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Bartha Maria Knoppers
Bartha Maria Knoppers
Verified email at mcgill.ca - Homepage
Title
Cited by
Cited by
Year
A global reference for human genetic variation
1000 Genomes Project Consortium
Nature 526 (7571), 68, 2015
187542015
A second generation human haplotype map of over 3.1 million SNPs
International HapMap Consortium
Nature 449 (7164), 851, 2007
9709*2007
An integrated map of genetic variation from 1,092 human genomes
1000 Genomes Project Consortium
Nature 491 (7422), 56, 2012
87912012
The international HapMap project
RA Gibbs, JW Belmont, P Hardenbol, TD Willis, FL Yu, HM Yang, ...
Nature Publishing Group, 2003
66272003
A map of human genome variation from population scale sequencing
1000 Genomes Project Consortium
Nature 467 (7319), 1061, 2010
52322010
Pan-cancer analysis of whole genomes
Nature 578 (7793), 82-93, 2020
2972*2020
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
24742007
A haplotype map of the human genome
D Altshuler
Nature 437, 1299-1320, 2005
12332005
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
9182017
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
7892011
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
5872013
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
5322012
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
5062017
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
4952014
Human genetic research: emerging trends in ethics
BM Knoppers, R Chadwick
Nature Reviews Genetics 6 (1), 75-79, 2005
4082005
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
4022007
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
3442013
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
3392014
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
3392006
Proposed international guidelines on ethical issues in medical genetics and genetic services-report of a WHO Meeting on Ethical Issues and Medical Genetics
World Health Organization
318*2001
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Articles 1–20