Articoli con mandati relativi all'accesso pubblico - Aravinda ChakravartiUlteriori informazioni
TotaleNIHMRCBHFWellcomeNIHREuropean CommissionBBSRCDFGHHMICancer Research UKESRCZonMwNHMRCCIHRNSFCGovernment of SpainGoverno ItalianoSNSFNWOAHAARCVAFWFGenome CanadaDFFTelethonAutism Speaks Inc, USANSFDOEFRQSNSERCEMBLDNRFAcademy of FinlandINSERMSwedish Research CouncilVersus Arthritis, UKCSODiabetes UKDHFJDRFOICRUSDAMacArthurFWOCASHelmholtzDCTITekesHRBSFIA*StarAlzheimers's UKAction on Hearing Loss, UKRCNDoris Duke Charitable FoundationBMBFKNAWKWFNMRCResearch Grants Council, Hong KongRWJFLeducq Foundation, USAHealth Data Research, UKSusan G. Komen
Non disponibili pubblicamente: 2
Revealing rate‐limiting steps in complex disease biology: The crucial importance of studying rare, extreme‐phenotype families
A Chakravarti, TN Turner
Bioessays 38 (6), 578-586, 2016
Mandati: US National Institutes of Health
Magnitude of Mendelian versus complex inheritance of rare disorders
A Chakravarti
American Journal of Medical Genetics Part A 185 (11), 3287-3293, 2021
Mandati: US National Institutes of Health
Disponibili pubblicamente: 195
Heart disease and stroke statistics—2014 update: a report from the American Heart Association
AS Go, D Mozaffarian, VL Roger, EJ Benjamin, JD Berry, MJ Blaha, S Dai, ...
circulation 129 (3), e28-e292, 2014
Mandati: US National Institutes of Health
A global reference for human genetic variation
1000 Genomes Project Consortium
Nature 526 (7571), 68, 2015
Mandati: US National Institutes of Health, Howard Hughes Medical Institute, Canadian …
Finding the missing heritability of complex diseases
TA Manolio, FS Collins, NJ Cox, DB Goldstein, LA Hindorff, DJ Hunter, ...
Nature 461 (7265), 747-753, 2009
Mandati: US National Institutes of Health
A second generation human haplotype map of over 3.1 million SNPs
International HapMap Consortium
Nature 449 (7164), 851, 2007
Mandati: Genome Canada
A map of human genome variation from population scale sequencing
1000 Genomes Project Consortium
Nature 467 (7319), 1061, 2010
Mandati: Swiss National Science Foundation, US National Institutes of Health, Howard …
An integrated map of genetic variation from 1,092 human genomes
1000 Genomes Project Consortium
Nature 491 (7422), 56, 2012
Mandati: US National Institutes of Health, Howard Hughes Medical Institute, British …
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
Mandati: US National Institutes of Health, British Heart Foundation, Cancer Research …
Discovery and refinement of loci associated with lipid levels
CJ Willer, EM Schmidt, S Sengupta, GM Peloso, S Gustafsson, S Kanoni, ...
Nature genetics 45 (11), 1274, 2013
Mandati: US National Institutes of Health, British Heart Foundation, UK Economic and …
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
B Devlin, JR Kelsoe, P Sklar, MJ Daly, MC O'Donovan, N Craddock, ...
Nature genetics 45 (9), 984-994, 2013
Mandati: US National Institutes of Health, Australian Research Council, National …
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
CKDGen Consortium, KidneyGen Consortium, EchoGen consortium, ...
Nature 478 (7367), 103-109, 2011
Mandati: US National Institutes of Health, Howard Hughes Medical Institute, Austrian …
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
Mandati: US National Institutes of Health, British Heart Foundation, UK Medical …
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
Mandati: US National Institutes of Health, British Heart Foundation, Cancer Research …
Genome-wide association study of blood pressure and hypertension
D Levy, GB Ehret, K Rice, GC Verwoert, LJ Launer, A Dehghan, ...
Nature genetics 41 (6), 677-687, 2009
Mandati: US National Institutes of Health, German Research Foundation
Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits
E Evangelou, HR Warren, D Mosen-Ansorena, B Mifsud, R Pazoki, H Gao, ...
Nature genetics 50 (10), 1412-1425, 2018
Mandati: Swiss National Science Foundation, US National Institutes of Health, US …
Common variants associated with plasma triglycerides and risk for coronary artery disease
R Do, CJ Willer, EM Schmidt, S Sengupta, C Gao, GM Peloso, ...
Nature genetics 45 (11), 1345-1352, 2013
Mandati: US National Institutes of Health, Canadian Institutes of Health Research …
A genome-wide linkage and association scan reveals novel loci for autism
LA Weiss, DE Arking, ...
Nature 461 (7265), 802-808, 2009
Mandati: US National Institutes of Health, National Institute of Health and Medical …
The genetic basis of Mendelian phenotypes: discoveries, challenges, and opportunities
JX Chong, KJ Buckingham, SN Jhangiani, C Boehm, N Sobreira, ...
The American Journal of Human Genetics 97 (2), 199-215, 2015
Mandati: US National Institutes of Health, Howard Hughes Medical Institute
Demographic history and rare allele sharing among human populations
S Gravel, BM Henn, RN Gutenkunst, AR Indap, GT Marth, AG Clark, F Yu, ...
Proceedings of the National Academy of Sciences 108 (29), 11983-11988, 2011
Mandati: US National Institutes of Health
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