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Funder (15)
European Commission(669)Wellcome Trust(428)National Institutes of Health(400)Netherlands Organisation for Scientific Research (NWO)(251)Academy of Finland(241)Research Council UK(186)National Health and Medical Research Council (NHMRC)(166)Swiss National Science Foundation(98)Australian Research Council (ARC)(80)Austrian Science Fund (FWF)(26)Croatian Science Foundation (CSF)(23)Ministry of Science, Education and Sports of the Republic of Croatia (MSES)(20)National Science Foundation(14)Fundação para a Ciência e a Tecnologia, I.P.(5)Science Foundation Ireland(3)
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Project (99+)
ENGAGE(669)NCHA Subsidiebesluit 2008-2012(166)Genetics of cardiovascular risk factors in large founder population birth control(134)THE FRAMINGHAM HEART STUDY-268025195(126)Well-being and health: Research in the Northern Finland birth cohort 1966 (NFBC 1966) and 1985/86 (NFBC 1986)(124)GENETIC REGULATION OF THE TIMING OF PUBERTY: Characterization of Candidate Loci for Constitutional Delay of Puberty in the Finnish Population(118)Whole Genome Assoc. Analysis Strategies for Multi. Phenotypes(115)Institute for Clinical and Translational Research (UL1)(109)GMI(107)CORONARY HEART DISEASE AND STROKE(106)GWA for Gene-Environment Interaction Effects Influencing CHD(103)Genetic Influences on ADHD in a Finnish Birth Cohort(100)CENTRAL BLOOD ANALYSIS LABORATORY FOR CHS(98)Genome-Wide Association for Loci Influencing CHD and Other Heart, Lung and Blood(98)A Genome-Wide Association Study in Essential Hypertension (FEHGAS2)(90)GEFOS(89)The genetics of weight, BMI, adiposity and obesity(89)CHS-Transition Phase -268055222(88)tweeling onderzoek, met een focus op gedrag en depressie(87)Genome-wide combined linkage-association scan of multiply phenotyped twin sibships(83)Centre for molecular-based causal analyses in health and disease(83)CHARGE consortium: gene discovery for CVD and aging phenotypes(82)Validation and Replication of Genes Associated with Common Human Disease Using Australian Twin Families(79)A national DNA control series for genetic case-control studies based on the British 1958 birth cohort(79)Improved methods of lifestyle modification for patients at high risk for metabolic syndrome / Consortium: PrevMetSyn(78)Epidemiology of Venous Thrombosis &Pulmonary Embolism(78)NIMH Center for Collaborative Genetic Studies(78)Mapping Genes for typical migraine using twin families.(77)Cluster computing in genetic linkage studies on human complex traits(77)Genetics of melanoma risk factors(74)Center of Excellence in Complex Disease Genetics(73)Genetics of melanoma risk factors(73)Dissecting genetic complexity of Alzheimer's disease and cognitive function(72)Twin-family database for behavior genetics and genomics studies(72)CoE in Complex Disease Genetics(71)Assessment of biomedical risk factors and disease outcomes in the British 1958 cohort(71)Cardiovascular diseases and psychiatric disorders in the general population: a prospective follow-up study(71)Investigating the role of pigmentation pathway genes in moliness and melanoma risk(70)Association Screen of High Priority Positional Candidate Genes for Migraine(70)CHS Events Follow-up Study(69)AGES STUDY-THE REYKJAVIK STUDY OF HEALTHY AGING FOR THE NEW MILLENNIUM-260012100(66)WGA Study to Identify Genetic Variants Associated with CV Events in CHS(65)CORONARY HEART DISEASE &STROKE IN THE ELDERLY(64)Type 1 Diabetes Genetics Consortium(63)The Cardiovascular Risk in Young Finns Study - the 27-year follow-up.(62)Statistical Methods and Algorithms for Analysis of High-throughput Genetics and Genomics Platforms(62)CORONARY HEART DISEASE AND STROKE(62)CORONARY HEART DISEASE &STROKE IN PEOPLE AGED 65-84(62)Roles of inflammation, oxidation, sex hormones and genetic variation in vascular aging and the development of atherosclerosis over the life-course.(61)Research Fellowship - Grant ID:442915(60)UCLA Clinical and Translational Science Institute(60)CORONARY HEART DISEASE &STROKE IN PEOPLE AGED 65-84(60)CCSP - FIELD CENTER AND ULTRASOUND READING CENTER(60)CCSP-FIELD CENTER(58)COMMUNITY AND COHORT SURVEILLANCE PROGRAM(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)Develop & improve methodology in gene mapping, targetting localisation of genes underlying migraine & other disorders(54)CCSP - FIELD CENTER(54)FIELD CENTER FOR CCSP(53)BIOSHARE-EU(51)CARDIOVASCULAR HEALTH STUDY--ECHOCARDIOGRAPHY(51)COMMUNITY AND COHORT SURVEILLANCE PROGRAMS(51)MRI READING CENTER FOR THE CARDIOVASCULAR HEALTH STUDY(50)CANDIDATE GENE STUDIES OF OBESITY GUIDED BY WHOLE GENOME ASSOCIATION DATA(49)Integration of Genomics &Transcriptomics in Normal Twins &Major Depression(49)BBMRI-NL(49)CENTRAL HEMOSTATIS LABORATORY FOR CCSP(48)Major Depression: Stage 1 Genomewide Association in Population-Based Samples(48)Understanding the genetic basis of common human diseases: core funding for the Wellcome Trust Centre for Human Genetics.