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Motee Ashhab

Observed names: Lina Motee Ashhab, Motee Al-Ashhab, Motee Al‐Ashhab
ORCID: 0009-0005-4610-0482
Observed ORCID: 0009-0005-4610-0482
OpenAlex ID: A5011453477
Mutations in SLC1A4, encoding the brain serine transporter, are associated with developmental delay, microcephaly and hypomyelination
2015 · Nadirah Damseh, Alexandre Simonin, et al. · Journal of Medical Genetics · 86
A defect in the retromer accessory protein, SNX27, manifests by infantile myoclonic epilepsy and neurodegeneration
2015 · Nadirah Damseh, Chris M. Danson, et al. · Neurogenetics · 42
PARP10 deficiency manifests by severe developmental delay and DNA repair defect
2016 · Maher Awni Shahrour, Claudia M. Nicolae, et al. · Neurogenetics · 21
Pontocerebellar hypoplasia associated with p. Arg183Trp homozygous variant in EXOSC1 gene: A case report
2023 · Nadirah S. Damseh, Ali N. Obeidat, et al. · American Journal of Medical Genetics Part A · 13
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A novel variant of the human mitochondrial DnaJ protein, Tid1, associates with a human disease exhibiting developmental delay and polyneuropathy
2019 · Malay Patra, Celeste Weiss, et al. · European Journal of Human Genetics · 12
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Homozygous frameshift variant in NTNG2, encoding a synaptic cell adhesion molecule, in individuals with developmental delay, hypotonia, and autistic features
2019 · Bassam Abu-Libdeh, Motee Ashhab, et al. · Neurogenetics · 11
Hypomyelinating leukodystrophy associated with a deleterious mutation in the ATRN gene
2017 · Maher Awni Shahrour, Motee Ashhab, et al. · Neurogenetics · 10
Broadening the phenotypic and molecular spectrum of FINCA syndrome: Biallelic NHLRC2 variants in 15 novel individuals
2023 · Henrike L. Sczakiel, Max Zhao, et al. · European Journal of Human Genetics · 8
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Recessive loss of DIAPH1 function causes a progressive neurodevelopmental syndrome with variable immunological involvement
2026 · Valentina Galassi Deforie, Reza Maroofian, et al. · Genetics in Medicine · 3
LSM1 c.231+4A>C hotspot variant is associated with a novel neurodevelopmental syndrome: first patient cohort
2025 · Sivan Reytan Miron, Alina Kurolap, et al. · Journal of Medical Genetics · 1
Characterization of Goal-Directed and Habitual Behavior in Children with Attention-Deficit/Hyperactivity Disorder
2019 · Joman Natsheh, Ashar Y. Natsheh, et al. · SSRN Electronic Journal · 1
Erratum to: PARP10 deficiency manifests by severe developmental delay and DNA repair defect
2016 · Maher Awni Shahrour, Claudia M. Nicolae, et al. · Neurogenetics · 1
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Recurrent homozygous GLRB p.Arg472Ter variant in Palestinian hereditary hyperekplexia: a retrospective genotype–phenotype case series of nine children
2026 · Samir Nasser, Omar Emad Salah, et al. · BMC Medical Genomics
Clinical and genetic spectrum of congenital myasthenic syndromes in Palestine: a retrospective cohort of 35 genetically confirmed patients
2026 · Motee Ashhab, Omar Abusenenh, et al. · Research Square
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Clinical Characteristics, and current perspectives of Kernicterus Spectrum Disorder in Palestine
2026 · Ahmed Khammash, Mohammad Ghannam, et al. · Research Square
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A founder variant in TANGO2 p.(Leu148Trp) in ten Palestinian families: clinical characterization and haplotype analysis of TANGO2 deficiency disorder
2026 · Christina Canavati, Motee Ashhab, et al. · BMC Medical Genomics
Public Awareness of Chronic Kidney Disease Among Adults in Palestine: Knowledge Gaps and Determinants of Higher Awareness in a Resource Constrained Setting
2026 · Omar G. Nasereddin, Hamza Y. Hassouneh, et al. · Research Square
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MOG Antibody‐Associated Disease With Bilateral Deep Gray Matter Involvement in a Child: Unique MRI Findings and Therapeutic Response
2026 · Abdulkareem Saymeh, Hamza A. Abdul-Hafez, et al. · Case Reports in Pediatrics
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Clinical characteristics of pediatric epilepsy in Palestine: a cross-sectional study
2025 · Reem Sawafta, Zaher Nazzal, et al. · BMC Neurology
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Erratum to: PARP10 deficiency manifests by severe developmental delay and DNA repair defect
2017 · Maher Awni Shahrour, Claudia M. Nicolae, et al. · Neurogenetics
Works count: 20
Citation count: 209
H-index: 8
I10-index: 7
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