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Connection

Graeme Bell to Genetic Markers

This is a "connection" page, showing publications Graeme Bell has written about Genetic Markers.
Connection Strength

0.457
  1. Dinucleotide repeat polymorphism at D9S328E (EST hbc220). Hum Mol Genet. 1994 Feb; 3(2):387.
    View in: PubMed
    Score: 0.111
  2. Genetic variation in the gene encoding calpain-10 is associated with type 2 diabetes mellitus. Nat Genet. 2000 Oct; 26(2):163-75.
    View in: PubMed
    Score: 0.044
  3. Searching for NIDDM susceptibility genes: studies of genes with triplet repeats expressed in skeletal muscle. Diabetologia. 1996 Jun; 39(6):725-30.
    View in: PubMed
    Score: 0.033
  4. A yeast artificial chromosome-based map of the region of chromosome 20 containing the diabetes-susceptibility gene, MODY1, and a myeloid leukemia related gene. Proc Natl Acad Sci U S A. 1996 Apr 30; 93(9):3937-41.
    View in: PubMed
    Score: 0.032
  5. Chromosomal assignment and tissue distribution of novel expressed sequence tags from a human pancreatic islet cDNA library. Genomics. 1995 Sep 01; 29(1):276-81.
    View in: PubMed
    Score: 0.031
  6. Localization of the glucagon receptor gene to human chromosome band 17q25. Genomics. 1994 Mar 15; 20(2):327-8.
    View in: PubMed
    Score: 0.028
  7. Human somatostatin receptor genes: localization of SSTR5 to human chromosome 20p11.2. Genomics. 1993 Sep; 17(3):785-6.
    View in: PubMed
    Score: 0.027
  8. Identification of a simple tandem repeat DNA polymorphism in the human glycogen synthase gene and linkage to five markers on chromosome 19q. Diabetes. 1993 Jun; 42(6):930-2.
    View in: PubMed
    Score: 0.026
  9. Mapping diabetes-susceptibility genes. Lessons learned from search for DNA marker for maturity-onset diabetes of the young. Diabetes. 1992 Apr; 41(4):401-7.
    View in: PubMed
    Score: 0.024
  10. The 31-cM region of chromosome 11 including the obesity gene tubby and ATP-sensitive potassium channel genes, SUR1 and Kir6.2, does not contain a major susceptibility locus for NIDDM in 127 non-Hispanic white affected sibships. Diabetes. 1997 Jul; 46(7):1227-9.
    View in: PubMed
    Score: 0.009
  11. Identification of nine novel mutations in the hepatocyte nuclear factor 1 alpha gene associated with maturity-onset diabetes of the young (MODY3). Hum Mol Genet. 1997 Apr; 6(4):583-6.
    View in: PubMed
    Score: 0.009
  12. Exclusion of epidermal growth factor and high-resolution physical mapping across the Rieger syndrome locus. Am J Hum Genet. 1996 Dec; 59(6):1288-96.
    View in: PubMed
    Score: 0.008
  13. Maturity onset diabetes of the young (MODY). Diabet Med. 1996 Sep; 13(9 Suppl 6):S90-5.
    View in: PubMed
    Score: 0.008
  14. A genome-wide search for human non-insulin-dependent (type 2) diabetes genes reveals a major susceptibility locus on chromosome 2. Nat Genet. 1996 Jun; 13(2):161-6.
    View in: PubMed
    Score: 0.008
  15. Identification of microsatellite markers near the human genes encoding the beta-cell ATP-sensitive K+ channel and linkage studies with NIDDM in Japanese. Diabetes. 1996 Feb; 45(2):267-9.
    View in: PubMed
    Score: 0.008
  16. Linkage studies in NIDDM with markers near the sulphonylurea receptor gene. Diabetologia. 1995 Dec; 38(12):1479-81.
    View in: PubMed
    Score: 0.008
  17. Candidate gene studies in pedigrees with maturity-onset diabetes of the young not linked with glucokinase. Diabetologia. 1995 Sep; 38(9):1055-60.
    View in: PubMed
    Score: 0.008
  18. Identification of microsatellite markers near the human ob gene and linkage studies in NIDDM-affected sib pairs. Diabetes. 1995 Aug; 44(8):999-1001.
    View in: PubMed
    Score: 0.008
  19. Linkage and association between insulin-dependent diabetes mellitus (IDDM) susceptibility and markers near the glucokinase gene on chromosome 7. Nat Genet. 1995 Jun; 10(2):240-2.
    View in: PubMed
    Score: 0.008
  20. Localization of the gene encoding a neutral amino acid transporter-like protein to human chromosome band 19q13.3 and characterization of a simple sequence repeat DNA polymorphism. Genomics. 1994 Sep 15; 23(2):490-1.
    View in: PubMed
    Score: 0.007
  21. Abnormal insulin secretion, not insulin resistance, is the genetic or primary defect of MODY in the RW pedigree. Diabetes. 1994 Jan; 43(1):40-6.
    View in: PubMed
    Score: 0.007
  22. Linkage of Rieger syndrome to the region of the epidermal growth factor gene on chromosome 4. Nat Genet. 1992 Sep; 2(1):46-9.
    View in: PubMed
    Score: 0.006
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.