BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

144 related articles for article (PubMed ID: 21690246)

  • 1. Linkage and association analysis of hyperthyrotropinaemia in an Alpine population reveal two novel loci on chromosomes 3q28-29 and 6q26-27.
    Volpato CB; De Grandi A; Gögele M; Taliun D; Fuchsberger C; Facheris MF; Minelli C; Pattaro C; Pramstaller PP; Hicks AA
    J Med Genet; 2011 Aug; 48(8):549-56. PubMed ID: 21690246
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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]  

  • 3. Distinct loci on chromosome 1q21 and 6q22 predispose to familial nonmedullary thyroid cancer: a SNP array-based linkage analysis of 38 families.
    Suh I; Filetti S; Vriens MR; Guerrero MA; Tumino S; Wong M; Shen WT; Kebebew E; Duh QY; Clark OH
    Surgery; 2009 Dec; 146(6):1073-80. PubMed ID: 19958934
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Susceptibility locus on chromosome 1q23-25 for a schizophrenia subtype resembling deficit schizophrenia identified by latent class analysis.
    Holliday EG; McLean DE; Nyholt DR; Mowry BJ
    Arch Gen Psychiatry; 2009 Oct; 66(10):1058-67. PubMed ID: 19805696
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Objective prioritization of positional candidate genes at a quantitative trait locus for pre-eclampsia on 2q22.
    Moses EK; Fitzpatrick E; Freed KA; Dyer TD; Forrest S; Elliott K; Johnson MP; Blangero J; Brennecke SP
    Mol Hum Reprod; 2006 Aug; 12(8):505-12. PubMed ID: 16809377
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Evidence for a colorectal cancer susceptibility locus on chromosome 3q21-q24 from a high-density SNP genome-wide linkage scan.
    Kemp Z; Carvajal-Carmona L; Spain S; Barclay E; Gorman M; Martin L; Jaeger E; Brooks N; Bishop DT; Thomas H; Tomlinson I; Papaemmanuil E; Webb E; Sellick GS; Wood W; Evans G; Lucassen A; Maher ER; Houlston RS;
    Hum Mol Genet; 2006 Oct; 15(19):2903-10. PubMed ID: 16923799
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Linkage and association analyses of glaucoma related traits in a large pedigree from a Dutch genetically isolated population.
    Axenovich T; Zorkoltseva I; Belonogova N; van Koolwijk LM; Borodin P; Kirichenko A; Babenko V; Ramdas WD; Amin N; Despriet DD; Vingerling JR; Lemij HG; Oostra BA; Klaver CC; Aulchenko Y; van Duijn CM
    J Med Genet; 2011 Dec; 48(12):802-9. PubMed ID: 22058429
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetic mapping of a 17q chromosomal region linked to obesity phenotypes in the IRAS family study.
    Sutton BS; Langefeld CD; Campbell JK; Haffner SM; Norris JM; Scherzinger AL; Wagenknecht LE; Bowden DW
    Int J Obes (Lond); 2006 Sep; 30(9):1433-41. PubMed ID: 16520807
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Dissecting the locus heterogeneity of autism: significant linkage to chromosome 12q14.
    Ma DQ; Cuccaro ML; Jaworski JM; Haynes CS; Stephan DA; Parod J; Abramson RK; Wright HH; Gilbert JR; Haines JL; Pericak-Vance MA
    Mol Psychiatry; 2007 Apr; 12(4):376-84. PubMed ID: 17179998
    [TBL] [Abstract][Full Text] [Related]  

