Pilot corpus: NIH-funded biomedical datasets. Any DOI can be scored on demand — network effects sharpen as coverage grows.

Localizing Components of Shared Transethnic Genetic Architecture of Complex Traits from GWAS Summary Data

The American Journal of Human Genetics(2020)10.1016/j.ajhg.2020.04.012Source: DataRank Database

Localizing Components of Shared Transethnic Genetic Architecture of Complex Traits from GWAS Summary Data is a research paper published in The American Journal of Human Genetics (2020). On theSindex it has a DataRank of 0.714. It has been cited 116 times.

N/A

0.714DataRank · unranked

Scored on demand from live citation data

Open Access116 citations

Download PDF

Cite:

Linked data & code

doi

DataRank reads this dataset's downstream impact straight off the citation graph — no black box, no proprietary weighting. How is this computed?

›Methodology & internals

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Pipeline:MetadataData-paper checkEnrichmentCitation networkScoring

Enrichment:Funding (14 grants)Impact (FWCI 12.64)OA: bronzeTopics (62)Linked Datasets (25)DataCite Reuse (25)IDs (PubMed, PMC, OpenAlex)Annotations (1)

FAIR Checklist

Context only (not used in score)

Findable (2/2)

Has DOI
Indexed in repositories

Accessible (1/2)

Open Access

Interoperable (2/2)

DataCite relations
Linked datasets

Reusable (0/3)

FAIR checklist signals are shown for context only and do not affect DataRank scoring.

Run a calibrated FAIR evaluation for this paper →

We only score data papers we can read in full — never from an abstract alone.

DataRank Breakdown

Base Score 100%Citation Network 0%

Base Score Contribution

0.714

From this paper's citation signal

Citation Network Contribution

Citation network not refreshed for this result

This paper's DataRank is currently driven only by its base citation score. Citation network data was not refreshed for this result.

Learn more about DataRank methodology →

Authors (9)

Kathryn S. Burch ORCID,Ruth Johnson ORCID,Malika Freund ORCID,Gleb Kichaev ORCID,Nicholas Mancuso ORCID

Live enrichment

PubMed:32442408 PMC:PMC7273527 OpenAlex:https://openalex.org/W3026380245

NHGRI NIH HHS

Grant: T32 HG002536

NHGRI NIH HHS

Grant: R01 HG009120

NCI NIH HHS

Grant: U01 CA194393

NIMH NIH HHS

Grant: T32 MH073526

NHGRI NIH HHS

Grant: R01 HG006399

NINDS NIH HHS

Grant: T32 NS048004

NIMH NIH HHS

Grant: R01 MH115676

National Institutes of Health

Grant: 3T32HG002536-06S1

Training Grant in Genomic Analysis and Interpretation

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: 5R01MH115676-03

Joint genomic and statistical analyses of schizophrenia and bipolar to decipher genetic susceptibility

National Institutes of Health

Grant: 5R01HG009120-04

Integrative approaches for mapping the genetic risk of complex traits

National Institutes of Health

Grant: 2T32MH073526-06

Training Grant in Neurobehavioral Genetics

National Institutes of Health

Grant: 5U01CA194393-04

Quantifying and Characterizing the shared genetic contribution to common cancers

National Institutes of Health

FWCI

12.64

Citation Percentile

1.0%

Citation Trend

2020

2021

2022

2023

2024

2025

2026

bronzeLicense: Elsevier Non-Commercial

journalhttp://www.cell.com/article/S000292972030121X/pdf

publisherhttp://www.cell.com/article/S000292972030121X/pdf

publisherhttps://api.elsevier.com/content/article/PII:S000292972030121X?httpAccept=text/xml

publisherhttps://api.elsevier.com/content/article/PII:S000292972030121X?httpAccept=text/plain

journalhttps://doi.org/10.1016/j.ajhg.2020.04.012

Fields of Study

Genetic Associations and EpidemiologyGenetic and phenotypic traits in livestockGenetic Mapping and Diversity in Plants and Animals0301 basic medicine0303 health sciences03 medical and health sciencesBayes TheoremEthnicityEuropeAsia, EasternGene FrequencyGenome-Wide Association StudyHumansLinkage DisequilibriumMultifactorial InheritanceOrgan SpecificityPolymorphism, Single Nucleotide

MeSH Terms

Bayes TheoremEthnicityEuropeAsia, EasternGene FrequencyHumansOrgan SpecificityLinkage DisequilibriumMultifactorial InheritancePolymorphism, Single NucleotideGenome-Wide Association Study

Keywords

Genome-wide association studyGenetic architectureSingle-nucleotide polymorphismBiologyGenetic associationGeneticsPopulationHeritabilityBayes' theoremQuantitative trait locusEvolutionary biologyStatisticsDemographyBayesian probabilityGeneGenotypeMathematicslinkage disequilibriumGwasComplex TraitsAncestryPrsFine-mappingTransethnicPolygenicityMultifactorial InheritanceAsia, EasternBayes TheoremPolymorphism, Single NucleotideEuropeGene FrequencyOrgan SpecificityEthnicityHumans

Additional file 1 of Polygenic transcriptome risk scores (PTRS) can improve portability of polygenic risk scores across ancestries

10.6084/m9.figshare.18393353.v1figshare

Additional file 1 of Polygenic transcriptome risk scores (PTRS) can improve portability of polygenic risk scores across ancestries

