Detalhe da pesquisa
1.
The genetic architecture of type 2 diabetes.
Nature;
536(7614): 41-47, 2016 08 04.
Artigo
em Inglês
| 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.
Artigo
em Inglês
| 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.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31064750
4.
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.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29279374
5.
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.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29481666
6.
Genetic Regulation of Adipose Gene Expression and Cardio-Metabolic Traits.
Am J Hum Genet;
100(3): 428-443, 2017 Mar 02.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28257690
7.
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.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29084231
8.
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.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28193859
9.
BoostMe accurately predicts DNA methylation values in whole-genome bisulfite sequencing of multiple human tissues.
BMC Genomics;
19(1): 390, 2018 May 23.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29792182
10.
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.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23152449
11.
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.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24127591
12.
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.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23314155
13.
The metabochip, a custom genotyping array for genetic studies of metabolic, cardiovascular, and anthropometric traits.
PLoS Genet;
8(8): e1002793, 2012.
Artigo
em Inglês
| MEDLINE
| ID: mdl-22876189
14.
Systematic comparison of three genomic enrichment methods for massively parallel DNA sequencing.
Genome Res;
20(10): 1420-31, 2010 Oct.
Artigo
em Inglês
| MEDLINE
| ID: mdl-20810667
15.
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.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37386251
16.
The ClinSeq Project: piloting large-scale genome sequencing for research in genomic medicine.
Genome Res;
19(9): 1665-74, 2009 Sep.
Artigo
em Inglês
| MEDLINE
| ID: mdl-19602640
17.
LocusZoom: regional visualization of genome-wide association scan results.
Bioinformatics;
26(18): 2336-7, 2010 Sep 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-20634204
18.
Multiomic Profiling Identifies cis-Regulatory Networks Underlying Human Pancreatic ß Cell Identity and Function.
Cell Rep;
26(3): 788-801.e6, 2019 01 15.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30650367
19.
Screening of 134 single nucleotide polymorphisms (SNPs) previously associated with type 2 diabetes replicates association with 12 SNPs in nine genes.
Diabetes;
56(1): 256-64, 2007 Jan.
Artigo
em Inglês
| MEDLINE
| ID: mdl-17192490
20.
Interactions between genetic variation and cellular environment in skeletal muscle gene expression.
PLoS One;
13(4): e0195788, 2018.
Artigo
em Inglês
| MEDLINE
| ID: mdl-29659628