Eimear Kenny

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Christopher R GignouxColorado Center for Personalized Medicine and Department of Biomedical InformaticsVerifisert e-postadresse på cuanschutz.edu
Mark DalyDirector, Institute for Molecular Medicine Finland (FIMM) & Chief, ATGU, MGH & Broad InstituteVerifisert e-postadresse på atgu.mgh.harvard.edu
Simon GravelAssociate Professor, McGill UniversityVerifisert e-postadresse på mcGill.ca
Alicia MartinAssistant Professor, MGH & Broad InstituteVerifisert e-postadresse på broadinstitute.org
Girish NadkarniIcahn School of Medicine at Mount SinaiVerifisert e-postadresse på mountsinai.org
Brian Keith MaplesStanford UniversityVerifisert e-postadresse på stanford.edu
Andres Moreno-EstradaCINVESTAV, MexicoVerifisert e-postadresse på cinvestav.mx
Hyun Min KangProfessor of Biostatistics, University of Michigan, Ann ArborVerifisert e-postadresse på umich.edu
Alexander (Sasha) GusevDana-Farber Cancer InstituteVerifisert e-postadresse på dfci.harvard.edu
Richard DurbinDept of Genetics, University of CambridgeVerifisert e-postadresse på cam.ac.uk
Steven A McCarrollHarvard Medical School; Broad Institute of MIT and HarvardVerifisert e-postadresse på genetics.med.harvard.edu
Goncalo AbecasisUniversity of Michigan School of Public HealthVerifisert e-postadresse på umich.edu
Marc ViaDepartment of Clinical Psychology and PsychobiologyVerifisert e-postadresse på ub.edu
Jake K ByrnesVice President, Data Science, Biobot AnalyticsVerifisert e-postadresse på biobot.io
Juan L Rodriguez-Flores, Ph.D.Regeneron Genetics Center & Weill Cornell MedicineVerifisert e-postadresse på med.cornell.edu
Francisco M. De La VegaStanford University School of MedicineVerifisert e-postadresse på stanford.edu
Vladimir Vacic23andMe, Inc.Verifisert e-postadresse på 23andme.com
Gabriel Bedoya BerríoProfessor of Population GeneticsVerifisert e-postadresse på udea.edu.co
Juan Carlos Martinez CruzadoUniversity of Puerto Rico at MayaguezVerifisert e-postadresse på upr.edu
Richa SaxenaProfessor of Anaesthesia, Harvard Medical School, Massachusetts General HospitalVerifisert e-postadresse på broadinstitute.org

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Eimear Kenny

Icahn School of Medicine at Mount Sinai

Verifisert e-postadresse på mssm.edu - Startside

Human Genomics Genomic Medicine Population Genetics Statistical Genetics


Tittel Sorter etter sitater Sorter etter år Sorter etter tittel	Sitert av Sitert av	År
A global reference for human genetic variation 1000 Genomes Project Consortium Nature 526 (7571), 68, 2015	16521	2015
An integrated map of genetic variation from 1,092 human genomes 1000 Genomes Project Consortium Nature 491 (7422), 56, 2012	8633	2012
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	1918	2012
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	1781	2021
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	1469	2015
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	1444	2017
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	938	2019
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	900	2013
Textpresso: an ontology-based information retrieval and extraction system for biological literature HM Müller, EE Kenny, PW Sternberg PLoS biology 2 (11), e309, 2004	878	2004
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	846	2021
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	708	2020
A draft human pangenome reference WW Liao, M Asri, J Ebler, D Doerr, M Haukness, G Hickey, S Lu, JK Lucas, ... Nature 617 (7960), 312-324, 2023	646	2023
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	581	2020
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	568	2014
A global reference for human genetic variation GP Consortium Nature 526 (7571), 68, 2015	532	2015
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	475	2014
The Human Pangenome Project: a global resource to map genomic diversity T Wang, L Antonacci-Fulton, K Howe, HA Lawson, JK Lucas, AM Phillippy, ... Nature 604 (7906), 437-446, 2022	361	2022
Personalized medicine and the power of electronic health records NS Abul-Husn, EE Kenny Cell 177 (1), 58-69, 2019	323	2019
Whole-genome sequencing reveals host factors underlying critical COVID-19 A Kousathanas, E Pairo-Castineira, K Rawlik, A Stuckey, CA Odhams, ... Nature 607 (7917), 97-103, 2022	307	2022
Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease W Zhou, M Kanai, KHH Wu, H Rasheed, K Tsuo, JB Hirbo, Y Wang, ... Cell genomics 2 (10), 2022	294	2022

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