Matthew Harms

7PUBLICATIONS

133CO-AUTHORS

Cancer geneticsNeurology and neuromuscular diseasesGene expression (incl. microarray and other genome-wide approaches)Craniofacial biologyNeurogenetics

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Publications (7)

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|Jun 29, 2026

Preparing Amyotrophic Lateral Sclerosis Clinics to Provide Longitudinal Care for Individuals Carrying ALS Risk Variants.

|May 18, 2026

The New York Genome Center ALS Consortium resource integrates postmortem tissue transcriptomics and whole genome sequencing to empower biological discovery.

|Mar 31, 2026

Large-scale exome analyses reveal new rare variant contributions in amyotrophic lateral sclerosis.

Paul J Hop, Maarten Kooyman, Brendan J Kenna

|Jan 07, 2026

Spectrum of dominant Charcot-Marie-Tooth disease due to <i>SLC12A6</i> variants.

Christopher J Record, Tiffany Grider, Adriana P Rebelo

|Oct 03, 2025

Reader Response: Genetic Associations With an Amyotrophic Lateral Sclerosis Reversal Phenotype.

Wouter van Rheenen, Matthew Harms, Michael A van Es

|Feb 19, 2021

Genetics of primary lateral sclerosis.

Vincenzo Silani, Philippe Corcia, Matthew B Harms

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Frequent Collaborators

Jan H Veldink

John E Landers

Nicola Ticozzi

Karen E Morrison

Guy Rouleau

Leonard H van den Berg

Vincenzo Silani

Pamela J Shaw

Ammar Al-Chalabi

Hemali Phatnani

Frequent Collaborators

Jan H Veldink

John E Landers

Nicola Ticozzi

Karen E Morrison