10.1038/Ejhg.2013.86  0.089
2011 Kraft M, Cirstea IC, Voss AK, Thomas T, Goehring I, Sheikh BN, Gordon L, Scott H, Smyth GK, Ahmadian MR, Trautmann U, Zenker M, Tartaglia M, Ekici A, Reis A, ... ... Rauch A, et al. Disruption of the histone acetyltransferase MYST4 leads to a Noonan syndrome-like phenotype and hyperactivated MAPK signaling in humans and mice. The Journal of Clinical Investigation. 121: 3479-91. PMID 21804188 DOI: 10.1172/Jci43428  0.088
2008 Rauch A, Cieza A, Stucki G. How to apply the International Classification of Functioning, Disability and Health (ICF) for rehabilitation management in clinical practice. European Journal of Physical and Rehabilitation Medicine. 44: 329-42. PMID 18762742  0.088
2015 Lim HW, Uhlenhaut NH, Rauch A, Weiner J, Hübner S, Hübner N, Won KJ, Lazar MA, Tuckermann J, Steger DJ. Genomic redistribution of GR monomers and dimers mediates transcriptional response to exogenous glucocorticoid in vivo. Genome Research. 25: 836-44. PMID 25957148 DOI: 10.1101/Gr.188581.114  0.086
2013 Aouri M, Calmy A, Hirschel B, Telenti A, Buclin T, Cavassini M, Rauch A, Decosterd LA. A validated assay by liquid chromatography-tandem mass spectrometry for the simultaneous quantification of elvitegravir and rilpivirine in HIV positive patients. Journal of Mass Spectrometry : Jms. 48: 616-25. PMID 23674286 DOI: 10.1002/jms.3200  0.085
2013 Rauch A, Fekete C, Cieza A, Geyh S, Meyer T. Participation in physical activity in persons with spinal cord injury: a comprehensive perspective and insights into gender differences. Disability and Health Journal. 6: 165-76. PMID 23769475 DOI: 10.1016/j.dhjo.2013.01.006  0.085
2019 Rauch A, Haakonsson AK, Madsen JGS, Larsen M, Forss I, Madsen MR, Van Hauwaert EL, Wiwie C, Jespersen NZ, Tencerova M, Nielsen R, Larsen BD, Röttger R, Baumbach J, Scheele C, et al. Osteogenesis depends on commissioning of a network of stem cell transcription factors that act as repressors of adipogenesis. Nature Genetics. PMID 30833796 DOI: 10.1038/s41588-019-0359-1  0.085
2006 Suslow T, Ohrmann P, Bauer J, Rauch AV, Schwindt W, Arolt V, Heindel W, Kugel H. Amygdala activation during masked presentation of emotional faces predicts conscious detection of threat-related faces. Brain and Cognition. 61: 243-8. PMID 16510224 DOI: 10.1016/j.bandc.2006.01.005  0.084
2009 Combescure C, Vallier N, Ledergerber B, Cavassini M, Furrer H, Rauch A, Battegay M, Bernasconi E, Vernazza P, Hirschel B. How reliable is an undetectable viral load? Hiv Medicine. 10: 470-6. PMID 19459990 DOI: 10.1111/J.1468-1293.2009.00714.X  0.084
2011 Jacquemont S, Reymond A, Zufferey F, Harewood L, Walters RG, Kutalik Z, Martinet D, Shen Y, Valsesia A, Beckmann ND, Thorleifsson G, Belfiore M, Bouquillon S, Campion D, de Leeuw N, ... ... Rauch A, et al. Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus. Nature. 478: 97-102. PMID 21881559 DOI: 10.1038/Nature10406  0.084
2012 Baune BT, Konrad C, Grotegerd D, Suslow T, Birosova E, Ohrmann P, Bauer J, Arolt V, Heindel W, Domschke K, Schöning S, Rauch AV, Uhlmann C, Kugel H, Dannlowski U. Interleukin-6 gene (IL-6): a possible role in brain morphology in the healthy adult brain. Journal of Neuroinflammation. 9: 125. PMID 22695063 DOI: 10.1186/1742-2094-9-125  0.083
2005 Jolivet R, Rauch A, Lüscher HR, Gerstner W. Integrate-and-Fire models with adaptation are good enough: Predicting spike times under random current injection Advances in Neural Information Processing Systems. 595-602.  0.083
2008 Rauch A, Thiel CT, Schindler D, Wick U, Crow YJ, Ekici AB, van Essen AJ, Goecke TO, Al-Gazali L, Chrzanowska KH, Zweier C, Brunner HG, Becker K, Curry CJ, Dallapiccola B, et al. Mutations in the pericentrin (PCNT) gene cause primordial dwarfism. Science (New York, N.Y.). 319: 816-9. PMID 18174396 DOI: 10.1126/Science.1151174  0.082
2012 Weber H, Rauch A, Adamski S, Chakravarthy K, Kulkarni A, Dogdas B, Bendtsen C, Kath G, Alves SE, Wilkinson HA, Chiu CS. Automated rodent in situ muscle contraction assay and myofiber organization analysis in sarcopenia animal models. Journal of Applied Physiology (Bethesda, Md. : 1985). 112: 2087-98. PMID 22461442 DOI: 10.1152/Japplphysiol.00871.2011  0.082
2021 Rauch A, Mandrup S. Transcriptional networks controlling stromal cell differentiation. Nature Reviews. Molecular Cell Biology. PMID 33837369 DOI: 10.1038/s41580-021-00357-7  0.082
2014 Hart L, Rauch A, Carr AM, Vermeesch JR, O'Driscoll M. LETM1 haploinsufficiency causes mitochondrial defects in cells from humans with Wolf-Hirschhorn syndrome: implications for dissecting the underlying pathomechanisms in this condition. Disease Models & Mechanisms. 7: 535-45. PMID 24626991 DOI: 10.1242/dmm.014464  0.082
2013 Aouri M, Moradpour D, Cavassini M, Mercier T, Buclin T, Csajka C, Telenti A, Rauch A, Decosterd LA. Multiplex liquid chromatography-tandem mass spectrometry assay for simultaneous therapeutic drug monitoring of ribavirin, boceprevir, and telaprevir. Antimicrobial Agents and Chemotherapy. 57: 3147-58. PMID 23629707 DOI: 10.1128/AAC.00281-13  0.081
2010 Rauch AV, Reker M, Ohrmann P, Pedersen A, Bauer J, Dannlowski U, Harding L, Koelkebeck K, Konrad C, Kugel H, Arolt V, Heindel W, Suslow T. Increased amygdala activation during automatic processing of facial emotion in schizophrenia. Psychiatry Research. 182: 200-6. PMID 20488680 DOI: 10.1016/J.Pscychresns.2010.03.005  0.081
2015 Yigit G, Brown KE, Kayserili H, Pohl E, Caliebe A, Zahnleiter D, Rosser E, Bögershausen N, Uyguner ZO, Altunoglu U, Nürnberg G, Nürnberg P, Rauch A, Li Y, Thiel CT, et al. Mutations in CDK5RAP2 cause Seckel syndrome. Molecular Genetics & Genomic Medicine. 3: 467-80. PMID 26436113 DOI: 10.1002/mgg3.158  0.08
2015 Weidemann A, Lovas A, Rauch A, Andreas N, von Maltzahn J, Riemann M, Weih F. Classical and alternative NF-κB signaling cooperate in regulating adipocyte differentiation and function. International Journal of Obesity (2005). PMID 26403432 DOI: 10.1038/ijo.2015.198  0.08
2002 La Camera G, Rauch A, Senn W, Lüscher HR, Fusi S. Firing rate adaptation without losing sensitivity to input fluctuations Lecture Notes in Computer Science (Including Subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics). 2415: 180-185.  0.08
2012 Putoux A, Nampoothiri S, Laurent N, Cormier-Daire V, Beales PL, Schinzel A, Bartholdi D, Alby C, Thomas S, Elkhartoufi N, Ichkou A, Litzler J, Munnich A, Encha-Razavi F, Kannan R, ... ... Rauch A, et al. Novel KIF7 mutations extend the phenotypic spectrum of acrocallosal syndrome. Journal of Medical Genetics. 49: 713-20. PMID 23125460 DOI: 10.1136/Jmedgenet-2012-101016  0.079
2004 Teber OA, Gillessen-Kaesbach G, Fischer S, Böhringer S, Albrecht B, Albert A, Arslan-Kirchner M, Haan E, Hagedorn-Greiwe M, Hammans C, Henn W, Hinkel GK, König R, Kunstmann E, Kunze J, ... ... Rauch A, et al. Genotyping in 46 patients with tentative diagnosis of Treacher Collins syndrome revealed unexpected phenotypic variation. European Journal of Human Genetics : Ejhg. 12: 879-90. PMID 15340364 DOI: 10.1038/sj.ejhg.5201260  0.079
2010 Scheuringer M, Kirchberger I, Boldt C, Eriks-Hoogland I, Rauch A, Velstra IM, Cieza A. Identification of problems in individuals with spinal cord injury from the health professional perspective using the ICF: a worldwide expert survey. Spinal Cord. 48: 529-36. PMID 20065988 DOI: 10.1038/sc.2009.176  0.079
2007 Zenker M, Horn D, Wieczorek D, Allanson J, Pauli S, van der Burgt I, Doerr HG, Gaspar H, Hofbeck M, Gillessen-Kaesbach G, Koch A, Meinecke P, Mundlos S, Nowka A, Rauch A, et al. SOS1 is the second most common Noonan gene but plays no major role in cardio-facio-cutaneous syndrome. Journal of Medical Genetics. 44: 651-6. PMID 17586837 DOI: 10.1136/Jmg.2007.051276  0.079
2013 Zahnleiter D, Uebe S, Ekici AB, Hoyer J, Wiesener A, Wieczorek D, Kunstmann E, Reis A, Doerr HG, Rauch A, Thiel CT. Rare copy number variants are a common cause of short stature. Plos Genetics. 9: e1003365. PMID 23516380 DOI: 10.1371/journal.pgen.1003365  0.079
2008 Bähring S, Kann M, Neuenfeld Y, Gong M, Chitayat D, Toka HR, Toka O, Plessis G, Maass P, Rauch A, Aydin A, Luft FC. Inversion region for hypertension and brachydactyly on chromosome 12p features multiple splicing and noncoding RNA. Hypertension. 51: 426-31. PMID 18086950 DOI: 10.1161/Hypertensionaha.107.101774  0.078
2014 Vulto-van Silfhout AT, Rajamanickam S, Jensik PJ, Vergult S, de Rocker N, Newhall KJ, Raghavan R, Reardon SN, Jarrett K, McIntyre T, Bulinski J, Ownby SL, Huggenvik JI, McKnight GS, Rose GM, ... ... Rauch A, et al. Mutations affecting the SAND domain of DEAF1 cause intellectual disability with severe speech impairment and behavioral problems. American Journal of Human Genetics. 94: 649-61. PMID 24726472 DOI: 10.1016/J.Ajhg.2014.03.013  0.077
2009 Kleefstra T, van Zelst-Stams WA, Nillesen WM, Cormier-Daire V, Houge G, Foulds N, van Dooren M, Willemsen MH, Pfundt R, Turner A, Wilson M, McGaughran J, Rauch A, Zenker M, Adam MP, et al. Further clinical and molecular delineation of the 9q subtelomeric deletion syndrome supports a major contribution of EHMT1 haploinsufficiency to the core phenotype. Journal of Medical Genetics. 46: 598-606. PMID 19264732 DOI: 10.1136/Jmg.2008.062950  0.077
2014 Rauch A, Hennig D, Schäfer C, Wirth M, Marx C, Heinzel T, Schneider G, Krämer OH. Survivin and YM155: how faithful is the liaison? Biochimica Et Biophysica Acta. 1845: 202-20. PMID 24440709 DOI: 10.1016/j.bbcan.2014.01.003  0.077
2009 Rauch A, Cieza A, Boonen A, Ewert T, Stucki G. Identification of similarities and differences in functioning in persons with rheumatoid arthritis and ankylosing spondylitis using the International Classification of Functioning, Disability and Health (ICF). Clinical and Experimental Rheumatology. 27: S92-101. PMID 19822053  0.076
2012 Pillai SK, Abdel-Mohsen M, Guatelli J, Skasko M, Monto A, Fujimoto K, Yukl S, Greene WC, Kovari H, Rauch A, Fellay J, Battegay M, Hirschel B, Witteck A, Bernasconi E, et al. Role of retroviral restriction factors in the interferon-α-mediated suppression of HIV-1 in vivo. Proceedings of the National Academy of Sciences of the United States of America. 109: 3035-40. PMID 22315404 DOI: 10.1073/Pnas.1111573109  0.075
2012 Pfeffer M, Rauch A, Korf HW, von Gall C. The endogenous melatonin (MT) signal facilitates reentrainment of the circadian system to light-induced phase advances by acting upon MT2 receptors. Chronobiology International. 29: 415-29. PMID 22489607 DOI: 10.3109/07420528.2012.667859  0.075
2023 Hansen MS, Søe K, Christensen LL, Fernandez-Guerra P, Hansen NW, Wyatt RA, Martin C, Hardy RS, Andersen TL, Olesen JB, Hartmann B, Rosenkilde MM, Kassem M, Rauch A, Gorvin CM, et al. GIP reduces osteoclast activity and improves osteoblast survival in primary human bone cells. European Journal of Endocrinology. 188. PMID 36747334 DOI: 10.1093/ejendo/lvac004  0.075
2005 Zweier C, Thiel CT, Dufke A, Crow YJ, Meinecke P, Suri M, Ala-Mello S, Beemer F, Bernasconi S, Bianchi P, Bier A, Devriendt K, Dimitrov B, Firth H, Gallagher RC, ... ... Rauch A, et al. Clinical and mutational spectrum of Mowat-Wilson syndrome. European Journal of Medical Genetics. 48: 97-111. PMID 16053902 DOI: 10.1016/j.ejmg.2005.01.003  0.075
2011 Hoischen A, van Bon BW, Rodríguez-Santiago B, Gilissen C, Vissers LE, de Vries P, Janssen I, van Lier B, Hastings R, Smithson SF, Newbury-Ecob R, Kjaergaard S, Goodship J, McGowan R, Bartholdi D, ... Rauch A, et al. De novo nonsense mutations in ASXL1 cause Bohring-Opitz syndrome. Nature Genetics. 43: 729-31. PMID 21706002 DOI: 10.1038/Ng.868  0.075
2012 Rauch A, Zhao X, Li H. Cross-country differences in entrepreneurial activity: The role of cultural practice and national wealth Frontiers of Business Research in China. 6: 447-474. DOI: 10.3868/s070-001-012-0021-0  0.074
2010 Alizon S, von Wyl V, Stadler T, Kouyos RD, Yerly S, Hirschel B, Böni J, Shah C, Klimkait T, Furrer H, Rauch A, Vernazza PL, Bernasconi E, Battegay M, Bürgisser P, et al. Phylogenetic approach reveals that virus genotype largely determines HIV set-point viral load. Plos Pathogens. 6: e1001123. PMID 20941398 DOI: 10.1371/Journal.Ppat.1001123  0.074
2014 Regoes RR, McLaren PJ, Battegay M, Bernasconi E, Calmy A, Günthard HF, Hoffmann M, Rauch A, Telenti A, Fellay J. Disentangling human tolerance and resistance against HIV. Plos Biology. 12: e1001951. PMID 25226169 DOI: 10.1371/journal.pbio.1001951  0.074
2008 Koolen DA, Sharp AJ, Hurst JA, Firth HV, Knight SJ, Goldenberg A, Saugier-Veber P, Pfundt R, Vissers LE, Destrée A, Grisart B, Rooms L, Van der Aa N, Field M, Hackett A, ... ... Rauch A, et al. Clinical and molecular delineation of the 17q21.31 microdeletion syndrome. Journal of Medical Genetics. 45: 710-20. PMID 18628315 DOI: 10.1136/Jmg.2008.058701  0.073
2024 Nielsen SSR, Pedersen JAZ, Sharma N, Wasehuus PK, Hansen MS, Møller AMJ, Borggaard XG, Rauch A, Frost M, Sondergaard TE, Søe K. Human osteoclasts in vitro are dose dependently both inhibited and stimulated by cannabidiol (CBD) and Δ9-tetrahydrocannabinol (THC). Bone. 181: 117035. PMID 38342278 DOI: 10.1016/j.bone.2024.117035  0.073
