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A polygenic biomarker to identify patients with severe hypercholesterolemia of polygenic origin

Molecular Genetics & Genomic Medicine(2020)10.1002/mgg3.1248Source: DataRank Database

A polygenic biomarker to identify patients with severe hypercholesterolemia of polygenic origin is a research paper published in Molecular Genetics & Genomic Medicine (2020). On theSindex it has a DataRank of 0. It has been cited 16 times.

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Scored on demand from live citation data

Open Access16 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

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Enrichment:Funding (40 grants)OA: goldTopics (41)IDs (PubMed, PMC)Annotations (4)SDGs (1)

FAIR Checklist

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Findable (1/2)

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Accessible (1/2)

Open Access

Interoperable (0/2)

Reusable (0/3)

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Authors (6)

Clive Hoggart ORCID,Marjo-Riitta Järvelin,Karl‐Heinz Herzig ORCID,Michael J.E. Sternberg ORCID,Alessia David ORCID

Live enrichment

PubMed:32307928 PMC:PMC7284038

Horizon 2020 Framework Programme

Grant: 668303

Personalised Risk assessment in febrile illness to Optimise Real-life Management across the European Union

Wellcome Trust

Grant: WT/104955/Z/14/Z

Academy of Finland

Grant: 104781

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

Academy of Finland

Grant: 120315

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

Academy of Finland

Grant: 129269

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

Academy of Finland

Grant: 1114194

Academy of Finland

Grant: 24300796

National Heart, Lung, and Blood Institute

Grant: 5R01HL087679‐ 02

National Institute of General Medical Sciences

Grant: U01‐HG‐004610

National Institute of General Medical Sciences

Grant: U01‐ HG‐004608

National Institute of General Medical Sciences

Grant: U01‐HG‐04599

National Institute of General Medical Sciences

Grant: U01HG004609

National Institute of General Medical Sciences

Grant: U01‐HG‐04603

National Institute of General Medical Sciences

Grant: U01HG004438

National Institute of General Medical Sciences

Grant: U01HG004424

NIMH NIH HHS

Grant: RL1 MH083268

Medical Research Council

Grant: MR/M013138/1

Methods and tools for structural models integrating multiple high-throughput omics data sets in genetic epidemiology

NHGRI NIH HHS

Grant: U01 HG004608

NHGRI NIH HHS

Grant: U01 HG004610

NIMH NIH HHS

Grant: R01 MH063706

Medical Research Council

Grant: MR/M013138/2

NHLBI NIH HHS

Grant: R01 HL087679

National Institutes of Health

Grant: 5R01HL087679-02

Genetics of cardiovascular risk factors in large founder population birth control

National Institutes of Health

Grant: 1R01MH063706-01

Genetic Influences on ADHD in a Finnish Birth Cohort

National Institutes of Health

Grant: 1U01HG004608-01

Genome-Wide Study of Cataract and Low HDL in the Personalized Medicine Research P

Wellcome Trust

Grant: 104955

Development and dissemination of a community tool for structure-based annotations of proteins in disease networks.

Research Council of Finland

Grant: 285547

Northern Finland Birth Cohort (NFBC) Programme: Exposomic, Genomic and Epigenomic Approach to Prediction of Metabolic and Cardiorespiratory function and Ill-Health (EGEA)

National Institutes of Health

Grant: 1RL1MH083268-01

Whole Genome Assoc. Analysis Strategies for Multi. Phenotypes

National Institutes of Health

Grant: 1U01HG004610-01

Development and Use of Network Infrastructure for High-Throughput GWA Studies

National Institutes of Health

Grant: 1U01HG004599-01

EMR Phenotypes and Community Engaged Genomic Associations

Wellcome Trust

Grant: unidentified

unidentified

European Commission

Grant: 633595

Understanding the dynamic determinants of glucose homeostasis and social capability to promote Healthy and active aging

National Institutes of Health

Grant: 5U01HG004438-04

JH/CIDR Genotyping for Genome-Wide Association Studies

National Institutes of Health

Grant: 5U01HG004610-03

Development and Use of Network Infrastructure for High-Throughput GWA Studies

National Institutes of Health

Grant: 1U01HG004603-01

Vanderbilt Genome-Electronic Records Project

National Institutes of Health

Grant: 5RL1MH083268-04

Whole Genome Assoc. Analysis Strategies for Multi. Phenotypes

National Institutes of Health

Grant: 1U01HG004609-01

Genome-wide Studies from the NUgene Biorespository

National Institutes of Health

Grant: 3U01HG004599-03S1

EMR Phenotypes and Community Engaged Genomic Associations

National Institutes of Health

Grant: 5U01HG004424-02

A Center for GEI Association Studies

Wellcome Trust

goldLicense: cc-by

publisherhttps://onlinelibrary.wiley.com/doi/pdfdirect/10.1002/mgg3.1248

publisherhttps://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1002%2Fmgg3.1248

publisherhttps://onlinelibrary.wiley.com/doi/pdf/10.1002/mgg3.1248

publisherhttps://onlinelibrary.wiley.com/doi/full-xml/10.1002/mgg3.1248

repositoryhttps://doaj.org/article/c1899659dec54d3393d256b9caa83a51

Fields of Study

0301 basic medicine03 medical and health sciences0302 clinical medicine

MeSH Terms

HumansHypercholesterolemiaMultifactorial InheritancePolymorphism, Single NucleotideAgedMiddle AgedUnited StatesFinlandFemaleMaleCholesterol, LDL

Keywords

LipidsHypercholesterolemiaRisk stratificationPolygenic Risk ScoreMaleMultifactorial Inheritance610QH426-470Polymorphism, Single NucleotideDISEASEMONOGENIC FAMILIAL HYPERCHOLESTEROLEMIAGeneticsHumansFinlandAgedGenetics & HeredityGENETIC RISK SCORE0604 GeneticsScience & Technology0304 Medicinal and Biomolecular Chemistry1103 Clinical SciencesOriginal ArticlesCholesterol, LDLMiddle AgedUnited StatesFemaleLife Sciences & Biomedicine

Sustainable Development Goals

SDG 3: 3. Good health

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