Hamad Alzaidan

2.6k citations

39 papers · 578 indexed · h-index 14

Co-authors: Mohammed Al‐Owain Zuhair N. Al‐Hassnan Alya Qari Faiqa Imtiaz Namik Kaya Albandary AlBakheet Zuhair Rahbeeni Fowzan S. Alkuraya
Topics: Metabolism and Genetic Disorders (13 papers)Genomics and Rare Diseases (6 papers)Mitochondrial Function and Pathology (5 papers)
Cited by: Clinical Biochemistry Neurology Genetics
Journals: PLoS ONE The American Journal of Human Genetics Human Genetics
Partner nations: Saudi Arabia United States France

In The Last Decade

Hamad Alzaidan

36 papers receiving 569 citations

Peers

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

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20 of 20 papers shown

#	Work	Indexed citations
1	Natural history of SPTBN4-related neurodevelopmental disorder with hypotonia, neuropathy, and deafness 2025 ·Orphanet Journal of Rare Diseases ·(unknown),Mohammad A. Al–Muhaizea,(unknown),(unknown),(unknown),(unknown),Anoud Albader,(unknown),Rawan Almass,Albandary AlBakheet,Tarfa Al‐Sheddi,Eman Alobeid,Maha Al‐Rasheed,Ali Al‐Odaib,Hamad Alzaidan,Moeenaldeen AlSayed,Namik Kaya	0
2	PRSS8, encoding prostasin, is mutated in patients with autosomal recessive ichthyosis 2023 ·Human Genetics ·Hanan E. Shamseldin,Nada Derar,Hamad Alzaidan,Naif Alhathal,(unknown),Firdous Abdulwahab,Tariq Al‐Zaid,(unknown),(unknown),Fowzan S. Alkuraya	4
3	Clinical, radiological, and genetic characterization of SLC13A5 variants in Saudi families: Genotype phenotype correlation and brief review of the literature 2023 ·Frontiers in Pediatrics ·(unknown),Hesham Aldhalaan,(unknown),(unknown),(unknown),(unknown),Albandary AlBakheet,(unknown),(unknown),(unknown),Moeen Al-Sayed,Hamad Alzaidan,Maha Al‐Rasheed,Ali Al‐Odaib,Namik Kaya	2
4	Children's Oral Health Status Among Urban and Rural Areas of Qassim Region, Saudi Arabia: A Cross-Sectional Study 2023 ·Cureus ·(unknown),(unknown),Hamad Alzaidan,(unknown)	0
5	Further delineation of van den Ende‐Gupta syndrome: Genetic heterogeneity and overlap with congenital heart defects and skeletal malformations syndrome 2021 ·American Journal of Medical Genetics Part A ·(unknown),Nisha Patel,John M. Graham,Michael J. Bamshad,Deborah A. Nickerson,Janson J. White,Colby T. Marvin,Danny E. Miller,Katheryn Grand,Pedro A. Sanchez‐Lara,(unknown),Hamad Alzaidan,(unknown),Fowzan S. Alkuraya,Angela E. Lin	3
6	Further delineation of MYO18B‐related autosomal recessive Klippel‐Feil syndrome with myopathy and facial dysmorphism 2020 ·American Journal of Medical Genetics Part A ·(unknown),Chad Haldeman‐Englert,Edward Cupler,(unknown),Hamad Alzaidan,Mais Hashem,Fowzan S. Alkuraya	2
7	Phenotypic delineation of the retinal arterial macroaneurysms with supravalvular pulmonic stenosis syndrome 2019 ·Clinical Genetics ·Hisham Alkuraya,Nisha Patel,Niema Ibrahim,(unknown),Sulaiman M. Alsulaiman,Sawsan R. Nowilaty,Emad B. Abboud,(unknown),Abdullah S. Al-Kharashi,Wafaa Eyaid,(unknown),Hamad Alzaidan,(unknown),Ahmed M. Abu El‐Asrar,(unknown),(unknown),(unknown),Naif A. M. Almontashiri,Abdulrahman Al‐Hussaini,Fowzan S. Alkuraya	5
8	Bi-allelic Mutations in FAM149B1 Cause Abnormal Primary Cilium and a Range of Ciliopathy Phenotypes in Humans 2019 ·The American Journal of Human Genetics ·Ranad Shaheen,Nan Jiang,Fatema Alzahrani,Nour Ewida,Tarfa Al‐Sheddi,Eman Alobeid,Damir Musaev,Valentina Stanley,Mais Hashem,Niema Ibrahim,Firdous Abdulwahab,(unknown),Fatma Müjgan Sönmez,(unknown),Hamad Alzaidan,Mohammad M. Al‐Qattan,Futwan Al‐Mohanna,Joseph G. Gleeson,Fowzan S. Alkuraya	21
9	Spectrum of mutations underlying Propionic acidemia and further insight into a genotype-phenotype correlation for the common mutation in Saudi Arabia 2019 ·Molecular Genetics and Metabolism Reports ·Mohamed H. Al‐Hamed,Faiqa Imtiaz,Zuhair N. Al‐Hassnan,Mohammed Al‐Owain,Hamad Alzaidan,Mohamed Al‐Amoudi,Eissa Faqeih,Majid Alfadhel,Ali Alasmari,Mohammed M. Saleh,Fuad Al Mutairi,Nabil Moghrabi,Moeenaldeen AlSayed	12
10	The phenotype, genotype, and outcome of infantile-onset Pompe disease in 18 Saudi patients 2018 ·Molecular Genetics and Metabolism Reports ·Zuhair N. Al‐Hassnan,Ola Khalifa,Dalal Bubshait,(unknown),(unknown),Hamad Alzaidan,Mohammed Al‐Owain,Zuhair Rahbeeni,Moeen Al-Sayed	6
11	Exome sequencing identifies novel NTRK1 mutations in patients with HSAN‐IV phenotype 2017 ·American Journal of Medical Genetics Part A ·Ruqaiah Altassan,(unknown),Tariq Masoodi,(unknown),Ola Khalifa,Hamad Alzaidan,Nadia Sakati,(unknown),Zuhair N. Al‐Hassnan,Yousef Binamer,(unknown),William J. Wade,Zayed Al‐Zayed,(unknown),(unknown),Brian F. Meyer,(unknown),Salma M. Wakil	15
12	Spectrum of Mutations in 60 Saudi Patients with Mut Methylmalonic Acidemia 2014 ·JIMD Reports ·Faiqa Imtiaz,(unknown),(unknown),Mohamed H. Al‐Hamed,(unknown),Zuhair N. Al‐Hassnan,Mohammed Al‐Owain,Hamad Alzaidan,Zuhair Rahbeeni,Alya Qari,Eissa Faqeih,Ali Alasmari,(unknown),Majid Alfadhel,Wafaa Eyaid,Mohamed S. Rashed,Moeenaldeen AlSayed	5
13	New Findings in a Global Approach to Dissect the Whole Phenotype of PLA2G6 Gene Mutations 2013 ·PLoS ONE ·Mustafa A. Salih,Emeline Mundwiller,Arif O. Khan,Abdulmajeed AlDrees,Salah A. Elmalik,Hamdy H. Hassan,Mohammed Al‐Owain,Hisham Alkhalidi,István Katona,Mohammad M. Kabiraj,Roman Chrast,Amal Y. Kentab,Hamad Alzaidan,Richard J. Rodenburg,Thomas M. Bosley,Joachim Weis,M. Kœnig,Giovanni Stévanin,Hamid Azzedine	38
14	Correction: New Findings in a Global Approach to Dissect the Whole Phenotype of PLA2G6 Gene Mutations 2013 ·PLoS ONE ·Mustafa A. Salih,Emeline Mundwiller,Arif O. Khan,Abdulmajeed AlDrees,Salah A. Elmalik,Hamdy H. Hassan,Mohammed Al‐Owain,Hisham Alkhalidi,István Katona,Mohammad M. Kabiraj,Roman Chrast,Amal Y. Kentab,Hamad Alzaidan,Richard J. Rodenburg,Thomas M. Bosley,Joachim Weis,Michel Kœnig,Giovanni Stévanin,Hamid Azzedine	6