(48)The Application of 'Omics' to Public Health Epidemiology: Prospective Analysis of the FINRISK 1997 Cohort(47)Genome Wide Association Coordinating Center(47)Candidate gene variation and the association between early growth and adult disease: studies in the 1966 Northern Finland Birth Cohort(47)Maximising knowledge from dense SNP (single nucleotide polymorphisms) data using multi-locus analysis(46)Wellcome Trust Sanger Institute - generic account for deposition of all core- funded research papers(46)MSDs@LIFECOURSE CONSORTIU Subproject: Shared Risk Factors Study Group Turku University Central Hospital / Consortium: MSDs@LIFE(45)PHASE(45)OPENGENE(45)Prospective meta-analyses of drug-gene interactions: CHARGE GWAS consortium(45)CHS-ULTRASOUND READING(45)Genetic analysis of type II diabetes in Finnish populati(44)Exceptional aging: 12 year trajectories to function(44)Sustainable Innovative Materials in High Tech Applications. An Interdisciplinary Approach to Design,Engineering Technology and Chemistry of Environmentally Sound Products and Production.(43)ATHEROREMO(43)Genome-wide association studies of biomedical traits and endophenotypes for complex disease(43)Identifying Genes for Type 2 Diabetes: FUSION(43)CHS RETINAL READING CENTER(43)Public Health Genomics to Practice in Cardiovascular Diseases / Consortium: PUBGENSENS(42)CORE--ADIPOSE TISSUE BIOLOGY AND BASIC MECHANISMS(42)Genetic and environmental predictors of tobacco, drug and alcohol addiction in adolescence and young adulthood ¿ a lifecourse twin and population approach / Consortium: addictgene(41)EURHEALTHAGEING(41)Identification of genetic risk factors for asthma: genome-wide association and the role of epigenetics(41)Identification of new genes for type 2 diabetes(40)TRIAL OF ASPIRIN AND VITAMIN E IN WOMEN(40)Cambridge Institute for Medical Research (CIMR).(40)SUBCLINICAL CARDIOVASCULAR DISEASE COORDINATING CENTER-268995159(39)Locating genes for elementary and complex cognitive abilities using genetic linkage and association analysis(38)HYPERGENES(38)VARIATION IN THE EFFECTS OF ALCOHOL ON LIVER FUNCTION(38)SUBCLINICAL CARDIOVASCULAR DISEASE STUDY--EBCT READING(38)
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Publication Date (11)
2012(126)2013(91)2011(89)2014(63)2010(58)2017(58)2015(53)2009(45)2016(45)2018(24)2008(9)
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Access Mode (3)
Open Access(593)Closed Access(73)Restricted(3)
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Type (11)
Article(660)Other literature type(124)Preprint(12)Review(11)Doctoral thesis(3)Book(1)Collection(1)Conference object(1)External research report(1)Report(1)Unknown(1)
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Language (2)
English(649)Undetermined(15)
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Community (2)
EGI Federation(24)FET FP7(1)
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Content Provider (100+)
Europe PubMed Central(385)Unknown Repository(360)Erasmus University Institutional Repository(79)Edinburgh Research Explorer(74)UCL Discovery(51)Digital Access to Scholarship at Harvard(41)PLoS Genetics(39)PLoS ONE(34)SpringerOpen(33)Enlighten(30)University of Groningen Digital Archive(30)DSpace at VU(27)St George's Online Research Archive(27)LSHTM Research Online(24)MPG.PuRe(23)TamPub Julkaisuarkisto - TamPub Institutional Repository(19)Publikationer från Uppsala Universitet(19)King's Research Portal(19)BASE (Open Access Aggregator)(16)Explore Bristol Research(16)Radboud Repository(15)Open Access LMU(14)Serveur académique lausannois(14)Queen's University Research Portal(13)Online Research @ Cardiff(13)University of Southern Denmark Research Output(11)Lund University Publications(11)Hyper Article en Ligne(11)Norwegian Open Research Archives(10)Copenhagen University Research Information System(10)INRIA a CCSD electronic archive server(10)Ghent University Academic Bibliography(10)Oxford University Research Archive(9)Brunel University Research Archive(9)bioRxiv(9)Helsingin yliopiston digitaalinen arkisto(8)Utrecht University Repository(7)University of Liverpool Repository(7)DSpace@MIT(6)eScholarship - University of