Author

Stephen E. Hamby

Glenfield HospitalORCID 0000-0002-6215-5791Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

Click to filter author papers

Signature Assays, Organisms & Methods

Click to filter · or open tag

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

Frequent Co-Authors

Adrien B. GeorgesiD· 2 shared Anna BaranowskaiD· 2 shared Daniella L. Kadian‐DodoviD· 2 shared David AdlamiD· 2 shared Jason Ciril KovaciciD· 2 shared Jeffrey W. OliniD· 2 shared Min‐Lee YangiD· 2 shared Nabila Bouatia‐NajiiD· 2 shared

Activity by Year

2020-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

Click any collaborator node to inspect or filter shared papers

Focal author (center)Selected co-authorORCID co-authorUnlinked name

Curved chords = mutual co-authorship

2 shared papersGenetic & Genomic Medicine

Adrien B. GeorgesORCID

Mutual co-authors in cluster

Author profile →

2 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

𝕏 PostBluesky

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

𝕏 PostBluesky