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Connection

T. Conrad Gilliam to Muscular Atrophy, Spinal

This is a "connection" page, showing publications T. Conrad Gilliam has written about Muscular Atrophy, Spinal.
Connection Strength

1.319
  1. Extensive DNA deletion associated with severe disease alleles on spinal muscular atrophy homologues. Ann Neurol. 1997 Jul; 42(1):41-9.
    View in: PubMed
    Score: 0.153
  2. Characterization of survival motor neuron (SMNT) gene deletions in asymptomatic carriers of spinal muscular atrophy. Hum Mol Genet. 1996 Mar; 5(3):359-65.
    View in: PubMed
    Score: 0.140
  3. Autosomal dominant distal spinal muscular atrophy in four generations. Neurology. 1995 Apr; 45(4):699-704.
    View in: PubMed
    Score: 0.131
  4. Is the spinal muscular atrophy gene found? Nat Med. 1995 Feb; 1(2):124-7.
    View in: PubMed
    Score: 0.130
  5. Linkage disequilibrium and haplotype analysis among Polish families with spinal muscular atrophy. Am J Hum Genet. 1995 Jan; 56(1):210-5.
    View in: PubMed
    Score: 0.129
  6. Refinement of the spinal muscular atrophy locus to the interval between D5S435 and MAP1B. Genomics. 1993 Feb; 15(2):365-71.
    View in: PubMed
    Score: 0.113
  7. Spinal muscular atrophy is not the result of mutations at the beta-hexosaminidase or GM2-activator locus. Neurology. 1991 Sep; 41(9):1418-22.
    View in: PubMed
    Score: 0.102
  8. Genetic analysis of childhood-onset spinal muscular atrophy. Adv Neurol. 1991; 56:181-7.
    View in: PubMed
    Score: 0.098
  9. Genetic homogeneity between acute and chronic forms of spinal muscular atrophy. Nature. 1990 Jun 28; 345(6278):823-5.
    View in: PubMed
    Score: 0.094
  10. Differential SMN2 expression associated with SMA severity. Nat Genet. 1998 Nov; 20(3):230-1.
    View in: PubMed
    Score: 0.042
  11. A multicopy transcription-repair gene, BTF2p44, maps to the SMA region and demonstrates SMA associated deletions. Hum Mol Genet. 1997 Feb; 6(2):229-36.
    View in: PubMed
    Score: 0.037
  12. Expressed cadherin pseudogenes are localized to the critical region of the spinal muscular atrophy gene. Proc Natl Acad Sci U S A. 1995 Apr 25; 92(9):3702-6.
    View in: PubMed
    Score: 0.033
  13. An investigation of genetic heterogeneity and linkage disequilibrium in 161 families with spinal muscular atrophy. Genomics. 1994 May 01; 21(1):27-33.
    View in: PubMed
    Score: 0.031
  14. Assessment of nonallelic genetic heterogeneity of chronic (type II and III) spinal muscular atrophy. Hum Hered. 1993 Nov-Dec; 43(6):380-7.
    View in: PubMed
    Score: 0.030
  15. High resolution physical map of the region surrounding the spinal muscular atrophy gene. Hum Mol Genet. 1993 Aug; 2(8):1169-76.
    View in: PubMed
    Score: 0.029
  16. Mapping of human microtubule-associated protein 1B in proximity to the spinal muscular atrophy locus at 5q13. Proc Natl Acad Sci U S A. 1991 Sep 01; 88(17):7873-6.
    View in: PubMed
    Score: 0.026
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.