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Bartha Maria Knoppers
Bartha Maria Knoppers
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A second generation human haplotype map of over 3.1 million SNPs
International HapMap Consortium
Nature 449 (7164), 851, 2007
9368*2007
A map of human genome variation from population scale sequencing
1000 Genomes Project Consortium
Nature 467 (7319), 1061, 2010
87902010
An integrated map of genetic variation from 1,092 human genomes
1000 Genomes Project Consortium
Nature 491 (7422), 56, 2012
82782012
The international HapMap project
RA Gibbs, JW Belmont, P Hardenbol, TD Willis, FL Yu, HM Yang, ...
Nature Publishing Group, 2003
62142003
International network of cancer genome projects
Data coordination centre Kasprzyk (Leader) Arek 1 Stein (Leader) Lincoln D ...
Nature 464 (7291), 993-998, 2010
22692010
Genome-wide detection and characterization of positive selection in human populations
PC Sabeti, P Varilly, B Fry, J Lohmueller, E Hostetter, C Cotsapas, X Xie, ...
Nature 449 (7164), 913-918, 2007
22192007
A haplotype map of the human genome
D Altshuler
Nature 437, 1299-1320, 2005
11892005
Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder
RK C Yuen, D Merico, M Bookman, J L Howe, B Thiruvahindrapuram, ...
Nature neuroscience 20 (4), 602-611, 2017
7752017
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
7092011
Whole-genome sequencing in health care
CG Van El, MC Cornel, P Borry, RJ Hastings, F Fellmann, SV Hodgson, ...
European Journal of Human Genetics 21 (6), 580-584, 2013
5372013
Managing incidental findings and research results in genomic research involving biobanks and archived data sets
SM Wolf, BN Crock, B Van Ness, F Lawrenz, JP Kahn, LM Beskow, ...
Genetics in Medicine 14 (4), 361-384, 2012
5062012
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
4392014
Human genetic research: emerging trends in ethics
BM Knoppers, R Chadwick
Nature Reviews Genetics 6 (1), 75-79, 2005
4012005
International cooperation to enable the diagnosis of all rare genetic diseases
KM Boycott, A Rath, JX Chong, T Hartley, FS Alkuraya, G Baynam, ...
The American Journal of Human Genetics 100 (5), 695-705, 2017
3892017
Trends in ethical and legal frameworks for the use of human biobanks
A Cambon-Thomsen, E Rial-Sebbag, BM Knoppers
European Respiratory Journal 30 (2), 373-382, 2007
3852007
Recommendations for returning genomic incidental findings? We need to talk!
W Burke, AH Matheny Antommaria, R Bennett, J Botkin, EW Clayton, ...
Genetics in Medicine 15 (11), 854-859, 2013
3392013
The emergence of an ethical duty to disclose genetic research results: international perspectives
BM Knoppers, Y Joly, J Simard, F Durocher
European Journal of Human Genetics 14 (11), 1170-1178, 2006
3232006
Research ethics recommendations for whole-genome research: consensus statement
T Caulfield, AL McGuire, M Cho, JA Buchanan, MM Burgess, U Danilczyk, ...
PLoS biology 6 (3), e73, 2008
3032008
FORGE Canada Consortium: outcomes of a 2-year national rare-disease gene-discovery project
CL Beaulieu, J Majewski, J Schwartzentruber, ME Samuels, ...
The American Journal of Human Genetics 94 (6), 809-817, 2014
2782014
DataSHIELD: taking the analysis to the data, not the data to the analysis
A Gaye, Y Marcon, J Isaeva, P LaFlamme, A Turner, EM Jones, J Minion, ...
International journal of epidemiology 43 (6), 1929-1944, 2014
2732014
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Artikelen 1–20