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Project:ENGAGE

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Funder (16)
European Commi... (705)
Wellcome Trust (442)
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Project (98)
ENGAGE (705)
NCHA Subsidieb... (165)
Genetics of ca... (149)
Well-being and... (134)
THE FRAMINGHAM... (129)
GENETIC REGULA... (127)
Whole Genome A... (123)
GMI (111)
Genetic Influe... (110)
Institute for ... (109)
CORONARY HEART... (105)
GWA for Gene-E... (104)
Genome-Wide Ass... (99)
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tweeling onderz... (95)
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A Genome-Wide A... (93)
GEFOS (91)
CHS-Transition ... (87)
Centre for mole... (87)
A national DNA ... (87)
Improved method... (83)
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CHARGE consorti... (78)
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Mapping Genes f... (75)
Genetics of mel... (74)
Genetics of mel... (73)
Investigating t... (69)
AGES STUDY-THE ... (69)
CHS Events Foll... (69)
Type 1 Diabetes... (68)
Association Scr... (67)
Dissecting gene... (67)
The Cardiovascu... (65)
WGA Study to Id... (63)
Roles of inflam... (62)
Statistical Met... (61)
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CORONARY HEART ... (60)
CCSP - FIELD CE... (60)
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CORONARY HEART ... (58)
CORONARY HEART ... (57)
COMMUNITY AND C... (55)
UCLA Clinical a... (55)
CANDIDATE GENE ... (55)
Role of early l... (54)
CARDIOVASCULAR ... (54)
CCSP-FIELD CENTER (54)
MRI READING CEN... (54)
Understanding t... (54)
The Application... (51)
COMMUNITY AND C... (51)
CCSP - FIELD CE... (51)
Public Health G... (50)
Develop & impro... (50)
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BIOSHARE-EU (49)
FIELD CENTER FO... (49)
Major Depressio... (49)
BBMRI-NL (49)
CENTRAL HEMOSTA... (48)
OPENGENE (47)
Wellcome Trust ... (47)
CORE--ADIPOSE T... (46)
Genetic and env... (45)
MSDs@LIFECOURSE... (45)
Maximising know... (45)
PHASE (45)
CHS-ULTRASOUND ... (45)
Integration of ... (45)
Sustainable Inn... (43)
EURHEALTHAGEING (43)
CHS RETINAL REA... (43)
Exceptional agi... (43)
Prospective met... (43)
Cambridge Insti... (43)
Genome-wide ass... (42)
Genetic analysi... (42)
Identifying Gen... (42)
HYPERGENES (40)
ATHEROREMO (40)
TRIAL OF ASPIRI... (40)
Identification ... (39)
Predictors, neu... (39)
AN NCRR CENTER ... (39)
VARIATION IN TH... (39)
Oxygenology of ... (38)

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2012 (130)
2013 (102)
2011 (92)
2010 (69)
2017 (63)
2014 (58)
2015 (53)
2009 (47)
2016 (42)
2018 (27)
2008 (8)
2019 (8)

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Open Access (611)
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Type (11)
Article (699)
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English (685)

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PLoS Genetics (34)
PLoS ONE (34)
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MPG.PuRe (20)
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Collected From (100+)
PubMed Central (359)
HEALTH FP7 Pub... (332)
SESAM Publicat... (249)
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NARCIS (171)
CORE (RIOXX-UK... (127)
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HELDA - Digital... (60)
Spiral - Imperi... (57)
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INRIA a CCSD el... (11)
Norwegian Open ... (10)
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edoc (3)
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Project:ENGAGE

Funder (16)
European Commi... (705)
Wellcome Trust (442)
National Insti... (421)
Netherlands Or... (262)
Academy of Fin... (256)
View more
Funder
European Commission (705)
Wellcome Trust (442)
National Institutes of Health (421)
Netherlands Organisation for Scientific Research (NWO) (262)
Academy of Finland (256)
Research Council UK (205)
National Health and Medical Research Council (NHMRC) (179)
Swiss National Science Foundation (102)
Australian Research Council (ARC) (80)
Canadian Institutes of Health Research (74)
Austrian Science Fund (FWF) (27)
Ministry of Science, Education and Sports of the Republic of Croatia (MSES) (23)
Croatian Science Foundation (CSF) (22)
National Science Foundation (15)
Fundação para a Ciência e a Tecnologia, I.P. (5)
Science Foundation Ireland (3)

