Concepedia
Statistics
Publications
16
Citations
383
H-Index
13
Active since
2012
Affiliations
Queensland University of Technology(Current)
Griffith University
Sydney Children's Hospital
University of Oxford
Neven Maksemous is an author at Queensland University of Technology specializing in genetics, life sciences, and genomics.
Publications per year
2012–2023
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 · 81 citations · Full text
Life Sciences, Genetics, Neurology +16
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
Life Sciences, Genetics, Molecular Genetics +17
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 · 34 citations · Full text
Life Sciences, Genetics, Neurology +17
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
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 · 31 citations · Full text
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