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
31851999
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
20012001
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
19152010
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
18122012
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, 2013
17322013
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
17162014
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
16342012
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
11782011
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
8412015
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
8262014
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
7542014
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
6642013
The Heritability of IQ
B Devlin, M Daniels, K Roeder
Nature 388 (6641), 468-471, 1997
6601997
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
6472010
Practical Bayesian density estimation using mixtures of normals
K Roeder, L Wasserman
Journal of the American Statistical Association 92 (439), 894-902, 1997
6261997
Testing for an unusual distribution of rare variants
BM Neale, MA Rivas, BF Voight, D Altshuler, B Devlin, M Orho-Melander, ...
PLoS Genet 7 (3), e1001322, 2011
6192011
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
5932010
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
5722016
Genomic control, a new approach to genetic-based association studies
B Devlin, K Roeder, L Wasserman
Theoretical population biology 60 (3), 155-166, 2001
5602001
High dimensional variable selection
L Wasserman, K Roeder
Annals of statistics 37 (5A), 2178, 2009
5292009
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Makaleler 1–20