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- 2018
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Mark
Genetic inactivation of ANGPTL4 improves glucose homeostasis and is associated with reduced risk of diabetes
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- Contribution to journal › Article
- 2017
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Mark
Functional investigations of HNF1A identify rare variants as risk factors for type 2 diabetes in the general population
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- Contribution to journal › Article
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Mark
Variation in maturity-onset diabetes of the young genes influence response to interventions for diabetes prevention
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- Contribution to journal › Article
- 2016
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Mark
Association of Exome Sequences with Cardiovascular Traits among Blacks in the Jackson Heart Study
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- Contribution to journal › Article
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Mark
A reference panel of 64,976 haplotypes for genotype imputation
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- Contribution to journal › Article
- 2015
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Mark
Identification and Functional Characterization of G6PC2 Coding Variants Influencing Glycemic Traits Define an Effector Transcript at the G6PC2-ABCB11 Locus.
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- Contribution to journal › Article
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Mark
Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci.
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- Contribution to journal › Article
- 2014
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Mark
Simulation of Finnish population history, guided by empirical genetic data, to assess power of rare-variant tests in Finland
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- Contribution to journal › Article
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Mark
Rare variants in PPARG with decreased activity in adipocyte differentiation are associated with increased risk of type 2 diabetes
2014) In Proceedings of the National Academy of Sciences of the United States of America 111(36). p.32-13127(
- Contribution to journal › Article
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Mark
A Novel Test for Recessive Contributions to Complex Diseases Implicates Bardet-Biedl Syndrome Gene BBS10 in Idiopathic Type 2 Diabetes and Obesity
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- Contribution to journal › Article
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Mark
Age-Related Clonal Hematopoiesis Associated with Adverse Outcomes.
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- Contribution to journal › Article
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Mark
Distribution and Medical Impact of Loss-of-Function Variants in the Finnish Founder Population.
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- Contribution to journal › Article
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Mark
Loss-of-function mutations in SLC30A8 protect against type 2 diabetes.
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- Contribution to journal › Article
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Mark
Loss-of-Function Mutations in APOC3, Triglycerides, and Coronary Disease
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- Contribution to journal › Article
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Mark
Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol.
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- Contribution to journal › Article
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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
- 2013
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Mark
Assessing the phenotypic effects in the general population of rare variants in genes for a dominant Mendelian form of diabetes
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- Contribution to journal › Article
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Mark
Exome Sequencing and Directed Clinical Phenotyping Diagnose Cholesterol Ester Storage Disease Presenting as Autosomal Recessive Hypercholesterolemia.
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- Contribution to journal › Article
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Mark
Large-scale association analysis identifies new risk loci for coronary artery disease
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- Contribution to journal › Article
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Mark
Common variants associated with plasma triglycerides and risk for coronary artery disease
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- Contribution to journal › Article
- 2012
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Mark
Genetic Modulation of Lipid Profiles following Lifestyle Modification or Metformin Treatment: The Diabetes Prevention Program
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- Contribution to journal › Article
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Mark
Analysis of case-control association studies with known risk variants
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- Contribution to journal › Article
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Mark
Hypothesis-Based Analysis of Gene-Gene Interactions and Risk of Myocardial Infarction
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- Contribution to journal › Article
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Mark
Informed Conditioning on Clinical Covariates Increases Power in Case-Control Association Studies
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- Contribution to journal › Article
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Mark
Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study
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- Contribution to journal › Article
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Mark
Large-Scale Gene-Centric Meta-Analysis across 39 Studies Identifies Type 2 Diabetes Loci
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- 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
- 2011
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Mark
Testing for an Unusual Distribution of Rare Variants
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- Contribution to journal › Article
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Mark
Updated Genetic Score Based on 34 Confirmed Type 2 Diabetes Loci Is Associated With Diabetes Incidence and Regression to Normoglycemia in the Diabetes Prevention Program
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- Contribution to journal › Article
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Mark
Comparing strategies to fine-map the association of common SNPs at chromosome 9p21 with type 2 diabetes and myocardial infarction
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- Contribution to journal › Article
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Mark
Power in the Phenotypic Extremes: A Simulation Study of Power in Discovery and Replication of Rare Variants
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- Contribution to journal › Article
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Mark
A Genome-Wide Association Study Identifies LIPA as a Susceptibility Gene for Coronary Artery Disease
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- Contribution to journal › Article
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Mark
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease
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- Contribution to journal › Article
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Mark
Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure
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- 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
Common Inherited Variation in Mitochondrial Genes Is Not Enriched for Associations with Type 2 Diabetes or Related Glycemic Traits
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- Contribution to journal › Article
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Mark
Testing for an unusual distribution of rare variation
(
- Contribution to journal › Published meeting abstract
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Mark
Common Genetic Variants and Modification of Penetrance of BRCA2-Associated Breast Cancer
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- Contribution to journal › Article
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Mark
Genome-wide meta-analyses identify multiple loci associated with smoking behavior
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- 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
Twelve type 2 diabetes susceptibility loci identified through large-scale association analysis
(
- Contribution to journal › Article
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Mark
Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge
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- Contribution to journal › Article
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Mark
A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general population
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- Contribution to journal › Article
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Mark
Biological, clinical and population relevance of 95 loci for blood lipids
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- 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
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- Contribution to journal › Article
- 2009
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Mark
Tissue-specific alternative splicing of TCF7L2
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- Contribution to journal › Article
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Mark
Common variant in MTNR1B associated with increased risk of type 2 diabetes and impaired early insulin secretion.
(
- Contribution to journal › Article
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Mark
The T-381C SNP in BNP gene may be modestly associated with type 2 diabetes: an updated meta-analysis in 49 279 subjects
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- Contribution to journal › Article
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Mark
Underlying Genetic Models of Inheritance in Established Type 2 Diabetes Associations
(
- Contribution to journal › Scientific review
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Mark
New susceptibility locus for coronary artery disease on chromosome 3q22.3
(
- Contribution to journal › Article