Anas M. Alazami

3.9k citations

55 papers · 1.5k indexed · h-index 22

Impact in

Genetics top 5%
- Connective tissue disorders research
- Genomics and Rare Diseases
- Genetic and Kidney Cyst Diseases
Neurology top 5%
- Neurological diseases and metabolism

Papers in

Genetics 24
- Genetics and Neurodevelopmental Disorders 7
- Genomics and Rare Diseases 6
- Genetic and Kidney Cyst Diseases 4
Immunology 15
- Immunodeficiency and Autoimmune Disorders 11
- Immune Cell Function and Interaction 6

Co-authors: Fowzan S. Alkuraya Hadia Hijazi Fatema Alzahrani Ranad Shaheen Amal Y. Kentab Eissa Faqeih Saad S. M. Hassan Coralie Poizat
Journals: Journal of Clinical Immunology (5 papers)Frontiers in Immunology (4 papers)The American Journal of Human Genetics (4 papers)Journal of Medical Genetics (4 papers)Clinical Genetics (4 papers)
Partner nations: Saudi Arabia United States United Kingdom

In The Last Decade

Anas M. Alazami

52 papers receiving 1.5k citations

Peers

Countries citing papers authored by Anas M. Alazami

Since Specialization

Citations

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

Fields of papers citing papers by Anas M. Alazami

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Anas M. Alazami. 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 Anas M. Alazami. The network helps show where Anas M. Alazami may publish in the future.

