BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

474 related articles for article (PubMed ID: 19198613)

  • 1. Common variants on 9q22.33 and 14q13.3 predispose to thyroid cancer in European populations.
    Gudmundsson J; Sulem P; Gudbjartsson DF; Jonasson JG; Sigurdsson A; Bergthorsson JT; He H; Blondal T; Geller F; Jakobsdottir M; Magnusdottir DN; Matthiasdottir S; Stacey SN; Skarphedinsson OB; Helgadottir H; Li W; Nagy R; Aguillo E; Faure E; Prats E; Saez B; Martinez M; Eyjolfsson GI; Bjornsdottir US; Holm H; Kristjansson K; Frigge ML; Kristvinsson H; Gulcher JR; Jonsson T; Rafnar T; Hjartarsson H; Mayordomo JI; de la Chapelle A; Hrafnkelsson J; Thorsteinsdottir U; Kong A; Stefansson K
    Nat Genet; 2009 Apr; 41(4):460-4. PubMed ID: 19198613
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Common variants at 9q22.33, 14q13.3, and ATM loci, and risk of differentiated thyroid cancer in the French Polynesian population.
    Maillard S; Damiola F; Clero E; Pertesi M; Robinot N; Rachédi F; Boissin JL; Sebbag J; Shan L; Bost-Bezeaud F; Petitdidier P; Doyon F; Xhaard C; Rubino C; Blanché H; Drozdovitch V; Lesueur F; de Vathaire F
    PLoS One; 2015; 10(4):e0123700. PubMed ID: 25849217
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Fine-mapping of two differentiated thyroid carcinoma susceptibility loci at 9q22.33 and 14q13.3 detects novel candidate functional SNPs in Europeans from metropolitan France and Melanesians from New Caledonia.
    Tcheandjieu C; Lesueur F; Sanchez M; Baron-Dubourdieu D; Guizard AV; Mulot C; Laurent-Puig P; Schvartz C; Truong T; Guenel P
    Int J Cancer; 2016 Aug; 139(3):617-27. PubMed ID: 26991144
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Confirmation of papillary thyroid cancer susceptibility loci identified by genome-wide association studies of chromosomes 14q13, 9q22, 2q35 and 8p12 in a Chinese population.
    Wang YL; Feng SH; Guo SC; Wei WJ; Li DS; Wang Y; Wang X; Wang ZY; Ma YY; Jin L; Ji QH; Wang JC
    J Med Genet; 2013 Oct; 50(10):689-95. PubMed ID: 23847140
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Common variants at the 9q22.33, 14q13.3 and ATM loci, and risk of differentiated thyroid cancer in the Cuban population.
    Pereda CM; Lesueur F; Pertesi M; Robinot N; Lence-Anta JJ; Turcios S; Velasco M; Chappe M; Infante I; Bustillo M; García A; Clero E; Xhaard C; Ren Y; Maillard S; Damiola F; Rubino C; Salazar S; Rodriguez R; Ortiz RM; de Vathaire F
    BMC Genet; 2015 Mar; 16():22. PubMed ID: 25879635
    [TBL] [Abstract][Full Text] [Related]  

  • 6. rs965513 polymorphism as a common risk marker is associated with papillary thyroid cancer.
    Wang F; Yan D; Ji X; Han J; Chen M; Qiao H; Zhang S
    Oncotarget; 2016 Jul; 7(27):41336-41345. PubMed ID: 27191655
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Age at diagnosis and gender modify the risk of 9q22 and 14q13 polymorphisms for papillary thyroid carcinoma.
    Kula D; Kalemba M; Puch Z; Polańska J; Świerniak M; Rusinek D; Żebracka-Gala J; Kowalska M; Handkiewicz-Junak D; Kowal M; Tyszkiewicz T; Piasna E; Czarniecka A; Pawlaczek A; Krajewska J; Szpak-Ulczok S; Jarząb B
    Endokrynol Pol; 2017; 68(3):283-289. PubMed ID: 28660995
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Genome-wide association study identifies a novel susceptibility gene for serum TSH levels in Chinese populations.
    Zhan M; Chen G; Pan CM; Gu ZH; Zhao SX; Liu W; Wang HN; Ye XP; Xie HJ; Yu SS; Liang J; Gao GQ; Yuan GY; Zhang XM; Zuo CL; Su B; Huang W; Ning G; Chen SJ; Chen JL; Song HD;
    Hum Mol Genet; 2014 Oct; 23(20):5505-17. PubMed ID: 24852370
    [TBL] [Abstract][Full Text] [Related]  

