Agnes Bloch-Zupan

Professeur des Universités - Praticien Hospitalier

University of Strasbourg

France

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Research Interests

Orthodontics

60%

Oral Pathology

50%

Dentistry

60%

Rare Disease

60%

Osteogenesis Imperfecta

60%

Medical Science

50%

Birth Defect

40%

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Articles18

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

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Year:

2024

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

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Year:

2024

Rare dentin defects: Understanding the pathophysiological mechanisms of COLXVA1 mutations

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Year:

2024

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

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Year:

2024

Orofacial Anomalies in Kindler Epidermolysis Bullosa

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Year:

2024

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

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Year:

2024

La dent : un marqueur d’anomalies génétiques du développement

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Year:

2024

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

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Year:

2023

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

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Year:

2023

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

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Year:

2023

Primary failure of eruption: From molecular diagnosis to therapeutic management

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Year:

2023

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

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Year:

2022

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

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Year:

2021

Robert Frank: A Pioneer and Visionary Scientist in Oral Medicine

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Year:

2021

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

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Year:

2021

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

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Year:

2021

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

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Year:

2021

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

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Year:

2020

Collaborators11

Marie-Christine Birling

University of Strasbourg

FRANCE

Naji Kharouf

Professor (Assoc.)

University of Strasbourg

FRANCE

Pascal Dollé

Associate Professor in Biochemistry, Group Leader at IGBMC

University of Strasbourg

FRANCE

Thibault Canceill

Senior Lecturer (MCU-PH)

Université Toulouse III - Paul Sabatier

FRANCE

olivier etienne

Assistant professor - Head of post-graduate in esthetic dentistry

University of Strasbourg

FRANCE

Kenneth Myers

Assistant Professor

McGill University Health Centre

CANADA

Claire Smith

Lecturer in Biomineralisation in Oral Health

University of Leeds

UNITED KINGDOM

Sophie Jung

Professeur des Universités

University of Strasbourg

FRANCE

jerome bouchet

Associate Professor

Université Paris-Saclay

FRANCE

Jane Waite

Aston University

UNITED KINGDOM

kazutoyo yasukawa

Associate Professor - Hospital Practitioner

FRANCE

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