| Year |
Citation |
Score |
| 2020 |
Morales F, Vásquez M, Corrales E, Vindas-Smith R, Santamaría-Ulloa C, Zhang B, Sirito M, Estecio MR, Krahe R, Monckton DG. Longitudinal increases in somatic mosaicism of the expanded CTG repeat in myotonic dystrophy type 1 are associated with variation in age-at-onset. Human Molecular Genetics. PMID 32601694 DOI: 10.1093/Hmg/Ddaa123 |
0.313 |
|
| 2020 |
Kurkiewicz A, Cooper A, McIlwaine E, Cumming SA, Adam B, Krahe R, Puymirat J, Schoser B, Timchenko L, Ashizawa T, Thornton CA, Rogers S, McClure JD, Monckton DG. Towards development of a statistical framework to evaluate myotonic dystrophy type 1 mRNA biomarkers in the context of a clinical trial. Plos One. 15: e0231000. PMID 32287265 DOI: 10.1371/Journal.Pone.0231000 |
0.337 |
|
| 2019 |
Corrales E, Vásquez M, Zhang B, Santamaría-Ulloa C, Cuenca P, Krahe R, Monckton DG, Morales F. Analysis of mutational dynamics at the DMPK (CTG)n locus identifies saliva as a suitable DNA sample source for genetic analysis in myotonic dystrophy type 1. Plos One. 14: e0216407. PMID 31048891 DOI: 10.1371/Journal.Pone.0216407 |
0.32 |
|
| 2017 |
Yenigun VB, Sirito M, Amcheslavky A, Czernuszewicz T, Colonques-Bellmunt J, García-Alcover I, Wojciechowska M, Bolduc C, Chen Z, López Castel A, Krahe R, Bergmann A. (CCUG)n RNA toxicity in a Drosophila model for myotonic dystrophy type 2 (DM2) activates apoptosis. Disease Models & Mechanisms. PMID 28623239 DOI: 10.1242/Dmm.026179 |
0.333 |
|
| 2016 |
Chakraborty S, Vatta M, Bachinski LL, Krahe R, Dlouhy S, Bai S. Molecular Diagnosis of Myotonic Dystrophy. Current Protocols in Human Genetics. 91: 9.29.1-9.29.19. PMID 27727437 DOI: 10.1002/Cphg.22 |
0.408 |
|
| 2014 |
Screen M, Jonson PH, Raheem O, Palmio J, Laaksonen R, Lehtimäki T, Sirito M, Krahe R, Hackman P, Udd B. Abnormal splicing of NEDD4 in myotonic dystrophy type 2: possible link to statin adverse reactions. The American Journal of Pathology. 184: 2322-32. PMID 24907641 DOI: 10.1016/J.Ajpath.2014.04.013 |
0.375 |
|
| 2014 |
Bachinski LL, Baggerly KA, Neubauer VL, Nixon TJ, Raheem O, Sirito M, Unruh AK, Zhang J, Nagarajan L, Timchenko LT, Bassez G, Eymard B, Gamez J, Ashizawa T, Mendell JR, ... ... Krahe R, et al. Most expression and splicing changes in myotonic dystrophy type 1 and type 2 skeletal muscle are shared with other muscular dystrophies. Neuromuscular Disorders : Nmd. 24: 227-40. PMID 24332166 DOI: 10.1016/J.Nmd.2013.11.001 |
0.373 |
|
| 2013 |
Vihola A, Sirito M, Bachinski LL, Raheem O, Screen M, Suominen T, Krahe R, Udd B. Altered expression and splicing of Ca(2+) metabolism genes in myotonic dystrophies DM1 and DM2. Neuropathology and Applied Neurobiology. 39: 390-405. PMID 22758909 DOI: 10.1111/J.1365-2990.2012.01289.X |
0.329 |
|
| 2012 |
Udd B, Krahe R. The myotonic dystrophies: molecular, clinical, and therapeutic challenges. The Lancet. Neurology. 11: 891-905. PMID 22995693 DOI: 10.1016/S1474-4422(12)70204-1 |
0.366 |
|
| 2012 |
Izaguirre DI, Zhu W, Hai T, Cheung HC, Krahe R, Cote GJ. PTBP1-dependent regulation of USP5 alternative RNA splicing plays a role in glioblastoma tumorigenesis. Molecular Carcinogenesis. 51: 895-906. PMID 21976412 DOI: 10.1002/Mc.20859 |
0.318 |
|
| 2011 |
Fang S, Krahe R, Bachinski LL, Zhang B, Amos CI, Strong LC. Sex-specific effect of the TP53 PIN3 polymorphism on cancer risk in a cohort study of TP53 germline mutation carriers. Human Genetics. 130: 789-94. PMID 21688173 DOI: 10.1007/S00439-011-1039-0 |
0.326 |
|
| 2011 |
Udd B, Meola G, Krahe R, Wansink DG, Bassez G, Kress W, Schoser B, Moxley R. Myotonic dystrophy type 2 (DM2) and related disorders report of the 180th ENMC workshop including guidelines on diagnostics and management 3-5 December 2010, Naarden, The Netherlands. Neuromuscular Disorders : Nmd. 21: 443-50. PMID 21543227 DOI: 10.1016/J.Nmd.2011.03.013 |
0.444 |
|
| 2011 |
Suominen T, Bachinski LL, Auvinen S, Hackman P, Baggerly KA, Angelini C, Peltonen L, Krahe R, Udd B. Population frequency of myotonic dystrophy: higher than expected frequency of myotonic dystrophy type 2 (DM2) mutation in Finland. European Journal of Human Genetics : Ejhg. 19: 776-82. PMID 21364698 DOI: 10.1038/Ejhg.2011.23 |
0.379 |
|
| 2011 |
Wu CC, Krahe R, Lozano G, Zhang B, Wilson CD, Jo EJ, Amos CI, Shete S, Strong LC. Joint effects of germ-line TP53 mutation, MDM2 SNP309, and gender on cancer risk in family studies of Li-Fraumeni syndrome. Human Genetics. 129: 663-73. PMID 21305319 DOI: 10.1007/S00439-011-0957-1 |
0.336 |
|
| 2010 |
Bachinski LL, Sirito M, Böhme M, Baggerly KA, Udd B, Krahe R. Altered MEF2 isoforms in myotonic dystrophy and other neuromuscular disorders. Muscle & Nerve. 42: 856-63. PMID 21104860 DOI: 10.1002/Mus.21789 |
0.363 |
|
| 2010 |
Raheem O, Olufemi SE, Bachinski LL, Vihola A, Sirito M, Holmlund-Hampf J, Haapasalo H, Li YP, Udd B, Krahe R. Mutant (CCTG)n expansion causes abnormal expression of zinc finger protein 9 (ZNF9) in myotonic dystrophy type 2. The American Journal of Pathology. 177: 3025-36. PMID 20971734 DOI: 10.2353/Ajpath.2010.100179 |
0.401 |
|
| 2010 |
Fang S, Krahe R, Lozano G, Han Y, Chen W, Post SM, Zhang B, Wilson CD, Bachinski LL, Strong LC, Amos CI. Effects of MDM2, MDM4 and TP53 codon 72 polymorphisms on cancer risk in a cohort study of carriers of TP53 germline mutations. Plos One. 5: e10813. PMID 20520810 DOI: 10.1371/Journal.Pone.0010813 |
0.324 |
|
| 2010 |
Sammons MA, Antons AK, Bendjennat M, Udd B, Krahe R, Link AJ. ZNF9 activation of IRES-mediated translation of the human ODC mRNA is decreased in myotonic dystrophy type 2. Plos One. 5: e9301. PMID 20174632 DOI: 10.1371/Journal.Pone.0009301 |