Co-authors

The 25 scholars most cited alongside Anas M. Alazami, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Anas M. Alazami Line = papers co-authored together Anas M. Alazami links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Expanding the clinical spectrum of interleukin-2 receptor alpha chain deficiency: two novel cases with long-term hematopoietic stem cell transplantation outcome and literature review Frontiers in Immunology ·Maha Alzubedy, Ahmed Sayed Osman, Huda Alajlan, Anas M. Alazami, (unknown)	2026	0
2	Homozygous Loss of Function PIK3CD Mutation in Multiple Siblings Leading To B Cell Dysregulation and Autoimmunity Journal of Clinical Immunology ·Huda Alajlan, Amer Al‐Mazrou, Hibah Alruwaili, Safia Sumayli, Ali Almehaidib, Khalid A. Alsaleem, Sawsan Abu Awwad, Hazem Ghebeh, Monther Al‐Alwan, Anas M. Alazami, Hamoud Al‐Mousa	2025	0
3	A unique STK4 mutation truncating only the C-terminal SARAH domain results in a mild clinical phenotype despite severe T cell lymphopenia: Case report Frontiers in Immunology ·Bandar Al‐Saud, Huda Alajlan, Hibah Alruwaili, Latifa Almoaibed, Amer Al‐Mazrou, Hazem Ghebeh, Monther Al‐Alwan, Anas M. Alazami	2024	2
4	Severe Combined Immunodeficiency from a Homozygous DNA Ligase 1 Mutant with Reduced Catalytic Activity but Increased Ligation Fidelity Journal of Clinical Immunology ·Huda Alajlan, Vlad‐Stefan Raducanu, Yossef López de los Santos, Muhammad Tehseen, Hibah Alruwaili, Amer Al‐Mazrou, Reem Mohammad, Monther Al‐Alwan, Alfredo De Biasio, Jasmeen S. Merzaban, Hamoud Al‐Mousa, Samir M. Hamdan, Anas M. Alazami	2024	4
5	A homozygous truncating mutation of FGL2 is associated with immune dysregulation Journal of Allergy and Clinical Immunology ·Erin Janssen, Mohammad F Alosaimi, Anas M. Alazami, Abdullah Alsuliman, Ayodele Alaiya, Bandar Al‐Saud, Hamoud Al‐Mousa, Tariq Al‐Zaid, Emma Smith, Craig D. Platt, Hibah Alruwaili, Sarah Albanyan, Sulaiman M. Al‐Mayouf, Raif S. Geha	2022	2
6	Phenotypic and Genotypic Characterization of Hereditary Angioedema in Saudi Arabia Journal of Clinical Immunology ·Farrukh Sheikh, Huda Alajlan, Maram Albanyan, Hibah Alruwaili, Fatimah Alawami, Safia Sumayli, Sulaiman Al Gazlan, Sawsan Abu Awwad, Hasan Al‐Dhekri, Bandar Al‐Saud, Rand Arnaout, Hassan Al-Rayes, Najla Sayes, Mohamed H. Al‐Hamed, Hamoud Al‐Mousa, Saad Mohammed AlShareef, Anas M. Alazami	2022	0
7	PUS7 mutations impair pseudouridylation in humans and cause intellectual disability and microcephaly Human Genetics ·Ranad Shaheen, Monika Tasak, Sateesh Maddirevula, Ghada M. H. Abdel‐Salam, Inas S. M. Sayed, Anas M. Alazami, Tarfa Al‐Sheddi, Eman Alobeid, Eric M. Phizicky, Fowzan S. Alkuraya	2019	68
8	Deletion of DDB1- and CUL4- associated factor-17 (Dcaf17) gene causes spermatogenesis defects and male infertility in mice Scientific Reports ·Asmaa Ali, Bhavesh V. Mistry, Hala Ahmed, Razan Abdulla, Hassan Amer, Abdelbary Prince, Anas M. Alazami, Fowzan S. Alkuraya, Abdullah M. Assiri	2018	20
9	A first-line diagnostic assay for limb-girdle muscular dystrophy and other myopathies Human Genomics ·Dorota Monies, Hindi Al‐Hindi, Mohamed Almuhaizea, Mohamed Abouelhoda, Anas M. Alazami, Ewa Goljan, Banan Al‐Younes, Dyala Jaroudi, Abdulelah AlIssa, Khalid Alabdulrahman, Shazia Subhani, Mohamed El-Kalioby, Tariq Faquih, Salma M. Wakil, Nada Al Tassan, Brian F. Meyer, Saeed Bohlega	2016	29
10	The many faces of KIF7 Human Genome Variation ·Duna Barakeh, Eissa Faqeih, Shams Anazi, Mohammed S. Al‐Dosari, Ameen Softah, Fahad Albadr, Hamdy H. Hassan, Anas M. Alazami, Fowzan S. Alkuraya	2015	14
11	TLE6 mutation causes the earliest known human embryonic lethality Genome biology ·Anas M. Alazami, Salma Awad, Serdar Coşkun, Saad S. M. Hassan, Hadia Hijazi, Firdous Abdulwahab, Coralie Poizat, Fowzan S. Alkuraya	2015	147
12	Report of a case of Raine syndrome and literature review American Journal of Medical Genetics Part A ·Mohammed Zain Seidahmed, Anas M. Alazami, Omer Bashir Abdelbasit, Khalid Al Hussein, Abeer M. Miqdad, Omar Abu‐Sa'da, Tareq Mustafa, Sarah Bahjat, Fowzan S. Alkuraya	2015	18
13	Novel compound heterozygous frameshift mutations of C2orf37 in a familial Indian case of Woodhouse–Sakati syndrome Journal of Genetics ·Mansoor C. Abdulla, Anas M. Alazami, Jemshad Alungal, JASSIM M. KOYA, Mohthash Musambil	2015	8
14	The clinical utility of molecular karyotyping for neurocognitive phenotypes in a consanguineous population Genetics in Medicine ·Sarah M. Al-Qattan, Salma M. Wakil, Shamsa Anazi, Anas M. Alazami, Nisha Patel, Ranad Shaheen, Hanan E. Shamseldin, Samya Hagos, Haya M. AlDossari, Mustafa A. Salih, Heba Y. El Khashab, Amal Y. Kentab, Mohammed N. Al-Nasser, Fahad A. Bashiri, Namik Kaya, Mais Hashem, Fowzan S. Alkuraya	2014	11
15	Study of autosomal recessive osteogenesis imperfecta in Arabia reveals a novel locus defined by TMEM38B mutation Journal of Medical Genetics ·Ranad Shaheen, Anas M. Alazami, Muneera Alshammari, Eissa Faqeih, Nadia Alhashmi, Noon Mousa, Aisha Al-Sinani, Shinu Ansari, Fatema Alzahrani, Mohammed Al‐Owain, Zayed Al‐Zayed, Fowzan S. Alkuraya	2012	108
16	Loss of function mutation in LARP7, chaperone of 7SK ncRNA, causes a syndrome of facial dysmorphism, intellectual disability, and primordial dwarfism Human Mutation ·Anas M. Alazami, Mohammad Al-Owain, Fatema Alzahrani, Taghreed Shuaib, Hussain Al-Shamrani, Yahya H. Al‐Falki, Saleh M. Al‐Qahtani, Tarfa Al‐Sheddi, Dilek Çolak, Fowzan S. Alkuraya	2012	64
17	Molecular characterization of Joubert syndrome in Saudi Arabia Human Mutation ·Anas M. Alazami, Muneera Alshammari, Mustafa A. Salih, Fatema Alzahrani, Hadia Hijazi, Mohammed Zain Seidahmed, Leen Abu Safieh, Mazhor Aldosary, Arif O. Khan, Fowzan S. Alkuraya	2012	45
18	Mutations in C2orf37, Encoding a Nucleolar Protein, Cause Hypogonadism, Alopecia, Diabetes Mellitus, Mental Retardation, and Extrapyramidal Syndrome The American Journal of Human Genetics ·Anas M. Alazami, Amr Al‐Saif, Abdulaziz Alsemari, Saeed Bohlega, Soumaya Zlitni, Fatema Alzahrani, Prashant Bavi, Namik Kaya, Dilek Çolak, Hanif Khalak, Andy Baltus, Borut Peterlin, Sumita Danda, Kailash P. Bhatia, Susanne A. Schneider, Nadia Sakati, Christopher A. Walsh, Futwan Al‐Mohanna, Brian F. Meyer, Fowzan S. Alkuraya	2008	94
19	Novel PRG4 mutations underlie CACP in Saudi families Human Mutation ·Anas M. Alazami, Sulaiman M. Al‐Mayouf, Carol-Ann Wyngaard, Brian F. Meyer	2006	30
20	Human artificial chromosomes containing chromosome 17 alphoid DNA maintain an active centromere in murine cells but are not stable Genomics ·Anas M. Alazami, José Enrique Mejía, Zoia L. Monaco	2004	21