  • 9. The common genetic variant rs944289 on chromosome 14q13.3 associates with risk of both malignant and benign thyroid tumors in the Japanese population.
    Rogounovitch TI; Bychkov A; Takahashi M; Mitsutake N; Nakashima M; Nikitski AV; Hayashi T; Hirokawa M; Ishigaki K; Shigematsu K; Bogdanova T; Matsuse M; Nishihara E; Minami S; Yamanouchi K; Ito M; Kawaguchi T; Kondo H; Takamura N; Ito Y; Miyauchi A; Matsuda F; Yamashita S; Saenko VA
    Thyroid; 2015 Mar; 25(3):333-40. PubMed ID: 25562676
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Discovery of common variants associated with low TSH levels and thyroid cancer risk.
    Gudmundsson J; Sulem P; Gudbjartsson DF; Jonasson JG; Masson G; He H; Jonasdottir A; Sigurdsson A; Stacey SN; Johannsdottir H; Helgadottir HT; Li W; Nagy R; Ringel MD; Kloos RT; de Visser MC; Plantinga TS; den Heijer M; Aguillo E; Panadero A; Prats E; Garcia-Castaño A; De Juan A; Rivera F; Walters GB; Bjarnason H; Tryggvadottir L; Eyjolfsson GI; Bjornsdottir US; Holm H; Olafsson I; Kristjansson K; Kristvinsson H; Magnusson OT; Thorleifsson G; Gulcher JR; Kong A; Kiemeney LA; Jonsson T; Hjartarson H; Mayordomo JI; Netea-Maier RT; de la Chapelle A; Hrafnkelsson J; Thorsteinsdottir U; Rafnar T; Stefansson K
    Nat Genet; 2012 Jan; 44(3):319-22. PubMed ID: 22267200
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Replication and Meta-Analysis of Common Gene Mutations in TTF1 and TTF2 with Papillary Thyroid Cancer.
    Gao Y; Chen F; Niu S; Lin S; Li S
    Medicine (Baltimore); 2015 Sep; 94(36):e1246. PubMed ID: 26356687
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genetic predisposition to papillary thyroid carcinoma: involvement of FOXE1, TSHR, and a novel lincRNA gene, PTCSC2.
    He H; Li W; Liyanarachchi S; Jendrzejewski J; Srinivas M; Davuluri RV; Nagy R; de la Chapelle A
    J Clin Endocrinol Metab; 2015 Jan; 100(1):E164-72. PubMed ID: 25303483
    [TBL] [Abstract][Full Text] [Related]  

  • 13. FOXE1 polymorphisms are associated with familial and sporadic nonmedullary thyroid cancer susceptibility.
    Tomaz RA; Sousa I; Silva JG; Santos C; Teixeira MR; Leite V; Cavaco BM
    Clin Endocrinol (Oxf); 2012 Dec; 77(6):926-33. PubMed ID: 22882326
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Fine mapping of 14q13 reveals novel variants associated with different histological subtypes of papillary thyroid carcinoma.
    Jendrzejewski J; Liyanarachchi S; Eiterman A; Thomas A; He H; Nagy R; Senter L; Sworczak K; de la Chapelle A
    Int J Cancer; 2019 Feb; 144(3):503-512. PubMed ID: 30350351
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Multiple functional variants in long-range enhancer elements contribute to the risk of SNP rs965513 in thyroid cancer.
    He H; Li W; Liyanarachchi S; Srinivas M; Wang Y; Akagi K; Wang Y; Wu D; Wang Q; Jin V; Symer DE; Shen R; Phay J; Nagy R; de la Chapelle A
    Proc Natl Acad Sci U S A; 2015 May; 112(19):6128-33. PubMed ID: 25918370
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genotype Analyses in the Japanese and Belarusian Populations Reveal Independent Effects of rs965513 and rs1867277 but Do Not Support the Role of FOXE1 Polyalanine Tract Length in Conferring Risk for Papillary Thyroid Carcinoma.
    Nikitski AV; Rogounovitch TI; Bychkov A; Takahashi M; Yoshiura KI; Mitsutake N; Kawaguchi T; Matsuse M; Drozd VM; Demidchik Y; Nishihara E; Hirokawa M; Miyauchi A; Rubanovich AV; Matsuda F; Yamashita S; Saenko VA
    Thyroid; 2017 Feb; 27(2):224-235. PubMed ID: 27824288
    [TBL] [Abstract][Full Text] [Related]  

  • 17. The polymorphism rs944289 predisposes to papillary thyroid carcinoma through a large intergenic noncoding RNA gene of tumor suppressor type.
    Jendrzejewski J; He H; Radomska HS; Li W; Tomsic J; Liyanarachchi S; Davuluri RV; Nagy R; de la Chapelle A
    Proc Natl Acad Sci U S A; 2012 May; 109(22):8646-51. PubMed ID: 22586128
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Thyroid cancer susceptibility polymorphisms: confirmation of loci on chromosomes 9q22 and 14q13, validation of a recessive 8q24 locus and failure to replicate a locus on 5q24.
    Jones AM; Howarth KM; Martin L; Gorman M; Mihai R; Moss L; Auton A; Lemon C; Mehanna H; Mohan H; Clarke SE; Wadsley J; Macias E; Coatesworth A; Beasley M; Roques T; Martin C; Ryan P; Gerrard G; Power D; Bremmer C; ; Tomlinson I; Carvajal-Carmona LG
    J Med Genet; 2012 Mar; 49(3):158-63. PubMed ID: 22282540
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Common genetic variant on 14q13.3 contributes to thyroid cancer susceptibility: evidence based on 12 studies.
    Zheng J; Li C; Wang C; Ai Z
    Mol Genet Genomics; 2015 Jun; 290(3):1125-33. PubMed ID: 25552255
    [TBL] [Abstract][Full Text] [Related]  

  • 20. MYH9 binds to lncRNA gene PTCSC2 and regulates FOXE1 in the 9q22 thyroid cancer risk locus.
    Wang Y; He H; Li W; Phay J; Shen R; Yu L; Hancioglu B; de la Chapelle A
    Proc Natl Acad Sci U S A; 2017 Jan; 114(3):474-479. PubMed ID: 28049826
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 24.