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Phased Whole-Genome Genetic Risk in a Family Quartet Using a Major Allele Reference Sequence

PLoS Genetics(2011)10.1371/journal.pgen.1002280Source: DataRank Database

Phased Whole-Genome Genetic Risk in a Family Quartet Using a Major Allele Reference Sequence is a research paper published in PLoS Genetics (2011). On theSindex it has a DataRank of 7.5. It has been cited 148 times, with 99 citing works in its 1-hop citation network.

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7.5DataRank · unranked

Scored on demand from live citation data

Open Access148 citations · 99 citing works in its network

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Linked data & code

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (22 grants)Impact (FWCI 13.36)OA: goldTopics (126)IDs (PubMed, PMC, OpenAlex)Annotations (1)SDGs (2)

FAIR Checklist

Context only (not used in score)

Findable (1/2)

Has DOI

Accessible (1/2)

Open Access

Interoperable (0/2)

Reusable (0/3)

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DataRank Breakdown

Base Score 10%Citation Network 90%

Base Score Contribution

0.751

From this paper's citation signal

Citation Network Contribution

6.7

From 87 citing papers with measurable signal

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Authors (38)

Rong Chen ORCID,Sergio P. Cordero,Kelly E. Ormond ORCID,Colleen Caleshu ORCID,Konrad J. Karczewski ORCID

Live enrichment

PubMed:21935354 PMC:PMC3174201 OpenAlex:https://openalex.org/W2150933237

NHLBI NIH HHS

Grant: F32 HL097462

NIH HHS

Grant: OD004613

NIGMS NIH HHS

Grant: R01 GM079719

NHLBI NIH HHS

Grant: T32 HL094274-01A2

NHGRI NIH HHS

Grant: P50 HG003389

NHGRI NIH HHS

Grant: U01HG005715

NHLBI NIH HHS

Grant: T32 HL094274

NIGMS NIH HHS

Grant: U01 GM061374

NHGRI NIH HHS

Grant: 5 P50 HG003389-05

NLM NIH HHS

Grant: T15 LM007033

NHLBI NIH HHS

Grant: K08 HL083914

NIGMS NIH HHS

Grant: U01 GM61374

NHGRI NIH HHS

Grant: R01 HG003229

National Institutes of Health

Grant: 1F32HL097462-01

Effect of Cholesterol Anabolism on Network Signaling in Cardiac Hypertrophy

National Institutes of Health

Grant: 5U01GM061374-02

THE STANFORD PHARMACOGENETICS KNOWLEDGE BASE

National Institutes of Health

Grant: 3U01HG005715-02S1

Population Structure Admixture and Selection across the 1000 Genomes Data Set

National Institutes of Health

Grant: 5K08HL083914-04

Integrative Cardiovascular Biology of Apelin-APJ

National Institutes of Health

Grant: 5P50HG003389-03

Center for Integrating Ethics &Genetic Research

National Institutes of Health

Grant: 1T32HL094274-01A2

Research Training in Myocardial Biology at Stanford

National Institutes of Health

Grant: 5R01GM079719-04

Enabling new discoveries in pharmacogenomics through a genomic date-driven nosolo

National Institutes of Health

Grant: 5T15LM007033-36

Biomedical Informatics Training at Stanford

National Institutes of Health

Grant: 5T32HL094274-13

Training in Myocardial Biology at Stanford

FWCI

13.36

Citation Percentile

1.0%

Citation Trend

2012

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2021

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2026

goldLicense: cc-by

journalhttps://journals.plos.org/plosgenetics/article/file?id=10.1371/journal.pgen.1002280&type=printable

publisherhttps://journals.plos.org/plosgenetics/article/file?id=10.1371/journal.pgen.1002280&type=printable

publisherhttp://dx.plos.org/10.1371/journal.pgen.1002280

journalhttps://doi.org/10.1371/journal.pgen.1002280

repositoryhttps://pubmed.ncbi.nlm.nih.gov/21935354

Fields of Study

Genetic Associations and EpidemiologyGenomics and Rare DiseasesPlatelet Disorders and Treatments0301 basic medicine0303 health sciences03 medical and health sciencesAllelesBase SequenceDNA Mutational AnalysisFemaleGenes, SyntheticGenetic Predisposition to DiseaseGenetic VariationGenome, HumanGenome-Wide Association StudyGenotypeHaplotypesHumansMalePedigreeReference StandardsRisk AssessmentSequence AlignmentSequence Analysis, DNAThrombophilia

MeSH Terms

AllelesBase SequenceDNA Mutational AnalysisFemaleGenes, SyntheticGenotypeHaplotypesHumansMalePedigreeReference StandardsGenetic VariationGenome, HumanSequence AlignmentSequence Analysis, DNARisk AssessmentThrombophiliaGenetic Predisposition to DiseaseGenome-Wide Association Study

Keywords

BiologyGeneticsHaplotype1000 Genomes ProjectWhole genome sequencingGenomeHuman genomeReference genomeComputational biologyAlleleGenotypeGeneSingle-nucleotide polymorphismPrevention (rcdc)MaleDNA Mutational AnalysisBase Sequence (mesh)QH426-470Human (mesh)3105 Genetics (for-2020)0604 Genetics (for)2.5 Research design and methodologies (aetiology)Synthetic (mesh)Thrombophilia (mesh)Genes, Synthetic2.1 Biological and endogenous factorsThrombophiliaReference Standards (mesh)Sequence Alignment (mesh)Male (mesh)Genetic Predisposition to Disease (mesh)Developmental Biology (science-metrix)Humans (mesh)Generic health relevance (hrcs-hc)2.5 Research design and methodologies (aetiology) (hrcs-rac)Genome-Wide Association Study - methodsBiological SciencesReference StandardsThrombophilia - geneticsPedigreePedigree (mesh)Alleles (mesh)Genome-Wide Association Study (mesh)Risk Assessment (mesh)FemaleSequence AnalysisHaplotypes (mesh)BiotechnologyHumanGenetics; Molecular Biology; Ecology, Evolution, Behavior and Systematics; Cancer Research; Genetics (clinical)Research Article570610DNA Mutational Analysis - methodsBiotechnology (rcdc)Risk AssessmentHumansResearch Subject Categories::NATURAL SCIENCES::Biology::Cell and molecular biology::GeneticsGenetic Predisposition to DiseaseGenetic Variation (mesh)Alleles31 Biological Sciences (for-2020)Base SequenceGenetics (rcdc)Genotype (mesh)Genome, HumanPreventionSyntheticGenetic VariationDNA2.1 Biological and endogenous factors (hrcs-rac)Sequence Analysis, DNAHuman Genome (rcdc)GenesHaplotypesFemale (mesh)Generic health relevanceDNA (mesh)DNA Mutational Analysis (mesh)Sequence AlignmentDevelopmental BiologyGenome-Wide Association Study

Sustainable Development Goals

SDG 3: 3. Good healthSDG 0: Good health and well-being