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A missense variant in Mitochondrial Amidoxime Reducing Component 1 gene and protection against liver disease

PLoS Genetics(2020)10.1371/journal.pgen.1008629Source: DataRank Database

A missense variant in Mitochondrial Amidoxime Reducing Component 1 gene and protection against liver disease is a research paper published in PLoS Genetics (2020). On theSindex it has a DataRank of 0. It has been cited 169 times.

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Scored on demand from live citation data

Open Access169 citations

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›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (36 grants)Impact (FWCI 13.81)OA: goldTopics (97)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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Authors (42)

Mary E. Haas ORCID,Amit V. Khera ORCID,Krishna G. Aragam ORCID,Mark Chaffin ORCID,Derek Klarin ORCID

Live enrichment

PubMed:32282858 PMC:PMC7200007 OpenAlex:https://openalex.org/W3016050178

British Heart Foundation

Grant: CS/14/2/30841

Medical Research Council

Grant: HDR-9004

NHLBI NIH HHS

Grant: R01 HL127564

NIGMS NIH HHS

Grant: U54 GM115428

NHGRI NIH HHS

Grant: U54 HG003067

NHLBI NIH HHS

Grant: HHSN268201300046C

National Institute for Health Research (NIHR)

Grant: NF-SI-0611-10170

NIDDK NIH HHS

Grant: R56 DK101478

NHLBI NIH HHS

Grant: RC2 HL102925

NHLBI NIH HHS

Grant: RC2 HL103010

National Institute for Health Research (NIHR)

Grant: IS_BRU_0211_20033

NIDDK NIH HHS

Grant: R01 DK101478

NHGRI NIH HHS

Grant: UM1 HG008895

NHLBI NIH HHS

Grant: HHSN268201300050C

NHLBI NIH HHS

Grant: RC2 HL102923

British Heart Foundation

Grant: RG/18/10/33842

British Heart Foundation

Grant: RG2000010

NHLBI NIH HHS

Grant: HHSN268201300047C

NHLBI NIH HHS

Grant: HHSN268201300048C

NHLBI NIH HHS

Grant: HHSN268201300049C

NHLBI NIH HHS

Grant: RC2 HL102924

NHGRI NIH HHS

Grant: K08 HG010155

NHLBI NIH HHS

Grant: RC2 HL102926

National Institutes of Health

Grant: 1RC2HL103010-01

Human Exome Sequencing in Six Well-Phenotyped NHLBI Cohorts

National Institutes of Health

Grant: 1RC2HL102925-01

Comprehensive Sequencing and Analysis of Variation in NHLBI Cohorts

National Institutes of Health

Grant: 5UM1HG008895-04

Center for Common Disease Genetics

National Institutes of Health

Grant: 3U54HG003067-07S1

Large Scale Sequencing and Analysis of Genomes

National Institutes of Health

Grant: 1RC2HL102923-01

ARRA - NHLBI Lung Cohorts Sequencing Project

National Institutes of Health

Grant: 1RC2HL102924-01

WHI Sequencing Project (WHISP)

National Institutes of Health

Grant: 5U54GM115428-07

Mississippi Center for Clinical and Translational Research

Wellcome Trust

Grant: unidentified

unidentified

National Institutes of Health

Grant: 1RC2HL102926-01

Northwest Genomics Center

European Commission

Grant: 261123

Sharing capacity across Europe in high-throughput sequencing technology to explore genetic variation in health and disease

National Institutes of Health

Grant: 5R01HL127564-06

Using genetic variation to study biology of blood lipids & coronary heart disease

National Institutes of Health

Grant: 1K08HG010155-01

Polygenic prediction of common, complex diseases

Deutsche Forschungsgemeinschaft

Grant: 238187445/SFB 1123

Atherosclerosis: Mechanisms and Networks of Novel Therapeutic Targets

FWCI

13.81

Citation Percentile

1.0%

Citation Trend

2015

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2026

goldLicense: cc-by

journalhttps://journals.plos.org/plosgenetics/article/file?id=10.1371/journal.pgen.1008629&type=printable

publisherhttps://journals.plos.org/plosgenetics/article/file?id=10.1371/journal.pgen.1008629&type=printable

publisherhttps://dx.plos.org/10.1371/journal.pgen.1008629

journalhttps://doi.org/10.1371/journal.pgen.1008629

repositoryhttps://pubmed.ncbi.nlm.nih.gov/32282858

Fields of Study

Liver Disease Diagnosis and TreatmentLiver Disease and TransplantationDrug-Induced Hepatotoxicity and Protection0301 basic medicine03 medical and health sciences0303 health sciencesAllelesCholesterol, LDLCoronary Artery DiseaseDatasets as TopicFatty LiverFemaleGenetic Predisposition to DiseaseHomozygoteHumansLiverLiver CirrhosisLiver Cirrhosis, AlcoholicLoss of Function MutationMaleMiddle AgedMitochondrial ProteinsMutation, MissenseOxidoreductases

MeSH Terms

Loss of Function MutationAllelesCoronary Artery DiseaseFatty LiverFemaleHomozygoteHumansCholesterol, LDLLiverLiver CirrhosisLiver Cirrhosis, AlcoholicMaleMiddle AgedOxidoreductasesGenetic Predisposition to DiseaseMutation, MissenseMitochondrial ProteinsDatasets as Topic

Keywords

Missense mutationCirrhosisBiologyHepatologyInternal medicineLiver diseaseFatty liverAlanine transaminaseEndocrinologyGastroenterologyGeneDiseaseGeneticsMedicineBiochemistryMutationLiver CirrhosisMaleCirrosi hepàticaMutation, MissensePROTEINDatasets as TopicCoronary Artery DiseaseQH426-470Fetge -- MalaltiesTM6SF2Social sciencesMitochondrial ProteinsANGPTL3Liver Cirrhosis, AlcoholicLoss of Function MutationHumansGenetic Predisposition to DiseaseGENOME-WIDE ASSOCIATIONCONFERS SUSCEPTIBILITYPNPLA3AllelesMedicine and health sciencesBiology and life sciencesMORTALITYHomozygoteFOS: Social sciencesCholesterol, LDLMiddle AgedRISK LOCIBiomedicineYIELDLiverGenetics, developmental biology, physiologyFemaleOxidoreductasesENZYMESColesterolProteïnesResearch Article

Sustainable Development Goals

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