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ENGAGE

(649)

NCHA Subsidiebesluit 2008-2012

(157)

Genetics of cardiovascular risk factors in large founder population birth control

(128)

Well-being and health: Research in the Northern Finland birth cohort 1966 (NFBC 1966) and 1985/86 (NFBC 1986)

(120)

THE FRAMINGHAM HEART STUDY-268025195

(114)

GENETIC REGULATION OF THE TIMING OF PUBERTY: Characterization of Candidate Loci for Constitutional Delay of Puberty in the Finnish Population

(113)

Whole Genome Assoc. Analysis Strategies for Multi. Phenotypes

(111)

GMI

(107)

Institute for Clinical and Translational Research (UL1)

(102)

CORONARY HEART DISEASE AND STROKE

(98)

Genetic Influences on ADHD in a Finnish Birth Cohort

(96)

GWA for Gene-Environment Interaction Effects Influencing CHD

(96)

CENTRAL BLOOD ANALYSIS LABORATORY FOR CHS

(90)

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

(90)

GEFOS

(88)

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

(87)

The genetics of weight, BMI, adiposity and obesity

(84)

CHS-Transition Phase -268055222

(81)

tweeling onderzoek, met een focus op gedrag en depressie

(81)

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

(80)

Centre for molecular-based causal analyses in health and disease

(78)

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

(78)

CHARGE consortium: gene discovery for CVD and aging phenotypes

(77)

NIMH Center for Collaborative Genetic Studies

(77)

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

(76)

Improved methods of lifestyle modification for patients at high risk for metabolic syndrome / Consortium: PrevMetSyn

(75)

Mapping Genes for typical migraine using twin families.

(75)

Epidemiology of Venous Thrombosis &Pulmonary Embolism

(75)

Cluster computing in genetic linkage studies on human complex traits

(74)

Genetics of melanoma risk factors

(72)

Genetics of melanoma risk factors

(72)

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

(72)

Center of Excellence in Complex Disease Genetics

(71)

Twin-family database for behavior genetics and genomics studies

(71)

CoE in Complex Disease Genetics

(69)

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

(69)

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

(68)

Association Screen of High Priority Positional Candidate Genes for Migraine

(68)

Dissecting genetic complexity of Alzheimer's disease and cognitive function

(67)

CHS Events Follow-up Study

(64)

Type 1 Diabetes Genetics Consortium

(61)

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

(61)

The Cardiovascular Risk in Young Finns Study - the 27-year follow-up.

(60)

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

(60)

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

(59)

Research Fellowship - Grant ID:442915

(58)

CORONARY HEART DISEASE &STROKE IN THE ELDERLY

(58)

CORONARY HEART DISEASE &STROKE IN PEOPLE AGED 65-84

(57)

Roles of inflammation, oxidation, sex hormones and genetic variation in vascular aging and the development of atherosclerosis over the life-course.

(56)

CORONARY HEART DISEASE AND STROKE

(56)

UCLA Clinical and Translational Science Institute

(54)

CORONARY HEART DISEASE &STROKE IN PEOPLE AGED 65-84

(54)

CCSP - FIELD CENTER AND ULTRASOUND READING CENTER

(54)

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

(52)

CCSP-FIELD CENTER

(51)

Role of early life risk factors in associations between work, cardiovascular disease and depression: A life course approach based on two prospective cohorts. / Consortium: ELRFWCDD

(49)

CARDIOVASCULAR HEALTH STUDY--ECHOCARDIOGRAPHY

(49)

CANDIDATE GENE STUDIES OF OBESITY GUIDED BY WHOLE GENOME ASSOCIATION DATA

(49)

Major Depression: Stage 1 Genomewide Association in Population-Based Samples

(49)

BIOSHARE-EU

(48)

COMMUNITY AND COHORT SURVEILLANCE PROGRAM

(48)

MRI READING CENTER FOR THE CARDIOVASCULAR HEALTH STUDY

(48)

Integration of Genomics &Transcriptomics in Normal Twins &Major Depression

(48)

BBMRI-NL

(48)

CCSP - FIELD CENTER

(47)

Understanding the genetic basis of common human diseases: core funding for the Wellcome Trust Centre for Human Genetics.

