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Katarzyna (Kasia) Bryc
Katarzyna (Kasia) Bryc
Senior Scientist, 23andMe
Verified email at genetics.med.harvard.edu - Homepage
Title
Cited by
Cited by
Year
A high-coverage genome sequence from an archaic Denisovan individual
M Meyer, M Kircher, MT Gansauge, H Li, F Racimo, S Mallick, ...
Science 338 (6104), 222-226, 2012
18312012
Genes mirror geography within Europe
J Novembre, T Johnson, K Bryc, Z Kutalik, AR Boyko, A Auton, A Indap, ...
Nature 456 (7218), 98-101, 2008
16192008
Genome-wide survey of SNP variation uncovers the genetic structure of cattle breeds
Bovine HapMap Consortium, RA Gibbs, JF Taylor, CP Van Tassell, ...
Science 324 (5926), 528-532, 2009
9012009
Genome-wide SNP and haplotype analyses reveal a rich history underlying dog domestication
BM Vonholdt, JP Pollinger, KE Lohmueller, E Han, HG Parker, P Quignon, ...
Nature 464 (7290), 898-902, 2010
7972010
Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies
MA Nalls, C Blauwendraat, CL Vallerga, K Heilbron, S Bandres-Ciga, ...
The Lancet Neurology 18 (12), 1091-1102, 2019
6992019
The genetic ancestry of african americans, latinos, and european Americans across the United States
K Bryc, EY Durand, JM Macpherson, D Reich, JL Mountain
The American Journal of Human Genetics 96 (1), 37-53, 2015
5262015
Genome-wide patterns of population structure and admixture in West Africans and African Americans
K Bryc, A Auton, MR Nelson, JR Oksenberg, SL Hauser, S Williams, ...
Proceedings of the National Academy of Sciences 107 (2), 786-791, 2010
4852010
Genome-wide patterns of population structure and admixture among Hispanic/Latino populations
K Bryc, C Velez, T Karafet, A Moreno-Estrada, A Reynolds, A Auton, ...
Proceedings of the National Academy of Sciences 107 (supplement_2), 8954-8961, 2010
4212010
Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences
R Karlsson Linnér, P Biroli, E Kong, SFW Meddens, R Wedow, ...
Nature genetics 51 (2), 245-257, 2019
3592019
An atlas of genetic influences on osteoporosis in humans and mice
JA Morris, JP Kemp, SE Youlten, L Laurent, JG Logan, RC Chai, ...
Nature genetics 51 (2), 258-266, 2019
3502019
The Population Reference Sample, POPRES: a resource for population, disease, and pharmacological genetics research
MR Nelson, K Bryc, KS King, A Indap, AR Boyko, J Novembre, LP Briley, ...
The American Journal of Human Genetics 83 (3), 347-358, 2008
2892008
Global distribution of genomic diversity underscores rich complex history of continental human populations
A Auton, K Bryc, AR Boyko, KE Lohmueller, J Novembre, A Reynolds, ...
Genome research 19 (5), 795-803, 2009
2042009
PCAdmix: principal components-based assignment of ancestry along each chromosome in individuals with admixed ancestry from two or more populations
A Brisbin, K Bryc, J Byrnes, F Zakharia, L Omberg, J Degenhardt, ...
Human biology 84 (4), 343, 2012
1792012
Identification of novel risk loci for restless legs syndrome in genome-wide association studies in individuals of European ancestry: a meta-analysis
B Schormair, C Zhao, S Bell, E Tilch, AV Salminen, B Pütz, Y Dauvilliers, ...
The Lancet Neurology 16 (11), 898-907, 2017
1552017
A genetic investigation of sex bias in the prevalence of attention-deficit/hyperactivity disorder
J Martin, RK Walters, D Demontis, M Mattheisen, SH Lee, E Robinson, ...
Biological psychiatry 83 (12), 1044-1053, 2018
1282018
Population genetic inference from personal genome data: impact of ancestry and admixture on human genomic variation
JM Kidd, S Gravel, J Byrnes, A Moreno-Estrada, S Musharoff, K Bryc, ...
The American Journal of Human Genetics 91 (4), 660-671, 2012
1152012
Genetic consequences of the transatlantic slave trade in the Americas
SJ Micheletti, K Bryc, SGA Esselmann, WA Freyman, ME Moreno, ...
The American Journal of Human Genetics 107 (2), 265-277, 2020
712020
Common variant burden contributes to the familial aggregation of migraine in 1,589 families
P Gormley, MI Kurki, ME Hiekkala, K Veerapen, P Häppölä, AA Mitchell, ...
Neuron 98 (4), 743-753. e4, 2018
652018
On identifying the optimal number of population clusters via the deviance information criterion
H Gao, K Bryc, CD Bustamante
PloS one 6 (6), e21014, 2011
592011
Characterization of prevalence and health consequences of uniparental disomy in four million individuals from the general population
P Nakka, SP Smith, AH O’Donnell-Luria, KF McManus, M Agee, A Auton, ...
The American Journal of Human Genetics 105 (5), 921-932, 2019
442019
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