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 *

169 related articles for article (PubMed ID: 23372565)

  • 1. Genome-wide assessment of the association of rare and common copy number variations to testicular germ cell cancer.
    Edsgärd D; Dalgaard MD; Weinhold N; Wesolowska-Andersen A; Rajpert-De Meyts E; Ottesen AM; Juul A; Skakkebæk NE; Skøt Jensen T; Gupta R; Leffers H; Brunak S
    Front Endocrinol (Lausanne); 2013; 4():2. PubMed ID: 23372565
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Accuracy of CNV Detection from GWAS Data.
    Zhang D; Qian Y; Akula N; Alliey-Rodriguez N; Tang J; ; Gershon ES; Liu C
    PLoS One; 2011 Jan; 6(1):e14511. PubMed ID: 21249187
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genome-wide association study of copy number variation with lung function identifies a novel signal of association near BANP for forced vital capacity.
    Shrine N; Tobin MD; Schurmann C; Soler Artigas M; Hui J; Lehtimäki T; Raitakari OT; Pennell CE; Ang QW; Strachan DP; Homuth G; Gläser S; Felix SB; Evans DM; Henderson J; Granell R; Palmer LJ; Huffman J; Hayward C; Scotland G; Malarstig A; Musk B; James AL; ; Wain LV
    BMC Genet; 2016 Aug; 17(1):116. PubMed ID: 27514831
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder.
    Jarick I; Volckmar AL; Pütter C; Pechlivanis S; Nguyen TT; Dauvermann MR; Beck S; Albayrak Ö; Scherag S; Gilsbach S; Cichon S; Hoffmann P; Degenhardt F; Nöthen MM; Schreiber S; Wichmann HE; Jöckel KH; Heinrich J; Tiesler CM; Faraone SV; Walitza S; Sinzig J; Freitag C; Meyer J; Herpertz-Dahlmann B; Lehmkuhl G; Renner TJ; Warnke A; Romanos M; Lesch KP; Reif A; Schimmelmann BG; Hebebrand J; Scherag A; Hinney A
    Mol Psychiatry; 2014 Jan; 19(1):115-21. PubMed ID: 23164820
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Genome-wide association and targeted analysis of copy number variants with psoriatic arthritis in German patients.
    Uebe S; Ehrlicher M; Ekici AB; Behrens F; Böhm B; Homuth G; Schurmann C; Völker U; Jünger M; Nauck M; Völzke H; Traupe H; Krawczak M; Burkhardt H; Reis A; Hüffmeier U
    BMC Med Genet; 2017 Aug; 18(1):92. PubMed ID: 28835222
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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]  

