J B Kerrison

Summary

Affiliation: Johns Hopkins University
Country: USA

Publications

  1. ncbi request reprint A case-control study of tobacco and alcohol consumption in Leber hereditary optic neuropathy
    J B Kerrison
    Wilmer Ophthalmological Institute, Johns Hopkins Hospital, Baltimore, Maryland 21287, USA
    Am J Ophthalmol 130:803-12. 2000
  2. ncbi request reprint Neuro-ophthalmology of the phacomatoses
    J B Kerrison
    Wilmer Eye Institute, Johns Hopkins Hospital, Baltimore, Maryland, USA
    Curr Opin Ophthalmol 11:413-20. 2000
  3. ncbi request reprint Hereditary optic neuropathies
    J B Kerrison
    Wilmer Ophthalmological Institute, Johns Hopkins Hospital, Baltimore, Maryland, USA
    Ophthalmol Clin North Am 14:99-107. 2001
  4. ncbi request reprint A gene for autosomal dominant congenital nystagmus localizes to 6p12
    J B Kerrison
    Johns Hopkins Center for Hereditary Eye Diseases, Wilmer Ophthalmological Institute, Maumenee 517, Baltimore, Maryland, 21287 9237, USA
    Genomics 33:523-6. 1996
  5. ncbi request reprint Leber hereditary optic neuropathy. Electron microscopy and molecular genetic analysis of a case
    J B Kerrison
    Wilmer Eye Institute, Department of Pathology, Johns Hopkins Medical Institutions, Baltimore, Maryland, USA
    Ophthalmology 102:1509-16. 1995
  6. ncbi request reprint Genetic heterogeneity of dominant optic atrophy, Kjer type: Identification of a second locus on chromosome 18q12.2-12.3
    J B Kerrison
    Johns Hopkins Center for Hereditary Eye Diseases, Wilmer Eye Institute, Baltimore, MD, USA
    Arch Ophthalmol 117:805-10. 1999
  7. ncbi request reprint Clinical features of autosomal dominant congenital nystagmus linked to chromosome 6p12
    J B Kerrison
    Johns Hopkins Center for Hereditary Eye Diseases, Wilmer Ophthalmological Institute, Johns Hopkins Hospital, Baltimore, MD 21287 9237, USA
    Am J Ophthalmol 125:64-70. 1998
  8. ncbi request reprint Quantification of optic nerve axon loss associated with a relative afferent pupillary defect in the monkey
    J B Kerrison
    Wilmer Ophthalmological Institute, Johns Hopkins Hospital, Baltimore, MD, USA
    Arch Ophthalmol 119:1333-41. 2001
  9. ncbi request reprint Clinical and genetic analysis of a family with X-linked congenital nystagmus (NYS1)
    J B Kerrison
    Wilmer Ophthalmological Institute, Johns Hopkins Hospital, Baltimore, MD, USA
    Ophthalmic Genet 22:241-8. 2001

Detail Information

Publications9

  1. ncbi request reprint A case-control study of tobacco and alcohol consumption in Leber hereditary optic neuropathy
    J B Kerrison
    Wilmer Ophthalmological Institute, Johns Hopkins Hospital, Baltimore, Maryland 21287, USA
    Am J Ophthalmol 130:803-12. 2000
    ..To determine if tobacco or alcohol consumption is associated with vision loss among sibships harboring pathogenic mitochondrial mutations associated with Leber hereditary optic neuropathy...
  2. ncbi request reprint Neuro-ophthalmology of the phacomatoses
    J B Kerrison
    Wilmer Eye Institute, Johns Hopkins Hospital, Baltimore, Maryland, USA
    Curr Opin Ophthalmol 11:413-20. 2000
    ..This review provides an overview of the phacomatoses with emphasis on recent reports of significance to neuro-ophthalmology...
  3. ncbi request reprint Hereditary optic neuropathies
    J B Kerrison
    Wilmer Ophthalmological Institute, Johns Hopkins Hospital, Baltimore, Maryland, USA
    Ophthalmol Clin North Am 14:99-107. 2001
    ..Though a combination of family history, clinical presentation, age of onset, and associated findings may distinguish disorders, diagnosis may be facilitated by genetic testing...
  4. ncbi request reprint A gene for autosomal dominant congenital nystagmus localizes to 6p12
    J B Kerrison
    Johns Hopkins Center for Hereditary Eye Diseases, Wilmer Ophthalmological Institute, Maumenee 517, Baltimore, Maryland, 21287 9237, USA
    Genomics 33:523-6. 1996
    ..Haplotype analysis localizes the gene for autosomal dominant congenital motor nystagmus to an 18-cM region between D6S271 and D6S455...
  5. ncbi request reprint Leber hereditary optic neuropathy. Electron microscopy and molecular genetic analysis of a case
    J B Kerrison
    Wilmer Eye Institute, Department of Pathology, Johns Hopkins Medical Institutions, Baltimore, Maryland, USA
    Ophthalmology 102:1509-16. 1995
    ..Homoplasmy for mitochondrial mutations 4160 and 14484 in the leukocyte/platelet fraction of whole blood may correlate with homoplasmy in the optic nerve...
  6. ncbi request reprint Genetic heterogeneity of dominant optic atrophy, Kjer type: Identification of a second locus on chromosome 18q12.2-12.3
    J B Kerrison
    Johns Hopkins Center for Hereditary Eye Diseases, Wilmer Eye Institute, Baltimore, MD, USA
    Arch Ophthalmol 117:805-10. 1999
    ..To evaluate a family with autosomal dominant optic atrophy, which has been previously linked to the Kidd blood group...
  7. ncbi request reprint Clinical features of autosomal dominant congenital nystagmus linked to chromosome 6p12
    J B Kerrison
    Johns Hopkins Center for Hereditary Eye Diseases, Wilmer Ophthalmological Institute, Johns Hopkins Hospital, Baltimore, MD 21287 9237, USA
    Am J Ophthalmol 125:64-70. 1998
    ..To describe the clinical features of a large pedigree with autosomal dominant congenital nystagmus linked to chromosome 6p12...
  8. ncbi request reprint Quantification of optic nerve axon loss associated with a relative afferent pupillary defect in the monkey
    J B Kerrison
    Wilmer Ophthalmological Institute, Johns Hopkins Hospital, Baltimore, MD, USA
    Arch Ophthalmol 119:1333-41. 2001
    ..To quantify the amount of optic nerve axonal loss associated with the presence of a mild relative afferent pupillary defect (RAPD) in an experimental monkey model...
  9. ncbi request reprint Clinical and genetic analysis of a family with X-linked congenital nystagmus (NYS1)
    J B Kerrison
    Wilmer Ophthalmological Institute, Johns Hopkins Hospital, Baltimore, MD, USA
    Ophthalmic Genet 22:241-8. 2001
    ..To describe a family with X-linked congenital nystagmus and identify the genetic interval within which the gene is located...