0.342 |
|
| 2010 |
Vihola A, Bachinski LL, Sirito M, Olufemi SE, Hajibashi S, Baggerly KA, Raheem O, Haapasalo H, Suominen T, Holmlund-Hampf J, Paetau A, Cardani R, Meola G, Kalimo H, Edström L, ... Krahe R, et al. Differences in aberrant expression and splicing of sarcomeric proteins in the myotonic dystrophies DM1 and DM2. Acta Neuropathologica. 119: 465-79. PMID 20066428 DOI: 10.1007/S00401-010-0637-6 |
0.383 |
|
| 2010 |
Suominen T, Bachinski LL, Auvinen S, Hackman P, Angelini C, Peltonen L, Krahe R, Udd B. P2.32 The frequency of myotonic dystrophy type 2 (DM2) and type 1 (DM1) mutations in the population Neuromuscular Disorders. 20: 628-628. DOI: 10.1016/J.Nmd.2010.07.104 |
0.33 |
|
| 2009 |
Bachinski LL, Czernuszewicz T, Ramagli LS, Suominen T, Shriver MD, Udd B, Siciliano MJ, Krahe R. Premutation allele pool in myotonic dystrophy type 2. Neurology. 72: 490-7. PMID 19020295 DOI: 10.1212/01.Wnl.0000333665.01888.33 |
0.321 |
|
| 2008 |
Auvinen S, Suominen T, Hannonen P, Bachinski LL, Krahe R, Udd B. Myotonic dystrophy type 2 found in two of sixty-three persons diagnosed as having fibromyalgia. Arthritis and Rheumatism. 58: 3627-31. PMID 18975316 DOI: 10.1002/Art.24037 |
0.371 |
|
| 2008 |
Suominen T, Schoser B, Raheem O, Auvinen S, Walter M, Krahe R, Lochmüller H, Kress W, Udd B. High frequency of co-segregating CLCN1 mutations among myotonic dystrophy type 2 patients from Finland and Germany. Journal of Neurology. 255: 1731-6. PMID 18807109 DOI: 10.1007/S00415-008-0010-Z |
0.36 |
|
| 2008 |
Cheung HC, Baggerly KA, Tsavachidis S, Bachinski LL, Neubauer VL, Nixon TJ, Aldape KD, Cote GJ, Krahe R. Global analysis of aberrant pre-mRNA splicing in glioblastoma using exon expression arrays. Bmc Genomics. 9: 216. PMID 18474104 DOI: 10.1186/1471-2164-9-216 |
0.316 |
|
| 2007 |
Müller JS, Herczegfalvi A, Vilchez JJ, Colomer J, Bachinski LL, Mihaylova V, Santos M, Schara U, Deschauer M, Shevell M, Poulin C, Dias A, Soudo A, Hietala M, Aärimaa T, ... Krahe R, et al. Phenotypical spectrum of DOK7 mutations in congenital myasthenic syndromes. Brain : a Journal of Neurology. 130: 1497-506. PMID 17439981 DOI: 10.1093/Brain/Awm068 |
0.375 |
|
| 2007 |
Vihola A, Sirito M, Bachinski L, Olufemi S, Raheem O, Suominen T, Udd B, Krahe R. G.P.14.14 Differences in aberrant expression and splicing of genes involved in Ca2+ metabolism between myotonic dystrophy type 2 (DM2) and type 1 (DM1) Neuromuscular Disorders. 17: 858. DOI: 10.1016/J.Nmd.2007.06.323 |
0.325 |
|
| 2006 |
Suominen T, Raheem O, Vihola A, Haapasalo H, Krahe R, Udd B. P.P.2 06 ClC1 chloride channel gene mutations in myotonic dystrophy type 2 patients Neuromuscular Disorders. 16: 672. DOI: 10.1016/J.Nmd.2006.05.100 |
0.336 |
|
| 2005 |
Maurage CA, Udd B, Ruchoux MM, Vermersch P, Kalimo H, Krahe R, Delacourte A, Sergeant N. Similar brain tau pathology in DM2/PROMM and DM1/Steinert disease. Neurology. 65: 1636-8. PMID 16301494 DOI: 10.1212/01.Wnl.0000184585.93864.4E |
0.31 |
|
| 2005 |
Ruteshouser EC, Hendrickson BW, Colella S, Krahe R, Pinto L, Huff V. Genome-wide loss of heterozygosity analysis of WT1-wild-type and WT1-mutant Wilms tumors. Genes, Chromosomes & Cancer. 43: 172-80. PMID 15761866 DOI: 10.1002/Gcc.20169 |
0.378 |
|
| 2004 |
Van Goethem G, Luoma P, Rantamäki M, Al Memar A, Kaakkola S, Hackman P, Krahe R, Löfgren A, Martin JJ, De Jonghe P, Suomalainen A, Udd B, Van Broeckhoven C. POLG mutations in neurodegenerative disorders with ataxia but no muscle involvement. Neurology. 63: 1251-7. PMID 15477547 DOI: 10.1212/01.Wnl.0000140494.58732.83 |
0.375 |
|
| 2004 |
Grewal RP, Zhang S, Ma W, Rosenberg M, Krahe R. Clinical and genetic analysis of a family with PROMM. Journal of Clinical Neuroscience : Official Journal of the Neurosurgical Society of Australasia. 11: 603-5. PMID 15261229 DOI: 10.1016/J.Jocn.2003.09.014 |
0.577 |
|
| 2004 |
Tanner SM, Li Z, Bisson R, Acar C, Oner C, Oner R, Cetin M, Abdelaal MA, Ismail EA, Lissens W, Krahe R, Broch H, Gräsbeck R, de la Chapelle A. Genetically heterogeneous selective intestinal malabsorption of vitamin B12: founder effects, consanguinity, and high clinical awareness explain aggregations in Scandinavia and the Middle East. Human Mutation. 23: 327-33. PMID 15024727 DOI: 10.1002/Humu.20014 |
0.375 |
|
| 2004 |
Sallinen R, Vihola A, Bachinski LL, Huoponen K, Haapasalo H, Hackman P, Zhang S, Sirito M, Kalimo H, Meola G, Horelli-Kuitunen N, Wessman M, Krahe R, Udd B. New methods for molecular diagnosis and demonstration of the (CCTG)n mutation in myotonic dystrophy type 2 (DM2). Neuromuscular Disorders : Nmd. 14: 274-83. PMID 15019706 DOI: 10.1016/J.Nmd.2004.01.002 |
0.588 |
|
| 2003 |
Meola G, Sansone V, Perani D, Scarone S, Cappa S, Dragoni C, Cattaneo E, Cotelli M, Gobbo C, Fazio F, Siciliano G, Mancuso M, Vitelli E, Zhang S, Krahe R, et al. Executive dysfunction and avoidant personality trait in myotonic dystrophy type 1 (DM-1) and in proximal myotonic myopathy (PROMM/DM-2). Neuromuscular Disorders : Nmd. 13: 813-21. PMID 14678804 DOI: 10.1016/S0960-8966(03)00137-8 |
0.515 |
|
| 2003 |
Miller BJ, Wang D, Krahe R, Wright FA. Pooled analysis of loss of heterozygosity in breast cancer: a genome scan provides comparative evidence for multiple tumor suppressors and identifies novel candidate regions. American Journal of Human Genetics. 73: 748-67. PMID 13680524 DOI: 10.1086/378522 |
0.341 |
|
| 2003 |
