Author

Haikel Dridi

Columbia UniversityORCID 0000-0001-9533-7367Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Cell Biology· 1 Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Organism:human· 2 Research Focus:benchmarking· 1 Research Focus:cell type annotation· 1 Approach:experimental assay· 1 Assay:proteomics· 1 Approach:statistical model· 1

Frequent Co-Authors

Andrew R. MarksiD· 2 shared Alain LacampagneiD· 1 shared Albano C. MéliiD· 1 shared Alex R. ChangiD· 1 shared Azzouz Charrabi· 1 shared Carolyn Martinez JorgeiD· 1 shared Eleonora TorreiD· 1 shared Giuseppe AngeliniiD· 1 shared

Activity by Year

2024-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 25 mutual co-author links

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2 shared papersCell Biology

Andrew R. MarksORCID

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2 papers

Recent·Most cited

Validation of differentiated sinoatrial-like hiPSCs as a model of native sinus node myocytes

Eleonora Torre, Yvonne Sleiman, Haikel Dridi, Azzouz Charrabi, Nadia Mekrane, Giuseppe Angelini, Leïla Talssi, Rajesh Kumar Soni, Valentina Di Biase, Héloïse Faure-Gautron, Pascal Seyer, Pieter P. de Tombe, Andrew R. Marks, Jean‐Luc Pasquié, Alain Lacampagne, , Albano C. Méli

The paper validates a protocol to generate sinoatrial-like hiPSC-derived cardiomyocytes that mimic native SAN myocytes in function and protein expression.

bioRxiv · Jan 23, 2026 · PreprintCell Biology

Location of ryanodine receptor type 2 mutation predicts age of onset of sudden death in catecholaminergic polymorphic ventricular tachycardia. A systematic review and meta analysis of case based literature

Halil Beqaj, Leah R. Sittenfeld, Alex R. Chang, Marco Miotto, Haikel Dridi, Gloria Willson, Carolyn Martinez Jorge, Jaan Altosaar Li, Steven R. Reiken, Yang Liu, Zonglin Dai, Andrew R. Marks

This study identifies that RyR2 mutation locations in CPVT patients predict earlier onset of sudden death, based on a meta-analysis of 1008 patients from 227 papers.

medRxiv · Mar 15, 2024 · PreprintGenetic & Genomic Medicine