Human Genome Epidemiology Literature Finder
Records 1 - 21 (of 21 Records) |
Query Trace: DYRK1A[original query] |
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Genome-wide association scan for five major dimensions of personality.
Molecular psychiatry 2010 Jun 15 (6): 647-56. Terracciano A, Sanna S, Uda M, Deiana B, Usala G, Busonero F, Maschio A, Scally M, Patriciu N, Chen W-M, Distel M A, Slagboom E P, Boomsma D I, Villafuerte S, Sliwerska E, Burmeister M, Amin N, Janssens A C J W, van Duijn C M, Schlessinger D, Abecasis G R, Costa P |
DYRK1A genetic variants are not linked to Alzheimer's disease in a Spanish case-control cohort. BMC medical genetics 2009 10 (1): 129. Vázquez-Higuera José Luis, Sánchez-Juan Pascual, Rodríguez-Rodríguez Eloy, Mateo Ignacio, Pozueta Ana, Frank Ana, Sastre Isabel, Valdivieso Fernando, Berciano José, Bullido María J, Combarros Onof |
Genome-wide association study identifies single nucleotide polymorphism in DYRK1A associated with replication of HIV-1 in monocyte-derived macrophages.
PloS one 2011 6 (2): e17190. Bol Sebastiaan M, Moerland Perry D, Limou Sophie, van Remmerden Yvonne, Coulonges Cédric, van Manen Daniëlle, Herbeck Joshua T, Fellay Jacques, Sieberer Margit, Sietzema Jantine G, van 't Slot Ruben, Martinson Jeremy, Zagury Jean-François, Schuitemaker Hanneke, van 't Wout Angélique |
Unraveling the genetic etiology of adult antisocial behavior: a genome-wide association study. PloS one 2012 7 (10): 10. Tielbeek JJ, Medland SE, Benyamin B, Byrne EM, Heath AC, Madden PA, Martin NG, Wray NR, Verweij KJ |
A pilot study examining associations between DYRK1A and a-synuclein dementias. Neuro-degenerative diseases 2012 10 (1-4): 229-31. Jones Emma L, Aarsland Dag, Londos Elisabet, Ballard Cli |
DYRK1A mutations in two unrelated patients. European journal of medical genetics 2015 Mar 58 (3): 168-74. Ruaud Lyse, Mignot Cyril, Guët Agnès, Ohl Christelle, