Hamad Alzaidan

2.6k total citations
39 papers, 578 citations indexed

About

Hamad Alzaidan is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Hamad Alzaidan has authored 39 papers receiving a total of 578 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 17 papers in Genetics and 13 papers in Clinical Biochemistry. Recurrent topics in Hamad Alzaidan's work include Metabolism and Genetic Disorders (13 papers), Genomics and Rare Diseases (6 papers) and Mitochondrial Function and Pathology (5 papers). Hamad Alzaidan is often cited by papers focused on Metabolism and Genetic Disorders (13 papers), Genomics and Rare Diseases (6 papers) and Mitochondrial Function and Pathology (5 papers). Hamad Alzaidan collaborates with scholars based in Saudi Arabia, United States and France. Hamad Alzaidan's co-authors include Mohammed Al‐Owain, Zuhair N. Al‐Hassnan, Faiqa Imtiaz, Alya Qari, Namik Kaya, Albandary AlBakheet, Zuhair Rahbeeni, Fowzan S. Alkuraya, Moeenaldeen AlSayed and Firdous Abdulwahab and has published in prestigious journals such as PLoS ONE, The American Journal of Human Genetics and Human Genetics.

In The Last Decade

Hamad Alzaidan

36 papers receiving 569 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Hamad Alzaidan Saudi Arabia 14 283 173 132 67 66 39 578
Matias Wagner Germany 16 447 1.6× 225 1.3× 133 1.0× 37 0.6× 73 1.1× 83 792
Fuad Al Mutairi Saudi Arabia 16 342 1.2× 225 1.3× 195 1.5× 44 0.7× 70 1.1× 47 674
Nouriya Al‐Sannaa Saudi Arabia 13 290 1.0× 150 0.9× 96 0.7× 67 1.0× 64 1.0× 27 611
Joan E. Pellegrino United States 11 256 0.9× 215 1.2× 133 1.0× 69 1.0× 116 1.8× 19 492
Dalia Kasperavičiūtė United Kingdom 20 274 1.0× 356 2.1× 39 0.3× 78 1.2× 106 1.6× 27 942
Geetha Anand United Kingdom 13 303 1.1× 105 0.6× 77 0.6× 34 0.5× 36 0.5× 34 565
Davide Tonduti Italy 19 728 2.6× 183 1.1× 106 0.8× 27 0.4× 81 1.2× 64 1.1k
Yaping Yang United States 16 322 1.1× 292 1.7× 76 0.6× 39 0.6× 84 1.3× 37 654
Maja Hempel Germany 19 511 1.8× 342 2.0× 112 0.8× 58 0.9× 116 1.8× 58 855
Ralitza H. Gavrilova United States 14 309 1.1× 97 0.6× 57 0.4× 37 0.6× 35 0.5× 52 824

Countries citing papers authored by Hamad Alzaidan

Since Specialization
Citations

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

Fields of papers citing papers by Hamad Alzaidan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hamad Alzaidan

