Ahlam A. Hamed

420 total citations
15 papers, 102 citations indexed

About

Ahlam A. Hamed is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, Ahlam A. Hamed has authored 15 papers receiving a total of 102 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 5 papers in Pediatrics, Perinatology and Child Health and 5 papers in Genetics. Recurrent topics in Ahlam A. Hamed's work include Epilepsy research and treatment (4 papers), Genomics and Rare Diseases (3 papers) and Metabolism and Genetic Disorders (3 papers). Ahlam A. Hamed is often cited by papers focused on Epilepsy research and treatment (4 papers), Genomics and Rare Diseases (3 papers) and Metabolism and Genetic Disorders (3 papers). Ahlam A. Hamed collaborates with scholars based in Sudan, Saudi Arabia and United States. Ahlam A. Hamed's co-authors include Mustafa A. Salih, Salah A. Ibrahim, Liena E. O. Elsayed, Mahmoud Koko, Mustafa I. Elbashir, Manar E. Abdel‐Rahman, Ammar Ahmed, Sarah El-Sadig, Elicia Estrella and Christina A. Pacak and has published in prestigious journals such as Frontiers in Psychiatry, Physiological Genomics and Epilepsy & Behavior.

In The Last Decade

Ahlam A. Hamed

14 papers receiving 101 citations

Peers

Countries citing papers authored by Ahlam A. Hamed

Since Specialization

Citations

This map shows the geographic impact of Ahlam A. Hamed's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Ahlam A. Hamed with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ahlam A. Hamed more than expected).

Fields of papers citing papers by Ahlam A. Hamed

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ahlam A. Hamed. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Ahlam A. Hamed. The network helps show where Ahlam A. Hamed may publish in the future.

Co-authorship network of co-authors of Ahlam A. Hamed

This figure shows the co-authorship network connecting the top 25 collaborators of Ahlam A. Hamed. A scholar is included among the top collaborators of Ahlam A. Hamed based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Ahlam A. Hamed. Ahlam A. Hamed is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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15 of 15 papers shown

#	Work	Indexed citations
1	Case report: Clinical and genetic characterization of a novel ALDH7A1 variant causing pyridoxine-dependent epilepsy, developmental delay, and intellectual disability in two siblings 2024 ·Frontiers in Psychiatry ·Mustafa A. Salih, Albandary AlBakheet, Rawan Almass, Ahlam A. Hamed, Ali Al‐Odaib, Namik Kaya	2
2	A novel missense variant in the ATPase domain of ATP8A2 and review of phenotypic variability of ATP8A2-related disorders caused by missense changes 2024 ·Neurogenetics ·(unknown), (unknown), (unknown), (unknown), Ahlam A. Hamed, (unknown), (unknown), Mahmoud Koko, (unknown), (unknown), Liena E. O. Elsayed, Vikram Bhise, Robert S. Molday, Mustafa A. Salih, (unknown), M. Chiara Manzini	0
3	A novel homozygous mutation in TRAPPC9 gene causing autosomal recessive non-syndromic intellectual disability 2022 ·BMC Medical Genomics ·Mutaz Amin, (unknown), (unknown), (unknown), Ahlam A. Hamed, (unknown), (unknown), (unknown), (unknown), (unknown), Mohamed Mustafa, Séverine Drunat, Liena E. O. Elsayed, Ammar Ahmed, Odile Boespflug‐Tanguy, Imen Dorboz	4
4	A children’s epilepsy diagnosis aid: Development and early validation using a Bayesian approach 2021 ·Epilepsy & Behavior ·(unknown), (unknown), Ahlam A. Hamed, (unknown), Victor Patterson	4
5	Intelligence quotient (IQ) among children with epilepsy: National epidemiological study – Sudan 2020 ·Epilepsy & Behavior ·(unknown), (unknown), (unknown), (unknown), Ahlam A. Hamed, (unknown), (unknown), Moiz Bakhiet, Sarah El-Sadig, (unknown)	9
6	Novel Homozygous Missense Mutation in the ARG1 Gene in a Large Sudanese Family 2020 ·Frontiers in Neurology ·Liena E. O. Elsayed, (unknown), Ahlam A. Hamed, (unknown), Mustafa A. Salih, (unknown), (unknown), Mahmoud Koko, (unknown), Mustafa I. Elbashir, Muntaser E. Ibrahim, Alexis Brice, Ammar Ahmed, Giovanni Stévanin	5
7	Overlap of polymicrogyria, hydrocephalus, and Joubert syndrome in a family with novel truncating mutations in ADGRG1/GPR56 and KIAA0556 2019 ·Neurogenetics ·(unknown), Ahlam A. Hamed, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Mahmoud Koko, Liena E. O. Elsayed, Xianhua Piao, Mustafa A. Salih, M. Chiara Manzini	14
8	Classification and management of epilepsy and epileptic syndromes in a cohort of 202 school children- a 2 year follow up study- Sudan 2019 ·BMC Neurology ·(unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Moiz Bakhiet, Ahlam A. Hamed	2
9	Case report of a novel homozygous splice site mutation in PLA2G6 gene causing infantile neuroaxonal dystrophy in a Sudanese family 2018 ·BMC Medical Genetics ·Liena E. O. Elsayed, (unknown), Ahlam A. Hamed, (unknown), Mustafa A. Salih, (unknown), (unknown), Mutaz Amin, Mahmoud Koko, Mustafa I. Elbashir, Muntaser E. Ibrahim, Alexis Brice, Ammar Ahmed, Giovanni Stévanin	8
10	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 2018 ·Epilepsy & Behavior ·(unknown), Kebreab Ghebremeskel, Manar E. Abdel‐Rahman, (unknown), (unknown), (unknown), (unknown), Ahlam A. Hamed, Adrián L. Rabinowicz, Mohamed Salih, Mustafa I. Elbashir, Ahmed Daak	15
11	Impact of PYROXD1 deficiency on cellular respiration and correlations with genetic analyses of limb-girdle muscular dystrophy in Saudi Arabia and Sudan 2018 ·Physiological Genomics ·Madhurima Saha, Hemakumar M. Reddy, Mustafa A. Salih, Elicia Estrella, Michael D. Jones, Satomi Mitsuhashi, (unknown), (unknown), (unknown), Muddathir H. Hamad, Maowia M. Mukhtar, Ahlam A. Hamed, (unknown), Monkol Lek, Elise Valkanas, Daniel G. MacArthur, Louis M. Kunkel, Christina A. Pacak, Isabelle Draper, Peter B. Kang	15
12	Brain tuberculoma, an unusual cause of stroke in a child with trisomy 21: a case report 2017 ·Journal of Medical Case Reports ·(unknown), Salah A. Ibrahim, Ahlam A. Hamed, (unknown), (unknown)	10
13	Prevalence of epilepsy in 74,949 school children in Khartoum State, Sudan 2017 ·Paediatrics and International Child Health ·(unknown), (unknown), Ahlam A. Hamed, Manar E. Abdel‐Rahman, Sarah El-Sadig, (unknown), (unknown), Ammar Ahmed, Z. A. Karrar, Mustafa A. Salih	11
14	Paediatric neurology service in Sudan: Current situation and future challenges 2015 ·Europe PMC (PubMed Central) ·(unknown), (unknown), Ahlam A. Hamed	2
15	Epidemiology of epilepsy among school children in Khartoum State-2014. 2015 ·Europe PMC (PubMed Central) ·Ahlam A. Hamed, (unknown), (unknown)	1

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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