Melina Ellis

6PUBLICATIONS
74CO-AUTHORS
Neurology and neuromuscular diseasesGene expression (incl. microarray and other genome-wide approaches)Cell and nuclear divisionGene mappingMedical infection agents (incl. prions)
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Publications (6)

|Jun 09, 2026
Monoallelic POLR3A Variants Cause Early-Onset Peripheral Neuropathy.

|Dec 08, 2025
Novel and rare variants in amyotrophic lateral sclerosis genes identified in Malaysian patients.

Nurul Angelyn Zulhairy-Liong, Suzanna Edgar, Melina Ellis

|Oct 14, 2025
Pseudodominant Inheritance of Biallelic RFC1 Expansions-Revisiting the 3p22-p24 HSN1B Locus.

Bianca R Grosz, Melina Ellis, Shuchi Trivedi

|Jul 30, 2024
Team Science Approaches to Unravel Monogenic Parkinson's Disease on a Global Scale.

Johanna Junker, Lara M Lange, Eva-Juliane Vollstedt

|Jun 11, 2024
A deep intronic variant in MME causes autosomal recessive Charcot-Marie-Tooth neuropathy through aberrant splicing.

Bianca R Grosz, Jevin M Parmar, Melina Ellis

|Mar 26, 2024
Understanding monogenic Parkinson's disease at a global scale.

Johanna Junker, Lara M Lange, Eva-Juliane Vollstedt

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Frequent Collaborators

5 joint publications

Kishore R Kumar

4 joint publications

Marina L Kennerson

3 joint publications

Steve Vucic

3 joint publications

Bianca R Grosz