About Anas M. Alazami

Anas M. Alazami is a scholar working on Genetics, Immunology, Clinical Biochemistry, Genetics and Cell Biology, having authored 55 papers that have together received 1.5k indexed citations. Recurring topics across this work include Immunodeficiency and Autoimmune Disorders (11 papers), Genetics and Neurodevelopmental Disorders (7 papers), Immune Cell Function and Interaction (6 papers), Genomics and Rare Diseases (6 papers), RNA regulation and disease (5 papers), RNA modifications and cancer (5 papers), Genetic and Kidney Cyst Diseases (4 papers) and Lysosomal Storage Disorders Research (4 papers). The work is most often cited by research in Genetics (584 citations), Neurology (156 citations), Molecular Biology (857 citations), Genetics (127 citations) and Rheumatology (129 citations). Anas M. Alazami has collaborated with scholars based in Saudi Arabia, United States and United Kingdom. Frequent co-authors include Fowzan S. Alkuraya, Hadia Hijazi, Fatema Alzahrani, Ranad Shaheen, Amal Y. Kentab, Eissa Faqeih, Saad S. M. Hassan, Coralie Poizat, Mustafa A. Salih and Muneera Alshammari. Their work appears in journals such as Journal of Clinical Immunology, Frontiers in Immunology, The American Journal of Human Genetics, Journal of Medical Genetics and Clinical 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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