Bachinski LL, Udd B, Meola G, Sansone V, Bassez G, Eymard B, Thornton CA, Moxley RT, Harper PS, Rogers MT, Jurkat-Rott K, Lehmann-Horn F, Wieser T, Gamez J, Navarro C, ... ... Krahe R, et al. Confirmation of the type 2 myotonic dystrophy (CCTG)n expansion mutation in patients with proximal myotonic myopathy/proximal myotonic dystrophy of different European origins: a single shared haplotype indicates an ancestral founder effect. American Journal of Human Genetics. 73: 835-48. PMID 12970845 DOI: 10.1086/378566 |
0.602 |
|
| 2003 |
Udd B, Meola G, Krahe R, Thornton C, Ranum L, Day J, Bassez G, Ricker K. Report of the 115th ENMC workshop: DM2/PROMM and other myotonic dystrophies. 3rd Workshop, 14-16 February 2003, Naarden, The Netherlands. Neuromuscular Disorders : Nmd. 13: 589-96. PMID 12921797 DOI: 10.1016/S0960-8966(03)00092-0 |
0.413 |
|
| 2003 |
Vihola A, Bassez G, Meola G, Zhang S, Haapasalo H, Paetau A, Mancinelli E, Rouche A, Hogrel JY, Laforêt P, Maisonobe T, Pellissier JF, Krahe R, Eymard B, Udd B. Histopathological differences of myotonic dystrophy type 1 (DM1) and PROMM/DM2. Neurology. 60: 1854-7. PMID 12796551 DOI: 10.1212/01.Wnl.0000065898.61358.09 |
0.517 |
|
| 2002 |
Lemon WJ, Palatini JJ, Krahe R, Wright FA. Theoretical and experimental comparisons of gene expression indexes for oligonucleotide arrays. Bioinformatics (Oxford, England). 18: 1470-6. PMID 12424118 DOI: 10.1093/Bioinformatics/18.11.1470 |
0.309 |
|
| 2002 |
Miano JM, Kitchen CM, Chen J, Maltby KM, Kelly LA, Weiler H, Krahe R, Ashworth LK, Garcia E. Expression of human smooth muscle calponin in transgenic mice revealed with a bacterial artificial chromosome. American Journal of Physiology. Heart and Circulatory Physiology. 282: H1793-803. PMID 11959645 DOI: 10.1152/Ajpheart.00875.2001 |
0.332 |
|
| 2002 |
Zhang S, Krahe R. Physical and transcript map of a 2-Mb region in Xp22.1 containing candidate genes for X-linked mental retardation and short stature. Genomics. 79: 274-7. PMID 11863356 DOI: 10.1006/Geno.2002.6702 |
0.532 |
|
| 2001 |
Karacay B, O'Dorisio MS, Kasow K, Hollenback C, Krahe R. Expression and fine mapping of murine vasoactive intestinal peptide receptor 1. Journal of Molecular Neuroscience : Mn. 17: 311-24. PMID 11859927 DOI: 10.1385/Jmn:17:3:311 |
0.341 |
|
| 2001 |
Rush LJ, Dai Z, Smiraglia DJ, Gao X, Wright FA, Frühwald M, Costello JF, Held WA, Yu L, Krahe R, Kolitz JE, Bloomfield CD, Caligiuri MA, Plass C. Novel methylation targets in de novo acute myeloid leukemia with prevalence of chromosome 11 loci. Blood. 97: 3226-33. PMID 11342453 DOI: 10.1182/Blood.V97.10.3226 |
0.315 |
|
| 2001 |
Zhuo D, Zhao WD, Wright FA, Yang HY, Wang JP, Sears R, Baer T, Kwon DH, Gordon D, Gibbs S, Dai D, Yang Q, Spitzner J, Krahe R, Stredney D, et al. Assembly, annotation, and integration of UNIGENE clusters into the human genome draft. Genome Research. 11: 904-18. PMID 11337484 DOI: 10.1101/Gr.Gr-1645R |
0.303 |
|
| 2001 |
Virtaneva K, Wright FA, Tanner SM, Yuan B, Lemon WJ, Caligiuri MA, Bloomfield CD, de La Chapelle A, Krahe R. Expression profiling reveals fundamental biological differences in acute myeloid leukemia with isolated trisomy 8 and normal cytogenetics. Proceedings of the National Academy of Sciences of the United States of America. 98: 1124-9. PMID 11158605 DOI: 10.1073/Pnas.98.3.1124 |
0.339 |
|
| 2001 |
Frühwald MC, O'Dorisio MS, Dai Z, Rush LJ, Krahe R, Smiraglia DJ, Pietsch T, Elsea SH, Plass C. Aberrant hypermethylation of the major breakpoint cluster region in 17p11.2 in medulloblastomas but not supratentorial PNETs. Genes, Chromosomes & Cancer. 30: 38-47. PMID 11107174 DOI: 10.1002/1098-2264(2000)9999:9999<::Aid-Gcc1052>3.0.Co;2-S |
0.325 |
|
| 2001 |
Virtaneva KI, Wright FA, Tanner SM, Yuan B, Lemon WJ, Caligiuri MA, Bloomfield CD, Chapelle Adl, Krahe R. Gene expression profiling reveals fundamental biological differences in AML with trisomy 8 and normal cytogenetics Nature Genetics. 27: 65-65. DOI: 10.1038/87158 |
0.319 |
|
| 2000 |
Wise DO, Krahe R, Oakley BR. The gamma-tubulin gene family in humans. Genomics. 67: 164-70. PMID 10903841 DOI: 10.1006/Geno.2000.6247 |
0.323 |
|
| 2000 |
Kristiansen M, Aminoff M, Jacobsen C, de La Chapelle A, Krahe R, Verroust PJ, Moestrup SK. Cubilin P1297L mutation associated with hereditary megaloblastic anemia 1 causes impaired recognition of intrinsic factor-vitamin B(12) by cubilin. Blood. 96: 405-9. PMID 10887099 DOI: 10.1182/Blood.V96.2.405.014K16_405_409 |
0.338 |
|
| 2000 |
Pellegata NS, Dieguez-Lucena JL, Joensuu T, Lau S, Montgomery KT, Krahe R, Kivelä T, Kucherlapati R, Forsius H, de la Chapelle A. Mutations in KERA, encoding keratocan, cause cornea plana. Nature Genetics. 25: 91-5. PMID 10802664 DOI: 10.1038/75664 |
0.39 |
|
| 2000 |
Ashizawa T, Gonzales I, Ohsawa N, Singer RH, Devillers M, Balasubramanyam A, Cooper TA, Khajavi M, Lia-Baldini AS, Miller G, Philips AV, Timchenko LT, Waring J, Yamagata H, Barbet JP, ... ... Krahe R, et al. New nomenclature and DNA testing guidelines for myotonic dystrophy type 1 (DM1) Neurology. 54: 1218-1221. PMID 10746587 DOI: 10.1212/Wnl.54.6.1218 |
0.383 |
|
| 2000 |
Kourlas PJ, Strout MP, Becknell B, Veronese ML, Croce CM, Theil KS, Krahe R, Ruutu T, Knuutila S, Bloomfield CD, Caligiuri MA. Identification of a gene at 11q23 encoding a guanine nucleotide exchange factor: evidence for its fusion with MLL in acute myeloid leukemia. Proceedings of the National Academy of Sciences of the United States of America. 97: 2145-50. PMID 10681437 DOI: 10.1073/Pnas.040569197 |
0.358 |
|
| 1999 |
Miano JM, Garcia E, Krahe R. Radiation Hybrid (RH) Mapping of Human Smooth Muscle-Restricted Genes. Methods in Molecular Medicine. 30: 25-35. PMID 21341013 DOI: 10.1385/1-59259-247-3:25 |
0.408 |
|
| 1999 |