2015 Rauch AK, Rosskothen-Kuhl N, Illing RB. Counter-regulation of the AP-1 monomers pATF2 and Fos: Molecular readjustment of brainstem neurons in hearing and deaf adult rats after electrical intracochlear stimulation. Neuroscience. PMID 26601778 DOI: 10.1016/j.neuroscience.2015.11.025  0.073
2012 Mühlethaler K, Bögli-Stuber K, Wasmer S, von Garnier C, Dumont P, Rauch A, Mühlemann K, Garzoni C. Quantitative PCR to diagnose Pneumocystis pneumonia in immunocompromised non-HIV patients. The European Respiratory Journal. 39: 971-8. PMID 21920890 DOI: 10.1183/09031936.00095811  0.073
2006 Gaudieri S, Rauch A, Park LP, Freitas E, Herrmann S, Jeffrey G, Cheng W, Pfafferott K, Naidoo K, Chapman R, Battegay M, Weber R, Telenti A, Furrer H, James I, et al. Evidence of viral adaptation to HLA class I-restricted immune pressure in chronic hepatitis C virus infection. Journal of Virology. 80: 11094-104. PMID 17071929 DOI: 10.1128/JVI.00912-06  0.072
2019 Tencerova M, Frost M, Figeac F, Nielsen TK, Ali D, Lauterlein JL, Andersen TL, Haakonsson AK, Rauch A, Madsen JS, Ejersted C, Højlund K, Kassem M. Obesity-Associated Hypermetabolism and Accelerated Senescence of Bone Marrow Stromal Stem Cells Suggest a Potential Mechanism for Bone Fragility. Cell Reports. 27: 2050-2062.e6. PMID 31091445 DOI: 10.1016/j.celrep.2019.04.066  0.072
2013 Bartha I, Carlson JM, Brumme CJ, McLaren PJ, Brumme ZL, John M, Haas DW, Martinez-Picado J, Dalmau J, López-Galíndez C, Casado C, Rauch A, Günthard HF, Bernasconi E, Vernazza P, et al. A genome-to-genome analysis of associations between human genetic variation, HIV-1 sequence diversity, and viral control. Elife. 2: e01123. PMID 24171102 DOI: 10.7554/Elife.01123  0.072
2011 Sanders JM, Rauch A, Mendelsberg RJ, Anders A. A synchronized emissive probe for time-resolved plasma potential measurements of pulsed discharges. The Review of Scientific Instruments. 82: 093505. PMID 21974585 DOI: 10.1063/1.3640408  0.071
2008 Zweier C, Sticht H, Bijlsma EK, Clayton-Smith J, Boonen SE, Fryer A, Greally MT, Hoffmann L, den Hollander NS, Jongmans M, Kant SG, King MD, Lynch SA, McKee S, Midro AT, ... ... Rauch A, et al. Further delineation of Pitt-Hopkins syndrome: phenotypic and genotypic description of 16 novel patients. Journal of Medical Genetics. 45: 738-44. PMID 18728071 DOI: 10.1136/jmg.2008.060129  0.071
2007 Chitayat D, Sroka H, Keating S, Colby RS, Ryan G, Toi A, Blaser S, Viero S, Devisme L, Boute-Bénéjean O, Manouvrier-Hanu S, Mortier G, Loeys B, Rauch A, Bitoun P. The PDAC syndrome (pulmonary hypoplasia/agenesis, diaphragmatic hernia/eventration, anophthalmia/microphthalmia, and cardiac defect) (Spear syndrome, Matthew-Wood syndrome): report of eight cases including a living child and further evidence for autosomal recessive inheritance. American Journal of Medical Genetics. Part A. 143: 1268-81. PMID 17506106 DOI: 10.1002/Ajmg.A.31788  0.071
2014 Abdel-Mohsen M, Deng X, Liegler T, Guatelli JC, Salama MS, Ghanem Hel-D, Rauch A, Ledergerber B, Deeks SG, Günthard HF, Wong JK, Pillai SK. Effects of alpha interferon treatment on intrinsic anti-HIV-1 immunity in vivo. Journal of Virology. 88: 763-7. PMID 24155399 DOI: 10.1128/Jvi.02687-13  0.071
2010 Rauch A, Nazarova E, Vogel J. Analysis of microtubules in budding yeast. Methods in Cell Biology. 97: 277-306. PMID 20719277 DOI: 10.1016/S0091-679X(10)97016-7  0.071
2005 Thiel CT, Horn D, Zabel B, Ekici AB, Salinas K, Gebhart E, Rüschendorf F, Sticht H, Spranger J, Müller D, Zweier C, Schmitt ME, Reis A, Rauch A. Severely incapacitating mutations in patients with extreme short stature identify RNA-processing endoribonuclease RMRP as an essential cell growth regulator. American Journal of Human Genetics. 77: 795-806. PMID 16252239 DOI: 10.1086/497708  0.07
2004 Zenker M, Rauch A, Winterpacht A, Tagariello A, Kraus C, Rupprecht T, Sticht H, Reis A. A dual phenotype of periventricular nodular heterotopia and frontometaphyseal dysplasia in one patient caused by a single FLNA mutation leading to two functionally different aberrant transcripts. American Journal of Human Genetics. 74: 731-7. PMID 14988809 DOI: 10.1086/383094  0.07
2002 La Camera G, Fusi S, Senn W, Rauch A, Lüscher HR. When NMDA receptor conductances increase inter-spike interval variability Lecture Notes in Computer Science (Including Subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics). 2415: 235-240.  0.07
2012 Rauch A, Wieczorek D, Graf E, Wieland T, Endele S, Schwarzmayr T, Albrecht B, Bartholdi D, Beygo J, Di Donato N, Dufke A, Cremer K, Hempel M, Horn D, Hoyer J, et al. Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study. Lancet (London, England). 380: 1674-82. PMID 23020937 DOI: 10.1016/S0140-6736(12)61480-9  0.07
2006 Martin A, Nolan D, Almeida CA, Rauch A, Mallal S. Predicting and diagnosing abacavir and nevirapine drug hypersensitivity: from bedside to bench and back again. Pharmacogenomics. 7: 15-23. PMID 16354121 DOI: 10.2217/14622416.7.1.15  0.07
2012 Jaureguiberry G, De la Dure-Molla M, Parry D, Quentric M, Himmerkus N, Koike T, Poulter J, Klootwijk E, Robinette SL, Howie AJ, Patel V, Figueres ML, Stanescu HC, Issler N, Nicholson JK, ... ... Rauch A, et al. Nephrocalcinosis (enamel renal syndrome) caused by autosomal recessive FAM20A mutations. Nephron. Physiology. 122: 1-6. PMID 23434854 DOI: 10.1159/000349989  0.069
2013 Rauch A. Clinical research in osteopathy - Part 2: Neuronal and organic disorders | Klinische Forschung in der Osteopathie - Teil 2: neuronale und organische Störungen Osteopathische Medizin. 14: 19-25. DOI: 10.1016/S1615-9071(13)60060-X  0.069
2013 Wieczorek D, Bögershausen N, Beleggia F, Steiner-Haldenstätt S, Pohl E, Li Y, Milz E, Martin M, Thiele H, Altmüller J, Alanay Y, Kayserili H, Klein-Hitpass L, Böhringer S, Wollstein A, ... ... Rauch A, et al. A comprehensive molecular study on Coffin-Siris and Nicolaides-Baraitser syndromes identifies a broad molecular and clinical spectrum converging on altered chromatin remodeling. Human Molecular Genetics. 22: 5121-35. PMID 23906836 DOI: 10.1093/Hmg/Ddt366  0.068
2010 Allanson JE, Bohring A, Dörr HG, Dufke A, Gillessen-Kaesbach G, Horn D, König R, Kratz CP, Kutsche K, Pauli S, Raskin S, Rauch A, Turner A, Wieczorek D, Zenker M. The face of Noonan syndrome: Does phenotype predict genotype. American Journal of Medical Genetics. Part A. 152: 1960-6. PMID 20602484 DOI: 10.1002/ajmg.a.33518  0.068
2011 Hofmann K, Becker J, Heller R, Boute O, Andrieux J, Hoyer J, Ekici AB, Reis A, Rauch A. 7 Mb de novo deletion within 8q21 in a patient with distal arthrogryposis type 2B (DA2B). European Journal of Medical Genetics. 54: e495-500. PMID 21722758 DOI: 10.1016/j.ejmg.2011.06.002  0.068
2011 Valero A, Braschler T, Rauch A, Demierre N, Barral Y, Renaud P. Tracking and synchronization of the yeast cell cycle using dielectrophoretic opacity. Lab On a Chip. 11: 1754-60. PMID 21445448 DOI: 10.1039/C1Lc00007A  0.067
2010 Rauch R, Hofbeck M, Zweier C, Koch A, Zink S, Trautmann U, Hoyer J, Kaulitz R, Singer H, Rauch A. Comprehensive genotype-phenotype analysis in 230 patients with tetralogy of Fallot. Journal of Medical Genetics. 47: 321-31. PMID 19948535 DOI: 10.1136/jmg.2009.070391  0.067
2014 Hasse B, Iff M, Ledergerber B, Calmy A, Schmid P, Hauser C, Cavassini M, Bernasconi E, Marzolini C, Tarr PE, Aubert V, Barth J, Battegay M, Bernasconi E, ... ... Rauch A, et al. Obesity Trends and Body Mass Index Changes After Starting Antiretroviral Treatment: The Swiss HIV Cohort Study. Open Forum Infectious Diseases. 1: ofu040. PMID 25734114 DOI: 10.1093/ofid/ofu040  0.066
2007 Zweier C, Sticht H, Aydin-Yaylagül I, Campbell CE, Rauch A. Human TBX1 missense mutations cause gain of function resulting in the same phenotype as 22q11.2 deletions. American Journal of Human Genetics. 80: 510-7. PMID 17273972 DOI: 10.1086/511993  0.066
2011 Kouyos RD, von Wyl V, Yerly S, Böni J, Rieder P, Joos B, Taffé P, Shah C, Bürgisser P, Klimkait T, Weber R, Hirschel B, Cavassini M, Rauch A, Battegay M, et al. Ambiguous nucleotide calls from population-based sequencing of HIV-1 are a marker for viral diversity and the age of infection. Clinical Infectious Diseases : An Official Publication of the Infectious Diseases Society of America. 52: 532-9. PMID 21220770 DOI: 10.1093/Cid/Ciq164  0.066
2011 Nguyen A, Calmy A, Delhumeau C, Mercier IK, Cavassini M, Fayet-Mello A, Elzi L, Genné D, Rauch A, Bernasconi E, Hirschel B. A randomized crossover study to compare efavirenz and etravirine treatment. Aids (London, England). 25: 57-63. PMID 21076278 DOI: 10.1097/Qad.0B013E32833F9F63  0.065
2014 Dalmau J, Rotger M, Erkizia I, Rauch A, Reche P, Pino M, Esteve A, Palou E, Brander C, Paredes R, Phung P, Clotet B, Telenti A, Martinez-Picado J, Prado JG, et al. Highly pathogenic adapted HIV-1 strains limit host immunity and dictate rapid disease progression. Aids (London, England). 28: 1261-72. PMID 24732774 DOI: 10.1097/QAD.0000000000000293  0.065
2011 Rauch A, Gossye V, Bracke D, Gevaert E, Jacques P, Van Beneden K, Vandooren B, Rauner M, Hofbauer LC, Haegeman G, Elewaut D, Tuckermann JP, De Bosscher K. An anti-inflammatory selective glucocorticoid receptor modulator preserves osteoblast differentiation. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 25: 1323-32. PMID 21233489 DOI: 10.1096/Fj.10-173393  0.065
2010 Rauch A, Escorpizo R, Riddle DL, Eriks-Hoogland I, Stucki G, Cieza A. Using a case report of a patient with spinal cord injury to illustrate the application of the International Classification of Functioning, Disability and Health during multidisciplinary patient management. Physical Therapy. 90: 1039-52. PMID 20508027 DOI: 10.2522/ptj.20090327  0.065
2011 Busche A, Graul-Neumann LM, Zweier C, Rauch A, Klopocki E, Horn D. Microdeletions of chromosome 7p21, including TWIST1, associated with significant microcephaly, facial dysmorphism, and short stature. European Journal of Medical Genetics. 54: 256-61. PMID 21333765 DOI: 10.1016/j.ejmg.2011.02.002  0.064
2008 Schlicker C, Rauch A, Hess KC, Kachholz B, Levin LR, Buck J, Steegborn C. Structure-based development of novel adenylyl cyclase inhibitors. Journal of Medicinal Chemistry. 51: 4456-64. PMID 18630896 DOI: 10.1021/Jm800481Q  0.063
2014 Grotegerd D, Stuhrmann A, Kugel H, Schmidt S, Redlich R, Zwanzger P, Rauch AV, Heindel W, Zwitserlood P, Arolt V, Suslow T, Dannlowski U. Amygdala excitability to subliminally presented emotional faces distinguishes unipolar and bipolar depression: an fMRI and pattern classification study. Human Brain Mapping. 35: 2995-3007. PMID 24038516 DOI: 10.1002/Hbm.22380  0.063
2014 Abdel-Mohsen M, Deng X, Danesh A, Liegler T, Jacobs ES, Rauch A, Ledergerber B, Norris PJ, Günthard HF, Wong JK, Pillai SK. Role of microRNA modulation in the interferon-α/ribavirin suppression of HIV-1 in vivo. Plos One. 9: e109220. PMID 25275557 DOI: 10.1371/Journal.Pone.0109220  0.063
2015 Giarrana ML, Joset P, Sticht H, Robb S, Steindl K, Rauch A, Klein A. A severe congenital myasthenic syndrome with "dropped head" caused by novel MUSK mutations. Muscle & Nerve. PMID 25900532 DOI: 10.1002/mus.24687  0.061
2009 Gaudieri S, Rauch A, Pfafferott K, Barnes E, Cheng W, McCaughan G, Shackel N, Jeffrey GP, Mollison L, Baker R, Furrer H, Günthard HF, Freitas E, Humphreys I, Klenerman P, et al. Hepatitis C virus drug resistance and immune-driven adaptations: relevance to new antiviral therapy. Hepatology (Baltimore, Md.). 49: 1069-82. PMID 19263475 DOI: 10.1002/hep.22773  0.061
2005 Hüffmeier U, Hausser I, Reis A, Rauch A. Novel autosomal recessive progressive hyperpigmentation syndrome. American Journal of Medical Genetics. Part A. 135: 195-9. PMID 15852476 DOI: 10.1002/ajmg.a.30668  0.061
2014 Oneda B, Baldinger R, Reissmann R, Reshetnikova I, Krejci P, Masood R, Ochsenbein-Kölble N, Bartholdi D, Steindl K, Morotti D, Faranda M, Baumer A, Asadollahi R, Joset P, Niedrist D, ... ... Rauch A, et al. High-resolution chromosomal microarrays in prenatal diagnosis significantly increase diagnostic power. Prenatal Diagnosis. 34: 525-33. PMID 24919595 DOI: 10.1002/pd.4342  0.061
2015 Rauch A, Rosenbusch N, Unger J, Frese M. The effectiveness of cohesive and diversified networks: A meta-analysis Journal of Business Research. DOI: 10.1016/j.jbusres.2015.05.011  0.06
2014 Rohrbach J, Stickel F, Schmid P, Thormann W, Kovari H, Scherrer A, Günthard HF, Vuichard D, Cavassini M, Ambrosioni J, Bernasconi E, Furrer H, Rauch A. Changes in biomarkers of liver disease during successful combination antiretroviral therapy in HIV-HCV-coinfected individuals. Antiviral Therapy. 19: 149-59. PMID 24036684 DOI: 10.3851/IMP2686  0.06
2004 Zenker M, Buheitel G, Rauch R, Koenig R, Bosse K, Kress W, Tietze HU, Doerr HG, Hofbeck M, Singer H, Reis A, Rauch A. Genotype-phenotype correlations in Noonan syndrome. The Journal of Pediatrics. 144: 368-74. PMID 15001945 DOI: 10.1016/j.jpeds.2003.11.032  0.06
2013 Cosgrove C, Ussher JE, Rauch A, Gärtner K, Kurioka A, Hühn MH, Adelmann K, Kang YH, Fergusson JR, Simmonds P, Goulder P, Hansen TH, Fox J, Günthard HF, Khanna N, et al. Early and nonreversible decrease of CD161++ /MAIT cells in HIV infection. Blood. 121: 951-61. PMID 23255555 DOI: 10.1182/Blood-2012-06-436436  0.06
