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Allelic imbalance of chromatin accessibility in cancer identifies candidate causal risk variants and their mechanisms

Nature Genetics(2022)10.1038/s41588-022-01075-2Source: DataRank Database

Allelic imbalance of chromatin accessibility in cancer identifies candidate causal risk variants and their mechanisms is a research paper published in Nature Genetics (2022). On theSindex it has a DataRank of 0.561. It has been cited 41 times.

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0.561DataRank · unranked

Scored on demand from live citation data

Open Access41 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (11 grants)Impact (FWCI 6.33)OA: greenTopics (43)IDs (PubMed, OpenAlex)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 100%Citation Network 0%

Base Score Contribution

0.561

From this paper's citation signal

Citation Network Contribution

Citation network not refreshed for this result

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Authors (2)

Alexander Gusev ORCID,Dennis Grishin ORCID

Live enrichment

PubMed:35697866 OpenAlex:https://openalex.org/W4282549610

U.S. Department of Health & Human Services | National Institutes of Health

Grant: R01 MH115676

U.S. Department of Health & Human Services | National Institutes of Health

Grant: R01 CA227237

U.S. Department of Health & Human Services | National Institutes of Health

Grant: R01 CA244569

U.S. Department of Health & Human Services | National Institutes of Health

Grant: R01 CA259200

National Institutes of Health

Grant: 3R01CA259200-04S2

Genomic and Genomic Variation in Prostate Cancer

National Institutes of Health

Grant: 5R01MH115676-08

Integrating case-control transcriptomic and genetic data in admixed individuals to identify disease genes for schizophrenia and bipolar disorder

National Institutes of Health

Grant: 5R01CA227237-03

(PQ3) A functional genomic approach to identification and interpretation of germline-tumor genetic interactions

National Institutes of Health

Grant: 1R01CA244569-01A1

Characterizing non-coding somatic and germline variant interactions in ovarian cancer

NHGRI NIH HHS

Grant: R01 HG006399

NIMH NIH HHS

Grant: R01 MH125252

NCI NIH HHS

Grant: R01 CA262577

FWCI

6.33

Citation Percentile

1.0%

Citation Trend

2023

2024

2025

2026

greenLicense: Springer TDM

repositoryhttps://www.ncbi.nlm.nih.gov/pmc/articles/9886437

publisherhttps://www.nature.com/articles/s41588-022-01075-2.pdf

publisherhttps://www.nature.com/articles/s41588-022-01075-2

journalhttps://doi.org/10.1038/s41588-022-01075-2

Fields of Study

Genetic Associations and EpidemiologyEpigenetics and DNA MethylationBioinformatics and Genomic Networks0301 basic medicine0303 health sciences03 medical and health sciencesAllelic ImbalanceChromatinGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansMaleNeoplasmsPolymorphism, Single Nucleotide

MeSH Terms

ChromatinHumansMaleNeoplasmsGenetic Predisposition to DiseasePolymorphism, Single NucleotideAllelic ImbalanceGenome-Wide Association Study

Keywords

BiologyGenome-wide association studyGeneticsGermlineProstate cancerCancerComputational biologyGenetic architectureAlleleBreast cancerGeneQuantitative trait locusSingle-nucleotide polymorphismGenotypeMaleNeoplasmsHumansGenetic Predisposition to DiseaseAllelic ImbalancePolymorphism, Single NucleotideChromatin

Sustainable Development Goals

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