Search details
1.
The genetic architecture of type 2 diabetes.
Nature
; 536(7614): 41-47, 2016 08 04.
Article
in English
| MEDLINE | ID: mdl-27398621
2.
Integrative analysis of gene expression, DNA methylation, physiological traits, and genetic variation in human skeletal muscle.
Proc Natl Acad Sci U S A
; 116(22): 10883-10888, 2019 05 28.
Article
in English
| MEDLINE | ID: mdl-31076557
3.
Hydroa vacciniforme-like lymphoproliferative disorder: an EBV disease with a low risk of systemic illness in whites.
Blood
; 133(26): 2753-2764, 2019 06 27.
Article
in English
| MEDLINE | ID: mdl-31064750
4.
An integrated map of structural variation in 2,504 human genomes.
Nature
; 526(7571): 75-81, 2015 Oct 01.
Article
in English
| MEDLINE | ID: mdl-26432246
5.
Evaluating the contribution of rare variants to type 2 diabetes and related traits using pedigrees.
Proc Natl Acad Sci U S A
; 115(2): 379-384, 2018 01 09.
Article
in English
| MEDLINE | ID: mdl-29279374
6.
Identification of seven novel loci associated with amino acid levels using single-variant and gene-based tests in 8545 Finnish men from the METSIM study.
Hum Mol Genet
; 27(9): 1664-1674, 2018 05 01.
Article
in English
| MEDLINE | ID: mdl-29481666
7.
Genetic Regulation of Adipose Gene Expression and Cardio-Metabolic Traits.
Am J Hum Genet
; 100(3): 428-443, 2017 Mar 02.
Article
in English
| MEDLINE | ID: mdl-28257690
8.
Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study.
PLoS Genet
; 13(10): e1007079, 2017 Oct.
Article
in English
| MEDLINE | ID: mdl-29084231
9.
Genetic regulatory signatures underlying islet gene expression and type 2 diabetes.
Proc Natl Acad Sci U S A
; 114(9): 2301-2306, 2017 02 28.
Article
in English
| MEDLINE | ID: mdl-28193859
10.
BoostMe accurately predicts DNA methylation values in whole-genome bisulfite sequencing of multiple human tissues.
BMC Genomics
; 19(1): 390, 2018 May 23.
Article
in English
| MEDLINE | ID: mdl-29792182
11.
A novel somatic mutation achieves partial rescue in a child with Hutchinson-Gilford progeria syndrome.
J Med Genet
; 54(3): 212-216, 2017 03.
Article
in English
| MEDLINE | ID: mdl-27920058
12.
A systems genetics approach identifies CXCL14, ITGAX, and LPCAT2 as novel aggressive prostate cancer susceptibility genes.
PLoS Genet
; 10(11): e1004809, 2014 Nov.
Article
in English
| MEDLINE | ID: mdl-25411967
13.
Putative Prostate Cancer Risk SNP in an Androgen Receptor-Binding Site of the Melanophilin Gene Illustrates Enrichment of Risk SNPs in Androgen Receptor Target Sites.
Hum Mutat
; 37(1): 52-64, 2016 Jan.
Article
in English
| MEDLINE | ID: mdl-26411452
14.
Correlated alterations in genome organization, histone methylation, and DNA-lamin A/C interactions in Hutchinson-Gilford progeria syndrome.
Genome Res
; 23(2): 260-9, 2013 Feb.
Article
in English
| MEDLINE | ID: mdl-23152449
15.
Chromatin stretch enhancer states drive cell-specific gene regulation and harbor human disease risk variants.
Proc Natl Acad Sci U S A
; 110(44): 17921-6, 2013 Oct 29.
Article
in English
| MEDLINE | ID: mdl-24127591
16.
Use of microarray hybrid capture and next-generation sequencing to identify the anatomy of a transgene.
Nucleic Acids Res
; 41(6): e70, 2013 Apr 01.
Article
in English
| MEDLINE | ID: mdl-23314155
17.
The metabochip, a custom genotyping array for genetic studies of metabolic, cardiovascular, and anthropometric traits.
PLoS Genet
; 8(8): e1002793, 2012.
Article
in English
| MEDLINE | ID: mdl-22876189
18.
Integrative genetic analysis of allergic inflammation in the murine lung.
Am J Respir Cell Mol Biol
; 51(3): 436-45, 2014 Sep.
Article
in English
| MEDLINE | ID: mdl-24693920
19.
Systematic comparison of three genomic enrichment methods for massively parallel DNA sequencing.
Genome Res
; 20(10): 1420-31, 2010 Oct.
Article
in English
| MEDLINE | ID: mdl-20810667
20.
Noncoding variants alter GATA2 expression in rhombomere 4 motor neurons and cause dominant hereditary congenital facial paresis.
Nat Genet
; 55(7): 1149-1163, 2023 07.
Article
in English
| MEDLINE | ID: mdl-37386251