2006 Tagariello A, Heller R, Greven A, Kalscheuer VM, Molter T, Rauch A, Kress W, Winterpacht A. Balanced translocation in a patient with craniosynostosis disrupts the SOX6 gene and an evolutionarily conserved non-transcribed region. Journal of Medical Genetics. 43: 534-40. PMID 16258006 DOI: 10.1136/jmg.2005.037820  0.06
2012 March S, Rauch A, Thomas D, Bender S, Swart E. [Procedures according to data protection laws for coupling primary and secondary data in a cohort study: the lidA study]. Gesundheitswesen (Bundesverband Der ã„Rzte Des ã–Ffentlichen Gesundheitsdienstes (Germany)). 74: e122-9. PMID 22297825 DOI: 10.1055/s-0031-1301276  0.06
2013 Bartholdi D, Asadollahi R, Oneda B, Schmitt-Mechelke T, Tonella P, Baumer A, Rauch A. Further delineation of genotype-phenotype correlation in homozygous 2p21 deletion syndromes: first description of patients without cystinuria. American Journal of Medical Genetics. Part A. 161: 1853-9. PMID 23794250 DOI: 10.1002/ajmg.a.35994  0.06
2010 Ferry T, Hirschel B, Dang T, Meylan P, Delhumeau C, Rauch A, Weber R, Elzi L, Bernasconi E, Schmid P, Calmy A. Infrequent replication of parvovirus B19 and erythrovirus genotypes 2 and 3 among HIV-infected patients with chronic anemia. Clinical Infectious Diseases : An Official Publication of the Infectious Diseases Society of America. 50: 115-8. PMID 19951110 DOI: 10.1086/649004  0.06
2011 Wandeler G, Furrer H, Rauch A. Sustained virological response to a raltegravir-containing salvage therapy in an HIV-2-infected patient. Aids (London, England). 25: 2306-8. PMID 22067200 DOI: 10.1097/QAD.0b013e32834cdb89  0.06
2021 Huang LO, Rauch A, Mazzaferro E, Preuss M, Carobbio S, Bayrak CS, Chami N, Wang Z, Schick UM, Yang N, Itan Y, Vidal-Puig A, den Hoed M, Mandrup S, Kilpeläinen TO, et al. Genome-wide discovery of genetic loci that uncouple excess adiposity from its comorbidities. Nature Metabolism. 3: 228-243. PMID 33619380 DOI: 10.1038/s42255-021-00346-2  0.06
2023 Caratti G, Stifel U, Caratti B, Jamil AJM, Chung KJ, Kiehntopf M, Gräler MH, Blüher M, Rauch A, Tuckermann JP. Glucocorticoid activation of anti-inflammatory macrophages protects against insulin resistance. Nature Communications. 14: 2271. PMID 37080971 DOI: 10.1038/s41467-023-37831-z  0.059
2010 Rauch A, Seitz S, Baschant U, Schilling AF, Illing A, Stride B, Kirilov M, Mandic V, Takacz A, Schmidt-Ullrich R, Ostermay S, Schinke T, Spanbroek R, Zaiss MM, Angel PE, et al. Glucocorticoids suppress bone formation by attenuating osteoblast differentiation via the monomeric glucocorticoid receptor. Cell Metabolism. 11: 517-31. PMID 20519123 DOI: 10.1016/J.Cmet.2010.05.005  0.059
2015 Kovari H, Russmann S, Ledergerber B, Müller D, Rotger M, Velli P, Cavassini M, Ambrosioni J, Bregenzer A, Stöckle M, Bernasconi E, Rauch A, Speck RF. Ribavirin Concentrations Do Not Predict Sustained Virological Response in HIV/HCV-Coinfected Patients Treated with Ribavirin and Pegylated Interferon in the Swiss HIV Cohort Study. Plos One. 10: e0133879. PMID 26218843 DOI: 10.1371/journal.pone.0133879  0.059
2003 Heller R, Rauch A, Lüttgen S, Schröder B, Winterpacht A. Partial deletion of the critical 1.5 Mb interval in Williams-Beuren syndrome. Journal of Medical Genetics. 40: e99. PMID 12920091  0.058
2019 Søndergaard E, Rauch A, Michaut M, Rapin N, Rehn M, Wilhelmson AS, Camponeschi A, Hasemann MS, Bagger FO, Jendholm J, Knudsen KJ, Mandrup S, Mårtensson IL, Porse BT. ERG Controls B Cell Development by Promoting Igh V-to-DJ Recombination. Cell Reports. 29: 2756-2769.e6. PMID 31775043 DOI: 10.1016/j.celrep.2019.10.098  0.058
2014 Arab-Alameddine M, Lubomirov R, Fayet-Mello A, Aouri M, Rotger M, Buclin T, Widmer N, Gatri M, Ledergerber B, Rentsch K, Cavassini M, Panchaud A, Guidi M, Telenti A, Décosterd LA, ... ... Rauch A, et al. Population pharmacokinetic modelling and evaluation of different dosage regimens for darunavir and ritonavir in HIV-infected individuals Journal of Antimicrobial Chemotherapy. 69: 2489-2498. PMID 24821595 DOI: 10.1093/jac/dku131  0.058
2012 Soemedi R, Wilson IJ, Bentham J, Darlay R, Töpf A, Zelenika D, Cosgrove C, Setchfield K, Thornborough C, Granados-Riveron J, Blue GM, Breckpot J, Hellens S, Zwolinkski S, Glen E, ... ... Rauch A, et al. Contribution of global rare copy-number variants to the risk of sporadic congenital heart disease. American Journal of Human Genetics. 91: 489-501. PMID 22939634 DOI: 10.1016/J.Ajhg.2012.08.003  0.058
2015 Van Gorkom KJ, Wardle JFC, Rauch AP, Gobeille DB. Comparing different indicators of quasar orientation Monthly Notices of the Royal Astronomical Society. 450: 4240-4247. DOI: 10.1093/Mnras/Stv912  0.058
2014 Avila D, Keiser O, Egger M, Kouyos R, Böni J, Yerly S, Klimkait T, Vernazza PL, Aubert V, Rauch A, Bonhoeffer S, Günthard HF, Stadler T, Spycher BD. Social meets molecular: Combining phylogenetic and latent class analyses to understand HIV-1 transmission in Switzerland. American Journal of Epidemiology. 179: 1514-25. PMID 24821749 DOI: 10.1093/Aje/Kwu076  0.058
2013 Pajarola S, Bachmann R, Niedrist D, Rauch A. [Basic aspects of medical genetics]. Praxis. 102: 1457-65. PMID 24280602 DOI: 10.1024/1661-8157/a001487  0.057
2013 Zweier C, Kraus C, Brueton L, Cole T, Degenhardt F, Engels H, Gillessen-Kaesbach G, Graul-Neumann L, Horn D, Hoyer J, Just W, Rauch A, Reis A, Wollnik B, Zeschnigk M, et al. A new face of Borjeson-Forssman-Lehmann syndrome? De novo mutations in PHF6 in seven females with a distinct phenotype. Journal of Medical Genetics. 50: 838-47. PMID 24092917 DOI: 10.1136/jmedgenet-2013-101918  0.057
2011 Schüpbach J, Bisset LR, Regenass S, Bürgisser P, Gorgievski M, Steffen I, Andreutti C, Martinetti G, Shah C, Yerly S, Klimkait T, Gebhardt M, Schöni-Affolter F, Rickenbach M, ... ... Rauch A, et al. High specificity of line-immunoassay based algorithms for recent HIV-1 infection independent of viral subtype and stage of disease. Bmc Infectious Diseases. 11: 254. PMID 21943091 DOI: 10.1186/1471-2334-11-254  0.057
2007 Crisponi L, Crisponi G, Meloni A, Toliat MR, Nurnberg G, Usala G, Uda M, Masala M, Hohne W, Becker C, Marongiu M, Chiappe F, Kleta R, Rauch A, Wollnik B, et al. Crisponi syndrome is caused by mutations in the CRLF1 gene and is allelic to cold-induced sweating syndrome type 1. American Journal of Human Genetics. 80: 971-81. PMID 17436252 DOI: 10.1086/516843  0.057
2004 Hennies HC, Rauch A, Seifert W, Schumi C, Moser E, Al-Taji E, Tariverdian G, Chrzanowska KH, Krajewska-Walasek M, Rajab A, Giugliani R, Neumann TE, Eckl KM, Karbasiyan M, Reis A, et al. Allelic heterogeneity in the COH1 gene explains clinical variability in Cohen syndrome. American Journal of Human Genetics. 75: 138-45. PMID 15154116 DOI: 10.1086/422219  0.057
2011 Gianella S, von Wyl V, Fischer M, Niederoest B, Battegay M, Bernasconi E, Cavassini M, Rauch A, Hirschel B, Vernazza P, Weber R, Joos B, Günthard HF. Effect of early antiretroviral therapy during primary HIV-1 infection on cell-associated HIV-1 DNA and plasma HIV-1 RNA. Antiviral Therapy. 16: 535-45. PMID 21685541 DOI: 10.3851/IMP1776  0.056
2014 Rauch A, Legendre P, Christophe OD, Goudemand J, van Belle E, Vincentelli A, Denis CV, Susen S, Lenting PJ. Antibody-based prevention of von Willebrand factor degradation mediated by circulatory assist devices. Thrombosis and Haemostasis. 112: 1014-23. PMID 25030452 DOI: 10.1160/TH14-02-0148  0.056
2010 Rauch AC, Schöttle PB, Beitzel K, Imhoff AB. [Double-bundle technique--anatomic reconstruction of the posterior cruciate ligament]. Operative Orthopã¤Die Und Traumatologie. 22: 387-401. PMID 20931318 DOI: 10.1007/s00064-010-9037-2  0.056
2013 Rauch AS, Fleischhacker WW. Long-acting injectable formulations of new-generation antipsychotics: a review from a clinical perspective. Cns Drugs. 27: 637-52. PMID 23780619 DOI: 10.1007/s40263-013-0083-9  0.056
2015 Braun DL, Rauch A, Aouri M, Durisch N, Eberhard N, Anagnostopoulos A, Ledergerber B, Müllhaupt B, Metzner KJ, Decosterd L, Böni J, Weber R, Fehr J. A Lead-In with Silibinin Prior to Triple-Therapy Translates into Favorable Treatment Outcomes in Difficult-To-Treat HIV/Hepatitis C Coinfected Patients. Plos One. 10: e0133028. PMID 26176696 DOI: 10.1371/journal.pone.0133028  0.055
2015 Kouyos RD, Hasse B, Calmy A, Cavassini M, Furrer H, Stöckle M, Vernazza PL, Bernasconi E, Weber R, Günthard HF, Aubert V, Battegay M, Bernasconi E, Böni J, ... ... Rauch A, et al. Increases in Condomless Sex in the Swiss HIV Cohort Study. Open Forum Infectious Diseases. 2: ofv077. PMID 26180827 DOI: 10.1093/ofid/ofv077  0.055
2015 Vinikoor MJ, Zürcher S, Musukuma K, Kachuwaire O, Rauch A, Chi BH, Gorgievski M, Zwahlen M, Wandeler G. Hepatitis B viral load in dried blood spots: A validation study in Zambia. Journal of Clinical Virology : the Official Publication of the Pan American Society For Clinical Virology. 72: 20-4. PMID 26356987 DOI: 10.1016/j.jcv.2015.08.019  0.055
2012 Smit C, Sterne JAC, Monforte ADA, Puotti M, De Wolf F, Peters L, Ledergerber B, De Wit S, Sambatakou H, Rauch A, Dabis F. Effect of hepatitis C treatment on CD4+ T-cell counts and the risk of death in HIV-HCV-coinfected patients: The COHERE collaboration Antiviral Therapy. 17: 1541-1550. PMID 22869294 DOI: 10.3851/Imp2263  0.055
2014 Thiele S, Baschant U, Rauch A, Rauner M. Instructions for producing a mouse model of glucocorticoid-induced osteoporosis. Bonekey Reports. 3: 552. PMID 25120909 DOI: 10.1038/bonekey.2014.47  0.055
2012 Fekete C, Rauch A. Correlates and determinants of physical activity in persons with spinal cord injury: A review using the International Classification of Functioning, Disability and Health as reference framework. Disability and Health Journal. 5: 140-50. PMID 22726854 DOI: 10.1016/j.dhjo.2012.04.003  0.054
2004 Wolff B, Cieza A, Parentin A, Rauch A, Sigl T, Brockow T, Stucki A. Identifying the concepts contained in outcome measures of clinical trials on four internal disorders using the International Classification of Functioning, Disability and Health as a reference. Journal of Rehabilitation Medicine. 37-42. PMID 15370746 DOI: 10.1080/16501960410015407  0.054
2016 Rauch A, Teixeira PA, Gillet R, Perez M, Clerc-Urmes I, Lombard C, Blum A. Analysis of the position of the branches of the ulnar nerve in Guyon's canal using high-resolution MRI in positions adopted by cyclists. Surgical and Radiologic Anatomy : Sra. PMID 26740001 DOI: 10.1007/s00276-015-1612-7  0.054
2015 Ussher JE, Phalora P, Cosgrove C, Hannaway RF, Rauch A, Günthard HF, Goulder P, Phillips RE, Willberg CB, Klenerman P. Molecular Analyses Define Vα7.2-Jα33+ MAIT Cell Depletion in HIV Infection: A Case-Control Study. Medicine. 94: e1134. PMID 26200614 DOI: 10.1097/MD.0000000000001134  0.054
2022 Figeac F, Tencerova M, Ali D, Andersen TL, Appadoo DRC, Kerckhofs G, Ditzel N, Kowal JM, Rauch A, Kassem M. Impaired Bone Fracture Healing in Type 2 Diabetes Is Caused by Defective Functions of Skeletal Progenitor Cells. Stem Cells (Dayton, Ohio). 40: 149-164. PMID 35257177 DOI: 10.1093/stmcls/sxab011  0.054
2013 Peters L, Mocroft A, Soriano V, Rockstroh J, Rauch A, Karlsson A, Knysz B, Pradier C, Zilmer K, Lundgren JD. Hyaluronic acid levels predict risk of hepatic encephalopathy and liver-related death in HIV/viral hepatitis coinfected patients. Plos One. 8: e64283. PMID 23724041 DOI: 10.1371/journal.pone.0064283  0.054
2010 Casado C, Colombo S, Rauch A, Martínez R, Günthard HF, Garcia S, Rodríguez C, Del Romero J, Telenti A, López-Galíndez C. Host and viral genetic correlates of clinical definitions of HIV-1 disease progression. Plos One. 5: e11079. PMID 20552027 DOI: 10.1371/journal.pone.0011079  0.053
2010 Zweier M, Gregor A, Zweier C, Engels H, Sticht H, Wohlleber E, Bijlsma EK, Holder SE, Zenker M, Rossier E, Grasshoff U, Johnson DS, Robertson L, Firth HV, ... ... Rauch A, et al. Mutations in MEF2C from the 5q14.3q15 microdeletion syndrome region are a frequent cause of severe mental retardation and diminish MECP2 and CDKL5 expression. Human Mutation. 31: 722-33. PMID 20513142 DOI: 10.1002/humu.21253  0.053
2006 Jung R, Rauch A, Salomons GS, Verhoeven NM, Jakobs C, Michael Gibson K, Lachmann E, Sass JO, Trautmann U, Zweier C, Staatz G, Knerr I. Clinical, cytogenetic and molecular characterization of a patient with combined succinic semialdehyde dehydrogenase deficiency and incomplete WAGR syndrome with obesity. Molecular Genetics and Metabolism. 88: 256-60. PMID 16545979 DOI: 10.1016/j.ymgme.2006.02.003  0.053
2011 Zollino M, Garavelli L, Rauch A. Clinical utility gene card for: Mowat-Wilson syndrome. European Journal of Human Genetics : Ejhg. 19. PMID 21343952 DOI: 10.1038/ejhg.2011.12  0.053
2015 Wandeler G, Schlauri M, Jaquier ME, Rohrbach J, Metzner KJ, Fehr J, Ambrosioni J, Cavassini M, Stöckle M, Schmid P, Bernasconi E, Keiser O, Salazar-Vizcaya L, Furrer H, Rauch A, ... ... Rauch A, et al. Incident Hepatitis C Virus Infections in the Swiss HIV Cohort Study: Changes in Treatment Uptake and Outcomes Between 1991 and 2013. Open Forum Infectious Diseases. 2: ofv026. PMID 26034775 DOI: 10.1093/ofid/ofv026  0.052
2010 Smigiel R, Szafranska A, Czyzewska M, Rauch A, Zweier Ch, Patkowski D. Severe clinical course of Hirschsprung disease in a Mowat-Wilson syndrome patient. Journal of Applied Genetics. 51: 111-3. PMID 20145308  0.052
