Stéphanie Millecamps

Sorbonne Université

France

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Articles (10)

Year:

2023

Year:

2022

Year:

2022

Year:

2021

Year:

2021

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2021

Year:

2021

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2021

Year:

2020

Year:

2020

Collaborators (22)

danielle seilhean

Professor

Assistance Publique - Hôpitaux de Paris

FRANCE

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Delphine Bohl

associate professor (Neuroscience)

Institut du Cerveau et de la Moelle Épinière

FRANCE

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Deniz Yilmazer-Hanke

Professor, Section Head

Universität Ulm

GERMANY

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Dominique Langui

INSERM

FRANCE

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Charles Curtis

King’s College London

UNITED KINGDOM

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Dominic Rowe

Macquarie University

AUSTRALIA

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Bradley Smith

King’s College London

UNITED KINGDOM

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Sandra D'Alfonso

Università degli Studi del Piemonte Orientale Amedeo Avogadro

ITALY

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Pascal Leblanc

FRANCE

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Michael Sendtner

Professor for Clinical Neurobiology

University of Würzburg

GERMANY

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Viviana Pensato

Fondazione IRCCS Istituto Neurologico Carlo Besta

ITALY

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simon topp

King’s College London

UNITED KINGDOM

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Alberto Catanese

Université Paris Descartes

FRANCE

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William Duddy

University of Ulster

UNITED KINGDOM

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Ewout J. N. Groen

NETHERLANDS

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Kelly Williams

Macquarie University

AUSTRALIA

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Mark K Bakker

NETHERLANDS

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Julia Kraft

Charité - Universitätsmedizin Berlin

GERMANY

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Sarah Furlong

Macquarie University

AUSTRALIA

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Luc Dupuis

University of Strasbourg

FRANCE

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Julie Dumonceaux

University College London Institute of Child Health

UNITED KINGDOM

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Angelica Nordin

University Hospital of Umeå

SWEDEN

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Stéphanie Millecamps

Research Interests

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Articles (10)

Integrative genetic analysis illuminates ALS heritability and identifies risk genes

The Amyotrophic Lateral Sclerosis M114T PFN1 Mutation Deregulates Alternative Autophagy Pathways and Mitochondrial Homeostasis.

Muscle cells of sporadic amyotrophic lateral sclerosis patients secrete neurotoxic vesicles

Common and rare variant association analyses in amyotrophic lateral sclerosis identify 15 risk loci with distinct genetic architectures and neuron-specific biology

Impact of a frequent nearsplice <i>SOD1</i> variant in amyotrophic lateral sclerosis: optimising <i>SOD1</i> genetic screening for gene therapy opportunities

Deletion of the inflammatory S100-A9/MRP14 protein does not influence survival in hSOD1G93A ALS mice

Phenoconversion from Spastic Paraplegia to ALS/FTD Associated with CYP7B1 Compound Heterozygous Mutations

New advances in Amyotrophic Lateral Sclerosis genetics: Towards gene therapy opportunities for familial and young cases

Modifying macrophages at the periphery has the capacity to change microglial reactivity and to extend ALS survival.

Genetic screening of ANXA11 revealed novel mutations linked to amyotrophic lateral sclerosis.

Collaborators (22)

danielle seilhean

Delphine Bohl

Deniz Yilmazer-Hanke

Dominique Langui

Charles Curtis

Dominic Rowe

Bradley Smith

Sandra D'Alfonso

Pascal Leblanc

Michael Sendtner

Viviana Pensato

simon topp

Alberto Catanese

William Duddy

Ewout J. N. Groen

Kelly Williams

Mark K Bakker

Julia Kraft

Sarah Furlong

Luc Dupuis

Julie Dumonceaux

Angelica Nordin

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