Adam E. Locke

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Michael BoehnkeProfessor of Biostatistics, University of MichiganAdresse e-mail validée de umich.edu
Laura J ScottDepartment of Biostatistics, Center for Statistical Genetics, University of MichiganAdresse e-mail validée de umich.edu
Christian FuchsbergerEurac Research, Bozen/Bolzano, ItalyAdresse e-mail validée de eurac.edu
Shawn LevyCSO, Element BiosciencesAdresse e-mail validée de elembio.com
Stephanie L. ShermanProfessor of Human Genetics, Emory University School of MedicineAdresse e-mail validée de emory.edu
Matt McGueProfessor, University of MinnesotaAdresse e-mail validée de umn.edu
Goncalo AbecasisUniversity of Michigan School of Public HealthAdresse e-mail validée de umich.edu
Lora J. H. BeanAssociate Professor, Emory University; Senior Molecular Director, EGL GeneticsAdresse e-mail validée de emory.edu
Felix DayMRC Epidemiology UnitAdresse e-mail validée de mrc-epid.cam.ac.uk
Scott VriezeUniversity of MinnesotaAdresse e-mail validée de umn.edu
Ruth LoosNovo Nordisk Foundation Center for Basic Metabolic Research, University of CopenhagenAdresse e-mail validée de sund.ku.dk
Bratati KahaliCentre for Brain Research, Indian Institute of ScienceAdresse e-mail validée de iisc.ac.in
Stuart W. TinkerEmory Genetics LaboratoryAdresse e-mail validée de emory.edu
Emily AllenEmory UniversityAdresse e-mail validée de emory.edu
Zoltán KutalikUniversity of Lausanne / UnisanteAdresse e-mail validée de unil.ch
Carlo SidoreRegeneron Genetics CenterAdresse e-mail validée de irgb.cnr.it
Sebastian SchoenherrMedical University of InnsbruckAdresse e-mail validée de i-med.ac.at
Sayantan Das23andMeAdresse e-mail validée de 23andme.com
Dr Joshua C RandallGenomics plcAdresse e-mail validée de alum.mit.edu
Tõnu EskoUniversity of TartuAdresse e-mail validée de ut.ee

Suivre

Adam E. Locke

Senior Director, Statistical Genetics, Regeneron Genetics Center

Adresse e-mail validée de regeneron.com

Human and Statistical Genetics/Genomics Sequencing Down Syndrome Obesity and Diabetes


Titre Trier par citations Trier par année Trier par titre	Citée par Citée par	Année
Genetic studies of body mass index yield new insights for obesity biology AE Locke, B Kahali, SI Berndt, AE Justice, TH Pers, FR Day, C Powell, ... Nature 518 (7538), 197-206, 2015	5019	2015
Next-generation genotype imputation service and methods S Das, L Forer, S Schönherr, C Sidore, AE Locke, A Kwong, SI Vrieze, ... Nature genetics 48 (10), 1284-1287, 2016	3715	2016
Defining the role of common variation in the genomic and biological architecture of adult human height AR Wood, T Esko, J Yang, S Vedantam, TH Pers, S Gustafsson, AY Chu, ... Nature genetics 46 (11), 1173-1186, 2014	2188	2014
Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps A Mahajan, D Taliun, M Thurner, NR Robertson, JM Torres, NW Rayner, ... Nature genetics 50 (11), 1505-1513, 2018	1750	2018
New genetic loci link adipose and insulin biology to body fat distribution D Shungin, TW Winkler, DC Croteau-Chonka, T Ferreira, AE Locke, ... Nature 518 (7538), 187-196, 2015	1735	2015
The genetic architecture of type 2 diabetes C Fuchsberger, J Flannick, TM Teslovich, A Mahajan, V Agarwala, ... Nature 536 (7614), 41-47, 2016	1301	2016
Rare and low-frequency coding variants alter human adult height E Marouli, M Graff, C Medina-Gomez, KS Lo, AR Wood, TR Kjaer, RS Fine, ... Nature 542 (7640), 186-190, 2017	683	2017
Exome sequencing and analysis of 454,787 UK Biobank participants JD Backman, AH Li, A Marcketta, D Sun, J Mbatchou, MD Kessler, ... Nature 599 (7886), 628-634, 2021	673	2021
The power of genetic diversity in genome-wide association studies of lipids SE Graham, SL Clarke, KHH Wu, S Kanoni, GJM Zajac, S Ramdas, ... Nature 600 (7890), 675-679, 2021	615	2021
Quality control and conduct of genome-wide association meta-analyses TW Winkler, FR Day, DC Croteau-Chonka, AR Wood, AE Locke, R Mägi, ... Nature protocols 9 (5), 1192-1212, 2014	570	2014
A saturated map of common genetic variants associated with human height L Yengo, S Vedantam, E Marouli, J Sidorenko, E Bartell, S Sakaue, ... Nature 610 (7933), 704-712, 2022	530	2022
Sex-stratified genome-wide association studies including 270,000 individuals show sexual dimorphism in genetic loci for anthropometric traits JC Randall, TW Winkler, Z Kutalik, SI Berndt, AU Jackson, KL Monda, ... PLoS genetics 9 (6), e1003500, 2013	482	2013
Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation A Mahajan, CN Spracklen, W Zhang, MCY Ng, LE Petty, H Kitajima, ... Nature genetics 54 (5), 560-572, 2022	448	2022
Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci KJ Gaulton, T Ferreira, Y Lee, A Raimondo, R Mägi, ME Reschen, ... Nature genetics 47 (12), 1415-1425, 2015	433	2015
Ethnicity, sex, and the incidence of congenital heart defects: a report from the National Down Syndrome Project SB Freeman, LH Bean, EG Allen, SW Tinker, AE Locke, C Druschel, ... Genetics in Medicine 10 (3), 173-180, 2008	403	2008
Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations CG Boer, K Hatzikotoulas, L Southam, L Stefánsdóttir, Y Zhang, ... Cell 184 (18), 4784-4818. e17, 2021	395	2021
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity V Turcot, Y Lu, HM Highland, C Schurmann, AE Justice, RS Fine, ... Nature genetics 50 (1), 26-41, 2018	370	2018
Genetic evidence of assortative mating in humans MR Robinson, A Kleinman, M Graff, AAE Vinkhuyzen, D Couper, ... Nature Human Behaviour 1 (1), 0016, 2017	346	2017
New loci for body fat percentage reveal link between adiposity and cardiometabolic disease risk Y Lu, FR Day, S Gustafsson, ML Buchkovich, J Na, V Bataille, ... Nature communications 7 (1), 10495, 2016	313	2016
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	246	2014

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