These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

102 related articles for article (PubMed ID: 15047638)

  • 21. Evidence for linkage of migraine in Rolandic epilepsy to known 1q23 FHM2 and novel 17q22 genetic loci.
    Addis L; Chiang T; Clarke T; Hardison H; Kugler S; Mandelbaum DE; Novotny E; Wolf S; Strug LJ; Pal DK
    Genes Brain Behav; 2014 Mar; 13(3):333-40. PubMed ID: 24286483
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Linkage analysis of factors underlying insulin resistance: Strong Heart Family Study.
    North KE; Almasy L; Göring HH; Cole SA; Diego VP; Laston S; Cantu T; Williams JT; Howard BV; Lee ET; Best LG; Fabsitz RR; MacCluer JW
    Obes Res; 2005 Nov; 13(11):1877-84. PubMed ID: 16339117
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Variation in the lamin A/C gene: associations with metabolic syndrome.
    Steinle NI; Kazlauskaite R; Imumorin IG; Hsueh WC; Pollin TI; O'Connell JR; Mitchell BD; Shuldiner AR
    Arterioscler Thromb Vasc Biol; 2004 Sep; 24(9):1708-13. PubMed ID: 15205219
    [TBL] [Abstract][Full Text] [Related]  

  • 24. The metabolic syndrome in overweight Hispanic youth and the role of insulin sensitivity.
    Cruz ML; Weigensberg MJ; Huang TT; Ball G; Shaibi GQ; Goran MI
    J Clin Endocrinol Metab; 2004 Jan; 89(1):108-13. PubMed ID: 14715836
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Expanded genomewide scan implicates a novel locus at 3q28 among Caribbean hispanics with familial Alzheimer disease.
    Lee JH; Cheng R; Santana V; Williamson J; Lantigua R; Medrano M; Arriaga A; Stern Y; Tycko B; Rogaeva E; Wakutani Y; Kawarai T; St George-Hyslop P; Mayeux R
    Arch Neurol; 2006 Nov; 63(11):1591-8. PubMed ID: 17101828
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Genome-wide linkage scans for fasting glucose, insulin, and insulin resistance in the National Heart, Lung, and Blood Institute Family Blood Pressure Program: evidence of linkages to chromosome 7q36 and 19q13 from meta-analysis.
    An P; Freedman BI; Hanis CL; Chen YD; Weder AB; Schork NJ; Boerwinkle E; Province MA; Hsiung CA; Wu X; Quertermous T; Rao DC
    Diabetes; 2005 Mar; 54(3):909-14. PubMed ID: 15734873
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Heritability, parental transmission and environment correlation of pediatric-onset type 2 diabetes mellitus and metabolic syndrome-related traits.
    Miranda-Lora AL; Vilchis-Gil J; Molina-Díaz M; Flores-Huerta S; Klünder-Klünder M
    Diabetes Res Clin Pract; 2017 Apr; 126():151-159. PubMed ID: 28242438
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Strong evidence for a novel schizophrenia risk locus on chromosome 1p31.1 in homogeneous pedigrees from Tamil Nadu, India.
    Holliday EG; Nyholt DR; Tirupati S; John S; Ramachandran P; Ramamurti M; Ramadoss AJ; Jeyagurunathan A; Kottiswaran S; Smith HJ; Filippich C; Nertney DA; Nancarrow DJ; Hayward NK; Watkins WS; Jorde LB; Thara R; Mowry BJ
    Am J Psychiatry; 2009 Feb; 166(2):206-15. PubMed ID: 18829870
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Exclusion of chromosome 1q21-q31 from linkage to three pedigrees affected by the pigment-dispersion syndrome.
    Paglinauan C; Haines JL; Del Bono EA; Schuman J; Stawski S; Wiggs JL
    Am J Hum Genet; 1995 May; 56(5):1240-3. PubMed ID: 7726183
    [No Abstract]   [Full Text] [Related]  

