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Alexandre Reymond

University of Lausanne

Switzerland

Research Interests

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Professors in Switzerland Professors in Cell Biology Cell Biology professors in Switzerland

Articles (10)

Year:

2022

Year:

2021

Year:

2021

Year:

2021

Year:

2021

Year:

2021

Year:

2021

Year:

2021

Year:

2021

Year:

2021

Collaborators (13)

Caroline Schluth-Bolard

University of Lyon

FRANCE

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Michael Craig

Professor

King’s College London

UNITED KINGDOM

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Benjamin Delprat

Research Director

INSERM Délégation Régionale Occitanie Méditerranée

FRANCE

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Mohamad Mikati

Duke University

UNITED STATES

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Carlos Prieto

Head of Bioinformatics

Universidad de Salamanca

SPAIN

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Sissy Bassani

University of Zurich

SWITZERLAND

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Tangui Maurice

University of Montpellier

FRANCE

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Danny Miller

Assistant Professor

University of Washington

UNITED STATES

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Christopher Ching

Assistant Professor

University of Southern California Keck School of Medicine

UNITED STATES

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Vincent Bonagura

Jack Hausman Professor of Pediatrics, Professor of Molecular Medicine

Donald & Barbara Zucker School of Medicine at Hofstra/Northwell

UNITED STATES

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Francesca Amati

Professor, MD PhD

University of Lausanne

SWITZERLAND

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Mireille Rossel

University of Montpellier

FRANCE

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Miroslava Hancarova

Charles University

CZECH REPUBLIC

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Alexandre Reymond

Research Interests

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Articles (10)

Effects of copy number variations on brain structure and risk for psychiatric illness

Alpha satellite insertion close to an ancestral centromeric region.

Variants in USP48 encoding ubiquitin hydrolase are associated with autosomal dominant non-syndromic hereditary hearing loss.

Variants in the degron of AFF3 are associated with intellectual disability, mesomelic dysplasia, horseshoe kidney, and epileptic encephalopathy

Mutation-specific pathophysiological mechanisms define different neurodevelopmental disorders associated with SATB1 dysfunction

Biallelic truncation variants in ATP9A are associated with a novel autosomal recessive neurodevelopmental disorder

Differentially expressed genes reflect disease-induced rather than disease-causing changes in the transcriptome.

Rare and de novo coding variants in chromodomain genes in Chiari I malformation.

Ophthalmic phenotypes associated with biallelic loss-of-function PCDH12 variants.

Rare and de novo coding variants in chromodomain genes in Chiari I malformation.

Collaborators (13)

Caroline Schluth-Bolard

Michael Craig

Benjamin Delprat

Mohamad Mikati

Carlos Prieto

Sissy Bassani

Tangui Maurice

Danny Miller

Christopher Ching

Vincent Bonagura

Francesca Amati

Mireille Rossel

Miroslava Hancarova

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