Project (98)
ENGAGE (705)
NCHA Subsidieb... (165)
Genetics of ca... (149)
Well-being and... (134)
THE FRAMINGHAM... (129)
View more
Project
ENGAGE (705)
NCHA Subsidiebesluit 2008-2012 (165)
Genetics of cardiovascular risk factors in large founder population birth control (149)
Well-being and health: Research in the Northern Finland birth cohort 1966 (NFBC 1966) and 1985/86 (NFBC 1986) (134)
THE FRAMINGHAM HEART STUDY-268025195 (129)
GENETIC REGULATION OF THE TIMING OF PUBERTY: Characterization of Candidate Loci for Constitutional Delay of Puberty in the Finnish Population (127)
Whole Genome Assoc. Analysis Strategies for Multi. Phenotypes (123)
GMI (111)
Genetic Influences on ADHD in a Finnish Birth Cohort (110)
Institute for Clinical and Translational Research (UL1) (109)
CORONARY HEART DISEASE AND STROKE (105)
GWA for Gene-Environment Interaction Effects Influencing CHD (104)
Genome-Wide Association for Loci Influencing CHD and Other Heart, Lung and Blood (99)
CENTRAL BLOOD ANALYSIS LABORATORY FOR CHS (96)
tweeling onderzoek, met een focus op gedrag en depressie (95)
The genetics of weight, BMI, adiposity and obesity (94)
A Genome-Wide Association Study in Essential Hypertension (FEHGAS2) (93)
GEFOS (91)
CHS-Transition Phase -268055222 (87)
Centre for molecular-based causal analyses in health and disease (87)
A national DNA control series for genetic case-control studies based on the British 1958 birth cohort (87)
Improved methods of lifestyle modification for patients at high risk for metabolic syndrome / Consortium: PrevMetSyn (83)
Twin-family database for behavior genetics and genomics studies (83)
Assessment of biomedical risk factors and disease outcomes in the British 1958 cohort (83)
Center of Excellence in Complex Disease Genetics (80)
Genome-wide combined linkage-association scan of multiply phenotyped twin sibships (80)
Epidemiology of Venous Thrombosis &Pulmonary Embolism (80)
CoE in Complex Disease Genetics (78)
CHARGE consortium: gene discovery for CVD and aging phenotypes (78)
Validation and Replication of Genes Associated with Common Human Disease Using Australian Twin Families (77)
NIMH Center for Collaborative Genetic Studies (77)
Cluster computing in genetic linkage studies on human complex traits (76)
Cardiovascular diseases and psychiatric disorders in the general population: a prospective follow-up study (76)
Mapping Genes for typical migraine using twin families. (75)
Genetics of melanoma risk factors (74)
Genetics of melanoma risk factors (73)
Investigating the role of pigmentation pathway genes in moliness and melanoma risk (69)
AGES STUDY-THE REYKJAVIK STUDY OF HEALTHY AGING FOR THE NEW MILLENNIUM-260012100 (69)
CHS Events Follow-up Study (69)
Type 1 Diabetes Genetics Consortium (68)
Association Screen of High Priority Positional Candidate Genes for Migraine (67)
Dissecting genetic complexity of Alzheimer's disease and cognitive function (67)
The Cardiovascular Risk in Young Finns Study - the 27-year follow-up. (65)
WGA Study to Identify Genetic Variants Associated with CV Events in CHS (63)
Roles of inflammation, oxidation, sex hormones and genetic variation in vascular aging and the development of atherosclerosis over the life-course. (62)
Statistical Methods and Algorithms for Analysis of High-throughput Genetics and Genomics Platforms (61)
Research Fellowship - Grant ID:442915 (60)
