Human Genome Epidemiology Literature Finder
Records 1 - 25 (of 25 Records) |
Query Trace: RIT2[original query] |
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Strong synaptic transmission impact by copy number variations in schizophrenia. Proceedings of the National Academy of Sciences of the United States of America 2010 Jun 107 (23): 10584-9. Glessner Joseph T, Reilly Muredach P, Kim Cecilia E, Takahashi Nagahide, Albano Anthony, Hou Cuiping, Bradfield Jonathan P, Zhang Haitao, Sleiman Patrick M A, Flory James H, Imielinski Marcin, Frackelton Edward C, Chiavacci Rosetta, Thomas Kelly A, Garris Maria, Otieno Frederick G, Davidson Michael, Weiser Mark, Reichenberg Abraham, Davis Kenneth L, Friedman Joseph I, Cappola Thomas P, Margulies Kenneth B, Rader Daniel J, Grant Struan F A, Buxbaum Joseph D, Gur Raquel E, Hakonarson Hak |
[Genome-wide association study of allergic diseases in Russians of Western Siberia]. Molekuliarnaia biologiia 0 45 (3): 464-72. Fre?din M B, Bragina E Iu, Fedorova O S, Deev I A, Kulikov E S, Ogorodova L M, Puzyrev V |
Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2.
Annals of neurology 2012 Mar 71 (3): 3. Pankratz N, Beecham GW, Destefano AL, Dawson TM, Doheny KF, Factor SA, Hamza TH, Hung AY, Hyman BT, Ivinson AJ, Krainc D, Latourelle JC, Clark LN, Marder K, Martin ER, Mayeux R, Ross OA, Scherzer CR, Simon DK, Tanner C, Vance JM, Wszolek ZK, Zabetian CP, Myers RH, Payami H, Scott WK, Foroud T |
RIT2 variant is not associated with Parkinson's disease in a Taiwanese population. Neurobiology of aging 2013 Sep 34 (9): 2236.e1-3. Lin Chin-Hsien, Chen Meng-Ling, Yu Chin-Yi, Wu Ruey-Me |
RIT2 polymorphism is associated with Parkinson's disease in a Han Chinese population. Neurobiology of aging 2015 Mar 36 (3): 1603.e15-7. Nie Kun, Feng Shu-jun, Tang Hong-mei, Ma Gui-xian, Gan Rong, Zhao Xin, Zhao Jie-hao, Wang Li-min, Huang Zhi-heng, Huang Jing, Gao Liang, Zhang You-wen, Zhu Rui-ming, Duan Zhen-peng, Zhang Yu-hu, Wang Li-ju |
The RIT2 and STX1B polymorphisms are associated with Parkinson's disease. Parkinsonism & related disorders 2015 Mar 21 (3): 300-2. Wang Jian-Yong, Gong Mei-Ying, Ye Yang-Lie, Ye Jin-Min, Lin Guo-Liang, Zhuang Qing-Qing, Zhang Xiong, Zhu Jian-Ho |
Genetic association of RIT2 rs12456492 polymorphism and Parkinson's disease susceptibility in Asian populations: a meta-analysis. Scientific reports 2015 5 13805. Lu Yanjun, Liu Wei, Tan Kun, Peng Jing, Zhu Yaowu, Wang Xio |
Genome-wide Association Study of Autism Spectrum Disorder in the East Asian Populations.
