172 related articles for article (PubMed ID: 31080157)
1. Copy number variant syndromes are frequent in schizophrenia: Progressing towards a CNV-schizophrenia model.
Sriretnakumar V; Zai CC; Wasim S; Barsanti-Innes B; Kennedy JL; So J
Schizophr Res; 2019 Jul; 209():171-178. PubMed ID: 31080157
[TBL] [Abstract][Full Text] [Related]
2. Identifying schizophrenia patients who carry pathogenic genetic copy number variants using standard clinical assessment: retrospective cohort study.
Foley C; Heron EA; Harold D; Walters J; Owen M; O'Donovan M; Sebat J; Kelleher E; Mooney C; Durand A; Pinto C; Cormican P; Morris D; Donohoe G; Gill M; Gallagher L; Corvin A
Br J Psychiatry; 2020 May; 216(5):275-279. PubMed ID: 31964429
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. 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]
5. 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]
6. Copy number variants in German patients with schizophrenia.
Priebe L; Degenhardt F; Strohmaier J; Breuer R; Herms S; Witt SH; Hoffmann P; Kulbida R; Mattheisen M; Moebus S; Meyer-Lindenberg A; Walter H; Mössner R; Nenadic I; Sauer H; Rujescu D; Maier W; Rietschel M; Nöthen MM; Cichon S
PLoS One; 2013; 8(7):e64035. PubMed ID: 23843933
[TBL] [Abstract][Full Text] [Related]
7. Accurately assessing the risk of schizophrenia conferred by rare copy-number variation affecting genes with brain function.
Raychaudhuri S; Korn JM; McCarroll SA; ; Altshuler D; Sklar P; Purcell S; Daly MJ
PLoS Genet; 2010 Sep; 6(9):e1001097. PubMed ID: 20838587
[TBL] [Abstract][Full Text] [Related]
8. Polygenic risk scores in schizophrenia with clinically significant copy number variants.
Taniguchi S; Ninomiya K; Kushima I; Saito T; Shimasaki A; Sakusabe T; Momozawa Y; Kubo M; Kamatani Y; Ozaki N; Ikeda M; Iwata N
Psychiatry Clin Neurosci; 2020 Jan; 74(1):35-39. PubMed ID: 31461559
[TBL] [Abstract][Full Text] [Related]
9. 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]
10. Copy number variants in siblings of Mexican origin concordant for schizophrenia or bipolar disorder.
Vega-Sevey JG; Martínez-Magaña JJ; Genis-Mendoza AD; Escamilla M; Lanzagorta N; Tovilla-Zarate CA; Nicolini H
Psychiatry Res; 2020 Sep; 291():113018. PubMed ID: 32540681
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. Dysregulation of post-transcriptional modification by copy number variable microRNAs in schizophrenia with enhanced glycation stress.
Yoshikawa A; Kushima I; Miyashita M; Toriumi K; Suzuki K; Horiuchi Y; Kawaji H; Takizawa S; Ozaki N; Itokawa M; Arai M
Transl Psychiatry; 2021 May; 11(1):331. PubMed ID: 34050135
[TBL] [Abstract][Full Text] [Related]
13. Cognitive Performance Among Carriers of Pathogenic Copy Number Variants: Analysis of 152,000 UK Biobank Subjects.
Kendall KM; Rees E; Escott-Price V; Einon M; Thomas R; Hewitt J; O'Donovan MC; Owen MJ; Walters JTR; Kirov G
Biol Psychiatry; 2017 Jul; 82(2):103-110. PubMed ID: 27773354
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Copy number variation meta-analysis reveals a novel duplication at 9p24 associated with multiple neurodevelopmental disorders.
Glessner JT; Li J; Wang D; March M; Lima L; Desai A; Hadley D; Kao C; Gur RE; Cohen N; Sleiman PMA; Li Q; Hakonarson H;
Genome Med; 2017 Nov; 9(1):106. PubMed ID: 29191242
[TBL] [Abstract][Full Text] [Related]
16. A review of the cognitive impact of neurodevelopmental and neuropsychiatric associated copy number variants.
Molloy CJ; Quigley C; McNicholas Á; Lisanti L; Gallagher L
Transl Psychiatry; 2023 Apr; 13(1):116. PubMed ID: 37031194
[TBL] [Abstract][Full Text] [Related]
17. Gender differences in CNV burden do not confound schizophrenia CNV associations.
Han J; Walters JT; Kirov G; Pocklington A; Escott-Price V; Owen MJ; Holmans P; O'Donovan MC; Rees E
Sci Rep; 2016 May; 6():25986. PubMed ID: 27185616
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. 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]
20. Clinical and parental age characteristics of rare copy number variant burden in patients with schizophrenia.
Martin AK; Robinson G; Reutens D; Mowry B
Am J Med Genet B Neuropsychiatr Genet; 2015 Jul; 168B(5):374-82. PubMed ID: 25943776
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