2016 Vinikoor MJ, Zürcher S, Musukuma K, Kachuwaire O, Rauch A, Chi BH, Gorgievski M, Zwahlen M, Wandeler G. Corrigendum to "Hepatitis B viral load in dried blood spots: A validation study in Zambia" [J. Clin. Virol. 72 (2015) 20-24] Doi: 10.1016/j.jcv.2015.08.019 Journal of Clinical Virology. 74: 88. DOI: 10.1016/j.jcv.2015.10.019  0.052
2012 Stern M, Czaja K, Rauch A, Rickenbach M, Günthard HF, Battegay M, Fellay J, Hirschel B, Hess C. HLA-Bw4 identifies a population of HIV-infected patients with an increased capacity to control viral replication after structured treatment interruption. Hiv Medicine. 13: 589-95. PMID 22500819 DOI: 10.1111/j.1468-1293.2012.01019.x  0.052
2009 Harmsen MB, Azzarello-Burri S, García González MM, Gillessen-Kaesbach G, Meinecke P, Müller D, Rauch A, Rossier E, Seemanova E, Spaich C, Steiner B, Wieczorek D, Zenker M, Kutsche K. Goltz-Gorlin (focal dermal hypoplasia) and the microphthalmia with linear skin defects (MLS) syndrome: no evidence of genetic overlap. European Journal of Human Genetics : Ejhg. 17: 1207-15. PMID 19277062 DOI: 10.1038/ejhg.2009.40  0.052
2011 Wyl Vv, Gianella S, Fischer M, Niederoest B, Kuster H, Battegay M, Bernasconi E, Cavassini M, Rauch A, Hirschel B, Vernazza P, Weber R, Joos B, Günthard HF. Early antiretroviral therapy during primary HIV-1 infection results in a transient reduction of the viral setpoint upon treatment interruption. Plos One. 6: e27463. PMID 22102898 DOI: 10.1371/journal.pone.0027463  0.052
2009 Vandewalle J, Van Esch H, Govaerts K, Verbeeck J, Zweier C, Madrigal I, Mila M, Pijkels E, Fernandez I, Kohlhase J, Spaich C, Rauch A, Fryns JP, Marynen P, Froyen G. Dosage-dependent severity of the phenotype in patients with mental retardation due to a recurrent copy-number gain at Xq28 mediated by an unusual recombination. American Journal of Human Genetics. 85: 809-22. PMID 20004760 DOI: 10.1016/j.ajhg.2009.10.019  0.051
2011 Templin C, Ghadri JR, Rougier JS, Baumer A, Kaplan V, Albesa M, Sticht H, Rauch A, Puleo C, Hu D, Barajas-Martinez H, Antzelevitch C, Lüscher TF, Abriel H, Duru F. Identification of a novel loss-of-function calcium channel gene mutation in short QT syndrome (SQTS6). European Heart Journal. 32: 1077-88. PMID 21383000 DOI: 10.1093/Eurheartj/Ehr076  0.051
2011 Nguyen A, Calmy A, Delhumeau C, Mercier I, Cavassini M, Mello AF, Elzi L, Rauch A, Bernasconi E, Schmid P, Hirschel B. A randomized cross-over study to compare raltegravir and efavirenz (SWITCH-ER study). Aids (London, England). 25: 1481-7. PMID 21593661 DOI: 10.1097/Qad.0B013E328348Dab0  0.051
2015 Hasse B, Tarr PE, Marques-Vidal P, Waeber G, Preisig M, Mooser V, Valeri F, Djalali S, Andri R, Bernasconi E, Calmy A, Cavassini M, Vernazza P, Battegay M, Weber R, ... ... Rauch A, et al. Strong Impact of Smoking on Multimorbidity and Cardiovascular Risk Among Human Immunodeficiency Virus-Infected Individuals in Comparison With the General Population. Open Forum Infectious Diseases. 2: ofv108. PMID 26284258 DOI: 10.1093/ofid/ofv108  0.051
2015 Hoertnagl CM, Biedermann F, Yalcin-Siedentopf N, Muehlbacher M, Rauch AS, Baumgartner S, Kaufmann A, Kemmler G, Deisenhammer EA, Hausmann A, Hofer A. Prosodic and semantic affect perception in remitted patients with bipolar I disorder. The Journal of Clinical Psychiatry. 76: e779-86. PMID 26132686 DOI: 10.4088/JCP.14m08990  0.051
2014 Sobiech F, Eilermann B, Rauch A. On iteration optimization for non-cross-functional teams in Scrum Proceedings of the 2014 Research in Adaptive and Convergent Systems, Racs 2014. 266-271. DOI: 10.1145/2663761.2664198  0.051
2015 Popp B, Støve SI, Endele S, Myklebust LM, Hoyer J, Sticht H, Azzarello-Burri S, Rauch A, Arnesen T, Reis A. De novo missense mutations in the NAA10 gene cause severe non-syndromic developmental delay in males and females. European Journal of Human Genetics : Ejhg. 23: 602-9. PMID 25099252 DOI: 10.1038/ejhg.2014.150  0.051
2006 Hüffmeier U, Zenker M, Hoyer J, Fahsold R, Rauch A. A variable combination of features of Noonan syndrome and neurofibromatosis type I are caused by mutations in the NF1 gene. American Journal of Medical Genetics. Part A. 140: 2749-56. PMID 17103458 DOI: 10.1002/ajmg.a.31547  0.051
2004 Cerruti Mainardi P, Pastore G, Zweier C, Rauch A. Mowat-Wilson syndrome and mutation in the zinc finger homeo box 1B gene: a well defined clinical entity. Journal of Medical Genetics. 41: e16. PMID 14757866  0.05
2012 Peter C, Rauch A, Cieza A, Geyh S. Stress, internal resources and functioning in a person with spinal cord disease. Neurorehabilitation. 30: 119-30. PMID 22430577 DOI: 10.3233/NRE-2012-0735  0.05
2007 Lucas M, Ulsenheimer A, Pfafferot K, Heeg MH, Gaudieri S, Grüner N, Rauch A, Gerlach JT, Jung MC, Zachoval R, Pape GR, Schraut W, Santantonio T, Nitschko H, Obermeier M, et al. Tracking virus-specific CD4+ T cells during and after acute hepatitis C virus infection. Plos One. 2: e649. PMID 17653276 DOI: 10.1371/journal.pone.0000649  0.05
2009 Rauch A, Kirchberger I, Stucki G, Cieza A. Validation of the Comprehensive ICF Core Set for obstructive pulmonary diseases from the perspective of physiotherapists. Physiotherapy Research International : the Journal For Researchers and Clinicians in Physical Therapy. 14: 242-59. PMID 19764071 DOI: 10.1002/pri.448  0.05
2006 Zweier C, Horn D, Kraus C, Rauch A. Atypical ZFHX1B mutation associated with a mild Mowat-Wilson syndrome phenotype. American Journal of Medical Genetics. Part A. 140: 869-72. PMID 16532472 DOI: 10.1002/ajmg.a.31196  0.05
2004 Horn D, Weschke B, Zweier C, Rauch A. Facial phenotype allows diagnosis of Mowat-Wilson syndrome in the absence of Hirschsprung disease. American Journal of Medical Genetics. Part A. 124: 102-4. PMID 14679597 DOI: 10.1002/ajmg.a.20298  0.05
2008 Rauch A, Gaudieri S, Evison J, Nolan D, Cavassini M, Weber R, James I, Furrer H. Low current and nadir CD4+ T-cell counts are associated with higher hepatitis C virus RNA levels in the Swiss HIV cohort study. Antiviral Therapy. 13: 455-60. PMID 18572759  0.05
2014 Buetikofer S, Wandeler G, Kouyos R, Weber R, Ledergerber B, Aubert V, Barth J, Battegay M, Bernasconi E, Böni J, Bucher HC, Burton-Jeangros C, Calmy A, Cavassini M, Egger M, ... ... Rauch A, et al. Prevalence and risk factors of late presentation for HIV diagnosis and care in a tertiary referral centre in Switzerland: Presenting late with HIV-1 Swiss Medical Weekly. 144. PMID 24723302 DOI: 10.4414/smw.2014.13961  0.05
2008 Fux CA, Rauch A, Simcock M, Bucher HC, Hirschel B, Opravil M, Vernazza P, Cavassini M, Bernasconi E, Elzi L, Furrer H. Tenofovir use is associated with an increase in serum alkaline phosphatase in the Swiss HIV Cohort Study. Antiviral Therapy. 13: 1077-82. PMID 19195333  0.05
2014 Drescher SM, Von Wyl V, Yang WL, Böni J, Yerly S, Shah C, Aubert V, Klimkait T, Taffé P, Furrer H, Battegay M, Ambrosioni J, Cavassini M, Bernasconi E, Vernazza PL, ... ... Rauch A, et al. Treatment-naive individuals are the major source of transmitted HIV-1 drug resistance in men who have sex with men in the Swiss HIV cohort study Clinical Infectious Diseases. 58: 285-294. PMID 24145874 DOI: 10.1093/cid/cit694  0.05
2006 Heinritz W, Zweier C, Froster UG, Strenge S, Kujat A, Syrbe S, Rauch A, Schuster V. A missense mutation in the ZFHX1B gene associated with an atypical Mowat-Wilson syndrome phenotype. American Journal of Medical Genetics. Part A. 140: 1223-7. PMID 16688751 DOI: 10.1002/ajmg.a.31267  0.049
2013 Egli A, Schäfer J, Osthoff M, Thiel S, Mikkelsen C, Rauch A, Hirsch HH, Bucher HC, Young J, Jensenius JC, Battegay M, Trendelenburg M. Low levels of mannan-binding lectin or ficolins are not associated with an increased risk of cytomegalovirus disease in HIV-infected patients. Plos One. 8: e51983. PMID 23308103 DOI: 10.1371/journal.pone.0051983  0.049
2014 Young J, Wang Q, Fux CA, Bernasconi E, Furrer H, Vernazza P, Calmy A, Cavassini M, Weber R, Battegay M, Bucher HC, Aubert V, Barth J, Böni J, Burton-Jeangros C, ... ... Rauch A, et al. The rate of recovery in renal function when patients with HIV infection discontinue treatment with tenofovir Hiv Medicine. 15: 505-510. PMID 24641488 DOI: 10.1111/hiv.12149  0.049
2015 Schmid P, Bregenzer A, Huber M, Rauch A, Jochum W, Müllhaupt B, Vernazza P, Opravil M, Weber R. Progression of Liver Fibrosis in HIV/HCV Co-Infection: A Comparison between Non-Invasive Assessment Methods and Liver Biopsy. Plos One. 10: e0138838. PMID 26418061 DOI: 10.1371/journal.pone.0138838  0.049
2015 Guidi M, Foletti G, McLaren P, Cavassini M, Rauch A, Tarr PE, Lamy O, Panchaud A, Telenti A, Csajka C, Rotger M. Vitamin D time profile based on the contribution of non-genetic and genetic factors in HIV-infected individuals of European ancestry. Antiviral Therapy. 20: 261-9. PMID 25032819 DOI: 10.3851/IMP2823  0.049
2009 Zweier C, de Jong EK, Zweier M, Orrico A, Ousager LB, Collins AL, Bijlsma EK, Oortveld MA, Ekici AB, Reis A, Schenck A, Rauch A. CNTNAP2 and NRXN1 are mutated in autosomal-recessive Pitt-Hopkins-like mental retardation and determine the level of a common synaptic protein in Drosophila. American Journal of Human Genetics. 85: 655-66. PMID 19896112 DOI: 10.1016/j.ajhg.2009.10.004  0.049
2013 Rotger M, Glass TR, Junier T, Lundgren J, Neaton JD, Poloni ES, van 't Wout AB, Lubomirov R, Colombo S, Martinez R, Rauch A, Günthard HF, Neuhaus J, Wentworth D, van Manen D, et al. Contribution of genetic background, traditional risk factors, and HIV-related factors to coronary artery disease events in HIV-positive persons. Clinical Infectious Diseases : An Official Publication of the Infectious Diseases Society of America. 57: 112-21. PMID 23532479 DOI: 10.1093/Cid/Cit196  0.049
2014 Braun DL, Rauch A, Durisch N, Eberhard N, Anagnostopoulos A, Ledergerber B, Metzner KJ, Böni J, Weber R, Fehr J. Efficacy of lead-in silibinin and subsequent triple therapy in difficult-to-treat HIV/hepatitis C virus-coinfected patients. Hiv Medicine. 15: 625-30. PMID 24894776 DOI: 10.1111/hiv.12166  0.048
2013 Wandeler G, Gsponer T, Bihl F, Bernasconi E, Cavassini M, Kovari H, Schmid P, Battegay M, Calmy A, Egger M, Furrer H, Rauch A. Hepatitis B virus infection is associated with impaired immunological recovery during antiretroviral therapy in the Swiss HIV cohort study. The Journal of Infectious Diseases. 208: 1454-8. PMID 23901088 DOI: 10.1093/infdis/jit351  0.048
2010 Kovari H, Ledergerber B, Battegay M, Rauch A, Hirschel B, Foguena AK, Vernazza P, Bernasconi E, Mueller NJ, Weber R. Incidence and risk factors for chronic elevation of alanine aminotransferase levels in HIV-infected persons without hepatitis b or c virus co-infection. Clinical Infectious Diseases : An Official Publication of the Infectious Diseases Society of America. 50: 502-11. PMID 20085465 DOI: 10.1086/649922  0.048
2011 Pfafferott K, Gaudieri S, Ulsenheimer A, James I, Heeg M, Nolan D, John M, Rauch A, Mallal S, Lucas A, Klenerman P, Diepolder HM, Lucas M. Constrained pattern of viral evolution in acute and early HCV infection limits viral plasticity. Plos One. 6: e16797. PMID 21347433 DOI: 10.1371/journal.pone.0016797  0.048
2014 Neukam K, Munteanu D, Haubitz S, Mira JA, Ingiliz P, Rivero-Juárez A, Lutz T, de Los Santos-Gil I, Scholten S, Márquez M, Rauch A, Rockstroh JK, Pineda JA. Impact of IL28B genotype on first-week response to telaprevir-based therapy in HIV-HCV coinfection. Antiviral Therapy. PMID 25470790 DOI: 10.3851/IMP2921  0.048
2013 Gasser O, Brander C, Wolbers M, Brown NV, Rauch A, Günthard HF, Battegay M, Hess C. Expansion of interferon-γ-secreting HIV-specific T cells during successful antiretroviral therapy. Hiv Medicine. 14: 241-6. PMID 22934786 DOI: 10.1111/j.1468-1293.2012.01040.x  0.048
2008 Thiel CT, Dörr HG, Trautmann U, Hoyer J, Hofmann K, Kraus C, Ekici AB, Reis A, Rauch A. A de novo 7.6Mb tandem duplication of 14q32.2-qter associated with primordial short stature with neurosecretory growth hormone dysfunction, distinct facial anomalies and mild developmental delay. European Journal of Medical Genetics. 51: 362-7. PMID 18434272 DOI: 10.1016/j.ejmg.2008.03.001  0.048
2007 Zweier C, Peippo MM, Hoyer J, Sousa S, Bottani A, Clayton-Smith J, Reardon W, Saraiva J, Cabral A, Gohring I, Devriendt K, de Ravel T, Bijlsma EK, Hennekam RC, Orrico A, ... ... Rauch A, et al. Haploinsufficiency of TCF4 causes syndromal mental retardation with intermittent hyperventilation (Pitt-Hopkins syndrome). American Journal of Human Genetics. 80: 994-1001. PMID 17436255 DOI: 10.1086/515583  0.048
2015 Rosin N, Elcioglu NH, Beleggia F, Isgüven P, Altmüller J, Thiele H, Steindl K, Joset P, Rauch A, Nürnberg P, Wollnik B, Yigit G. Mutations in XRCC4 cause primary microcephaly, short stature and increased genomic instability. Human Molecular Genetics. 24: 3708-17. PMID 25839420 DOI: 10.1093/hmg/ddv115  0.048
2012 Soemedi R, Topf A, Wilson IJ, Darlay R, Rahman T, Glen E, Hall D, Huang N, Bentham J, Bhattacharya S, Cosgrove C, Brook JD, Granados-Riveron J, Setchfield K, Bu'lock F, ... ... Rauch A, et al. Phenotype-specific effect of chromosome 1q21.1 rearrangements and GJA5 duplications in 2436 congenital heart disease patients and 6760 controls. Human Molecular Genetics. 21: 1513-20. PMID 22199024 DOI: 10.1093/Hmg/Ddr589  0.047
