BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

628 related articles for article (PubMed ID: 30208311)

  • 1. Comparative Analyses of Copy-Number Variation in Autism Spectrum Disorder and Schizophrenia Reveal Etiological Overlap and Biological Insights.
    Kushima I; Aleksic B; Nakatochi M; Shimamura T; Okada T; Uno Y; Morikawa M; Ishizuka K; Shiino T; Kimura H; Arioka Y; Yoshimi A; Takasaki Y; Yu Y; Nakamura Y; Yamamoto M; Iidaka T; Iritani S; Inada T; Ogawa N; Shishido E; Torii Y; Kawano N; Omura Y; Yoshikawa T; Uchiyama T; Yamamoto T; Ikeda M; Hashimoto R; Yamamori H; Yasuda Y; Someya T; Watanabe Y; Egawa J; Nunokawa A; Itokawa M; Arai M; Miyashita M; Kobori A; Suzuki M; Takahashi T; Usami M; Kodaira M; Watanabe K; Sasaki T; Kuwabara H; Tochigi M; Nishimura F; Yamasue H; Eriguchi Y; Benner S; Kojima M; Yassin W; Munesue T; Yokoyama S; Kimura R; Funabiki Y; Kosaka H; Ishitobi M; Ohmori T; Numata S; Yoshikawa T; Toyota T; Yamakawa K; Suzuki T; Inoue Y; Nakaoka K; Goto YI; Inagaki M; Hashimoto N; Kusumi I; Son S; Murai T; Ikegame T; Okada N; Kasai K; Kunimoto S; Mori D; Iwata N; Ozaki N
    Cell Rep; 2018 Sep; 24(11):2838-2856. PubMed ID: 30208311
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Cross-Disorder Analysis of Genic and Regulatory Copy Number Variations in Bipolar Disorder, Schizophrenia, and Autism Spectrum Disorder.
    Kushima I; Nakatochi M; Aleksic B; Okada T; Kimura H; Kato H; Morikawa M; Inada T; Ishizuka K; Torii Y; Nakamura Y; Tanaka S; Imaeda M; Takahashi N; Yamamoto M; Iwamoto K; Nawa Y; Ogawa N; Iritani S; Hayashi Y; Lo T; Otgonbayar G; Furuta S; Iwata N; Ikeda M; Saito T; Ninomiya K; Okochi T; Hashimoto R; Yamamori H; Yasuda Y; Fujimoto M; Miura K; Itokawa M; Arai M; Miyashita M; Toriumi K; Ohi K; Shioiri T; Kitaichi K; Someya T; Watanabe Y; Egawa J; Takahashi T; Suzuki M; Sasaki T; Tochigi M; Nishimura F; Yamasue H; Kuwabara H; Wakuda T; Kato TA; Kanba S; Horikawa H; Usami M; Kodaira M; Watanabe K; Yoshikawa T; Toyota T; Yokoyama S; Munesue T; Kimura R; Funabiki Y; Kosaka H; Jung M; Kasai K; Ikegame T; Jinde S; Numata S; Kinoshita M; Kato T; Kakiuchi C; Yamakawa K; Suzuki T; Hashimoto N; Ishikawa S; Yamagata B; Nio S; Murai T; Son S; Kunii Y; Yabe H; Inagaki M; Goto YI; Okumura Y; Ito T; Arioka Y; Mori D; Ozaki N
    Biol Psychiatry; 2022 Sep; 92(5):362-374. PubMed ID: 35667888
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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]  

  • 4. 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]  

