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 *

338 related articles for article (PubMed ID: 19536264)

  • 1. Copy number variation at 1q21.1 associated with neuroblastoma.
    Diskin SJ; Hou C; Glessner JT; Attiyeh EF; Laudenslager M; Bosse K; Cole K; Mossé YP; Wood A; Lynch JE; Pecor K; Diamond M; Winter C; Wang K; Kim C; Geiger EA; McGrady PW; Blakemore AI; London WB; Shaikh TH; Bradfield J; Grant SF; Li H; Devoto M; Rappaport ER; Hakonarson H; Maris JM
    Nature; 2009 Jun; 459(7249):987-91. PubMed ID: 19536264
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Novel submicroscopic chromosomal abnormalities detected in autism spectrum disorder.
    Christian SL; Brune CW; Sudi J; Kumar RA; Liu S; Karamohamed S; Badner JA; Matsui S; Conroy J; McQuaid D; Gergel J; Hatchwell E; Gilliam TC; Gershon ES; Nowak NJ; Dobyns WB; Cook EH
    Biol Psychiatry; 2008 Jun; 63(12):1111-7. PubMed ID: 18374305
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Autism genome-wide copy number variation reveals ubiquitin and neuronal genes.
    Glessner JT; Wang K; Cai G; Korvatska O; Kim CE; Wood S; Zhang H; Estes A; Brune CW; Bradfield JP; Imielinski M; Frackelton EC; Reichert J; Crawford EL; Munson J; Sleiman PM; Chiavacci R; Annaiah K; Thomas K; Hou C; Glaberson W; Flory J; Otieno F; Garris M; Soorya L; Klei L; Piven J; Meyer KJ; Anagnostou E; Sakurai T; Game RM; Rudd DS; Zurawiecki D; McDougle CJ; Davis LK; Miller J; Posey DJ; Michaels S; Kolevzon A; Silverman JM; Bernier R; Levy SE; Schultz RT; Dawson G; Owley T; McMahon WM; Wassink TH; Sweeney JA; Nurnberger JI; Coon H; Sutcliffe JS; Minshew NJ; Grant SF; Bucan M; Cook EH; Buxbaum JD; Devlin B; Schellenberg GD; Hakonarson H
    Nature; 2009 May; 459(7246):569-73. PubMed ID: 19404257
    [TBL] [Abstract][Full Text] [Related]  

  • 4. On the analysis of copy-number variations in genome-wide association studies: a translation of the family-based association test.
    Ionita-Laza I; Perry GH; Raby BA; Klanderman B; Lee C; Laird NM; Weiss ST; Lange C
    Genet Epidemiol; 2008 Apr; 32(3):273-84. PubMed ID: 18228561
    [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. Copy Number Variation in
    Wang Y; Li L; Yang Y; Feng J; Wang L; Zhang H
    Genet Test Mol Biomarkers; 2020 Apr; 24(4):173-180. PubMed ID: 32208937
    [No Abstract]   [Full Text] [Related]  

  • 7. What a difference copy number variation makes.
    Kehrer-Sawatzki H
    Bioessays; 2007 Apr; 29(4):311-3. PubMed ID: 17373652
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Large recurrent microdeletions associated with schizophrenia.
    Stefansson H; Rujescu D; Cichon S; Pietiläinen OP; Ingason A; Steinberg S; Fossdal R; Sigurdsson E; Sigmundsson T; Buizer-Voskamp JE; Hansen T; Jakobsen KD; Muglia P; Francks C; Matthews PM; Gylfason A; Halldorsson BV; Gudbjartsson D; Thorgeirsson TE; Sigurdsson A; Jonasdottir A; Jonasdottir A; Bjornsson A; Mattiasdottir S; Blondal T; Haraldsson M; Magnusdottir BB; Giegling I; Möller HJ; Hartmann A; Shianna KV; Ge D; Need AC; Crombie C; Fraser G; Walker N; Lonnqvist J; Suvisaari J; Tuulio-Henriksson A; Paunio T; Toulopoulou T; Bramon E; Di Forti M; Murray R; Ruggeri M; Vassos E; Tosato S; Walshe M; Li T; Vasilescu C; Mühleisen TW; Wang AG; Ullum H; Djurovic S; Melle I; Olesen J; Kiemeney LA; Franke B; ; Sabatti C; Freimer NB; Gulcher JR; Thorsteinsdottir U; Kong A; Andreassen OA; Ophoff RA; Georgi A; Rietschel M; Werge T; Petursson H; Goldstein DB; Nöthen MM; Peltonen L; Collier DA; St Clair D; Stefansson K
    Nature; 2008 Sep; 455(7210):232-6. PubMed ID: 18668039
    [TBL] [Abstract][Full Text] [Related]  