2007 Thiel CT, Mortier G, Kaitila I, Reis A, Rauch A. Type and level of RMRP functional impairment predicts phenotype in the cartilage hair hypoplasia-anauxetic dysplasia spectrum. American Journal of Human Genetics. 81: 519-29. PMID 17701897 DOI: 10.1086/521034  0.047
2014 Yalcin-Siedentopf N, Hoertnagl CM, Biedermann F, Baumgartner S, Deisenhammer EA, Hausmann A, Kaufmann A, Kemmler G, Mühlbacher M, Rauch AS, Fleischhacker WW, Hofer A. Facial affect recognition in symptomatically remitted patients with schizophrenia and bipolar disorder. Schizophrenia Research. 152: 440-5. PMID 24361305 DOI: 10.1016/j.schres.2013.11.024  0.047
2010 Göhring I, Tagariello A, Endele S, Stolt CC, Ghassibé M, Fisher M, Thiel CT, Trautmann U, Vikkula M, Winterpacht A, FitzPatrick DR, Rauch A. Disruption of ST5 is associated with mental retardation and multiple congenital anomalies. Journal of Medical Genetics. 47: 91-8. PMID 19843505 DOI: 10.1136/jmg.2009.069799  0.047
2014 Hoertnagl CM, Yalcin-Siedentopf N, Baumgartner S, Biedermann F, Deisenhammer EA, Hausmann A, Kaufmann A, Kemmler G, Mühlbacher M, Rauch AS, Fleischhacker WW, Hofer A. Affective prosody perception in symptomatically remitted patients with schizophrenia and bipolar disorder. Schizophrenia Research. 158: 100-4. PMID 25096540 DOI: 10.1016/j.schres.2014.07.019  0.047
2006 Tanteles GA, Kurup B, Rauch A, Splitt MP. Microcephaly, lissencephaly, Hirschsprung disease and tetralogy of Fallot: a new syndrome? Clinical Dysmorphology. 15: 107-10. PMID 16531738 DOI: 10.1097/01.mcd.0000198927.78835.6a  0.047
2011 Scherrer AU, Ledergerber B, von Wyl V, Böni J, Yerly S, Klimkait T, Bürgisser P, Rauch A, Hirschel B, Cavassini M, Elzi L, Vernazza PL, Bernasconi E, Held L, Günthard HF, et al. Improved virological outcome in White patients infected with HIV-1 non-B subtypes compared to subtype B. Clinical Infectious Diseases : An Official Publication of the Infectious Diseases Society of America. 53: 1143-52. PMID 21998284 DOI: 10.1093/cid/cir669  0.046
2017 Liu P, Lee S, Knoll J, Rauch A, Ostermay S, Luther J, Malkusch N, Lerner UH, Zaiss MM, Neven M, Wittig R, Rauner M, David JP, Bertolino P, Zhang CX, et al. Loss of menin in osteoblast lineage affects osteocyte-osteoclast crosstalk causing osteoporosis. Cell Death and Differentiation. PMID 28106886 DOI: 10.1038/cdd.2016.165  0.046
2009 May M, Wood R, Myer L, Taffé P, Rauch A, Battegay M, Egger M. CD4(+) T cell count decreases by ethnicity among untreated patients with HIV infection in South Africa and Switzerland. The Journal of Infectious Diseases. 200: 1729-35. PMID 19848608 DOI: 10.1086/648096  0.046
2005 Rauch A, Egger M, Reichen J, Furrer H. Chronic hepatitis C in HIV-infected patients: low eligibility and applicability of therapy with pegylated interferon-alpha plus ribavirin. Journal of Acquired Immune Deficiency Syndromes (1999). 38: 238-40. PMID 15671812  0.046
2009 Rauch A, James I, Pfafferott K, Nolan D, Klenerman P, Cheng W, Mollison L, McCaughan G, Shackel N, Jeffrey GP, Baker R, Freitas E, Humphreys I, Furrer H, Günthard HF, et al. Divergent adaptation of hepatitis C virus genotypes 1 and 3 to human leukocyte antigen-restricted immune pressure. Hepatology (Baltimore, Md.). 50: 1017-29. PMID 19670417 DOI: 10.1002/hep.23101  0.046
2012 Wandeler G, Gsponer T, Bregenzer A, Günthard HF, Clerc O, Calmy A, Stöckle M, Bernasconi E, Furrer H, Rauch A. Hepatitis C virus infections in the Swiss HIV Cohort Study: a rapidly evolving epidemic. Clinical Infectious Diseases : An Official Publication of the Infectious Diseases Society of America. 55: 1408-16. PMID 22893583 DOI: 10.1093/cid/cis694  0.046
2005 Rauch A, Zink S, Zweier C, Thiel CT, Koch A, Rauch R, Lascorz J, Hüffmeier U, Weyand M, Singer H, Hofbeck M. Systematic assessment of atypical deletions reveals genotype-phenotype correlation in 22q11.2. Journal of Medical Genetics. 42: 871-6. PMID 15831592 DOI: 10.1136/jmg.2004.030619  0.046
2005 Haimerl J, Freitag-Krikovic A, Rauch A, Sauer E. Quantification of aortic valve area and left ventricular muscle mass in healthy subjects and patients with symptomatic aortic valve stenosis by MRI. Zeitschrift Fã¼R Kardiologie. 94: 173-81. PMID 15747039 DOI: 10.1007/s00392-005-0198-1  0.046
2014 Rauch A, van Doorn R, Hulsink W. A Qualitative Approach to Evidence-Based Entrepreneurship: Theoretical Considerations and an Example Involving Business Clusters Entrepreneurship: Theory and Practice. 38: 333-368. DOI: 10.1111/etap.12093  0.046
2008 Zweier C, Trautmann U, Ekici A, Rauch A. A 15Mb duplication of 6q24.1-q25.3 associated with typical but milder features of the duplication 6q syndrome. European Journal of Medical Genetics. 51: 358-61. PMID 18342594 DOI: 10.1016/j.ejmg.2008.01.005  0.046
2015 Van Belle E, Rauch A, Vincentelli A, Jeanpierre E, Legendre P, Juthier F, Hurt C, Banfi C, Rousse N, Godier A, Caron C, Elkalioubie A, Corseaux D, Dupont A, Zawadzki C, et al. Von Willebrand factor as a biological sensor of blood flow to monitor percutaneous aortic valve interventions. Circulation Research. 116: 1193-201. PMID 25670067 DOI: 10.1161/CIRCRESAHA.116.305046  0.046
2013 Müller R, Rauch A, Cieza A, Geyh S. Social support and functioning in a patient with spinal cord injury: the role of social skills. International Journal of Rehabilitation Research. Internationale Zeitschrift Fã¼R Rehabilitationsforschung. Revue Internationale De Recherches De Rã©Adaptation. 36: 236-45. PMID 23337323 DOI: 10.1097/MRR.0b013e32835dd5ff  0.046
2011 Chiu CS, Weber H, Adamski S, Rauch A, Gentile MA, Alves SE, Kath G, Flores O, Wilkinson HA. Non-invasive muscle contraction assay to study rodent models of sarcopenia. Bmc Musculoskeletal Disorders. 12: 246. PMID 22035016 DOI: 10.1186/1471-2474-12-246  0.046
2015 Robinson K, Rauch A, Hannan L. Salicylate poisoning following topical administration of methylsalicylate. Emergency Medicine Australasia : Ema. 27: 374-5. PMID 26073053 DOI: 10.1111/1742-6723.12423  0.046
2004 Rauch R, Rauch A, Koch A, Zink S, Kaulitz R, Girisch M, Singer H, Hofbeck M. Laterality of the aortic arch and anomalies of the subclavian artery-reliable indicators for 22q11.2 deletion syndromes? European Journal of Pediatrics. 163: 642-5. PMID 15300432 DOI: 10.1007/s00431-004-1518-6  0.045
2009 Kesselring AM, Wit FW, Sabin CA, Lundgren JD, Gill MJ, Gatell JM, Rauch A, Montaner JS, de Wolf F, Reiss P, Mocroft A. Risk factors for treatment-limiting toxicities in patients starting nevirapine-containing antiretroviral therapy. Aids (London, England). 23: 1689-99. PMID 19487907 DOI: 10.1097/QAD.0b013e32832d3b54  0.045
2013 Rauch A, Rijsdijk SA. The Effects of General and Specific Human Capital on Long-Term Growth and Failure of Newly Founded Businesses Entrepreneurship: Theory and Practice. 37: 923-941. DOI: 10.1111/j.1540-6520.2011.00487.x  0.045
2007 Wimplinger I, Rauch A, Orth U, Schwarzer U, Trautmann U, Kutsche K. Mother and daughter with a terminal Xp deletion: implication of chromosomal mosaicism and X-inactivation in the high clinical variability of the microphthalmia with linear skin defects (MLS) syndrome. European Journal of Medical Genetics. 50: 421-31. PMID 17845869 DOI: 10.1016/j.ejmg.2007.07.004  0.045
2010 Bedeschi MF, Colombo L, Mari F, Hofmann K, Rauch A, Gentilin B, Renieri A, Clerici D. Unmasking of a Recessive SCARF2 Mutation by a 22q11.12 de novo Deletion in a Patient with Van den Ende-Gupta Syndrome. Molecular Syndromology. 1: 239-245. PMID 22140376 DOI: 10.1159/000328135  0.044
2009 Riedel HP, Ellger-Rüttgardt S, Karbe H, Niehaus M, Rauch A, Schian HM, Schmidt C, Schott T, Schröder H, Spijkers W, Wittwer U. [Shaping the future of vocational rehabilitation of adults: eight fields of action as starting points for a cross-actor innovation process]. Die Rehabilitation. 48: 375-82. PMID 20069522 DOI: 10.1055/s-0029-1241829  0.044
2015 Boillat-Blanco N, Darling KEA, Schoni-Affolter F, Vuichard D, Rougemont M, Fulchini R, Bernasconi E, Aouri M, Clerc O, Furrer H, Günthard HF, Cavassini M, Aubert V, Battegay M, Böni J, ... ... Rauch A, et al. Virological outcome and management of persistent low-level viraemia in HIV-1-infected patients: 11 years of the Swiss HIV cohort study Antiviral Therapy. 20: 165-175. DOI: 10.3851/IMP2815  0.044
2008 Rauch A, Nolan D, Thurnheer C, Fux CA, Cavassini M, Chave JP, Opravil M, Phillips E, Mallal S, Furrer H. Refining abacavir hypersensitivity diagnoses using a structured clinical assessment and genetic testing in the Swiss HIV Cohort Study. Antiviral Therapy. 13: 1019-28. PMID 19195327  0.044
2014 Metzner KJ, Scherrer AU, Von Wyl V, Böni J, Yerly S, Klimkait T, Aubert V, Furrer H, Hirsch HH, Vernazza PL, Cavassini M, Calmy A, Bernasconi E, Weber R, Gunthard HF, ... ... Rauch A, et al. Limited clinical benefit of minority K103N and Y181C-variant detection in addition to routine genotypic resistance testing in antiretroviral therapy-naive patients Aids. 28: 2231-2239. PMID 25036184 DOI: 10.1097/QAD.0000000000000397  0.044
2010 Schwinger E, Devriendt K, Rauch A, Philip N. Clinical utility gene card for: DiGeorge syndrome, velocardiofacial syndrome, Shprintzen syndrome, chromosome 22q11.2 deletion syndrome (22q11.2, TBX1). European Journal of Human Genetics : Ejhg. 18. PMID 20125192 DOI: 10.1038/ejhg.2010.5  0.044
2013 Weber R, Ruppik M, Rickenbach M, Spoerri A, Furrer H, Battegay M, Cavassini M, Calmy A, Bernasconi E, Schmid P, Flepp M, Kowalska J, Ledergerber B, Barth J, Böni J, ... ... Rauch A, et al. Decreasing mortality and changing patterns of causes of death in the Swiss HIV Cohort Study Hiv Medicine. 14: 195-207. PMID 22998068 DOI: 10.1111/j.1468-1293.2012.01051.x  0.043
2015 Migliavacca E, Golzio C, Männik K, Blumenthal I, Oh EC, Harewood L, Kosmicki JA, Loviglio MN, Giannuzzi G, Hippolyte L, Maillard AM, Alfaiz AA, Witwicki R, Didelot G, Van Der Werf I, ... ... Rauch A, et al. A potential contributory role for ciliary dysfunction in the 16p11.2 600 kb BP4-BP5 pathology American Journal of Human Genetics. 96: 784-796. DOI: 10.1016/j.ajhg.2015.04.002  0.043
2009 Segel R, Levy-Lahad E, Pasutto F, Picard E, Rauch A, Alterescu G, Schimmel MS. Pulmonary hypoplasia-diaphragmatic hernia-anophthalmia-cardiac defect (PDAC) syndrome due to STRA6 mutations--what are the minimal criteria? American Journal of Medical Genetics. Part A. 149: 2457-63. PMID 19839040 DOI: 10.1002/ajmg.a.33038  0.043
2005 Garavelli L, Cerruti-Mainardi P, Virdis R, Pedori S, Pastore G, Godi M, Provera S, Rauch A, Zweier C, Zollino M, Banchini G, Longo N, Mowat D, Neri G, Bernasconi S. Genitourinary anomalies in Mowat-Wilson syndrome with deletion/mutation in the zinc finger homeo box 1B gene (ZFHX1B). Report of three Italian cases with hypospadias and review. Hormone Research. 63: 187-92. PMID 15908750 DOI: 10.1159/000085894  0.043
2013 Rauch A, Baschant U, Tuckermann J. Lessons from glucocorticoid receptor action in bone: New ways to avoid side effects of steroid therapy Osteoimmunology: Interactions of the Immune and Skeletal Systems. 31-48. DOI: 10.1007/978-1-4614-5366-6_5  0.043
2010 Rauch A, Kutalik Z, Descombes P, Cai T, Di Iulio J, Mueller T, Bochud M, Battegay M, Bernasconi E, Borovicka J, Colombo S, Cerny A, Dufour JF, Furrer H, Günthard HF, et al. Genetic variation in IL28B is associated with chronic hepatitis C and treatment failure: a genome-wide association study. Gastroenterology. 138: 1338-45, 1345.e1-7. PMID 20060832 DOI: 10.1053/j.gastro.2009.12.056  0.043
2005 Rauch A, Rickenbach M, Weber R, Hirschel B, Tarr PE, Bucher HC, Vernazza P, Bernasconi E, Zinkernagel AS, Evison J, Furrer H. Unsafe sex and increased incidence of hepatitis C virus infection among HIV-infected men who have sex with men: the Swiss HIV Cohort Study. Clinical Infectious Diseases : An Official Publication of the Infectious Diseases Society of America. 41: 395-402. PMID 16007539 DOI: 10.1086/431486  0.042
2019 Rauch A, Haakonsson AK, Madsen JGS, Larsen M, Forss I, Madsen MR, Van Hauwaert EL, Wiwie C, Jespersen NZ, Tencerova M, Nielsen R, Larsen BD, Röttger R, Baumbach J, Scheele C, et al. Author Correction: Osteogenesis depends on commissioning of a network of stem cell transcription factors that act as repressors of adipogenesis. Nature Genetics. PMID 30911162 DOI: 10.1038/s41588-019-0400-4  0.042
2009 Cardinale J, Rauch A, Barral Y, Szèkely G, Sbalzarini IF. Bayesian image analysis with on-line confidence estimates and its application to microtubule tracking Proceedings - 2009 Ieee International Symposium On Biomedical Imaging: From Nano to Macro, Isbi 2009. 1091-1094. DOI: 10.1109/ISBI.2009.5193246  0.042
2014 Hackenberg A, Baumer A, Sticht H, Schmitt B, Kroell-Seger J, Wille D, Joset P, Papuc S, Rauch A, Plecko B. Infantile epileptic encephalopathy, transient choreoathetotic movements, and hypersomnia due to a De Novo missense mutation in the SCN2A gene. Neuropediatrics. 45: 261-4. PMID 24710820 DOI: 10.1055/s-0034-1372302  0.042
2015 Zollino M, Marangi G, Ponzi E, Orteschi D, Ricciardi S, Lattante S, Murdolo M, Battaglia D, Contaldo I, Mercuri E, Stefanini MC, Caumes R, Edery P, Rossi M, Piccione M, ... ... Rauch A, et al. Intragenic KANSL1 mutations and chromosome 17q21.31 deletions: broadening the clinical spectrum and genotype-phenotype correlations in a large cohort of patients. Journal of Medical Genetics. PMID 26424144 DOI: 10.1136/jmedgenet-2015-103184  0.042