California(6)UPF Digital Repository(6)Landspítali University Hospital Research Archive(6)Archive ouverte UNIGE(6)Lirias(6)e-Prints Soton(5)Publikationer från Umeå universitet(5)HAL-Inserm(5)University of Lincoln Institutional Repository(5)BMC Genomics(4)Translational Psychiatry(4)Norsk Epidemiologi(4)NTNU Open(4)Juelich Shared Electronic Resources(4)Publikationer från Högskolan i Jönköping(4)Wageningen Yield(4)MediaTUM(4)BMC Bioinformatics(3)BMC Medical Genomics(3)Scientific Reports(3)Keele Research Repository(3)edoc(3)Nottingham ePrints(3)UEF eRepository(3)Nucleic Acids Research(2)BMC Medical Genetics(2)PLoS Medicine(2)HAL-Rennes 1(2)Hal-Diderot(2)Diposit Digital de la Universitat de Barcelona(2)Kingston University Research Repository(2)Bergen Open Research Archive - UiB(2)Apollo(2)HAL AMU(2)Archivio istituzionale della ricerca - Università di Trieste(2)arXiv.org e-Print Archive(2)RERO DOC Digital Library(2)Archivio Istituzionale(2)Universiteit Twente Repository(2)Archivio istituzionale della ricerca - Università dell'Insubria(2)HAL-UPMC(2)University of Oulu Repository - Jultika(2)Central Archive at the University of Reading(2)Universiteit van Amsterdam Digital Academic Repository(2)Digital.CSIC(2)HKU Scholars Hub(2)Journal of the Renin-Angiotensin-Aldosterone System(1)PLoS Computational Biology(1)G3: Genes, Genomes, Genetics(1)Aging Cell(1)BMC Genetics(1)Investigative Genetics(1)GigaScience(1)Disease Models & Mechanisms(1)Biology of Sex Differences(1)Schizophrenia Research: Cognition(1)Genome Biology(1)Cancer Management and Research(1)Frontiers(1)PURE Aarhus University(1)Publikationer från Örebro universitet(1)
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Collected From (100+)
PubMed Central(385)HEALTH FP7 Publications Database(334)SESAM Publication Database - FP7 HEALTH(249)Crossref(245)NARCIS(151)CORE (RIOXX-UK Aggregator)(126)DOAJ-Articles(89)Edinburgh Research Explorer(74)UCL Discovery(51)Digital Access to Scholarship at Harvard(41)European Research Council (ERC)(31)MPG.PuRe(23)TamPub Julkaisuarkisto - TamPub Institutional Repository(19)Publikationer från Uppsala Universitet(19)King's Research Portal(19)BASE (Open Access Aggregator)(17)Explore Bristol Research(16)Open Access LMU(14)Serveur académique lausannois(14)Queen's University Research Portal(13)University of Southern Denmark Research Output(11)Lund University Publications(11)Hyper Article en Ligne(11)Norwegian Open Research Archives(10)Copenhagen University Research Information System(10)INRIA a CCSD electronic archive server(10)Ghent University Academic Bibliography(10)Oxford University Research Archive(9)Brunel University Research Archive(9)bioRxiv(9)Helsingin yliopiston digitaalinen arkisto(8)Sygma(7)DSpace@MIT(6)eScholarship - University of California(6)UPF Digital Repository(6)Landspítali University Hospital Research Archive(6)Archive ouverte UNIGE(6)Lirias(6)e-Prints Soton(5)Publikationer från Umeå universitet(5)HAL-Inserm(5)University of Lincoln Institutional Repository(5)NTNU Open(4)Juelich Shared Electronic Resources(4)Publikationer från Högskolan i Jönköping(4)MediaTUM(4)Scientific Reports(3)Web Crawl(3)edoc(3)UEF eRepository(3)SESAM Publication Database - FP7 KBBE(2)HAL-Rennes 1(2)Hal-Diderot(2)Diposit Digital de la Universitat de Barcelona(2)Bergen Open Research Archive - UiB(2)Apollo(2)HAL AMU(2)Archivio istituzionale della ricerca - Università di Trieste(2)arXiv.org e-Print Archive(2)RERO DOC Digital Library(2)Archivio Istituzionale(2)Archivio istituzionale della ricerca - Università dell'Insubria(2)HAL-UPMC(2)University of Oulu Repository - Jultika(2)Digital.CSIC(2)HKU Scholars Hub(2)Frontiers(1)PURE Aarhus University(1)Publikationer från Örebro universitet(1)Flore (Florence Research Repository)(1)OPUS FAU - Online-Publikationssystem der Friedrich-Alexander-Universität Erlangen-Nürnberg(1)Zurich Open Repository and Archive(1)Online Research Database In Technology(1)Archivio Istituzionale della Ricerca dell'Università degli Studi di Milano(1)Diposit Digital de Documents de la UAB(1)Open Repository and Bibliography - Luxembourg(1)Archivio istituzionale della ricerca - Università di Brescia(1)ZENODO(1)Theses@asb(1)Research Papers in Economics(1)HAL-CEA(1)Repositori d'Objectes Digitals per a l'Ensenyament la Recerca i la Cultura(1)Open Archive: Publications from Karolinska Institutet(1)Bern Open Repository and Information System (BORIS)(1)University of East Anglia digital repository(1)Nottingham eTheses(1)Cork Open Research Archive(1)Open Repository and Bibliography - University of Liège(1)Research Repository of Catalonia(1)LSE Research Online(1)Biblos-e Archivo(1)Opin visindi(1)ECNIS-NIOM Repository (Environmental Cancer Risk, Nutrition and Individual Susceptibility)(1)St Andrews Research Repository(1)Institutional Repository of the Freie Universität Berlin(1)Repositório Científico do Instituto Nacional de Saúde(1)e-publications@RCSI(1)Spiral - Imperial College Digital Repository(1)OceanRep(1)Institutional Repository Universiteit Antwerpen(1)