  • 9. A Genome Wide Study of Copy Number Variation Associated with Nasopharyngeal Carcinoma in Malaysian Chinese Identifies CNVs at 11q14.3 and 6p21.3 as Candidate Loci.
    Low JS; Chin YM; Mushiroda T; Kubo M; Govindasamy GK; Pua KC; Yap YY; Yap LF; Subramaniam SK; Ong CA; Tan TY; Khoo AS; ; Ng CC
    PLoS One; 2016; 11(1):e0145774. PubMed ID: 26730743
    [TBL] [Abstract][Full Text] [Related]  

  • 10. A gender-specific association of CNV at 6p21.3 with NPC susceptibility.
    Tse KP; Su WH; Yang ML; Cheng HY; Tsang NM; Chang KP; Hao SP; Yao Shugart Y; Chang YS
    Hum Mol Genet; 2011 Jul; 20(14):2889-96. PubMed ID: 21536588
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 12. Absence of AVPR2 copy number variation in eunatremic and dysnatremic subjects in non-Hispanic Caucasian populations.
    Fu Y; Chen Z; Blakemore AI; Orwoll E; Cohen DM
    Physiol Genomics; 2010 Feb; 40(3):121-7. PubMed ID: 19996159
    [TBL] [Abstract][Full Text] [Related]  

  • 13. Copy number variation in schizophrenia in Sweden.
    Szatkiewicz JP; O'Dushlaine C; Chen G; Chambert K; Moran JL; Neale BM; Fromer M; Ruderfer D; Akterin S; Bergen SE; Kähler A; Magnusson PK; Kim Y; Crowley JJ; Rees E; Kirov G; O'Donovan MC; Owen MJ; Walters J; Scolnick E; Sklar P; Purcell S; Hultman CM; McCarroll SA; Sullivan PF
    Mol Psychiatry; 2014 Jul; 19(7):762-73. PubMed ID: 24776740
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Systematic prediction and validation of breakpoints associated with copy-number variants in the human genome.
    Korbel JO; Urban AE; Grubert F; Du J; Royce TE; Starr P; Zhong G; Emanuel BS; Weissman SM; Snyder M; Gerstein MB
    Proc Natl Acad Sci U S A; 2007 Jun; 104(24):10110-5. PubMed ID: 17551006
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Integrative genomics identifies LMO1 as a neuroblastoma oncogene.
    Wang K; Diskin SJ; Zhang H; Attiyeh EF; Winter C; Hou C; Schnepp RW; Diamond M; Bosse K; Mayes PA; Glessner J; Kim C; Frackelton E; Garris M; Wang Q; Glaberson W; Chiavacci R; Nguyen L; Jagannathan J; Saeki N; Sasaki H; Grant SF; Iolascon A; Mosse YP; Cole KA; Li H; Devoto M; McGrady PW; London WB; Capasso M; Rahman N; Hakonarson H; Maris JM
    Nature; 2011 Jan; 469(7329):216-20. PubMed ID: 21124317
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Copy number variation on chromosome 10q26.3 for obesity identified by a genome-wide study.
    Yang TL; Guo Y; Shen H; Li J; Glessner JT; Qiu C; Deng FY; Tian Q; Yu P; Liu YZ; Liu YJ; Hakonarson H; Grant SF; Deng HW
    J Clin Endocrinol Metab; 2013 Jan; 98(1):E191-5. PubMed ID: 23175694
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Genetics and genomics of neuroblastoma.
    Capasso M; Diskin SJ
    Cancer Treat Res; 2010; 155():65-84. PubMed ID: 20517688
    [TBL] [Abstract][Full Text] [Related]  

  • 18. 1q23 gain is associated with progressive neuroblastoma resistant to aggressive treatment.
    Hirai M; Yoshida S; Kashiwagi H; Kawamura T; Ishikawa T; Kaneko M; Ohkawa H; Nakagawara A; Miwa M; Uchida K
    Genes Chromosomes Cancer; 1999 Jul; 25(3):261-9. PubMed ID: 10379872
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Clinical and molecular cytogenetic analyses of four families with 1q21.1 microdeletion or microduplication.
    Wang HD; Liu L; Wu D; Li T; Cui CY; Zhang LZ; Wang CZ
    J Gene Med; 2017 Apr; 19(4):. PubMed ID: 28220983
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Common variants in the BCL9 gene conferring risk of schizophrenia.
    Li J; Zhou G; Ji W; Feng G; Zhao Q; Liu J; Li T; Li Y; Chen P; Zeng Z; Wang T; Hu Z; Zheng L; Wang Y; Shen Y; He L; Shi Y
    Arch Gen Psychiatry; 2011 Mar; 68(3):232-40. PubMed ID: 21383261
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 17.