2014 Kouyos RD, Rauch A, Braun DL, Yang WL, Böni J, Yerly S, Klimkait T, Aubert V, Shah C, Kovari H, Calmy A, Cavassini M, Battegay M, Vernazza PL, Bernasconi E, et al. Higher risk of incident hepatitis C virus coinfection among men who have sex with men, in whom the HIV genetic bottleneck at transmission was wide. The Journal of Infectious Diseases. 210: 1555-61. PMID 24943723 DOI: 10.1093/infdis/jiu315  0.042
2015 Bihl F, Martinetti G, Wandeler G, Weber R, Ledergeber B, Calmy A, Battegay M, Cavassini M, Vernazza P, Caminada AP, Rickenbach M, Bernasconi E, Barth J, Böni J, Bucher HC, ... ... Rauch A, et al. HBV genotypes and response to tenofovir disoproxil fumarate in HIV/HBV-coinfected persons Bmc Gastroenterology. 15. DOI: 10.1186/s12876-015-0308-0  0.042
2014 Kouyos RD, Rauch A, Böni J, Yerly S, Shah C, Aubert V, Klimkait T, Kovari H, Calmy A, Cavassini M, Battegay M, Vernazza PL, Bernasconi E, Ledergerber B, Günthard HF, et al. Clustering of HCV coinfections on HIV phylogeny indicates domestic and sexual transmission of HCV. International Journal of Epidemiology. 43: 887-96. PMID 24453237 DOI: 10.1093/ije/dyt276  0.041
2013 Cordell HJ, Töpf A, Mamasoula C, Postma AV, Bentham J, Zelenika D, Heath S, Blue G, Cosgrove C, Granados Riveron J, Darlay R, Soemedi R, Wilson IJ, Ayers KL, Rahman TJ, ... ... Rauch A, et al. Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of Fallot. Human Molecular Genetics. 22: 1473-81. PMID 23297363 DOI: 10.1093/Hmg/Dds552  0.041
2016 Beguelin C, Vazquez M, Moradpour D, Sahli R, Suter F, Rauch A, Wandeler G. Uncontrolled hepatitis delta virus infection after initial suppression on tenofovir in a HIV/HBV-coinfected patient Aids. 30: 530-532. DOI: 10.1097/QAD.0000000000000972  0.041
2014 Nitschke K, Barriga A, Schmidt J, Timm J, Viazov S, Kuntzen T, Kim AY, Lauer GM, Allen TM, Gaudieri S, Rauch A, Lange CM, Sarrazin C, Eiermann T, Sidney J, et al. HLA-B*27 subtype specificity determines targeting and viral evolution of a hepatitis C virus-specific CD8+ T cell epitope. Journal of Hepatology. 60: 22-9. PMID 23978718 DOI: 10.1016/J.Jhep.2013.08.009  0.041
2015 Elkalioubie A, Haulon S, Duhamel A, Rosa M, Rauch A, Staels B, Susen S, Van Belle E, Dupont A. Meta-Analysis of Abdominal Aortic Aneurysm in Patients With Coronary Artery Disease. The American Journal of Cardiology. 116: 1451-6. PMID 26347003 DOI: 10.1016/j.amjcard.2015.07.074  0.041
2008 Graul-Neumann LM, Hausser I, Essayie M, Rauch A, Kraus C. Highly variable cutis laxa resulting from a dominant splicing mutation of the elastin gene. American Journal of Medical Genetics. Part A. 146: 977-83. PMID 18348261 DOI: 10.1002/ajmg.a.32242  0.041
2014 Asadollahi R, Oneda B, Joset P, Azzarello-Burri S, Bartholdi D, Steindl K, Vincent M, Cobilanschi J, Sticht H, Baldinger R, Reissmann R, Sudholt I, Thiel CT, Ekici AB, Reis A, ... ... Rauch A, et al. The clinical significance of small copy number variants in neurodevelopmental disorders. Journal of Medical Genetics. 51: 677-88. PMID 25106414 DOI: 10.1136/Jmedgenet-2014-102588  0.04
2012 Wolff D, Endele S, Azzarello-Burri S, Hoyer J, Zweier M, Schanze I, Schmitt B, Rauch A, Reis A, Zweier C. In-Frame Deletion and Missense Mutations of the C-Terminal Helicase Domain of SMARCA2 in Three Patients with Nicolaides-Baraitser Syndrome. Molecular Syndromology. 2: 237-244. PMID 22822383  0.04
2010 Boldt C, Grill E, Bartholomeyczik S, Brach M, Rauch A, Eriks-Hoogland I, Stucki G. Combined application of the International Classification of Functioning, Disability and Health and the NANDA-International Taxonomy II. Journal of Advanced Nursing. 66: 1885-98. PMID 20557378 DOI: 10.1111/j.1365-2648.2010.05359.x  0.04
2006 Rauch A, Hoyer J, Guth S, Zweier C, Kraus C, Becker C, Zenker M, Hüffmeier U, Thiel C, Rüschendorf F, Nürnberg P, Reis A, Trautmann U. Diagnostic yield of various genetic approaches in patients with unexplained developmental delay or mental retardation. American Journal of Medical Genetics. Part A. 140: 2063-74. PMID 16917849 DOI: 10.1002/ajmg.a.31416  0.039
2007 Patronek GJ, Rauch A. Systematic review of comparative studies examining alternatives to the harmful use of animals in biomedical education. Journal of the American Veterinary Medical Association. 230: 37-43. PMID 17199490 DOI: 10.2460/javma.230.1.37  0.039
2015 Schaerer V, Haubitz S, Kovari H, Ledergerber B, Ambrosioni J, Cavassini M, Stoeckle M, Schmid P, Decosterd L, Aouri M, Böni J, Günthard HF, Furrer H, Metzner KJ, Fehr J, ... Rauch A, et al. Protease inhibitors to treat hepatitis C in the Swiss HIV Cohort Study: high efficacy but low treatment uptake. Hiv Medicine. 16: 599-607. PMID 26135140 DOI: 10.1111/hiv.12269  0.039
2015 Schaerer V, Haubitz S, Kovari H, Ledergerber B, Ambrosioni J, Cavassini M, Stoeckle M, Schmid P, Decosterd L, Aouri M, Böni J, Günthard H, Furrer H, Metzner K, Fehr J, ... Rauch A, et al. Protease inhibitors to treat hepatitis C in the Swiss HIV Cohort Study: High efficacy but low treatment uptake Hiv Medicine. DOI: 10.1111/hiv.12269  0.039
2010 Rohrbach J, Robinson N, Harcourt G, Hammond E, Gaudieri S, Gorgievski M, Telenti A, Keiser O, Günthard HF, Hirschel B, Hoffmann M, Bernasconi E, Battegay M, Furrer H, Klenerman P, ... Rauch A, et al. Cellular immune responses to HCV core increase and HCV RNA levels decrease during successful antiretroviral therapy. Gut. 59: 1252-8. PMID 20660698 DOI: 10.1136/gut.2009.205971  0.039
2011 Gregor A, Albrecht B, Bader I, Bijlsma EK, Ekici AB, Engels H, Hackmann K, Horn D, Hoyer J, Klapecki J, Kohlhase J, Maystadt I, Nagl S, Prott E, Tinschert S, ... ... Rauch A, et al. Expanding the clinical spectrum associated with defects in CNTNAP2 and NRXN1. Bmc Medical Genetics. 12: 106. PMID 21827697 DOI: 10.1186/1471-2350-12-106  0.039
2015 Rauch A, Hummel CA. How to stop the race to the bottom: Empirical evidence from North Rhine-Westphalia International Tax and Public Finance. 1-23. DOI: 10.1007/s10797-015-9387-7  0.039
2011 Kantaputra P, Tanpaiboon P, Porntaveetus T, Ohazama A, Sharpe P, Rauch A, Hussadaloy A, Thiel CT. The smallest teeth in the world are caused by mutations in the PCNT gene. American Journal of Medical Genetics. Part A. 155: 1398-403. PMID 21567919 DOI: 10.1002/ajmg.a.33984  0.039
2008 Clifford GM, Rickenbach M, Polesel J, Dal Maso L, Steffen I, Ledergerber B, Rauch A, Probst-Hensch NM, Bouchardy C, Levi F, Franceschi S. Influence of HIV-related immunodeficiency on the risk of hepatocellular carcinoma. Aids (London, England). 22: 2135-41. PMID 18832877 DOI: 10.1097/QAD.0b013e32831103ad  0.038
2015 Carballo D, Delhumeau C, Carballo S, Bähler C, Radovanovic D, Hirschel B, Clerc O, Bernasconi E, Fasel D, Schmid P, Cusini A, Fehr J, Erne P, Keller PF, Ledergerber B, ... ... Rauch A, et al. Increased mortality after a first myocardial infarction in human immunodeficiency virus-infected patients; a nested cohort study Aids Research and Therapy. 12. DOI: 10.1186/s12981-015-0045-z  0.038
2010 Isidor B, Pichon O, Redon R, Day-Salvatore D, Hamel A, Siwicka KA, Bitner-Glindzicz M, Heymann D, Kjellén L, Kraus C, Leroy JG, Mortier GR, Rauch A, Verloes A, David A, et al. Mesomelia-synostoses syndrome results from deletion of SULF1 and SLCO5A1 genes at 8q13. American Journal of Human Genetics. 87: 95-100. PMID 20602915 DOI: 10.1016/j.ajhg.2010.05.012  0.038
2015 Bülow L, Lissewski C, Bressel R, Rauch A, Stark Z, Zenker M, Bartsch O. Hydrops, fetal pleural effusions and chylothorax in three patients with CBL mutations. American Journal of Medical Genetics. Part A. 167: 394-9. PMID 25358541 DOI: 10.1002/ajmg.a.36838  0.038
2013 Rosenbusch N, Rauch A, Bausch A. The Mediating Role of Entrepreneurial Orientation in the Task Environment-Performance Relationship: A Meta-Analysis Journal of Management. 39: 633-659. DOI: 10.1177/0149206311425612  0.038
2014 Bartholdi D, Stray-Pedersen A, Azzarello-Burri S, Kibaek M, Kirchhoff M, Oneda B, Rødningen O, Schmitt-Mechelke T, Rauch A, Kjaergaard S. A newly recognized 13q12.3 microdeletion syndrome characterized by intellectual disability, microcephaly, and eczema/atopic dermatitis encompassing the HMGB1 and KATNAL1 genes. American Journal of Medical Genetics. Part A. 164: 1277-83. PMID 24664804 DOI: 10.1002/ajmg.a.36439  0.037
2015 Schäfer J, Young J, Bernasconi E, Ledergerber B, Nicca D, Calmy A, Cavassini M, Furrer H, Battegay M, Bucher HC, Barth J, Böni J, Burton-Jeangros C, Cellerai C, Egger M, ... ... Rauch A, et al. Predicting smoking cessation and its relapse in HIV-infected patients: The Swiss HIV Cohort Study Hiv Medicine. 16: 3-14. DOI: 10.1111/hiv.12165  0.037
2011 Zahnleiter D, Trautmann U, Ekici AB, Goehring I, Reis A, Dörr HG, Rauch A, Thiel CT. Familial short stature due to a 5q22.1-q23.2 duplication refines the 5q duplication spectrum. European Journal of Medical Genetics. 54: e521-4. PMID 21777705 DOI: 10.1016/j.ejmg.2011.06.007  0.037
2008 Simm D, Degenhardt K, Gerdemann C, Völkl TM, Rauch A, Dörr HG. [Chronological age of patients with Turner syndrome at diagnosis]. Klinische Pã¤Diatrie. 220: 16-20. PMID 18095252 DOI: 10.1055/s-2007-972569  0.037
2015 Hirsenkorn N, Hanke T, Rauch A, Dehlink B, Rasshofer R, Biebl E. A non-parametric approach for modeling sensor behavior Proceedings International Radar Symposium. 2015: 131-136. DOI: 10.1109/IRS.2015.7226346  0.037
2008 Göhring I, Blümlein HM, Hoyer J, Ekici AB, Trautmann U, Rauch A. 6.7 Mb interstitial duplication in chromosome band 11q24.2q25 associated with infertility, minor dysmorphic features and normal psychomotor development. European Journal of Medical Genetics. 51: 666-71. PMID 18757044 DOI: 10.1016/j.ejmg.2008.07.009  0.037
2022 Ali D, Figeac F, Caci A, Ditzel N, Schmal C, Kerckhofs G, Havelund J, Faergeman N, Rauch A, Tencerova M, Kassem M. High-fat diet-induced obesity augments the deleterious effects of estrogen deficiency on bone: Evidence from ovariectomized mice. Aging Cell. e13726. PMID 36217558 DOI: 10.1111/acel.13726  0.037
2015 Rauch A, Hinrichs T, Oberhauser C, Cieza A. Do people with spinal cord injury meet the WHO recommendations on physical activity? International Journal of Public Health. PMID 26303072 DOI: 10.1007/s00038-015-0724-5  0.036
2016 Ryom L, Boesecke C, Gisler V, Manzardo C, Rockstroh JK, Puoti M, Furrer H, Miro JM, Gatell JM, Pozniak A, Behrens G, Battegay M, Lundgren JD, Monforte AdA, Arribas J, ... ... Rauch A, et al. Essentials from the 2015 European AIDS Clinical Society (EACS) guidelines for the treatment of adult HIV-positive persons Hiv Medicine. 17: 83-88. DOI: 10.1111/hiv.12322  0.036
2006 Weidemann F, Wacker C, Rauch A, Bauer WR, Bijnens B, Sutherland GR, Ertl G, Voelker W, Fidler F, Strotmann JM. Sequential changes of myocardial function during acute myocardial infarction, in the early and chronic phase after coronary intervention described by ultrasonic strain rate imaging. Journal of the American Society of Echocardiography : Official Publication of the American Society of Echocardiography. 19: 839-47. PMID 16824992 DOI: 10.1016/j.echo.2006.01.024  0.036
2015 Klein A, Rauch A, Sattiraju RR, Schotten HD. Achievable performance gains using movement prediction and advanced 3D system modeling Ieee Vehicular Technology Conference. 2015. DOI: 10.1109/VTCSpring.2014.7023153  0.036
2011 Merani S, Petrovic D, James I, Chopra A, Cooper D, Freitas E, Rauch A, di Iulio J, John M, Lucas M, Fitzmaurice K, McKiernan S, Norris S, Kelleher D, Klenerman P, et al. Effect of immune pressure on hepatitis C virus evolution: insights from a single-source outbreak. Hepatology (Baltimore, Md.). 53: 396-405. PMID 21246583 DOI: 10.1002/hep.24076  0.036
2008 Huehne K, Zweier C, Raab K, Odent S, Bonnaure-Mallet M, Sixou JL, Landrieu P, Goizet C, Sarlangue J, Baumann M, Eggermann T, Rauch A, Ruppert S, Stettner GM, Rautenstrauss B. Novel missense, insertion and deletion mutations in the neurotrophic tyrosine kinase receptor type 1 gene (NTRK1) associated with congenital insensitivity to pain with anhidrosis. Neuromuscular Disorders : Nmd. 18: 159-66. PMID 18077166 DOI: 10.1016/j.nmd.2007.10.005  0.036
2007 Strenge S, Heinritz W, Zweier C, Rauch A, Rolle U, Merkenschlager A, Froster UG. Pulmonary artery sling and congenital tracheal stenosis in another patient with Mowat-Wilson syndrome. American Journal of Medical Genetics. Part A. 143: 1528-30. PMID 17567886 DOI: 10.1002/ajmg.a.31801  0.035
2015 Alhenc-Gelas M, Plu-Bureau G, Horellou MH, Rauch A, Suchon P. PROS1 genotype phenotype relationships in a large cohort of adults with suspicion of inherited quantitative protein S deficiency. Thrombosis and Haemostasis. 115. PMID 26466767 DOI: 10.1160/TH15-05-0391  0.035
2012 Keiser O, Spycher B, Rauch A, Calmy A, Cavassini M, Glass TR, Nicca D, Ledergerber B, Egger M. Outcomes of antiretroviral therapy in the Swiss HIV Cohort Study: latent class analysis. Aids and Behavior. 16: 245-55. PMID 21630013 DOI: 10.1007/s10461-011-9971-5  0.034
2009 Thiel C, Wilken M, Zenker M, Sticht H, Fahsold R, Gusek-Schneider GC, Rauch A. Independent NF1 and PTPN11 mutations in a family with neurofibromatosis-Noonan syndrome. American Journal of Medical Genetics. Part A. 149: 1263-7. PMID 19449407 DOI: 10.1002/ajmg.a.32837  0.034