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Funder (15)
European Commission(669)Wellcome Trust(428)National Institutes of Health(400)Netherlands Organisation for Scientific Research (NWO)(251)Academy of Finland(241)Funder
European Commission(669)Wellcome Trust(428)National Institutes of Health(400)Netherlands Organisation for Scientific Research (NWO)(251)Academy of Finland(241)Research Council UK(186)National Health and Medical Research Council (NHMRC)(166)Swiss National Science Foundation(98)Australian Research Council (ARC)(80)Austrian Science Fund (FWF)(26)Croatian Science Foundation (CSF)(23)Ministry of Science, Education and Sports of the Republic of Croatia (MSES)(20)National Science Foundation(14)Fundação para a Ciência e a Tecnologia, I.P.(5)Science Foundation Ireland(3)
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Project (99+)
ENGAGE(669)NCHA Subsidiebesluit 2008-2012(166)Genetics of cardiovascular risk factors in large founder population birth control(134)THE FRAMINGHAM HEART STUDY-268025195(126)Well-being and health: Research in the Northern Finland birth cohort 1966 (NFBC 1966) and 1985/86 (NFBC 1986)(124)Project
Showing top 99 values.ENGAGE(669)
NCHA Subsidiebesluit 2008-2012(166)Genetics of cardiovascular risk factors in large founder population birth control(134)THE FRAMINGHAM HEART STUDY-268025195(126)Well-being and health: Research in the Northern Finland birth cohort 1966 (NFBC 1966) and 1985/86 (NFBC 1986)(124)GENETIC REGULATION OF THE TIMING OF PUBERTY: Characterization of Candidate Loci for Constitutional Delay of Puberty in the Finnish Population(118)Whole Genome Assoc. Analysis Strategies for Multi. Phenotypes(115)Institute for Clinical and Translational Research (UL1)(109)GMI(107)CORONARY HEART DISEASE AND STROKE(106)GWA for Gene-Environment Interaction Effects Influencing CHD(103)Genetic Influences on ADHD in a Finnish Birth Cohort(100)CENTRAL BLOOD ANALYSIS LABORATORY FOR CHS(98)Genome-Wide Association for Loci Influencing CHD and Other Heart, Lung and Blood(98)A Genome-Wide Association Study in Essential Hypertension (FEHGAS2)(90)GEFOS(89)The genetics of weight, BMI, adiposity and obesity(89)CHS-Transition Phase -268055222(88)tweeling onderzoek, met een focus op gedrag en depressie(87)Genome-wide combined linkage-association scan of multiply phenotyped twin sibships(83)Centre for molecular-based causal analyses in health and disease(83)CHARGE consortium: gene discovery for CVD and aging phenotypes(82)Validation and Replication of Genes Associated with Common Human Disease Using Australian Twin Families(79)A national DNA control series for genetic case-control studies based on the British 1958 birth cohort(79)Improved methods of lifestyle modification for patients at high risk for metabolic syndrome / Consortium: PrevMetSyn(78)Epidemiology of Venous Thrombosis &Pulmonary Embolism(78)NIMH Center for Collaborative Genetic Studies(78)Mapping Genes for typical migraine using twin families.(77)Cluster computing in genetic linkage studies on human complex traits(77)Genetics of melanoma risk factors(74)Center of Excellence in Complex Disease Genetics(73)Genetics of melanoma risk factors(73)Dissecting genetic complexity of Alzheimer's disease and cognitive function(72)Twin-family database for behavior genetics and genomics studies(72)CoE in Complex Disease Genetics(71)Assessment of biomedical risk factors and disease outcomes in the British 1958 cohort(71)Cardiovascular diseases and psychiatric disorders in the general population: a prospective follow-up study(71)Investigating the role of pigmentation pathway genes in moliness and melanoma risk(70)Association Screen of High Priority Positional Candidate Genes for Migraine(70)CHS Events Follow-up Study(69)AGES STUDY-THE REYKJAVIK STUDY OF HEALTHY AGING FOR THE NEW MILLENNIUM-260012100(66)WGA Study to Identify Genetic Variants Associated with CV Events in CHS(65)CORONARY HEART DISEASE &STROKE IN THE ELDERLY(64)Type 1 Diabetes Genetics Consortium(63)The Cardiovascular Risk in Young Finns Study - the 27-year follow-up.