BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

204 related articles for article (PubMed ID: 25943776)

  • 21. Rare copy number variants: a point of rarity in genetic risk for bipolar disorder and schizophrenia.
    Grozeva D; Kirov G; Ivanov D; Jones IR; Jones L; Green EK; St Clair DM; Young AH; Ferrier N; Farmer AE; McGuffin P; Holmans PA; Owen MJ; O'Donovan MC; Craddock N;
    Arch Gen Psychiatry; 2010 Apr; 67(4):318-27. PubMed ID: 20368508
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Genome-wide analysis shows increased frequency of copy number variation deletions in Dutch schizophrenia patients.
    Buizer-Voskamp JE; Muntjewerff JW; ; Strengman E; Sabatti C; Stefansson H; Vorstman JA; Ophoff RA
    Biol Psychiatry; 2011 Oct; 70(7):655-62. PubMed ID: 21489405
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Impact of IQ on the diagnostic yield of chromosomal microarray in a community sample of adults with schizophrenia.
    Lowther C; Merico D; Costain G; Waserman J; Boyd K; Noor A; Speevak M; Stavropoulos DJ; Wei J; Lionel AC; Marshall CR; Scherer SW; Bassett AS
    Genome Med; 2017 Nov; 9(1):105. PubMed ID: 29187259
    [TBL] [Abstract][Full Text] [Related]  

  • 24. A genome wide survey supports the involvement of large copy number variants in schizophrenia with and without intellectual disability.
    Derks EM; Ayub M; Chambert K; Del Favero J; Johnstone M; MacGregor S; Maclean A; McKechanie AG; McRae AF; Moran JL; Pickard BS; Purcell S; Sklar P; StClair DM; Wray NR; Visscher PM; Blackwood DH
    Am J Med Genet B Neuropsychiatr Genet; 2013 Dec; 162B(8):847-54. PubMed ID: 24115684
    [TBL] [Abstract][Full Text] [Related]  

  • 25. Prevalence of Pathogenic Copy Number Variation in Adults With Pediatric-Onset Epilepsy and Intellectual Disability.
    Borlot F; Regan BM; Bassett AS; Stavropoulos DJ; Andrade DM
    JAMA Neurol; 2017 Nov; 74(11):1301-1311. PubMed ID: 28846756
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Genetic copy number variants, cognition and psychosis: a meta-analysis and a family study.
    Thygesen JH; Presman A; Harju-Seppänen J; Irizar H; Jones R; Kuchenbaecker K; Lin K; Alizadeh BZ; Austin-Zimmerman I; Bartels-Velthuis A; Bhat A; Bruggeman R; Cahn W; Calafato S; Crespo-Facorro B; de Haan L; de Zwarte SMC; Di Forti M; Díez-Revuelta Á; Hall J; Hall MH; Iyegbe C; Jablensky A; Kahn R; Kalaydjieva L; Kravariti E; Lawrie S; Luykx JJ; Mata I; McDonald C; McIntosh AM; McQuillin A; Muir R; Ophoff R; Picchioni M; Prata DP; Ranlund S; Rujescu D; Rutten BPF; Schulze K; Shaikh M; Schirmbeck F; Simons CJP; Toulopoulou T; van Amelsvoort T; van Haren N; van Os J; van Winkel R; Vassos E; Walshe M; Weisbrod M; Zartaloudi E; Bell V; Powell J; Lewis CM; Murray RM; Bramon E
    Mol Psychiatry; 2021 Sep; 26(9):5307-5319. PubMed ID: 32719466
    [TBL] [Abstract][Full Text] [Related]  