CORONARY HEART DISEASE &STROKE IN THE ELDERLY (60)
CCSP - FIELD CENTER AND ULTRASOUND READING CENTER (60)
CORONARY HEART DISEASE &STROKE IN PEOPLE AGED 65-84 (59)
CORONARY HEART DISEASE AND STROKE (58)
CORONARY HEART DISEASE &STROKE IN PEOPLE AGED 65-84 (57)
COMMUNITY AND COHORT SURVEILLANCE PROGRAM (55)
UCLA Clinical and Translational Science Institute (55)
CANDIDATE GENE STUDIES OF OBESITY GUIDED BY WHOLE GENOME ASSOCIATION DATA (55)
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 (54)
CARDIOVASCULAR HEALTH STUDY--ECHOCARDIOGRAPHY (54)
CCSP-FIELD CENTER (54)
MRI READING CENTER FOR THE CARDIOVASCULAR HEALTH STUDY (54)
Understanding the genetic basis of common human diseases: core funding for the Wellcome Trust Centre for Human Genetics. (54)
The Application of 'Omics' to Public Health Epidemiology: Prospective Analysis of the FINRISK 1997 Cohort (51)
COMMUNITY AND COHORT SURVEILLANCE PROGRAMS (51)
CCSP - FIELD CENTER (51)
Public Health Genomics to Practice in Cardiovascular Diseases / Consortium: PUBGENSENS (50)
Develop & improve methodology in gene mapping, targetting localisation of genes underlying migraine & other disorders (50)
Genome Wide Association Coordinating Center (50)
Candidate gene variation and the association between early growth and adult disease: studies in the 1966 Northern Finland Birth Cohort (50)
BIOSHARE-EU (49)
FIELD CENTER FOR CCSP (49)
Major Depression: Stage 1 Genomewide Association in Population-Based Samples (49)
BBMRI-NL (49)
CENTRAL HEMOSTATIS LABORATORY FOR CCSP (48)
OPENGENE (47)
Wellcome Trust Sanger Institute - generic account for deposition of all core- funded research papers (47)
CORE--ADIPOSE TISSUE BIOLOGY AND BASIC MECHANISMS (46)
Genetic and environmental predictors of tobacco, drug and alcohol addiction in adolescence and young adulthood ¿ a lifecourse twin and population approach / Consortium: addictgene (45)
MSDs@LIFECOURSE CONSORTIU Subproject: Shared Risk Factors Study Group Turku University Central Hospital / Consortium: MSDs@LIFE (45)
Maximising knowledge from dense SNP (single nucleotide polymorphisms) data using multi-locus analysis (45)
PHASE (45)
CHS-ULTRASOUND READING (45)
Integration of Genomics &Transcriptomics in Normal Twins &Major Depression (45)
Sustainable Innovative Materials in High Tech Applications. An Interdisciplinary Approach to Design,Engineering Technology and Chemistry of Environmentally Sound Products and Production. (43)
EURHEALTHAGEING (43)
CHS RETINAL READING CENTER (43)
Exceptional aging: 12 year trajectories to function (43)
Prospective meta-analyses of drug-gene interactions: CHARGE GWAS consortium (43)
Cambridge Institute for Medical Research (CIMR). (43)
Genome-wide association studies of biomedical traits and endophenotypes for complex disease (42)
Genetic analysis of type II diabetes in Finnish populati (42)
Identifying Genes for Type 2 Diabetes: FUSION (42)
HYPERGENES (40)
ATHEROREMO (40)
TRIAL OF ASPIRIN AND VITAMIN E IN WOMEN (40)
Identification of new genes for type 2 diabetes (39)
Predictors, neuropsychological correlates, and consequences of cannabis and alcohol use among Finnish young adults. A twin and population approach (39)
AN NCRR CENTER FOR HIGH THROUGHPUT SNP GENOTYPING AND ANALYSIS: GAIN NETWORK (39)
VARIATION IN THE EFFECTS OF ALCOHOL ON LIVER FUNCTION (39)
Oxygenology of soil (38)

