Nebal Waill Saadi

4PUBLICATIONS
57CO-AUTHORS
Neurology and neuromuscular diseasesGene expression (incl. microarray and other genome-wide approaches)Cellular nervous systemGene mapping
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Publications (4)

|Apr 02, 2026
Neurological manifestations and genotype-phenotype correlations in NDUFAF6-associated mitochondrial disease.

Alessandra Torraco, Charlotte L Alston, Giulia Barcia

|Dec 01, 2025
Clinical and Genetic Spectrum of SCN8A-Related Disorders: A Retrospective Study From the Gulf Region.

Osama Muthaffar, Mashael Alsubhan, Ali Mir

|Apr 02, 2024
Mono and biallelic variants in HCN2 cause severe neurodevelopmental disorders.

Clara Houdayer, A Marie Phillips, Marie Chabbert

|Apr 02, 2021
A novel homozygous SLC13A5 whole-gene deletion generated by Alu/Alu-mediated rearrangement in an Iraqi family with epileptic encephalopathy.

Ruizhi Duan, Nebal Waill Saadi, Christopher M Grochowski

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Frequent Collaborators

2 joint publications

Henry Houlden

1 joint publications

Hind Alsharhan

1 joint publications

Ahmed Bamaga

1 joint publications

Anas Alyazidi