Autism research : official journal of the International Society for Autism Research 2015 Aug . Liu Xiaoxi, Shimada Takafumi, Otowa Takeshi, Wu Yu-Yu, Kawamura Yoshiya, Tochigi Mamoru, Iwata Yasuhide, Umekage Tadashi, Toyota Tomoko, Maekawa Motoko, Iwayama Yoshimi, Suzuki Katsuaki, Kakiuchi Chihiro, Kuwabara Hitoshi, Kano Yukiko, Nishida Hisami, Sugiyama Toshiro, Kato Nobumasa, Chen Chia-Hsiang, Mori Norio, Yamada Kazuo, Yoshikawa Takeo, Kasai Kiyoto, Tokunaga Katsushi, Sasaki Tsukasa, Gau Susan Shur-F |
RIT2 rs12456492 polymorphism and the risk of Parkinson's disease: A meta-analysis. Neuroscience letters 2015 Aug 602 167-71. Zhang Xiaona, Niu Mengyue, Li Hong, Xie An |
Personal exposure to PM2.5, genetic variants and DNA damage: a multi-center population-based study in Chinese. Toxicology letters 2015 Jun 235 (3): 172-8. Chu Minjie, Sun Chongqi, Chen Weihong, Jin Guangfu, Gong Jianhang, Zhu Meng, Yuan Jing, Dai Juncheng, Wang Meilin, Pan Yun, Song Yuanchao, Ding Xiaojie, Guo Xuejiang, Du Mulong, Xia Yankai, Kan Haidong, Zhang Zhengdong, Hu Zhibin, Wu Tangchun, Shen Hongbi |
Assessment of RIT2 rs12456492 association with Parkinson's disease in Mainland China. Neurobiology of aging 2015 Mar 36 (3): 1600.e9-11. Liu Zhen-hua, Guo Ji-feng, Wang Ya-qin, Li Kai, Sun Qi-ying, Xu Qian, Yan Xin-xiang, Xu Chang-shui, Tang Bei-s |
Trans-pQTL study identifies immune crosstalk between Parkinson and Alzheimer loci. Neurology. Genetics 2016 Aug 2 (4): e90. Chan Gail, White Charles C, Winn Phoebe A, Cimpean Maria, Replogle Joseph M, Glick Laura R, Cuerdon Nicole E, Ryan Katie J, Johnson Keith A, Schneider Julie A, Bennett David A, Chibnik Lori B, Sperling Reisa A, De Jager Philip L, Bradshaw Elizabeth |
RIT2 Polymorphisms: Is There a Differential Association? Molecular neurobiology 2016 Mar . Emamalizadeh Babak, Jamshidi Javad, Movafagh Abolfazl, Ohadi Mina, Khaniani Mahmoud Shekari, Kazeminasab Somayyeh, Biglarian Akbar, Taghavi Shaghayegh, Motallebi Marzieh, Fazeli Atena, Ahmadifard Azadeh, Shahidi Gholam-Ali, Petramfar Peyman, Shahmohammadibeni Neda, Dadkhah Tahereh, Khademi Ehteram, Tafakhori Abbas, Khaligh Ali, Safaralizadeh Tannaz, Kowsari Ali, Mirabzadeh Arash, Zarneh Amir Ehtesham Shafiei, Khorrami Mehdi, Shokraeian Parasto, Banavandi Mohammad Javad Soltani, Lima Behnam Safarpour, Andarva Monavvar, Alehabib Elham, Atakhorrami Minoo, Darvish Hosse |
Genome-wide association study of Parkinson's disease in East Asians.
