153 related articles for article (PubMed ID: 35967956)
1. Investigation of
Furuta S; Aleksic B; Nawa Y; Kimura H; Kushima I; Ishizuka K; Kato H; Toyama M; Arioka Y; Mori D; Morikawa M; Inada T; Ozaki N
Nagoya J Med Sci; 2022 May; 84(2):260-268. PubMed ID: 35967956
[TBL] [Abstract][Full Text] [Related]
2. Mutation screening of GRIN2B in schizophrenia and autism spectrum disorder in a Japanese population.
Takasaki Y; Koide T; Wang C; Kimura H; Xing J; Kushima I; Ishizuka K; Mori D; Sekiguchi M; Ikeda M; Aizawa M; Tsurumaru N; Iwayama Y; Yoshimi A; Arioka Y; Yoshida M; Noma H; Oya-Ito T; Nakamura Y; Kunimoto S; Aleksic B; Uno Y; Okada T; Ujike H; Egawa J; Kuwabara H; Someya T; Yoshikawa T; Iwata N; Ozaki N
Sci Rep; 2016 Sep; 6():33311. PubMed ID: 27616045
[TBL] [Abstract][Full Text] [Related]
3. Sequencing of selected chromatin remodelling genes reveals increased burden of rare missense variants in ASD patients from the Japanese population.
Lo T; Kushima I; Aleksic B; Kato H; Nawa Y; Hayashi Y; Otgonbayar G; Kimura H; Arioka Y; Mori D; Ozaki N
Int Rev Psychiatry; 2022 Feb; 34(2):154-167. PubMed ID: 35699097
[TBL] [Abstract][Full Text] [Related]
4. Identification of ultra-rare disruptive variants in voltage-gated calcium channel-encoding genes in Japanese samples of schizophrenia and autism spectrum disorder.
Wang C; Horigane SI; Wakamori M; Ueda S; Kawabata T; Fujii H; Kushima I; Kimura H; Ishizuka K; Nakamura Y; Iwayama Y; Ikeda M; Iwata N; Okada T; Aleksic B; Mori D; Yoshida T; Bito H; Yoshikawa T; Takemoto-Kimura S; Ozaki N
Transl Psychiatry; 2022 Feb; 12(1):84. PubMed ID: 35220405
[TBL] [Abstract][Full Text] [Related]
5. A novel rare variant R292H in RTN4R affects growth cone formation and possibly contributes to schizophrenia susceptibility.
Kimura H; Fujita Y; Kawabata T; Ishizuka K; Wang C; Iwayama Y; Okahisa Y; Kushima I; Morikawa M; Uno Y; Okada T; Ikeda M; Inada T; Branko A; Mori D; Yoshikawa T; Iwata N; Nakamura H; Yamashita T; Ozaki N
Transl Psychiatry; 2017 Aug; 7(8):e1214. PubMed ID: 28892071
[TBL] [Abstract][Full Text] [Related]
6. Functional characterization of rare NRXN1 variants identified in autism spectrum disorders and schizophrenia.
Ishizuka K; Yoshida T; Kawabata T; Imai A; Mori H; Kimura H; Inada T; Okahisa Y; Egawa J; Usami M; Kushima I; Morikawa M; Okada T; Ikeda M; Branko A; Mori D; Someya T; Iwata N; Ozaki N
J Neurodev Disord; 2020 Sep; 12(1):25. PubMed ID: 32942984
[TBL] [Abstract][Full Text] [Related]
7. Investigation of Rare Single-Nucleotide PCDH15 Variants in Schizophrenia and Autism Spectrum Disorders.
Ishizuka K; Kimura H; Wang C; Xing J; Kushima I; Arioka Y; Oya-Ito T; Uno Y; Okada T; Mori D; Aleksic B; Ozaki N
PLoS One; 2016; 11(4):e0153224. PubMed ID: 27058588
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Rare genetic variants in the gene encoding histone lysine demethylase 4C (KDM4C) and their contributions to susceptibility to schizophrenia and autism spectrum disorder.