Aminoff M, Carter JE, Chadwick RB, Johnson C, Gräsbeck R, Abdelaal MA, Broch H, Jenner LB, Verroust PJ, Moestrup SK, de la Chapelle A, Krahe R. Mutations in CUBN, encoding the intrinsic factor-vitamin B12 receptor, cubilin, cause hereditary megaloblastic anaemia 1. Nature Genetics. 21: 309-13. PMID 10080186 DOI: 10.1038/6831 |
0.362 |
|
| 1997 |
Miano JM, Krahe R, Garcia E, Elliott JM, Olson EN. Expression, genomic structure and high resolution mapping to 19p13.2 of the human smooth muscle cell calponin gene. Gene. 197: 215-24. PMID 9332369 DOI: 10.1016/S0378-1119(97)00265-5 |
0.376 |
|
| 1997 |
Udd B, Krahe R, Wallgren-Pettersson C, Falck B, Kalimo H. Proximal myotonic dystrophy--a family with autosomal dominant muscular dystrophy, cataracts, hearing loss and hypogonadism: heterogeneity of proximal myotonic syndromes? Neuromuscular Disorders : Nmd. 7: 217-28. PMID 9196902 DOI: 10.1016/S0960-8966(97)00041-2 |
0.368 |
|
| 1997 |
Virtaneva K, D'Amato E, Miao J, Koskiniemi M, Norio R, Avanzini G, Franceschetti S, Michelucci R, Tassinari CA, Omer S, Pennacchio LA, Myers RM, Dieguez-Lucena JL, Krahe R, de la Chapelle A, et al. Unstable minisatellite expansion causing recessively inherited myoclonus epilepsy, EPM1. Nature Genetics. 15: 393-6. PMID 9090386 DOI: 10.1038/Ng0497-393 |
0.429 |
|
| 1997 |
Bachinski LL, Abchee A, Durand JB, Roberts R, Krahe R, Hobson GM. Polymorphic trinucleotide repeat in the MEF2A gene at 15q26 is not expanded in familial cardiomyopathies. Molecular and Cellular Probes. 11: 55-8. PMID 9076715 DOI: 10.1006/Mcpr.1996.0076 |
0.347 |
|
| 1996 |
Abbruzzese C, Krahe R, Liguori M, Tessarolo D, Siciliano MJ, Ashizawa T, Giacanelli M. Myotonic dystrophy phenotype without expansion of (CTG)n repeat: an entity distinct from proximal myotonic myopathy (PROMM)? Journal of Neurology. 243: 715-21. PMID 8923304 DOI: 10.1007/Bf00873977 |
0.409 |
|
| 1995 |
Boucher CA, King SK, Carey N, Krahe R, Winchester CL, Rahman S, Creavin T, Meghji P, Bailey ME, Chartier FL. A novel homeodomain-encoding gene is associated with a large CpG island interrupted by the myotonic dystrophy unstable (CTG)n repeat. Human Molecular Genetics. 4: 1919-25. PMID 8595416 DOI: 10.1093/Hmg/4.10.1919 |
0.405 |
|
| 1995 |
Hobson GM, Krahe R, Garcia E, Siciliano MJ, Funanage VL. Regional chromosomal assignments for four members of the MADS domain transcription enhancer factor 2 (MEF2) gene family to human chromosomes 15q26, 19p12, 5q14, and 1q12-q23. Genomics. 29: 704-11. PMID 8575763 DOI: 10.1006/Geno.1995.9007 |
0.374 |
|
| 1995 |
Krahe R, Ashizawa T, Abbruzzese C, Roeder E, Carango P, Giacanelli M, Funanage VL, Siciliano MJ. Effect of myotonic dystrophy trinucleotide repeat expansion on DMPK transcription and processing. Genomics. 28: 1-14. PMID 7590731 DOI: 10.1006/Geno.1995.1099 |
0.366 |
|
| Low-probability matches (unlikely to be authored by this person) |
| 2003 |
Colella S, Shen L, Baggerly KA, Issa JP, Krahe R. Sensitive and quantitative universal Pyrosequencing methylation analysis of CpG sites. Biotechniques. 35: 146-50. PMID 12866414 DOI: 10.2144/03351Md01 |
0.298 |
|
| 2009 |
Salisbury E, Schoser B, Schneider-Gold C, Wang GL, Huichalaf C, Jin B, Sirito M, Sarkar P, Krahe R, Timchenko NA, Timchenko LT. Expression of RNA CCUG repeats dysregulates translation and degradation of proteins in myotonic dystrophy 2 patients. The American Journal of Pathology. 175: 748-62. PMID 19590039 DOI: 10.2353/Ajpath.2009.090047 |
0.294 |
|
| 2009 |
Hu J, He X, Cote GJ, Krahe R. Singular Value Decomposition-based Alternative Splicing Detection. Journal of the American Statistical Association. 104: 944-953. PMID 20305737 DOI: 10.1198/Jasa.2009.Ap08283 |
0.293 |
|
| 2018 |
Larsson CA, Moyer SM, Liu B, Michel KA, Pant V, Yang P, Wong J, El-Naggar AK, Krahe R, Lozano G. Synergistic and additive effect of retinoic acid in circumventing resistance to p53 restoration. Proceedings of the National Academy of Sciences of the United States of America. PMID 29440484 DOI: 10.1073/Pnas.1719001115 |
0.29 |
|
| 1996 |
Iyer GS, Krahe R, Goodwin LA, Doggett NA, Siciliano MJ, Funanage VL, Proujansky R. Identification of a testis-expressed creatine transporter gene at 16p11.2 and confirmation of the X-linked locus to Xq28. Genomics. 34: 143-6. PMID 8661037 DOI: 10.1006/Geno.1996.0254 |
0.289 |
|
| 2017 |
Jonson P, Krahe R, Richard I, Peng B, Hackman P, Udd B. Unexpected gene expression findings in the titinopathy mouse model FINmaj-KI using RNA-Seq Neuromuscular Disorders. 27: S237. DOI: 10.1016/J.Nmd.2017.06.512 |
0.289 |
|
| 1999 |
Krahe R, Palatini J, Ashizawa T, Virtaneva K. DNA microarray-based profiling of global gene-expression changes in myotonic dystrophy Nature Genetics. 23: 56-56. DOI: 10.1038/14342 |
0.287 |
|
| 2009 |
Cheung HC, Hai T, Zhu W, Baggerly KA, Tsavachidis S, Krahe R, Cote GJ. Splicing factors PTBP1 and PTBP2 promote proliferation and migration of glioma cell lines. Brain : a Journal of Neurology. 132: 2277-88. PMID 19506066 DOI: 10.1093/Brain/Awp153 |
0.285 |
|
| 1995 |
Krahe R, Eckhart M, Ogunniyi AO, Osuntokun BO, Siciliano MJ, Ashizawa T. De novo myotonic dystrophy mutation in a Nigerian kindred. American Journal of Human Genetics. 56: 1067-74. PMID 7726160 |
0.282 |
|
| 2001 |
Zhuo D, Zhao W, Yang HY, Wang JP, Sears R, Kwon DH, Gordon D, Gibbs S, Dean D, Baer T, Stredney D, Stutz A, Krahe R, Wright F, Yuan B. Physical mapping and functional annotation of 60, 000 human genes Nature Genetics. 27: 98. DOI: 10.1038/87378 |
0.28 |
|
| 2005 |
Bachinski LL, Olufemi SE, Zhou X, Wu CC, Yip L, Shete S, Lozano G, Amos CI, Strong LC, Krahe R. Genetic mapping of a third Li-Fraumeni syndrome predisposition locus to human chromosome 1q23. Cancer Research. 65: 427-31. PMID 15695383 |