This figure shows the co-authorship network connecting the top 25 collaborators of Hamad Alzaidan. A scholar is included among the top collaborators of Hamad Alzaidan 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 Hamad Alzaidan. Hamad Alzaidan 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.
Coucke, Paul, Firdous Abdulwahab, Lama AlAbdi, et al.. (2025). Structure-Activity Analysis Reveals Perturbed Cilia-Jun N-Terminal Kinase Signaling in MAPKBP1-Associated Kidney Disease. Kidney International Reports. 10(8). 2836–2851.
2.
Shamseldin, Hanan E., Nada Derar, Hamad Alzaidan, et al.. (2023). PRSS8, encoding prostasin, is mutated in patients with autosomal recessive ichthyosis. Human Genetics. 142(4). 477–482. 4 indexed citations
3.
Aldhalaan, Hesham, Albandary AlBakheet, Moeen Al-Sayed, et al.. (2023). Clinical, radiological, and genetic characterization of SLC13A5 variants in Saudi families: Genotype phenotype correlation and brief review of the literature. Frontiers in Pediatrics. 10. 1051534–1051534. 2 indexed citations
4.
5.
Patel, Nisha, John M. Graham, Michael J. Bamshad, et al.. (2021). Further delineation of van den Ende‐Gupta syndrome: Genetic heterogeneity and overlap with congenital heart defects and skeletal malformations syndrome. American Journal of Medical Genetics Part A. 185(7). 2136–2149. 3 indexed citations
6.
Haldeman‐Englert, Chad, et al.. (2020). Further delineation of MYO18B‐related autosomal recessive Klippel‐Feil syndrome with myopathy and facial dysmorphism. American Journal of Medical Genetics Part A. 185(2). 370–376. 2 indexed citations
7.
Alkuraya, Hisham, Nisha Patel, Niema Ibrahim, et al.. (2019). Phenotypic delineation of the retinal arterial macroaneurysms with supravalvular pulmonic stenosis syndrome. Clinical Genetics. 97(3). 447–456. 5 indexed citations
8.
Shaheen, Ranad, Nan Jiang, Fatema Alzahrani, et al.. (2019). Bi-allelic Mutations in FAM149B1 Cause Abnormal Primary Cilium and a Range of Ciliopathy Phenotypes in Humans. The American Journal of Human Genetics. 104(4). 731–737. 21 indexed citations
9.
Al‐Hamed, Mohamed H., Faiqa Imtiaz, Zuhair N. Al‐Hassnan, et al.. (2019). Spectrum of mutations underlying Propionic acidemia and further insight into a genotype-phenotype correlation for the common mutation in Saudi Arabia. Molecular Genetics and Metabolism Reports. 18. 22–29. 12 indexed citations
10.
Maddirevula, Sateesh, Talal Algoufi, Hessa S. Alsaif, et al.. (2018). Identification of novel loci for pediatric cholestatic liver disease defined by KIF12, PPM1F, USP53, LSR, and WDR83OS pathogenic variants. Genetics in Medicine. 21(5). 1164–1172. 69 indexed citations
11.
Altassan, Ruqaiah, Tariq Masoodi, Ola Khalifa, et al.. (2017). Exome sequencing identifies novel NTRK1 mutations in patients with HSAN‐IV phenotype. American Journal of Medical Genetics Part A. 173(4). 1009–1016. 15 indexed citations
12.
Khalifa, Ola, Faiqa Imtiaz, Khushnooda Ramzan, et al.. (2015). Variable expression pattern in Donnai-Barrow syndrome: Report of two novel LRP2 mutations and review of the literature. European Journal of Medical Genetics. 58(5). 293–299. 30 indexed citations
13.
Imtiaz, Faiqa, Mohamed H. Al‐Hamed, Zuhair N. Al‐Hassnan, et al.. (2014). Spectrum of Mutations in 60 Saudi Patients with Mut Methylmalonic Acidemia. JIMD Reports. 29. 39–46. 5 indexed citations
14.
Salih, Mustafa A., Emeline Mundwiller, Arif O. Khan, et al.. (2013). Correction: New Findings in a Global Approach to Dissect the Whole Phenotype of PLA2G6 Gene Mutations. PLoS ONE. 8(11). 6 indexed citations
15.
Salih, Mustafa A., Emeline Mundwiller, Arif O. Khan, et al.. (2013). New Findings in a Global Approach to Dissect the Whole Phenotype of PLA2G6 Gene Mutations. PLoS ONE. 8(10). e76831–e76831. 38 indexed citations
16.
AlSayed, Moeenaldeen, Hamad Alzaidan, Albandary AlBakheet, et al.. (2013). Mutations in NALCN Cause an Autosomal-Recessive Syndrome with Severe Hypotonia, Speech Impairment, and Cognitive Delay. The American Journal of Human Genetics. 93(4). 721–726. 69 indexed citations
17.
Al‐Owain, Mohammed, Hamad Alzaidan, & Zuhair N. Al‐Hassnan. (2012). Map of autosomal recessive genetic disorders in Saudi Arabia: Concepts and future directions. American Journal of Medical Genetics Part A. 158A(10). 2629–2640. 71 indexed citations
18.
Al‐Owain, Mohammed, et al.. (2010). Novel intragenic deletion in OPHN1 in a family causing XLMR with cerebellar hypoplasia and distinctive facial appearance. Clinical Genetics. 79(4). 363–370. 24 indexed citations
19.
Al‐Owain, Mohammed, Namik Kaya, Hamad Alzaidan, et al.. (2010). Renal Failure Associated with APECED and Terminal 4q Deletion: Evidence of Autoimmune Nephropathy. Journal of Immunology Research. 2010(1). 586342–586342. 12 indexed citations
20.
Al‐Owain, Mohammed, et al.. (2009). Munchausen syndrome by proxy mimicking as Gaucher disease. European Journal of Pediatrics. 169(8). 1029–1032. 5 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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