Mohammad Othman

7.6k total citations
47 papers, 2.6k citations indexed

About

Mohammad Othman is a scholar working on Molecular Biology, Ophthalmology and Radiology, Nuclear Medicine and Imaging. According to data from OpenAlex, Mohammad Othman has authored 47 papers receiving a total of 2.6k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 23 papers in Ophthalmology and 10 papers in Radiology, Nuclear Medicine and Imaging. Recurrent topics in Mohammad Othman's work include Retinal Development and Disorders (19 papers), Retinal Diseases and Treatments (16 papers) and Glaucoma and retinal disorders (8 papers). Mohammad Othman is often cited by papers focused on Retinal Development and Disorders (19 papers), Retinal Diseases and Treatments (16 papers) and Glaucoma and retinal disorders (8 papers). Mohammad Othman collaborates with scholars based in United States, France and Netherlands. Mohammad Othman's co-authors include Anand Swaroop, Kari Branham, Gonçalo R. Abecasis, Ritu Khanna, Julia E. Richards, Patrick Couvreur, Ruxandra Gref, Douglas Vollrath, Atsuhiro Kanda and Matthew Brooks and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and ACS Nano.

In The Last Decade

Mohammad Othman

47 papers receiving 2.6k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Mohammad Othman United States	26	1.5k	1.3k	733	267	228	47	2.6k
Aparna Lakkaraju United States	19	693 0.4×	1.3k 1.0×	254 0.3×	72 0.3×	265 1.2×	34	1.8k
Ricardo F. Frausto United States	23	192 0.1×	1.3k 1.0×	492 0.7×	162 0.6×	199 0.9×	49	2.6k
Haiyan Gong United States	32	1.7k 1.1×	1.4k 1.1×	893 1.2×	110 0.4×	1.2k 5.3×	113	4.4k
Sven Schnichels Germany	21	718 0.5×	775 0.6×	405 0.6×	46 0.2×	85 0.4×	85	1.8k
Mark J. Cooper United States	31	268 0.2×	2.2k 1.6×	171 0.2×	672 2.5×	121 0.5×	55	2.8k
Renee C. Ryals United States	19	335 0.2×	1.4k 1.1×	127 0.2×	549 2.1×	34 0.1×	36	1.7k
Kyoko Okada Japan	24	186 0.1×	872 0.7×	184 0.3×	112 0.4×	728 3.2×	89	2.1k
Dayle H. Geroski United States	22	1.1k 0.7×	515 0.4×	1.1k 1.4×	50 0.2×	49 0.2×	48	2.0k
Eduardo H. Moriyama Canada	19	236 0.2×	519 0.4×	439 0.6×	87 0.3×	66 0.3×	39	2.0k
David M. Maurice United States	25	905 0.6×	279 0.2×	1.1k 1.5×	48 0.2×	60 0.3×	47	1.9k

Countries citing papers authored by Mohammad Othman

Since Specialization

Citations

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

Fields of papers citing papers by Mohammad Othman

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mohammad Othman

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

All Works

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20 of 20 papers shown

Ratnapriya, Rinki, İlhan E. Acar, Maartje J. Geerlings, et al.. (2020). Family-based exome sequencing identifies rare coding variants in age-related macular degeneration. Human Molecular Genetics. 29(12). 2022–2034. 24 indexed citations

Othman, Mohammad, et al.. (2020). Living Donor Liver Transplant in Patients With Budd-Chiari Syndrome: A Single-Center Experience at Our University Hospital. Experimental and Clinical Transplantation. 18(7). 796–802. 1 indexed citations

Fahim, Abigail T., Lori S. Sullivan, Sara J. Bowne, et al.. (2019). X-Chromosome Inactivation is a Biomarker of Clinical Severity in Female Carriers of X-linked Retinitis Pigmentosa. Investigative Ophthalmology & Visual Science. 60(9). 2961–2961. 1 indexed citations

Fahim, Abigail T., Lori S. Sullivan, Sara J. Bowne, et al.. (2019). X-Chromosome Inactivation Is a Biomarker of Clinical Severity in Female Carriers of RPGR-Associated X-Linked Retinitis Pigmentosa. Ophthalmology Retina. 4(5). 510–520. 33 indexed citations