15	Mutations in NALCN Cause an Autosomal-Recessive Syndrome with Severe Hypotonia, Speech Impairment, and Cognitive Delay 2013 ·The American Journal of Human Genetics ·Moeenaldeen AlSayed,Hamad Alzaidan,Albandary AlBakheet,(unknown),(unknown),Yusra Alyafee,Mazhor Aldosary,Alya Qari,Tarfa Al‐Sheddi,(unknown),(unknown),(unknown),Hindi Al‐Hindi,(unknown),Dilek Çolak,Namik Kaya	69
16	Novel PHKG2 mutation causing GSD IX with prominent liver disease: report of three cases and review of literature 2013 ·European Journal of Pediatrics ·(unknown),Faiqa Imtiaz,Hamad Alzaidan,(unknown),(unknown),(unknown),(unknown),Mohammed Al‐Owain	24
17	Identification of mutations causing hereditary tyrosinemia type I in patients of Middle Eastern origin 2011 ·Molecular Genetics and Metabolism ·Faiqa Imtiaz,Mohamed S. Rashed,Bashayer Al‐Mubarak,(unknown),Hanaa El-Karaksy,Zuhair N. Al‐Hassnan,Mohammed Al‐Owain,Hamad Alzaidan,Zuhair Rahbeeni,Alya Qari,Brian F. Meyer,Moeen Al-Sayed	16
18	Renal Failure Associated with APECED and Terminal 4q Deletion: Evidence of Autoimmune Nephropathy 2010 ·Journal of Immunology Research ·Mohammed Al‐Owain,Namik Kaya,Hamad Alzaidan,Ibrahim Hussain,(unknown),Hindi Al‐Hindi,Shelley Kennedy,M. Anwar Iqbal,Hamad Al‐Mojalli,Albandary AlBakheet,Anne Puel,Jean‐Laurent Casanova,Saleh Al‐Muhsen	12
19	Novel FBP1 gene mutations in Arab patients with fructose-1,6-bisphosphatase deficiency 2009 ·European Journal of Pediatrics ·Muhammad Faiyaz‐Ul‐Haque,Mohammed Al‐Owain,Fouad Al‐Dayel,Zuhair N. Al‐Hassnan,Hamad Alzaidan,Zuhair Rahbeeni,Moeen Al-Sayed,(unknown),Ahmad A. Cluntun,(unknown),(unknown),(unknown),Syed Hassan Ejaz Zaidi	26
20	Munchausen syndrome by proxy mimicking as Gaucher disease 2009 ·European Journal of Pediatrics ·Mohammed Al‐Owain,Hamad Alzaidan,Amal Alhashem,(unknown),(unknown)	5

About Hamad Alzaidan

Hamad Alzaidan is a scholar working on Clinical Biochemistry, Genetics and Rheumatology, having authored 39 papers that have together received 578 indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (13 papers), Genomics and Rare Diseases (6 papers) and Mitochondrial Function and Pathology (5 papers). The work is most often cited by research in Clinical Biochemistry (132 citations), Neurology (52 citations) and Genetics (173 citations). Hamad Alzaidan has collaborated with scholars based in Saudi Arabia, United States and France. Frequent co-authors include Mohammed Al‐Owain, Zuhair N. Al‐Hassnan, Alya Qari, Faiqa Imtiaz, Namik Kaya, Albandary AlBakheet, Zuhair Rahbeeni, Fowzan S. Alkuraya, Firdous Abdulwahab and Niema Ibrahim. Their work appears in journals such as PLoS ONE, The American Journal of Human Genetics and Human Genetics.

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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