Human Genome Epidemiology Literature Finder
Records 1 - 16 (of 16 Records) |
Query Trace: RTN4R[original query] |
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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 |
Mutations and novel polymorphisms in coding regions and UTRs of CDK5R1 and OMG genes in patients with non-syndromic mental retardation. Neurogenetics 2006 Mar 7 (1): 59-66. Venturin Marco, Moncini Silvia, Villa Valentina, Russo Silvia, Bonati Maria Teresa, Larizza Lidia, Riva Pao |
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 |
A common functional allele of the Nogo receptor gene, reticulon 4 receptor (RTN4R), is associated with sporadic amyotrophic lateral sclerosis in a French population. Amyotrophic lateral sclerosis & frontotemporal degeneration 2015 Jun 1-7. Amy Maïté, Staehlin Oliver, René Frédérique, Blasco Hélène, Marouillat Sylviane, Daoud Hussein, Vourc'h Patrick, Gordon Paul H, Camu William, Corcia Philippe, Loeffler Jean-Philippe, Palkovits Miklós, Sommer Wolfgang H, Andres Christian |
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 |
Genetic variation is associated with RTN4R expression and working memory processing in healthy humans. Brain research bulletin 2017 Jul 134 162-167. Lo Bianco Luciana, Attrotto Maria Teresa, Torretta Silvia, Masellis Rita, Rampino Antonio, D'Ambrosio Enrico, Di Giorgio Annabella, Ferranti Laura, Fazio Leonardo, Gelao Barbara, Blasi Giuseppe, Bertolino Alessand |
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 |
The rs696880 Polymorphism in the Nogo-A Receptor Gene (RTN4R) Is Associated With Susceptibility to Sporadic Amyotrophic Lateral Sclerosis in the Chinese Population. Frontiers in aging neuroscience 2018 10 108. Xu Lianping, Li Jiao, Tian Danyang, Chen Lu, Tang Lu, Fan Dongshe |
Genetic Screening of Plasticity Regulating Nogo-Type Signaling Genes in Migraine. Brain sciences 2019 12 10 (1): . Smedfors Gabriella, Liesecke Franziska, Ran Caroline, Olson Lars, Karlsson Tobias E, Carmine Belin Andr |
Genetic Variants Were Associated With the Prognosis of Head and Neck Squamous Carcinoma.
Frontiers in oncology 2020 10 372. He Yingzheng, Ji Pei, Li Yuancheng, Wang Ruixia, Ma Hongxia, Yuan H |
A Comprehensive Analysis of Unique and Recurrent Copy Number Variations in Alzheimer's Disease and its Related Disorders. Current Alzheimer research 2020 Nov . El Bitar Fadia, Al Sudairy Nourah, Qadi Najeeb, Al Rajeh Saad, Alghamdi Fatimah, Al Amari Hala, Al Dawsari Ghadeer, Alsubaie Sahar, Al Sudairi Mishael, Abdulaziz Sara, Al Tassan Na |
An in-depth analysis reveals two new genetic variants on 22q11.2 associated with vitiligo in the Chinese Han population. Molecular biology reports 2021 Aug . Tang Xianfa, Cheng Hui, Cheng Lu, Liang Bo, Chen Mengyun, Zheng Xiaodong, Xiao Feng |
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- Page last updated:Apr 22, 2024
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