  • 5. Association of copy number variation across the genome with neuropsychiatric traits in the general population.
    Guyatt AL; Stergiakouli E; Martin J; Walters J; O'Donovan M; Owen M; Thapar A; Kirov G; Rodriguez S; Rai D; Zammit S; Gaunt TR
    Am J Med Genet B Neuropsychiatr Genet; 2018 Jul; 177(5):489-502. PubMed ID: 29687944
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Rare recurrent copy number variations in metabotropic glutamate receptor interacting genes in children with neurodevelopmental disorders.
    Glessner JT; Khan ME; Chang X; Liu Y; Otieno FG; Lemma M; Slaby I; Hain H; Mentch F; Li J; Kao C; Sleiman PMA; March ME; Connolly J; Hakonarson H
    J Neurodev Disord; 2023 Apr; 15(1):14. PubMed ID: 37120522
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The landscape of copy number variations in Finnish families with autism spectrum disorders.
    Kanduri C; Kantojärvi K; Salo PM; Vanhala R; Buck G; Blancher C; Lähdesmäki H; Järvelä I
    Autism Res; 2016 Jan; 9(1):9-16. PubMed ID: 26052927
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Psychotic symptoms in 16p11.2 copy-number variant carriers.
    Jutla A; Turner JB; Green Snyder L; Chung WK; Veenstra-VanderWeele J
    Autism Res; 2020 Feb; 13(2):187-198. PubMed ID: 31724820
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Attention-deficit hyperactivity disorder shares copy number variant risk with schizophrenia and autism spectrum disorder.
    Gudmundsson OO; Walters GB; Ingason A; Johansson S; Zayats T; Athanasiu L; Sonderby IE; Gustafsson O; Nawaz MS; Jonsson GF; Jonsson L; Knappskog PM; Ingvarsdottir E; Davidsdottir K; Djurovic S; Knudsen GPS; Askeland RB; Haraldsdottir GS; Baldursson G; Magnusson P; Sigurdsson E; Gudbjartsson DF; Stefansson H; Andreassen OA; Haavik J; Reichborn-Kjennerud T; Stefansson K
    Transl Psychiatry; 2019 Oct; 9(1):258. PubMed ID: 31624239
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Synaptic and Gene Regulatory Mechanisms in Schizophrenia, Autism, and 22q11.2 Copy Number Variant-Mediated Risk for Neuropsychiatric Disorders.
    Forsyth JK; Nachun D; Gandal MJ; Geschwind DH; Anderson AE; Coppola G; Bearden CE
    Biol Psychiatry; 2020 Jan; 87(2):150-163. PubMed ID: 31500805
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The phenotypic manifestations of rare genic CNVs in autism spectrum disorder.
    Merikangas AK; Segurado R; Heron EA; Anney RJ; Paterson AD; Cook EH; Pinto D; Scherer SW; Szatmari P; Gill M; Corvin AP; Gallagher L
    Mol Psychiatry; 2015 Nov; 20(11):1366-72. PubMed ID: 25421404
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Rare copy number variants in tourette syndrome disrupt genes in histaminergic pathways and overlap with autism.
    Fernandez TV; Sanders SJ; Yurkiewicz IR; Ercan-Sencicek AG; Kim YS; Fishman DO; Raubeson MJ; Song Y; Yasuno K; Ho WS; Bilguvar K; Glessner J; Chu SH; Leckman JF; King RA; Gilbert DL; Heiman GA; Tischfield JA; Hoekstra PJ; Devlin B; Hakonarson H; Mane SM; Günel M; State MW
    Biol Psychiatry; 2012 Mar; 71(5):392-402. PubMed ID: 22169095
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The penetrance of copy number variations for schizophrenia and developmental delay.
    Kirov G; Rees E; Walters JT; Escott-Price V; Georgieva L; Richards AL; Chambert KD; Davies G; Legge SE; Moran JL; McCarroll SA; O'Donovan MC; Owen MJ
    Biol Psychiatry; 2014 Mar; 75(5):378-85. PubMed ID: 23992924
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Copy number variants in autism spectrum disorders.
    Vicari S; Napoli E; Cordeddu V; Menghini D; Alesi V; Loddo S; Novelli A; Tartaglia M
    Prog Neuropsychopharmacol Biol Psychiatry; 2019 Jun; 92():421-427. PubMed ID: 30797015
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Genome-wide analysis of copy number variations identifies PARK2 as a candidate gene for autism spectrum disorder.
    Yin CL; Chen HI; Li LH; Chien YL; Liao HM; Chou MC; Chou WJ; Tsai WC; Chiu YN; Wu YY; Lo CZ; Wu JY; Chen YT; Gau SS
    Mol Autism; 2016; 7():23. PubMed ID: 27042285
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Association between copy number variations in parkin (PRKN) and schizophrenia and autism spectrum disorder: A case-control study.
    Lo T; Kushima I; Kimura H; Aleksic B; Okada T; Kato H; Inada T; Nawa Y; Torii Y; Yamamoto M; Kimura R; Funabiki Y; Kosaka H; Numata S; Kasai K; Sasaki T; Yokoyama S; Munesue T; Hashimoto R; Yasuda Y; Fujimoto M; Usami M; Itokawa M; Arai M; Ohi K; Someya T; Watanabe Y; Egawa J; Takahashi T; Suzuki M; Yamasue H; Iwata N; Ikeda M; Ozaki N
    Neuropsychopharmacol Rep; 2024 Mar; 44(1):42-50. PubMed ID: 37915257
    [TBL] [Abstract][Full Text] [Related]  

  • 17. 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]  

  • 18. Rare Genome-Wide Copy Number Variation and Expression of Schizophrenia in 22q11.2 Deletion Syndrome.
    Bassett AS; Lowther C; Merico D; Costain G; Chow EWC; van Amelsvoort T; McDonald-McGinn D; Gur RE; Swillen A; Van den Bree M; Murphy K; Gothelf D; Bearden CE; Eliez S; Kates W; Philip N; Sashi V; Campbell L; Vorstman J; Cubells J; Repetto GM; Simon T; Boot E; Heung T; Evers R; Vingerhoets C; van Duin E; Zackai E; Vergaelen E; Devriendt K; Vermeesch JR; Owen M; Murphy C; Michaelovosky E; Kushan L; Schneider M; Fremont W; Busa T; Hooper S; McCabe K; Duijff S; Isaev K; Pellecchia G; Wei J; Gazzellone MJ; Scherer SW; Emanuel BS; Guo T; Morrow BE; Marshall CR;
    Am J Psychiatry; 2017 Nov; 174(11):1054-1063. PubMed ID: 28750581
    [TBL] [Abstract][Full Text] [Related]  

  • 19. High resolution analysis of rare copy number variants in patients with autism spectrum disorder from Taiwan.
    Chen CH; Chen HI; Chien WH; Li LH; Wu YY; Chiu YN; Tsai WC; Gau SS
    Sci Rep; 2017 Sep; 7(1):11919. PubMed ID: 28931914
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Analysis of common genetic variation and rare CNVs in the Australian Autism Biobank.
    Yap CX; Alvares GA; Henders AK; Lin T; Wallace L; Farrelly A; McLaren T; Berry J; Vinkhuyzen AAE; Trzaskowski M; Zeng J; Yang Y; Cleary D; Grove R; Hafekost C; Harun A; Holdsworth H; Jellett R; Khan F; Lawson L; Leslie J; Levis Frenk M; Masi A; Mathew NE; Muniandy M; Nothard M; Visscher PM; Dawson PA; Dissanayake C; Eapen V; Heussler HS; Whitehouse AJO; Wray NR; Gratten J
    Mol Autism; 2021 Feb; 12(1):12. PubMed ID: 33568206
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 32.