Neven Maksemous

Eye movement disorders are an early manifestation of <i><scp>CACNA</scp>1A</i> mutations in children

Esther Tantsis, Deepak Gill, Lyn R. Griffiths et al. · Developmental Medicine & Child Neurology · 2016 · 79 citations · Full text

Exome Sequencing Diagnoses X-Linked Moesin-Associated Immunodeficiency in a Primary Immunodeficiency Case

Gabrielle Bradshaw, Robbie R. Lualhati, Cassie L. Albury et al. · Frontiers in Immunology · 2018 · 34 citations · Full text

Next‐generation sequencing identifies novel <i><scp>CACNA</scp>1A</i> gene mutations in episodic ataxia type 2

Neven Maksemous, Bishakha Roy, Robert A. Smith et al. · Molecular Genetics & Genomic Medicine · 2016 · 33 citations · Full text

Comprehensive Exonic Sequencing of Hemiplegic Migraine-Related Genes in a Cohort of Suspected Probands Identifies Known and Potential Pathogenic Variants

Heidi G. Sutherland, Neven Maksemous, Cassie L. Albury et al. · Cells · 2020 · 31 citations · Full text

Targeted next generation sequencing identifies novel NOTCH3 gene mutations in CADASIL diagnostics patients

Neven Maksemous, Robert A. Smith, Larisa M. Haupt et al. · Human Genomics · 2016 · 30 citations · Full text