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Christoph Preuss - Publications

Affiliations: 
The Jackson Laboratory, Bar Harbor, ME, United States 
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43 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2024 Sasner M, Preuss C, Pandey RS, Uyar A, Garceau D, Kotredes KP, Williams H, Oblak AL, Lin PB, Perkins B, Soni D, Ingraham C, Lee-Gosselin A, Lamb BT, Howell GR, et al. In vivo validation of late-onset Alzheimer's disease genetic risk factors. Alzheimer's & Dementia : the Journal of the Alzheimer's Association. PMID 38687251 DOI: 10.1002/alz.13840  0.642
2023 Sasner M, Preuss C, Pandey RS, Uyar A, Garceau D, Kotredes KP, Williams H, Oblak AL, Lin PB, Perkins B, Soni D, Ingraham C, Lee-Gosselin A, Lamb BT, Howell GR, et al. validation of late-onset Alzheimer's disease genetic risk factors. Biorxiv : the Preprint Server For Biology. PMID 38187758 DOI: 10.1101/2023.12.21.572849  0.641
2023 Barendrecht S, Schreurs A, Geissler S, Sabanov V, Ilse V, Rieckmann V, Eichentopf R, Künemund A, Hietel B, Wussow S, Hoffmann K, Körber-Ferl K, Pandey R, Carter GW, Demuth HU, ... ... Preuss C, et al. A novel human tau knock-in mouse model reveals interaction of Abeta and human tau under progressing cerebral amyloidosis in 5xFAD mice. Alzheimer's Research & Therapy. 15: 16. PMID 36641439 DOI: 10.1186/s13195-022-01144-y  0.477
2021 Li Y, Haber A, Preuss C, John C, Uyar A, Yang HS, Logsdon BA, Philip V, Karuturi RKM, Carter GW. Transfer learning-trained convolutional neural networks identify novel MRI biomarkers of Alzheimer's disease progression. Alzheimer's & Dementia (Amsterdam, Netherlands). 13: e12140. PMID 34027015 DOI: 10.1002/dad2.12140  0.604
2020 Mukherjee S, Heath L, Preuss C, Jayadev S, Garden GA, Greenwood AK, Sieberts SK, De Jager PL, Ertekin-Taner N, Carter GW, Mangravite LM, Logsdon BA. Author Correction: Molecular estimation of neurodegeneration pseudotime in older brains. Nature Communications. 11: 6307. PMID 33273466 DOI: 10.1038/s41467-020-20261-6  0.394
2020 Mukherjee S, Heath L, Preuss C, Jayadev S, Garden GA, Greenwood AK, Sieberts SK, De Jager PL, Ertekin-Taner N, Carter GW, Mangravite LM, Logsdon BA. Molecular estimation of neurodegeneration pseudotime in older brains. Nature Communications. 11: 5781. PMID 33188183 DOI: 10.1038/s41467-020-19622-y  0.564
2020 Preuss C, Pandey R, Piazza E, Fine A, Uyar A, Perumal T, Garceau D, Kotredes KP, Williams H, Mangravite LM, Lamb BT, Oblak AL, Howell GR, Sasner M, Logsdon BA, et al. A novel systems biology approach to evaluate mouse models of late-onset Alzheimer's disease. Molecular Neurodegeneration. 15: 67. PMID 33172468 DOI: 10.1186/s13024-020-00412-5  0.639
2020 Wan YW, Al-Ouran R, Mangleburg CG, Perumal TM, Lee TV, Allison K, Swarup V, Funk CC, Gaiteri C, Allen M, Wang M, Neuner SM, Kaczorowski CC, Philip VM, Howell GR, ... ... Preuss C, et al. Meta-Analysis of the Alzheimer's Disease Human Brain Transcriptome and Functional Dissection in Mouse Models. Cell Reports. 32: 107908. PMID 32668255 DOI: 10.1016/J.Celrep.2020.107908  0.604
2020 Milind N, Preuss C, Haber A, Ananda G, Mukherjee S, John C, Shapley S, Logsdon BA, Crane PK, Carter GW. Transcriptomic stratification of late-onset Alzheimer's cases reveals novel genetic modifiers of disease pathology. Plos Genetics. 16: e1008775. PMID 32492070 DOI: 10.1371/Journal.Pgen.1008775  0.609