  • 30. Suggestive linkage of familial primary cutaneous amyloidosis to a locus on chromosome 1q23.
    Lin MW; Lee DD; Lin CH; Huang CY; Wong CK; Chang YT; Liu HN; Hsiao KJ; Tsai SF
    Br J Dermatol; 2005 Jan; 152(1):29-36. PubMed ID: 15656797
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Comparison of linkage analysis methods for genome-wide scanning of extended pedigrees, with application to the TG/HDL-C ratio in the Framingham Heart Study.
    Horne BD; Malhotra A; Camp NJ;
    BMC Genet; 2003 Dec; 4 Suppl 1(Suppl 1):S93. PubMed ID: 14975161
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Evidence for a major gene for type II diabetes and linkage analyses with selected candidate genes in Mexican-Americans.
    Stern MP; Mitchell BD; Blangero J; Reinhart L; Krammerer CM; Harrison CR; Shipman PA; O'Connell P; Frazier ML; MacCluer JW
    Diabetes; 1996 May; 45(5):563-8. PubMed ID: 8621004
    [TBL] [Abstract][Full Text] [Related]  

  • 33. Evidence for linkage of postchallenge insulin levels with intestinal fatty acid-binding protein (FABP2) in Mexican-Americans.
    Mitchell BD; Kammerer CM; O'Connell P; Harrison CR; Manire M; Shipman P; Moyer MP; Stern MP; Frazier ML
    Diabetes; 1995 Sep; 44(9):1046-53. PubMed ID: 7657027
    [TBL] [Abstract][Full Text] [Related]  

  • 34. A gene for congenital generalized lipodystrophy maps to human chromosome 9q34.
    Garg A; Wilson R; Barnes R; Arioglu E; Zaidi Z; Gurakan F; Kocak N; O'Rahilly S; Taylor SI; Patel SB; Bowcock AM
    J Clin Endocrinol Metab; 1999 Sep; 84(9):3390-4. PubMed ID: 10487716
    [TBL] [Abstract][Full Text] [Related]  

  • 35. A new look at the genetic and environmental coherence of metabolic syndrome components.
    Panizzon MS; Hauger RL; Sailors M; Lyons MJ; Jacobson KC; Murray McKenzie R; Rana B; Vasilopoulos T; Vuoksimaa E; Xian H; Kremen WS; Franz CE
    Obesity (Silver Spring); 2015 Dec; 23(12):2499-507. PubMed ID: 26524476
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Metabolic syndrome and related variables, insulin resistance, leptin levels, and PPAR-γ2 and leptin gene polymorphisms in a pedigree of subjects with bipolar disorder.
    Baptista T; Sandia I; Fernandez E; Balzán L; Connell L; Uzcátegui E; Serrano A; Pabón A; Angeles F; Araque Y; Delgado H; González A; Alviarez Y; Piãero J; Baptista EA
    Braz J Psychiatry; 2015; 37(2):106-12. PubMed ID: 26083812
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Prevalence and characteristics of the metabolic syndrome in the San Antonio Heart and Framingham Offspring Studies.
    Meigs JB; Wilson PW; Nathan DM; D'Agostino RB; Williams K; Haffner SM
    Diabetes; 2003 Aug; 52(8):2160-7. PubMed ID: 12882936
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Correspondence between the adult treatment panel III criteria for metabolic syndrome and insulin resistance.
    Sierra-Johnson J; Johnson BD; Allison TG; Bailey KR; Schwartz GL; Turner ST
    Diabetes Care; 2006 Mar; 29(3):668-72. PubMed ID: 16505524
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Genome-wide scan for serum ghrelin detects linkage on chromosome 1p36 in Hispanic children: results from the Viva La Familia study.
    Voruganti VS; Göring HH; Diego VP; Cai G; Mehta NR; Haack K; Cole SA; Butte NF; Comuzzie AG
    Pediatr Res; 2007 Oct; 62(4):445-50. PubMed ID: 17667848
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Familial partial lipodystrophy: a monogenic form of the insulin resistance syndrome.
    Hegele RA
    Mol Genet Metab; 2000 Dec; 71(4):539-44. PubMed ID: 11136544
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 6.