  • 11. [Linkage analysis of susceptibility loci in 2 target chromosomes in pedigrees with paranoid schizophrenia and undifferentiated schizophrenia].
    Zeng LP; Hu ZM; Mu LL; Mei GS; Lu XL; Zheng YJ; Li PJ; Zhang YX; Pan Q; Long ZG; Dai HP; Zhang ZH; Xia JH; Zhao JP; Xia K
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Jun; 28(3):256-60. PubMed ID: 21644218
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genome-wide linkage analysis in families with infantile hypertrophic pyloric stenosis indicates novel susceptibility loci.
    Svenningsson A; Söderhäll C; Persson S; Lundberg F; Luthman H; Chung E; Gardiner M; Kockum I; Nordenskjöld A
    J Hum Genet; 2012 Feb; 57(2):115-21. PubMed ID: 22158425
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Alcoholism susceptibility loci: confirmation studies in a replicate sample and further mapping.
    Foroud T; Edenberg HJ; Goate A; Rice J; Flury L; Koller DL; Bierut LJ; Conneally PM; Nurnberger JI; Bucholz KK; Li TK; Hesselbrock V; Crowe R; Schuckit M; Porjesz B; Begleiter H; Reich T
    Alcohol Clin Exp Res; 2000 Jul; 24(7):933-45. PubMed ID: 10923994
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Mapping a new familial thyroid epithelial neoplasia susceptibility locus to chromosome 8p23.1-p22 by high-density single-nucleotide polymorphism genome-wide linkage analysis.
    Cavaco BM; Batista PF; Sobrinho LG; Leite V
    J Clin Endocrinol Metab; 2008 Nov; 93(11):4426-30. PubMed ID: 18765515
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Identification and replication of a novel obesity locus on chromosome 1q24 in isolated populations of Cilento.
    Ciullo M; Nutile T; Dalmasso C; Sorice R; Bellenguez C; Colonna V; Persico MG; Bourgain C
    Diabetes; 2008 Mar; 57(3):783-90. PubMed ID: 18162505
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Linkage and potential association of obesity-related phenotypes with two genes on chromosome 12q24 in a female dizygous twin cohort.
    Wilson SG; Adam G; Langdown M; Reneland R; Braun A; Andrew T; Surdulescu GL; Norberg M; Dudbridge F; Reed PW; Sambrook PN; Kleyn PW; Spector TD
    Eur J Hum Genet; 2006 Mar; 14(3):340-8. PubMed ID: 16391564
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Identification of a major locus for Paget's disease on chromosome 10p13 in families of British descent.
    Lucas GJ; Riches PL; Hocking LJ; Cundy T; Nicholson GC; Walsh JP; Ralston SH
    J Bone Miner Res; 2008 Jan; 23(1):58-63. PubMed ID: 17907922
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genome-wide analysis of extended pedigrees confirms IL2-IL21 linkage and shows additional regions of interest potentially influencing coeliac disease risk.
    Einarsdottir E; Koskinen LL; de Kauwe AL; Dukes E; Mustalahti K; Balogh M; Korponay-Szabo IR; Kaukinen K; Kurppa K; Adány R; Pocsai Z; Széles G; Mäki M; Kere J; Saavalainen P
    Tissue Antigens; 2011 Dec; 78(6):428-37. PubMed ID: 22077623
    [TBL] [Abstract][Full Text] [Related]  

  • 19. A genome-wide association study of thyroid stimulating hormone and free thyroxine in Danish children and adolescents.
    Nielsen TR; Appel EV; Svendstrup M; Ohrt JD; Dahl M; Fonvig CE; Hollensted M; Have CT; Kadarmideen HN; Pedersen O; Hansen T; Holm JC; Grarup N
    PLoS One; 2017; 12(3):e0174204. PubMed ID: 28333968
    [TBL] [Abstract][Full Text] [Related]  

  • 20. An SNP linkage scan identifies significant Crohn's disease loci on chromosomes 13q13.3 and, in Jewish families, on 1p35.2 and 3q29.
    Shugart YY; Silverberg MS; Duerr RH; Taylor KD; Wang MH; Zarfas K; Schumm LP; Bromfield G; Steinhart AH; Griffiths AM; Kane SV; Barmada MM; Rotter JI; Mei L; Bernstein CN; Bayless TM; Langelier D; Cohen A; Bitton A; Rioux JD; Cho JH; Brant SR
    Genes Immun; 2008 Mar; 9(2):161-7. PubMed ID: 18246054
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 8.