دنبال کردن
Deborah A. Nickerson
Deborah A. Nickerson
University of Washington
ایمیل تأیید شده در uw.edu
عنوان
نقل شده توسط
نقل شده توسط
سال
Heart disease and stroke statistics—2016 update: a report from the American Heart Association‏
D Mozaffarian, EJ Benjamin, AS Go, DK Arnett, MJ Blaha, M Cushman, ...‏
circulation 133 (4), e38-e360, 2016‏
71712*2016
A global reference for human genetic variation‏
1000 Genomes Project Consortium‏
Nature 526 (7571), 68, 2015‏
164982015
A map of human genome variation from population scale sequencing‏
1000 Genomes Project Consortium‏
Nature 467 (7319), 1061, 2010‏
90392010
An integrated map of genetic variation from 1,092 human genomes‏
1000 Genomes Project Consortium‏
Nature 491 (7422), 56, 2012‏
84892012
The international HapMap project‏
RA Gibbs, JW Belmont, P Hardenbol, TD Willis, FL Yu, HM Yang, ...‏
Nature Publishing Group, 2003‏
63352003
Biological, clinical and population relevance of 95 loci for blood lipids‏
TM Teslovich, K Musunuru, AV Smith, AC Edmondson, IM Stylianou, ...‏
Nature 466 (7307), 707-713, 2010‏
41642010
A reference panel of 64,976 haplotypes for genotype imputation‏
Nature genetics 48 (10), 1279-1283, 2016‏
31632016
The contribution of de novo coding mutations to autism spectrum disorder‏
I Iossifov, BJ O’roak, SJ Sanders, M Ronemus, N Krumm, D Levy, ...‏
Nature 515 (7526), 216-221, 2014‏
27692014
Targeted capture and massively parallel sequencing of 12 human exomes‏
SB Ng, EH Turner, PD Robertson, SD Flygare, AW Bigham, C Lee, ...‏
Nature 461 (7261), 272-276, 2009‏
27272009
Exome sequencing identifies the cause of a mendelian disorder‏
SB Ng, KJ Buckingham, C Lee, AW Bigham, HK Tabor, KM Dent, CD Huff, ...‏
Nature genetics 42 (1), 30-35, 2010‏
25862010
Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations‏
BJ O’Roak, L Vives, S Girirajan, E Karakoc, N Krumm, BP Coe, R Levy, ...‏
Nature 485 (7397), 246-250, 2012‏
24912012
Exome sequencing as a tool for Mendelian disease gene discovery‏
MJ Bamshad, SB Ng, AW Bigham, HK Tabor, MJ Emond, DA Nickerson, ...‏
Nature Reviews Genetics 12 (11), 745-755, 2011‏
22202011
Evolution and functional impact of rare coding variation from deep sequencing of human exomes‏
JA Tennessen, AW Bigham, TD O’connor, W Fu, EE Kenny, S Gravel, ...‏
science 337 (6090), 64-69, 2012‏
19182012
Selecting a maximally informative set of single-nucleotide polymorphisms for association analyses using linkage disequilibrium‏
CS Carlson, MA Eberle, MJ Rieder, Q Yi, L Kruglyak, DA Nickerson‏
The American Journal of Human Genetics 74 (1), 106-120, 2004‏
18572004
Effect of VKORC1 haplotypes on transcriptional regulation and warfarin dose‏
MJ Rieder, AP Reiner, BF Gage, DA Nickerson, CS Eby, HL McLeod, ...‏
New England Journal of Medicine 352 (22), 2285-2293, 2005‏
18402005
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
17752021
Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome‏
SB Ng, AW Bigham, KJ Buckingham, MC Hannibal, MJ McMillin, ...‏
Nature genetics 42 (9), 790-793, 2010‏
16702010
Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders‏
BJ O’Roak, L Vives, W Fu, JD Egertson, IB Stanaway, IG Phelps, G Carvill, ...‏
Science 338 (6114), 1619-1622, 2012‏
14602012
Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations‏
BJ O'Roak, P Deriziotis, C Lee, L Vives, JJ Schwartz, S Girirajan, ...‏
Nature genetics 43 (6), 585-589, 2011‏
14572011
Mapping and sequencing of structural variation from eight human genomes‏
JM Kidd, GM Cooper, WF Donahue, HS Hayden, N Sampas, T Graves, ...‏
Nature 453 (7191), 56-64, 2008‏
14462008
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مقاله‌ها 1–20