  • 27. High-resolution copy number variation analysis of schizophrenia in Japan.
    Kushima I; Aleksic B; Nakatochi M; Shimamura T; Shiino T; Yoshimi A; Kimura H; Takasaki Y; Wang C; Xing J; Ishizuka K; Oya-Ito T; Nakamura Y; Arioka Y; Maeda T; Yamamoto M; Yoshida M; Noma H; Hamada S; Morikawa M; Uno Y; Okada T; Iidaka T; Iritani S; Yamamoto T; Miyashita M; Kobori A; Arai M; Itokawa M; Cheng MC; Chuang YA; Chen CH; Suzuki M; Takahashi T; Hashimoto R; Yamamori H; Yasuda Y; Watanabe Y; Nunokawa A; Someya T; Ikeda M; Toyota T; Yoshikawa T; Numata S; Ohmori T; Kunimoto S; Mori D; Iwata N; Ozaki N
    Mol Psychiatry; 2017 Mar; 22(3):430-440. PubMed ID: 27240532
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications.
    Levinson DF; Duan J; Oh S; Wang K; Sanders AR; Shi J; Zhang N; Mowry BJ; Olincy A; Amin F; Cloninger CR; Silverman JM; Buccola NG; Byerley WF; Black DW; Kendler KS; Freedman R; Dudbridge F; Pe'er I; Hakonarson H; Bergen SE; Fanous AH; Holmans PA; Gejman PV
    Am J Psychiatry; 2011 Mar; 168(3):302-16. PubMed ID: 21285140
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Copy number variations and risk for schizophrenia in 22q11.2 deletion syndrome.
    Bassett AS; Marshall CR; Lionel AC; Chow EW; Scherer SW
    Hum Mol Genet; 2008 Dec; 17(24):4045-53. PubMed ID: 18806272
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. Copy Number Variant Risk Scores Associated With Cognition, Psychopathology, and Brain Structure in Youths in the Philadelphia Neurodevelopmental Cohort.
    Alexander-Bloch A; Huguet G; Schultz LM; Huffnagle N; Jacquemont S; Seidlitz J; Saci Z; Moore TM; Bethlehem RAI; Mollon J; Knowles EK; Raznahan A; Merikangas A; Chaiyachati BH; Raman H; Schmitt JE; Barzilay R; Calkins ME; Shinohara RT; Satterthwaite TD; Gur RC; Glahn DC; Almasy L; Gur RE; Hakonarson H; Glessner J
    JAMA Psychiatry; 2022 Jul; 79(7):699-709. PubMed ID: 35544191
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Double hits in schizophrenia.
    Vorstman JAS; Olde Loohuis LM; ; Kahn RS; Ophoff RA;
    Hum Mol Genet; 2018 Aug; 27(15):2755-2761. PubMed ID: 29767709
    [TBL] [Abstract][Full Text] [Related]  

  • 33. No association between general cognitive ability and rare copy number variation.
    McRae AF; Wright MJ; Hansell NK; Montgomery GW; Martin NG
    Behav Genet; 2013 May; 43(3):202-7. PubMed ID: 23417127
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Characterization of Single Gene Copy Number Variants in Schizophrenia.
    Szatkiewicz JP; Fromer M; Nonneman RJ; Ancalade N; Johnson JS; Stahl EA; Rees E; Bergen SE; Hultman CM; Kirov G; O'Donovan M; Owen M; Holmans P; Sklar P; Sullivan PF; Purcell SM; Crowley JJ; Ruderfer DM
    Biol Psychiatry; 2020 Apr; 87(8):736-744. PubMed ID: 31767120
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Increased rare duplication burden genomewide in patients with treatment-resistant schizophrenia.
    Martin AK; Mowry B
    Psychol Med; 2016 Feb; 46(3):469-76. PubMed ID: 26349998
    [TBL] [Abstract][Full Text] [Related]  

  • 36. De novo copy number variants and parental age: Is there an association?
    Wadhawan I; Hai Y; Foyouzi Yousefi N; Guo X; Graham JM; Rosenfeld JA
    Eur J Med Genet; 2020 Apr; 63(4):103829. PubMed ID: 31883480
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Strong synaptic transmission impact by copy number variations in schizophrenia.
    Glessner JT; Reilly MP; Kim CE; Takahashi N; Albano A; Hou C; Bradfield JP; Zhang H; Sleiman PM; Flory JH; Imielinski M; Frackelton EC; Chiavacci R; Thomas KA; Garris M; Otieno FG; Davidson M; Weiser M; Reichenberg A; Davis KL; Friedman JI; Cappola TP; Margulies KB; Rader DJ; Grant SF; Buxbaum JD; Gur RE; Hakonarson H
    Proc Natl Acad Sci U S A; 2010 Jun; 107(23):10584-9. PubMed ID: 20489179
    [TBL] [Abstract][Full Text] [Related]  

  • 38. Increased paternal age and the influence on burden of genomic copy number variation in the general population.
    Buizer-Voskamp JE; Blauw HM; Boks MP; van Eijk KR; Veldink JH; Hennekam EA; Vorstman JA; Mulder F; Tiemeier H; Uitterlinden AG; Kiemeney LA; van den Berg LH; Kahn RS; Sabatti C; Ophoff RA
    Hum Genet; 2013 Apr; 132(4):443-50. PubMed ID: 23315237
    [TBL] [Abstract][Full Text] [Related]  

  • 39. CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1.
    Rees E; Walters JT; Chambert KD; O'Dushlaine C; Szatkiewicz J; Richards AL; Georgieva L; Mahoney-Davies G; Legge SE; Moran JL; Genovese G; Levinson D; Morris DW; Cormican P; Kendler KS; O'Neill FA; Riley B; Gill M; Corvin A; ; Sklar P; Hultman C; Pato C; Pato M; Sullivan PF; Gejman PV; McCarroll SA; O'Donovan MC; Owen MJ; Kirov G
    Hum Mol Genet; 2014 Mar; 23(6):1669-76. PubMed ID: 24163246
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Whole genome sequencing of 91 multiplex schizophrenia families reveals increased burden of rare, exonic copy number variation in schizophrenia probands and genetic heterogeneity.
    Khan FF; Melton PE; McCarthy NS; Morar B; Blangero J; Moses EK; Jablensky A
    Schizophr Res; 2018 Jul; 197():337-345. PubMed ID: 29486958
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 11.