Agnes Bloch-Zupan

Professeur des Universités - Praticien Hospitalier

University of Strasbourg

France

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Articles (18)

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2024

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2024

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2024

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2024

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2024

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2022

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2021

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2021

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2021

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2021

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2021

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2020

Collaborators (14)

Marie-Christine Birling

University of Strasbourg

FRANCE

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Naji Kharouf

Professor (Assoc.)

University of Strasbourg

FRANCE

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Pascal Dollé

Associate Professor in Biochemistry, Group Leader at IGBMC

University of Strasbourg

FRANCE

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Thibault Canceill

Senior Lecturer (MCU-PH)

Université Toulouse III - Paul Sabatier

FRANCE

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olivier etienne

Assistant professor - Head of post-graduate in esthetic dentistry

University of Strasbourg

FRANCE

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Kenneth Myers

Assistant Professor

McGill University Health Centre

CANADA

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Claire Smith

Lecturer in Biomineralisation in Oral Health

University of Leeds

UNITED KINGDOM

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Michiel van Wijk

Visiting Professor

Catholic University of Leuven

BELGIUM

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Sophie Jung

Professeur des Universités

University of Strasbourg

FRANCE

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jerome bouchet

Associate Professor

Université Paris-Saclay

FRANCE

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Jane Waite

Aston University

UNITED KINGDOM

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Michael Cheetham

University College London

UNITED KINGDOM

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kazutoyo yasukawa

Associate Professor - Hospital Practitioner

FRANCE

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Alan Mighell

University of Leeds School of Medicine

UNITED KINGDOM

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Agnes Bloch-Zupan

Research Interests

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Articles (18)

Diagnosis and management in Rubinstein-Taybi syndrome: first international consensus statement

Biallelic variants in Plexin B2 ( PLXNB2 ) cause amelogenesis imperfecta, hearing loss and intellectual disability

Rare dentin defects: Understanding the pathophysiological mechanisms of COLXVA1 mutations

i-Dent: A virtual assistant to diagnose rare genetic dental diseases

Orofacial Anomalies in Kindler Epidermolysis Bullosa

The Rogdi knockout mouse is a model for Kohlschütter–Tönz syndrome

La dent : un marqueur d’anomalies génétiques du développement

Association between malocclusions and amelogenesis imperfecta genotype and phenotype: A systematic review

GenIDA, a participatory patient registry for genetic forms of intellectual disability provides detailed caregiver-reported information on 237 individuals with Koolen-de Vries syndrome

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

Primary failure of eruption: From molecular diagnosis to therapeutic management

Author Correction: EMPReSS: standardized phenotype screens for functional annotation of the mouse genome

COVID-19 and Dentistry in 72 Questions: An Overview of the Literature

Robert Frank: A Pioneer and Visionary Scientist in Oral Medicine

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

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

Periodontal (formerly type VIII) Ehlers-Danlos syndrome: Description of 13 novel cases and expansion of the clinical phenotype.

Deficiency of the SMOC2 matricellular protein impairs bone healing and produces age-dependent bone loss

Collaborators (14)

Marie-Christine Birling

Naji Kharouf

Pascal Dollé

Thibault Canceill

olivier etienne

Kenneth Myers

Claire Smith

Michiel van Wijk

Sophie Jung

jerome bouchet

Jane Waite

Michael Cheetham

kazutoyo yasukawa

Alan Mighell

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