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Eimear Kenny
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A global reference for human genetic variation
1000 Genomes Project Consortium
Nature 526 (7571), 68, 2015
132042015
An integrated map of genetic variation from 1,092 human genomes
1000 Genomes Project Consortium
Nature 491 (7422), 56, 2012
80212012
Evolution and functional impact of rare coding variation from deep sequencing of human exomes
JA Tennessen, AW Bigham, TD O’connor, W Fu, EE Kenny, S Gravel, ...
science 337 (6090), 64-69, 2012
18182012
Modeling linkage disequilibrium increases accuracy of polygenic risk scores
BJ Vilhjálmsson, J Yang, HK Finucane, A Gusev, S Lindström, S Ripke, ...
The american journal of human genetics 97 (4), 576-592, 2015
12002015
Human demographic history impacts genetic risk prediction across diverse populations
AR Martin, CR Gignoux, RK Walters, GL Wojcik, BM Neale, S Gravel, ...
The American Journal of Human Genetics 100 (4), 635-649, 2017
11362017
Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program
D Taliun, DN Harris, MD Kessler, J Carlson, ZA Szpiech, R Torres, ...
Nature 590 (7845), 290-299, 2021
10562021
Textpresso: an ontology-based information retrieval and extraction system for biological literature
HM Müller, EE Kenny, PW Sternberg
PLoS biology 2 (11), e309, 2004
8622004
RFMix: a discriminative modeling approach for rapid and robust local-ancestry inference
BK Maples, S Gravel, EE Kenny, CD Bustamante
The American Journal of Human Genetics 93 (2), 278-288, 2013
7042013
Genetic analyses of diverse populations improves discovery for complex traits
GL Wojcik, M Graff, KK Nishimura, R Tao, J Haessler, CR Gignoux, ...
Nature 570 (7762), 514-518, 2019
6662019
Mapping the human genetic architecture of COVID-19
Writing group Writing group leaders Pathak Gita A. 6 Andrews Shea J. 7 Kanai ...
Nature 600 (7889), 472-477, 2021
6042021
The genetics of Mexico recapitulates Native American substructure and affects biomedical traits
A Moreno-Estrada, CR Gignoux, JC Fernández-López, F Zakharia, ...
Science 344 (6189), 1280-1285, 2014
5282014
A brief history of human disease genetics
M Claussnitzer, JH Cho, R Collins, NJ Cox, ET Dermitzakis, ME Hurles, ...
Nature 577 (7789), 179-189, 2020
4522020
A global reference for human genetic variation
GP Consortium
Nature 526 (7571), 68, 2015
4312015
Integrating sequence and array data to create an improved 1000 Genomes Project haplotype reference panel
O Delaneau, J Marchini
Nature communications 5 (1), 3934, 2014
4172014
Inherited causes of clonal haematopoiesis in 97,691 whole genomes
AG Bick, JS Weinstock, SK Nandakumar, CP Fulco, EL Bao, SM Zekavat, ...
Nature 586 (7831), 763-768, 2020
3542020
WormBase: a multi‐species resource for nematode biology and genomics
TW Harris, N Chen, F Cunningham, M Tello‐Ruiz, I Antoshechkin, ...
Nucleic acids research 32 (suppl_1), D411-D417, 2004
2562004
ImmunoChip study implicates antigen presentation to T cells in narcolepsy
J Faraco, L Lin, BR Kornum, EE Kenny, G Trynka, M Einen, TJ Rico, ...
PLoS genetics 9 (2), e1003270, 2013
2422013
WormBase: a comprehensive data resource for Caenorhabditis biology and genomics
N Chen, TW Harris, I Antoshechkin, C Bastiani, T Bieri, D Blasiar, ...
Nucleic acids research 33 (suppl_1), D383-D389, 2005
2412005
Genome‐wide association study of schizophrenia in Ashkenazi Jews
FS Goes, J McGrath, D Avramopoulos, P Wolyniec, M Pirooznia, ...
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 168 …, 2015
2292015
Whole-exome sequencing identifies rare and low-frequency coding variants associated with LDL cholesterol
LA Lange, Y Hu, H Zhang, C Xue, EM Schmidt, ZZ Tang, C Bizon, ...
The American Journal of Human Genetics 94 (2), 233-245, 2014
2252014
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Articles 1–20