(62)Statistical Methods and Algorithms for Analysis of High-throughput Genetics and Genomics Platforms(62)CORONARY HEART DISEASE AND STROKE(62)CORONARY HEART DISEASE &STROKE IN PEOPLE AGED 65-84(62)Roles of inflammation, oxidation, sex hormones and genetic variation in vascular aging and the development of atherosclerosis over the life-course.(61)Research Fellowship - Grant ID:442915(60)UCLA Clinical and Translational Science Institute(60)CORONARY HEART DISEASE &STROKE IN PEOPLE AGED 65-84(60)CCSP - FIELD CENTER AND ULTRASOUND READING CENTER(60)CCSP-FIELD CENTER(58)COMMUNITY AND COHORT SURVEILLANCE PROGRAM(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)Develop & improve methodology in gene mapping, targetting localisation of genes underlying migraine & other disorders(54)CCSP - FIELD CENTER(54)FIELD CENTER FOR CCSP(53)BIOSHARE-EU(51)CARDIOVASCULAR HEALTH STUDY--ECHOCARDIOGRAPHY(51)COMMUNITY AND COHORT SURVEILLANCE PROGRAMS(51)MRI READING CENTER FOR THE CARDIOVASCULAR HEALTH STUDY(50)CANDIDATE GENE STUDIES OF OBESITY GUIDED BY WHOLE GENOME ASSOCIATION DATA(49)Integration of Genomics &Transcriptomics in Normal Twins &Major Depression(49)BBMRI-NL(49)CENTRAL HEMOSTATIS LABORATORY FOR CCSP(48)Major Depression: Stage 1 Genomewide Association in Population-Based Samples(48)Understanding the genetic basis of common human diseases: core funding for the Wellcome Trust Centre for Human Genetics.(48)The Application of 'Omics' to Public Health Epidemiology: Prospective Analysis of the FINRISK 1997 Cohort(47)Genome Wide Association Coordinating Center(47)Candidate gene variation and the association between early growth and adult disease: studies in the 1966 Northern Finland Birth Cohort(47)Maximising knowledge from dense SNP (single nucleotide polymorphisms) data using multi-locus analysis(46)Wellcome Trust Sanger Institute - generic account for deposition of all core- funded research papers(46)MSDs@LIFECOURSE CONSORTIU Subproject: Shared Risk Factors Study Group Turku University Central Hospital / Consortium: MSDs@LIFE(45)PHASE(45)OPENGENE(45)Prospective meta-analyses of drug-gene interactions: CHARGE GWAS consortium(45)CHS-ULTRASOUND READING(45)Genetic analysis of type II diabetes in Finnish populati(44)Exceptional aging: 12 year trajectories to function(44)Sustainable Innovative Materials in High Tech Applications. An Interdisciplinary Approach to Design,Engineering Technology and Chemistry of Environmentally Sound Products and Production.(43)ATHEROREMO(43)Genome-wide association studies of biomedical traits and endophenotypes for complex disease(43)Identifying Genes for Type 2 Diabetes: FUSION(43)CHS RETINAL READING CENTER(43)Public Health Genomics to Practice in Cardiovascular Diseases / Consortium: PUBGENSENS(42)CORE--ADIPOSE TISSUE BIOLOGY AND BASIC MECHANISMS(42)Genetic and environmental predictors of tobacco, drug and alcohol addiction in adolescence and young adulthood ¿ a lifecourse twin and population approach / Consortium: addictgene(41)EURHEALTHAGEING(41)Identification of genetic risk factors for asthma: genome-wide association and the role of epigenetics(41)Identification of new genes for type 2 diabetes(40)TRIAL OF ASPIRIN AND VITAMIN E IN WOMEN(40)Cambridge Institute for Medical Research (CIMR).(40)SUBCLINICAL CARDIOVASCULAR DISEASE COORDINATING CENTER-268995159(39)Locating genes for elementary and complex cognitive abilities using genetic linkage and association analysis(38)HYPERGENES(38)VARIATION IN THE EFFECTS OF ALCOHOL ON LIVER FUNCTION(38)SUBCLINICAL CARDIOVASCULAR DISEASE STUDY--EBCT READING(38)
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Publication Date (11)
2012(126)2013(91)2011(89)2014(63)2010(58)Publication Date
2012(126)2013(91)2011(89)2014(63)2010(58)2017(58)2015(53)2009(45)2016(45)2018(24)2008(9)
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Access Mode (3)
Open Access(593)Closed Access(73)Restricted(3)Access Mode
Open Access(593)Closed Access(73)Restricted(3)
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Type (11)
Article(660)Other literature type(124)Preprint(12)Review(11)Doctoral thesis(3)Type
Article(660)Other literature type(124)Preprint(12)Review(11)Doctoral thesis(3)Book(1)Collection(1)Conference object(1)External research report(1)Report(1)Unknown(1)
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Language (2)
English(649)Undetermined(15)Language
English(649)Undetermined(15)
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Community (2)
EGI Federation(24)FET FP7(1)Community
EGI Federation(24)FET FP7(1)
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Content Provider (100+)
