Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 33 Records) |
Query Trace: NR4A2[original query] |
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NURR1 promoter polymorphisms: Parkinson's disease, schizophrenia, and personality traits. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2003 Jul 120B (1): 51-7. Carmine Andrea, Buervenich Silvia, Galter Dagmar, Jönsson Erik G, Sedvall Göran C, Farde Lars, Gustavsson J Petter, Bergman Hans, Chowdari Kodavali V, Nimgaonkar Vishwajit L, Anvret Maria, Sydow Olof, Olson La |
Distribution of haplotypes derived from three common variants of the NR4A2 gene in Japanese patients with schizophrenia. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2003 Apr 118B (1): 20-4. Iwayama-Shigeno Yoshimi, Yamada Kazuo, Toyota Tomoko, Shimizu Hiromitsu, Hattori Eiji, Yoshitsugu Kiyoshi, Fujisawa Tetsuya, Yoshida Yukako, Kobayashi Toshio, Toru Michio, Kurumaji Akeo, Detera-Wadleigh Sevilla, Yoshikawa Tak |
NR4A2 and schizophrenia: lack of association in a Portuguese/Brazilian study. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2004 Jul 128B (1): 41-5. Ruano Dina, Macedo António, Dourado Ana, Soares Maria João, Valente José, Coelho Isabel, Santos Vítor, Azevedo Maria Helena, Goodman Ann, Hutz Mara Helena, Gama Clarissa, Lobato Maria Inês, Belmonte-de-Abreu Paulo, Palha Joana Almei |
Identification and characterization of human NR4A2 polymorphisms in attention deficit hyperactivity disorder. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2005 Feb 133B (1): 57-63. Smith Karen Müller, Bauer Lorri, Fischer Mariellen, Barkley Russell, Navia Bradford |
NR4A2 genetic variation in sporadic Parkinson's disease: a genewide approach. Movement disorders : official journal of the Movement Disorder Society 2006 Nov 21 (11): 1960-3. Healy Daniel G, Abou-Sleiman Patrick M, Ahmadi Kourosh R, Gandhi Sonia, Muqit Miratul M, Bhatia Kailash P, Quinn Niall P, Lees Andrew J, Holton Janice L, Revesz Tamas, Wood Nicholas |
Association analysis of 15 polymorphisms within 10 candidate genes for antisocial behavioural traits. Psychiatric genetics 2007 Oct 17 (5): 299-303. Prichard Zoë M, Jorm Anthony F, Mackinnon Andrew, Easteal Sim |
Nuclear receptor NR4A2 IVS6 +18insG and brain derived neurotrophic factor (BDNF) V66M polymorphisms and risk of Taiwanese Parkinson's disease. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2007 Jun 144B (4): 458-62. Chen Chiung-Mei, Chen I-Cheng, Chang Kuo-Hsuan, Chen Yi-Chun, Lyu Rong-Kuo, Liu Yen-Tzu, Hu Fen-Ju, Chao Chih-Ying, Lee-Chen Guey-Jen, Wu Yih- |
Genotype patterns that contribute to increased risk for or protection from developing heroin addiction. Molecular psychiatry 2008 Apr 13 (4): 417-28. Nielsen D A, Ji F, Yuferov V, Ho A, Chen A, Levran O, Ott J, Kreek M |
Dopamine genes and nicotine dependence in treatment-seeking and community smokers. Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology 2009 Sep 34 (10): 2252-64. Bergen Andrew W, Conti David V, Van Den Berg David, Lee Wonho, Liu Jinghua, Li Dalin, Guo Nan, Mi Huaiyu, Thomas Paul D, Lessov-Schlaggar Christina N, Krasnow Ruth, He Yungang, Nishita Denise, Jiang Ruhong, McClure Jennifer B, Tildesley Elizabeth, Hops Hyman, Tyndale Rachel F, Benowitz Neal L, Lerman Caryn, Swan Gary |
Do polymorphisms in the familial Parkinsonism genes contribute to risk for sporadic Parkinson's disease? Movement disorders : official journal of the Movement Disorder Society 2009 Apr 24 (6): 833-8. Sutherland Greg T, Halliday Glenda M, Silburn Peter A, Mastaglia Frank L, Rowe Dominic B, Boyle Richard S, O'Sullivan John D, Ly Tina, Wilton Steve D, Mellick George |
