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Connection

Nancy Jean Cox to Genetic Linkage

This is a "connection" page, showing publications Nancy Jean Cox has written about Genetic Linkage.
Connection Strength

3.187
  1. MERLIN...and the geneticist's stone? Nat Genet. 2002 Jan; 30(1):3-4.
    View in: PubMed
    Score: 0.183
  2. Computational issues in mapping variation affecting susceptibility to complex disorders: the chicken and the egg. Theor Popul Biol. 2001 Nov; 60(3):221-5.
    View in: PubMed
    Score: 0.181
  3. Seven regions of the genome show evidence of linkage to type 1 diabetes in a consensus analysis of 767 multiplex families. Am J Hum Genet. 2001 Oct; 69(4):820-30.
    View in: PubMed
    Score: 0.178
  4. Allele-sharing models: LOD scores and accurate linkage tests. Am J Hum Genet. 1997 Nov; 61(5):1179-88.
    View in: PubMed
    Score: 0.137
  5. Accurate inference of relationships in sib-pair linkage studies. Am J Hum Genet. 1997 Aug; 61(2):423-9.
    View in: PubMed
    Score: 0.135
  6. Pharmacogenomic variants have larger effect sizes than genetic variants associated with other dichotomous complex traits. Pharmacogenomics J. 2016 08; 16(4):388-92.
    View in: PubMed
    Score: 0.117
  7. Importance sampling. I. Computing multimodel p values in linkage analysis. Am J Hum Genet. 1992 Dec; 51(6):1413-29.
    View in: PubMed
    Score: 0.098
  8. Identifying plausible genetic models based on association and linkage results: application to type 2 diabetes. Genet Epidemiol. 2012 Dec; 36(8):820-8.
    View in: PubMed
    Score: 0.095
  9. Linkage studies on NIDDM and the insulin and insulin-receptor genes. Diabetes. 1989 May; 38(5):653-8.
    View in: PubMed
    Score: 0.076
  10. Segregation and linkage analyses of bipolar and major depressive illnesses in multigenerational pedigrees. J Psychiatr Res. 1989; 23(2):109-23.
    View in: PubMed
    Score: 0.074
  11. Linkage disequilibrium in the human insulin/insulin-like growth factor II region of human chromosome II. Am J Hum Genet. 1988 Oct; 43(4):495-501.
    View in: PubMed
    Score: 0.073
  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: 0.069
  13. Some effects of selection strategies on linkage analysis. Genet Epidemiol. 1988; 5(4):289-97.
    View in: PubMed
    Score: 0.069
  14. 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: 0.066
  15. Meta-analysis of 23 type 2 diabetes linkage studies from the International Type 2 Diabetes Linkage Analysis Consortium. Hum Hered. 2008; 66(1):35-49.
    View in: PubMed
    Score: 0.065
  16. Combined analysis of three whole genome linkage scans for Ankylosing Spondylitis. Rheumatology (Oxford). 2007 May; 46(5):763-71.
    View in: PubMed
    Score: 0.065
  17. Genetic studies of stuttering in a founder population. J Fluency Disord. 2007; 32(1):33-50.
    View in: PubMed
    Score: 0.065
  18. Coverage and characteristics of the Affymetrix GeneChip Human Mapping 100K SNP set. PLoS Genet. 2006 May; 2(5):e67.
    View in: PubMed
    Score: 0.062
  19. Haplotype structure and phylogenetic shadowing of a hypervariable region in the CAPN10 gene. Hum Genet. 2005 Jul; 117(2-3):258-66.
    View in: PubMed
    Score: 0.058
  20. Genomewide significant linkage to stuttering on chromosome 12. Am J Hum Genet. 2005 Apr; 76(4):647-51.
    View in: PubMed
    Score: 0.057
  21. Linkage analysis for psychiatric disorders. II. Methodological considerations. Psychiatr Dev. 1985; 3(4):369-82.
    View in: PubMed
    Score: 0.056
  22. Linkage analysis for psychiatric disorders. I. Basic concepts. Psychiatr Dev. 1985; 3(3):219-43.
    View in: PubMed
    Score: 0.056
  23. Human genetics: an expression of interest. Nature. 2004 Aug 12; 430(7001):733-4.
    View in: PubMed
    Score: 0.055
  24. Loci on chromosomes 6q and 6p interact to increase susceptibility to bipolar affective disorder in the national institute of mental health genetics initiative pedigrees. Biol Psychiatry. 2004 Jul 01; 56(1):18-23.
