J BronwynBatemanMD

PubMed

• 1 citations
  Gender Diversity on Corporate Boards Associated with Ophthalmology.
  Dominique Alexis, Corrinne Fahl, Eve Higginbotham, J Bronwyn Bateman> ;American Journal of Ophthalmology. 2022 Jul 1
• 18 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, J. Bronwyn Bateman> ;JAMA Ophthalmology. 2013 Aug 1
• 7 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 Jul 8
• 12 citations
  Recombinational event between Norrie disease and DXS7 loci.
  Julielani T. Ngo, M. Anne Spence, Victoria K. Cortessis, Robert S. Sparkes, J. Bronwyn Bateman> ;Clinical Genetics. 2008 Jun 28
• 39 citations
  Clinical variability of autosomal dominant cataract, microcornea and corneal opacity and novel mutation in the alpha A crystallin gene (CRYAA).
  L. Richter, Pamela Flodman, Fernando Barria von-Bischhoffshausen, D. Burch, Sandra E. Brown, Linda Nguyen, Julia Turner, M. Anne Spence, J. Bronwyn Bateman> ;American Journal of Medical Genetics. Part A. 2008 Apr 1
• 141 citations
  Multiple and Additive Functions of ALDH3A1 and ALDH1A1: CATARACT PHENOTYPE AND OCULAR OXIDATIVE DAMAGE IN Aldh3a1(−/−)/Aldh1a1(−/−) KNOCK-OUT MICE
  Natalie Lassen, J. Bronwyn Bateman, Tia Estey, Jer R. Kuszak, David W. Nees, Joram Piatigorsky, Gregg Duester, Brian J. Day, Jie Huang, Lisa M. Hines, Vasilis Vasiliou> ;The Journal of Biological Chemistry. 2007 Aug 31
• 29 citations
  Gene Conversion Mutation in Crystallin, β-B2 (CRYBB2) in a Chilean Family with Autosomal Dominant Cataract
  J. Bronwyn Bateman, Fernando R. Barria von-Bischhoffshaunsen, Leslie Richter, Pamela Flodman, Douglas Burch, M. Anne Spence> ;Ophthalmology. 2007 Mar 1
• 8 citations
  A new locus for autosomal dominant cataract on chromosome 19: linkage analyses and screening of candidate genes.
  J. Bronwyn Bateman, L. Richter, Pamela Flodman, D. Burch, Sandra E. Brown, Philip Penrose, Otis Paul, David D. Geyer, David G. Brooks, M. Anne Spence> ;Investigative Ophthalmology & Visual Science. 2006 Aug 1
• 53 citations
  Novel single-base deletional mutation in major intrinsic protein (MIP) in autosomal dominant cataract.
  David D. Geyer, M. Anne Spence, Meriam Johannes, Pamela Flodman, Kevin P. Clancy, Rebecca Berry, Robert S. Sparkes, Matthew D. Jonsen, Sherwin J. Isenberg, J. Bronwyn ...> ;American Journal of Ophthalmology. 2006 Apr 1
• 8 citations
  Autosomal Dominant Cataract: Intrafamilial Phenotypic Variability, Interocular Asymmetry, and Variable Progression in Four Chilean Families
  Suraiya M. Shafie, Fernando Barria von-Bischhoffshausen, J. Bronwyn Bateman> ;American Journal of Ophthalmology. 2006 Apr 1
• 1 citations
  The Pan American Association of Ophthalmology
  J. Bronwyn Bateman> ;Archives of Ophthalmology. 2004 Oct 1
• 41 citations
  Infantile Cataract in the Collaborative Perinatal Project: Prevalence and Risk Factors
  John Paul SanGiovanni, Emily Y. Chew, George F. Reed, Nancy A. Remaley, J. Bronwyn Bateman, Tina A. Sugimoto, Mark A. Klebanoff> ;Archives of Ophthalmology. 2002 Nov 1
• 23 citations
  Eye disease and care in Latin America and the Caribbean.
  Juan Carlos Silva, J. Bronwyn Bateman, Francisco Ganga Contreras> ;Survey of Ophthalmology. 2002 May 1
• 2 citations
  Comparison of measured astigmatic retinoscopies from different lid specula.
  Caroline J. Shea, Kelly Cooper Westfall, Todd MacKenzie, J. Bronwyn Bateman> ;Journal of AAPOS. 2001 Dec 1
• 87 citations
  Identification and functional consequences of a new mutation (E155G) in the gene for GCAP1 that causes autosomal dominant cone dystrophy.
  Susan E. Wilkie, Yang Li, Evelyne Deery, Richard J. Newbold, Daniel C. Garibaldi, J. Bronwyn Bateman, Heidi Zhang, Wei Lin, Donald J. Zack, Shomi S. Bhattacharya, Mart...> ;American Journal of Human Genetics. 2001 Sep 1
• 65 citations
  A New βA1-Crystallin Splice Junction Mutation in Autosomal Dominant Cataract
  J. Bronwyn Bateman, David D. Geyer, Pamela Flodman, Meriam Johannes, James M. Sikela, Nicole A.R. Walter, Ana Teresa Moreira, Kevin P. Clancy, M. Anne Spence> ;Investigative Ophthalmology & Visual Science. 2000 Oct 1
• 7 citations
  Acute megakaryoblastic leukemia in Down syndrome: orbital infiltration
  Jeffrey L. Olson, Michael J May, Linda C. Stork, Nina Kadan, J. Bronwyn Bateman> ;American Journal of Ophthalmology. 2000 Jul 1
• 3 citations
  Selective B-wave reduction with congenital cataract in neurofibromatosis-2.
  John T Tong, J. Bronwyn Bateman> ;Ophthalmology. 1999 Sep 1
• 8 citations
  Menkes disease: New ocular and electroretinographic findings
  Rosane C. Ferreira, John R. Heckenlively, John H. Menkes, J. Bronwyn Bateman> ;Ophthalmology. 1998 Jun 1
• 1 citations
  Electroretinography in incontinentia pigmenti.
  Rosane C. Ferreira, Caroline J. Shea, David W. Johnson, J. Bronwyn Bateman> ;Journal of AAPOS. 1997 Sep 1
• 11 citations
  Endogenous Endophthalmitis Caused by Streptococcus mitis
  Steven A. Harrison, J. Bronwyn Bateman> ;American Journal of Ophthalmology. 1997 Feb 1
• 17 citations
  Ophthalmologic Findings in Patients With Ataxia
  Peter Rabiah, J. Bronwyn Bateman, Joseph L. Demer, Susan Perlman> ;American Journal of Ophthalmology. 1997 Jan 1
• 2 citations
  Autosomal-dominant anomalies of the iris pigment epithelium
  Brian L. Lee, Andrea B. Lamer, J. Bronwyn Bateman> ;Ophthalmology. 1996 Oct 1
• 12 citations
  Posterior Segment Neovascularization Associated With Optic Nerve Aplasia
  Brian L. Lee, J. Bronwyn Bateman, Steven D. Schwartz> ;American Journal of Ophthalmology. 1996 Jul 1
• 26 citations
  Orbital Lesions in the Blue Rubber Bleb Nevus Syndrome
  Colin A. McCannel, Jonathan Hoenig, James Umlas, John J. Woog, Anita Newman, J. Bronwyn Bateman> ;Ophthalmology. 1996 Jun 1
• Join now to see all

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
• Join now to see all