J BronwynBatemanMD

PubMed

• 2 citations
  Gender Diversity on Corporate Boards Associated with Ophthalmology.
  Dominique Alexis, Corrinne Fahl, Eve Higginbotham, J Bronwyn Bateman
  American Journal of Ophthalmology. 2022-07-01
• 19 citations
  Distinct ocular expression in infants and children with Down syndrome in Cairo, Egypt: myopia and heart disease.
  Hanan H. Afifi, Amira A. Abdel Azeem, Hala T. El-Bassyouni, Moataz E. Gheith, Akmal Rizk
  JAMA Ophthalmology. 2013-08-01
• 8 citations
  Duane retraction syndrome, nystagmus, retinal pigment epitheliopathy and epiretinal membrane with micro- and pachygyria, developmental delay, hearing loss and cranioph...
  Savino D'Amelio, Natalie Lassen, Vasilis Vasiliou, J. Bronwyn Bateman
  Ophthalmic Genetics. 2009-07-08

Journal Articles

• Distinct ocular expression in infants and children with down syndrome in Cairo, Egypt: myopia and heart disease  
  Afifi HH, Abdel Azeem AA, El-Bassyouni HT, Gheith ME, Rizk A, Bateman JB, JAMA Ophthalmol, 1/1/2013
• Duane retraction syndrome, nystagmus, retinal pigment epitheliopathy and epiretinal membrane with micro-and pachygyria, developmental delay, hearing loss and craniopha...  
  D'Amelio S, Lassen N, Vasiliou V, Bateman JB, Ophthalmic Genet, 1/1/2009
• Clinical variability of autosomal dominant cataract, microcornea and corneal opacity and novel mutation in the alpha A crystallin gene (CRYAA)  
  Richter L, Flodman P, Barria von-Bischhoffshaunsen FR, Brown S, Nguyen L, Turner J, Burch D, Spence MA, Bateman JB, Am J Med Genet A, 1/1/2008
• Multiple and additive functions of ALDH3A1 and ALDH1A1: cataract phenotype and ocular oxidative damage in Aldh3a1(-/-)/Aldh1a1(-/-) knock-out mice  
  Lassen N, Bateman JB, Estey T, Kuszak JR, Nees DW, Piatigorsky J, Duester G, Day BJ, Huang J, Hines LM, Vasiliou V, J Biol Chem, 6/13/2007
• Gene conversion mutation in crystallin, beta-B2 (CRYBB2) in a Chilean family with autosomal dominant cataract  
  Bateman JB, Barría von Bischoffshausen FR, Richter L, Flodman P, Burch D, Spence MA, Ophthalmology, 1/1/2007
• Autosomal dominant cataract: Intrafamilial phenotypic variability, interocular asymmetry, and variable progression in four Chilean families  
  Shafie, SM, Barria von-Bischhoffshaunsen FR, Bateman JB, Am J Ophthalmol, 1/1/2006
• Novel single-base deletional mutation in major intrinsic protein (MIP) in autosomal dominant cataract  
  Geyer DD, Spence MA, Johannes M, Flodman P, Clancy KP, Berry R, Sparkes RS, Jonsen MD, Isenberg SJ, Bateman JB, Am J Ophthalmol, 1/1/2006
• Erratum in: A new locus for autosomal dominant cataract on chromosome 19: Linkage analyses and screening of candidate gene  
  Bateman JB, Richter L, Flodman P, Burch D, Brown S, Penrose, Paul O, Geyer DD, Brooks DG, Spence MA, Invest Ophthalmol Vis Sci, 1/1/2006
• A new locus for autosomal dominant cataract on chromosome 19: Linkage analyses and screening of candidate genes  
  Bateman JB, Richter L, Flodman P, Burch D, Brown S, Penrose P, Paul O, Geyer DD, Brooks DG, Spence MA, Invest Ophthalmol Vis Sci, 1/1/2006
• Glycosylation type Ic disorder: idiopathic intracranial hypertension and retinal degeneration  
  Kahook MY, Thomas JA, Mandava N, Bateman JB, Br J Ophthalmol, 1/1/2005
• The Pan American Association of Ophthalmology  
  Bateman JB, Arch Ophthalmol, 10/1/2004
• Genetic aspects of strabismus  
  Ferreira R, Oelrich F, Bateman B, Arq Bras Oftalmol, 1/1/2002
• Infantile cataract in the Collaborative Perinatal Project: Prevalence and risk factors  
  San Giovanni JP, Chew EY, Reed GF, Remaley NA, Bateman JB, Sugimoto TA, Klebanoff MA, Arch Ophthalmol, 1/1/2002
• Eye disease and care in Latin America and the Caribbean  
  Silva JC, Bateman JB, Contreras F, Surv Ophthalmol, 1/1/2002
• Identification and functional consequences of a new mutation (E155G) in the gene for GCAP1 that causes autosomal dominant cone dystrophy  
  Wilkie SE, Li G, Deery EC, Newbold RJ, Garibaldi D, Bateman JB, Zhang H, Lin W, Zack DJ, Bhattacharya SS, Warren MJ, Hunt DM, Zhang K, Am J Hum Genet, 1/1/2001
• Comparison of measured astigmatic retinoscopies from different lid specula  
  Shea CJ, Westfall KC, MacKenzie T, Bateman JB, J Am Assoc Pediatr Ophthalmol Strab, 1/1/2001
• Acute megakayoblastic leukemia in Down syndrome  
  Olson JL, May MJ, Stork L, Kadan N, Bateman JB, Am J Ophthalmol, 1/1/2000
• A new bettaA1-crystallin splice junction mutation in autosomal dominant cataract  
  Bateman JB, Geyer DD, Flodman P, Johannes M, Sikela J, Walter N, Moreira AT, Clancy K, Spence MA, Invest Ophthalmol Vis Sci, 1/1/2000
• A new locus for autosomal dominant cataract on chromosome 12q13  
  Bateman JB, Johannes M, Flodman P, Geyer DD, Clancy KP, Heinzmann C, Kojis T, Berry R, Sparkes RS, Spence MA, Invest Ophthalmol Vis Sci, 1/1/2000
• Ocular colobomata  
  Onwochei BC, Simon JW, Bateman JB, Couture KC, Mir E, Surv Ophthalmol, 1/1/2000
• Selective B-wave reduction with congenital catatact in neurofibromatosis-2  
  Tong JT, Bateman JB, Ophthalmology, 1/1/1999
• Menkes disease: New ocular and electroretinographic findings  
  Ferreira RC, Heckenlively JR, Menkes JH, Bateman JB, Ophthalmology, 1/1/1998
• Comparison of fluorescent genotyping methods  
  Johannes M, Geyer DD, Berry R, Walter NAR, Sikela JM, Bateman JB, Anal Biochem, 1/1/1998
• Ophthalmologic findings in patients with ataxia  
  Rabiah PK, Bateman JB, Demer JL, Perlman S, Am J Ophthalmol, 1/1/1997
• Endogenous endophthalmitits caused by Streptococcus mitis  
  Harrison SA, Bateman, JB, Am J Ophthalmol, 1/1/1997
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