Branham, Kari, Igor Kozak, Pooja Biswas, et al.. (2018). Identification of Novel Deletions as the Underlying Cause of Retinal Degeneration in Two Pedigrees. Advances in experimental medicine and biology. 1074. 229–236. 2 indexed citations

Lundy, Steven K., Enayat Nikoopour, Athanasios J. Karoukis, et al.. (2018). T Helper 1 Cellular Immunity Toward Recoverin Is Enhanced in Patients With Active Autoimmune Retinopathy. Frontiers in Medicine. 5. 249–249. 4 indexed citations

Zahid, Sarwar, Naheed Khan, Kari Branham, et al.. (2013). Phenotypic Conservation in Patients With X-Linked Retinitis Pigmentosa Caused byRPGRMutations. JAMA Ophthalmology. 131(8). 1016–1016. 30 indexed citations

Oliver, Verity F., Maria Franchina, Andrew E. Jaffe, et al.. (2013). Hypomethylation of the IL17RC Promoter in Peripheral Blood Leukocytes Is Not A Hallmark of Age-Related Macular Degeneration. Cell Reports. 5(6). 1527–1535. 37 indexed citations

Othman, Mohammad, Kari Branham, & John R. Heckenlively. (2011). Genetic Basis of Age-related Macular Degeneration. 4(2). 119–119. 1 indexed citations

10.

Branham, Kari, Mohammad Othman, Richard G. Weleber, et al.. (2010). X-Linked Recessive Mutations in Simplex Males With Retinitis Pigmentosa. Investigative Ophthalmology & Visual Science. 51(13). 1399–1399. 1 indexed citations

11.

Parapuram, Sunil K., Radu Cojocaru, Jessica R. Chang, et al.. (2010). Distinct Signature of Altered Homeostasis in Aging Rod Photoreceptors: Implications for Retinal Diseases. PLoS ONE. 5(11). e13885–e13885. 33 indexed citations

12.

Wu, David M., Pelin Atmaca-Sönmez, Paul A. Sieving, et al.. (2009). Long-term follow-up of a family with dominant X-linked retinitis pigmentosa. Eye. 24(5). 764–774. 26 indexed citations

13.

Iannaccone, Alessandro, et al.. (2007). Retinal Phenotype of an X-Linked Pseudo-usher Syndrome in Association with the G173R Mutation in the RPGR Gene. Advances in experimental medicine and biology. 613. 221–227. 3 indexed citations

14.

Rozsa, Frank W., David M. Reed, Kathleen M. Scott, et al.. (2006). Gene expression profile of human trabecular meshwork cells in response to long-term dexamethasone exposure.. PubMed. 12. 125–41. 103 indexed citations

15.

Friedman, James S., Bo Chang, Chitra Kannabiran, et al.. (2006). Premature Truncation of a Novel Protein, RD3, Exhibiting Subnuclear Localization Is Associated with Retinal Degeneration. The American Journal of Human Genetics. 79(6). 1059–1070. 95 indexed citations

16.

Brooks, Brian P., Sayoko E. Moroi, Catherine A. Downs, et al.. (2004). A novel mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome. Ophthalmic Genetics. 25(1). 57–62. 24 indexed citations

17.

Thompson, Debra A., Christina L. McHenry, Yun Li, et al.. (2002). Retinal Dystrophy Due to Paternal Isodisomy for Chromosome 1 or Chromosome 2, with Homoallelism for Mutations in RPE65 or MERTK, Respectively. The American Journal of Human Genetics. 70(1). 224–229. 103 indexed citations

18.

Shimizu, Satoko, Paul R. Lichter, A. Tim Johnson, et al.. (2000). Age-dependent prevalence of mutations at the GLC1A locus in primary open-angle glaucoma. American Journal of Ophthalmology. 130(2). 165–177. 158 indexed citations

19.

Rozsa, Frank W., Satoko Shimizu, Paul R. Lichter, et al.. (1998). GLC1A mutations point to regions of potential functional importance on the TIGR/MYOC protein.. PubMed. 4. 20–20. 89 indexed citations

20.

Chensue, Stephen W., Kelly Warmington, S D Hershey, et al.. (1993). Evolving T cell responses in murine schistosomiasis. Th2 cells mediate secondary granulomatous hypersensitivity and are regulated by CD8+ T cells in vivo.. The Journal of Immunology. 151(3). 1391–1400. 62 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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