Haplotypes of the NR4A2/NURR1 gene and cardiovascular disease: the Rotterdam Study. Human mutation 2009 Mar 30 (3): 417-23. Kardys Isabella, van Tiel Claudia M, de Vries Carlie J M, Pannekoek Hans, Uitterlinden André G, Hofman Albert, Witteman Jacqueline C M, de Maat Moniek P |
Replicated association of the NR4A3 gene with smoking behaviour in schizophrenia and in bipolar disorder. Genes, brain, and behavior 2010 Nov 9 (8): 910-7. Novak G, Zai C C, Mirkhani M, Shaikh S, Vincent J B, Meltzer H, Lieberman J A, Strauss J, Lévesque D, Kennedy J L, Le Foll |
Response to methadone maintenance treatment is associated with the MYOCD and GRM6 genes. Molecular diagnosis & therapy 2010 Jun 14 (3): 171-8. Fonseca Francina, Gratacòs Mònica, Escaramís Geòrgia, De Cid Rafael, Martín-Santos Rocío, Fernández-Espejo Emilio, Estivill Xavier, Torrens Mar |
Genetic analysis of NR4A2 gene in a large population of Han Chinese patients with Parkinson's disease. European journal of neurology : the official journal of the European Federation of Neurological Societies 2012 Jul . Liu H, Tao Q, Deng H, Ming M, Ding Y, Xu P, Chen S, Song Z, Le W |
NR4A2: effects of an "orphan" receptor on sustained attention in a schizophrenic population. Schizophrenia bulletin 2013 May 39 (3): 555-63. Ancín Inés, Cabranes José A, Vázquez-Álvarez Blanca, Santos José Luis, Sánchez-Morla Eva, Alaerts Maaike, Del-Favero Jurgen, Barabash A |
Somatic ATP1A1, ATP2B3, and KCNJ5 mutations in aldosterone-producing adenomas. Hypertension 2014 Jan 63 (1): 188-95. Williams Tracy Ann, Monticone Silvia, Schack Vivien R, Stindl Julia, Burrello Jacopo, Buffolo Fabrizio, Annaratone Laura, Castellano Isabella, Beuschlein Felix, Reincke Martin, Lucatello Barbara, Ronconi Vanessa, Fallo Francesco, Bernini Giampaolo, Maccario Mauro, Giacchetti Gilberta, Veglio Franco, Warth Richard, Vilsen Bente, Mulatero Pao |
Association between NR4A2 genetic variation and schizophrenia: A comprehensive systematic review and meta-analysis. Neuroscience letters 2015 Jun 598 85-90. Liu Hongmei, Fu Yingmei, Ren Juanjuan, Yu Shunying, Liu Hongbo, Jiang Ping, Dong Yi, Li Huafa |
Rare Inherited and De Novo CNVs Reveal Complex Contributions to ASD Risk in Multiplex Families. American journal of human genetics 2016 Sep 99 (3): 540-54. Leppa Virpi M, Kravitz Stephanie N, Martin Christa Lese, Andrieux Joris, Le Caignec Cedric, Martin-Coignard Dominique, DyBuncio Christina, Sanders Stephan J, Lowe Jennifer K, Cantor Rita M, Geschwind Daniel |
Pharmacogenetic analysis of cinacalcet response in secondary hyperparathyroidism patients. Drug design, development and therapy 2016 10 2211-25. Jeong Sohyun, Kim In-Wha, Oh Kook-Hwan, Han Nayoung, Joo Kwon Wook, Kim Hyo Jin, Oh Jung |
Association of polymorphisms and reduced expression levels of the NR4A2 gene with Parkinson's disease in a Mexican population. Journal of the neurological sciences 2017 Aug 379 58-63. Ruiz-Sánchez Elizabeth, Yescas Petra, Rodríguez-Violante Mayela, Martínez-Rodríguez Nancy, Díaz-López Jesica N, Ochoa Adriana, Valdes-Rojas Sergio S, Magos-Rodríguez Daniel, Rojas-Castañeda Julio C, Cervantes-Arriaga Amin, Canizales-Quinteros Samuel, Rojas Patric |
NR4A2 genetic variation and Parkinson's disease: Evidence from a systematic review and meta-analysis. Neuroscience letters 2017 Apr . Liu Hongmei, Liu Hongbo, Li Ting, Cui Jiayi, Fu Yingmei, Ren Juanjuan, Sun Xiujia, Jiang Ping, Yu Shunying, Li Chun |
