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)

|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

3 joint publications

Jan H Veldink

2 joint publications

John E Landers

2 joint publications

Nicola Ticozzi

2 joint publications

Karen E Morrison