10.6084/m9.figshare.18393353figshare

Additional file 6 of Polygenic transcriptome risk scores (PTRS) can improve portability of polygenic risk scores across ancestries

10.6084/m9.figshare.18393368.v1figshare

Additional file 6 of Polygenic transcriptome risk scores (PTRS) can improve portability of polygenic risk scores across ancestries

10.6084/m9.figshare.18393368figshare

Additional file 2 of Similarity and diversity of genetic architecture for complex traits between East Asian and European populations

10.6084/m9.figshare.23505079.v1figshare

Additional file 2 of Similarity and diversity of genetic architecture for complex traits between East Asian and European populations

10.6084/m9.figshare.23505079figshare

Additional file 1 of Robust identification of regulatory variants (eQTLs) using a differential expression framework developed for RNA-sequencing

10.6084/m9.figshare.26582303.v1figshare

Additional file 1 of Robust identification of regulatory variants (eQTLs) using a differential expression framework developed for RNA-sequencing

10.6084/m9.figshare.26582303figshare

Additional file 3 of Robust identification of regulatory variants (eQTLs) using a differential expression framework developed for RNA-sequencing

10.6084/m9.figshare.26582309.v1figshare

Additional file 3 of Robust identification of regulatory variants (eQTLs) using a differential expression framework developed for RNA-sequencing

10.6084/m9.figshare.26582309figshare

Additional file 1 of Genetic correlation for alcohol consumption between Europeans and East Asians

10.6084/m9.figshare.26634024.v1figshare

Additional file 1 of Genetic correlation for alcohol consumption between Europeans and East Asians

10.6084/m9.figshare.26634024figshare

Additional file 6 of Robust identification of regulatory variants (eQTLs) using a differential expression framework developed for RNA-sequencing

10.6084/m9.figshare.26582318.v1figshare

Additional file 6 of Robust identification of regulatory variants (eQTLs) using a differential expression framework developed for RNA-sequencing

10.6084/m9.figshare.26582318figshare

Additional file 7 of Robust identification of regulatory variants (eQTLs) using a differential expression framework developed for RNA-sequencing

10.6084/m9.figshare.26582321.v1figshare

Additional file 4 of Robust identification of regulatory variants (eQTLs) using a differential expression framework developed for RNA-sequencing

10.6084/m9.figshare.26582312figshare

Additional file 9 of Robust identification of regulatory variants (eQTLs) using a differential expression framework developed for RNA-sequencing

10.6084/m9.figshare.26582327.v1figshare

Additional file 4 of Robust identification of regulatory variants (eQTLs) using a differential expression framework developed for RNA-sequencing

10.6084/m9.figshare.26582312.v1figshare

Additional file 7 of Robust identification of regulatory variants (eQTLs) using a differential expression framework developed for RNA-sequencing

10.6084/m9.figshare.26582321figshare

Additional file 8 of Robust identification of regulatory variants (eQTLs) using a differential expression framework developed for RNA-sequencing

10.6084/m9.figshare.26582324figshare

Related Papers (10)

Multi-ancestry fine-mapping improves precision to identify causal genes in transcriptome-wide association studies

N/A

0.624DataRank · unranked

The American Journal of Human Genetics(2022)

co-citedsame journal

10.1016/j.ajhg.2022.07.002

Worldwide trends in body-mass index, underweight, overweight, and obesity from 1975 to 2016: a pooled analysis of 2416 population-based measurement studies in 128·9 million children, adolescents, and adults

N/A

1.3DataRank · unranked

The Lancet(2017)

co-cited

10.1016/s0140-6736(17)32129-3

Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases

N/A

1.0DataRank · unranked

Nature Genetics(2018)

co-cited

10.1038/s41588-018-0047-6

Clinical use of current polygenic risk scores may exacerbate health disparities

N/A

1.2DataRank · unranked

Nature Genetics(2019)

co-cited

10.1038/s41588-019-0379-x

The exposome and health: Where chemistry meets biology

N/A

1.0DataRank · unranked

Science(2020)

co-cited

10.1126/science.aay3164

High-depth African genomes inform human migration and health

N/A

0.889DataRank · unranked

Nature(2020)

co-cited

10.1038/s41586-020-2859-7

Mapping gene flow between ancient hominins through demography-aware inference of the ancestral recombination graph

N/A

3.7DataRank · unranked

PLoS Genetics(2020)

co-cited

10.1371/journal.pgen.1008895

Assessment of polygenic architecture and risk prediction based on common variants across fourteen cancers

N/A

0.735DataRank · unranked

Nature Communications(2020)

co-cited

10.1038/s41467-020-16483-3

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

Top 3%

7.0DataRank

Nature(2021)

co-cited

10.1038/s41586-021-03205-y

Population-specific causal disease effect sizes in functionally important regions impacted by selection

N/A

0.741DataRank · unranked

Nature Communications(2021)

co-cited

10.1038/s41467-021-21286-1

Localizing Components of Shared Transethnic Genetic Architecture of Complex Traits from GWAS Summary Data

FAIR Checklist

DataRank Breakdown

Authors (9)

Funding (14 grants)

Impact

Open Access

Topics

Linked Datasets (25)

Annotations (Europe PMC)

Related Papers (10)