Kathryn Roeder
Kathryn Roeder
Professor of Statistics, Carnegie Mellon University
andrew.cmu.edu üzerinde doğrulanmış e-posta adresine sahip - Ana Sayfa
Başlık
Alıntı yapanlar
Alıntı yapanlar
Yıl
Genomic control for association studies
B Devlin, K Roeder
Biometrics 55 (4), 997-1004, 1999
33021999
A SAS procedure based on mixture models for estimating developmental trajectories
BL Jones, DS Nagin, K Roeder
Sociological methods & research 29 (3), 374-393, 2001
21622001
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
20162010
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
19562012
Synaptic, transcriptional and chromatin genes disrupted in autism
S De Rubeis, X He, AP Goldberg, CS Poultney, K Samocha, AE Cicek, ...
Nature 515 (7526), 209-215, 2014
19542014
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
17642012
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
SH Lee, S Ripke, BM Neale, SV Faraone, SM Purcell, RH Perlis, ...
Nature genetics 45 (9), 984-995, 2013
13442013
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
12662011
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
9902015
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
9552014
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
8242014
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
7852019
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
7382013
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
7062016
The Heritability of IQ
B Devlin, M Daniels, K Roeder
Nature 388 (6641), 468-471, 1997
6811997
Genome-wide association identifies multiple ulcerative colitis susceptibility loci
DPB McGovern, A Gardet, L Törkvist, P Goyette, J Essers, KD Taylor, ...
Nature genetics 42 (4), 332-337, 2010
6632010
Practical Bayesian density estimation using mixtures of normals
K Roeder, L Wasserman
Journal of the American Statistical Association 92 (439), 894-902, 1997
6561997
Testing for an unusual distribution of rare variants
BM Neale, MA Rivas, BF Voight, D Altshuler, B Devlin, M Orho-Melander, ...
PLoS genetics 7 (3), e1001322, 2011
6482011
A genome-wide scan for common alleles affecting risk for autism
R Anney, L Klei, D Pinto, R Regan, J Conroy, TR Magalhaes, C Correia, ...
Human molecular genetics 19 (20), 4072-4082, 2010
6212010
Genomic control, a new approach to genetic-based association studies
B Devlin, K Roeder, L Wasserman
Theoretical population biology 60 (3), 155-166, 2001
5832001
Sistem, işlemi şu anda gerçekleştiremiyor. Daha sonra yeniden deneyin.
Makaleler 1–20