Mohammad Othman

Genetic variants near TIMP3 and high-density lipoprotein–associated loci influence susceptibility to age-related macular degeneration

Margaret A. Pericak-Vance, Nirubol Tosakulwong, Emily Y. Chew, 2010, Proceedings of the National Academy of Sciences.

Evidence of association of APOE with age‐related macular degeneration ‐ a pooled analysis of 15 studies

Lars G Fritsche, Ammarin Thakkinstian, Wei Chen, 2011, Human mutation.

Premature truncation of a novel protein, RD3, exhibiting subnuclear localization is associated with retinal degeneration.

Subhadra Jalali, Anand Swaroop, S. Jacobson, 2006, American journal of human genetics.

A variant of mitochondrial protein LOC387715/ARMS2, not HTRA1, is strongly associated with age-related macular degeneration

Gonçalo R. Abecasis, Anand Swaroop, Wei Chen, 2007, Proceedings of the National Academy of Sciences.

Phenotypic conservation in patients with X-linked retinitis pigmentosa caused by RPGR mutations.

Anand Swaroop, Paul A Sieving, P. Sieving, 2013, JAMA ophthalmology.

Identification of a Rare Coding Variant in Complement 3 Associated with Age-related Macular Degeneration

Margaret A. Pericak-Vance, David E. Larson, Elaine R. Mardis, 2013, Nature Genetics.

CFH haplotypes without the Y402H coding variant show strong association with susceptibility to age-related macular degeneration

Yun Li, Liming Liang, Anand Swaroop, 2006, Nature Genetics.