OpenAIRE | Search Publications

HYPERGENES

(382)

EPLORE

(55)

ENGAGE

(24)

HOMAGE

(24)

EU-MASCARA

(22)

GWA for Gene-Environment Interaction Effects Influencing CHD

(18)

Investigating the role of pigmentation pathway genes in moliness and melanoma risk

(17)

Genetics of melanoma risk factors

(17)

Genetics of melanoma risk factors

(17)

Validation and Replication of Genes Associated with Common Human Disease Using Australian Twin Families

(17)

Genome-wide combined linkage-association scan of multiply phenotyped twin sibships

(17)

Mapping Genes for typical migraine using twin families.

(17)

Institute for Clinical and Translational Research (UL1)

(16)

Genome-Wide Association for Loci Influencing CHD and Other Heart, Lung and Blood

(16)

Cardiovascular diseases and psychiatric disorders in the general population: a prospective follow-up study

(16)

Research Fellowship - Grant ID:442915

(15)

Association Screen of High Priority Positional Candidate Genes for Migraine

(15)

A Genome-Wide Association Study in Essential Hypertension (FEHGAS2)

(15)

NCHA Subsidiebesluit 2008-2012

(15)

CORONARY HEART DISEASE AND STROKE

(14)

AGES STUDY-THE REYKJAVIK STUDY OF HEALTHY AGING FOR THE NEW MILLENNIUM-260012100

(14)

Genetics of cardiovascular risk factors in large founder population birth control

(14)

WGA Study to Identify Genetic Variants Associated with CV Events in CHS

(14)

A national DNA control series for genetic case-control studies based on the British 1958 birth cohort

(14)

GEFOS

(13)

Statistical Methods and Algorithms for Analysis of High-throughput Genetics and Genomics Platforms

(13)

Epidemiology of Venous Thrombosis &Pulmonary Embolism

(13)

Genetic Influences on ADHD in a Finnish Birth Cohort

(13)

Type 1 Diabetes Genetics Consortium

(13)

CANDIDATE GENE STUDIES OF OBESITY GUIDED BY WHOLE GENOME ASSOCIATION DATA

(13)

THE FRAMINGHAM HEART STUDY-268025195

(13)

CHS Events Follow-up Study

(13)

Identification of genetic variants underlying coronary artery disease and associated phenotypes in Indian Asians.

(13)

Maximising knowledge from dense SNP (single nucleotide polymorphisms) data using multi-locus analysis

(12)

CENTRAL BLOOD ANALYSIS LABORATORY FOR CHS

(12)

Whole Genome Assoc. Analysis Strategies for Multi. Phenotypes

(12)

Cluster computing in genetic linkage studies on human complex traits

(12)

Twin-family database for behavior genetics and genomics studies

(12)

Assessment of biomedical risk factors and disease outcomes in the British 1958 cohort

(12)

The genetics of weight, BMI, adiposity and obesity

(12)

ATHEROREMO

(11)

Explaining the Dark Matter of Genome-wide Association Studies for Complex Disease

(11)

Accurate prediction of individual risk to disease from genome-wide association studies

(11)

CORONARY HEART DISEASE AND STROKE

(11)

CORONARY HEART DISEASE &STROKE IN THE ELDERLY

(11)

tweeling onderzoek, met een focus op gedrag en depressie

(11)

CORE--ADIPOSE TISSUE BIOLOGY AND BASIC MECHANISMS

(10)

Genetic analysis of type II diabetes in Finnish populati

(10)

Identifying Genes for Type 2 Diabetes: FUSION

(10)

Genetic Architecture of Adiposity in Multiple Large Cohorts

(10)

CCSP - FIELD CENTER AND ULTRASOUND READING CENTER

(10)

CHARGE consortium: gene discovery for CVD and aging phenotypes

(10)

NIMH Center for Collaborative Genetic Studies

(10)

Genome-wide Association in Families: Data Integrity, Design and Methods Issue

(10)

CCSP-FIELD CENTER

(9)

FIELD CENTER FOR CCSP

(9)

CORONARY HEART DISEASE &STROKE IN PEOPLE AGED 65-84

(9)

TRIAL OF ASPIRIN AND VITAMIN E IN WOMEN

(9)

AN NCRR CENTER FOR HIGH THROUGHPUT SNP GENOTYPING AND ANALYSIS: GAIN NETWORK

(9)

From modules to models: towards a better understanding of disease through advanced analysis of large-scale data

(9)

Cambridge Institute for Medical Research (CIMR).

