Mohammed Al‐Owain
Impact in
- Clinical Biochemistry top 1%
- Metabolism and Genetic Disorders
- Rheumatology top 2%
- Systemic Lupus Erythematosus Research
Papers in
-
- Mitochondrial Function and Pathology 6
- Genetics 29
- Genetics and Neurodevelopmental Disorders 10
- Connective tissue disorders research 8
- Genomics and Rare Diseases 8
- Neurogenetic and Muscular Disorders Research 7
- Genomic variations and chromosomal abnormalities 6
- Co-authors
- Fowzan S. Alkuraya (24 shared papers)Zuhair N. Al‐Hassnan (18 shared papers)Nadia Alhashmi (7 shared papers)Hamad Alzaidan (18 shared papers)Eissa Faqeih (11 shared papers)Sulaiman M. Al‐Mayouf (4 shared papers)Mohammad Ghaziuddin (3 shared papers)Namik Kaya (13 shared papers)
- Journals
- Clinical Genetics (5 papers)Journal of Medical Genetics (5 papers)European Journal of Pediatrics (4 papers)European Journal of Medical Genetics (4 papers)Journal of Child Neurology (3 papers)
- Partner nations
- Saudi ArabiaUnited StatesCanada
In The Last Decade
Mohammed Al‐Owain
87 papers receiving 2.2k citations
Peers
Comparison fields: 5 of 102
- Clinical Biochemistry 241
- Rheumatology 315
- Sensory Systems 103
- Genetics 574
- Immunology 341
Countries citing papers authored by Mohammed Al‐Owain
This map shows the geographic impact of Mohammed Al‐Owain'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 Mohammed Al‐Owain with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mohammed Al‐Owain more than expected).
Fields of papers citing papers by Mohammed Al‐Owain
This network shows the impact of papers produced by Mohammed Al‐Owain. 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 Mohammed Al‐Owain. The network helps show where Mohammed Al‐Owain may publish in the future.
Co-authors
The 25 scholars most cited alongside Mohammed Al‐Owain, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 88 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2011 | 345 | |
| 2 | 2012 | 208 | |
| 3 | 2012 | 110 | |
| 4 | 2016 | 72 | |
| 5 | 2012 | 70 | |
| 6 | Molecular characterization of retinitis pigmentosa in Saudi Arabia. | 2009 | 68 |
| 7 | 2016 | 64 | |
| 8 | 2012 | 59 | |
| 9 | 2011 | 57 | |
| 10 | 2011 | 54 | |
| 11 | 2012 | 52 | |
| 12 | 2012 | 48 | |
| 13 | 2016 | 44 | |
| 14 | 2013 | 40 | |
| 15 | 2013 | 38 | |
| 16 | 2017 | 37 | |
| 17 | A null mutation in CABP4 causes Leber's congenital amaurosis-like phenotype. | 2010 | 35 |
| 18 | 2017 | 35 | |
| 19 | 2012 | 28 | |
| 20 | 2010 | 28 |
About Mohammed Al‐Owain
Mohammed Al‐Owain is a scholar working on Molecular Biology, Genetics, Clinical Biochemistry, Rheumatology and Physiology, having authored 88 papers that have together received 2.2k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (21 papers), Genetics and Neurodevelopmental Disorders (10 papers), Connective tissue disorders research (8 papers), Genomics and Rare Diseases (8 papers), Hearing, Cochlea, Tinnitus, Genetics (7 papers), Neurogenetic and Muscular Disorders Research (7 papers), Genomic variations and chromosomal abnormalities (6 papers) and Mitochondrial Function and Pathology (6 papers). The work is most often cited by research in Clinical Biochemistry (241 citations), Rheumatology (315 citations), Sensory Systems (103 citations), Genetics (574 citations) and Immunology (341 citations). Mohammed Al‐Owain has collaborated with scholars based in Saudi Arabia, United States and Canada. Frequent co-authors include Fowzan S. Alkuraya, Zuhair N. Al‐Hassnan, Nadia Alhashmi, Hamad Alzaidan, Eissa Faqeih, Sulaiman M. Al‐Mayouf, Mohammad Ghaziuddin, Namik Kaya, Faiqa Imtiaz and Hanif Khalak. Their work appears in journals such as Clinical Genetics, Journal of Medical Genetics, European Journal of Pediatrics, European Journal of Medical Genetics and Journal of Child Neurology.
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.