Kato H; Kushima I; Mori D; Yoshimi A; Aleksic B; Nawa Y; Toyama M; Furuta S; Yu Y; Ishizuka K; Kimura H; Arioka Y; Tsujimura K; Morikawa M; Okada T; Inada T; Nakatochi M; Shinjo K; Kondo Y; Kaibuchi K; Funabiki Y; Kimura R; Suzuki T; Yamakawa K; Ikeda M; Iwata N; Takahashi T; Suzuki M; Okahisa Y; Takaki M; Egawa J; Someya T; Ozaki N
Transl Psychiatry; 2020 Dec; 10(1):421. PubMed ID: 33279929
[TBL] [Abstract][Full Text] [Related]
10. Rare genetic variants in CX3CR1 and their contribution to the increased risk of schizophrenia and autism spectrum disorders.
Ishizuka K; Fujita Y; Kawabata T; Kimura H; Iwayama Y; Inada T; Okahisa Y; Egawa J; Usami M; Kushima I; Uno Y; Okada T; Ikeda M; Aleksic B; Mori D; Someya T; Yoshikawa T; Iwata N; Nakamura H; Yamashita T; Ozaki N
Transl Psychiatry; 2017 Aug; 7(8):e1184. PubMed ID: 28763059
[TBL] [Abstract][Full Text] [Related]
11. 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]
12. 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]
13. Damaging coding variants within kainate receptor channel genes are enriched in individuals with schizophrenia, autism and intellectual disabilities.
Koromina M; Flitton M; Blockley A; Mellor IR; Knight HM
Sci Rep; 2019 Dec; 9(1):19215. PubMed ID: 31844109
[TBL] [Abstract][Full Text] [Related]
14. Common vs. Distinct Visuomotor Control Deficits in Autism Spectrum Disorder and Schizophrenia.
Carment L; Khoury E; Dupin L; Guedj L; Bendjemaa N; Cuenca M; Maier MA; Krebs MO; Lindberg PG; Amado I
Autism Res; 2020 Jun; 13(6):885-896. PubMed ID: 32157824
[TBL] [Abstract][Full Text] [Related]
15. Investigation of SHANK3 in schizophrenia.
de Sena Cortabitarte A; Degenhardt F; Strohmaier J; Lang M; Weiss B; Roeth R; Giegling I; Heilmann-Heimbach S; Hofmann A; Rujescu D; Fischer C; Rietschel M; Nöthen MM; Rappold GA; Berkel S
Am J Med Genet B Neuropsychiatr Genet; 2017 Jun; 174(4):390-398. PubMed ID: 28371232
[TBL] [Abstract][Full Text] [Related]
16. Rare single-nucleotide DAB1 variants and their contribution to Schizophrenia and autism spectrum disorder susceptibility.
Nawa Y; Kimura H; Mori D; Kato H; Toyama M; Furuta S; Yu Y; Ishizuka K; Kushima I; Aleksic B; Arioka Y; Morikawa M; Okada T; Inada T; Kaibuchi K; Ikeda M; Iwata N; Suzuki M; Okahisa Y; Egawa J; Someya T; Nishimura F; Sasaki T; Ozaki N
Hum Genome Var; 2020 Nov; 7(1):37. PubMed ID: 33298905
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. Gain-of-function missense variant in SLC12A2, encoding the bumetanide-sensitive NKCC1 cotransporter, identified in human schizophrenia.
Merner ND; Mercado A; Khanna AR; Hodgkinson A; Bruat V; Awadalla P; Gamba G; Rouleau GA; Kahle KT
J Psychiatr Res; 2016 Jun; 77():22-6. PubMed ID: 26955005
[TBL] [Abstract][Full Text] [Related]
19. Rare loss of function mutations in N-methyl-D-aspartate glutamate receptors and their contributions to schizophrenia susceptibility.
Yu Y; Lin Y; Takasaki Y; Wang C; Kimura H; Xing J; Ishizuka K; Toyama M; Kushima I; Mori D; Arioka Y; Uno Y; Shiino T; Nakamura Y; Okada T; Morikawa M; Ikeda M; Iwata N; Okahisa Y; Takaki M; Sakamoto S; Someya T; Egawa J; Usami M; Kodaira M; Yoshimi A; Oya-Ito T; Aleksic B; Ohno K; Ozaki N
Transl Psychiatry; 2018 Jan; 8(1):12. PubMed ID: 29317596
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
