Mohammad Al-Owain

464 total citations
15 papers, 264 citations indexed

About

Mohammad Al-Owain is a scholar working on Molecular Biology, Clinical Biochemistry and Surgery. According to data from OpenAlex, Mohammad Al-Owain has authored 15 papers receiving a total of 264 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 5 papers in Clinical Biochemistry and 4 papers in Surgery. Recurrent topics in Mohammad Al-Owain's work include Metabolism and Genetic Disorders (5 papers), Mitochondrial Function and Pathology (2 papers) and RNA regulation and disease (2 papers). Mohammad Al-Owain is often cited by papers focused on Metabolism and Genetic Disorders (5 papers), Mitochondrial Function and Pathology (2 papers) and RNA regulation and disease (2 papers). Mohammad Al-Owain collaborates with scholars based in Saudi Arabia, United States and United Kingdom. Mohammad Al-Owain's co-authors include Fowzan S. Alkuraya, Dilek Çolak, Taghreed Shuaib, Cathrine Broberg Vågbø, Dorota Monies, Tarfa Al‐Sheddi, Saleh M. Al‐Qahtani, Anas M. Alazami, Fatema Alzahrani and Namik Kaya and has published in prestigious journals such as The American Journal of Human Genetics, Human Mutation and Genetics in Medicine.

In The Last Decade

Mohammad Al-Owain

15 papers receiving 260 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Mohammad Al-Owain Saudi Arabia	10	170	65	41	39	34	15	264
Eyby Leon United States	9	263 1.5×	104 1.6×	60 1.5×	22 0.6×	41 1.2×	29	379
Taghreed Shuaib Saudi Arabia	9	133 0.8×	74 1.1×	25 0.6×	19 0.5×	27 0.8×	13	243
Sara Bertok Slovenia	10	166 1.0×	122 1.9×	42 1.0×	25 0.6×	18 0.5×	35	354
Yu Ding China	12	219 1.3×	170 2.6×	38 0.9×	35 0.9×	22 0.6×	38	359
Michael Yourshaw United States	9	166 1.0×	86 1.3×	32 0.8×	48 1.2×	34 1.0×	10	347
Leigh B. Waddell Australia	9	314 1.8×	45 0.7×	68 1.7×	22 0.6×	47 1.4×	16	371
Julie A. Jurgens United States	11	148 0.9×	124 1.9×	17 0.4×	16 0.4×	38 1.1×	14	298
Yo Okizuka Japan	10	307 1.8×	66 1.0×	28 0.7×	21 0.5×	13 0.4×	18	363
Laila Mahmoud Qatar	6	100 0.6×	136 2.1×	31 0.8×	16 0.4×	35 1.0×	6	254
Minal Menezes Australia	10	195 1.1×	65 1.0×	83 2.0×	17 0.4×	16 0.5×	17	290

Countries citing papers authored by Mohammad Al-Owain

Since Specialization

Citations

This map shows the geographic impact of Mohammad 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 Mohammad 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 Mohammad Al-Owain more than expected).

Fields of papers citing papers by Mohammad Al-Owain

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Mohammad 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 Mohammad Al-Owain. The network helps show where Mohammad Al-Owain may publish in the future.

Co-authorship network of co-authors of Mohammad Al-Owain

This figure shows the co-authorship network connecting the top 25 collaborators of Mohammad Al-Owain. A scholar is included among the top collaborators of Mohammad Al-Owain 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 Mohammad Al-Owain. Mohammad Al-Owain is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

15 of 15 papers shown

AlBakheet, Albandary, Rawan Almass, Alya Qari, et al.. (2024). Novel UBE3B mutations: report of eight patients with Kaufman oculocerebrofacial syndrome with additional clinical findings from a highly consanguineous population. Clinical Dysmorphology. 33(2). 55–62. 1 indexed citations

Altassan, Ruqaiah, Dimpna C. Albert, Mohammad Al-Owain, et al.. (2022). Successful heart transplantation in an infant with phosphoglucomutase 1 deficiency (PGM1‐CDG). JIMD Reports. 64(2). 123–128. 3 indexed citations

