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Connection

Susannah Spiess to Polymorphism, Genetic

This is a "connection" page, showing publications Susannah Spiess has written about Polymorphism, Genetic.
Connection Strength

1.557
  1. Hypertriglyceridemia and the apolipoprotein CIII gene locus: lack of association with the variant insulin response element in Italian school children. Hum Genet. 1996 Nov; 98(5):557-66.
    View in: PubMed
    Score: 0.104
  2. An approach for identifying simple sequence repeat DNA polymorphisms near cloned cDNAs and genes. Linkage studies of the islet amyloid polypeptide/amylin and liver glycogen synthase genes and NIDDM. Diabetes. 1996 Mar; 45(3):291-4.
    View in: PubMed
    Score: 0.099
  3. Identification of a functional polymorphism of the human type 5 17beta-hydroxysteroid dehydrogenase gene associated with polycystic ovary syndrome. J Clin Endocrinol Metab. 2006 Jan; 91(1):270-6.
    View in: PubMed
    Score: 0.097
  4. Genetic variants in the calpain-10 gene and the development of type 2 diabetes in the Japanese population. J Hum Genet. 2005; 50(2):92-98.
    View in: PubMed
    Score: 0.092
  5. cDNA sequence and localization of polymorphic human cytosolic phosphoenolpyruvate carboxykinase gene (PCK1) to chromosome 20, band q13.31: PCK1 is not tightly linked to maturity-onset diabetes of the young. Hum Mol Genet. 1993 Jan; 2(1):1-4.
    View in: PubMed
    Score: 0.080
  6. Relationship of insulin receptor substrate-1 and -2 genotypes to phenotypic features of polycystic ovary syndrome. J Clin Endocrinol Metab. 2002 Sep; 87(9):4297-300.
    View in: PubMed
    Score: 0.078
  7. Insulin resistance is attenuated in women with polycystic ovary syndrome with the Pro(12)Ala polymorphism in the PPARgamma gene. J Clin Endocrinol Metab. 2002 Feb; 87(2):772-5.
    View in: PubMed
    Score: 0.075
  8. Germline polymorphisms discovered via a cell-based, genome-wide approach predict platinum response in head and neck cancers. Transl Res. 2011 May; 157(5):265-72.
    View in: PubMed
    Score: 0.070
  9. Parent-of-origin effects of the serotonin transporter gene associated with autism. Am J Med Genet B Neuropsychiatr Genet. 2011 Mar; 156(2):139-44.
    View in: PubMed
    Score: 0.069
  10. HLA-DR typing "at the DNA level": RFLPs and subtypes detected with a DR beta cDNA probe. Am J Hum Genet. 1988 Dec; 43(6):954-63.
    View in: PubMed
    Score: 0.060
  11. Variation of apolipoprotein-B gene is associated with obesity, high blood cholesterol levels, and increased risk of coronary heart disease. Lancet. 1988 Dec 24-31; 2(8626-8627):1442-6.
    View in: PubMed
    Score: 0.060
  12. Insulin-gene sharing in sib pairs with insulin-dependent diabetes mellitus: no evidence for linkage. Am J Hum Genet. 1988 Jan; 42(1):167-72.
    View in: PubMed
    Score: 0.056
  13. Identification of type 2 diabetes genes in Mexican Americans through genome-wide association studies. Diabetes. 2007 Dec; 56(12):3033-44.
    View in: PubMed
    Score: 0.055
  14. Influenza A virus haemagglutinin polymorphism: pleiotropic antigenic variants of A/Shanghai/11/87 (H3N2) virus selected as high yield reassortants. J Gen Virol. 1993 Jul; 74 ( Pt 7):1311-6.
    View in: PubMed
    Score: 0.041
  15. A study of CNVs as trait-associated polymorphisms and as expression quantitative trait loci. PLoS Genet. 2011 Feb 03; 7(2):e1001292.
    View in: PubMed
    Score: 0.035
  16. Polymorphisms of GLUT2 and GLUT4 genes. Use in evaluation of genetic susceptibility to NIDDM in blacks. Diabetes. 1990 Dec; 39(12):1534-42.
    View in: PubMed
    Score: 0.035
  17. 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: 0.034
  18. A calpain-10 gene polymorphism is associated with reduced muscle mRNA levels and insulin resistance. J Clin Invest. 2000 Oct; 106(7):R69-73.
    View in: PubMed
    Score: 0.034
  19. Apa I and Sst I RFLPs at the insulin-like growth factor II (IGF2) locus on chromosome 11. Nucleic Acids Res. 1988 Apr 25; 16(8):3599.
    View in: PubMed
    Score: 0.029
  20. Bgl II RFLP at the human erythrocyte/HepG2-type glucose transporter (GLUT) locus on chromosome 1. Nucleic Acids Res. 1987 Nov 11; 15(21):9101.
