Skip to content

Home Search Authors Pakistan News Saved

SciRah

SciRah does not host or store research papers. Results come live from free, official scholarly APIs, and every paper links back to its original source.

Data sources

OpenAlex
Semantic Scholar
Crossref
CORE
arXiv
PubMed

Privacy policy Terms of service

Ahlam A. A. Hamed · SciRah

Researcher profile · Semantic Scholar

Ahlam A. A. Hamed

Share profile

Ahlam A. A. Hamed — researcher profile on SciRah

h-index: 9
Works: 23
Citations: 315

Most-cited papers

A Novel Nonsense Mutation in DNAJC6 Expands the Phenotype of Autosomal‐Recessive Juvenile‐Onset Parkinson's Disease
Liena E. O. Elsayed, Valérie Drouet, T. Usenko, Inaam N. Mohammed +13 more
2016Annals of Neurology73 citations
Semantic Scholar
Expanding the phenome and variome of skeletal dysplasia
S. Maddirevula, S. Alsahli, Lamees Alhabeeb, N. Patel +52 more
2018Genetics in Medicine71 citations Open access
Semantic Scholar
Hereditary spastic paraplegias: identification of a novel SPG57 variant affecting TFG oligomerization and description of HSP subtypes in Sudan
Liena E. O. Elsayed, Inaam N. Mohammed, Ahlam A. A. Hamed, Maha A. Elseed +30 more
2016European Journal of Human Genetics31 citations Open access
Semantic Scholar
The impact of PYROXD1 deficiency on cellular respiration and correlations with genetic analyses of limb-girdle muscular dystrophy in Saudi Arabia and Sudan.
Madhurima Saha, Hemakumar M. Reddy, M. Salih, E. Estrella +16 more
2018Physiological Genomics24 citations Open access
Semantic Scholar
The differential effects of eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) on seizure frequency in patients with drug-resistant epilepsy - A randomized, double-blind, placebo-controlled trial.
F. Ibrahim, K. Ghebremeskel, M. Abdel-Rahman, Amar Ahmed +8 more
2018Epilepsy & Behavior20 citations Open access
Semantic Scholar
Intelligence quotient (IQ) among children with epilepsy: National epidemiological study - Sudan.
I. Mohamed, A. H. Osman, S. Mohamed, E. K. Hamid +6 more
2020Epilepsy & Behavior17 citations
Semantic Scholar
Case report of a novel homozygous splice site mutation in PLA2G6 gene causing infantile neuroaxonal dystrophy in a Sudanese family
Liena E. O. Elsayed, Inaam N. Mohammed, Ahlam A. A. Hamed, Maha A. Elseed +10 more
2018BMC Medical Genetics13 citations Open access
Semantic Scholar
Clinical phenotyping and genetic diagnosis of a large cohort of Sudanese families with hereditary spinocerebellar degenerations
Ashraf Yahia, Ahlam A. A. Hamed, I. Mohamed, Maha A. Elseed +40 more
2023European Journal of Human Genetics12 citations Open access
Semantic Scholar
Pathogenic Variants in ABHD16A Cause a Novel Psychomotor Developmental Disorder With Spastic Paraplegia
Ashraf Yahia, Liena E. O. Elsayed, Rémi Valter, Ahlam A. A. Hamed +25 more
2021Frontiers in Neurology10 citations Open access
Semantic Scholar
Novel Homozygous Missense Mutation in the ARG1 Gene in a Large Sudanese Family
Liena E. O. Elsayed, Inaam N. Mohammed, Ahlam A. A. Hamed, Maha A. Elseed +10 more
2020Frontiers in Neurology8 citations Open access
Semantic Scholar
Genetic diagnosis in Sudanese and Tunisian families with syndromic intellectual disability through exome sequencing
Ashraf Yahia, I. Ben Ayed, Ahlam A. A. Hamed, Inaam N. Mohammed +20 more
2022Annals of Human Genetics7 citations
Semantic Scholar
Novel variants causing megalencephalic leukodystrophy in Sudanese families
M. Amin, Cédric Vignal, Ahlam A. A. Hamed, Inaam N. Mohammed +19 more
2021Journal of Human Genetics7 citations
Semantic Scholar