2011 Schick B, Wemmert S, Willnecker V, Dlugaiczyk J, Nicolai P, Siwiec H, Thiel CT, Rauch A, Wendler O. Genome-wide copy number profiling using a 100K SNP array reveals novel disease-related genes BORIS and TSHZ1 in juvenile angiofibroma. International Journal of Oncology. 39: 1143-51. PMID 21874228 DOI: 10.3892/ijo.2011.1166  0.034
2015 Fitzmaurice K, Hurst J, Dring M, Rauch A, McLaren PJ, Günthard HF, Gardiner C, Klenerman P. Additive effects of HLA alleles and innate immune genes determine viral outcome in HCV infection. Gut. 64: 813-9. PMID 24996883 DOI: 10.1136/gutjnl-2013-306287  0.034
2015 Kovari H, Ledergerber B, Cavassini M, Ambrosioni J, Bregenzer A, Stöckle M, Bernasconi E, Kouyos R, Weber R, Rauch A. High Hepatic and Extrahepatic Mortality and Low Treatment Uptake in HCV-coinfected Persons in the Swiss HIV Cohort Study between 2001 and 2013. Journal of Hepatology. PMID 25937433 DOI: 10.1016/j.jhep.2015.04.019  0.034
2004 Rauch A, Devriendt K, Koch A, Rauch R, Gewillig M, Kraus C, Weyand M, Singer H, Reis A, Hofbeck M. Assessment of association between variants and haplotypes of the remaining TBX1 gene and manifestations of congenital heart defects in 22q11.2 deletion patients. Journal of Medical Genetics. 41: e40. PMID 15060116  0.033
2012 Zweier M, Rauch A. The MEF2C-Related and 5q14.3q15 Microdeletion Syndrome. Molecular Syndromology. 2: 164-170. PMID 22670137  0.033
2005 Thiel CT, Rosanowski F, Kohlhase J, Reis A, Rauch A. Exclusion of TCOF1 mutations in a case of bilateral Goldenhar syndrome and one familial case of microtia with meatal atresia. Clinical Dysmorphology. 14: 67-71. PMID 15770127  0.033
2015 Roma-Lavisse C, Tagzirt M, Zawadzki C, Lorenzi R, Vincentelli A, Haulon S, Juthier F, Rauch A, Corseaux D, Staels B, Jude B, Van Belle E, Susen S, Chinetti-Gbaguidi G, Dupont A. M1 and M2 macrophage proteolytic and angiogenic profile analysis in atherosclerotic patients reveals a distinctive profile in type 2 diabetes. Diabetes & Vascular Disease Research. 12: 279-89. PMID 25966737 DOI: 10.1177/1479164115582351  0.033
2014 Fehr J, Schärer V, Hirzel C, Rauch A. [Hepatitis B and C in HIV coinfection]. Therapeutische Umschau. Revue Thã©Rapeutique. 71: 490-6. PMID 25093314 DOI: 10.1024/0040-5930/a000542  0.033
2005 Wick U, Kirsch M, Rauch A, Chudoba I, Lausen B, Efferth T, Gebhart E. FISH studies on the telomeric regions of the T-cell acute lymphoblastic leukemia cell line CCRF-CEM. Cytogenetic and Genome Research. 111: 34-40. PMID 16093718 DOI: 10.1159/000085667  0.032
2009 Tschochner M, Chopra A, Maiden TM, Ahmad IF, James I, Furrer H, Günthard HF, Mallal S, Rauch A, John M. Effects of HIV type-1 immune selection on susceptability to integrase inhibitor resistance. Antiviral Therapy. 14: 953-64. PMID 19918099 DOI: 10.3851/IMP1419  0.032
2011 Rauch A, Baumberger M, Moise FG, von Elm E, Reinhardt JD. Rehabilitation needs assessment in persons with spinal cord injury following the 2010 earthquake in Haiti: a pilot study using an ICF-based tool. Journal of Rehabilitation Medicine. 43: 969-75. PMID 22031341 DOI: 10.2340/16501977-0896  0.032
2011 Boillat Blanco N, Probst A, Da Costa VW, Giulieri S, Bernasconi E, Calmy A, Elzi L, Rauch A, Weber R, Bertisch B, Cavassini M, Bochud PY. Impact of a nurse vaccination program on hepatitis B immunity in a Swiss HIV clinic. Journal of Acquired Immune Deficiency Syndromes (1999). 58: 472-4. PMID 21963937 DOI: 10.1097/QAI.0b013e318237915e  0.031
2006 Rauch A, Nolan D, Martin A, McKinnon E, Almeida C, Mallal S. Prospective genetic screening decreases the incidence of abacavir hypersensitivity reactions in the Western Australian HIV cohort study. Clinical Infectious Diseases : An Official Publication of the Infectious Diseases Society of America. 43: 99-102. PMID 16758424 DOI: 10.1086/504874  0.03
2013 Schnyder B, Adam J, Rauch A, Thurnheer MC, Pichler WJ. HLA-B*57:01(+) abacavir-naive individuals have specific T cells but no patch test reactivity. The Journal of Allergy and Clinical Immunology. 132: 756-8. PMID 23706613 DOI: 10.1016/j.jaci.2013.04.013  0.03
2007 Hoyer J, Dreweke A, Becker C, Göhring I, Thiel CT, Peippo MM, Rauch R, Hofbeck M, Trautmann U, Zweier C, Zenker M, Hüffmeier U, Kraus C, Ekici AB, Rüschendorf F, ... ... Rauch A, et al. Molecular karyotyping in patients with mental retardation using 100K single-nucleotide polymorphism arrays. Journal of Medical Genetics. 44: 629-36. PMID 17601928 DOI: 10.1136/jmg.2007.050914  0.03
2009 Hoyer J, Kraus C, Hammersen G, Geppert JP, Rauch A. Lethal cutis laxa with contractural arachnodactyly, overgrowth and soft tissue bleeding due to a novel homozygous fibulin-4 gene mutation. Clinical Genetics. 76: 276-81. PMID 19664000 DOI: 10.1111/j.1399-0004.2009.01204.x  0.03
2007 Rauch A, Laird R, McKinnon E, Telenti A, Furrer H, Weber R, Smillie D, Gaudieri S. Influence of inhibitory killer immunoglobulin-like receptors and their HLA-C ligands on resolving hepatitis C virus infection. Tissue Antigens. 69: 237-40. PMID 17445209 DOI: 10.1111/j.1399-0039.2006.773_4.x  0.03
2014 Sprenger K, Evison JM, Zwahlen M, Vogt CM, Elzi MV, Hauser C, Furrer H, Low N, Hubert V, Barth J, Battegay M, Bernasconi E, Böni J, Bucher HC, Burton-Jeangros C, ... ... Rauch A, et al. Sexually transmitted infections in HIV-infected people in Switzerland: Cross-sectional study Peerj. 2014. DOI: 10.7717/peerj.537  0.03
2012 Glässel A, Rauch A, Selb M, Emmenegger K, Lückenkemper M, Escorpizo R. A case study on the application of International Classification of Functioning, Disability and Health (ICF)-based tools for vocational rehabilitation in spinal cord injury. Work (Reading, Mass.). 41: 465-74. PMID 22495418 DOI: 10.3233/WOR-2012-1310  0.03
2014 Béguelin C, Vázquez M, Bertschi M, Yerly S, de Jong D, Rauch A, Cusini A. Viral escape in the CNS with multidrug-resistant HIV-1. Journal of the International Aids Society. 17: 19745. PMID 25397490  0.03
2012 Poretti A, Mall V, Smitka M, Grunt S, Risen S, Toelle SP, Benson JE, Yoshida S, Jung NH, Tinschert S, Neuhann TM, Rauch A, Steinlin M, Meoded A, Huisman TA, et al. Macrocerebellum: significance and pathogenic considerations. Cerebellum (London, England). 11: 1026-36. PMID 22528964 DOI: 10.1007/s12311-012-0379-1  0.03
2006 Krause FS, Rauch A, Schrott KM, Engehausen DG. Clinical decisions for treatment of different staged bladder cancer based on multitarget fluorescence in situ hybridization assays? World Journal of Urology. 24: 418-22. PMID 16688457 DOI: 10.1007/s00345-006-0086-y  0.029
2006 Völkl TM, Langer T, Aigner T, Greess H, Beck JD, Rauch AM, Dörr HG. Klinefelter syndrome and mediastinal germ cell tumors. American Journal of Medical Genetics. Part A. 140: 471-81. PMID 16470792 DOI: 10.1002/ajmg.a.31103  0.029
2015 Keith N, Unger JM, Rauch A, Frese M. Informal Learning and Entrepreneurial Success: A Longitudinal Study of Deliberate Practice among Small Business Owners Applied Psychology. DOI: 10.1111/apps.12054  0.029
2011 di Iulio J, Ciuffi A, Fitzmaurice K, Kelleher D, Rotger M, Fellay J, Martinez R, Pulit S, Furrer H, Günthard HF, Battegay M, Bernasconi E, Schmid P, Hirschel B, Barnes E, ... ... Rauch A, et al. Estimating the net contribution of interleukin-28B variation to spontaneous hepatitis C virus clearance. Hepatology (Baltimore, Md.). 53: 1446-54. PMID 21360716 DOI: 10.1002/hep.24263  0.029
2011 Rauch A. The shortest of the short: pericentrin mutations and beyond. Best Practice & Research. Clinical Endocrinology & Metabolism. 25: 125-30. PMID 21396579 DOI: 10.1016/j.beem.2010.10.015  0.029
2006 Zimmermann T, Brasch F, Rauch A, Stachel D, Holter W, Beck JD. CR10/80--Lymphoid interstitial pneumonia and Kabuki-Syndrome in a young man. Paediatric Respiratory Reviews. 7: S329. PMID 17036410  0.028
2013 Follmann R, Kother D, Campo MA, Franke T, Gabler A, Jakoby R, Manabe A, Rabe T, Heunisch A, Rauch A, Kasser T. Liquida-Sky - A tunable liquid crystal filter for space applications Proceedings of the 2013 Ieee-Aps Topical Conference On Antennas and Propagation in Wireless Communications, Ieee Apwc 2013. 90-93. DOI: 10.1109/APWC.2013.6624872  0.028
2008 Thiel CT, Knebel B, Knerr I, Sticht H, Müller-Wieland D, Zenker M, Reis A, Dörr HG, Rauch A. Two novel mutations in the insulin binding subunit of the insulin receptor gene without insulin binding impairment in a patient with Rabson-Mendenhall syndrome. Molecular Genetics and Metabolism. 94: 356-62. PMID 18411068 DOI: 10.1016/j.ymgme.2008.02.013  0.028
2022 Rauch A. [Knee injuries in winter sports]. Orthopadie (Heidelberg, Germany). 51: 870-881. PMID 36239771 DOI: 10.1007/s00132-022-04317-7  0.027
2008 Colombo S, Rauch A, Rotger M, Fellay J, Martinez R, Fux C, Thurnheer C, Günthard HF, Goldstein DB, Furrer H, Telenti A. The HCP5 single-nucleotide polymorphism: a simple screening tool for prediction of hypersensitivity reaction to abacavir. The Journal of Infectious Diseases. 198: 864-7. PMID 18684101 DOI: 10.1086/591184  0.027
2006 Trouillier H, Birkenmaier C, Rauch A, Weiler C, Kauschke T, Refior HJ. Posterior lumbar interbody fusion (PLIF) with cages and local bone graft in the treatment of spinal stenosis. Acta Orthopaedica Belgica. 72: 460-6. PMID 17009828  0.026
2005 Zenker M, Wermuth B, Trautmann U, Knerr I, Kraus C, Rauch A, Reis A. Severe, neonatal-onset OTC deficiency in twin sisters with a de novo balanced reciprocal translocation t(X;5)(p21.1;q11). American Journal of Medical Genetics. Part A. 132: 185-8. PMID 15578616 DOI: 10.1002/ajmg.a.30414  0.026
2013 Rauch A. Clinical research in osteopathy - Part 1: Musculoskeletal disorders | Klinische Forschung in der Osteopathie - Teil 1: Muskuloskelettale Störungen Osteopathische Medizin. 14: 27-32. DOI: 10.1016/S1615-9071(13)60035-0  0.026
2015 Rauch A, Mandrup S. A Genome-Wide Perspective on Metabolism. Handbook of Experimental Pharmacology. PMID 25903411 DOI: 10.1007/164_2015_2  0.026
2005 Zweier C, Guth S, Schulte-Mattler U, Rauch A, Trautmann U. 9 Mb deletion including chromosome band 3q24 associated with unsuspicious facial gestalt, persistent ductus omphaloentericus, mild mental retardation and tic. European Journal of Medical Genetics. 48: 360-2. PMID 16179233 DOI: 10.1016/j.ejmg.2005.04.016  0.026
2013 Gregor A, Oti M, Kouwenhoven EN, Hoyer J, Sticht H, Ekici AB, Kjaergaard S, Rauch A, Stunnenberg HG, Uebe S, Vasileiou G, Reis A, Zhou H, Zweier C. De novo mutations in the genome organizer CTCF cause intellectual disability. American Journal of Human Genetics. 93: 124-31. PMID 23746550 DOI: 10.1016/j.ajhg.2013.05.007  0.025
2013 Asadollahi R, Oneda B, Sheth F, Azzarello-Burri S, Baldinger R, Joset P, Latal B, Knirsch W, Desai S, Baumer A, Houge G, Andrieux J, Rauch A. Dosage changes of MED13L further delineate its role in congenital heart defects and intellectual disability. European Journal of Human Genetics : Ejhg. 21: 1100-4. PMID 23403903 DOI: 10.1038/ejhg.2013.17  0.025
2004 Rauch A, Hofbeck M, Cesnjevar R, Koch A, Rauch R, Buheitel G, Singer H, Weyand M. Search for somatic 22q11.2 deletions in patients with conotruncal heart defects. American Journal of Medical Genetics. Part A. 124: 165-9. PMID 14699615 DOI: 10.1002/ajmg.a.20323  0.025
2004 Bähring S, Rauch A, Toka O, Schroeder C, Hesse C, Siedler H, Fesüs G, Haefeli WE, Busjahn A, Aydin A, Neuenfeld Y, Mühl A, Toka HR, Gollasch M, Jordan J, et al. Autosomal-dominant hypertension with type E brachydactyly is caused by rearrangement on the short arm of chromosome 12. Hypertension. 43: 471-6. PMID 14707163 DOI: 10.1161/01.HYP.0000111808.08715.ec  0.025
2015 Wandeler G, Dufour JF, Bruggmann P, Rauch A. Hepatitis C: a changing epidemic. Swiss Medical Weekly. 145: w14093. PMID 25658972 DOI: 10.4414/smw.2015.14093  0.025
2014 Rauch A, Caron C, Susen S, Goudemand J. Von Willebrand factor and von Willebrand disease: Novel insights | Facteur von Willebrand et maladie de Willebrand: nouvelles approches Revue Francophone Des Laboratoires. 2014: 53-63. DOI: 10.1016/S1773-035X(14)72524-9  0.025
2007 Hüffmeier U, Tietze HU, Rauch A. Severe skeletal dysplasia caused by undiagnosed hypothyroidism. European Journal of Medical Genetics. 50: 209-15. PMID 17433800 DOI: 10.1016/j.ejmg.2007.02.002  0.024
2014 Rauch AF. Recovery at Kingston Power Engineering. 118.  0.024
2014 Hasselhorn HM, Peter R, Rauch A, Schröder H, Swart E, Bender S, du Prel JB, Ebener M, March S, Trappmann M, Steinwede J, Müller BH. Cohort profile: the lidA Cohort Study-a German Cohort Study on Work, Age, Health and Work Participation. International Journal of Epidemiology. 43: 1736-49. PMID 24618186 DOI: 10.1093/ije/dyu021  0.024
2015 Unger JM, Rauch A, Weis SE, Frese M. Biology (prenatal testosterone), psychology (achievement need) and entrepreneurial impact Journal of Business Venturing Insights. 4: 1-5. DOI: 10.1016/j.jbvi.2015.05.001  0.024
2013 Rauch A, Singhose W, Fujioka D, Jones T. Tip-over stability analysis of mobile boom cranes with swinging payloads Journal of Dynamic Systems, Measurement and Control, Transactions of the Asme. 135. DOI: 10.1115/1.4023276  0.024
2012 Simmons R, Sharp C, McClure CP, Rohrbach J, Kovari H, Frangou E, Simmonds P, Irving W, Rauch A, Bowness P, Klenerman P. Parvovirus 4 infection and clinical outcome in high-risk populations. The Journal of Infectious Diseases. 205: 1816-20. PMID 22492853 DOI: 10.1093/infdis/jis291  0.024