0.277 |
|
| 2016 |
Suominen T, Bachinski L, Raheem O, Haapasalo H, Kress W, Krahe R, Udd B. DM2-linked myopathy caused by uninterrupted short (CCTG)50–70 repeat expansion in CNBP Neuromuscular Disorders. 26. DOI: 10.1016/J.Nmd.2016.06.392 |
0.276 |
|
| 2006 |
Raheem O, Holmlund-Hampf J, Suominen T, Vihola A, Haapasalo H, Krahe R, Udd B. P.P.2 02 Aberrant DMPK expression in DM1 and DM2 patients Neuromuscular Disorders. 16: 670-671. DOI: 10.1016/J.Nmd.2006.05.096 |
0.272 |
|
| 2007 |
Suominen T, Auvinen S, Hannonen P, Kontula K, Krahe R, Udd B. G.P.14.16 Myotonic dystrophy type 2 (DM2) may be misdiagnosed as fibromyalgia Neuromuscular Disorders. 17: 858-859. DOI: 10.1016/J.Nmd.2007.06.325 |
0.269 |
|
| 2009 |
Edwards SF, Sirito M, Krahe R, Sinden RR. A Z-DNA sequence reduces slipped-strand structure formation in the myotonic dystrophy type 2 (CCTG) x (CAGG) repeat. Proceedings of the National Academy of Sciences of the United States of America. 106: 3270-5. PMID 19218442 DOI: 10.1073/Pnas.0807699106 |
0.268 |
|
| 2007 |
Raheem O, Holmlund-Hapf J, Vihola A, Suominen T, Haapasalo H, Krahe R, Udd B. G.P.14.17 Abnormal expression of DMPK substrate phospholamban in DM2 Neuromuscular Disorders. 17: 859. DOI: 10.1016/J.Nmd.2007.06.326 |
0.253 |
|
| 2009 |
Richards KL, Zhang B, Baggerly KA, Colella S, Lang JC, Schuller DE, Krahe R. Genome-wide hypomethylation in head and neck cancer is more pronounced in HPV-negative tumors and is associated with genomic instability. Plos One. 4: e4941. PMID 19293934 DOI: 10.1371/Journal.Pone.0004941 |
0.251 |
|
| 2009 |
Lott ST, Chen N, Chandler DS, Yang Q, Wang L, Rodriguez M, Xie H, Balasenthil S, Buchholz TA, Sahin AA, Chaung K, Zhang B, Olufemi SE, Chen J, Adams H, ... ... Krahe R, et al. DEAR1 is a dominant regulator of acinar morphogenesis and an independent predictor of local recurrence-free survival in early-onset breast cancer. Plos Medicine. 6: e1000068. PMID 19536326 DOI: 10.1371/Journal.Pmed.1000068 |
0.246 |
|
| 2009 |
Wang Y, Carlton VE, Karlin-Neumann G, Sapolsky R, Zhang L, Moorhead M, Wang ZC, Richardson AL, Warren R, Walther A, Bondy M, Sahin A, Krahe R, Tuna M, Thompson PA, et al. High quality copy number and genotype data from FFPE samples using Molecular Inversion Probe (MIP) microarrays. Bmc Medical Genomics. 2: 8. PMID 19228381 DOI: 10.1186/1755-8794-2-8 |
0.245 |
|
| 2001 |
Wright FA, Lemon WJ, Zhao WD, Sears R, Zhuo D, Wang JP, Yang HY, Baer T, Stredney D, Spitzner J, Stutz A, Krahe R, Yuan B. A draft annotation and overview of the human genome. Genome Biology. 2: RESEARCH0025. PMID 11516338 DOI: 10.1186/Gb-2001-2-7-Research0025 |
0.239 |
|
| 2015 |
Chen Q, Zhang L, de Crombrugghe B, Krahe R. Mesenchyme-specific overexpression of nucleolar protein 66 in mice inhibits skeletal growth and bone formation. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 29: 2555-65. PMID 25746793 DOI: 10.1096/Fj.14-258970 |
0.238 |
|
| 2001 |
Barkardottir RB, Sarantaus L, Arason A, Vehmanen P, Bendahl PO, Kainu T, Syrjäkoski K, Krahe R, Huusko P, Pyrhönen S, Holli K, Kallioniemi OP, Egilsson V, Kere J, Nevanlinna H. Haplotype analysis in Icelandic and Finnish BRCA2 999del5 breast cancer families. European Journal of Human Genetics : Ejhg. 9: 773-9. PMID 11781689 DOI: 10.1038/sj.ejhg.5200717 |
0.235 |
|
| 1998 |
Virtaneva K, Paulin L, Krahe R, de la Chapelle A, Lehesjoki AE. The minisatellite expansion mutation in EPM1: resolution of an initial discrepancy. Mutatations in brief no. 186. Online. Human Mutation. 12: 218. PMID 10660338 |
0.223 |
|
| 2011 |
Richards KL, Zhang B, Sun M, Dong W, Churchill J, Bachinski LL, Wilson CD, Baggerly KA, Yin G, Hayes DN, Wistuba II, Krahe R. Methylation of the candidate biomarker TCF21 is very frequent across a spectrum of early-stage nonsmall cell lung cancers. Cancer. 117: 606-17. PMID 20945327 DOI: 10.1002/Cncr.25472 |
0.223 |
|
| 2001 |
Rantamäki M, Krahe R, Paetau A, Cormand B, Mononen I, Udd B. Adult-onset autosomal recessive ataxia with thalamic lesions in a Finnish family. Neurology. 57: 1043-9. PMID 11571332 DOI: 10.1212/Wnl.57.6.1043 |
0.221 |
|
| 2000 |
Sarantaus L, Huusko P, Eerola H, Launonen V, Vehmanen P, Rapakko K, Gillanders E, Syrjäkoski K, Kainu T, Vahteristo P, Krahe R, Pääkkönen K, Hartikainen J, Blomqvist C, Löppönen T, et al. Multiple founder effects and geographical clustering of BRCA1 and BRCA2 families in Finland. European Journal of Human Genetics : Ejhg. 8: 757-63. PMID 11039575 DOI: 10.1038/Sj.Ejhg.5200529 |
0.22 |
|
| 2005 |
Rotondo G, Sansone V, Cardani R, Mancinelli E, Krahe R, Stangalini D, Meola G. Proximal myotonic dystrophy mimicking progressive muscular atrophy. European Journal of Neurology : the Official Journal of the European Federation of Neurological Societies. 12: 160-1. PMID 15679706 DOI: 10.1111/J.1468-1331.2004.01032.X |
0.22 |
|
| 2022 |
Morales F, Corrales E, Vásquez M, Zhang B, Fernández H, Alvarado F, Cortés S, Santamaría-Ulloa C, Krahe R, Monckton DG. Individual-specific levels of CTG•CAG somatic instability are shared across multiple tissues in myotonic dystrophy type 1. Human Molecular Genetics. PMID 36099027 DOI: 10.1093/hmg/ddac231 |
0.22 |
|
| 2006 |
Simeone AM, Colella S, Krahe R, Johnson MM, Mora E, Tari AM. N-(4-Hydroxyphenyl)retinamide and nitric oxide pro-drugs exhibit apoptotic and anti-invasive effects against bone metastatic breast cancer cells. Carcinogenesis. 27: 568-77. PMID 16199439 DOI: 10.1093/Carcin/Bgi233 |
0.215 |
|
| 1999 |
