🏆 Finalist — NIH Data Sharing Index (“S-Index”) Challenge

Raehoon Jeong

Brigham and Women's Hospital

ORCID: 0000-0001-9840-4692

Also affiliated with Harvard University, Harvard University Press, Institut thématique Génétique, génomique et bioinformatique

Biochemistry, Genetics and Molecular BiologyMedicineImmunology and Microbiology

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile
0Author DataRank

Indexed papers

0in pilot corpus
datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 10 papers. Top paper: “Blood cell traits’ GWAS loci colocalization with variation in PU.1 genomic occupancy prioritizes causal noncoding regulatory variants”.

Blood cell traits’ GWAS loci colocalization with variation in PU.1 genomic occupancy prioritizes causal noncoding regulatory variants

Cell Genomics(2023)10.1016/j.xgen.2023.100327
N/A
0DataRank · unranked
10 citations

Martha L. Bulyk, Raehoon Jeong

Colocalization of blood cell traits GWAS associations and variation in PU.1 genomic occupancy prioritizes causal noncoding regulatory variants

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.03.29.534582
N/A
0DataRank · unranked
2 citations

Martha L. Bulyk, Raehoon Jeong

DNA binding analysis of rare variants in homeodomains reveals novel homeodomain specificity-determining residues

bioRxiv (Cold Spring Harbor Laboratory)(2023)10.1101/2023.06.16.545320
N/A
0DataRank · unranked
2 citations

Patrick K. Kimes, Stephen S. Gisselbrecht, Sachi Inukai, Sabrina K. Phanor, James T. Anderson +10 more

DNA binding analysis of rare variants in homeodomains reveals homeodomain specificity-determining residues

Nature Communications(2024)10.1038/s41467-024-47396-0
N/A
0DataRank · unranked
25 citations

Patrick K. Kimes, Stephen S. Gisselbrecht, Sachi Inukai, Sabrina K. Phanor, James T. Anderson +10 more

Chromatin accessibility variation provides insights into missing regulation underlying immune-mediated diseases

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.04.12.589213
N/A
0DataRank · unranked
4 citations

Martha L. Bulyk, Raehoon Jeong

Chromatin accessibility variation provides insights into missing regulation underlying immune-mediated diseases

eLife(2024)10.7554/elife.98289.1
N/A
0DataRank · unranked
4 citations

Martha L. Bulyk, Raehoon Jeong

Gene identification for ocular congenital cranial motor neuron disorders using human sequencing, zebrafish screening, and protein binding microarrays

bioRxiv (Cold Spring Harbor Laboratory)(2024)10.1101/2024.09.12.612713
N/A
0DataRank · unranked
2 citations

Paola M. Matos Ruiz, Jessica King, Emma E. Foster, Lindsay Berube, Wai‐Man Chan +23 more

Meta-analysis reveals transcription factors and DNA binding domain variants associated with congenital heart defect and orofacial cleft

npj Genomic Medicine(2025)10.1038/s41525-025-00525-0
N/A
0DataRank · unranked
1 citations

Martha L. Bulyk, Raehoon Jeong

Missense variants in human forkhead transcription factors reveal determinants of forkhead DNA bispecificity

Cell Reports(2025)10.1016/j.celrep.2025.116427
N/A
0DataRank · unranked
1 citations

Stephen S. Gisselbrecht, Julie‐Alexia Dias, Raehoon Jeong, Elisabeth Rothman, Martha L. Bulyk +1 more

Meta-analysis reveals transcription factors and DNA binding domain variants associated with congenital heart defect and orofacial cleft

medRxiv(2025)10.1101/2025.01.30.25321274
N/A
0DataRank · unranked
0 citations

Martha L. Bulyk, Raehoon Jeong