Mohammed Al‐Owain

7.2k total citations
87 papers, 2.0k citations indexed

About

Mohammed Al‐Owain is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Mohammed Al‐Owain has authored 87 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 48 papers in Molecular Biology, 33 papers in Genetics and 23 papers in Clinical Biochemistry. Recurrent topics in Mohammed Al‐Owain's work include Metabolism and Genetic Disorders (23 papers), Genetics and Neurodevelopmental Disorders (12 papers) and Genomics and Rare Diseases (9 papers). Mohammed Al‐Owain is often cited by papers focused on Metabolism and Genetic Disorders (23 papers), Genetics and Neurodevelopmental Disorders (12 papers) and Genomics and Rare Diseases (9 papers). Mohammed Al‐Owain collaborates with scholars based in Saudi Arabia, United States and Canada. Mohammed Al‐Owain's co-authors include Fowzan S. Alkuraya, Nadia Alhashmi, Hamad Alzaidan, Zuhair N. Al‐Hassnan, Mais Hashem, Mohammad Ghaziuddin, Eissa Faqeih, Sulaiman M. Al‐Mayouf, Namik Kaya and Faiqa Imtiaz and has published in prestigious journals such as Journal of Biological Chemistry, Nature Genetics and SHILAP Revista de lepidopterología.

In The Last Decade

Mohammed Al‐Owain

84 papers receiving 2.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mohammed Al‐Owain Saudi Arabia 25 1.1k 595 356 350 267 87 2.0k
Eissa Faqeih Saudi Arabia 28 1.5k 1.3× 920 1.5× 143 0.4× 181 0.5× 222 0.8× 80 2.2k
Daniel Grinberg Spain 33 1.6k 1.4× 512 0.9× 112 0.3× 410 1.2× 115 0.4× 180 3.3k
Maja Di Rocco Italy 34 1.5k 1.4× 860 1.4× 205 0.6× 778 2.2× 254 1.0× 147 3.6k
Mordechai Shohat Israel 26 1.7k 1.5× 540 0.9× 129 0.4× 79 0.2× 331 1.2× 83 2.9k
Hammadi Ayadi Tunisia 29 1.3k 1.1× 673 1.1× 298 0.8× 152 0.4× 34 0.1× 137 2.6k
Dusica Babovic‐Vuksanovic United States 27 863 0.8× 540 0.9× 122 0.3× 176 0.5× 154 0.6× 99 2.2k
Anita Farhi United States 12 2.3k 2.1× 1.1k 1.8× 144 0.4× 162 0.5× 95 0.4× 14 3.5k
Steffen Uebe Germany 22 819 0.7× 507 0.9× 138 0.4× 76 0.2× 69 0.3× 58 1.3k
Maha S. Zaki Egypt 27 1.2k 1.1× 679 1.1× 175 0.5× 127 0.4× 81 0.3× 147 2.4k
Philipp Rentzsch Germany 3 1.3k 1.2× 1.1k 1.9× 134 0.4× 75 0.2× 69 0.3× 6 2.2k