Kozyraki R, Fyfe J, Kristiansen M, Gerdes C, Jacobsen C, Cui S, Christensen EI, Aminoff M, de la Chapelle A, Krahe R, Verroust PJ, Moestrup SK. The intrinsic factor-vitamin B12 receptor, cubilin, is a high-affinity apolipoprotein A-I receptor facilitating endocytosis of high-density lipoprotein. Nature Medicine. 5: 656-61. PMID 10371504 DOI: 10.1038/9504 |
0.211 |
|
| 2006 |
Udd B, Meola G, Krahe R, Thornton C, Ranum LP, Bassez G, Kress W, Schoser B, Moxley R. 140th ENMC International Workshop: Myotonic Dystrophy DM2/PROMM and other myotonic dystrophies with guidelines on management. Neuromuscular Disorders : Nmd. 16: 403-13. PMID 16684600 DOI: 10.1016/J.Nmd.2006.03.010 |
0.208 |
|
| 2008 |
Colella S, Richards KL, Bachinski LL, Baggerly KA, Tsavachidis S, Lang JC, Schuller DE, Krahe R. Molecular signatures of metastasis in head and neck cancer. Head & Neck. 30: 1273-83. PMID 18642293 DOI: 10.1002/Hed.20871 |
0.205 |
|
| 1993 |
Bachinski LL, Krahe R, White BF, Wieringa B, Shaw D, Korneluk R, Thompson LH, Johnson K, Siciliano MJ. An informative panel of somatic cell hybrids for physical mapping on human chromosome 19q. American Journal of Human Genetics. 52: 375-87. PMID 8430698 |
0.196 |
|
| 2000 |
Frühwald MC, O'Dorisio MS, Rush LJ, Reiter JL, Smiraglia DJ, Wenger G, Costello JF, White PS, Krahe R, Brodeur GM, Plass C. Gene amplification in PNETs/medulloblastomas: mapping of a novel amplified gene within the MYCN amplicon. Journal of Medical Genetics. 37: 501-9. PMID 10882752 DOI: 10.1136/jmg.37.7.501 |
0.193 |
|
| 2017 |
Qian DC, Molfese DL, Jin JL, Titus AJ, He Y, Li Y, Vaissié M, Viswanath H, Baldwin PR, Krahe R, Salas R, Amos CI. Genome-wide imaging association study implicates functional activity and glial homeostasis of the caudate in smoking addiction. Bmc Genomics. 18: 740. PMID 28927378 DOI: 10.1186/S12864-017-4124-5 |
0.183 |
|
| 2021 |
Morales F, Corrales E, Zhang B, Vásquez M, Santamaría-Ulloa C, Quesada H, Sirito M, Estecio MR, Monckton DG, Krahe R. Myotonic dystrophy type 1 (DM1) clinical sub-types and CTCF site methylation status flanking the CTG expansion are mutant allele length-dependent. Human Molecular Genetics. PMID 34432028 DOI: 10.1093/hmg/ddab243 |
0.174 |
|
| 2001 |
Pääkkönen K, Sauramo S, Sarantaus L, Vahteristo P, Hartikainen A, Vehmanen P, Ignatius J, Ollikainen V, Kääriäinen H, Vauramo E, Nevanlinna H, Krahe R, Holli K, Kere J. Involvement of BRCA1 and BRCA2 in breast cancer in a western Finnish sub-population. Genetic Epidemiology. 20: 239-46. PMID 11180449 DOI: 10.1002/1098-2272(200102)20:2<239::AID-GEPI6>3.0.CO;2-Y |
0.159 |
|
| 2019 |
Schoser B, Montagnese F, Bassez G, Fossati B, Gamez J, Heatwole C, Hilbert J, Kornblum C, Kostera-Pruszczyk A, Krahe R, Lusakowska A, Meola G, Moxley R, Thornton C, Udd B, et al. Consensus-based care recommendations for adults with myotonic dystrophy type 2. Neurology. Clinical Practice. 9: 343-353. PMID 31583190 DOI: 10.1212/CPJ.0000000000000645 |
0.15 |
|
| 2006 |
Krahe R, Bachinski LL, Udd B. Myotonic dystrophy type 2: Clinical and genetic aspects Genetic Instabilities and Neurological Diseases, Second Edition. 131-150. DOI: 10.1016/B978-012369462-1/50009-0 |
0.144 |
|
| 2003 |
Auvinen S, Vihola A, Krahe R, Kupila J, Hackman P, Hietaharju A, Udd B. [A new type of myotonic dystrophy]. Duodecim; Lã¤ã¤Ketieteellinen Aikakauskirja. 119: 707-13. PMID 12806729 |
0.127 |
|
| 2015 |
Chen Q, Sinha K, Deng JM, Yasuda H, Krahe R, Behringer RR, de Crombrugghe B. Mesenchymal Deletion of Histone Demethylase NO66 in Mice Promotes Bone Formation. Journal of Bone and Mineral Research : the Official Journal of the American Society For Bone and Mineral Research. PMID 25736226 DOI: 10.1002/jbmr.2494 |
0.111 |
|
| 2014 |
Picq S, Alda F, Krahe R, Bermingham E. Miocene and Pliocene colonization of the Central American Isthmus by the weakly electric fish Brachyhypopomus occidentalis (Hypopomidae, Gymnotiformes) Journal of Biogeography. 41: 1520-1532. DOI: 10.1111/Jbi.12309 |
0.108 |
|
| 2014 |
Krahe R, Maler L. Neural maps in the electrosensory system of weakly electric fish. Current Opinion in Neurobiology. 24: 13-21. PMID 24492073 DOI: 10.1016/j.conb.2013.08.013 |
0.095 |
|
| 2013 |
Toscano-Márquez B, Dunn RJ, Krahe R. Distribution of muscarinic acetylcholine receptor mRNA in the brain of the weakly electric fish Apteronotus leptorhynchus. The Journal of Comparative Neurology. 521: 1054-72. PMID 22911562 DOI: 10.1002/Cne.23218 |
0.088 |
|
| 2008 |
Krahe R, Bastian J, Chacron MJ. Temporal processing across multiple topographic maps in the electrosensory system. Journal of Neurophysiology. 100: 852-67. PMID 18509073 DOI: 10.1152/Jn.90300.2008 |
0.088 |
|
| 2002 |
Rantamäki M, Krahe R, Paetau A, Cormand B, Mononen I, Udd B. [New adult-onset ataxia in a Finnish family]. Duodecim; Lã¤ã¤Ketieteellinen Aikakauskirja. 118: 2115-22. PMID 12463002 |
0.083 |
|
| 2015 |
Vardanjani HM, Baneshi MR, Haghdoost A, Krahe R. Cancer visibility among iranian familial networks: To what extent can we rely on family history reports? Plos One. 10. DOI: 10.1371/journal.pone.0136038 |
0.081 |
|
| 2005 |
Richards KL, Colella S, Baggerly KA, Tsavachidis S, Jas LC, Schuller DE, Krahe R. Genomic and transcriptomic profiling of Human Papilloma Virus (HPV)-positive head and neck squamous cell carcinomas (HNSCC) identifies a genetically distinct subgroup of head and neck cancers. Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology. 23: 5507. PMID 27945461 DOI: 10.1200/jco.2005.23.16_suppl.5507 |
0.078 |
|
| 2023 |
Chen Q, Sinha KM, de Crombrugghe B, Krahe R. Osteoblast-Specific Overexpression of Nucleolar Protein /RIOX1 in Mouse Embryos Leads to Osteoporosis in Adult Mice. Journal of Osteoporosis. 2023: 8998556. PMID 36660551 DOI: 10.1155/2023/8998556 |
