دنبال کردن
Bernie Devlin
Bernie Devlin
University of Pittsburgh School of Medicine
ایمیل تأیید شده در upmc.edu
عنوان
نقل شده توسط
نقل شده توسط
سال
Genomic control for association studies‏
B Devlin, K Roeder‏
Biometrics 55 (4), 997-1004, 1999‏
37991999
Synaptic, transcriptional and chromatin genes disrupted in autism‏
S De Rubeis, X He, AP Goldberg, CS Poultney, K Samocha, ...‏
Nature 515 (7526), 209-215, 2014‏
29812014
De novo mutations revealed by whole-exome sequencing are strongly associated with autism‏
SJ Sanders, MT Murtha, AR Gupta, JD Murdoch, MJ Raubeson, ...‏
Nature 485 (7397), 237-241, 2012‏
24512012
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs‏
B Devlin, JR Kelsoe, P Sklar, MJ Daly, MC O'Donovan, N Craddock, ...‏
Nature genetics 45 (9), 984-994, 2013‏
24242013
Functional impact of global rare copy number variation in autism spectrum disorders‏
D Pinto, AT Pagnamenta, L Klei, R Anney, D Merico, R Regan, J Conroy, ...‏
Nature 466 (7304), 368-372, 2010‏
24092010
Identification of common genetic risk variants for autism spectrum disorder‏
J Grove, S Ripke, TD Als, M Mattheisen, RK Walters, H Won, J Pallesen, ...‏
Nature genetics 51 (3), 431-444, 2019‏
21832019
Patterns and rates of exonic de novo mutations in autism spectrum disorders‏
BM Neale, Y Kou, L Liu, A Ma’Ayan, KE Samocha, A Sabo, CF Lin, ...‏
Nature 485 (7397), 242-245, 2012‏
20932012
Large-scale exome sequencing study implicates both developmental and functional changes in the neurobiology of autism‏
FK Satterstrom, JA Kosmicki, J Wang, MS Breen, S De Rubeis, JY An, ...‏
Cell 180 (3), 568-584. e23, 2020‏
20372020
Mutations in SDHD, a Mitochondrial Complex II Gene, in Hereditary Paraganglioma‏
BE Baysal, RE Ferrell, JE Willett-Brozick, EC Lawrence, D Myssiorek, ...‏
Science 287 (5454), 848-851, 2000‏
20082000
Autism genome-wide copy number variation reveals ubiquitin and neuronal genes‏
JT Glessner, K Wang, G Cai, O Korvatska, CE Kim, S Wood, H Zhang, ...‏
Nature 459 (7246), 569-573, 2009‏
16472009
Mapping autism risk loci using genetic linkage and chromosomal rearrangements‏
Nature genetics 39 (3), 319-328, 2007‏
16452007
Insights into autism spectrum disorder genomic architecture and biology from 71 risk loci‏
SJ Sanders, X He, AJ Willsey, AG Ercan-Sencicek, KE Samocha, ...‏
Neuron 87 (6), 1215-1233, 2015‏
15832015
Multiple recurrent de novo CNVs, including duplications of the 7q11. 23 Williams syndrome region, are strongly associated with autism‏
SJ Sanders, AG Ercan-Sencicek, V Hus, R Luo, MT Murtha, ...‏
Neuron 70 (5), 863-885, 2011‏
15382011
Most genetic risk for autism resides with common variation‏
T Gaugler, L Klei, SJ Sanders, CA Bodea, AP Goldberg, AB Lee, ...‏
Nature genetics 46 (8), 881-885, 2014‏
14522014
A comparison of linkage disequilibrium measures for fine-scale mapping‏
B Devlin, N Risch‏
Genomics 29 (2), 311-322, 1995‏
13631995
Gene expression elucidates functional impact of polygenic risk for schizophrenia‏
M Fromer, P Roussos, SK Sieberts, JS Johnson, DH Kavanagh, ...‏
Nature neuroscience 19 (11), 1442-1453, 2016‏
11492016
A framework for the interpretation of de novo mutation in human disease‏
KE Samocha, EB Robinson, SJ Sanders, C Stevens, A Sabo, LM McGrath, ...‏
Nature genetics 46 (9), 944-950, 2014‏
11432014
Convergence of genes and cellular pathways dysregulated in autism spectrum disorders‏
D Pinto, E Delaby, D Merico, M Barbosa, A Merikangas, L Klei, ...‏
The American Journal of Human Genetics 94 (5), 677-694, 2014‏
11312014
Coexpression networks implicate human midfetal deep cortical projection neurons in the pathogenesis of autism‏
AJ Willsey, SJ Sanders, M Li, S Dong, AT Tebbenkamp, RA Muhle, ...‏
Cell 155 (5), 997-1007, 2013‏
10232013
Internalizing disorders in childhood‏
M Kovacs, B Devlin‏
The Journal of Child Psychology and Psychiatry and Allied Disciplines 39 (1 …, 1998‏
9681998
سیستم در حال حاضر قادر به انجام عملکرد نیست. بعداً دوباره امتحان کنید.
مقاله‌ها 1–20