Europe PubMed Central(385)Unknown Repository(360)Erasmus University Institutional Repository(79)Edinburgh Research Explorer(74)UCL Discovery(51)Content Provider
Showing top 100 values.Europe PubMed Central(385)Unknown Repository(360)Erasmus University Institutional Repository(79)Edinburgh Research Explorer(74)UCL Discovery(51)Digital Access to Scholarship at Harvard(41)PLoS Genetics(39)PLoS ONE(34)SpringerOpen(33)Enlighten(30)University of Groningen Digital Archive(30)DSpace at VU(27)St George's Online Research Archive(27)LSHTM Research Online(24)MPG.PuRe(23)TamPub Julkaisuarkisto - TamPub Institutional Repository(19)Publikationer från Uppsala Universitet(19)King's Research Portal(19)BASE (Open Access Aggregator)(16)Explore Bristol Research(16)Radboud Repository(15)Open Access LMU(14)Serveur académique lausannois(14)Queen's University Research Portal(13)Online Research @ Cardiff(13)University of Southern Denmark Research Output(11)Lund University Publications(11)Hyper Article en Ligne(11)Norwegian Open Research Archives(10)Copenhagen University Research Information System(10)INRIA a CCSD electronic archive server(10)Ghent University Academic Bibliography(10)Oxford University Research Archive(9)Brunel University Research Archive(9)bioRxiv(9)Helsingin yliopiston digitaalinen arkisto(8)Utrecht University Repository(7)University of Liverpool Repository(7)DSpace@MIT(6)eScholarship - University of California(6)UPF Digital Repository(6)Landspítali University Hospital Research Archive(6)Archive ouverte UNIGE(6)Lirias(6)e-Prints Soton(5)Publikationer från Umeå universitet(5)HAL-Inserm(5)University of Lincoln Institutional Repository(5)BMC Genomics(4)Translational Psychiatry(4)Norsk Epidemiologi(4)NTNU Open(4)Juelich Shared Electronic Resources(4)Publikationer från Högskolan i Jönköping(4)Wageningen Yield(4)MediaTUM(4)BMC Bioinformatics(3)BMC Medical Genomics(3)Scientific Reports(3)Keele Research Repository(3)edoc(3)Nottingham ePrints(3)UEF eRepository(3)Nucleic Acids Research(2)BMC Medical Genetics(2)PLoS Medicine(2)HAL-Rennes 1(2)Hal-Diderot(2)Diposit Digital de la Universitat de Barcelona(2)Kingston University Research Repository(2)Bergen Open Research Archive - UiB(2)Apollo(2)HAL AMU(2)Archivio istituzionale della ricerca - Università di Trieste(2)arXiv.org e-Print Archive(2)RERO DOC Digital Library(2)Archivio Istituzionale(2)Universiteit Twente Repository(2)Archivio istituzionale della ricerca - Università dell'Insubria(2)HAL-UPMC(2)University of Oulu Repository - Jultika(2)Central Archive at the University of Reading(2)Universiteit van Amsterdam Digital Academic Repository(2)Digital.CSIC(2)HKU Scholars Hub(2)Journal of the Renin-Angiotensin-Aldosterone System(1)PLoS Computational Biology(1)G3: Genes, Genomes, Genetics(1)Aging Cell(1)BMC Genetics(1)Investigative Genetics(1)GigaScience(1)Disease Models & Mechanisms(1)Biology of Sex Differences(1)Schizophrenia Research: Cognition(1)Genome Biology(1)Cancer Management and Research(1)Frontiers(1)PURE Aarhus University(1)Publikationer från Örebro universitet(1)
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A novel atlas of gene expression in human skeletal muscle reveals molecular changes associated with aging
Su, Jing; Ekman, Carl; Oskolkov, Nikolay; Lahti, Leo; Ström, Kristoffer; Brazma, Alvis; Groop, Leif; Rung, Johan; Hansson, Ola; (2015)Background Although high-throughput studies of gene expression have generated large amounts of data, most of which is freely available in public archives, the use of this valuable resource is limited by computational complications and non-homogenous annotation. To addre... -
Quality, quantity and harmony: the DataSHaPER approach to integrating data across bioclinical studies
Fortier, Isabel; Burton, Paul R; Robson, Paula J; Ferretti, Vincent; Little, Julian; L’Heureux, Francois; Deschênes, Mylène; Knoppers, Bartha M; Doiron, Dany; Keers, Joost C; Linksted, Pamela; Harris, Jennifer R; Lachance, Geneviève; Boileau, Catherine; Pedersen, Nancy L; ... (2010)Background Vast sample sizes are often essential in the quest to disentangle the complex interplay of the genetic, lifestyle, environmental and social factors that determine the aetiology and progression of chronic diseases. The pooling of information between studies is... -
Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes
Albrechtsen, A.; Grarup, N.; Li, Y.; Sparsø, T.; Tian, G.; Cao, H.; Jiang, T.; Kim, S. Y.; Korneliussen, T.; Li, Q.; Nie, C.; Wu, R.; Skotte, L.; Morris, A. P.; Ladenvall, C.; ... (2012)Project: RCUK | Assessment of biomedical ... (G0000934), WT | An investigation of genes... (083270), WT | Statistical methods for t... (081682), WT | The genetics of weight, B... (076113), WT | The UK Type 2 diabetes ge... (072960), EC | ENGAGE (201413)Aims/hypothesis Human complex metabolic traits are in part regulated by genetic determinants. Here we applied exome sequencing to identify novel associations of coding polymorphisms at minor allele frequencies (MAFs) >1% with common metabolic phenotypes. Methods The stu... -
Twin's Birth-Order Differences in Height and Body Mass Index From Birth to Old Age: A Pooled Study of 26 Twin Cohorts Participating in the CODATwins Project
Yokoyama, Yoshie; Jelenkovic, Aline; Sund, Reijo; Sung, Joohon; Hopper, John L.; Ooki, Syuichi; Heikkilä, Kauko; Aaltonen, Sari; Tarnoki, Adam D.; Tarnoki, David L.; Willemsen, Gonneke; Bartels, Meike; Van Beijsterveldt, Toos C. E. M.; Saudino, Kimberly J.; Cutler, Tessa L.; ... (2016)Project: NIH | Gene-environment Interact... (5R01MH081813-04), NIH | Familial Transmission of ... (1R03MH063851-01A1), NIH | The Effects of Estradiol ... (5R01MH092377-03), NHMRC | Mental Health Across Gene... (437015), NHMRC | Defining genetic and epig... (607358), NHMRC | Australian Centre of Exce... (1079102), AKA | Genetic and environmental... (141054), AKA | Oxygenology of soil (205585), AKA | Genomic epidemiology of a... (263278), AKA | Center of Excellence in C... (129680), AKA | Indicators of marginaliza... (264146), AKA | Predictors, neuropsycholo... (118555), AKA | Genomic epidemiology of a... (265240), AKA | CoE in Complex Disease Ge... (213506), EC | ENGAGE (201413), ...<p>We analyzed birth order differences in means and variances of height and body mass index (BMI) in monozygotic (MZ) and dizygotic (DZ) twins from infancy to old age. The data were derived from the international CODATwins database. The total number of height and BMI me... -
The Challenges of Genome-Wide Interaction Studies: Lessons to Learn from the Analysis of HDL Blood Levels
van Leeuwen, Elisabeth M.; Smouter, Françoise A. S.; Kam-Thong, Tony; Karbalai, Nazanin; Smith, Albert V.; Harris, Tamara B.; Launer, Lenore J.; Sitlani, Colleen M.; Li, Guo; Brody, Jennifer A.; Bis, Joshua C.; White, Charles C.; Jaiswal, Alok; Oostra, Ben A.; Hofman, Albert; ... (2014)Project: NIH | CORONARY HEART DISEASE AN... (N01HC085082-024), EC | CHANCES (242244), AKA | Predicting risk for coron... (251217), EC | ENGAGE (201413), NIH | CORONARY HEART DISEASE AN... (N01HC085079-023), NIH | CTSA INFRASTRUCTURE FOR A... (1UL1RR033176-01), NWO | Dissecting genetic comple... (2300137747), NWO | BBMRI-NL (2300154272), NWO | NCHA Subsidiebesluit 2008... (2300155116), WT, NIH | CORONARY HEART DISEASE &S... (N01HC085080-018), NIH | Diabetes Endocrinology Re... (3P30DK063491-04S1), NIH | CENTRAL BLOOD ANALYSIS LA... (N01HC085086-019), NIH | CORONARY HEART DISEASE &S... (N01HC085083-021), NIH | CORONARY HEART DISEASE &S... (N01HC085081-016), ...textabstractGenome-wide association studies (GWAS) have revealed 74 single nucleotide polymorphisms (SNPs) associated with high-density lipoprotein cholesterol (HDL) blood levels. This study is, to our knowledge, the first genome-wide interaction study (GWIS) to identif... -
The BioSample Database (BioSD) at the European Bioinformatics Institute
Gostev, M.; Faulconbridge, A.; Brandizi, M.; Fernandez-Banet, J.; Sarkans, U.; Brazma, A.; Parkinson, H.; (2012)The BioSample Database (http://www.ebi.ac.uk/biosamples) is a new database at EBI that stores information about biological samples used in molecular experiments, such as sequencing, gene expression or proteomics. The goals of the BioSample Database include: (i) recordin... -
Genome-wide association identifies ATOH7 as a major gene determining human optic disc size
Macgregor, Stuart; Hewitt, Alex W.; Hysi, Pirro G.; Ruddle, Jonathan B.; Medland, Sarah E.; Henders, Anjali K.; Gordon, Scott D.; Andrew, Toby; McEvoy, Brian; Sanfilippo, Paul G.; Carbonaro, Francis; Tah, Vikas; Li, Yi Ju; Bennett, Sonya L.; Craig, Jamie E.; ... (2010)Project: NIH | INVESTIGATION OF MAMMALIA... (5R01EY013612-04), EC | ENGAGE (201413), EC | GEFOS (201865), WT, NWO | Cluster computing in gene... (2300131050), NIH | International Collaborati... (5R01EY018246-03)Optic nerve assessment is important for many blinding diseases, with cup-to-disc ratio (CDR) assessments commonly used in both diagnosis and progression monitoring of glaucoma patients. Optic disc, cup, rim area and CDR measurements all show substantial variation betwee... -
Genetic loci associated with coronary artery disease harbor evidence of selection and antagonistic pleiotropy.
