249 related articles for article (PubMed ID: 33279929)
1. 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]
2. Novel germline variant in the histone demethylase and transcription regulator KDM4C induces a multi-cancer phenotype.
Katainen R; Donner I; Räisänen M; Berta D; Kuosmanen A; Kaasinen E; Hietala M; Aaltonen LA
J Med Genet; 2022 Jul; 59(7):644-651. PubMed ID: 34281993
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Focal structural variants revealed by whole genome sequencing disrupt the histone demethylase KDM4C in B-cell lymphomas.
Lopez C; Schleussner N; Bernhart SH; Kleinheinz K; Sungalee S; Sczakiel HL; Kretzmer H; Toprak UH; Glaser S; Wagener R; Ammerpohl O; Bens S; Giefing M; Sanchez JCG; Apic G; Hubschmann D; Janz M; Kreuz M; Mottok A; Muller JM; Seufert J; Hoffmann S; Korbel JO; Russell RB; Schule R; Trumper L; Klapper W; Radlwimmer B; Lichter P; Kuppers R; Schlesner M; Mathas S; Siebert R
Haematologica; 2023 Feb; 108(2):543-554. PubMed ID: 35522148
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. 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]
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. 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]
9. 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]
10. 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]
11. Positional cloning and comprehensive mutation analysis identified a novel KDM2B mutation in a Japanese family with minor malformations, intellectual disability, and schizophrenia.
Yokotsuka-Ishida S; Nakamura M; Tomiyasu Y; Nagai M; Kato Y; Tomiyasu A; Umehara H; Hayashi T; Sasaki N; Ueno SI; Sano A
J Hum Genet; 2021 Jun; 66(6):597-606. PubMed ID: 33402700
[TBL] [Abstract][Full Text] [Related]
12. Novel KDM5B splice variants identified in patients with developmental disorders: Functional consequences.
Lebrun N; Mehler-Jacob C; Poirier K; Zordan C; Lacombe D; Carion N; Billuart P; Bienvenu T
Gene; 2018 Dec; 679():305-313. PubMed ID: 30217758
[TBL] [Abstract][Full Text] [Related]
13. Natural variation in the histone demethylase, KDM4C, influences expression levels of specific genes including those that affect cell growth.
Gregory BL; Cheung VG
Genome Res; 2014 Jan; 24(1):52-63. PubMed ID: 24285722
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. Leveraging blood serotonin as an endophenotype to identify de novo and rare variants involved in autism.
Chen R; Davis LK; Guter S; Wei Q; Jacob S; Potter MH; Cox NJ; Cook EH; Sutcliffe JS; Li B
Mol Autism; 2017; 8():14. PubMed ID: 28344757
[TBL] [Abstract][Full Text] [Related]
17. 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]
18. 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]
19. Opposing Chromatin Signals Direct and Regulate the Activity of Lysine Demethylase 4C (KDM4C).
Pack LR; Yamamoto KR; Fujimori DG
J Biol Chem; 2016 Mar; 291(12):6060-70. PubMed ID: 26747609
[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]