(47)

FIELD CENTER FOR CCSP

(46)

COMMUNITY AND COHORT SURVEILLANCE PROGRAMS

(45)

Candidate gene variation and the association between early growth and adult disease: studies in the 1966 Northern Finland Birth Cohort

(45)

The Application of 'Omics' to Public Health Epidemiology: Prospective Analysis of the FINRISK 1997 Cohort

(44)

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

(44)

CENTRAL HEMOSTATIS LABORATORY FOR CCSP

(44)

Genome Wide Association Coordinating Center

(44)

Wellcome Trust Sanger Institute - generic account for deposition of all core- funded research papers

(44)

PHASE

(43)

CHS-ULTRASOUND READING

(43)

Public Health Genomics to Practice in Cardiovascular Diseases / Consortium: PUBGENSENS

(42)

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

(42)

CORE--ADIPOSE TISSUE BIOLOGY AND BASIC MECHANISMS

(42)

Genetic analysis of type II diabetes in Finnish populati

(42)

Exceptional aging: 12 year trajectories to function

(42)

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

(42)

MSDs@LIFECOURSE CONSORTIU Subproject: Shared Risk Factors Study Group Turku University Central Hospital / Consortium: MSDs@LIFE

(41)

OPENGENE

(41)

ATHEROREMO

(41)

Identifying Genes for Type 2 Diabetes: FUSION

(41)

CHS RETINAL READING CENTER

(41)

TRIAL OF ASPIRIN AND VITAMIN E IN WOMEN

(40)

Genetic and environmental predictors of tobacco, drug and alcohol addiction in adolescence and young adulthood ¿ a lifecourse twin and population approach / Consortium: addictgene

(39)

EURHEALTHAGEING

(39)

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

(39)

Identification of new genes for type 2 diabetes

(38)

Sustainable Innovative Materials in High Tech Applications. An Interdisciplinary Approach to Design,Engineering Technology and Chemistry of Environmentally Sound Products and Production.

(38)

SUBCLINICAL CARDIOVASCULAR DISEASE COORDINATING CENTER-268995159

(38)

VARIATION IN THE EFFECTS OF ALCOHOL ON LIVER FUNCTION

(38)

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

(38)

Cambridge Institute for Medical Research (CIMR).

(38)

HYPERGENES

(37)

SUBCLINICAL CARDIOVASCULAR DISEASE STUDY--EBCT READING

(37)

Funder (15)

Project (99+)

Publication Date (11)

Access Mode (3)

Type (10)

Language (2)

Community (2)

Content Provider (100+)

Collected From (100+)

Funder (15)

Project (99+)

Publication Date (11)

Access Mode (3)

Type (10)

Language (2)

Community (2)

Content Provider (100+)

Collected From (100+)

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

Variation at 2q35 (PNKD and TMBIM1) influences colorectal cancer risk and identifies a pleiotropic effect with inflammatory bowel disease

Differential gene expression patterns between smokers and non-smokers: cause or consequence?

Heritability of metabolic syndrome traits in a large population-based sample

A Meta-Analysis of Thyroid-Related Traits Reveals Novel Loci and Gender-Specific Differences in the Regulation of Thyroid Function

Novel Loci for Adiponectin Levels and Their Influence on Type 2 Diabetes and Metabolic Traits: A Multi-Ethnic Meta-Analysis of 45,891 Individuals

Genome-wide association study identifies multiple loci influencing human serum metabolite levels

Genetic Architecture of Vitamin B12 and Folate Levels Uncovered Applying Deeply Sequenced Large Datasets

Association of genetic Loci with glucose levels in childhood and adolescence: a meta-analysis of over 6,000 children.

Genotype-driven recruitment: a strategy whose time has come?