    View in: PubMed
    Score: 0.054
  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: 0.054
  26. Evidence for gene-environment interactions in a linkage study of asthma and smoking exposure. J Allergy Clin Immunol. 2003 Apr; 111(4):840-6.
    View in: PubMed
    Score: 0.050
  27. A statistical method for identification of polymorphisms that explain a linkage result. Am J Hum Genet. 2002 Feb; 70(2):399-411.
    View in: PubMed
    Score: 0.046
  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: 0.045
  29. Genomewide screen and identification of gene-gene interactions for asthma-susceptibility loci in three U.S. populations: collaborative study on the genetics of asthma. Am J Hum Genet. 2001 Jun; 68(6):1437-46.
    View in: PubMed
    Score: 0.044
  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: 0.042
  31. Genome-wide screen for atopy susceptibility alleles in the Hutterites. Clin Exp Allergy. 1999 Dec; 29 Suppl 4:11-5.
    View in: PubMed
    Score: 0.040
  32. Loci on chromosomes 2 (NIDDM1) and 15 interact to increase susceptibility to diabetes in Mexican Americans. Nat Genet. 1999 Feb; 21(2):213-5.
    View in: PubMed
    Score: 0.037
  33. The genetics of asthma. Mapping genes for complex traits in founder populations. Clin Exp Allergy. 1998 Apr; 28 Suppl 1:101-5; discussion 108-10.
    View in: PubMed
    Score: 0.035
  34. 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: 0.034
  35. Evidence of linkage between the serotonin transporter and autistic disorder. Mol Psychiatry. 1997 May; 2(3):247-50.
    View in: PubMed
    Score: 0.033
  36. Localization of MODY3 to a 5-cM region of human chromosome 12. Diabetes. 1995 Dec; 44(12):1408-13.
    View in: PubMed
    Score: 0.030
  37. Linkage studies in NIDDM with markers near the sulphonylurea receptor gene. Diabetologia. 1995 Dec; 38(12):1479-81.
    View in: PubMed
    Score: 0.030
  38. 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: 0.029
  39. A genome-wide sib-pair scan for quantitative language traits reveals linkage to chromosomes 10 and 13. Genes Brain Behav. 2015 Jun; 14(5):387-97.
    View in: PubMed
    Score: 0.029
  40. Linkage of familial dysalbuminemic hyperthyroxinemia to the albumin gene in a large Amish kindred. J Clin Endocrinol Metab. 1995 Jan; 80(1):116-21.
    View in: PubMed
    Score: 0.028
  41. Sequential imputation for multilocus linkage analysis. Proc Natl Acad Sci U S A. 1994 Nov 22; 91(24):11684-8.
    View in: PubMed
    Score: 0.028
  42. Stuttering: a complex behavioral disorder for our times? Am J Med Genet. 1993 Dec 15; 48(4):177-8.
    View in: PubMed
    Score: 0.026
  43. Sequential imputation and multipoint linkage analysis. Genet Epidemiol. 1993; 10(6):483-8.
    View in: PubMed
    Score: 0.025
  44. Linkage analysis with adjustment for covariates: a method combining peeling with Gibbs sampling. Cytogenet Cell Genet. 1992; 59(2-3):208-10.
    View in: PubMed
    Score: 0.023
  45. Germline BAP1 mutations predispose to malignant mesothelioma. Nat Genet. 2011 Aug 28; 43(10):1022-5.
    View in: PubMed
    Score: 0.022
  46. 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: 0.022
  47. Genetic linkage studies of thyroid peroxidase (TPO) gene in families with TPO deficiency. J Clin Endocrinol Metab. 1991 Feb; 72(2):471-6.
    View in: PubMed
    Score: 0.021
  48. Linkage studies of maturity onset diabetes of the young--R.W. pedigree. Diabetologia. 1988 Oct; 31(10):778.
    View in: PubMed
    Score: 0.018
  49. Insulin gene mutations as a cause of permanent neonatal diabetes. Proc Natl Acad Sci U S A. 2007 Sep 18; 104(38):15040-4.
