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Connection

Christopher Aston to Pedigree

This is a "connection" page, showing publications Christopher Aston has written about Pedigree.
Connection Strength

0.162
  1. Lung cancer risk in families of nonsmoking probands: heterogeneity by age at diagnosis. Genet Epidemiol. 1999 Nov; 17(4):253-73.
    View in: PubMed
    Score: 0.042
  2. Inter- and intrafamilial variability in premature pubarche and polycystic ovary syndrome. Fertil Steril. 2002 Sep; 78(3):473-8.
    View in: PubMed
    Score: 0.013
  3. Evidence for a susceptibility gene (SLEH1) on chromosome 11q14 for systemic lupus erythematosus (SLE) families with hemolytic anemia. Proc Natl Acad Sci U S A. 2002 Sep 03; 99(18):11766-71.
    View in: PubMed
    Score: 0.013
  4. SLEB3 in systemic lupus erythematosus (SLE) is strongly related to SLE families ascertained through neuropsychiatric manifestations. Hum Genet. 2002 Jul; 111(1):54-8.
    View in: PubMed
    Score: 0.012
  5. Evidence for a susceptibility gene, SLEV1, on chromosome 17p13 in families with vitiligo-related systemic lupus erythematosus. Am J Hum Genet. 2001 Dec; 69(6):1401-6.
    View in: PubMed
    Score: 0.012
  6. Expression and penetrance of the hereditary pancreatitis phenotype in monozygotic twins. Gut. 2001 Apr; 48(4):542-7.
    View in: PubMed
    Score: 0.011
  7. Mutations in the cationic trypsinogen gene are associated with recurrent acute and chronic pancreatitis. Gastroenterology. 1997 Oct; 113(4):1063-8.
    View in: PubMed
    Score: 0.009
  8. Clinical characteristics of hereditary pancreatitis in a large family, based on high-risk haplotype. The Midwest Multicenter Pancreatic Study Group (MMPSG) Am J Gastroenterol. 1997 Jul; 92(7):1113-6.
    View in: PubMed
    Score: 0.009
  9. Fine mapping of an imprinted gene for familial nonchromaffin paragangliomas, on chromosome 11q23. Am J Hum Genet. 1997 Jan; 60(1):121-32.
    View in: PubMed
    Score: 0.009
  10. A gene for hereditary pancreatitis maps to chromosome 7q35. Gastroenterology. 1996 Jun; 110(6):1975-80.
    View in: PubMed
    Score: 0.008
  11. Craniosynostosis with autosomal dominant transmission in New Zealand white rabbits. J Craniofac Genet Dev Biol. 1996 Jan-Mar; 16(1):52-63.
    View in: PubMed
    Score: 0.008
  12. A gene for Crouzon craniofacial dysostosis maps to the long arm of chromosome 10. Nat Genet. 1994 Jun; 7(2):149-53.
    View in: PubMed
    Score: 0.007
  13. Familial iron overload with possible autosomal dominant inheritance. Aust N Z J Med. 1990 Jun; 20(3):226-30.
    View in: PubMed
    Score: 0.005
  14. A segregation and linkage study of classical and nonclassical 21-hydroxylase deficiency. Am J Hum Genet. 1988 Jun; 42(6):830-8.
    View in: PubMed
    Score: 0.005
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.