Countries citing papers authored by Mohammed Al‐Owain

Since Specialization
Citations

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

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of Mohammed Al‐Owain

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

All Works

20 of 20 papers shown
1.
Johari, Mridul, Ana Töpf, Jennifer Duff, et al.. (2024). Loss-of-function variants in JPH1 cause congenital myopathy with prominent facial and ocular involvement. Journal of Medical Genetics. 61(10). 992–998.
2.
Hussein, Maged H., Mohammed Al‐Owain, Zuhair N. Al‐Hassnan, et al.. (2023). Clinical and molecular features of four families with CLDN10-related HELIX syndrome. European Journal of Medical Genetics. 66(12). 104886–104886. 2 indexed citations
3.
Aldosary, Mazhor, Maysoon Alsagob, Stefan T. Arold, et al.. (2022). A Novel Homozygous Founder Variant of RTN4IP1 in Two Consanguineous Saudi Families. Cells. 11(19). 3154–3154.
4.
Aldalaan, Abdullah M., et al.. (2021). Genetic basis of pulmonary arterial hypertension: a prospective study from a highly inbred population. Pulmonary Circulation. 11(3). 1–8.
5.
Ramzan, Khushnooda, Nouf S. Al‐Numair, Nadia Sakati, et al.. (2020). Identification of Novel CDH23 Variants Causing Moderate to Profound Progressive Nonsyndromic Hearing Loss. Genes. 11(12). 1474–1474. 12 indexed citations
6.
Alkhunaizi, Ebba, Ranad Shaheen, Sanjay Kumar Bharti, et al.. (2018). Warsaw breakage syndrome: Further clinical and genetic delineation. American Journal of Medical Genetics Part A. 176(11). 2404–2418. 16 indexed citations
7.
Derar, Nada, Zuhair N. Al‐Hassnan, Mohammed Al‐Owain, et al.. (2018). De novo truncating variants in WHSC1 recapitulate the Wolf–Hirschhorn (4p16.3 microdeletion) syndrome phenotype. Genetics in Medicine. 21(1). 185–188. 21 indexed citations
8.
Patel, Nisha, Deepti Anand, Dorota Monies, et al.. (2016). Novel phenotypes and loci identified through clinical genomics approaches to pediatric cataract. Human Genetics. 136(2). 205–225. 64 indexed citations
9.
Faqeih, Eissa, Mohammed Al‐Owain, Dilek Çolak, et al.. (2014). Novel homozygous DEAF1 variant suspected in causing white matter disease, intellectual disability, and microcephaly. American Journal of Medical Genetics Part A. 164(6). 1565–1570. 12 indexed citations
10.
Imtiaz, Faiqa, Mohamed H. Al‐Hamed, Zuhair N. Al‐Hassnan, et al.. (2014). Spectrum of Mutations in 60 Saudi Patients with Mut Methylmalonic Acidemia. JIMD Reports. 29. 39–46. 5 indexed citations
11.
Salih, Mustafa A., Emeline Mundwiller, Arif O. Khan, et al.. (2013). New Findings in a Global Approach to Dissect the Whole Phenotype of PLA2G6 Gene Mutations. PLoS ONE. 8(10). e76831–e76831. 38 indexed citations
12.
Salih, Mustafa A., Emeline Mundwiller, Arif O. Khan, et al.. (2013). Correction: New Findings in a Global Approach to Dissect the Whole Phenotype of PLA2G6 Gene Mutations. PLoS ONE. 8(11). 6 indexed citations
13.
Ramzan, Khushnooda, et al.. (2013). Homozygosity mapping identifies a novel GIPC3 mutation causing congenital nonsyndromic hearing loss in a Saudi family. Gene. 521(1). 195–199. 18 indexed citations
14.
Shaheen, Ranad, Anas M. Alazami, Muneera Alshammari, et al.. (2012). Study of autosomal recessive osteogenesis imperfecta in Arabia reveals a novel locus defined by TMEM38B mutation. Journal of Medical Genetics. 49(10). 630–635. 108 indexed citations
15.
Khalifa, Ola, Faiqa Imtiaz, Zuhair N. Al‐Hassnan, et al.. (2012). A recessive form of Marshall syndrome is caused by a mutation in the COL11A1 gene: Figure 1. Journal of Medical Genetics. 49(4). 246–248. 14 indexed citations
16.
Aldahmesh, Mohammed A., Arif O. Khan, Jawahir Y. Mohamed, et al.. (2012). Genomic analysis of pediatric cataract in Saudi Arabia reveals novel candidate disease genes. Genetics in Medicine. 14(12). 955–962. 47 indexed citations
17.
Al‐Owain, Mohammed, et al.. (2012). Autism Spectrum Disorder in a Child with Propionic Acidemia. JIMD Reports. 7. 63–66. 51 indexed citations
18.
Al‐Owain, Mohammed, Namik Kaya, Hamad Alzaidan, et al.. (2010). Renal Failure Associated with APECED and Terminal 4q Deletion: Evidence of Autoimmune Nephropathy. Journal of Immunology Research. 2010(1). 586342–586342. 12 indexed citations
19.
Shaheen, Ranad, Mohammed Al‐Owain, Mustafa A. Salih, et al.. (2010). Clinical, biochemical and molecular characterization of peroxisomal diseases in Arabs. Clinical Genetics. 79(1). 60–70. 14 indexed citations
20.
Al‐Owain, Mohammed, Salma M. Wakil, Mansoor A. Haider, et al.. (2010). Novel homozygous mutation in DSP causing skin fragility-woolly hair syndrome: report of a large family and review of the desmoplakin-related phenotypes. Clinical Genetics. 80(1). 50–58. 18 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.

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