Search details
1.
Low-coverage sequencing cost-effectively detects known and novel variation in underrepresented populations.
Am J Hum Genet
; 108(4): 656-668, 2021 04 01.
Article
in English
| MEDLINE | ID: mdl-33770507
2.
Low-pass sequencing increases the power of GWAS and decreases measurement error of polygenic risk scores compared to genotyping arrays.
Genome Res
; 31(4): 529-537, 2021 04.
Article
in English
| MEDLINE | ID: mdl-33536225
3.
Genome-wide association study identifies 74 loci associated with educational attainment.
Nature
; 533(7604): 539-42, 2016 05 26.
Article
in English
| MEDLINE | ID: mdl-27225129
4.
Comparing low-pass sequencing and genotyping for trait mapping in pharmacogenetics.
BMC Genomics
; 22(1): 197, 2021 Mar 20.
Article
in English
| MEDLINE | ID: mdl-33743587
5.
Identifying genetic variants that affect viability in large cohorts.
PLoS Biol
; 15(9): e2002458, 2017 Sep.
Article
in English
| MEDLINE | ID: mdl-28873088
6.
DNase I sensitivity QTLs are a major determinant of human expression variation.
Nature
; 482(7385): 390-4, 2012 Feb 05.
Article
in English
| MEDLINE | ID: mdl-22307276
7.
Toward a new history and geography of human genes informed by ancient DNA.
Trends Genet
; 30(9): 377-89, 2014 Sep.
Article
in English
| MEDLINE | ID: mdl-25168683
8.
Joint analysis of functional genomic data and genome-wide association studies of 18 human traits.
Am J Hum Genet
; 94(4): 559-73, 2014 Apr 03.
Article
in English
| MEDLINE | ID: mdl-24702953
9.
Approximately independent linkage disequilibrium blocks in human populations.
Bioinformatics
; 32(2): 283-5, 2016 Jan 15.
Article
in English
| MEDLINE | ID: mdl-26395773
10.
Ancient west Eurasian ancestry in southern and eastern Africa.
Proc Natl Acad Sci U S A
; 111(7): 2632-7, 2014 Feb 18.
Article
in English
| MEDLINE | ID: mdl-24550290
11.
Understanding mechanisms underlying human gene expression variation with RNA sequencing.
Nature
; 464(7289): 768-72, 2010 Apr 01.
Article
in English
| MEDLINE | ID: mdl-20220758
12.
Comparative RNA sequencing reveals substantial genetic variation in endangered primates.
Genome Res
; 22(4): 602-10, 2012 Apr.
Article
in English
| MEDLINE | ID: mdl-22207615
13.
Inference of population splits and mixtures from genome-wide allele frequency data.
PLoS Genet
; 8(11): e1002967, 2012.
Article
in English
| MEDLINE | ID: mdl-23166502
14.
The contribution of RNA decay quantitative trait loci to inter-individual variation in steady-state gene expression levels.
PLoS Genet
; 8(10): e1003000, 2012.
Article
in English
| MEDLINE | ID: mdl-23071454
15.
Natural selection for the Duffy-null allele in the recently admixed people of Madagascar.
Proc Biol Sci
; 281(1789): 20140930, 2014 Aug 22.
Article
in English
| MEDLINE | ID: mdl-24990677
16.
Low-pass sequencing plus imputation using avidity sequencing displays comparable imputation accuracy to sequencing by synthesis while reducing duplicates.
G3 (Bethesda)
; 14(2)2024 Feb 07.
Article
in English
| MEDLINE | ID: mdl-38038370
17.
Noisy splicing drives mRNA isoform diversity in human cells.
PLoS Genet
; 6(12): e1001236, 2010 Dec 09.
Article
in English
| MEDLINE | ID: mdl-21151575
18.
The CFTR Met 470 allele is associated with lower birth rates in fertile men from a population isolate.
PLoS Genet
; 6(6): e1000974, 2010 Jun 03.
Article
in English
| MEDLINE | ID: mdl-20532200
19.
Variance component estimates, phenotypic characterization, and genetic evaluation of bovine congestive heart failure in commercial feeder cattle.
Front Genet
; 14: 1148301, 2023.
Article
in English
| MEDLINE | ID: mdl-37359370
20.
False positive peaks in ChIP-seq and other sequencing-based functional assays caused by unannotated high copy number regions.
Bioinformatics
; 27(15): 2144-6, 2011 Aug 01.
Article
in English
| MEDLINE | ID: mdl-21690102