  • 7. Genome-wide copy number variation-, validation- and screening study implicates a new copy number polymorphism associated with suicide attempts in major depressive disorder.
    Rao S; Shi M; Han X; Lam MHB; Chien WT; Zhou K; Liu G; Wing YK; So HC; Waye MMY
    Gene; 2020 Sep; 755():144901. PubMed ID: 32554045
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Continuing difficulties in interpreting CNV data: lessons from a genome-wide CNV association study of Australian HNPCC/lynch syndrome patients.
    Talseth-Palmer BA; Holliday EG; Evans TJ; McEvoy M; Attia J; Grice DM; Masson AL; Meldrum C; Spigelman A; Scott RJ
    BMC Med Genomics; 2013 Mar; 6():10. PubMed ID: 23531357
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Heterozygous deletion at the RLN1 locus in a family with testicular germ cell cancer identified by integrating copy number variation data with phenome and interactome information.
    Edsgärd D; Scheel M; Hansen NT; Ralfkiaer U; Jensen TS; Skakkebaek NE; Brunak S; Gupta R; Rajpert-De Meyts E; Ottesen AM
    Int J Androl; 2011 Aug; 34(4 Pt 2):e122-32. PubMed ID: 21696394
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Genome-wide CNV analysis replicates the association between GSTM1 deletion and bladder cancer: a support for using continuous measurement from SNP-array data.
    Marenne G; Real FX; Rothman N; Rodríguez-Santiago B; Pérez-Jurado L; Kogevinas M; García-Closas M; Silverman DT; Chanock SJ; Génin E; Malats N
    BMC Genomics; 2012 Jul; 13():326. PubMed ID: 22817656
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Joint Contributions of Rare Copy Number Variants and Common SNPs to Risk for Schizophrenia.
    Bergen SE; Ploner A; Howrigan D; ; O'Donovan MC; Smoller JW; Sullivan PF; Sebat J; Neale B; Kendler KS
    Am J Psychiatry; 2019 Jan; 176(1):29-35. PubMed ID: 30392412
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Rare copy number variation in posttraumatic stress disorder.
    Maihofer AX; Engchuan W; Huguet G; Klein M; MacDonald JR; Shanta O; Thiruvahindrapuram B; Jean-Louis M; Saci Z; Jacquemont S; Scherer SW; Ketema E; Aiello AE; Amstadter AB; Avdibegović E; Babic D; Baker DG; Bisson JI; Boks MP; Bolger EA; Bryant RA; Bustamante AC; Caldas-de-Almeida JM; Cardoso G; Deckert J; Delahanty DL; Domschke K; Dunlop BW; Dzubur-Kulenovic A; Evans A; Feeny NC; Franz CE; Gautam A; Geuze E; Goci A; Hammamieh R; Jakovljevic M; Jett M; Jones I; Kaufman ML; Kessler RC; King AP; Kremen WS; Lawford BR; Lebois LAM; Lewis C; Liberzon I; Linnstaedt SD; Lugonja B; Luykx JJ; Lyons MJ; Mavissakalian MR; McLaughlin KA; McLean SA; Mehta D; Mellor R; Morris CP; Muhie S; Orcutt HK; Peverill M; Ratanatharathorn A; Risbrough VB; Rizzo A; Roberts AL; Rothbaum AO; Rothbaum BO; Roy-Byrne P; Ruggiero KJ; Rutten BPF; Schijven D; Seng JS; Sheerin CM; Sorenson MA; Teicher MH; Uddin M; Ursano RJ; Vinkers CH; Voisey J; Weber H; Winternitz S; Xavier M; Yang R; McD Young R; Zoellner LA; ; ; Salem RM; Shaffer RA; Wu T; Ressler KJ; Stein MB; Koenen KC; Sebat J; Nievergelt CM
    Mol Psychiatry; 2022 Dec; 27(12):5062-5069. PubMed ID: 36131047
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Comprehensive performance comparison of high-resolution array platforms for genome-wide Copy Number Variation (CNV) analysis in humans.
    Haraksingh RR; Abyzov A; Urban AE
    BMC Genomics; 2017 Apr; 18(1):321. PubMed ID: 28438122
    [TBL] [Abstract][Full Text] [Related]  

  • 15. 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]  

  • 16. Integrated Genome-Wide Analysis of Gene Expression and DNA Copy Number Variations Highlights Stem Cell-Related Pathways in Small Cell Esophageal Carcinoma.
    Liu D; Xu X; Wen J; Xie L; Zhang J; Shen Y; Jiang G; Chen J; Fan M
    Stem Cells Int; 2018; 2018():3481783. PubMed ID: 30228821
    [No Abstract]   [Full Text] [Related]  

  • 17. Genome-wide mapping of copy number variation in humans: comparative analysis of high resolution array platforms.
    Haraksingh RR; Abyzov A; Gerstein M; Urban AE; Snyder M
    PLoS One; 2011; 6(11):e27859. PubMed ID: 22140474
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 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]  

  • 19. Polymorphic variation in the androgen receptor gene: association with risk of testicular germ cell cancer and metastatic disease.
    Västermark Å; Giwercman YL; Hagströmer O; Rajpert De-Meyts E; Eberhard J; Ståhl O; Cedermark GC; Rastkhani H; Daugaard G; Arver S; Giwercman A
    Eur J Cancer; 2011 Feb; 47(3):413-9. PubMed ID: 20880698
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Copy number variation and cytidine analogue cytotoxicity: a genome-wide association approach.
    Kalari KR; Hebbring SJ; Chai HS; Li L; Kocher JP; Wang L; Weinshilboum RM
    BMC Genomics; 2010 Jun; 11():357. PubMed ID: 20525348
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 9.