Lindsay Wilson

6PUBLICATIONS
61CO-AUTHORS
Infant and child healthNeurology and neuromuscular diseasesEpigenetics (incl. genome methylation and epigenomics)Medical biotechnology diagnostics (incl. biosensors)Major global burdens of disease
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Publications (6)

|Jul 31, 2026
Spinal Muscular Atrophy in Adult Neurology Services in India.

|May 05, 2025
Kennedy's disease from India: An Indian Cohort with multisystemic manifestations.

Saranya B Gomathy, William L Macken, Nimita Rani

|Feb 18, 2025
Biallelic variants in RYR1 and STAC3 are predominant causes of King-Denborough Syndrome in an African cohort.

Maryke Schoonen, Mahmoud Fassad, Krutik Patel

|Nov 15, 2024
Overcoming genetic neuromuscular diagnostic pitfalls in a middle-income country.

Rodrigo Siqueira Soares Frezatti, Pedro José Tomaselli, Christopher J Record

|Apr 25, 2024
The first genetically confirmed cohort of Facioscapulohumeral Muscular Dystrophy from Northern India.

Venugopalan Y Vishnu, Richard J L F Lemmers, Alisha Reyaz

|Jul 30, 2023
Neuromuscular disease genetics in under-represented populations: increasing data diversity.

Lindsay A Wilson, William L Macken, Luke D Perry

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Frequent Collaborators

4 joint publications

Venugopalan Y Vishnu

3 joint publications

Henry Houlden

3 joint publications

Ashwin Dalal

3 joint publications

Stephanie Efthymiou