RELN c.474-9041T>A

Variant ID: 7-103426115-A-T

NM_005045.3(RELN):c.474-9041T>A

This variant was identified in 10 publications

View GRCh38 version.




Publications:


New Strategies for the Treatment of Neuropsychiatric Disorders Based on Reelin Dysfunction.

International Journal Of Molecular Sciences
Tsuneura, Yumi Y; Nakai, Tsuyoshi T; Mizoguchi, Hiroyuki H; Yamada, Kiyofumi K
Publication Date: 2022-02-06

Variant appearance in text: rs262355
PubMed Link: 35163751
Variant Present in the following documents:
  • Main text
  • ijms-23-01829.pdf
View BVdb publication page



New Strategies for the Treatment of Neuropsychiatric Disorders Based on Reelin Dysfunction.

International Journal Of Molecular Sciences
Tsuneura, Yumi Y; Nakai, Tsuyoshi T; Mizoguchi, Hiroyuki H; Yamada, Kiyofumi K
Publication Date: 2022-02-06

Variant appearance in text: rs262355
PubMed Link: 35163751
Variant Present in the following documents:
  • Main text
  • ijms-23-01829.pdf
View BVdb publication page



Rare single-nucleotide DAB1 variants and their contribution to Schizophrenia and autism spectrum disorder susceptibility.

Human Genome Variation
Nawa, Yoshihiro Y; Kimura, Hiroki H; Mori, Daisuke D; Kato, Hidekazu H; Toyama, Miho M; Furuta, Sho S; Yu, Yanjie Y; Ishizuka, Kanako K; Kushima, Itaru I; Aleksic, Branko B; Arioka, Yuko Y; Morikawa, Mako M; Okada, Takashi T; Inada, Toshiya T; Kaibuchi, Kozo K; Ikeda, Masashi M; Iwata, Nakao N; Suzuki, Michio M; Okahisa, Yuko Y; Egawa, Jun J; Someya, Toshiyuki T; Nishimura, Fumichika F; Sasaki, Tsukasa T; Ozaki, Norio N
Publication Date: 2020-11-10

Variant appearance in text: rs262355
PubMed Link: 33298905
Variant Present in the following documents:
  • 41439_2020_Article_125.pdf
View BVdb publication page



Two Novel Loci of RELN Associated With Antipsychotics Response in Chinese Han Population.

Frontiers In Pharmacology
Xu, Qingqing Q; Li, Mo M; Qin, Shengying S; Li, Yaojing Y; Ning, Ailing A; Fu, Yingmei Y; Wang, Dongxiang D; Zeng, Duan D; Li, Huafang H; Yu, Wenjuan W; Yu, Shunying S
Publication Date: 2020

Variant appearance in text: rs262355
PubMed Link: 32082176
Variant Present in the following documents:
  • Main text
  • fphar-11-00007.pdf
View BVdb publication page



Reelin Signaling Controls the Preference for Social Novelty in Zebrafish.

Frontiers In Behavioral Neuroscience
Dalla Vecchia, Elisa E; Di Donato, Vincenzo V; Young, Andrew M J AMJ; Del Bene, Filippo F; Norton, William H J WHJ
Publication Date: 2019

Variant appearance in text: rs262355
PubMed Link: 31607872
Variant Present in the following documents:
  • Main text
  • fnbeh-13-00214.pdf
View BVdb publication page



SNP Variation of RELN Gene and Schizophrenia in a Chinese Population: A Hospital-Based Case-Control Study.

Frontiers In Genetics
Luo, Xia X; Chen, Si S; Xue, Li L; Chen, Jian-Huan JH; Shi, Yan-Wei YW; Zhao, Hu H
Publication Date: 2019

Variant appearance in text: rs262355
PubMed Link: 30891068
Variant Present in the following documents:
  • Main text
  • fgene-10-00175.pdf
View BVdb publication page



Toward the Language Oscillogenome.

Frontiers In Psychology
Murphy, Elliot E; Benítez-Burraco, Antonio A
Publication Date: 2018

Variant appearance in text: rs262355
PubMed Link: 30405489
Variant Present in the following documents:
  • fpsyg-09-01999.pdf
View BVdb publication page



Genetic Consideration of Schizotypal Traits: A Review.

Frontiers In Psychology
Walter, Emma E EE; Fernandez, Francesca F; Snelling, Mollie M; Barkus, Emma E
Publication Date: 2016

Variant appearance in text: rs262355
PubMed Link: 27895608
Variant Present in the following documents:
  • Main text
  • fpsyg-07-01769.pdf
View BVdb publication page



Bridging the Gap between Genes and Language Deficits in Schizophrenia: An Oscillopathic Approach.

Frontiers In Human Neuroscience
Murphy, Elliot E; Benítez-Burraco, Antonio A
Publication Date: 2016

Variant appearance in text: rs262355
PubMed Link: 27601987
Variant Present in the following documents:
  • fnhum-10-00422.pdf
View BVdb publication page



Paradox of schizophrenia genetics: is a paradigm shift occurring?

Behavioral And Brain Functions : Bbf
Doi, Nagafumi N; Hoshi, Yoko Y; Itokawa, Masanari M; Yoshikawa, Takeo T; Ichikawa, Tomoe T; Arai, Makoto M; Usui, Chie C; Tachikawa, Hirokazu H
Publication Date: 2012-05-31

Variant appearance in text: rs262355
PubMed Link: 22650965
Variant Present in the following documents:
  • Main text
  • 1744-9081-8-28.pdf
View BVdb publication page



A genome-wide analysis identifies genetic variants in the RELN gene associated with otosclerosis.

American Journal Of Human Genetics
Schrauwen, Isabelle I; Ealy, Megan M; Huentelman, Matthew J MJ; Thys, Melissa M; Homer, Nils N; Vanderstraeten, Kathleen K; Fransen, Erik E; Corneveaux, Jason J JJ; Craig, David W DW; Claustres, Mireille M; Cremers, Cor W R J CW; Dhooge, Ingeborg I; Van de Heyning, Paul P; Vincent, Robert R; Offeciers, Erwin E; Smith, Richard J H RJ; Van Camp, Guy G
Publication Date: 2009-03

Variant appearance in text: rs262355
PubMed Link: 19230858
Variant Present in the following documents:
  • Main text
View BVdb publication page