Publication Date (12)
2012 (130)
2013 (102)
2011 (92)
2010 (69)
2017 (63)
View more
Publication Date
2012 (130)
2013 (102)
2011 (92)
2010 (69)
2017 (63)
2014 (58)
2015 (53)
2009 (47)
2016 (42)
2018 (27)
2008 (8)
2019 (8)

Access Mode (4)
Open Access (611)
Closed Access (88)
Restricted (5)
not available (1)
Access Mode
Open Access (611)
Closed Access (88)
Restricted (5)
not available (1)

Type (11)
Article (699)
Other literatu... (102)
Review (11)
Preprint (4)
Doctoral thesis (3)
View more
Type
Article (699)
Other literature type (102)
Review (11)
Preprint (4)
Doctoral thesis (3)
0044 (1)
Book (1)
Conference object (1)
Dataset (1)
External research report (1)
Report (1)

Language (1)
English (685)
Language
English (685)

Community (1)
EGI Federation (25)
Community
EGI Federation (25)

Content Provider (100+)
Unknown Reposi... (378)
Europe PubMed ... (359)
Erasmus Univers... (72)
Edinburgh Resea... (62)
HELDA - Digital... (60)
View more
Content Provider
Showing top 100 values.
Unknown Repository (378)
Europe PubMed Central (359)
Erasmus University Institutional Repository (72)
Edinburgh Research Explorer (62)
HELDA - Digital Repository of the University of Helsinki (60)
Spiral - Imperial College Digital Repository (57)
UCL Discovery (56)
DSpace at VU (41)
University of Groningen Digital Archive (39)
Digital Access to Scholarship at Harvard (35)
PLoS Genetics (34)
PLoS ONE (34)
SpringerOpen (33)
Enlighten (28)
St George's Online Research Archive (25)
Universiteit van Amsterdam Digital Academic Repository (24)
LSHTM Research Online (23)
MPG.PuRe (20)
Oxford University Research Archive (19)
Radboud Repository (18)
Trepo - Institutional Repository of Tampere University (17)
PURE Aarhus University (15)
BASE (Open Access Aggregator) (15)
UniSA Research Outputs Repository (15)
Hyper Article en Ligne (15)
King's Research Portal (14)
Open Access LMU (14)
Explore Bristol Research (14)
Publikationer från Uppsala Universitet (13)
Online Research @ Cardiff (13)
Queen's University Research Portal (12)
INRIA a CCSD electronic archive server (11)
Norwegian Open Research Archives (10)
Ghent University Academic Bibliography (10)
Copenhagen University Research Information System (9)
Serveur académique lausannois (9)
UPF Digital Repository (9)
University of Southern Denmark Research Output (8)
Brunel University Research Archive (7)
Lund University Publications (6)
University of Oulu Repository - Jultika (6)
Landspítali University Hospital Research Archive (6)
Translational Psychiatry (5)
University of Liverpool Repository (5)
UM Publications (5)
BMC Genomics (4)
Norsk Epidemiologi (4)
BMC Medical Genomics (4)
e-Prints Soton (4)
DSpace@MIT (4)
Aaltodoc Publication Archive (4)
Leiden University Repository (4)
eScholarship - University of California (4)
Institutional Repository Universiteit Antwerpen (4)
UEF eRepository (4)
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Wageningen Yield (4)
HAL-Inserm (4)
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BMC Bioinformatics (3)
Scientific Reports (3)
Jagiellonian University Repository (3)
Kingston University Research Repository (3)
Keele Research Repository (3)
Archivio istituzionale della ricerca - Università di Trieste (3)
edoc (3)
Nottingham ePrints (3)
Publikationer från Umeå universitet (3)
LAReferencia - Red Federada de Repositorios Institucionales de Publicaciones Científicas Latinoamericanas (3)
Archive ouverte UNIGE (3)
Lirias (3)
Nucleic Acids Research (2)
BMC Medical Genetics (2)
ARCHIVO DIGITAL PARA LA DOCENCIA Y LA INVESTIGACION (2)
Hal-Diderot (2)
Diposit Digital de la Universitat de Barcelona (2)
HAL AMU (2)
NTNU Open (2)
Archivio istituzionale della ricerca - Alma Mater Studiorum Università di Bologna (2)
arXiv.org e-Print Archive (2)
Open Repository and Bibliography - University of Liège (2)
Research Repository of Catalonia (2)
Opin visindi (2)
Juelich Shared Electronic Resources (2)
Universiteit Twente Repository (2)
Digital.CSIC (2)
HKU Scholars Hub (2)
MediaTUM (2)
Journal of the Renin-Angiotensin-Aldosterone System (1)
PLoS Computational Biology (1)
G3: Genes, Genomes, Genetics (1)
Aging Cell (1)
BMC Genetics (1)
Scientific Reports (1)
Investigative Genetics (1)
GigaScience (1)
Disease Models & Mechanisms (1)
Nature Communications (1)
Schizophrenia Research: Cognition (1)
PLoS Medicine (1)