2019 Pandey RS, Graham L, Uyar A, Preuss C, Howell GR, Carter GW. Genetic perturbations of disease risk genes in mice capture transcriptomic signatures of late-onset Alzheimer's disease. Molecular Neurodegeneration. 14: 50. PMID 31878951 DOI: 10.1186/S13024-019-0351-3  0.683
2019 Wünnemann F, Ta-Shma A, Preuss C, Leclerc S, van Vliet PP, Oneglia A, Thibeault M, Nordquist E, Lincoln J, Scharfenberg F, Becker-Pauly C, Hofmann P, Hoff K, Audain E, Kramer HH, et al. Loss of ADAMTS19 causes progressive non-syndromic heart valve disease. Nature Genetics. PMID 31844321 DOI: 10.1038/S41588-019-0536-2  0.422
2019 Mukherjee S, Perumal TM, Daily K, Sieberts SK, Omberg L, Preuss C, Carter GW, Mangravite LM, Logsdon BA. Identifying and ranking potential driver genes of Alzheimer's disease using multiview evidence aggregation. Bioinformatics (Oxford, England). 35: i568-i576. PMID 31510680 DOI: 10.1093/Bioinformatics/Btz365  0.622
2019 Buchanan RA, Foley KE, Pepper KW, Reagan AM, Keezer KJ, Hewes AA, Diemler CA, Preuss C, Soto I, John SWM, Howell GR. Meox2 Haploinsufficiency Accelerates Axonal Degeneration in DBA/2J Glaucoma. Investigative Ophthalmology & Visual Science. 60: 3283-3296. PMID 31369031 DOI: 10.1167/Iovs.18-26126  0.375
2019 Onos KD, Uyar A, Keezer KJ, Jackson HM, Preuss C, Acklin CJ, O'Rourke R, Buchanan R, Cossette TL, Sukoff Rizzo SJ, Soto I, Carter GW, Howell GR. Enhancing face validity of mouse models of Alzheimer's disease with natural genetic variation. Plos Genetics. 15: e1008155. PMID 31150388 DOI: 10.1371/Journal.Pgen.1008155  0.558
2019 Salimova E, Nowak KJ, Estrada AC, Furtado MB, McNamara E, Nguyen Q, Balmer L, Preuss C, Holmes JW, Ramialison M, Morahan G, Rosenthal NA. Variable outcomes of human heart attack recapitulated in genetically diverse mice. Npj Regenerative Medicine. 4: 5. PMID 30854227 DOI: 10.1038/S41536-019-0067-6  0.37
2019 Luyckx I, Kumar AA, Reyniers E, Dekeyser E, Vanderstraeten K, Vandeweyer G, Wünnemann F, Preuss C, Mazzella JM, Goudot G, Messas E, Albuisson J, Jeunemaitre X, Eriksson P, Mohamed SA, et al. Copy number variation analysis in bicuspid aortic valve-related aortopathy identifies TBX20 as a contributing gene. European Journal of Human Genetics : Ejhg. PMID 30820038 DOI: 10.1038/s41431-019-0364-y  0.356
2019 Mukherjee S, Preuss C, Greenwood AK, Jayadev S, Garden GA, Carter GW, Mangravite LM, Logsdon BA. P4-119: MOLECULAR ESTIMATION OF ALZHEIMER'S DISEASE PROGRESSION Alzheimer's & Dementia. 15: P1321-P1322. DOI: 10.1016/J.Jalz.2019.06.3780  0.442
2019 Uyar A, Oblak AL, Williams HM, Pandey RS, Kotredes KP, Preuss C, Logsdon BA, Sukoff Rizzo SJ, Howell G, Lamb BT, Sasner M, Carter GW. P4-098: TRANSCRIPTOMIC ALTERATIONS DRIVEN BY THE TREM2*R47H ALLELE VARY ACROSS DIFFERENT TRANSGENIC MOUSE MODELS Alzheimer's & Dementia. 15: P1312-P1313. DOI: 10.1016/J.Jalz.2019.06.3758  0.327
2019 Oblak AL, Williams HM, Jadhav V, Tsai A, Soni D, Ingraham C, Kotredes KP, Uyar A, Pandey RS, Preuss C, Logsdon B, Territo PR, Rizzo SJS, Sasner M, Carter GW, et al. P4-091: The Trem2*R47H Variant Alters Expression And Function In Mouse Models Of Alzheimer'S Disease Alzheimers & Dementia. 15. DOI: 10.1016/J.Jalz.2019.06.3751  0.492
2019 Preuss C, Logsdon BA, Milind N, Harber A, Uyar A, Pandey RS, Perumal TM, Mangravite LM, Howell G, Sasner M, Mukherjee S, Crane PK, Carter GW. P3-142: Stratification Of Alzheimer'S Patients Using Postmortem Brain Co-Expression Data Reveals Novel Genetic Modifiers Mediating Inflammatory Aging Alzheimers & Dementia. 15. DOI: 10.1016/J.Jalz.2019.06.3170  0.429
