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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 21, 2025. (Total: 235532Documents)
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Records 1 - 8 (of 8 Records)

Query Trace: Schizophrenia and RTN4R[original query]
Mutations of the Nogo-66 receptor (RTN4R) gene in schizophrenia.
Human mutation 2004 Dec 24 (6): 534-5.
Sinibaldi Lorenzo, De Luca Alessandro, Bellacchio Emanuele, Conti Emanuela, Pasini Augusto, Paloscia Claudio, Spalletta Gianfranco, Caltagirone Carlo, Pizzuti Antonio, Dallapiccola Bru
No association between the genetic polymorphisms in the RTN4R gene and schizophrenia in the Chinese population.
Journal of neural transmission (Vienna, Austria : 1996) 2007 Feb 114 (2): 249-54.
Meng J, Shi Y, Zhao X, Guo S, Wang H, Zheng Y, Tang R, Feng G, Gu N, Liu H, Zhu S, He
Genetic variants of Nogo-66 receptor with possible association to schizophrenia block myelin inhibition of axon growth.
The Journal of neuroscience : the official journal of the Society for Neuroscience 2008 Dec 28 (49): 13161-72.
Budel Stéphane, Padukkavidana Thihan, Liu Betty P, Feng Zeny, Hu Fenghua, Johnson Sam, Lauren Juha, Park James H, McGee Aaron W, Liao Ji, Stillman Althea, Kim Ji-Eun, Yang Bao-Zhu, Sodi Stefano, Gelernter Joel, Zhao Hongyu, Hisama Fuki, Arnsten Amy F T, Strittmatter Stephen
Association study of Nogo-related genes with schizophrenia in a Japanese case-control sample.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2011 Jul 156B (5): 581-92.
Jitoku Daisuke, Hattori Eiji, Iwayama Yoshimi, Yamada Kazuo, Toyota Tomoko, Kikuchi Mitsuru, Maekawa Motoko, Nishikawa Toru, Yoshikawa Tak
Lack of association of the RTN4R genetic variations with risk of schizophrenia and SPEM abnormality in a Korean population.
Psychiatry research 2011 Sep 189 (2): 312-4.
Pasaje Charisse Flerida A, Bae Joon Seol, Park Byung-Lae, Park Chul Soo, Kim Bong-Jo, Lee Cheol-Soon, Kim Jae Won, Choi Woo Hyuk, Shin Tae-Min, Koh In Song, Choi Ihn-Geun, Woo Sung-Ll, Shin Hyoung D
Identification of genetic variants of LGI1 and RTN4R (NgR1) linked to schizophrenia that are defective in NgR1-LGI1 signaling.
Molecular genetics & genomic medicine 2016 Jul 4 (4): 447-56.
Thomas Rhalena A, Ambalavanan Amirthagowri, Rouleau Guy A, Barker Philip
A novel rare variant R292H in RTN4R affects growth cone formation and possibly contributes to schizophrenia susceptibility.
Translational psychiatry 2017 9 7 (8): e1214.
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
Associations between neurodevelopmental genes, neuroanatomy, and ultra high risk symptoms of psychosis in 22q11.2 deletion syndrome.
American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2017 Jan .
Thompson Carlie A, Karelis Jason, Middleton Frank A, Gentile Karen, Coman Ioana L, Radoeva Petya D, Mehta Rashi, Fremont Wanda P, Antshel Kevin M, Faraone Stephen V, Kates Wendy
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