Michelle Daya
Michelle Daya
Genentech, Human Genetics Computational Scientist
E-mail confirmado em
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Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program
D Taliun, DN Harris, MD Kessler, J Carlson, ZA Szpiech, R Torres, ...
Nature 590 (7845), 290-299, 2021
Mapping the human genetic architecture of COVID-19
Writing group Writing group leaders Pathak Gita A. 6 Andrews Shea J. 7 Kanai ...
Nature 600 (7889), 472-477, 2021
Inherited causes of clonal haematopoiesis in 97,691 whole genomes
AG Bick, JS Weinstock, SK Nandakumar, CP Fulco, EL Bao, SM Zekavat, ...
Nature 586 (7831), 763-768, 2020
Assembly of a pan-genome from deep sequencing of 910 humans of African descent (vol 51, pg 30, 2018)
RM Sherman, J Forman, V Antonescu, D Puiu, M Daya, N Rafaels, ...
NATURE GENETICS 51 (2), 364-364, 2019
Assembly of a pan-genome from deep sequencing of 910 humans of African descent
RM Sherman, J Forman, V Antonescu, D Puiu, M Daya, N Rafaels, ...
Nature genetics 51 (1), 30-35, 2019
Use of> 100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in …
MH Kowalski, H Qian, Z Hou, JD Rosen, AL Tapia, Y Shan, D Jain, ...
PLoS genetics 15 (12), e1008500, 2019
Genome-wide association study of ancestry-specific TB risk in the South African Coloured population
ER Chimusa, N Zaitlen, M Daya, M Möller, PD van Helden, NJ Mulder, ...
Human molecular genetics 23 (3), 796-809, 2014
TLR1, 2, 4, 6 and 9 variants associated with tuberculosis susceptibility: a systematic review and meta-analysis
H Schurz, M Daya, M Möller, EG Hoal, M Salie
PloS one 10 (10), e0139711, 2015
Association study in African-admixed populations across the Americas recapitulates asthma risk loci in non-African populations
M Daya, N Rafaels, TM Brunetti, S Chavan, AM Levin, A Shetty, ...
Nature communications 10 (1), 1-13, 2019
Worldwide Frequencies of APOL1 Renal Risk Variants
GN Nadkarni, CR Gignoux, EP Sorokin, M Daya, R Rahman, KC Barnes, ...
New England Journal of Medicine 379 (26), 2571-2572, 2018
Association of toll-like receptors with susceptibility to tuberculosis suggests sex-specific effects of TLR8 polymorphisms
M Salie, M Daya, LA Lucas, RM Warren, GD van der Spuy, ...
Infection, genetics and evolution 34, 221-229, 2015
A panel of ancestry informative markers for the complex five-way admixed South African coloured population
M Daya, L Van Der Merwe, U Galal, M Möller, M Salie, ER Chimusa, ...
PloS one 8 (12), e82224, 2013
clustifyr: an R package for automated single-cell RNA sequencing cluster classification
R Fu, AE Gillen, RM Sheridan, C Tian, M Daya, Y Hao, JR Hesselberth, ...
F1000Research 9, 2020
Associations Between Human Leukocyte Antigen Class I Variants and the Mycobacterium tuberculosis Subtypes Causing Disease
M Salie, L Van Der Merwe, M Möller, M Daya, GD Van Der Spuy, ...
The Journal of infectious diseases 209 (2), 216-223, 2014
De novo mutations across 1,465 diverse genomes reveal mutational insights and reductions in the Amish founder population
MD Kessler, DP Loesch, JA Perry, NL Heard-Costa, D Taliun, BE Cade, ...
Proceedings of the National Academy of Sciences 117 (5), 2560-2569, 2020
Determining ancestry proportions in complex admixture scenarios in South Africa using a novel proxy ancestry selection method
ER Chimusa, M Daya, M Möller, R Ramesar, BM Henn, PD Van Helden, ...
PloS one 8 (9), e73971, 2013
Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMed
MA Taub, MP Conomos, R Keener, KR Iyer, JS Weinstock, LR Yanek, ...
Cell Genomics 2 (1), 100084, 2022
A functional toll-interacting protein variant is associated with Bacillus calmette-guérin–specific immune responses and tuberculosis
JA Shah, M Musvosvi, M Shey, DJ Horne, RD Wells, GJ Peterson, JS Cox, ...
American journal of respiratory and critical care medicine 196 (4), 502-511, 2017
The role of ancestry in TB susceptibility of an admixed South African population
M Daya, L van der Merwe, PD van Helden, M Möller, EG Hoal
Tuberculosis 94 (4), 413-420, 2014
Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease
JB Nielsen, O Rom, I Surakka, SE Graham, W Zhou, T Roychowdhury, ...
Nature communications 11 (1), 1-12, 2020
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