Tristan Rey

TSPEAR variants are primarily associated with ectodermal dysplasia and tooth agenesis but not hearing loss: A novel cohort study

V. Shashi, K. Schoch, B. Dallapiccola, 2021, American journal of medical genetics. Part A.

Primary failure of eruption: From molecular diagnosis to therapeutic management

M. Manière, A. Bloch-Zupan, M. Strub, 2023, Journal of oral biology and craniofacial research.

Protocol GenoDENT: Implementation of a New NGS Panel for Molecular Diagnosis of Genetic Disorders with Orodental Involvement.

Marzena Kawczynski, M. Manière, A. Bloch-Zupan, 2019, Methods in molecular biology.

Amelogenesis imperfecta: Next-generation sequencing sheds light on Witkop’s classification

Marzena Kawczynski, M. Manière, A. Bloch-Zupan, 2023, Frontiers in Physiology.

A Novel Homozygous Variant in GJA1 Causing a Hallermann-Streiff/Oculodentodigital Dysplasia Overlapping Phenotype: A Clinical Report

A. Bloch-Zupan, V. Laugel-Haushalter, S. El Arabi, 2021, Frontiers in Dental Medicine.