(9)

COMMUNITY AND COHORT SURVEILLANCE PROGRAM

(8)

VARIATION IN THE EFFECTS OF ALCOHOL ON LIVER FUNCTION

(8)

GENOTYPING FOR LOCATING HUMAN DISEASE GENES

(8)

Genome-wide Search for CVD Gene-Environment Interactions

(8)

Centre for molecular-based causal analyses in health and disease

(8)

CARDIOVASCULAR HEALTH STUDY--ECHOCARDIOGRAPHY

(7)

MOLECULAR GENETICS OF SCHIZOPHRENIA

(7)

ATN 004: HEALTHY CHOICES: MOTIVATIONAL ENHANCEMENT TO PROMOTE HEALTH AND REDU

(7)

CORONARY HEART DISEASE &STROKE IN PEOPLE AGED 65-84

(7)

CCSP - FIELD CENTER

(7)

PATHOLOGY MONITORING--F344 RAT COLONY

(7)

UCLA Clinical and Translational Science Institute

(7)

Genetic Epidemiology of Metabolic Diseases of Obesity

(7)

Molecular Genetics of Schizophrenia

(7)

FHS-SCAN Genome Wide Association Scan for Atherosclerosis Pathway Genes

(7)

MOLECULAR GENETICS OF SCHIZOPHRENIA

(7)

MOLECULAR GENETICS OF SCHIZOPHRENIA

(7)

Molecular Genetics of Schizophrenia

(7)

Prospective meta-analyses of drug-gene interactions: CHARGE GWAS consortium

(7)

A Genome-wide Association Study for Early-Onset Myocardial Infarction

(7)

MOLECULAR GENETICS OF SCHIZOPHRENIA

(7)

MOLECULAR GENETICS OF SCHIZOPHRENIA

(7)

Integration of Genomics &Transcriptomics in Normal Twins &Major Depression

(7)

Dissecting genetic complexity of Alzheimer's disease and cognitive function

(7)

Gender differences in pathways to depression: the interplay of genes, environment, and (endo)phenotype

(7)

Social and psychopathological developments during adolescence: The assessment of mental disorders and contextually rated life events in the large TRAILS cohort

(7)

Delineating risk factors for the initiation and maintenance of cannabis use, in comparison with tobacco use, in adolescence

(7)

A social component of the TRIAL study (a prospective longitudinal study of mental health and social development from pre-puberty into young adulthood) with the development of pro- and antisocial behavior over time

(7)

Cardiovascular diseases and psychiatric disorders in the general population: a prospective follow-up study

(7)

OPENGENE

(6)

EPI-MIGRANT

(6)

GMI

(6)

Develop & improve methodology in gene mapping, targetting localisation of genes underlying migraine & other disorders

(6)

Genome-wide association studies of biomedical traits and endophenotypes for complex disease

(6)

Identification of genetic risk factors for asthma: genome-wide association and the role of epigenetics

(6)

SUBCLINICAL CARDIOVASCULAR DISEASE COORDINATING CENTER-268995159

(6)

CENTRAL HEMOSTATIS LABORATORY FOR CCSP

(6)

JH/CIDR Genotyping for Genome-Wide Association Studies

(6)

Funder (11)

Project (99+)

Publication Date (18)

Access Mode (2)

Type (10)

Language (5)

Community (1)

Content Provider (100+)

Funder (11)

Project (99+)

Publication Date (18)

Access Mode (2)

Type (10)

Language (5)

Community (1)

Content Provider (100+)

Dementia and hypertension

Altered molecular weight forms of adiponectin in hypertension

Genome-wide Strategies for Discovering Genetic Influences on Cognition and Cognitive Disorders: Methodological Considerations

Genome-wide association study of kidney function decline in individuals of European descent

Blood pressure as a prognostic factor after acute stroke

The International Database of Ambulatory Blood Pressure in relation to Cardiovascular Outcome (IDACO): protocol and research perspectives

Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies

Progress report on the first sub-Saharan trial of newer versus older antihypertensive drugs in native black patients

Blood pressure phenotypes in relation to the beta-adducin C1797T polymorphism in the European Project on Genes in Hypertension (EPOGH)

Night-day blood pressure ratio and dipping pattern as predictors of death and cardiovascular events in hypertension