Human Genome Epidemiology Literature Finder
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Records 1 - 20 (of 20 Records) |
| Query Trace: Disease and NR4A2[original query] |
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| Mutations in NR4A2 associated with familial Parkinson disease. Nature genetics 2003 Jan 33 (1): 85-9. Le Wei-Dong, Xu Pingyi, Jankovic Joseph, Jiang Hong, Appel Stanley H, Smith Roy G, Vassilatis Demetrios |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
| 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 |
- Page last reviewed:Feb 1, 2024
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