Al-Owain, Mohammad, et al.. (2020). Prolactinoma as a Cause of Persistent Hyperprolactinemia in 6-Pyruvoyl-tetrahydropterin synthase Deficiency. Wolverhampton Intellectual Repository and E-Theses (University of Wolverhampton). 5(2). 1–5. 1 indexed citations

Monies, Dorota, et al.. (2019). Recessive Truncating Mutations in ALKBH8 Cause Intellectual Disability and Severe Impairment of Wobble Uridine Modification. The American Journal of Human Genetics. 104(6). 1202–1209. 40 indexed citations

Alsaif, Hessa S., Mohammad Al-Owain, Martin E. Barrios‐Llerena, et al.. (2019). Homozygous Loss-of-Function Mutations in AP1B1, Encoding Beta-1 Subunit of Adaptor-Related Protein Complex 1, Cause MEDNIK-like Syndrome. The American Journal of Human Genetics. 105(5). 1016–1022. 36 indexed citations

Imtiaz, Faiqa, Khushnooda Ramzan, Nada Al Tassan, et al.. (2017). Twenty novel mutations in BCKDHA, BCKDHB and DBT genes in a cohort of 52 Saudi Arabian patients with maple syrup urine disease. Molecular Genetics and Metabolism Reports. 11. 17–23. 17 indexed citations

Čuturilo, Goran, Cassandra Runke, Erik C. Thorland, et al.. (2015). Phenotype analysis impacts testing strategy in patients with Currarino syndrome. Clinical Genetics. 89(1). 109–114. 10 indexed citations

Alazami, Anas M., Mohammad Al-Owain, Fatema Alzahrani, et al.. (2012). Loss of function mutation in LARP7, chaperone of 7SK ncRNA, causes a syndrome of facial dysmorphism, intellectual disability, and primordial dwarfism. Human Mutation. 33(10). 1429–1434. 64 indexed citations

Al-Owain, Mohammad, Banan Al‐Younes, Hesham Aldhalaan, et al.. (2012). A novel syndrome of abnormal striatum and congenital cataract: evidence for linkage to chromosomes 11. Clinical Genetics. 84(3). 258–264. 5 indexed citations

10.

Al-Owain, Mohammad, Faiqa Imtiaz, Taghreed Shuaib, et al.. (2011). Smith–Lemli–Opitz syndrome among Arabs. Clinical Genetics. 82(2). 165–172. 8 indexed citations

11.

Al-Owain, Mohammad, Dilek Çolak, Taghreed Shuaib, et al.. (2011). Novel mutation in GLRB in a large family with hereditary hyperekplexia. Clinical Genetics. 81(5). 479–484. 26 indexed citations

12.

Faiyaz‐Ul‐Haque, Muhammad, et al.. (2011). Clinical and molecular findings of 13 families from Saudi Arabia and a family from Sudan with homocystinuria. Clinical Genetics. 81(6). 563–570. 12 indexed citations

13.

Kaya, Namik, Saleh Al‐Muhsen, Bandar Al‐Saud, et al.. (2010). ICF Syndrome in Saudi Arabia: Immunological, Cytogenetic and Molecular Analysis. Journal of Clinical Immunology. 31(2). 245–252. 10 indexed citations

14.

Kaya, Namik, Faiqa Imtiaz, Dilek Çolak, et al.. (2008). Genome-wide gene expression profiling and mutation analysis of Saudi patients with Canavan disease. Genetics in Medicine. 10(9). 675–684. 17 indexed citations

15.

Kaya, Namik, Mohammad Al-Owain, Albandary AlBakheet, et al.. (2008). Array comparative genomic hybridization (aCGH) reveals the largest novel deletion in PCCA found in a Saudi family with propionic acidemia. European Journal of Medical Genetics. 51(6). 558–565. 14 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.

Explore authors with similar magnitude of impact