Connection

John Kerrison to Pedigree

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This is a "connection" page, showing publications John Kerrison has written about Pedigree.
John Kerrison
Connection Strength
0.221
Pedigree
  1. Clinical and genetic analysis of a family with X-linked congenital nystagmus (NYS1). Ophthalmic Genet. 2001 Dec; 22(4):241-8.
    View in: PubMed
    Score: 0.047
  2. Genetic heterogeneity of dominant optic atrophy, Kjer type: Identification of a second locus on chromosome 18q12.2-12.3. Arch Ophthalmol. 1999 Jun; 117(6):805-10.
    View in: PubMed
    Score: 0.039
  3. Congenital motor nystagmus linked to Xq26-q27. Am J Hum Genet. 1999 Feb; 64(2):600-7.
    View in: PubMed
    Score: 0.038
  4. Clinical features of autosomal dominant congenital nystagmus linked to chromosome 6p12. Am J Ophthalmol. 1998 Jan; 125(1):64-70.
    View in: PubMed
    Score: 0.035
  5. A gene for autosomal dominant congenital nystagmus localizes to 6p12. Genomics. 1996 May 01; 33(3):523-6.
    View in: PubMed
    Score: 0.032
  6. Leber hereditary optic neuropathy. Electron microscopy and molecular genetic analysis of a case. Ophthalmology. 1995 Oct; 102(10):1509-16.
    View in: PubMed
    Score: 0.030
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.