Collected From (100+)
PubMed Central (359)
HEALTH FP7 Pub... (332)
SESAM Publicat... (249)
Crossref (243)
NARCIS (171)
View more
Collected From
Showing top 100 values.
PubMed Central (359)
HEALTH FP7 Publications Database (332)
SESAM Publication Database - FP7 HEALTH (249)
Crossref (243)
NARCIS (171)
CORE (RIOXX-UK Aggregator) (127)
DOAJ-Articles (84)
Edinburgh Research Explorer (62)
HELDA - Digital Repository of the University of Helsinki (60)
Spiral - Imperial College Digital Repository (57)
UCL Discovery (56)
Digital Access to Scholarship at Harvard (35)
European Research Council (ERC) (26)
MPG.PuRe (20)
Oxford University Research Archive (19)
Trepo - Institutional Repository of Tampere University (17)
BASE (Open Access Aggregator) (16)
PURE Aarhus University (15)
UniSA Research Outputs Repository (15)
Hyper Article en Ligne (15)
King's Research Portal (14)
Open Access LMU (14)
Explore Bristol Research (14)
Datacite (13)
Sygma (13)
Publikationer från Uppsala Universitet (13)
Queen's University Research Portal (12)
INRIA a CCSD electronic archive server (11)
Norwegian Open Research Archives (10)
Ghent University Academic Bibliography (10)
Copenhagen University Research Information System (9)
Serveur académique lausannois (9)
UPF Digital Repository (9)
University of Southern Denmark Research Output (8)
Brunel University Research Archive (7)
Lund University Publications (6)
University of Oulu Repository - Jultika (6)
Landspítali University Hospital Research Archive (6)
e-Prints Soton (4)
DSpace@MIT (4)
Aaltodoc Publication Archive (4)
eScholarship - University of California (4)
Institutional Repository Universiteit Antwerpen (4)
UEF eRepository (4)
Publikationer från Högskolan i Jönköping (4)
HAL-Inserm (4)
University of Lincoln Institutional Repository (4)
Scientific Reports (3)
Web Crawl (3)
Jagiellonian University Repository (3)
Archivio istituzionale della ricerca - Università di Trieste (3)
edoc (3)
Publikationer från Umeå universitet (3)
LAReferencia - Red Federada de Repositorios Institucionales de Publicaciones Científicas Latinoamericanas (3)
Archive ouverte UNIGE (3)
Lirias (3)
SESAM Publication Database - FP7 KBBE (2)
ARCHIVO DIGITAL PARA LA DOCENCIA Y LA INVESTIGACION (2)
Hal-Diderot (2)
Diposit Digital de la Universitat de Barcelona (2)
HAL AMU (2)
NTNU Open (2)
Archivio istituzionale della ricerca - Alma Mater Studiorum Università di Bologna (2)
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Variants in ADCY5 and near CCNL1 are associated with fetal growth and birth weight
Article English CLOSED
Freathy, Rachel M.; Mook-Kanamori, Dennis O.; Sovio, Ulla; Prokopenko, Inga; Timpson, Nicholas J.; Berry, Diane J.; Warrington, Nicole M.; Widen, Elisabeth; Hottenga, Jouke Jan; Kaakinen, Marika; Lange, Leslie A.; Bradfield, Jonathan P.; Kerkhof, Marjan; Marsh, Julie A.; Maegi, Reedik; ...
(2010)
Publisher: NATURE PUBLISHING GROUP

Project: NIH | CANDIDATE GENE STUDIES OF... (3R01DK075787-07S1), AKA | Developmental origins of ... (129255), AKA | GENETIC REGULATION OF THE... (120315), AKA | DOHaD-Pubertal growth and... (129287), AKA | Well-being and health: Re... (104781), AKA | Early growth, programming... (209072), EC | ENGAGE (201413), WT | The role of maternal and ... (085541), WT | Identifying multiple comm... (085301), WT | The genetics of weight, B... (076113), WT | A national DNA control se... (068545), RCUK | Assessment of biomedical ... (G0000934), RCUK | Centre for molecular-base... (G0600705), RCUK | Translating genome-wide a... (G0601261), NWO | Twin-family database for ... (2200125679),...
Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility
Article English OPEN
(2014)

