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Matthieu Egloff

université de poitiers inserm 1084

France

Research Interests

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Professors in France Professors in Neuropsychology Neuropsychology professors in France

Articles (11)

Year:

2026

Year:

2025

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2025

Year:

2025

Year:

2025

Year:

2025

Year:

2024

Year:

2024

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2023

Year:

2022

Year:

2020

Collaborators (17)

Abderaouf Hamza

Assistant Lecturer

Université Paris Cité

FRANCE

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Stefan Barakat

Associate professor

Erasmus MC

NETHERLANDS

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Nathalie Eduarda Marie-Jeanne Vanden Eynde

Vrije Universiteit Brussel

BELGIUM

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Benjamin Fournier

Professor

Université Paris-Saclay

FRANCE

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Agnes Bloch-Zupan

Subgroup LEADER : Craniofacial and oral developments, and their associated abnormalities; Teams : Pathophysiology of Down's syndrome and rare dose-effect diseases causing intellectual disabilities (ID) or autism spectrum disorders (ASD) and other comorbidities

University of Strasbourg

FRANCE

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Paul Kuentz

Professeur des Universités-Praticien Hospitalier

Centre Hospitalier Universitaire Vaudois

FRANCE

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Richard Redon

INSERM

FRANCE

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Louise-Marie CHEVALIER

Institut de Cancérologie de l'Ouest

FRANCE

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Caroline Rooryck

University of Bordeaux

FRANCE

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Eric Pasmant

Head

Institut Curie

FRANCE

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Sarah Baer

Chief of resident

Hôpitaux universitaires de Strasbourg

FRANCE

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Pierre Vande Perre

Institut Claudius Regaud

FRANCE

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Hélène Cavé

PUPH, Head of the molecular Genetics unit

Hôpital Robert-Debré

FRANCE

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Florence Petit

Université de Lille

FRANCE

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Carin C.D. Van der Rijt

Full professor

Erasmus University Rotterdam

NETHERLANDS

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Laurie Galvan

Associate professor

Université de Nîmes

FRANCE

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Annick Toutain

FRANCE

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Matthieu Egloff

Research Interests

Explore related searches

Articles (11)

Delineation of a Novel Mirror Syndrome: NFIC Variants Cause Syndromic Intellectual Disability With Macrocephaly.

<i>PFMG2025</i>-integrating genomic medicine into the national healthcare system in France.

Recruitment, follow-up and survival in an 11-country cohort study of patients at the end of life and their relatives

French Guidelines of the AchroPuce Network for the Interpretation and Reporting of Constitutional Copy Number Variants.

Heterozygous alterations of GTF2I at the Williams-Beuren syndrome's locus cause a neurodevelopmental disorder

RORA-neurodevelopmental disorder: A unique triad of developmental disabilities, cerebellar anomalies, and myoclonic seizures

Intriguing link between fetal intracranial hemorrhage and X‐linked recessive chondrodysplasia punctata

3q29 duplications: A cohort of 46 patients and a literature review

Clinical and genomic delineation of the new proximal 19p13.3 microduplication syndrome

Cerebellar and Striatal Implications in Autism Spectrum Disorders: From Clinical Observations to Animal Models

12q21 deletion syndrome: Narrowing the critical region down to 1.6 Mb including SYT1 and PPP1R12A

Collaborators (17)

Abderaouf Hamza

Stefan Barakat

Nathalie Eduarda Marie-Jeanne Vanden Eynde

Benjamin Fournier

Agnes Bloch-Zupan

Paul Kuentz

Richard Redon

Louise-Marie CHEVALIER

Caroline Rooryck

Eric Pasmant

Sarah Baer

Pierre Vande Perre

Hélène Cavé

Florence Petit

Carin C.D. Van der Rijt

Laurie Galvan

Annick Toutain

Make your next move.

Matthieu Egloff

Research Interests

Explore related searches

Articles (11)

Delineation of a Novel Mirror Syndrome: NFIC Variants Cause Syndromic Intellectual Disability With Macrocephaly.

&lt;i&gt;PFMG2025&lt;/i&gt;-integrating genomic medicine into the national healthcare system in France.

Recruitment, follow-up and survival in an 11-country cohort study of patients at the end of life and their relatives

French Guidelines of the AchroPuce Network for the Interpretation and Reporting of Constitutional Copy Number Variants.

Heterozygous alterations of GTF2I at the Williams-Beuren syndrome's locus cause a neurodevelopmental disorder

RORA-neurodevelopmental disorder: A unique triad of developmental disabilities, cerebellar anomalies, and myoclonic seizures

Intriguing link between fetal intracranial hemorrhage and X‐linked recessive chondrodysplasia punctata

3q29 duplications: A cohort of 46 patients and a literature review

Clinical and genomic delineation of the new proximal 19p13.3 microduplication syndrome

Cerebellar and Striatal Implications in Autism Spectrum Disorders: From Clinical Observations to Animal Models

12q21 deletion syndrome: Narrowing the critical region down to 1.6 Mb including SYT1 and PPP1R12A

Collaborators (17)

Abderaouf Hamza

Stefan Barakat

Nathalie Eduarda Marie-Jeanne Vanden Eynde

Benjamin Fournier

Agnes Bloch-Zupan

Paul Kuentz

Richard Redon

Louise-Marie CHEVALIER

Caroline Rooryck

Eric Pasmant

Sarah Baer

Pierre Vande Perre

Hélène Cavé

Florence Petit

Carin C.D. Van der Rijt

Laurie Galvan

Annick Toutain

Make your next move.

<i>PFMG2025</i>-integrating genomic medicine into the national healthcare system in France.