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Motee Ashhab · SciRah

Researcher profile · Semantic Scholar

Motee Ashhab

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Motee Ashhab — researcher profile on SciRah

h-index: 4
Works: 11
Citations: 59

Most-cited papers

PARP10 deficiency manifests by infantile neurodegeneration and DNA repair defect
M. Shahrour, Claudia M. Nicolae, S. Edvardson, Motee Ashhab +5 more
2016Neurogenetics20 citations Open access
Semantic Scholar
Homozygous frameshift variant in NTNG2, encoding a synaptic cell adhesion molecule, in individuals with developmental delay, hypotonia, and autistic features
B. Abu-Libdeh, Motee Ashhab, M. Shahrour, M. Daana +4 more
2019Neurogenetics11 citations
Semantic Scholar
A novel variant of the human mitochondrial DnaJ protein, Tid1, associates with a human disease exhibiting developmental delay and polyneuropathy
M. Patra, Celeste Weiss, B. Abu-Libdeh, Motee Ashhab +5 more
2019European Journal of Human Genetics11 citations Open access
Semantic Scholar
Hypomyelinating leukodystrophy associated with a deleterious mutation in the ATRN gene
M. Shahrour, Motee Ashhab, S. Edvardson, Michal Gur +2 more
2017Neurogenetics10 citations
Semantic Scholar
Erratum to: PARP10 deficiency manifests by severe developmental delay and DNA repair defect
M. Shahrour, Claudia M. Nicolae, S. Edvardson, Motee Ashhab +5 more
2017Neurogenetics3 citations Open access
Semantic Scholar
Erratum to: PARP10 deficiency manifests by severe developmental delay and DNA repair defect
M. Shahrour, Claudia M. Nicolae, S. Edvardson, Motee Ashhab +5 more
2016Neurogenetics2 citations Open access
Semantic Scholar
Recessive Loss of DIAPH1 Function Causes a Progressive Neurodevelopmental Syndrome with Variable Immunological Involvement.
V. G. Deforie, R. Maroofian, I. Karagoz, A. Godwin +62 more
2026Genetics in Medicine1 citations Open access
Semantic Scholar
Clinical characteristics of pediatric epilepsy in Palestine: a cross-sectional study
Reem Sawafta, Z. Nazzal, Motee Ashhab, Sofian Nassar +3 more
2025BMC Neurology1 citations Open access
Semantic Scholar
Recurrent homozygous GLRB p.Arg472Ter variant in Palestinian hereditary hyperekplexia: a retrospective genotype–phenotype case series of nine children
Samir A. Nasser, O. Salah, Majd Shehadeh, Raghad Waheed Khanfar +4 more
2026BMC Medical Genomics0 citations Open access
Semantic Scholar
MOG Antibody‐Associated Disease With Bilateral Deep Gray Matter Involvement in a Child: Unique MRI Findings and Therapeutic Response
A. Saymeh, H. Abdul-Hafez, Alaa Zayed, Maysa Alawneh +3 more
2026Case Reports in Pediatrics0 citations Open access
Semantic Scholar
A founder variant in TANGO2 p.(Leu148Trp) in ten Palestinian families: clinical characterization and haplotype analysis of TANGO2 deficiency disorder
Christina Canavati, Motee Ashhab, Grace Rabie, Lina Hreimat +11 more
2026BMC Medical Genomics0 citations Open access
Semantic Scholar

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B. Abu-Libdeh×7
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B. Abu-Libdeh — researcher profile on SciRah
O. Elpeleg×6
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O. Elpeleg — researcher profile on SciRah
M. Shahrour×5
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M. Shahrour — researcher profile on SciRah
S. Edvardson×5
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S. Edvardson — researcher profile on SciRah

Claudia M. Nicolae

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