2005 Rauch R, Rauch A, Kaulitz R, Koch A, Zink S, Girisch M, Singer H, Hofbeck M. [Cervical origin of the subclavian artery: echocardiographic diagnosis in patients with monosomy 22q11]. Ultraschall in Der Medizin (Stuttgart, Germany : 1980). 26: 36-41. PMID 15700226 DOI: 10.1055/s-2004-813938  0.024
2008 Apitz C, Schaefer J, Sieverding L, Rauch A, Hofbeck M. Spontaneous development and rupture of pulmonary artery aneurysm: a rare complication in an infant with peripheral pulmonary artery stenoses due to mutation of the elastin gene. Pediatric Cardiology. 29: 438-41. PMID 17912483 DOI: 10.1007/s00246-007-9096-9  0.023
2015 Susen S, Rauch A, Van Belle E, Vincentelli A, Lenting PJ. Circulatory support devices: fundamental aspects and clinical management of bleeding and thrombosis. Journal of Thrombosis and Haemostasis : Jth. 13: 1757-67. PMID 26302994 DOI: 10.1111/jth.13120  0.023
2013 Steinbusch CV, van Roozendaal KE, Tserpelis D, Smeets EE, Kranenburg-de Koning TJ, de Waal KH, Zweier C, Rauch A, Hennekam RC, Blok MJ, Schrander-Stumpel CT. Somatic mosaicism in a mother of two children with Pitt-Hopkins syndrome. Clinical Genetics. 83: 73-7. PMID 22335494 DOI: 10.1111/j.1399-0004.2012.01857.x  0.023
2009 Rauch A, Gaudieri S, Thio C, Bochud PY. Host genetic determinants of spontaneous hepatitis C clearance. Pharmacogenomics. 10: 1819-37. PMID 19891557 DOI: 10.2217/pgs.09.121  0.023
2015 Rauch A, Hulsink W. Putting entrepreneurship Education where the intention to Act lies: An investigation into the impact of entrepreneurship education on entrepreneurial behavior Academy of Management Learning and Education. 14: 187-204. DOI: 10.5465/amle.2012.0293  0.022
2007 Rauch A, Dörr HG. Chromosome 5q subtelomeric deletion syndrome. American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. 145: 372-6. PMID 17910075 DOI: 10.1002/ajmg.c.30151  0.022
2015 Tophoven S, Tisch A, Rauch A, Burghardt A. [Psychosocial working conditions and mental health status of the German babyboomer generation]. Gesundheitswesen (Bundesverband Der äRzte Des öFfentlichen Gesundheitsdienstes (Germany)). 77: e63-9. PMID 25760102 DOI: 10.1055/s-0034-1398596  0.022
2013 Mamasoula C, Prentice RR, Pierscionek T, Pangilinan F, Mills JL, Druschel C, Pass K, Russell MW, Hall D, Töpf A, Brown DL, Zelenika D, Bentham J, Cosgrove C, Bhattacharya S, ... ... Rauch A, et al. Association between C677T polymorphism of methylene tetrahydrofolate reductase and congenital heart disease: meta-analysis of 7697 cases and 13,125 controls. Circulation. Cardiovascular Genetics. 6: 347-53. PMID 23876493 DOI: 10.1161/Circgenetics.113.000191  0.022
2015 Imthurn B, Berger W, Macas E, Magyar I, Oneda B, Rauch A, Xie M. Polar body diagnosis (PBD): An alternative and supplement to preimplantation diagnosis for single embryo transfer Screening the Single Euploid Embryo: Molecular Genetics in Reproductive Medicine. 103-121. DOI: 10.1007/978-3-319-16892-0_8  0.022
2014 Dieks JK, Baumer A, Wilichowski E, Rauch A, Sigler M. Microcephalic osteodysplastic primordial dwarfism type II (MOPD II) with multiple vascular complications misdiagnosed as Dubowitz syndrome. European Journal of Pediatrics. 173: 1253-6. PMID 24973050 DOI: 10.1007/s00431-014-2368-5  0.022
2008 Baradaran-Heravi A, Thiel C, Rauch A, Zenker M, Boerkoel CF, Kaitila I. Clinical and genetic distinction of Schimke immuno-osseous dysplasia and cartilage-hair hypoplasia. American Journal of Medical Genetics. Part A. 146: 2013-7. PMID 18627050 DOI: 10.1002/ajmg.a.32406  0.022
2009 Rauch A, Kirchberger I, Boldt C, Cieza A, Stucki G. Does the Comprehensive International Classification of Functioning, Disability and Health (ICF) Core Set for rheumatoid arthritis capture nursing practice? A Delphi survey. International Journal of Nursing Studies. 46: 1320-34. PMID 19457481 DOI: 10.1016/j.ijnurstu.2009.04.006  0.022
2013 Rauch A, Frese M, Wang ZM, Unger J, Lozada M, Kupcha V, Spirina T. National culture and cultural orientations of owners affecting the innovation-growth relationship in five countries Entrepreneurship and Regional Development. 25: 732-755. DOI: 10.1080/08985626.2013.862972  0.021
2010 Rauch A, Rohrbach J, Bochud PY. The recent breakthroughs in the understanding of host genomics in hepatitis C. European Journal of Clinical Investigation. 40: 950-9. PMID 20624172 DOI: 10.1111/j.1365-2362.2010.02337.x  0.021
2008 Treon SP, Soumerai JD, Branagan AR, Hunter ZR, Patterson CJ, Ioakimidis L, Briccetti FM, Pasmantier M, Zimbler H, Cooper RB, Moore M, Hill J, Rauch A, Garbo L, Chu L, et al. Thalidomide and rituximab in Waldenstrom macroglobulinemia. Blood. 112: 4452-7. PMID 18713945 DOI: 10.1182/blood-2008-04-150854  0.02
2013 Rauch A, Maier S, Klanner F, Dietmayer K. Inter-vehicle object association for cooperative perception systems Ieee Conference On Intelligent Transportation Systems, Proceedings, Itsc. 893-898. DOI: 10.1109/ITSC.2013.6728345  0.02
2007 Aigner T, Rau T, Niederhagen M, Zaucke F, Schmitz M, Pöhls U, Stöss H, Rauch A, Thiel CT. Achondrogenesis Type IA (Houston-Harris): a still-unresolved molecular phenotype. Pediatric and Developmental Pathology : the Official Journal of the Society For Pediatric Pathology and the Paediatric Pathology Society. 10: 328-34. PMID 17638425 DOI: 10.2350/06-07-0134.1  0.019
2009 Türkkani-Asal G, Alanay Y, Turul-Ozgür T, Zenker M, Thiel C, Rauch A, Unal S, Gürgey A, Tezcan I. Mild clinical phenotype and subtle radiographic findings in an infant with cartilage-hair hypoplasia. The Turkish Journal of Pediatrics. 51: 493-6. PMID 20112607  0.019
2008 Rauch A, Nolan D, Furrer H, McKinnon E, John M, Mallal S, Gaudieri S, Günthard HF, Schmid P, Battegay M, Hirschel B, Telenti A, James I. HLA-Bw4 homozygosity is associated with an impaired CD4 T cell recovery after initiation of antiretroviral therapy. Clinical Infectious Diseases : An Official Publication of the Infectious Diseases Society of America. 46: 1921-5. PMID 18466093 DOI: 10.1086/588479  0.018
2009 Tibelius A, Marhold J, Zentgraf H, Heilig CE, Neitzel H, Ducommun B, Rauch A, Ho AD, Bartek J, Krämer A. Microcephalin and pericentrin regulate mitotic entry via centrosome-associated Chk1. The Journal of Cell Biology. 185: 1149-57. PMID 19546241 DOI: 10.1083/jcb.200810159  0.017
2008 Hurni Ch, Rauch A, Trost N, Perrig M, Bürgi U, Schoenenberger AW. [Pulmonary nodules in a patient on long-term steroid treatment]. Praxis. 97: 849-52. PMID 18754339  0.016
2004 Rohrer TR, Gassmann KF, Rauch A, Pfeiffer RA, Doerr HG. Growth of heterokaryotic monozygotic twins discordant for Ullrich-Turner syndrome during the first years of life. American Journal of Medical Genetics. Part A. 126: 78-83. PMID 15039976 DOI: 10.1002/ajmg.a.20446  0.016
2006 Schirmer-Zimmerman H, Hammersen G, Scheuerlen W, Griese M, Brasch F, Rauch A. CR3/108--Congenital alveolar capillary dysplasia with familiary microphthalmia. Paediatric Respiratory Reviews. 7: S326. PMID 17036407  0.016
2004 Rauch A, Rüschendorf F, Huang J, Trautmann U, Becker C, Thiel C, Jones KW, Reis A, Nürnberg P. Molecular karyotyping using an SNP array for genomewide genotyping. Journal of Medical Genetics. 41: 916-22. PMID 15591277 DOI: 10.1136/jmg.2004.022855  0.016
2014 Edlinger M, Rauch AS, Kemmler G, Yalcin-Siedentopf N, Fleischhacker WW, Hofer A. Risk of violence of inpatients with severe mental illness--do patients with schizophrenia pose harm to others? Psychiatry Research. 219: 450-6. PMID 25023366 DOI: 10.1016/j.psychres.2014.06.021  0.015
2007 Liehr T, Utine GE, Trautmann U, Rauch A, Kuechler A, Pietrzak J, Pietracz J, Bocian E, Kosyakova N, Mrasek K, Boduroglu K, Weise A, Aktas D. Neocentric small supernumerary marker chromosomes (sSMC)--three more cases and review of the literature. Cytogenetic and Genome Research. 118: 31-7. PMID 17901697 DOI: 10.1159/000106438  0.013
2015 Rauch A, Lianghai J, Klein A, Schotten HD. Fast algorithm for radio propagation modeling in realistic 3-D urban environment Advances in Radio Science. 13: 169-173. DOI: 10.5194/ars-13-169-2015  0.013
2014 Rauch A. Exome sequencing in unspecific intellectual disability and rare disorders. Molecular Cytogenetics. 7: I26. PMID 24940363 DOI: 10.1186/1755-8166-7-S1-I26  0.012
2015 Burr H, Rauch A, Rose U, Tisch A, Tophoven S. Employment status, working conditions and depressive symptoms among German employees born in 1959 and 1965. International Archives of Occupational and Environmental Health. 88: 731-41. PMID 25416510 DOI: 10.1007/s00420-014-0999-5  0.012
2007 Melichar VO, Guth S, Hellebrand H, Meindl A, von der Hardt K, Kraus C, Trautmann U, Rascher W, Rauch A, Zenker M. A male infant with a 9.6 Mb terminal Xp deletion including the OA1 locus: Limit of viability of Xp deletions in males. American Journal of Medical Genetics. Part A. 143: 135-41. PMID 17163525 DOI: 10.1002/ajmg.a.31451  0.012
2014 Rauch A, Fekete C, Oberhauser C, Marti A, Cieza A. Participation in sport in persons with spinal cord injury in Switzerland. Spinal Cord. 52: 706-11. PMID 24937697 DOI: 10.1038/sc.2014.102  0.012
2007 Vermeesch JR, Fiegler H, de Leeuw N, Szuhai K, Schoumans J, Ciccone R, Speleman F, Rauch A, Clayton-Smith J, Van Ravenswaaij C, Sanlaville D, Patsalis PC, Firth H, Devriendt K, Zuffardi O. Guidelines for molecular karyotyping in constitutional genetic diagnosis. European Journal of Human Genetics : Ejhg. 15: 1105-14. PMID 17637806 DOI: 10.1038/sj.ejhg.5201896  0.011
2015 Hanke T, Hirsenkorn N, Dehlink B, Rauch A, Rasshofer R, Biebl E. Generic architecture for simulation of ADAS sensors Proceedings International Radar Symposium. 2015: 125-130. DOI: 10.1109/IRS.2015.7226306  0.01
2015 Rauch A, Deker JS, Woodside AG. Consuming Alone: Broadening Putnam's "Bowling Alone" Thesis Psychology and Marketing. 32: 967-976. DOI: 10.1002/mar.20830  0.01
2013 Otte C, Rauch A. [Intellectual disability - a frequent reason for referral to medical genetics]. Praxis. 102: 1467-73. PMID 24280603 DOI: 10.1024/1661-8157/a001488  0.01
2013 Hasselhorn HM, Rauch A. [Perspectives of work, age, health, and labor market participation in Germany]. Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz. 56: 339-48. PMID 23455551 DOI: 10.1007/s00103-012-1614-0  0.01
2013 Hasselhorn HM, Rauch A, Burr H. [The health status of the German workforce and its role in labor market participation]. Bundesgesundheitsblatt, Gesundheitsforschung, Gesundheitsschutz. 56: 337-8. PMID 23455550 DOI: 10.1007/s00103-012-1610-4  0.01
2013 Nye AM, Hamrick I, Rauch A, Pound MW, Shelton PS. Documenting the use of calcium supplements with oral bisphosphonates. The Consultant Pharmacist : the Journal of the American Society of Consultant Pharmacists. 28: 31-8. PMID 23315280 DOI: 10.4140/TCP.n.2013.31  0.01
2013 Rauch A, Anders A. Estimating electron drift velocities in magnetron discharges Vacuum. 89: 53-56. DOI: 10.1016/j.vacuum.2012.09.002  0.01
2012 Rauch A, Mandrup S. Lighting the fat furnace without SFRP5. The Journal of Clinical Investigation. 122: 2349-52. PMID 22728932 DOI: 10.1172/JCI64196  0.01
2012 Hoyer J, Ekici AB, Endele S, Popp B, Zweier C, Wiesener A, Wohlleber E, Dufke A, Rossier E, Petsch C, Zweier M, Göhring I, Zink AM, Rappold G, Schröck E, ... ... Rauch A, et al. Haploinsufficiency of ARID1B, a member of the SWI/SNF-a chromatin-remodeling complex, is a frequent cause of intellectual disability. American Journal of Human Genetics. 90: 565-72. PMID 22405089 DOI: 10.1016/j.ajhg.2012.02.007  0.01
2012 Gaudieri S, Lucas M, Lucas A, McKinnon E, Albloushi H, Rauch A, di Iulio J, Martino D, Prescott SL, Tulic MK. Genetic variations in IL28B and allergic disease in children. Plos One. 7: e30607. PMID 22295096 DOI: 10.1371/journal.pone.0030607  0.01
2011 Rauch A, Fellay J. Personalized hepatitis C therapy: opportunities and pitfalls. Expert Review of Molecular Diagnostics. 11: 127-9. PMID 21405961 DOI: 10.1586/erm.10.116  0.01
2011 Thiel CT, Rauch A. The molecular basis of the cartilage-hair hypoplasia-anauxetic dysplasia spectrum. Best Practice & Research. Clinical Endocrinology & Metabolism. 25: 131-42. PMID 21396580 DOI: 10.1016/j.beem.2010.08.004  0.01
2008 Rauch A, Leipelt M, Russwurm M, Steegborn C. Crystal structure of the guanylyl cyclase Cya2. Proceedings of the National Academy of Sciences of the United States of America. 105: 15720-5. PMID 18840690 DOI: 10.1073/pnas.0808473105  0.01
2008 Rauch A, Krüger L, Miyamoto A, Bollwein H. Colour Doppler sonography of cystic ovarian follicles in cows. The Journal of Reproduction and Development. 54: 447-53. PMID 18787308 DOI: JST.JSTAGE/jrd/20025  0.01
2007 Sauerstein K, Schroth M, Amann K, Hoyer J, Singer H, Rauch A, Dötsch J. Pulmonary embolism--a rare complication of Schimke immunoosseous dysplasia. European Journal of Pediatrics. 166: 1285-8. PMID 17195070 DOI: 10.1007/s00431-006-0383-x  0.01
2006 Vermeesch JR, Rauch A. Reply to Hochstenbach et al. 'Molecular karyotyping'. European Journal of Human Genetics : Ejhg. 14: 1063-4. PMID 16736034 DOI: 10.1038/sj.ejhg.5201663  0.01
2006 Rauch A, Droz S, Zimmerli S, Leib SL. Dysphagia in elderly women: consider tetanus. Infection. 34: 35-8. PMID 16501901 DOI: 10.1007/s15010-006-4151-7  0.01
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