BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

179 related articles for article (PubMed ID: 31125406)

  • 1. TSC22D2 identified as a candidate susceptibility gene of multi-cancer pedigree using genome-wide linkage analysis and whole-exome sequencing.
    Xiao L; Wei F; Liang F; Li Q; Deng H; Tan S; Chen S; Xiong F; Guo C; Liao Q; Li X; Zhang W; Wu M; Zhou Y; Xiang B; Zhou M; Li X; Xiong W; Zeng Z; Li G
    Carcinogenesis; 2019 Jul; 40(7):819-827. PubMed ID: 31125406
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Linkage and exome analysis implicate multiple genes in non-syndromic intellectual disability in a large Swedish family.
    Lindholm Carlström E; Halvardson J; Etemadikhah M; Wetterberg L; Gustavson KH; Feuk L
    BMC Med Genomics; 2019 Nov; 12(1):156. PubMed ID: 31694657
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Pedigree with frontotemporal lobar degeneration--motor neuron disease and Tar DNA binding protein-43 positive neuropathology: genetic linkage to chromosome 9.
    Luty AA; Kwok JB; Thompson EM; Blumbergs P; Brooks WS; Loy CT; Dobson-Stone C; Panegyres PK; Hecker J; Nicholson GA; Halliday GM; Schofield PR
    BMC Neurol; 2008 Aug; 8():32. PubMed ID: 18755042
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genome-wide linkage scan of a pedigree with familial hypercholesterolemia suggests susceptibility loci on chromosomes 3q25-26 and 21q22.
    Wang X; Li X; Zhang YB; Zhang F; Sun L; Lin J; Wang DM; Wang LY
    PLoS One; 2011; 6(10):e24838. PubMed ID: 22022364
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Whole-Exome Sequencing Identifies Novel Variants that Co-segregates with Autosomal Recessive Retinal Degeneration in a Pakistani Pedigree.
    Biswas P; Naeem MA; Ali MH; Assir MZ; Khan SN; Riazuddin S; Hejtmancik JF; Riazuddin SA; Ayyagari R
    Adv Exp Med Biol; 2018; 1074():219-228. PubMed ID: 29721947
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Using linkage studies combined with whole-exome sequencing to identify novel candidate genes for familial colorectal cancer.
    Toma C; Díaz-Gay M; Franch-Expósito S; Arnau-Collell C; Overs B; Muñoz J; Bonjoch L; Soares de Lima Y; Ocaña T; Cuatrecasas M; Castells A; Bujanda L; Balaguer F; Cubiella J; Caldés T; Fullerton JM; Castellví-Bel S
    Int J Cancer; 2020 Mar; 146(6):1568-1577. PubMed ID: 31525256
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Evidence for rare and common genetic risk variants for schizophrenia at protein kinase C, alpha.
    Carroll LS; Williams NM; Moskvina V; Russell E; Norton N; Williams HJ; Peirce T; Georgieva L; Dwyer S; Grozeva D; Greene E; Farmer A; McGuffin P; Morris DW; Corvin A; Gill M; Rujescu D; Sham P; Holmans P; Jones I; Kirov G; Craddock N; O'Donovan MC; Owen MJ
    Mol Psychiatry; 2010 Nov; 15(11):1101-11. PubMed ID: 19786960
    [TBL] [Abstract][Full Text] [Related]  

  • 9. TGM6 identified as a novel causative gene of spinocerebellar ataxias using exome sequencing.
    Wang JL; Yang X; Xia K; Hu ZM; Weng L; Jin X; Jiang H; Zhang P; Shen L; Guo JF; Li N; Li YR; Lei LF; Zhou J; Du J; Zhou YF; Pan Q; Wang J; Wang J; Li RQ; Tang BS
    Brain; 2010 Dec; 133(Pt 12):3510-8. PubMed ID: 21106500
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Whole-genome Linkage Analysis and Sequence Analysis of Candidate Loci in Familial Breast Cancer.
    Marikkannu R; Aravidis C; Rantala J; Picelli S; Adamovic T; Keihas M; Liu T; Kontham V; Nilsson D; Lindblom A
    Anticancer Res; 2015 Jun; 35(6):3155-65. PubMed ID: 26026075
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Combinational analysis of linkage and exome sequencing identifies the causative mutation in a Chinese family with congenital cataract.
    Jia X; Zhang F; Bai J; Gao L; Zhang X; Sun H; Sun D; Guan R; Sun W; Xu L; Yue Z; Yu Y; Fu S
    BMC Med Genet; 2013 Oct; 14():107. PubMed ID: 24103489
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Positional cloning and comprehensive mutation analysis of a Japanese family with lithium-responsive bipolar disorder identifies a novel DOCK5 mutation.
    Umehara H; Nakamura M; Nagai M; Kato Y; Ueno SI; Sano A
    J Hum Genet; 2021 Mar; 66(3):243-249. PubMed ID: 32920599
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Functional Common and Rare
    Bao R; Ng A; Sasaki M; Esai Selvan M; Katti A; Lee H; Huang L; Skol AD; Lavarino C; Salvador H; Klein RJ; Gümüş ZH; Mora J; Onel K
    Cancer Prev Res (Phila); 2021 Apr; 14(4):441-454. PubMed ID: 33419763
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genome-wide scan for hypertension linkage to chromosome 12q23.1 - q23.3 in a Chinese family.
    Dong Y; Yang L; Fang F; Zhang J; Jiang G; Xu S
    Indian J Med Res; 2013 May; 137(5):935-41. PubMed ID: 23760380
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Novel susceptibility gene for late-onset NIDDM is localized to human chromosome 12q.
    Shaw JT; Lovelock PK; Kesting JB; Cardinal J; Duffy D; Wainwright B; Cameron DP
    Diabetes; 1998 Nov; 47(11):1793-6. PubMed ID: 9792550
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genetic analyses supporting colorectal, gastric, and prostate cancer syndromes.
    Wallander K; Liu W; von Holst S; Thutkawkorapin J; Kontham V; Forsberg A; Lindblom A; Lagerstedt-Robinson K
    Genes Chromosomes Cancer; 2019 Nov; 58(11):775-782. PubMed ID: 31334572
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. The locus for an inherited cataract in sheep maps to ovine chromosome 6.
    Wilson GR; Morton JD; Palmer DN; McEwan JC; Gately K; Anderson RM; Dodds KG
    Mol Vis; 2012; 18():1384-94. PubMed ID: 22690116
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genome-wide linkage scan for psoriasis susceptibility loci in multiplex Tunisian families.
    Ammar M; Bouchlaka-Souissi C; Helms CA; Zaraa I; Jordan CT; Anbunathan H; Bouhaha R; Kouidhi S; Doss N; Dhaoui R; Ben Osman A; Ben Ammar El Gaied A; Marrakchi R; Mokni M; Bowcock AM
    Br J Dermatol; 2013 Mar; 168(3):583-7. PubMed ID: 23013406
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Whole Exome Sequencing of Highly Aggregated Lung Cancer Families Reveals Linked Loci for Increased Cancer Risk on Chromosomes 12q, 7p, and 4q.
    Musolf AM; Moiz BA; Sun H; Pikielny CW; Bossé Y; Mandal D; de Andrade M; Gaba C; Yang P; Li Y; You M; Govindan R; Wilson RK; Kupert EY; Anderson MW; Schwartz AG; Pinney SM; Amos CI; Bailey-Wilson JE
    Cancer Epidemiol Biomarkers Prev; 2020 Feb; 29(2):434-442. PubMed ID: 31826912
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.