Muddathir H. Hamad

1.5k total citations
44 papers, 274 citations indexed

About

Muddathir H. Hamad is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, Muddathir H. Hamad has authored 44 papers receiving a total of 274 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 11 papers in Pediatrics, Perinatology and Child Health and 11 papers in Genetics. Recurrent topics in Muddathir H. Hamad's work include Epilepsy research and treatment (7 papers), Genomics and Rare Diseases (6 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Muddathir H. Hamad is often cited by papers focused on Epilepsy research and treatment (7 papers), Genomics and Rare Diseases (6 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Muddathir H. Hamad collaborates with scholars based in Saudi Arabia, United States and Sudan. Muddathir H. Hamad's co-authors include Mustafa A. Salih, Fahad A. Bashiri, Amal Y. Kentab, Hamdy H. Hassan, Mais Hashem, Fowzan S. Alkuraya, Reem Al Khalifah, Ali H. Alwadei, Sarar Mohamed and Shams Anazi and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Medicine.

In The Last Decade

Muddathir H. Hamad

40 papers receiving 267 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Muddathir H. Hamad Saudi Arabia 9 105 52 51 44 42 44 274
Pascal Sabouraud France 11 116 1.1× 143 2.8× 50 1.0× 67 1.5× 41 1.0× 25 385
Yasemin Topçu Türkiye 10 70 0.7× 56 1.1× 28 0.5× 39 0.9× 35 0.8× 38 262
Ryuki Matsuura Japan 10 72 0.7× 130 2.5× 62 1.2× 35 0.8× 36 0.9× 47 294
Yukiko Mogami Japan 11 86 0.8× 138 2.7× 52 1.0× 31 0.7× 45 1.1× 37 342
Cha Gon Lee South Korea 12 117 1.1× 72 1.4× 126 2.5× 34 0.8× 23 0.5× 35 353
Simona Domenica Marino Italy 9 68 0.6× 130 2.5× 82 1.6× 29 0.7× 21 0.5× 39 287
Carlotta Canavese Italy 11 54 0.5× 86 1.7× 24 0.5× 59 1.3× 105 2.5× 33 340
Soroor Inaloo Iran 9 53 0.5× 108 2.1× 31 0.6× 36 0.8× 30 0.7× 45 304
Verónica Cantarín Extremera Spain 9 34 0.3× 77 1.5× 23 0.5× 27 0.6× 59 1.4× 41 216
Taro Kitamura Japan 10 49 0.5× 68 1.3× 17 0.3× 24 0.5× 34 0.8× 19 247

Countries citing papers authored by Muddathir H. Hamad

Since Specialization
Citations

This map shows the geographic impact of Muddathir H. Hamad'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 Muddathir H. Hamad with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Muddathir H. Hamad more than expected).

Fields of papers citing papers by Muddathir H. Hamad

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Muddathir H. Hamad. 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 Muddathir H. Hamad. The network helps show where Muddathir H. Hamad may publish in the future.

