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Mohammad Othman

Research Profile

Chemicals & Drugs

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Physiology

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Heterozygote

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Debra A Thompson; Zhijian Wu; Bo Chang; Peter Colosi; Garrett Grahek; Suja Hiriyanna; Lin Jia; Naheed W Khan; Hemant Khanna; Tiansen Li; Jacob Nellissery; Mohammad I Othman; Anand Swaroop; John R Heckenlively
Rd9 is a naturally occurring mouse model of a common form of retinitis pigmentosa caused by mutations in RPGR-ORF15.
Thiran Jayasundera; Kari E H Branham; Mohammad I Othman; William R Rhoades; Athanasios J Karoukis; Babak Behnam; Anand Swaroop; John R Heckenlively
RP2 phenotype and pathogenetic correlations in X-linked retinitis pigmentosa.
D M Wu; Babak Behnam; Pelin Atmaca Sonmez; Paul Sieving; Kari E H Branham; Mohammad I Othman; Anand Swaroop; Stephen P Daiger; John R Heckenlively
Long-term follow-up of a family with dominant X-linked retinitis pigmentosa.

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All Publications

2012: Debra A Thompson; Zhijian Wu; Bo Chang; Peter Colosi; Garrett Grahek; Suja Hiriyanna; Lin Jia; Naheed W Khan; Hemant Khanna; Tiansen Li; Jacob Nellissery; Mohammad I Othman; Anand Swaroop; John R Heckenlively
Rd9 is a naturally occurring mouse model of a common form of retinitis pigmentosa caused by mutations in RPGR-ORF15.
PloS one 2012;7(5):e35865.
2010: Thiran Jayasundera; Kari E H Branham; Mohammad I Othman; William R Rhoades; Athanasios J Karoukis; Babak Behnam; Anand Swaroop; John R Heckenlively
RP2 phenotype and pathogenetic correlations in X-linked retinitis pigmentosa.
Archives of ophthalmology 2010;128(7):915-23.
2010: D M Wu; Babak Behnam; Pelin Atmaca Sonmez; Paul Sieving; Kari E H Branham; Mohammad I Othman; Anand Swaroop; Stephen P Daiger; John R Heckenlively
Long-term follow-up of a family with dominant X-linked retinitis pigmentosa.
Eye (London, England) 2010;24(5):764-74.
2008: Alessandro Iannaccone; Mohammad I Othman; April D Cantrell; Barbara J Jennings; Kari E H Branham; Anand Swaroop
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 2008;613():221-7.
2007: Atsuhiro Kanda; Wei Chen; Mohammad I Othman; Kari E H Branham; Matthew Brooks; Ritu Khanna; Shirley He; Robert H Lyons Jr; Goncalo Abecasis; Anand Swaroop
A variant of mitochondrial protein LOC387715/ARMS2, not HTRA1, is strongly associated with age-related macular degeneration.
Proceedings of the National Academy of Sciences of the United States of America 2007;104(41):16227-32.
2007: Tomas S Aleman; Artur Vahe Cideciyan; Alexander Sumaroka; Sharon B Schwartz; Alejandro J Roman; Elizabeth A M Windsor; Janet D Steinberg; Kari E H Branham; Mohammad I Othman; Anand Swaroop; Samuel G Jacobson
Inner retinal abnormalities in X-linked retinitis pigmentosa with RPGR mutations.
Investigative ophthalmology & visual science 2007;48(10):4759-65.
2007: Jacque L Duncan; Yuhua Zhang; Jarel Gandhi; Chiaki Nakanishi; Mohammad I Othman; Kari E H Branham; Anand Swaroop; Austin Roorda
High-resolution imaging with adaptive optics in patients with inherited retinal degeneration.
Investigative ophthalmology & visual science 2007;48(7):3283-91.
2006: James S Friedman; Bo Chang; Chitra Kannabiran; Christina F Chakarova; Hardeep Pal Singh; Subhadra Jalali; Norman L Hawes; Kari E H Branham; Mohammad I Othman; Elena Filippova; Debra A Thompson; Andrew R Webster; Sten Andréasson; Samuel G Jacobson; Shomi S Bhattacharya; John R Heckenlively; Anand Swaroop
Premature truncation of a novel protein, RD3, exhibiting subnuclear localization is associated with retinal degeneration.
American journal of human genetics 2006;79(6):1059-70.
