Author

Min‐Lee Yang

University of MichiganORCID 0000-0003-2823-8320Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 3 Approach:statistical model· 3 Research Focus:GWAS / association mapping· 2 Assay:GWAS summary statistics· 2 Research Focus:differential expression· 1 Research Focus:variant calling· 1 Assay:whole-exome sequencing· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

Adrien B. GeorgesiD· 3 shared Daniella L. Kadian‐DodoviD· 3 shared Jason Ciril KovaciciD· 3 shared Jeffrey W. OliniD· 3 shared Nabila Bouatia‐NajiiD· 3 shared Santhi K. GaneshiD· 3 shared Takiy-Eddine BerrandouiD· 3 shared Valentina d’Escamard· 3 shared

Activity by Year

2020-2022 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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3 shared papersGenetic & Genomic Medicine

Adrien B. GeorgesORCID

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3 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintJul 5, 2022

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

David Adlam, Takiy-Eddine Berrandou, Adrien B. Georges…·Nabila Bouatia‐Naji

This study identifies 17 genetic risk loci for spontaneous coronary artery dissection (SCAD), including 12 new ones, and highlights genes related to artery integrity and coagulation.

5 citations

humanGWAS summary statistics

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Genetic & Genomic MedicinemedRxivPreprintSep 16, 2020

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

Adrien B. Georges, Min‐Lee Yang, Takiy-Eddine Berrandou…·Nabila Bouatia‐Naji

DOI 10.1101/2020.09.16.20195701

humanGWAS summary statistics

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Genetic & Genomic MedicineCardiovascular ResearchPeer-reviewedJun 7, 2020

Rare Loss-of-Function Mutations of PTGIR identified in Fibromuscular Dysplasia and Spontaneous Coronary Artery Dissection

Adrien B. Georges, Juliette Albuisson, Takiy-Eddine Berrandou…·Nabila Bouatia‐Naji

The paper identifies rare loss-of-function mutations in PTGIR in FMD and SCAD patients, showing impaired prostacyclin receptor function and suggesting a role for prostacyclin signaling in these diseases.

33 citations

humanwhole-exome sequencing

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