Author

David Adlam

Glenfield HospitalORCID 0000-0002-0080-9884Unclaimed 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· 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 Jason Ciril KovaciciD· 2 shared Jeffrey W. OliniD· 2 shared Min‐Lee YangiD· 2 shared Nabila Bouatia‐NajiiD· 2 shared Nicolas CombaretiD· 2 shared

Activity by Year

2020-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Adrien B. GeorgesORCID

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2 papers

Recent·Most cited

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, Christopher P. Nelson, Eleni Giannoulatou, Joséphine Henry, Lijiang Ma, Montgomery Blencowe, Tamiel Nichole Turley, Min‐Lee Yang, Peter S. Braund, Inès Sadeg-Sayoud, Siiri E. Iismaa, Matthew Kosel, Xiang Zhou, , 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.

medRxiv · Jul 5, 2022 · PreprintGenetic & Genomic Medicine

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

Adrien B. Georges, Juliette Albuisson, Takiy-Eddine Berrandou, Délia Dupré, Aurélien Lorthioir, Valentina d’Escamard, Antonio Di Narzo, Daniella L. Kadian‐Dodov, Jeffrey W. Olin, Ewa Warchoł-Celińska, Aleksander Prejbisz, Andrzej Januszewicz, Patrick Bruneval, Anna Baranowska, Tom R. Webb, , 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.

Cardiovascular Research · Jun 7, 2020Peer-reviewedGenetic & Genomic Medicine