BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

128 related articles for article (PubMed ID: 29581771)

  • 1. Genome-wide Association Study (GWAS) of Germline Copy Number Variations (CNVs) Reveal Genetic Risks of Prostate Cancer in Chinese population.
    Wu Y; Chen H; Jiang G; Mo Z; Ye D; Wang M; Qi J; Lin X; Zheng SL; Zhang N; Na R; Ding Q; Xu J; Sun Y
    J Cancer; 2018; 9(5):923-928. PubMed ID: 29581771
    [No Abstract]   [Full Text] [Related]  

  • 2. Genome-wide copy number analysis reveals candidate gene loci that confer susceptibility to high-grade prostate cancer.
    Poniah P; Mohd Zain S; Abdul Razack AH; Kuppusamy S; Karuppayah S; Sian Eng H; Mohamed Z
    Urol Oncol; 2017 Sep; 35(9):545.e1-545.e11. PubMed ID: 28527622
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genome-wide copy number variation analysis identified deletions in SFMBT1 associated with fasting plasma glucose in a Han Chinese population.
    Chung RH; Chiu YF; Hung YJ; Lee WJ; Wu KD; Chen HL; Lin MW; Chen YI; Quertermous T; Hsiung CA
    BMC Genomics; 2017 Aug; 18(1):591. PubMed ID: 28789618
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Rare CNVs in Suicide Attempt include Schizophrenia-Associated Loci and Neurodevelopmental Genes: A Pilot Genome-Wide and Family-Based Study.
    Sokolowski M; Wasserman J; Wasserman D
    PLoS One; 2016; 11(12):e0168531. PubMed ID: 28030616
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Increased genomic burden of germline copy number variants is associated with early onset breast cancer: Australian breast cancer family registry.
    Walker LC; Pearson JF; Wiggins GA; Giles GG; Hopper JL; Southey MC
    Breast Cancer Res; 2017 Mar; 19(1):30. PubMed ID: 28302160
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Inter- and intra-breed genome-wide copy number diversity in a large cohort of European equine breeds.
    Solé M; Ablondi M; Binzer-Panchal A; Velie BD; Hollfelder N; Buys N; Ducro BJ; François L; Janssens S; Schurink A; Viklund Å; Eriksson S; Isaksson A; Kultima H; Mikko S; Lindgren G
    BMC Genomics; 2019 Oct; 20(1):759. PubMed ID: 31640551
    [TBL] [Abstract][Full Text] [Related]  

  • 7. Rare copy-number variants as modulators of common disease susceptibility.
    Auwerx C; Jõeloo M; Sadler MC; Tesio N; Ojavee S; Clark CJ; Mägi R; ; Reymond A; Kutalik Z
    Genome Med; 2024 Jan; 16(1):5. PubMed ID: 38185688
    [TBL] [Abstract][Full Text] [Related]  

  • 8. A Genome-Wide Association Study to Identify Potential Germline Copy Number Variants for Sporadic Breast Cancer Susceptibility.
    Sapkota Y; Narasimhan A; Kumaran M; Sehrawat BS; Damaraju S
    Cytogenet Genome Res; 2016; 149(3):156-164. PubMed ID: 27668787
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Copy number variations in Friesian horses and genetic risk factors for insect bite hypersensitivity.
    Schurink A; da Silva VH; Velie BD; Dibbits BW; Crooijmans RPMA; Franҫois L; Janssens S; Stinckens A; Blott S; Buys N; Lindgren G; Ducro BJ
    BMC Genet; 2018 Jul; 19(1):49. PubMed ID: 30060732
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Copy number variation associates with mortality in long-lived individuals: a genome-wide assessment.
    Nygaard M; Debrabant B; Tan Q; Deelen J; Andersen-Ranberg K; de Craen AJ; Beekman M; Jeune B; Slagboom PE; Christensen K; Christiansen L
    Aging Cell; 2016 Feb; 15(1):49-55. PubMed ID: 26446717
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Germline copy number variations are associated with breast cancer risk and prognosis.
    Kumaran M; Cass CE; Graham K; Mackey JR; Hubaux R; Lam W; Yasui Y; Damaraju S
    Sci Rep; 2017 Nov; 7(1):14621. PubMed ID: 29116104
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Genome-wide analysis identifies rare copy number variations associated with inflammatory bowel disease.
    Frenkel S; Bernstein CN; Sargent M; Kuang Q; Jiang W; Wei J; Thiruvahindrapuram B; Spriggs E; Scherer SW; Hu P
    PLoS One; 2019; 14(6):e0217846. PubMed ID: 31185018
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Copy Number Variation and Clinical Outcomes in Patients With Germline PTEN Mutations.
    Yehia L; Seyfi M; Niestroj LM; Padmanabhan R; Ni Y; Frazier TW; Lal D; Eng C
    JAMA Netw Open; 2020 Jan; 3(1):e1920415. PubMed ID: 32003824
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Genome-wide copy number variation (CNV) detection in Nelore cattle reveals highly frequent variants in genome regions harboring QTLs affecting production traits.
    da Silva JM; Giachetto PF; da Silva LO; Cintra LC; Paiva SR; Yamagishi ME; Caetano AR
    BMC Genomics; 2016 Jun; 17():454. PubMed ID: 27297173
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Population Structure, and Selection Signatures Underlying High-Altitude Adaptation Inferred From Genome-Wide Copy Number Variations in Chinese Indigenous Cattle.
    Zhang Y; Hu Y; Wang X; Jiang Q; Zhao H; Wang J; Ju Z; Yang L; Gao Y; Wei X; Bai J; Zhou Y; Huang J
    Front Genet; 2019; 10():1404. PubMed ID: 32117428
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Genome-wide rare copy number variation screening in ulcerative colitis identifies potential susceptibility loci.
    Saadati HR; Wittig M; Helbig I; Häsler R; Anderson CA; Mathew CG; Kupcinskas L; Parkes M; Karlsen TH; Rosenstiel P; Schreiber S; Franke A
    BMC Med Genet; 2016 Apr; 17():26. PubMed ID: 27037036
    [TBL] [Abstract][Full Text] [Related]  

  • 17. CNV-RF Is a Random Forest-Based Copy Number Variation Detection Method Using Next-Generation Sequencing.
    Onsongo G; Baughn LB; Bower M; Henzler C; Schomaker M; Silverstein KA; Thyagarajan B
    J Mol Diagn; 2016 Nov; 18(6):872-881. PubMed ID: 27597741
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genome-wide rare copy number variations contribute to genetic risk for transposition of the great arteries.
    Costain G; Lionel AC; Ogura L; Marshall CR; Scherer SW; Silversides CK; Bassett AS
    Int J Cardiol; 2016 Feb; 204():115-21. PubMed ID: 26655555
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Genome-wide CNV analysis reveals variants associated with growth traits in Bos indicus.
    Zhou Y; Utsunomiya YT; Xu L; Hay el HA; Bickhart DM; Alexandre PA; Rosen BD; Schroeder SG; Carvalheiro R; de Rezende Neves HH; Sonstegard TS; Van Tassell CP; Ferraz JB; Fukumasu H; Garcia JF; Liu GE
    BMC Genomics; 2016 Jun; 17():419. PubMed ID: 27245577
    [TBL] [Abstract][Full Text] [Related]  

  • 20. CNV discovery for milk composition traits in dairy cattle using whole genome resequencing.
    Gao Y; Jiang J; Yang S; Hou Y; Liu GE; Zhang S; Zhang Q; Sun D
    BMC Genomics; 2017 Mar; 18(1):265. PubMed ID: 28356085
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.