Khalid Hundallah

565 total citations
21 papers, 165 citations indexed

About

Khalid Hundallah is a scholar working on Molecular Biology, Genetics and Neurology. According to data from OpenAlex, Khalid Hundallah has authored 21 papers receiving a total of 165 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 5 papers in Genetics and 4 papers in Neurology. Recurrent topics in Khalid Hundallah's work include Metabolism and Genetic Disorders (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Genomics and Rare Diseases (2 papers). Khalid Hundallah is often cited by papers focused on Metabolism and Genetic Disorders (3 papers), Genetics and Neurodevelopmental Disorders (3 papers) and Genomics and Rare Diseases (2 papers). Khalid Hundallah collaborates with scholars based in Saudi Arabia, United Kingdom and United States. Khalid Hundallah's co-authors include Majid Alfadhel, Marwan Nashabat, Brahim Tabarki, Fowzan S. Alkuraya, Waleed Altwaijri, Sateesh Maddirevula, Fahad A. Bashiri, Saeed Al Tala, Adel Mahmoud and Fuad Al Mutairi and has published in prestigious journals such as SHILAP Revista de lepidopterología, Journal of Medical Genetics and Frontiers in Neurology.

In The Last Decade

Khalid Hundallah

17 papers receiving 164 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Khalid Hundallah Saudi Arabia 7 88 48 24 19 18 21 165
Taku Omata Japan 7 119 1.4× 57 1.2× 32 1.3× 13 0.7× 19 1.1× 29 221
Rodolphe Dard France 6 113 1.3× 63 1.3× 8 0.3× 27 1.4× 28 1.6× 19 233
Ilya Kanivets Russia 7 91 1.0× 61 1.3× 6 0.3× 29 1.5× 11 0.6× 39 162
Huifang Yan China 9 108 1.2× 79 1.6× 6 0.3× 23 1.2× 9 0.5× 23 201
İbrahim Öncel Türkiye 7 87 1.0× 18 0.4× 15 0.6× 10 0.5× 30 1.7× 23 153
Narayan Chandra Saha Bangladesh 6 55 0.6× 30 0.6× 17 0.7× 8 0.4× 21 1.2× 34 192
Ting Bai China 10 99 1.1× 101 2.1× 43 1.8× 4 0.2× 13 0.7× 29 301
Hanène Benrhouma Tunisia 8 62 0.7× 21 0.4× 9 0.4× 35 1.8× 25 1.4× 37 150
İhsan Turan Türkiye 10 98 1.1× 110 2.3× 22 0.9× 6 0.3× 11 0.6× 34 242

Countries citing papers authored by Khalid Hundallah

Since Specialization
Citations

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

Fields of papers citing papers by Khalid Hundallah

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Khalid Hundallah. 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 Khalid Hundallah. The network helps show where Khalid Hundallah may publish in the future.

Co-authorship network of co-authors of Khalid Hundallah

This figure shows the co-authorship network connecting the top 25 collaborators of Khalid Hundallah. A scholar is included among the top collaborators of Khalid Hundallah 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 Khalid Hundallah. Khalid Hundallah 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.
Johari, Mridul, Ana Töpf, Jennifer Duff, et al.. (2024). Loss-of-function variants in JPH1 cause congenital myopathy with prominent facial and ocular involvement. Journal of Medical Genetics. 61(10). 992–998.
2.
Bashiri, Fahad A., Khalid Hundallah, Raidah Albaradie, et al.. (2024). Diagnosis and management of infantile epileptic spasms syndrome (IESS) in Gulf Cooperation Council (GCC) countries: Expert consensus statement. Seizure. 117. 174–182. 2 indexed citations
3.
Alhashem, Amal, et al.. (2024). Multiplex Consanguineous Family Highlights CLASP1 as a Candidate Gene for Lissencephaly. Neurology Genetics. 10(4). e200172–e200172. 1 indexed citations
4.
Alghamdi, Malak, Khalid Hundallah, Jehan Suleiman, et al.. (2023). Aromatic L-amino acid decarboxylase deficiency in countries in the Middle East: a case series and literature review. European Journal of Pediatrics. 182(6). 2535–2545.
5.
Hundallah, Khalid, et al.. (2023). Effectiveness of intra-thecal methotrexate in refractory Anti-N-methyl-d-aspartate receptor encephalitis. BMC Neurology. 23(1). 261–261. 2 indexed citations
6.
Hundallah, Khalid, et al.. (2023). Novel TLR7 hemizygous variant in post-COVID-19 neurological deterioration: a case report with literature review. Frontiers in Neurology. 14. 1268035–1268035. 2 indexed citations
7.
Hundallah, Khalid, et al.. (2022). Beyond the caudate nucleus: Early atypical neuroimaging findings in biotin-thiamine- responsive basal ganglia disease. Brain and Development. 44(9). 618–622. 1 indexed citations
8.
Bamaga, Ahmed K., Waleed Altwaijri, Fahad A. Bashiri, et al.. (2021). Consensus Statement on the Management of Duchenne Muscular Dystrophy in Saudi Arabia During the Coronavirus Disease 2019 Pandemic. Frontiers in Pediatrics. 9. 629549–629549. 12 indexed citations
9.
Bashiri, Fahad A., Mohamad‐Hani Temsah, Khalid Hundallah, Fahad Alsohime, & Yazed AlRuthia. (2021). 2020 Update to Spinal Muscular Atrophy Management in Saudi Arabia. Frontiers in Pediatrics. 9. 684134–684134. 2 indexed citations
10.
Hundallah, Khalid & Brahim Tabarki. (2021). Treatable inherited metabolic epilepsies. Neurosciences. 26(3). 229–235. 4 indexed citations
11.
Maroofian, Reza, Andrea Gubaš, Rauan Kaiyrzhanov, et al.. (2021). Homozygous missense WIPI2 variants cause a congenital disorder of autophagy with neurodevelopmental impairments of variable clinical severity and disease course. Brain Communications. 3(3). fcab183–fcab183. 11 indexed citations
12.
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
13.
Hundallah, Khalid, et al.. (2020). Editorial Message. Neurosciences. 1–3.
14.
Nashabat, Marwan, Waleed Altwaijri, Khalid Hundallah, et al.. (2019). The landscape of early infantile epileptic encephalopathy in a consanguineous population. Seizure. 69. 154–172. 38 indexed citations
15.
Hundallah, Khalid, et al.. (2019). Tuberous sclerosis. Neurosciences. 24(4). 335–337.
16.
Hundallah, Khalid, et al.. (2018). A novel variant in ATM gene causes ataxia telangiectasia revealed by whole-exome sequencing. Neurosciences. 23(2). 162–164. 4 indexed citations
17.
Alhashem, Amal, Eissa Faqeih, Majid Alfadhel, et al.. (2017). Congenital disorders of glycosylation: The Saudi experience. American Journal of Medical Genetics Part A. 173(10). 2614–2621. 29 indexed citations
18.
Hundallah, Khalid, et al.. (2017). Pantothenate kinase-associated neurodegeneration. Neurosciences. 22(2). 156–157. 3 indexed citations
19.
Alfadhel, Majid, et al.. (2017). Mitochondrial iron-sulfur cluster biogenesis from molecular understanding to clinical disease. Neurosciences. 22(1). 4–13. 21 indexed citations
20.
Hundallah, Khalid, et al.. (2016). Sulfite oxidase deficiency. PubMed Central. 21(4). 376–378. 1 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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