2019 Sasner M, Oblak AL, Preuss C, Garceau D, Williams H, Kotredes KP, Ingraham C, Pandey RS, Uyar A, Soni D, Logsdon BA, Lamb BT, Carter GW, Howell G. P2-133: Initial Characterization Of Novel Mouse Models Of Late Onset Alzheimer'S Disease Based On Human Genetic Associations Alzheimers & Dementia. 15. DOI: 10.1016/J.Jalz.2019.06.2540  0.554
2019 Kotredes KP, Preuss C, Pandey RS, Williams HM, Territo PR, Oblak AL, Lamb BT, Rizzo SJS, Carter GW, Sasner M, Howell G. P2-131: Novel Apoe4.Trem2*R47H Mouse Model: A Better Tool For Late-Onset Alzheimer'S Disease Alzheimers & Dementia. 15. DOI: 10.1016/J.Jalz.2019.06.2538  0.495
2019 Preuss C, Pandey RS, Fine A, Uyar A, Logsdon BA, Perumal TM, Piazza E, Rullo E, Kuhar J, Bailey C, Mangravite LM, Howell G, Sasner M, Carter GW. P2-105: A Novel Systems Biology Approach To Evaluate Mouse Models Of Late Onset Alzheimer'S Disease: Ncounter Mouse Ad Panel Alzheimers & Dementia. 15. DOI: 10.1016/J.Jalz.2019.06.2512  0.461
2018 Nelson D, Moreau C, de Vriendt M, Zeng Y, Preuss C, Vézina H, Milot E, Andelfinger G, Labuda D, Gravel S. Inferring Transmission Histories of Rare Alleles in Population-Scale Genealogies. American Journal of Human Genetics. 103: 893-906. PMID 30526866 DOI: 10.1016/J.Ajhg.2018.10.017  0.343
2018 Gould RA, Aziz H, Woods CE, Seman-Senderos MA, Sparks E, Preuss C, Wünnemann F, Bedja D, Moats CR, McClymont SA, Rose R, Sobreira N, Ling H, MacCarrick G, Kumar AA, et al. ROBO4 variants predispose individuals to bicuspid aortic valve and thoracic aortic aneurysm. Nature Genetics. PMID 30455415 DOI: 10.1038/S41588-018-0265-Y  0.389
2018 Pandey RS, Graham L, Uyar A, Preuss C, Howell G, Carter GW. P4-046: Transcriptomic Analysis Of Mouse Models Based On Candidate Genes Associated With Alzheimer'S Disease Alzheimers & Dementia. 14. DOI: 10.1016/J.Jalz.2018.06.2448  0.511
2018 Sasner M, Williams HM, Oblak AL, O'Rourke R, Preuss C, Saykin AJ, Rizzo SJS, Ananda G, Philip V, Carter GW, Lamb BT, Howell G. P4-031: Novel Models Of Late-Onset Alzheimer'S Disease Based On Gwas Alzheimers & Dementia. 14. DOI: 10.1016/J.Jalz.2018.06.2433  0.496
2017 Gillis E, Kumar AA, Luyckx I, Preuss C, Cannaerts E, van de Beek G, Wieschendorf B, Alaerts M, Bolar N, Vandeweyer G, Meester J, Wünnemann F, Gould RA, Zhurayev R, Zerbino D, et al. Candidate Gene Resequencing in a Large Bicuspid Aortic Valve-Associated Thoracic Aortic Aneurysm Cohort: SMAD6 as an Important Contributor. Frontiers in Physiology. 8: 400. PMID 28659821 DOI: 10.3389/Fphys.2017.00400  0.378
2017 Wu JW, Preuss C, Wang SP, Yang H, Ji B, Carter GW, Gladdy R, Andelfinger G, Mitchell GA. Epistatic interaction between the lipase-encoding genes Pnpla2 and Lipe causes liposarcoma in mice. Plos Genetics. 13: e1006716. PMID 28459858 DOI: 10.1371/Journal.Pgen.1006716  0.489
2017 Wang X, Preuss C, Philip V, Ananda G, Acklin C, Karuturi KM, Sasner M, Howell G, Carter GW. Novel Candidate Loci For Late-Onset Alzheimer’S Disease From Bayesian Mixed Modeling Of Whole-Genome And Whole-Exome Sequencing Alzheimers & Dementia. 13: 1490. DOI: 10.1016/J.Jalz.2017.07.574  0.434
2017 Sasner M, Carter GW, Howell G, Rizzo SJ, Williams HM, Preuss C, Wang X, Philip V, Ananda G, Uyar A, Onos K, Logsdon B, Omberg L, Mangravite LM, Lamb BT, et al. [P4-060]: MODEL ORGANISM DEVELOPMENT AND EVALUATION FOR LATE-ONSET ALZHEIMER's DISEASE: MODEL-AD Alzheimer's & Dementia. 13: P1280-P1281. DOI: 10.1016/J.Jalz.2017.06.1925  0.423