A novel homozygous mutation in TRAPPC9 gene causing autosomal recessive non-syndromic intellectual disability
M. Amin, Cédric Vignal, Esraa Eltaraifee, Inaam N. Mohammed +12 more
2022BMC Medical Genomics6 citations Open access
Semantic Scholar
An identical‐by‐descent novel splice‐donor variant in PRUNE1 causes a neurodevelopmental syndrome with prominent dystonia in two consanguineous Sudanese families
M. Koko, Ashraf Yahia, Liena E. O. Elsayed, Ahlam A. A. Hamed +17 more
2021Annals of Human Genetics6 citations
Semantic Scholar
A novel missense variant in the ATPase domain of ATP8A2 and review of phenotypic variability of ATP8A2-related disorders caused by missense changes
Kyle P. Flannery, Sylvia Safwat, Eli Matsell, Namarata Battula +12 more
2024Neurogenetics3 citations Open access
Semantic Scholar
Case report: Clinical and genetic characterization of a novel ALDH7A1 variant causing pyridoxine-dependent epilepsy, developmental delay, and intellectual disability in two siblings
Mustafa A. Salih, Albandary Albakheet, Rawan Almass, Ahlam A. A. Hamed +2 more
2024Frontiers in Psychiatry3 citations
Semantic Scholar
Bi-allelic PRRT2 variants may predispose to Self-limited Familial Infantile Epilepsy
M. Koko, Maha A. Elseed, Inaam N. Mohammed, Ahlam A. A. Hamed +23 more
2024European Journal of Human Genetics2 citations Open access
Semantic Scholar
A novel missense variant in the ATPase domain of ATP8A2 and review of phenotypic variability of ATP8A2-related disorders caused by missense changes
Kyle P. Flannery, Sylvia Safwat, Eli Matsell, Namarata Battula +12 more
2024medRxiv2 citations Open access
Semantic Scholar
Bi-allelic variants in WDR47 cause a complex neurodevelopmental syndrome
E. Bayam, Peggy Tilly, Stephan C. Collins, José Rivera Alvarez +27 more
2024EMBO Molecular Medicine1 citations Open access
Semantic Scholar
Bi-allelic variants in WDR47 lead to neuronal loss causing a rare neurodevelopmental syndrome with corpus callosum dysgenesis in humans
E. Bayam, Peggy Tilly, Stephan C. Collins, José R. Álvarez +22 more
2023bioRxiv0 citations Open access
Semantic Scholar
Exome Sequencing Revealed Mutations in ADAT3 and HERC2 Genes in two Sudanese Families with Syndromic Mental Retardation
Ashraf Yahia, Aisha M. Bakhiet, Ahlam A. A. Hamed, Fatima Abozar +8 more
20200 citations Open access
Semantic Scholar
Exploring the molecular basis of hereditary spinocerebellar degeneration in a large Sudanese family
Arwa Babai, Liena E. O. Elsayed, Inaam N. Mohammed, Maha A. Elseed +4 more
2019Journal of Neurological Sciences0 citations
Semantic Scholar
A novel variant of the GCDH gene causes glutaric aciduria type 1 in a Sudanese family: a case report -
Ahlam A. A. Hamed, Maha Abd El Moneim Elseed, Inaam Noureldyme Mohmed Masoud, K. Yararbaş +1 more
20170 citations Open access
Semantic Scholar

Frequent co-authors

Invite them to SciRah by sharing their profile.

Liena E. O. Elsayed×15
Invite
Liena E. O. Elsayed — researcher profile on SciRah
Maha A. Elseed×14
Invite
Maha A. Elseed — researcher profile on SciRah
Inaam N. Mohammed×11
Invite
Inaam N. Mohammed — researcher profile on SciRah
M. Koko×11
Invite
M. Koko — researcher profile on SciRah

×11

Invite

A. Ahmed — researcher profile on SciRah

Ashraf Yahia×11

Invite

Ashraf Yahia — researcher profile on SciRah

Invite

G. Stevanin — researcher profile on SciRah

Mustafa A. Salih×8

Invite

Mustafa A. Salih — researcher profile on SciRah

Invite

R. Abubaker — researcher profile on SciRah

Invite

M. Ibrahim — researcher profile on SciRah

Invite

M. Salih — researcher profile on SciRah

Invite

Arwa Babai — researcher profile on SciRah