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1
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Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis.
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Nat Genet
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2010
|
16.96
|
|
2
|
Genome-wide analysis of transcript isoform variation in humans.
|
Nat Genet
|
2008
|
6.70
|
|
3
|
Genome-wide association study for early-onset and morbid adult obesity identifies three new risk loci in European populations.
|
Nat Genet
|
2009
|
6.39
|
|
4
|
Novel loci for adiponectin levels and their influence on type 2 diabetes and metabolic traits: a multi-ethnic meta-analysis of 45,891 individuals.
|
PLoS Genet
|
2012
|
3.21
|
|
5
|
Seventy-five genetic loci influencing the human red blood cell.
|
Nature
|
2012
|
2.77
|
|
6
|
Heritability of alternative splicing in the human genome.
|
Genome Res
|
2007
|
2.76
|
|
7
|
Genomewide association study of an AIDS-nonprogression cohort emphasizes the role played by HLA genes (ANRS Genomewide Association Study 02).
|
J Infect Dis
|
2009
|
2.53
|
|
8
|
Stratifying type 2 diabetes cases by BMI identifies genetic risk variants in LAMA1 and enrichment for risk variants in lean compared to obese cases.
|
PLoS Genet
|
2012
|
2.34
|
|
9
|
A survey of genes differentially expressed in subcutaneous and visceral adipose tissue in men.
|
Obes Res
|
2004
|
2.33
|
|
10
|
TFCat: the curated catalog of mouse and human transcription factors.
|
Genome Biol
|
2009
|
2.06
|
|
11
|
A genome-wide association search for type 2 diabetes genes in African Americans.
|
PLoS One
|
2012
|
1.72
|
|
12
|
Genomewide association study of a rapid progression cohort identifies new susceptibility alleles for AIDS (ANRS Genomewide Association Study 03).
|
J Infect Dis
|
2009
|
1.57
|
|
13
|
cnvHap: an integrative population and haplotype-based multiplatform model of SNPs and CNVs.
|
Nat Methods
|
2010
|
1.41
|
|
14
|
Small deletion variants have stable breakpoints commonly associated with alu elements.
|
PLoS One
|
2008
|
1.30
|
|
15
|
Analysis of beta-cell gene expression reveals inflammatory signaling and evidence of dedifferentiation following human islet isolation and culture.
|
PLoS One
|
2012
|
1.13
|
|
16
|
Identification of novel chromosomal regions associated with airway hyperresponsiveness in recombinant congenic strains of mice.
|
Mamm Genome
|
2009
|
0.94
|
|
17
|
Rare genomic structural variants in complex disease: lessons from the replication of associations with obesity.
|
PLoS One
|
2013
|
0.88
|
|
18
|
Analysis of early C2C12 myogenesis identifies stably and differentially expressed transcriptional regulators whose knock-down inhibits myoblast differentiation.
|
Physiol Genomics
|
2011
|
0.86
|
|
19
|
Modulation of the allergic asthma transcriptome following resiquimod treatment.
|
Physiol Genomics
|
2009
|
0.86
|
|
20
|
The living microarray: a high-throughput platform for measuring transcription dynamics in single cells.
|
BMC Genomics
|
2011
|
0.84
|
|
21
|
Novel association approach for variable number tandem repeats (VNTRs) identifies DOCK5 as a susceptibility gene for severe obesity.
|
Hum Mol Genet
|
2012
|
0.83
|
|
22
|
Analysis of KLF transcription factor family gene variants in type 2 diabetes.
|
BMC Med Genet
|
2007
|
0.76
|