2016 Preuss C, Capredon M, Wünnemann F, Chetaille P, Prince A, Godard B, Leclerc S, Sobreira N, Ling H, Awadalla P, Thibeault M, Khairy P, Samuels ME, Andelfinger G. Family Based Whole Exome Sequencing Reveals the Multifaceted Role of Notch Signaling in Congenital Heart Disease. Plos Genetics. 12: e1006335. PMID 27760138 DOI: 10.1371/Journal.Pgen.1006335  0.356
2014 Greenway SC, McLeod R, Hume S, Roslin NM, Alvarez N, Giuffre M, Zhan SH, Shen Y, Preuss C, Andelfinger G, Jones SJ, Gerull B. Exome sequencing identifies a novel variant in ACTC1 associated with familial atrial septal defect. The Canadian Journal of Cardiology. 30: 181-7. PMID 24461919 DOI: 10.1016/J.Cjca.2013.12.003  0.446
2013 Preuss C, Andelfinger G. Genetics of Heart Failure in Congenital Heart Disease Canadian Journal of Cardiology. 29: 803-810. PMID 23706783 DOI: 10.1016/J.Cjca.2013.03.011  0.334
2013 Capredon M, Preuss C, Grenier J, Bruat V, de Malliard T, Leclerc S, Privé C, Thibeault M, Chetaille P, Samuel M, Awadalla P, Andelfinger G. Impact of Rare Genetic Variations on Left Ventricular Outflow Tract Obstruction: Lessons From Whole Exome Sequencing Canadian Journal of Cardiology. 29: S243. DOI: 10.1016/J.Cjca.2013.07.393  0.345
2013 Preuss C, Capredon M, Asselin G, Dubé M, Samuels M, Awadalla P, Chetaille P, Andelfinger G. Linkage Mapping and Whole-Exome Sequencing in a Family With Left Ventricular Outflow Tract Obstruction Canadian Journal of Cardiology. 29: S88. DOI: 10.1016/J.Cjca.2013.07.098  0.409
2013 Preuss C, Yang S, Capredon M, Samuels M, Awadalla P, Chetaille P, Andelfinger G. Composite Effects of Rare Variants in a Novel X-Linked Form of Congenital Heart Disease in the Québec Founder Population Canadian Journal of Cardiology. 29: S87. DOI: 10.1016/J.Cjca.2013.07.097  0.364
2012 Preuss C, Riemenschneider M, Wiedmann D, Stoll M. Evolutionary dynamics of co-segregating gene clusters associated with complex diseases. Plos One. 7: e36205. PMID 22606245 DOI: 10.1371/Journal.Pone.0036205  0.442
2011 Preuss C, Stoll M. Inherited risk factors for thrombotic diseases in children: the genome-wide perspective. Seminars in Thrombosis and Hemostasis. 37: 848-55. PMID 22187409 DOI: 10.1055/S-0031-1297177  0.417
2008 Reusch TB, Veron AS, Preuss C, Weiner J, Wissler L, Beck A, Klages S, Kube M, Reinhardt R, Bornberg-Bauer E. Comparative analysis of expressed sequence tag (EST) libraries in the seagrass Zostera marina subjected to temperature stress. Marine Biotechnology (New York, N.Y.). 10: 297-309. PMID 18239962 DOI: 10.1007/S10126-007-9065-6  0.31
2006 Preuss C, Wang X, Ananda G, Neuner SM, Philip V, Nho K, Logsdon B, Lamb BT, Kaczorowski CC, Sasner M, Howell GR, Carter GW. O4-01-06: WHOLE-EXOME ANALYSIS OF LATE-ONSET ALZHEIMER'S DISEASE REVEALS NOVEL CANDIDATE GENES INVOLVED IN COGNITIVE FUNCTION Alzheimer's & Dementia. 14: P1402-P1402. DOI: 10.1016/J.Jalz.2018.06.2914  0.435
2006 Logsdon BA, Perumal TM, Daily K, Sieberts SK, Omberg L, Mangravite LM, Preuss C, Carter GW. O3-03-02: SYSTEMS BIOLOGY RANKING OF CANDIDATE ALZHEIMER'S DRIVER GENES IDENTIFIES NEW GENETIC DRIVERS OF ALZHEIMER'S DISEASE ETIOLOGY Alzheimer's & Dementia. 14: P1015-P1015. DOI: 10.1016/J.Jalz.2018.06.2783  0.494
2006 Onos KD, Keezer KJ, Williams HM, Preuss C, Acklin C, O'Rourke R, Buchanan R, Cossette TL, Carter GW, Sukoff Rizzo SJ, Soto I, Howell GR. O1-01-03: GENETICALLY DIVERSE MOUSE MODELS OF ALZHEIMER'S DISEASE EXHIBIT DIFFERENTIAL MYELOID CELL RESPONSE AND NEURODEGENERATION Alzheimer's & Dementia. 14: P212-P213. DOI: 10.1016/J.Jalz.2018.06.2332  0.468
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