Yun Li
Titel
Zitiert von
Zitiert von
Jahr
A map of human genome variation from population scale sequencing
DM Altshuler, ES Lander, L Ambrogio, T Bloom, K Cibulskis, TJ Fennell, ...
Nature 467 (7319), 1061-1073, 2010
7089*2010
An integrated map of genetic variation from 1,092 human genomes
1000 Genomes Project Consortium
Nature 491 (7422), 56-65, 2012
66222012
A global reference for human genetic variation
1000 Genomes Project Consortium
Nature 526 (7571), 68-74, 2015
65022015
The variant call format and VCFtools
P Danecek, A Auton, G Abecasis, CA Albers, E Banks, MA DePristo, ...
Bioinformatics 27 (15), 2156-2158, 2011
55122011
A second generation human haplotype map of over 3.1 million SNPs
KA Frazer, DG Ballinger, DR Cox, DA Hinds, LL Stuve, RA Gibbs, ...
Nature 449 (7164), 851-861, 2007
46622007
A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants
LJ Scott, KL Mohlke, LL Bonnycastle, CJ Willer, Y Li, WL Duren, MR Erdos, ...
science 316 (5829), 1341-1345, 2007
30002007
METAL: fast and efficient meta-analysis of genomewide association scans
CJ Willer, Y Li, GR Abecasis
Bioinformatics 26 (17), 2190-2191, 2010
27222010
Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes
E Zeggini, LJ Scott, R Saxena, BF Voight, JL Marchini, T Hu, ...
Nature genetics 40 (5), 638-645, 2008
20142008
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk
J Dupuis, C Langenberg, I Prokopenko, R Saxena, N Soranzo, ...
Nature genetics 42 (2), 105-116, 2010
19862010
MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes
Y Li, CJ Willer, J Ding, P Scheet, GR Abecasis
Genetic epidemiology 34 (8), 816-834, 2010
19462010
Rare-variant association testing for sequencing data with the sequence kernel association test
MC Wu, S Lee, T Cai, Y Li, M Boehnke, X Lin
The American Journal of Human Genetics 89 (1), 82-93, 2011
19222011
Newly identified loci that influence lipid concentrations and risk of coronary artery disease
CJ Willer, S Sanna, AU Jackson, A Scuteri, LL Bonnycastle, R Clarke, ...
Nature genetics 40 (2), 161-169, 2008
16482008
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
15862007
Common variants at 30 loci contribute to polygenic dyslipidemia
S Kathiresan, CJ Willer, GM Peloso, S Demissie, K Musunuru, EE Schadt, ...
Nature genetics 41 (1), 56-65, 2009
13452009
Genome-wide scan reveals association of psoriasis with IL-23 and NF-κB pathways
RP Nair, KC Duffin, C Helms, J Ding, PE Stuart, D Goldgar, ...
Nature genetics 41 (2), 199, 2009
12642009
Genotype imputation
Y Li, C Willer, S Sanna, G Abecasis
Annual review of genomics and human genetics 10, 387-406, 2009
10532009
A systematic survey of loss-of-function variants in human protein-coding genes
DG MacArthur, S Balasubramanian, A Frankish, N Huang, J Morris, ...
Science 335 (6070), 823-828, 2012
10402012
Mapping copy number variation by population-scale genome sequencing
RE Mills, K Walter, C Stewart, RE Handsaker, K Chen, C Alkan, A Abyzov, ...
Nature 470 (7332), 59-65, 2011
10292011
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression
NR Wray, S Ripke, M Mattheisen, M Trzaskowski, EM Byrne, A Abdellaoui, ...
Nature genetics 50 (5), 668-681, 2018
9042018
An Abundance of Rare Functional Variants in 202 Drug Target Genes Sequenced in 14,002 People
MR Nelson, D Wegmann, MG Ehm, D Kessner, P St Jean, C Verzilli, ...
Science, 2012
6712012
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