0.072 |
|
| 2007 |
Simeone AM, Nieves-Alicea R, McMurtry VC, Colella S, Krahe R, Tari AM. Cyclooxygenase-2 uses the protein kinase C/ interleukin-8/urokinase-type plasminogen activator pathway to increase the invasiveness of breast cancer cells. International Journal of Oncology. 30: 785-92. PMID 17332916 |
0.068 |
|
| 2007 |
Ellis LD, Krahe R, Bourque CW, Dunn RJ, Chacron MJ. Muscarinic receptors control frequency tuning through the downregulation of an A-type potassium current. Journal of Neurophysiology. 98: 1526-37. PMID 17615127 DOI: 10.1152/Jn.00564.2007 |
0.068 |
|
| 2016 |
Picq S, Alda F, Bermingham E, Krahe R. Drift-driven evolution of electric signals in a Neotropical knifefish. Evolution; International Journal of Organic Evolution. PMID 27436179 DOI: 10.1111/Evo.13010 |
0.061 |
|
| 2016 |
Dunlap KD, Tran A, Ragazzi MA, Krahe R, Salazar VL. Predators inhibit brain cell proliferation in natural populations of electric fish, Brachyhypopomus occidentalis. Proceedings. Biological Sciences / the Royal Society. 283. PMID 26842566 DOI: 10.1098/rspb.2015.2113 |
0.061 |
|
| 1994 |
Heller KG, Krahe R. SOUND PRODUCTION AND HEARING IN THE PYRALID MOTH SYMMORACMA MINORALIS The Journal of Experimental Biology. 187: 101-11. PMID 9317421 |
0.059 |
|
| 2010 |
Stamper SA, Carrera-G E, Tan EW, Fugère V, Krahe R, Fortune ES. Species differences in group size and electrosensory interference in weakly electric fishes: implications for electrosensory processing. Behavioural Brain Research. 207: 368-76. PMID 19874855 DOI: 10.1016/j.bbr.2009.10.023 |
0.057 |
|
| 2008 |
Mehaffey WH, Ellis LD, Krahe R, Dunn RJ, Chacron MJ. Ionic and neuromodulatory regulation of burst discharge controls frequency tuning. Journal of Physiology, Paris. 102: 195-208. PMID 18992813 DOI: 10.1016/J.Jphysparis.2008.10.019 |
0.056 |
|
| 2012 |
Cuddy M, Aubin-Horth N, Krahe R. Electrocommunication behaviour and non invasively-measured androgen changes following induced seasonal breeding in the weakly electric fish, Apteronotus leptorhynchus. Hormones and Behavior. 61: 4-11. PMID 21944946 DOI: 10.1016/J.Yhbeh.2011.09.003 |
0.053 |
|
| 2000 |
Kreiman G, Krahe R, Metzner W, Koch C, Gabbiani F. Robustness and variability of neuronal coding by amplitude-sensitive afferents in the weakly electric fish eigenmannia. Journal of Neurophysiology. 84: 189-204. PMID 10899196 DOI: 10.1152/Jn.2000.84.1.189 |
0.052 |
|
| 2002 |
Krahe R, Budinger E, Ronacher B. Coding of a sexually dimorphic song feature by auditory interneurons of grasshoppers: the role of leading inhibition. Journal of Comparative Physiology. a, Neuroethology, Sensory, Neural, and Behavioral Physiology. 187: 977-85. PMID 11913816 DOI: 10.1007/s00359-001-0268-4 |
0.052 |
|
| 2013 |
Márquez BT, Krahe R, Chacron MJ. Neuromodulation of early electrosensory processing in gymnotiform weakly electric fish. The Journal of Experimental Biology. 216: 2442-50. PMID 23761469 DOI: 10.1242/Jeb.082370 |
0.052 |
|
| 2005 |
Chen L, House JL, Krahe R, Nelson ME. Modeling signal and background components of electrosensory scenes. Journal of Comparative Physiology. a, Neuroethology, Sensory, Neural, and Behavioral Physiology. 191: 331-45. PMID 15800793 DOI: 10.1007/s00359-004-0587-3 |
0.05 |
|
| 2013 |
Salazar VL, Krahe R, Lewis JE. The energetics of electric organ discharge generation in gymnotiform weakly electric fish. The Journal of Experimental Biology. 216: 2459-68. PMID 23761471 DOI: 10.1242/Jeb.082735 |
0.049 |
|
| 2000 |
Krahe R, Larsen ON, Ronacher B. Directional hearing is only weakly dependent on the rise time of acoustic stimuli. The Journal of the Acoustical Society of America. 107: 1067-70. PMID 10687720 DOI: 10.1121/1.428289 |
0.048 |
|
| 2013 |
Alda F, Picq S, de León LF, González R, Walz H, Bermingham E, Krahe R. First record of Gymnotus henni (Albert, Crampton and Maldonado, 2003) in Panama: Phylogenetic position and electric signal characterization Check List. 9: 655-659. DOI: 10.15560/9.3.655 |
0.047 |
|
| 2016 |
Metzen MG, Krahe R, Chacron MJ. Burst Firing in the Electrosensory System of Gymnotiform Weakly Electric Fish: Mechanisms and Functional Roles. Frontiers in Computational Neuroscience. 10: 81. PMID 27531978 DOI: 10.3389/Fncom.2016.00081 |
0.046 |
|
| 2002 |
Krahe R, Kreiman G, Gabbiani F, Koch C, Metzner W. Stimulus encoding and feature extraction by multiple sensory neurons. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 22: 2374-82. PMID 11896176 DOI: 10.1523/Jneurosci.22-06-02374.2002 |
0.045 |
|
| 2013 |
Fotowat H, Harrison RR, Krahe R. Statistics of the electrosensory input in the freely swimming weakly electric fish Apteronotus leptorhynchus. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 33: 13758-72. PMID 23966697 DOI: 10.1523/Jneurosci.0998-13.2013 |
0.045 |
|
| 2011 |
Savard M, Krahe R, Chacron MJ. Neural heterogeneities influence envelope and temporal coding at the sensory periphery. Neuroscience. 172: 270-84. PMID 21035523 DOI: 10.1016/J.Neuroscience.2010.10.061 |
0.044 |
|
| 2010 |
Avila-Akerberg O, Krahe R, Chacron MJ. Neural heterogeneities and stimulus properties affect burst coding in vivo. Neuroscience. 168: 300-13. PMID 20298764 DOI: 10.1016/J.Neuroscience.2010.03.012 |
0.043 |
|
| 2011 |
Reardon EE, Parisi A, Krahe R, Chapman LJ. Energetic constraints on electric signalling in wave-type weakly electric fishes. The Journal of Experimental Biology. 214: 4141-50. PMID 22116756 DOI: 10.1242/jeb.059444 |
0.041 |
|
| 2000 |
