John Landers

University of Massachusetts Chan Medical School

United States

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Articles (10)

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2022

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Collaborators (22)

Claudia Fallini

Assistant Professor

University of Rhode Island

UNITED STATES

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Cleide Souza

University of Sheffield

UNITED KINGDOM

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Ian Blair

Macquarie University

AUSTRALIA

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Sarah Opie-Martin

King’s College London

UNITED KINGDOM

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Eilis Hannon

University of Exeter Medical School

UNITED KINGDOM

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Dina Simkin

Research Assistant Professor

Northwestern University Feinberg School of Medicine

UNITED STATES

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Dominic Rowe

Macquarie University

AUSTRALIA

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Kevin Talbot

University of Oxford

UNITED KINGDOM

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Ke Ning

Senior Lecturer in Translational Neuroscience

University of Sheffield

UNITED KINGDOM

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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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Frederik Steyn

Senior Lecturer/Group Leader

University of Queensland

AUSTRALIA

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Kelly Williams

Macquarie University

AUSTRALIA

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Julian Großkreutz

University of Lübeck

GERMANY

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Mark K Bakker

NETHERLANDS

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Lyndal Henden

Macquarie University

AUSTRALIA

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Jonathan Mill

Professor

University of Exeter

UNITED KINGDOM

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Sarah Furlong

Macquarie University

AUSTRALIA

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Alfredo Iacoangeli

King’s College London

UNITED KINGDOM

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Eran Elhaik

Associate Professor

Lund University

SWEDEN

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Angelica Nordin

University Hospital of Umeå

SWEDEN

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ALESSANDRA FERLINI

University of Ferrara

ITALY

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John Landers

Research Interests

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Articles (10)

Genome-wide identification of the genetic basis of amyotrophic lateral sclerosis

Genome-wide study of DNA methylation shows alterations in metabolic, inflammatory, and cholesterol pathways in ALS

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

The SOD1-mediated ALS phenotype shows a decoupling between age of symptom onset and disease duration

The impact of age on genetic testing decisions in amyotrophic lateral sclerosis

Homozygous might be hemizygous: CRISPR/Cas9 editing in iPSCs results in detrimental on-target defects that escape standard quality controls

ATXN2 intermediate expansions in amyotrophic lateral sclerosis.

ALS-associated KIF5A mutations abolish autoinhibition resulting in a toxic gain of function.

Role of Lysosomal Gene Variants in Modulating GBA-Associated Parkinson's Disease Risk.

Structural variation analysis of 6,500 whole genome sequences in amyotrophic lateral sclerosis.

Collaborators (22)

Claudia Fallini

Cleide Souza

Ian Blair

Sarah Opie-Martin

Eilis Hannon

Dina Simkin

Dominic Rowe

Kevin Talbot

Ke Ning

Viviana Pensato

simon topp

Frederik Steyn

Kelly Williams

Julian Großkreutz

Mark K Bakker

Lyndal Henden

Jonathan Mill

Sarah Furlong

Alfredo Iacoangeli

Eran Elhaik

Angelica Nordin

ALESSANDRA FERLINI

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