Takiy-eddine Berrandou
Paris, France
Last Updated: 09/26/2026
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Found 12 publications
Multi-trait and Gene-Based Analyses Identify Genetic Variants Associated with Spontaneous Coronary Artery Dissection.
Journal: medRxiv : the preprint server for health sciences
Published: April 29, 2026
Genome-wide association studies (GWAS) in 2026: From gene hunting to biological discovery in endocrine and cardiometabolic diseases.
Journal: Annales d'endocrinologie
Published: March 21, 2026
KLK15 alters connective tissues in hypermobile Ehlers-Danlos syndrome.
Journal: iScience
Published: February 25, 2025
Mass spectrometric proteome profiling using a deep spectral library reveals homogenization of right and left atrial proteomes in persistent atrial fibrillation patients.
Journal: Cardiovascular research
Published: January 07, 2025
Polymorphisms in circadian rhythm genes and the risk of differentiated thyroid cancer.
Journal: Frontiers in genetics
Published: December 15, 2024
Variants in the Kallikrein Gene Family and Hypermobile Ehlers-Danlos Syndrome.
Journal: Research square
Published: July 01, 2024
Genomic, Transcriptomic, and Proteomic Depiction of Induced Pluripotent Stem Cells-Derived Smooth Muscle Cells As Emerging Cellular Models for Arterial Diseases.
Journal: Hypertension (Dallas, Tex. : 1979)
Published: January 19, 2023
Fibromuscular dysplasia as a polygenic disease
Journal: Medecine sciences : M/S
Published: November 30, 2022
LDAK-GBAT: Fast and powerful gene-based association testing using summary statistics.
Journal: American journal of human genetics
Published: June 28, 2022
Genome-wide association meta-analysis of spontaneous coronary artery dissection identifies risk variants and genes related to artery integrity and tissue-mediated coagulation.
Journal: Nature genetics
Published: June 13, 2022
Author Correction: Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases.
Journal: Nature communications
Published: April 21, 2022
Genetic investigation of fibromuscular dysplasia identifies risk loci and shared genetics with common cardiovascular diseases.
Journal: Nature communications
Published: November 10, 2020
Showing 1-12 of 12
Last Updated: 09/26/2026