Ronacher B, Krahe R. Temporal integration vs. parallel processing: coping with the variability of neuronal messages in directional hearing of insects. The European Journal of Neuroscience. 12: 2147-56. PMID 10886354 DOI: 10.1046/j.1460-9568.2000.00102.x |
0.04 |
|
| 2011 |
Fugère V, Ortega H, Krahe R. Electrical signalling of dominance in a wild population of electric fish. Biology Letters. 7: 197-200. PMID 20980295 DOI: 10.1098/rsbl.2010.0804 |
0.039 |
|
| 2001 |
Machens CK, Stemmler MB, Prinz P, Krahe R, Ronacher B, Herz AV. Representation of acoustic communication signals by insect auditory receptor neurons. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 21: 3215-27. PMID 11312306 DOI: 10.1523/Jneurosci.21-09-03215.2001 |
0.038 |
|
| 1998 |
Ronacher B, Krahe R. Song recognition in the grasshopper Chorthippus biguttulus is not impaired by shortening song signals: Implications for neuronal encoding Journal of Comparative Physiology - a Sensory, Neural, and Behavioral Physiology. 183: 729-735. DOI: 10.1007/s003590050295 |
0.037 |
|
| 1993 |
Krahe R, Ronacher B. Long rise times of sound pulses in grasshopper songs improve the directionality cues received by the CNS from the auditory receptors Journal of Comparative Physiology A. 173: 425-434. DOI: 10.1007/BF00193515 |
0.036 |
|
| 2008 |
Ronacher B, Wohlgemuth S, Vogel A, Krahe R. Discrimination of acoustic communication signals by grasshoppers (Chorthippus biguttulus): temporal resolution, temporal integration, and the impact of intrinsic noise. Journal of Comparative Psychology (Washington, D.C. : 1983). 122: 252-63. PMID 18729653 DOI: 10.1037/0735-7036.122.3.252 |
0.034 |
|
| 2011 |
van der Sluijs I, Gray SM, Amorim MCP, Barber I, Candolin U, Hendry AP, Krahe R, Maan ME, Utne-Palm AC, Wagner HJ, Wong BBM. Communication in troubled waters: Responses of fish communication systems to changing environments Evolutionary Ecology. 25: 623-640. DOI: 10.1007/S10682-010-9450-X |
0.032 |
|
| 2008 |
Krahe R. Rooted in behaviour. Journal of Physiology, Paris. 102: 154-6. PMID 18992331 DOI: 10.1016/j.jphysparis.2008.10.014 |
0.031 |
|
| 1997 |
Ronacher B, Krahe R. Long rise times of acoustic stimuli improve directional hearing in grasshoppers Naturwissenschaften. 84: 168-170. DOI: 10.1007/s001140050374 |
0.031 |
|
| 2004 |
Krahe R, Gabbiani F. Burst firing in sensory systems. Nature Reviews. Neuroscience. 5: 13-23. PMID 14661065 DOI: 10.1038/nrn1296 |
0.031 |
|
| 2010 |
Fugère V, Krahe R. Electric signals and species recognition in the wave-type gymnotiform fish Apteronotus leptorhynchus. The Journal of Experimental Biology. 213: 225-36. PMID 20038655 DOI: 10.1242/jeb.034751 |
0.03 |
|
| 2000 |
Ronacher B, Krahe R, Hennig RM. Effects of signal duration on the recognition of masked communication signals by the grasshopper Chorthippus biguttulus. Journal of Comparative Physiology. a, Sensory, Neural, and Behavioral Physiology. 186: 1065-72. PMID 11195282 DOI: 10.1007/S003590000153 |
0.029 |
|
| 1995 |
Fadul F, Krahe R. Microprocessor based inverse-time multiple overcurrent relays Electric Power Systems Research. 35: 207-211. DOI: 10.1016/0378-7796(95)01004-1 |
0.028 |
|
| 2010 |
Pollack G, Krahe R. Signal Identification: Peripheral and Central Mechanisms Encyclopedia of Neuroscience. 799-804. DOI: 10.1016/B978-008045046-9.01818-0 |
0.028 |
|
| 2013 |
Krahe R, Fortune ES. Electric fishes: neural systems, behaviour and evolution. The Journal of Experimental Biology. 216: 2363-4. PMID 23761461 DOI: 10.1242/jeb.091322 |
0.026 |
|
| 1999 |
Fuhr G, Ronacher B, Krahe R, Fest S, Shirley SG, Rogaschewski S. UV-laser ablation of sensory cells in living insects Applied Physics a: Materials Science and Processing. 68: 379-385. DOI: 10.1007/s003390050909 |
0.017 |
|
| 1999 |
Marande RP, Krahe RP, Fadul FK. A self-tuning microcontroller-based glass measuring instrument Computers and Electrical Engineering. 25: 493-500. |
0.014 |
|
| 1996 |
Krahe RP, Russell TE. Low power embedded control design Asee Annual Conference Proceedings. 2185-2196. |
0.012 |
|
| 2003 |
Loker DR, Krahe RP. Visual C++ applications in an EET curriculum Asee Annual Conference Proceedings. 6779-6791. |
0.012 |
|
| 1994 |
Fadul FK, Krahe RP. A DSP-based power integrated circuit controller/driver board for stepper motors Mechatronics. 4: 393-399. DOI: 10.1016/0957-4158(94)90019-1 |
0.012 |
|
| 2009 |
Nitterright F, Krahe R. Development of a solid modeling course for Electrical and Computer Engineering Technology (ECET) students Asee Annual Conference and Exposition, Conference Proceedings. |
0.01 |
|
| 2005 |
Krahe R. Software engineering standards in the ECET curriculum Asee Annual Conference and Exposition, Conference Proceedings. 12811-12818. |
0.01 |
|
| 2004 |
Loker DR, Krahe RP, Kirsch J, Yowonske TJ, Cunningham RJ, Petrovich JR. Remote sensing with GPS sensor and cellular modem Asee Annual Conference Proceedings. 11987-12001. |
0.01 |
|
| 2003 |
Krahe RP. Teach less better Asee Annual Conference Proceedings. 11869-11876. |
0.01 |
|
| 2001 |
Bar-Cohen Y, Sherrit S, Dolgin BP, Bao X, Chang Z, Pal DS, Krahe R, Kroh J, Du S, Peterson T. Ultrasonic/sonic drilling/coring (USDC) for planetary applications Proceedings of Spie - the International Society For Optical Engineering. 4327: 441-448. DOI: 10.1117/12.436556 |
0.01 |
|
| 1996 |
Krahe RP, Fadul FK. Industrial electronic glaziometer using linear array detector Measurement: Journal of the International Measurement Confederation. 18: 27-33. DOI: 10.1016/0263-2241(96)00041-3 |
0.01 |
|
| 1993 |
Krahe RP. Design oriented microcomputer lab project Proceedings - Frontiers in Education Conference, Fie. 826. DOI: 10.1109/FIE.1993.405401 |
0.01 |
|
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