Project: WT | Understanding the genetic... (090532), WT | Characterising causal all... (098381), WT | Next-Generation Disease A... (090367), WT | Statistical methods for t... (098017), NIH | Identifying variants caus... (5U01DK085545-02),CIHR, EC | ENGAGE (201413), NIH | Identifying Genes for Typ... (1R01DK062370-01A1), NIH | Identification and Replic... (5U01DK085501-02), NIH | DESIGN AND ANALYSIS OF HU... (5R01HG000376-08), NIH | Genetics of Type 2 Diabet... (5R01DK073541-03), NIH | Identifying T2D Variants ... (1U01DK085584-01)
To further understanding of the genetic basis of type 2 diabetes (T2D) susceptibility, we aggregated published meta-analyses of genome-wide association studies (GWAS) including 26,488 cases and 83,964 controls of European, East Asian, South Asian, and Mexican and Mexica...
Hundreds of variants clustered in genomic loci and biological pathways affect human height
Article English CLOSED
Allen, Hana Lango; Estrada, Karol; Lettre, Guillaume; Berndt, Sonja I.; Weedon, Michael N.; Rivadeneira, Fernando; Willer, Cristen J.; Jackson, Anne U.; Vedantam, Sailaja; Raychaudhuri, Soumya; Ferreira, Teresa; Wood, Andrew R.; Weyant, Robert J.; Segre, Ayellet V.; Speliotes, Elizabeth K.; ...
(2010)
Publisher: NATURE PUBLISHING GROUP

Project: NIH | Whole Genome Assoc. Analy... (5RL1MH083268-04), NIH | CHS-ULTRASOUND READING (N01HC045133-004), NIH | THE FRAMINGHAM HEART STUD... (N01HC025195-005), NIH | DETECTING SUSCEPTIBILITY ... (1R01MH059160-01A1), NIH | WGA Study to Identify Gen... (5R01HL087652-03), NIH | GWA for Gene-Environment ... (5U01HG004402-02), NIH | A Genome-wide Association... (5R01HL087676-03), NIH | Genome-wide Search for CV... (5U01HL072515-06), NIH | GENOTYPING FOR LOCATING H... (N01HG065403-001), NIH | Institute for Clinical an... (3UL1RR025005-03S2), NIH | The international 1q type... (5R01DK073490-04), NIH | Analysis of Fatty Liver i... (5K23DK080145-03), NIH | Genetic determinants of p... (1R01CA104021-01A2), NIH | CANDIDATE GENE STUDIES OF... (3R01DK075787-07S1), NIH | Epidemiology of IGF's and... (5R01AG031890-04),...
The Role of Adiposity in Cardiometabolic Traits: A Mendelian Randomization Analysis
Article English OPEN
Fall, Tove; Hagg, Sara; Maegi, Reedik; Ploner, Alexander; Fischer, Krista; Horikoshi, Momoko; Sarin, Antti-Pekka; Thorleifsson, Gudmar; Ladenvall, Claes; Kals, Mart; Kuningas, Maris; Draisma, Harmen H. M.; Ried, Janina S.; van Zuydam, Natalie R.; Huikari, Ville; ...
(2013)
Publisher: PUBLIC LIBRARY SCIENCE

Project: EC | GMI (230374), EC | CEED3 (223211), AKA | CoE in Complex Disease Ge... (213506), AKA | Genetic and environmental... (141054), AKA | Center of Excellence in C... (129680), ARC | Maximising knowledge from... (DP0770096), ARC | Quantitative and Molecula... (DP0212016), EC | ENGAGE (201413), AKA | Improved methods of lifes... (129418), AKA | Well-being and health: Re... (104781), ARC | Locating genes for elemen... (DP0343921), AKA | GENETIC REGULATION OF THE... (120315), AKA | The Application of 'Omics... (139635), NIH | Integration of Genomics &... (1RC2MH089951-01), WT | The UK Type 2 diabetes ge... (072960),...
A genome-wide association study of corneal astigmatism: The CREAM Consortium
Article English OPEN
Shah, Rupal L.; Li, Qing; Zhao, Wanting; Tedja, Milly S.; Tideman, J. Willem L.; Khawaja, Anthony P.; Fan, Qiao; Yazar, Seyhan; Williams, Katie M.; Verhoeven, Virginie J.M.; Xie, Jing; Wang, Ya Xing; Hess, Moritz; Nickels, Stefan; Lackner, Karl J.; ...
(2018)
Publisher: Molecular Vision

