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 *

425 related articles for article (PubMed ID: 19197363)

  • 1. A genome-wide investigation of SNPs and CNVs in schizophrenia.
    Need AC; Ge D; Weale ME; Maia J; Feng S; Heinzen EL; Shianna KV; Yoon W; Kasperaviciūte D; Gennarelli M; Strittmatter WJ; Bonvicini C; Rossi G; Jayathilake K; Cola PA; McEvoy JP; Keefe RS; Fisher EM; St Jean PL; Giegling I; Hartmann AM; Möller HJ; Ruppert A; Fraser G; Crombie C; Middleton LT; St Clair D; Roses AD; Muglia P; Francks C; Rujescu D; Meltzer HY; Goldstein DB
    PLoS Genet; 2009 Feb; 5(2):e1000373. PubMed ID: 19197363
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis.
    Williams NM; Zaharieva I; Martin A; Langley K; Mantripragada K; Fossdal R; Stefansson H; Stefansson K; Magnusson P; Gudmundsson OO; Gustafsson O; Holmans P; Owen MJ; O'Donovan M; Thapar A
    Lancet; 2010 Oct; 376(9750):1401-8. PubMed ID: 20888040
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Genome-wide association study of multiplex schizophrenia pedigrees.
    Levinson DF; Shi J; Wang K; Oh S; Riley B; Pulver AE; Wildenauer DB; Laurent C; Mowry BJ; Gejman PV; Owen MJ; Kendler KS; Nestadt G; Schwab SG; Mallet J; Nertney D; Sanders AR; Williams NM; Wormley B; Lasseter VK; Albus M; Godard-Bauché S; Alexander M; Duan J; O'Donovan MC; Walsh D; O'Neill A; Papadimitriou GN; Dikeos D; Maier W; Lerer B; Campion D; Cohen D; Jay M; Fanous A; Eichhammer P; Silverman JM; Norton N; Zhang N; Hakonarson H; Gao C; Citri A; Hansen M; Ripke S; ; Dudbridge F; Holmans PA
    Am J Psychiatry; 2012 Sep; 169(9):963-73. PubMed ID: 22885689
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Recurrent CNVs disrupt three candidate genes in schizophrenia patients.
    Vrijenhoek T; Buizer-Voskamp JE; van der Stelt I; Strengman E; ; Sabatti C; Geurts van Kessel A; Brunner HG; Ophoff RA; Veltman JA
    Am J Hum Genet; 2008 Oct; 83(4):504-10. PubMed ID: 18940311
    [TBL] [Abstract][Full Text] [Related]  

  • 5. 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]  

  • 6. Rare chromosomal deletions and duplications increase risk of schizophrenia.
    International Schizophrenia Consortium
    Nature; 2008 Sep; 455(7210):237-41. PubMed ID: 18668038
    [TBL] [Abstract][Full Text] [Related]  

  • 7. 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]  

  • 8. New copy number variations in schizophrenia.
    Magri C; Sacchetti E; Traversa M; Valsecchi P; Gardella R; Bonvicini C; Minelli A; Gennarelli M; Barlati S
    PLoS One; 2010 Oct; 5(10):e13422. PubMed ID: 20967226
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Ohnologs are overrepresented in pathogenic copy number mutations.
    McLysaght A; Makino T; Grayton HM; Tropeano M; Mitchell KJ; Vassos E; Collier DA
    Proc Natl Acad Sci U S A; 2014 Jan; 111(1):361-6. PubMed ID: 24368850
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Pathogenic rare copy number variants in community-based schizophrenia suggest a potential role for clinical microarrays.
    Costain G; Lionel AC; Merico D; Forsythe P; Russell K; Lowther C; Yuen T; Husted J; Stavropoulos DJ; Speevak M; Chow EW; Marshall CR; Scherer SW; Bassett AS
    Hum Mol Genet; 2013 Nov; 22(22):4485-501. PubMed ID: 23813976
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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]  

  • 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. A genome-wide CNV analysis of schizophrenia reveals a potential role for a multiple-hit model.
    Rudd DS; Axelsen M; Epping EA; Andreasen NC; Wassink TH
    Am J Med Genet B Neuropsychiatr Genet; 2014 Dec; 165B(8):619-26. PubMed ID: 25228354
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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]  

  • 15. Support for the involvement of large copy number variants in the pathogenesis of schizophrenia.
    Kirov G; Grozeva D; Norton N; Ivanov D; Mantripragada KK; Holmans P; ; ; Craddock N; Owen MJ; O'Donovan MC
    Hum Mol Genet; 2009 Apr; 18(8):1497-503. PubMed ID: 19181681
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Copy number variation in schizophrenia in the Japanese population.
    Ikeda M; Aleksic B; Kirov G; Kinoshita Y; Yamanouchi Y; Kitajima T; Kawashima K; Okochi T; Kishi T; Zaharieva I; Owen MJ; O'Donovan MC; Ozaki N; Iwata N
    Biol Psychiatry; 2010 Feb; 67(3):283-6. PubMed ID: 19880096
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Copy number variations in the genome of the Qatari population.
    Fakhro KA; Yousri NA; Rodriguez-Flores JL; Robay A; Staudt MR; Agosto-Perez F; Salit J; Malek JA; Suhre K; Jayyousi A; Zirie M; Stadler D; Mezey JG; Crystal RG
    BMC Genomics; 2015 Oct; 16():834. PubMed ID: 26490036
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Genomic copy number variations: A breakthrough in our knowledge on schizophrenia etiology?
    Hosak L; Silhan P; Hosakova J
    Neuro Endocrinol Lett; 2012; 33(2):183-90. PubMed ID: 22592199
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Schizophrenia genetics: advancing on two fronts.
    Owen MJ; Williams HJ; O'Donovan MC
    Curr Opin Genet Dev; 2009 Jun; 19(3):266-70. PubMed ID: 19345090
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Association of common copy number variants at the glutathione S-transferase genes and rare novel genomic changes with schizophrenia.
    Rodríguez-Santiago B; Brunet A; Sobrino B; Serra-Juhé C; Flores R; Armengol L; Vilella E; Gabau E; Guitart M; Guillamat R; Martorell L; Valero J; Gutiérrez-Zotes A; Labad A; Carracedo A; Estivill X; Pérez-Jurado LA
    Mol Psychiatry; 2010 Oct; 15(10):1023-33. PubMed ID: 19528963
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 22.