Co-authorship network of co-authors of Muddathir H. Hamad

This figure shows the co-authorship network connecting the top 25 collaborators of Muddathir H. Hamad. A scholar is included among the top collaborators of Muddathir H. Hamad 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 Muddathir H. Hamad. Muddathir H. Hamad is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
2.
Hamad, Muddathir H., Abdullah Alhuzaimi, Fadi Aljamaan, et al.. (2024). Virtual Objective Structured Clinical Examination (OSCE) Training in the Pandemic Era: Feasibility, Satisfaction, and the Road Ahead. Cureus. 16(6). e61564–e61564. 1 indexed citations
3.
4.
Bashiri, Fahad A., et al.. (2024). Vitamin D Supplementation for Children with Epilepsy on Antiseizure Medications: A Randomized Controlled Trial. Children. 11(10). 1187–1187. 1 indexed citations
5.
Bashiri, Fahad A., et al.. (2023). Genotype–Phenotype Analysis of Children with Epilepsy Referred for Whole-Exome Sequencing at a Tertiary Care University Hospital. Children. 10(8). 1334–1334. 1 indexed citations
6.
Alosaimi, Mohammed F., et al.. (2023). Case report: A late and isolated presentation of meningoencephalomyelitis uncovers a novel pathogenic variant in the CIITA gene. Frontiers in Pediatrics. 11. 1269396–1269396.
7.
Abbas, Mohamed, et al.. (2022). The Pattern of Management of Nocturnal Enuresis in a Tertiary Hospital in Sudan. 16(1). 394–396. 2 indexed citations
8.
Salih, Mustafa A., Muddathir H. Hamad, Marco Savarese, et al.. (2021). Exome Sequencing Reveals Novel TTN Variants in Saudi Patients with Congenital Titinopathies. Genetic Testing and Molecular Biomarkers. 25(12). 757–764. 5 indexed citations
9.
Bashiri, Fahad A., et al.. (2021). Neurodevelopmental and epilepsy outcomes of patients with infantile spasms treated in a tertiary care center. Neurosciences. 26(1). 21–25. 5 indexed citations
10.
Bashiri, Fahad A., Muddathir H. Hamad, Amal Y. Kentab, et al.. (2020). Acute Necrotizing Encephalopathy of Childhood: A Multicenter Experience in Saudi Arabia. Frontiers in Pediatrics. 8. 526–526. 23 indexed citations
11.
Atwal, Paldeep S., Sarah Endemann, Mark Midei, et al.. (2020). The natural history of infantile neuroaxonal dystrophy. Orphanet Journal of Rare Diseases. 15(1). 109–109. 14 indexed citations
12.
Seidahmed, Mohammed Zain, Muddathir H. Hamad, Albandary AlBakheet, et al.. (2020). Ancient founder mutation in RUBCN: a second unrelated family confirms Salih ataxia (SCAR15). BMC Neurology. 20(1). 207–207. 11 indexed citations
13.
Bashiri, Fahad A., Saeed Hassan, Amal Y. Kentab, et al.. (2019). Pediatric intracranial hypertension. Neurosciences. 24(4). 257–263. 2 indexed citations
14.
Ramadan, Wafaa S., Nisha Patel, Shamsa Anazi, et al.. (2018). Confirming the recessive inheritance of SCN1B mutations in developmental epileptic encephalopathy. Journal of Neurology and Neuroscience. 4 indexed citations
15.
Khalifah, Reem Al, et al.. (2018). Vitamin D supplementation to prevent vitamin D deficiency for children with epilepsy. Medicine. 97(40). e12734–e12734. 18 indexed citations
16.
Bashiri, Fahad A., et al.. (2018). Assessment of physicians’ knowledge and attitudes in the management of febrile seizures. Neurosciences. 23(4). 314–319. 5 indexed citations
17.
Patel, Nisha, Shams Anazi, Amal Y. Kentab, et al.. (2017). Confirming the recessive inheritance of SCN1B mutations in developmental epileptic encephalopathy. Clinical Genetics. 92(3). 327–331. 38 indexed citations
18.
Hashem, Mais, Rüstem Yilmaz, Muddathir H. Hamad, et al.. (2017). Mutations of PTPN23 in developmental and epileptic encephalopathy. Human Genetics. 136(11-12). 1455–1461. 13 indexed citations
19.
Mohamed, Sarar, Muddathir H. Hamad, & Khaled K. Abu‐Amero. (2015). Identification of 2 novel homozygous mutations in the methylmalonyl-CoA mutase gene in Saudi patients. Saudi Medical Journal. 36(9). 1110–1114. 4 indexed citations
20.
Mohamed, Sarar, Muddathir H. Hamad, Altaf A. Kondkar, & Khaled K. Abu‐Amero. (2015). A novel mutation in ornithine transcarbamylase gene causing mild intermittent hyperammonemia. Saudi Medical Journal. 36(10). 1229–1232. 3 indexed citations

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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