Association of genetic variants and expression levels of porcine FABP4 and FABP5 genes. Animal genetics 2017 10 48 (6): 660-668. Ballester M, Puig-Oliveras A, Castelló A, Revilla M, Fernández A I, Folch J |
Genome sequencing identifies multiple deleterious variants in autism patients with more severe phenotypes. Genetics in medicine : official journal of the American College of Medical Genetics 2018 12 21 (7): 1611-1620. Guo Hui, Duyzend Michael H, Coe Bradley P, Baker Carl, Hoekzema Kendra, Gerdts Jennifer, Turner Tychele N, Zody Michael C, Beighley Jennifer S, Murali Shwetha C, Nelson Bradley J, , Bamshad Michael J, Nickerson Deborah A, Bernier Raphael A, Eichler Evan |
Analysis of rare variants of autosomal-dominant genes in a Chinese population with sporadic Parkinson's disease. Molecular genetics & genomic medicine 2020 Aug e1449. Zheng Ran, Jin Chong-Yao, Chen Ying, Ruan Yang, Gao Ting, Lin Zhi-Hao, Dong Jia-Xian, Yan Ya-Ping, Tian Jun, Pu Jia-Li, Zhang Bao-Ro |
De novo variants of NR4A2 are associated with neurodevelopmental disorder and epilepsy. Genetics in medicine : official journal of the American College of Medical Genetics 2020 5 22 (8): 1413-1417. Singh Sakshi, Gupta Aditi, Zech Michael, Sigafoos Ashley N, Clark Karl J, Dincer Yasemin, Wagner Matias, Humberson Jennifer B, Green Sarah, van Gassen Koen, Brandt Tracy, Schnur Rhonda E, Millan Francisca, Si Yue, Mall Volker, Winkelmann Juliane, Gavrilova Ralitza H, Klee Eric W, Engleman Kendra, Safina Nicole P, Slaugh Rachel, Bryant Emily M, Tan Wen-Hann, Granadillo Jorge, Misra Sunita N, Schaefer G Bradley, Towner Shelley, Brilstra Eva H, Koeleman Bobby P |
Gene discovery for high-density lipoprotein cholesterol level change over time in prospective family studies.
Atherosclerosis 2020 Feb 297 102-110. Feitosa Mary F, Lunetta Kathryn L, Wang Lihua, Wojczynski Mary K, Kammerer Candace M, Perls Thomas, Schupf Nicole, Christensen Kaare, Murabito Joanne M, Province Michael |
Association Between NR4A2 Gene Polymorphism and Depressive Symptoms and Antidepressant Effect. Neuropsychiatric disease and treatment 2021 17 2613-2623. Song Xiaotong, Sun Ning, Zhang Aixia, Lei Lei, Li Xinrong, Liu Zhifen, Wang Yanfang, Yang Chunxia, Zhang Kera |
Working memory deficits in schizophrenia are associated with the rs34884856 variant and expression levels of the NR4A2 gene in a sample Mexican population: a case control study. BMC psychiatry 2021 Feb 21 (1): 86. Ruiz-Sánchez Elizabeth, Jiménez-Genchi Janet, Alcántara-Flores Yessica M, Castañeda-González Carlos J, Aviña-Cervantes Carlos L, Yescas Petra, Del Socorro González-Valadez María, Martínez-Rodríguez Nancy, Ríos-Ortiz Antonio, González-González Martha, López-Navarro María E, Rojas Patric |
Genetic screening of Filipinos suspected with familial Parkinson's disease: A pilot study. Parkinsonism & related disorders 2023 2 108 105319. Caritativo Erin Camille A, Yu Jeryl Ritzi T, Bautista Juan Miguel P, Nishioka Kenya, Jamora Roland Dominic G, Yalung Patrick M, Ng Arlene R, Hattori Nobuta |
Prognostic Factors for Restenosis of Superficial Femoral Artery after Endovascular Treatment. Journal of clinical medicine 2023 10 12 (19): . Vinko Boc, Matija Kozak, Barbara Eržen, Mojca Boži? Mijovski, Anja Boc, Aleš Bli |
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- Page last updated:Apr 22, 2024
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