2006: Mingyao Li; Pelin Atmaca Sonmez; Mohammad I Othman; Kari E H Branham; Ritu Khanna; Michael S Wade; Yun Li; Liming Liang; Sepideh Zareparsi; Anand Swaroop; Goncalo Abecasis
CFH haplotypes without the Y402H coding variant show strong association with susceptibility to age-related macular degeneration.
Nature genetics 2006;38(9):1049-54.
2006: Frank W Rozsa; David Reed; Kathleen M Scott; Hemant Pawar; Sayoko E Moroi; Theresa Guckian Kijek; Charles M Krafchak; Mohammad I Othman; Douglas Vollrath; Victor M Elner; Julia E Richards
Gene expression profile of human trabecular meshwork cells in response to long-term dexamethasone exposure.
Molecular vision 2006;12():125-41.
2004: Brian P Brooks; Sayoko E Moroi; Catherine A Downs; Shannon Wiltse; Mohammad I Othman; Elena V Semina; Julia E Richards
A novel mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome.
Ophthalmic genetics 2004;25(1):57-62.
2002: Jindan YU; Mohammad I Othman; Rafal Farjo; Sepideh Zareparsi; Sean P MacNee; Shigeo Yoshida; Anand Swaroop
Evaluation and optimization of procedures for target labeling and hybridization of cDNA microarrays.
Molecular vision 2002;8():130-7.
2002: Rafal Farjo; Jindan YU; Mohammad I Othman; Shigeo Yoshida; Sujata Sheth; Thomas M Glaser; Wolfgang Baehr; Anand Swaroop
Mouse eye gene microarrays for investigating ocular development and disease.
Vision research 2002;42(4):463-70.
2002: Debra A Thompson; Christina L McHenry; Yun Li; Julia E Richards; Mohammad I Othman; Eberhard Schwinger; Douglas Vollrath; Samuel G Jacobson; Andreas Gal
Retinal dystrophy due to paternal isodisomy for chromosome 1 or chromosome 2, with homoallelism for mutations in RPE65 or MERTK, respectively.
American journal of human genetics 2002;70(1):224-9.
2000: Satoko Shimizu; Paul R Lichter; A Tim Johnson; Z Zhou; Misao Higashi; MS Gottfredsdottir; Mohammad I Othman; Sayoko E Moroi; Frank W Rozsa; Robert M Schertzer; M S Clarke; A L Schwartz; Catherine A Downs; Douglas Vollrath; Julia E Richards
Age-dependent prevalence of mutations at the GLC1A locus in primary open-angle glaucoma.
American journal of ophthalmology 2000;130(2):165-77.
1998: Mohammad I Othman; S A Sullivan; G L Skuta; D A Cockrell; Heather M Stringham; Catherine A Downs; A Fornés; A Mick; Michael Boehnke; Douglas Vollrath; Julia E Richards
Autosomal dominant nanophthalmos (NNO1) with high hyperopia and angle-closure glaucoma maps to chromosome 11.
American journal of human genetics 1998;63(5):1411-8.
1998: Frank W Rozsa; Satoko Shimizu; Paul R Lichter; A Tim Johnson; Mohammad I Othman; K Scott; Catherine A Downs; T D Nguyen; Jon R Polansky; Julia E Richards
GLC1A mutations point to regions of potential functional importance on the TIGR/MYOC protein.
Molecular vision 1998;4():20.
1998: Julia E Richards; Robert Ritch; Paul R Lichter; Frank W Rozsa; Heather M Stringham; R M Caronia; D Johnson; G P Abundo; J Willcockson; Catherine A Downs; Debra A Thompson; Maria A Musarella; N Gupta; Mohammad I Othman; D M Torrez; S B Herman; D J Wong; Misao Higashi; Michael Boehnke
Novel trabecular meshwork inducible glucocorticoid response mutation in an eight-generation juvenile-onset primary open-angle glaucoma pedigree.
Ophthalmology 1998;105(9):1698-707.
1997: Paul R Lichter; Julia E Richards; Michael Boehnke; Mohammad I Othman; B D Cameron; Heather M Stringham; Catherine A Downs; S B Lewis; B F Boyd
Juvenile glaucoma linked to the GLC1A gene on chromosome 1q in a Panamanian family.
American journal of ophthalmology 1997;123(3):413-6.
1996: Paul R Lichter; Julia E Richards; Michael Boehnke; Mohammad I Othman; B D Cameron; Heather M Stringham; Catherine A Downs; S B Lewis; B F Boyd
Juvenile glaucoma linked to GLCIA in a Panamanian family.
Transactions of the American Ophthalmological Society 1996;94():335-46; discussion 347-51.