    View in: PubMed
    Score: 0.028
  21. Multiple Taq I RFLPs at the human manganese superoxide dismutase (S0D2) locus on chromosome 6. Nucleic Acids Res. 1987 Sep 25; 15(18):7654.
    View in: PubMed
    Score: 0.028
  22. 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: 0.025
  23. Recombinant mapping of the familial hyperinsulinism gene to an 0.8 cM region on chromosome 11p15.1 and demonstration of a founder effect in Ashkenazi Jews. Hum Mol Genet. 1995 May; 4(5):879-86.
    View in: PubMed
    Score: 0.023
  24. Genome-wide interrogation of longitudinal FEV1 in children with asthma. Am J Respir Crit Care Med. 2014 Sep 15; 190(6):619-27.
    View in: PubMed
    Score: 0.022
  25. Genome scan for loci linked to mite sensitivity: the Collaborative Study on the Genetics of Asthma (CSGA). Genes Immun. 2004 May; 5(3):226-31.
    View in: PubMed
    Score: 0.022
  26. Association of the calpain-10 gene with type 2 diabetes mellitus in a Mexican population. Mol Genet Metab. 2004 Feb; 81(2):122-6.
    View in: PubMed
    Score: 0.022
  27. Variants within the calpain-10 gene on chromosome 2q37 (NIDDM1) and relationships to type 2 diabetes, insulin resistance, and impaired acute insulin secretion among Scandinavian Caucasians. Diabetes. 2002 Dec; 51(12):3561-7.
    View in: PubMed
    Score: 0.020
  28. The importance of genealogy in determining genetic associations with complex traits. Am J Hum Genet. 2001 Nov; 69(5):1146-8.
    View in: PubMed
    Score: 0.018
  29. Gene for non-insulin-dependent diabetes mellitus (maturity-onset diabetes of the young subtype) is linked to DNA polymorphism on human chromosome 20q. Proc Natl Acad Sci U S A. 1991 Feb 15; 88(4):1484-8.
    View in: PubMed
    Score: 0.018
  30. A second-generation genomewide screen for asthma-susceptibility alleles in a founder population. Am J Hum Genet. 2000 Nov; 67(5):1154-62.
    View in: PubMed
    Score: 0.017
  31. Four RFLPs of the human insulin receptor gene: PstI, KpnI, RsaI (2 RFLPs). Nucleic Acids Res. 1989 Jan 25; 17(2):820.
    View in: PubMed
    Score: 0.015
  32. Four RFLPs of the human insulin receptor gene: PstI, KpnI, RsaI (2 RFLPs). Nucleic Acids Res. 1988 Aug 25; 16(16):8204.
    View in: PubMed
    Score: 0.015
  33. Relationship of EGFR mutations, expression, amplification, and polymorphisms to epidermal growth factor receptor inhibitors in the NCI60 cell lines. Clin Cancer Res. 2007 Nov 15; 13(22 Pt 1):6788-95.
    View in: PubMed
    Score: 0.014
  34. Genetic polymorphisms in uridine diphospho-glucuronosyltransferase 1A1 and breast cancer risk in Africans. Breast Cancer Res Treat. 2008 Jul; 110(2):367-76.
    View in: PubMed
    Score: 0.014
  35. A German genome-wide linkage scan for type 2 diabetes supports the existence of a metabolic syndrome locus on chromosome 1p36.13 and a type 2 diabetes locus on chromosome 16p12.2. Diabetologia. 2007 Jul; 50(7):1418-22.
    View in: PubMed
    Score: 0.013
  36. Relationship of calpain-10 genotype to phenotypic features of polycystic ovary syndrome. J Clin Endocrinol Metab. 2002 Apr; 87(4):1669-73.
    View in: PubMed
    Score: 0.009
  37. beta-cell transcription factors and diabetes: no evidence for diabetes-associated mutations in the gene encoding the basic helix-loop-helix transcription factor neurogenic differentiation 4 (NEUROD4) in Japanese patients with MODY. Diabetes. 2000 Nov; 49(11):1955-7.
    View in: PubMed
    Score: 0.009
  38. Genome-wide search for asthma susceptibility loci in a founder population. The Collaborative Study on the Genetics of Asthma. Hum Mol Genet. 1998 Sep; 7(9):1393-8.
    View in: PubMed
    Score: 0.007
  39. 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: 0.006
  40. Inheritance of human platelet thermolabile phenol sulfotransferase (TL PST) activity. Genet Epidemiol. 1988; 5(1):1-15.
    View in: PubMed
    Score: 0.004
  41. Lithium ion transport and affective disorders within families of bipolar patients. Identification of a major gene locus. Arch Gen Psychiatry. 1983 May; 40(5):545-52.
    View in: PubMed
    Score: 0.003
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.