Project: WT, RCUK | Diet, lifestyle and biolo... (G1000143), NWO | Towards solving MYOPia: f... (2300187867), AKA | Center of Excellence in C... (129680), EC | ENGAGE (201413), EC | MYOP-PATH (648268), AKA | CoE in Complex Disease Ge... (213506), NHMRC | Stem Cell Bioinformatics ... (1111437), NHMRC | Genome-wide association s... (1021105), NHMRC | Pathways to precision med... (1138585)
Purpose To identify genes and genetic markers associated with corneal astigmatism. Methods A meta-analysis of genome-wide association studies (GWASs) of corneal astigmatism undertaken for 14 European ancestry (n=22,250) and 8 Asian ancestry (n=9,120) cohorts was perform...
Hundreds of variants clustered in genomic loci and biological pathways affect human height
Article English OPEN
Lango Allen, Hana; Estrada, Karol; Lettre, Guillaume; Berndt, Sonja I.; Weedon, Michael N.; Rivadeneira, Fernando; Willer, Cristen J.; Jackson, Anne U.; Vedantam, Sailaja; Raychaudhuri, Soumya; Ferreira, Teresa; Wood, Andrew R.; Weyant, Robert J.; Segrè, Ayellet V.; Speliotes, Elizabeth K.; ...
(2010)

Project: NIH | A Genome-Wide Association... (5U01MH079469-03), NIH | Genetic Variants Associat... (1K99HL094535-01A1), NIH | Genes and Environment Ini... (5U01HG004399-02), NIH | Genome-Wide Association f... (5R01HL087641-02), NIH | Genome-wide Association i... (5U01HL084756-03), NIH | A Genome-Wide Association... (5R01HL086694-05), NIH | Genome-wide Association S... (5U01MH079470-03), NIH | CHS Events Follow-up Stud... (1U01HL080295-01), NIH | Bioinformatics and Popula... (1K08AR055688-01A1), NIH | MOLECULAR GENETICS OF SCH... (5R01MH059588-04), NIH | MOLECULAR GENETICS OF SCH... (5R01MH059571-04), NIH | A Genome-wide Association... (5R01HL087676-03), NIH | GWA for Gene-Environment ... (5U01HG004402-02), NIH | Genetic determinants of p... (1R01CA104021-01A2), NIH | The international 1q type... (5R01DK073490-04),...
Most common human traits and diseases have a polygenic pattern of inheritance: DNA sequence variants at many genetic loci influence phenotype. Genome-wide association (GWA) studies have identified >600 variants associated with human traits1, but these typically explain ...
Impact of smoking and smoking cessation on cardiovascular events and mortality among older adults: meta-analysis of individual participant data from prospective cohort studies of the CHANCES consortium
Article English OPEN
Mons, U.; Müezzinler, A.; Gellert, C.; Schöttker, B.; Abnet, C. C.; Bobak, M.; de Groot, L.; Freedman, N. D.; Jansen, E.; Kee, F.; Kromhout, D.; Kuulasmaa, K.; Laatikainen, T.; O Doherty, M. G.; Bueno-de-Mesquita, B.; ...
(2015)

Project: NIH | Health disparities and ag... (5R01AG023522-04), EC | SHARE_M4 (261982), EC | SHARE_LEAP (227822), EC | SHARE-PREP (211909), EC | ENGAGE (201413), EC | BIOMARCARE (278913), EC | CHANCES (242244), NIH | DEVELOPING AN ISRAELI VER... (1R21AG025169-01), WT | Determinants of cardiovas... (081081), WT | Determinants of cardiovas... (064947), NIH | HEALTH AND ECONOMIC STATU... (5P01AG008291-19), NIH | FINANCIAL STATUS--RETIREM... (2P01AG005842-04), NIH | RAND CENTER FOR THE STUDY... (5P30AG012815-10), NIH | Health and Retirement Stu... (3U01AG009740-24S2)
To investigate the impact of smoking and smoking cessation on cardiovascular mortality, acute coronary events, and stroke events in people aged 60 and older, and to calculate and report risk advancement periods for cardiovascular mortality in addition to traditional epi...
A Genome-Wide Association Study Reveals Variants in ARL15 that Influence Adiponectin Levels
Article English OPEN
Richards, J. Brent; Waterworth, Dawn; O'Rahilly, Stephen; Hivert, Marie-France; Loos, Ruth J. F.; Perry, John R. B.; Tanaka, Toshiko; Timpson, Nicholas John; Semple, Robert K.; Soranzo, Nicole; Song, Kijoung; Rocha, Nuno; Grundberg, Elin; Dupuis, Josee; Florez, Jose C.; ...
(2009)
Publisher: PUBLIC LIBRARY SCIENCE