Human molecular genetics 2016 Dec . Foo Jia Nee, Tan Louis C, Irwan Ishak D, Au Wing-Lok, Low Hui Qi, Prakash Kumar-M, Ahmad-Annuar Azlina, Bei Jinxin, Chan Anne Yy, Chen Chiung Mei, Chen Yi-Chun, Chung Sun Ju, Deng Hao, Lim Shen-Yang, Mok Vincent, Pang Hao, Pei Zhong, Peng Rong, Shang Hui-Fang, Song Kyuyoung, Tan Ai Huey, Wu Yih-Ru, Aung Tin, Cheng Ching-Yu, Chew Fook Tim, Chew Soo-Hong, Chong Siow-Ann, Ebstein Richard P, Lee Jimmy, Saw Seang-Mei, Seow Adeline, Subramaniam Mythily, Tai E-Shyong, Vithana Eranga N, Wong Tien-Yin, Heng Khai Koon, Meah Wee-Yang, Khor Chiea Chuen, Liu Hong, Zhang Furen, Liu Jianjun, Tan Eng-Ki |
Genetic association study between RIT2 and Parkinson's disease in a Han Chinese population. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2017 Feb 38 (2): 343-347. Li Jun-Ying, Zhang Jin-Hong, Li Nan-Nan, Wang Ling, Lu Zhong-Jiao, Cheng Lan, Sun Xiao-Yi, Peng Ro |
Ras-like without CAAX 2 (RIT2): a susceptibility gene for autism spectrum disorder. Metabolic brain disease 2017 Feb . Hamedani Shima Yazdandoost, Gharesouran Jalal, Noroozi Rezvan, Sayad Arezou, Omrani Mir Davood, Mir Atefeh, Afjeh Sarah Sadat Aghabozrg, Toghi Mehdi, Manoochehrabadi Saba, Ghafouri-Fard Soudeh, Taheri Mohamm |
Association of RIT2 and RAB7L1 with Parkinson's disease: a case-control study in a Taiwanese cohort and a meta-analysis in Asian populations. Neurobiology of aging 2019 Nov . Liu Tsai-Wei, Wu Yih-Ru, Chen Yi-Chun, Fung Hon Chung, Chen Chiung-M |
Genetic Risk Factors for Essential Tremor: A Review. Tremor and other hyperkinetic movements (New York, N.Y.) 2020 Jun 10 4. Siokas Vasileios, Aloizou Athina-Maria, Tsouris Zisis, Liampas Ioannis, Aslanidou Paraskevi, Dastamani Metaxia, Brotis Alexandros G, Bogdanos Dimitrios P, Hadjigeorgiou Georgios M, Dardiotis Efthimi |
A pH-eQTL Interaction at the RIT2-SYT4 Parkinson's Disease Risk Locus in the Substantia Nigra. Frontiers in aging neuroscience 2021 7 13 690632. Patel Sejal, Howard Derek, French Le |
Genome-Wide Association Study Meta-Analysis for Parkinson Disease Motor Subtypes.
Neurology. Genetics 2021 Apr 7 (2): e557. Alfradique-Dunham Isabel, Al-Ouran Rami, von Coelln Rainer, Blauwendraat Cornelis, Hill Emily, Luo Lan, Stillwell Amanda, Young Emily, Kaw Anita, Tan Manuela, Liao Calwing, Hernandez Dena, Pihlstrom Lasse, Grosset Donald, Shulman Lisa M, Liu Zhandong, Rouleau Guy A, Nalls Mike, Singleton Andrew B, Morris Huw, Jankovic Joseph, Shulman Joshua |
MAO-B Polymorphism Associated with Progression in a Chinese Parkinson's Disease Cohort but Not in the PPMI Cohort. Parkinson's disease 2022 9 2022 3481102. Cui Shi-Shuang, Wu Ling-Yu, Li Gen, Du Juan-Juan, Huang Pei, Liu Jin, Ling Yun, Ren Kang, Chen Zhong-Lue, Chen Sheng- |
Polymorphism of neurodegeneration-related genes associated with Parkinson's disease risk. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2022 6 43 (9): 5301-5312. Li Jiaxin, Yi Minhan, Li Binbin, Yin Shujuan, Zhang Ying, Huang Zini, Shu Li, Zhang Yu |
Synthesis of genetic association studies on autism spectrum disorders using a genetic model-free approach. Psychiatric genetics 2022 3 32 (3): 91-104. Mpoulimari Ioanna, Zintzaras Eli |
Predominant monomorphism of the RIT2 and GPM6B exceptionally long GA blocks in human and enriched divergent alleles in the disease compartment. Genetica 2022 1 150 (1): 27-40. Khamse S, Arabfard M, Salesi M, Behmard E, Jafarian Z, Afshar H, Khazaei M, Ohadi |
Association between RIT2 rs16976358 Polymorphism and Autism Spectrum Disorder in Asian Populations: A Meta-analysis. BioMed research international 2023 2 2023 8886927. Wang Jing, Wei Shoupeng, Zhang Jin, Wang |
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- Page last updated:Apr 22, 2024
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