Articles with public access mandates - David AltshulerLearn more
OverallNIHBHFWellcomeMRCNIHRSwedish Research CouncilCIHRDFGHHMIDoris Duke Charitable FoundationCancer Research UKEuropean CommissionDFFAcademy of FinlandINSERMGenome CanadaVersus Arthritis, UKGovernment of SpainSNSFVANHMRCZonMwFWFRCNBMBFHelmholtzTekesBBSRCGovernment of ItalyFWOFRQSNWOKnut and Alice Wallenberg FoundationA*StarCSODiabetes UKDMTESRCAction on Hearing Loss, UKKWFNMRCResearch Grants Council, Hong KongAutism Speaks Inc, USANational Research Foundation, SingaporeLeducq Foundation, USAAHADCTIOTKACSIRParkinson's UKANRWorld Cancer Researh Fund, UKNordforskMinistry of Health, SingaporeSusan G. Komen
Not available anywhere: 1
Genome Sequencing of Multiple Primary Tumors Reveals a Novel PALB2 Variant
KA Schrader, KL Stratton, R Murali, Y Laitman, L Cavallone, L Offit, ...
Journal of Clinical Oncology 34 (8), e61-e67, 2016
Mandates: US National Institutes of Health, Susan G. Komen
Available somewhere: 164
The Genome Analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data
A McKenna, M Hanna, E Banks, A Sivachenko, K Cibulskis, A Kernytsky, ...
Genome research 20 (9), 1297-1303, 2010
Mandates: US National Institutes of Health
A framework for variation discovery and genotyping using next-generation DNA sequencing data
MA DePristo, E Banks, R Poplin, KV Garimella, JR Maguire, C Hartl, ...
Nature genetics 43 (5), 491-498, 2011
Mandates: US National Institutes of Health
Analysis of protein-coding genetic variation in 60,706 humans
M Lek, KJ Karczewski, EV Minikel, KE Samocha, E Banks, T Fennell, ...
Nature 536 (7616), 285-291, 2016
Mandates: US National Institutes of Health, Canadian Institutes of Health Research …
A map of human genome variation from population scale sequencing
1000 Genomes Project Consortium
Nature 467 (7319), 1061, 2010
Mandates: 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
Mandates: Swiss National Science Foundation, US National Institutes of Health, Howard …
From FastQ data to high‐confidence variant calls: the genome analysis toolkit best practices pipeline
GA Van der Auwera, MO Carneiro, C Hartl, R Poplin, G Del Angel, ...
Current protocols in bioinformatics 43 (1), 11.10. 1-11.10. 33, 2013
Mandates: US National Institutes of Health
A haplotype map of the human genome
International HapMap Consortium Altshuler David altshuler@ molbio. mgh ...
Nature 437 (7063), 1299-1320, 2005
Mandates: Genome Canada
Age-related clonal hematopoiesis associated with adverse outcomes
S Jaiswal, P Fontanillas, J Flannick, A Manning, PV Grauman, BG Mar, ...
New England Journal of Medicine 371 (26), 2488-2498, 2014
Mandates: US National Institutes of Health, UK Medical Research Council, Wellcome Trust
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
Mandates: US National Institutes of Health, British Heart Foundation
Integrating common and rare genetic variation in diverse human populations
International HapMap 3 Consortium
Nature 467 (7311), 52, 2010
Mandates: Swiss National Science Foundation, US National Institutes of Health
A reference panel of 64,976 haplotypes for genotype imputation
Nature genetics 48 (10), 1279-1283, 2016
Mandates: US National Institutes of Health, Canadian Institutes of Health Research …
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
Mandates: 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
Mandates: US National Institutes of Health, British Heart Foundation, Dunhill Medical …
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
CKDGen Consortium, KidneyGen Consortium, EchoGen consortium, ...
Nature 478 (7367), 103-109, 2011
Mandates: US National Institutes of Health, Howard Hughes Medical Institute, Austrian …
Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes
E Zeggini, LJ Scott, R Saxena, BF Voight, JL Marchini, T Hu, ...
Nature genetics 40 (5), 638-645, 2008
Mandates: US National Institutes of Health
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
H Schunkert, IR König, S Kathiresan, MP Reilly, TL Assimes, H Holm, ...
Nature genetics 43 (4), 333-338, 2011
Mandates: US National Institutes of Health, British Heart Foundation
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis
BF Voight, LJ Scott, V Steinthorsdottir, AP Morris, C Dina, RP Welch, ...
Nature genetics 42 (7), 579-589, 2010
Mandates: US National Institutes of Health, German Research Foundation, Swedish …
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes
Meta-Analyses of Glucose and Insulin-related traits Consortium (MAGIC ...
Nature genetics 44 (9), 981-990, 2012
Mandates: US National Institutes of Health, German Research Foundation, Swedish …
Six new loci associated with body mass index highlight a neuronal influence on body weight regulation
Nature genetics 41 (1), 25-34, 2009
Mandates: US National Institutes of Health, British Heart Foundation, Cancer Research UK
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