Mohammed Al‐Owain
Impact in
- Clinical Biochemistry top 1%
- Metabolism and Genetic Disorders
- Rheumatology top 5%
- Systemic Lupus Erythematosus Research
Papers in
-
- Mitochondrial Function and Pathology 7
- RNA regulation and disease 6
- Genetics 33
- Genetics and Neurodevelopmental Disorders 12
- Genomics and Rare Diseases 9
- Connective tissue disorders research 8
- Neurogenetic and Muscular Disorders Research 7
- Co-authors
- Fowzan S. Alkuraya (23 shared papers)Nadia Alhashmi (7 shared papers)Hamad Alzaidan (18 shared papers)Zuhair N. Al‐Hassnan (17 shared papers)Mais Hashem (7 shared papers)Eissa Faqeih (11 shared papers)Mohammad Ghaziuddin (3 shared papers)Sulaiman M. Al‐Mayouf (4 shared papers)
- Journals
- Journal of Medical Genetics (5 papers)Clinical Genetics (5 papers)European Journal of Medical Genetics (4 papers)European Journal of Pediatrics (4 papers)The American Journal of Human Genetics (3 papers)
- Partner nations
- Saudi ArabiaUnited StatesCanada
In The Last Decade
Mohammed Al‐Owain
84 papers receiving 2.0k citations
Peers
Comparison fields: 5 of 101
- Clinical Biochemistry 267
- Rheumatology 350
- Genetics 595
- Sensory Systems 103
- Immunology 356
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 87 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2011 | 339 | |
| 2 | 2012 | 108 | |
| 3 | 2012 | 71 | |
| 4 | 2016 | 68 | |
| 5 | Molecular characterization of retinitis pigmentosa in Saudi Arabia. | 2009 | 67 |
| 6 | 2016 | 64 | |
| 7 | 2012 | 58 | |
| 8 | 2011 | 55 | |
| 9 | 2011 | 53 | |
| 10 | 2012 | 51 | |
| 11 | 2012 | 47 | |
| 12 | 2016 | 44 | |
| 13 | 2013 | 39 | |
| 14 | 2013 | 38 | |
| 15 | 2017 | 37 | |
| 16 | 2017 | 35 | |
| 17 | A null mutation in CABP4 causes Leber's congenital amaurosis-like phenotype. | 2010 | 35 |
| 18 | 2010 | 28 | |
| 19 | 2012 | 28 | |
| 20 | 2010 | 27 |
About Mohammed Al‐Owain
Mohammed Al‐Owain is a scholar working on Molecular Biology, Genetics, Clinical Biochemistry, Rheumatology and Physiology, having authored 87 papers that have together received 2.0k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (23 papers), Genetics and Neurodevelopmental Disorders (12 papers), Genomics and Rare Diseases (9 papers), Connective tissue disorders research (8 papers), Mitochondrial Function and Pathology (7 papers), Hearing, Cochlea, Tinnitus, Genetics (7 papers), Neurogenetic and Muscular Disorders Research (7 papers) and RNA regulation and disease (6 papers). The work is most often cited by research in Clinical Biochemistry (267 citations), Rheumatology (350 citations), Genetics (595 citations), Sensory Systems (103 citations) and Immunology (356 citations). Mohammed Al‐Owain has collaborated with scholars based in Saudi Arabia, United States and Canada. Frequent co-authors include Fowzan S. Alkuraya, Nadia Alhashmi, Hamad Alzaidan, Zuhair N. Al‐Hassnan, Mais Hashem, Eissa Faqeih, Mohammad Ghaziuddin, Sulaiman M. Al‐Mayouf, Namik Kaya and Faiqa Imtiaz. Their work appears in journals such as Journal of Medical Genetics, Clinical Genetics, European Journal of Medical Genetics, European Journal of Pediatrics and The American Journal of 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.