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- 2015
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Mark
Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci.
(
- Contribution to journal › Article
- 2014
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Mark
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility
(
- Contribution to journal › Article
- 2012
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Mark
Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke
(
- Contribution to journal › Article
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Mark
Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study
(
- Contribution to journal › Article
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Mark
Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes
(
- Contribution to journal › Article
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Mark
A genome-wide approach accounting for body mass index identifies genetic variants influencing fasting glycemic traits and insulin resistance
(
- Contribution to journal › Article
- 2011
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Mark
Phenotype mining in CNV carriers from a population cohort
(
- Contribution to journal › Article
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Mark
An Evolutionary Genomic Approach to Identify Genes Involved in Human Birth Timing
(
- Contribution to journal › Article
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Mark
Genetic variation near IRS1 associates with reduced adiposity and an impaired metabolic profile
(
- Contribution to journal › Article
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Mark
Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk
(
- Contribution to journal › Article
- 2010
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Mark
A multilocus genetic risk score for coronary heart disease: case-control and prospective cohort analyses
(
- Contribution to journal › Article
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Mark
NordicDB: a Nordic pool and portal for genome-wide control data
(
- Contribution to journal › Article
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Mark
Primate-specific evolution of noncoding element insertion into PLA2G4C and human preterm birth
(
- Contribution to journal › Article
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Mark
Genetic loci influencing kidney function and chronic kidney disease
(
- Contribution to journal › Article
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Mark
Lack of Association Between the Trp719Arg Polymorphism in Kinesin-Like Protein-6 and Coronary Artery Disease in 19 Case-Control Studies
(
- Contribution to journal › Article
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Mark
Genome-Wide Association Scan Meta-Analysis Identifies Three Loci Influencing Adiposity and Fat Distribution
(
- Contribution to journal › Article
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Mark
Biological, clinical and population relevance of 95 loci for blood lipids
(
- Contribution to journal › Article
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Mark
Hundreds of variants clustered in genomic loci and biological pathways affect human height
(
- Contribution to journal › Article
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Mark
New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk
(
- Contribution to journal › Article
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Mark
Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution
(
- Contribution to journal › Article
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Mark
Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index
(
- Contribution to journal › Article
- 2009
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Mark
Functional Variant Disrupts Insulin Induction of USF1 Mechanism for USF1-Associated Dyslipidemias
(
- Contribution to journal › Article
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Mark
Association of common variants in NPPA and NPPB with circulating natriuretic peptides and blood pressure
(
- Contribution to journal › Article
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Mark
Mother's Genome or Maternally-Inherited Genes Acting in the Fetus Influence Gestational Age in Familial Preterm Birth
(
- Contribution to journal › Article
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Mark
New susceptibility locus for coronary artery disease on chromosome 3q22.3
(
- Contribution to journal › Article
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Mark
Common variants at 30 loci contribute to polygenic dyslipidemia
(
- Contribution to journal › Article
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Mark
A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium
(
- Contribution to journal › Article
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Mark
Variants in MTNR1B influence fasting glucose levels
(
- Contribution to journal › Article
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Mark
Six new loci associated with body mass index highlight a neuronal influence on body weight regulation
(
- Contribution to journal › Article
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Mark
Genome-wide association study identifies eight loci associated with blood pressure
(
- Contribution to journal › Article
- 2008
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Mark
Independent introduction of two lactase-persistence alleles into human populations reflects different history of adaptation to milk culture
(
- Contribution to journal › Article
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Mark
Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans
(
- Contribution to journal › Article
-
Mark
Identification of ten loci associated with height highlights new biological pathways in human growth
(
- Contribution to journal › Article
-
Mark
Common Missense Variant in the Glucokinase Regulatory Protein Gene Is Associated With Increased Plasma Triglyceride and C-Reactive Protein but Lower Fasting Glucose Concentrations
(
- Contribution to journal › Article
- 2007
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Mark
Evidence of still-ongoing convergence evolution of the lactase persistence T-13910 alleles in humans
(
- Contribution to journal › Article
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Mark
A common variant of HMGA2 is associated with adult and childhood height in the general population
(
- Contribution to journal › Article
- 2002
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Mark
ABCB6 (MTABC3) excluded as the causative gene for the growth retardation syndrome with aminoaciduria, cholestasis, iron overload, and lactacidosis
(
- Contribution to journal › Article
-
Mark
Antenatal diagnosis of hereditary fetal growth retardation with aminoaciduria, cholestasis, iron overload, and lactic acidosis in the newborn infant
(
- Contribution to journal › Article
-
Mark
GRACILE syndrome, a lethal metabolic disorder with iron overload, is caused by a point mutation in BCS1L
(
- Contribution to journal › Article
- 1994
-
Mark
An extra cysteine in one of the non calcium binding EGF-like motifs of the FBN1 polypeptide is connected to a novel variant of Marfan syndrome
(
- Contribution to journal › Article