Sean G Byars; Qin Qin Huang; Lesley-Ann Gray; Andrew Bakshi; Samuli Ripatti; Gad Abraham; Stephen C Stearns; Michael Inouye; (2017)Project: WT, EC | ePerMed (692145), EC | BIOSHARE-EU (261433), NHMRC | Large-Scale Multi-Omic An... (1090462), NHMRC | Integrative genomics and ... (1062227), NHMRC | Using systems biology to ... (1061435), AKA | Human model for genetic v... (285380), EC | ENGAGE (201413), AKA | Predicting risk for coron... (251217), AKA | CoE in Complex Disease Ge... (213506), NIH | THE FRAMINGHAM HEART STUD... (N01HC025195-005)Traditional genome-wide scans for positive selection have mainly uncovered selective sweeps associated with monogenic traits. While selection on quantitative traits is much more common, very few signals have been detected because of their polygenic nature. We searched f... -
Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies
Elks, Cathy E.; Perry, John R.B.; Sulem, Patrick; Chasman, Daniel I.; Franceschini, Nora; He, Chunyan; Lunetta, Kathryn L.; Visser, Jenny A.; Byrne, Enda M.; Cousminer, Diana L.; Gudbjartsson, Daniel F.; Esko, Tõnu; Feenstra, Bjarke; Hottenga, Jouke-Jan; Koller, Daniel L.; ... (2010)Project: NIH | Genetic Modulation on the... (5R03HD061437-02), NIH | GWA for Gene-Environment ... (5U01HG004402-02), NIH | THE FRAMINGHAM HEART STUD... (N01HC025195-005), NIH | GWA Mapping: Maternal Met... (1U01HG004415-01), NIH | CTSA INFRASTRUCTURE FOR A... (1UL1RR025774-01), EC | GEFOS (201865), EC | ENGAGE (201413), ARC | Quantitative and Molecula... (DP0212016), ARC | Maximising knowledge from... (DP0770096), ARC | Locating genes for elemen... (DP0343921), EC | BBMRI (212111), EC | GMI (230374), NHMRC | A genome-wide search for ... (572613), NHMRC | Association Screen of Hig... (442981), NIH | CORE--ADIPOSE TISSUE BIOL... (5P30DK072488-02), ...<p>To identify loci for age at menarche, we performed a meta-analysis of 32 genome-wide association studies in 87,802 women of European descent, with replication in up to 14,731 women. In addition to the known loci at LIN28B (P = 5.4 x 10(-60)) and 9q31.2 (P = 2.2 x 10(... -
Novel Approach Identifies SNPs in SLC2A10 and KCNK9 with Evidence for Parent-of-Origin Effect on Body Mass Index
Hoggart, Clive J; Venturini, Giulia; Mangino, Massimo; Gomez, Felicia; Ascari, Giulia; Zhao, Jing Hua; Teumer, Alexander; Winkler, Thomas W; Tšernikova, Natalia; Luan, Jian'an; Mihailov, Evelin; Ehret, Georg B; Zhang, Weihua; Lamparter, David; Esko, Tõnu; ... (2014)Project: EC | EPI-MIGRANT (279143), NHMRC | Mapping Genes for typical... (389938), NHMRC | Genetics of melanoma risk... (241944), NHMRC | Explaining the Dark Matte... (613672), NHMRC | Research Fellowship - Gra... (442915), NHMRC | Genome-wide combined link... (389891), NHMRC | Validation and Replicatio... (496739), NHMRC | Association Screen of Hig... (442981), NHMRC | Accurate prediction of in... (496688), NHMRC | Investigating the role of... (552485), NHMRC | Statistical Methods and A... (389892), NHMRC | Genetics of melanoma risk... (389875), EC | HYPERGENES (201550), AKA | Well-being and health: Re... (104781), ARC | Maximising knowledge from... (DP0770096), ...Author Summary Large genetic association studies have revealed many genetic factors influencing common traits, such as body mass index (BMI). These studies assume that the effect of genetic variants is the same regardless of whether they are inherited from the mother or...