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PrintBrian P. Brooks, M.D., Ph.D.
Adjunct Investigator, National Human Genome Research Institute
Investigator and Chief, Pediatric, Developmental and Genetic Ophthalmology, NEI
Chang L, Blain D, Bertuzzi S, Brooks BP. Uveal coloboma: clinical and basic science update. Current Opinions in Ophthalmology, 17::447-70. 2006. [PubMed]
Blain D and Brooks BP. Molecular testing and genetic counseling in ophthalmology. Archives of Ophthalmology, 125:196-203. 2007. [PubMed]
Brooks BP, Larson DM, Chan CC, Kjellstron S, Smith RS, Crawford MA, Lamoreux L, Huizing M, Hess R, Jiao X, Hejtmancik FJ, Maminishkis A, John SWM, Bush R, Pavan WJ. Analysis of ocular hypopigmentation in Rab38cht/cht mice. Inv Ophthal Vis Sci, 48:3905-13. 2007. [PubMed]
Alur RR, Cox TA, Crawford MA, Gong X, Brooks BP. Optic nerve axon number in mouse is regulated by Pax2 in mouse. J-AAPOS, 12:117-21. 2008. [PubMed]
Asai-Coakwell M, French CR, Ye M, Garcha K, Bigot K, Perera AG, Staehling-Hampton K, Mema SC, Chanda B, Mushegian A, Bamforth S, Doschak MR, Li G, Dobbs MB, Giampietro PF, Brooks BP, Vijayalakshmi P, Sauvé Y, Abitbol M, Sundaresan P, van Heyningen V, Pourquié O, Underhill TM, Waskiewicz AJ, Lehmann OJ. Incomplete penetrance and phenotypic variability characterize Gdf6-attributable oculo-skeletal phenotypes. Hum Mol Genet, 15;18(6):1110-21. 2009. [PubMed]
Brown JD, Duuta S, Bharti K, Bonner RF, Munson PJ, Dawid IB, Akhtar AL, Onojafe IF, Alur RP, Gross JM, Hejtmancik JF, Jiao X, Chan WY, Brooks BP. Expression profiling during ocular development identifies two Nlz genes with a critical role in optic fissure closure. Proc National Acad Sci, USA, 3;106(5):1462-7. 2009. [PubMed]
Salchow DJ, Kohlhase J, Miller M, Kadon N, FitzGibbon EJ, Caruso RC, Brooks BP. Absent optic chiasm presenting with horizontal nystagmus. JPOS, 47:187-91. 2010. [PubMed]
Alur RP, Camasamudram V, Brown JD, Onojafe IF, Sergeev YV, Jones M, Tang K, Lu H, Zia C, Gong X, Brooks BP. Papillorenal syndome-causing missense mutations in PAX2/Pax2 result in hypomorphic allelels in mouse and human. PloS Genetics, 6(3):e1000870. 2010. [PubMed]
Nichols L, Alur RP, Boobalan E, Caruso RC, Stone EM, Swaroop A, Johnson MA, Brooks BP. Two novel CRX mutant proteins causing autosomal dominant Leber congenital amaurosis interact differently with NRL. Human Mutation, 31:E1472-83. 2010. [PubMed]
Last Updated: October 31, 2010
