J B Kerrison

Summary

Affiliation: Johns Hopkins University
Country: USA

Publications

  1. ncbi 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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...