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

Min‐Lee Yang

University of Michigan

ORCID: 0000-0003-2823-8320

Also affiliated with Michigan United

Biochemistry, Genetics and Molecular BiologyMedicine

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 9 papers. Top paper: “Chromosome 1q21.2 and additional loci influence risk of spontaneous coronary artery dissection and myocardial infarction”.

Chromosome 1q21.2 and additional loci influence risk of spontaneous coronary artery dissection and myocardial infarction

Nature Communications(2020)10.1038/s41467-020-17558-x

N/A

2.7DataRank · unranked

103 citations

Min‐Lee Yang, Mark Trinder, Catherine Tcheandjieu, Chang Xu, Andrew Starovoytov +22 more

Fibromuscular Dysplasia and Abdominal Aortic Aneurysms Are Dimorphic Sex-Specific Diseases With Shared Complex Genetic Architecture

Circulation Genomic and Precision Medicine(2022)10.1161/circgen.121.003496

N/A

0.806DataRank · unranked

22 citations

Min‐Lee Yang, Michael G. Levin, Catherine Tcheandjieu, Michael R. Mathis, Kristina L. Hunker +86 more

Genome-wide association meta-analysis of spontaneous coronary artery dissection identifies risk variants and genes related to artery integrity and tissue-mediated coagulation

Nature Genetics(2023)10.1038/s41588-023-01410-1

N/A

0.680DataRank · unranked

92 citations

Takiy-Eddine Berrandou, Adrien Georges, Christopher P. Nelson, Eleni Giannoulatou, Joséphine Henry +52 more

An Asian-specific MPL genetic variant alters JAK–STAT signaling and influences platelet count in the population

Human Molecular Genetics(2021)10.1093/hmg/ddab062

N/A

0.312DataRank · unranked

7 citations

Wei Zhou, Yi Fu, Chloe Y. Y. Cheung, Yujun Dong, Min‐Lee Yang +15 more

Meta-analysis of rare and common exome chip variants identifies S1PR4 and other loci influencing blood cell traits

UNC Libraries(2020)10.17615/aapr-pr41

N/A

0.104DataRank · unranked

1 citations

Niels Grarup, Albert Hofman, Lenore J. Launer, David C. Liewald, Albert V. Smith +76 more

Genetic variation in CCDC93 is associated with elevated central systolic blood pressure, impaired arterial relaxation, and mitochondrial dysfunction

PLoS Genetics(2024)10.1371/journal.pgen.1011151

N/A

0.104DataRank · unranked

1 citations

Min‐Lee Yang, Pengfei Sun, Kristina L. Hunker, Jianping Li, Jia Jia +12 more

Genetic association studies of fibromuscular dysplasia identify new risk loci and shared genetic basis with more common vascular diseases

medRxiv(2020)10.1101/2020.09.16.20195701

N/A

0DataRank · unranked

0 citations

Min‐Lee Yang, Takiy-Eddine Berrandou, Mark K. Bakker, Ozan Dikilitas, Soto Romuald Kiando +47 more

Rare loss-of-function mutations of PTGIR are enriched in fibromuscular dysplasia

Cardiovascular Research(2020)10.1093/cvr/cvaa161

N/A

0DataRank · unranked

32 citations

Juliette Albuisson, Takiy-Eddine Berrandou, Délia Dupré, Aurélien Lorthioir, Valentina d’Escamard +32 more

Sex-specific genetic architecture of blood pressure

Nature Medicine(2024)10.1038/s41591-024-02858-2

N/A

0DataRank · unranked

46 citations

Chang Xu, Trisha Gupte, Thomas J. Hoffmann, Carlos Iribarren, Xiang Zhou +2 more