    View in: PubMed
    Score: 0.017
  50. Genomewide linkage scan of 409 European-ancestry and African American families with schizophrenia: suggestive evidence of linkage at 8p23.3-p21.2 and 11p13.1-q14.1 in the combined sample. Am J Hum Genet. 2006 Feb; 78(2):315-33.
    View in: PubMed
    Score: 0.015
  51. The linkage and association of the gene encoding upstream stimulatory factor 1 with type 2 diabetes and metabolic syndrome in the Chinese population. Diabetologia. 2005 Oct; 48(10):2018-24.
    View in: PubMed
    Score: 0.015
  52. Genome-wide scan for type 2 diabetes loci in Hong Kong Chinese and confirmation of a susceptibility locus on chromosome 1q21-q25. Diabetes. 2004 Jun; 53(6):1609-13.
    View in: PubMed
    Score: 0.014
  53. The detection of major loci by segregation and linkage analysis: a simulation study. Genet Epidemiol. 1984; 1(3):285-96.
    View in: PubMed
    Score: 0.013
  54. Genetic Analysis Workshop II: results of segregation analyses using POINTER and linkage analyses using LIPED. Genet Epidemiol. 1984; 1(2):167-70.
    View in: PubMed
    Score: 0.013
  55. Confirmed locus on chromosome 11p and candidate loci on 6q and 8p for the triglyceride and cholesterol traits of combined hyperlipidemia. Arterioscler Thromb Vasc Biol. 2003 Nov 01; 23(11):2070-7.
    View in: PubMed
    Score: 0.013
  56. Locus on chromosome 6p linked to elevated HDL cholesterol serum levels and to protection against premature atherosclerosis in a kindred with familial hypercholesterolemia. Circ Res. 2003 Mar 21; 92(5):569-76.
    View in: PubMed
    Score: 0.012
  57. Mapping genes influencing type 2 diabetes risk and BMI in Japanese subjects. Diabetes. 2003 Jan; 52(1):209-13.
    View in: PubMed
    Score: 0.012
  58. Genome-wide linkage analysis of families with obsessive-compulsive disorder ascertained through pediatric probands. Am J Med Genet. 2002 Jul 08; 114(5):541-52.
    View in: PubMed
    Score: 0.012
  59. Role of calpain-10 gene variants in familial type 2 diabetes in Caucasians. J Clin Endocrinol Metab. 2002 Feb; 87(2):650-4.
    View in: PubMed
    Score: 0.012
  60. Studies of association between the gene for calpain-10 and type 2 diabetes mellitus in the United Kingdom. Am J Hum Genet. 2001 Sep; 69(3):544-52.
    View in: PubMed
    Score: 0.011
  61. Comparative studies of wild-type and cold-mutant (temperature-sensitive) influenza viruses: nonrandom reassortment of genes during preparation of live virus vaccine candidates by recombination at 25 degrees between recent H3N2 and H1N1 epidemic strains and cold-adapted A/An Arbor/6/60. Virology. 1979 Aug; 97(1):190-4.
    View in: PubMed
    Score: 0.010
  62. Two different mutations in the thyroid peroxidase gene of a large inbred Amish kindred: power and limits of homozygosity mapping. J Clin Endocrinol Metab. 1999 Mar; 84(3):1061-71.
    View in: PubMed
    Score: 0.009
  63. 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: 0.009
  64. A second-generation screen of the human genome for susceptibility to insulin-dependent diabetes mellitus. Nat Genet. 1998 Jul; 19(3):292-6.
    View in: PubMed
    Score: 0.009
  65. 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
  66. 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: 0.008
  67. 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: 0.008
  68. 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: 0.007
  69. Isolation of a cDNA clone encoding a KATP channel-like protein expressed in insulin-secreting cells, localization of the human gene to chromosome band 21q22.1, and linkage studies with NIDDM. Diabetes. 1995 May; 44(5):592-6.
    View in: PubMed
    Score: 0.007
  70. 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: 0.006
  71. 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: 0.005
  72. 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: 0.004
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.