Project: EC | GEFOS (201865),CIHR, EC | ENGAGE (201413), NIH | THE FRAMINGHAM HEART STUD... (N01HC025195-005), NIH | Genetic variation in drug... (5K23DK065978-03), NIH | Rare Sequence Variation a... (2R01DK078616-08), NIH | Epidemiology of Precursor... (5K24DK080140-03),WT
A Genome-Wide Association Meta-Analysis of Circulating Sex Hormone–Binding Globulin Reveals Multiple Loci Implicated in Sex Steroid Hormone Regulation
Article English OPEN
Coviello, Andrea D.; Haring, Robin; Wellons, Melissa; Vaidya, Dhananjay; Lehtimäki, Terho; Keildson, Sarah; Lunetta, Kathryn L.; He, Chunyan; Fornage, Myriam; Lagou, Vasiliki; Mangino, Massimo; Onland-Moret, N. Charlotte; Chen, Brian; Eriksson, Joel; Garcia, Melissa; ...
(2012)
Publisher: Public Library of Science

Project: NIH | AN NCRR CENTER FOR HIGH T... (5U54RR020278-04), NIH | HEALTH ABC--COORDINATING ... (N01AG062106-019), NIH | Genetics of cardiovascula... (5R01HL087679-02), NIH | Genome Wide Association C... (5U01HG004446-04), NIH | STUDY CORONARY HEART DISE... (N01HC048048-002), NIH | A Center for GEI Associat... (5U01HG004424-02), NIH | COORDINATING CENTER FOR W... (N01WH022110-014), NIH | Genetic Influences on ADH... (1R01MH063706-01), NIH | CORONARY HEART DISEASE RI... (N01HC048047-022), NIH | DYNAMICS OF HEALTH .AGING... (N01AG062101-015), NIH | Genes of the CYP450-Deriv... (5R01HL084099-04), NIH | CARDIA-ECHOCARDIOGRAPHY R... (N01HC045134-001), NIH | CORONARY ARTERY DISEASE R... (N01HC095095-028), NIH | Characterizing Genetic Su... (5U01CA098233-06), NIH | SUBCLINICAL CARDIOVASCULA... (N01HC095168-000),...
Sex hormone-binding globulin (SHBG) is a glycoprotein responsible for the transport and biologic availability of sex steroid hormones, primarily testosterone and estradiol. SHBG has been associated with chronic diseases including type 2 diabetes (T2D) and with hormone-s...
Novel Approach Identifies SNPs in SLC2A10 and KCNK9 with Evidence for Parent-of-Origin Effect on Body Mass Index
Article English OPEN
Hoggart, C. J.; Venturini, G.; Ascari, G.; Lamparter, D.; Macé, A.; Rüeger, S.; Bergmann, S.; Rivolta, C.; Kutalik, Z.; Mangino, M.; Spector, T. D.; Yuan, W.; Bell, J. T.; Gomez, F.; Borecki, I. B.; ...
(2014)

Project: WT | Identification of genetic... (084723), SNSF | Cardiovascular diseases a... (33CSC0-122661), RCUK | Bayesian Discovery of Reg... (G1002319), RCUK | Centre for molecular-base... (G0600705), RCUK | Aetiology of type 2 diabe... (MC_U106179471), NIH | A Genome-Wide Association... (5R01HL086694-05), NIH | Genome-Wide Association f... (5R01HL087641-02), EC | ENGAGE (201413), AKA | Improved methods of lifes... (129269), AKA | Well-being and health: Re... (104781), AKA | GENETIC REGULATION OF THE... (120315), ARC | Maximising knowledge from... (DP0770096), EC | EPI-MIGRANT (279143), EC | HYPERGENES (201550), NIH | Genetics of cardiovascula... (5R01HL087679-02),...
The phenotypic effect of some single nucleotide polymorphisms (SNPs) depends on their parental origin. We present a novel approach to detect parent-of-origin effects (POEs) in genome-wide genotype data of unrelated individuals. The method exploits increased phenotypic v...

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