Artículos con órdenes de acceso público - Goncalo AbecasisMás información
TotalNIHMRCWellcomeBHFNIHRDFGCancer Research UKCIHREuropean CommissionSwedish Research CouncilGovernment of ItalyESRCVANHMRCBBSRCSNSFAHANWODoris Duke Charitable FoundationBMBFCSOZonMwLeducq Foundation, USANSFARCDFFAcademy of FinlandGobierno de EspañaVersus Arthritis, UKState of CalifoniaFWFINSERMRCNDoDGenome CanadaHHMIFWOFRQSHelmholtzDHFJDRFNSERCKnut and Alice Wallenberg FoundationOICRDCTIA*StarMacArthurNSFCTekesDiabetes UKAction on Hearing Loss, UKNMRCRWJFGBMFDNRFDSFDMTKWFResearch Grants Council, Hong KongNational Research Foundation, SingaporeRoyal Society UKSusan G. KomenCCSEMBLHRBCSIRFORTEParkinson's UKFondazione CariploKNAWUK Research & InnovationWorld Cancer Researh Fund, UKHealth Data Research, UKNordforskMinistry of Health, SingaporeUSDAHSFSFIDSTTelethonFCTMarianne and Marcus Wallenberg FoundationAlzheimers's UKProstate Cancer UKANRBusiness FinlandAIRC Foundation for Cancer Research in ItalyDamon Runyon Cancer Research FoundationCPRITJSTGobierno de Argentina
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SERPINH1 variants and thrombotic risk among middle-aged and older adults: a population-based cohort study
E Manderstedt, C Lind-Halldén, C Halldén, J Elf, PJ Svensson, ...
Journal of Thrombosis and Haemostasis 22 (3), 869-873, 2024
Órdenes: Swedish Research Council
Disponibles en algún lugar: 466
The sequence alignment/map format and SAMtools
H Li, B Handsaker, A Wysoker, T Fennell, J Ruan, N Homer, G Marth, ...
bioinformatics 25 (16), 2078-2079, 2009
Órdenes: US National Institutes of Health
Heart disease and stroke statistics—2017 update: a report from the American Heart Association
EJ Benjamin, MJ Blaha, SE Chiuve, M Cushman, SR Das, R Deo, ...
circulation 135 (10), e146-e603, 2017
Órdenes: US National Institutes of Health, American Heart Association
A global reference for human genetic variation
1000 Genomes Project Consortium
Nature 526 (7571), 68, 2015
Órdenes: US National Institutes of Health, Howard Hughes Medical Institute, Canadian …
The variant call format and VCFtools
P Danecek, A Auton, G Abecasis, CA Albers, E Banks, MA DePristo, ...
Bioinformatics 27 (15), 2156-2158, 2011
Órdenes: US National Institutes of Health, British Heart Foundation
A second generation human haplotype map of over 3.1 million SNPs
International HapMap Consortium
Nature 449 (7164), 851, 2007
Órdenes: Genome Canada
A map of human genome variation from population scale sequencing
1000 Genomes Project Consortium
Nature 467 (7319), 1061, 2010
Órdenes: 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
Órdenes: Swiss National Science Foundation, US National Institutes of Health, Howard …
Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project
Management Group Liefer Laura A. 51 Wetterstrand Kris A. 51 Good Peter J. 51 ...
nature 447 (7146), 799-816, 2007
Órdenes: German Research Foundation
METAL: fast and efficient meta-analysis of genomewide association scans
CJ Willer, Y Li, GR Abecasis
Bioinformatics 26 (17), 2190-2191, 2010
Órdenes: US National Institutes of Health
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
Órdenes: US National Institutes of Health, British Heart Foundation, Cancer Research …
Biological, clinical and population relevance of 95 loci for blood lipids
TM Teslovich, K Musunuru, AV Smith, AC Edmondson, IM Stylianou, ...
Nature 466 (7307), 707-713, 2010
Órdenes: US National Institutes of Health, British Heart Foundation
Genome-wide association studies for complex traits: consensus, uncertainty and challenges
MI McCarthy, GR Abecasis, LR Cardon, DB Goldstein, J Little, ...
Nature reviews genetics 9 (5), 356-369, 2008
Órdenes: US National Institutes of Health
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
EK Speliotes, CJ Willer, SI Berndt, KL Monda, G Thorleifsson, AU Jackson, ...
Nature genetics 42 (11), 937-948, 2010
Órdenes: Swiss National Science Foundation, US National Institutes of Health, German …
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
Órdenes: US National Institutes of Health, Austrian Science Fund
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
Órdenes: US National Institutes of Health, British Heart Foundation, UK Economic and …
A reference panel of 64,976 haplotypes for genotype imputation
Nature genetics 48 (10), 1279-1283, 2016
Órdenes: US National Institutes of Health, Canadian Institutes of Health Research …
LocusZoom: regional visualization of genome-wide association scan results
RJ Pruim, RP Welch, S Sanna, TM Teslovich, PS Chines, TP Gliedt, ...
Bioinformatics 26 (18), 2336-2337, 2010
Órdenes: US National Institutes of Health
Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study
BF Voight, GM Peloso, M Orho-Melander, R Frikke-Schmidt, M Barbalic, ...
The Lancet 380 (9841), 572-580, 2012
Órdenes: US National Institutes of Health, British Heart Foundation
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk
J Dupuis, C Langenberg, I Prokopenko, R Saxena, N Soranzo, ...
Nature genetics 42 (2), 105-116, 2010
Órdenes: US National Institutes of Health, British Heart Foundation, Dunhill Medical …
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