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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
9388*2007
A map of human genome variation from population scale sequencing
1000 Genomes Project Consortium
Nature 467 (7319), 1061, 2010
87832010
An integrated map of genetic variation from 1,092 human genomes
1000 Genomes Project Consortium
Nature 491 (7422), 56, 2012
83012012
The international HapMap project
RA Gibbs, JW Belmont, P Hardenbol, TD Willis, FL Yu, HM Yang, ...
Nature Publishing Group, 2003
63322003
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
22362007
A haplotype map of the human genome
D Altshuler
Nature 437, 1299-1320, 2005
11992005
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
7852017
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
7162011
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
5382013
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
5082012
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
4452014
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
4012017
Human genetic research: emerging trends in ethics
BM Knoppers, R Chadwick
Nature Reviews Genetics 6 (1), 75-79, 2005
3912005
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
3872007
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
3262006
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
3092008
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
2832014
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
2802014
Cohort profile of the CARTaGENE study: Quebec’s population-based biobank for public health and personalized genomics
P Awadalla, C Boileau, Y Payette, Y Idaghdour, JP Goulet, B Knoppers, ...
International journal of epidemiology 42 (5), 1285-1299, 2013
2292013
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Artikelen 1–20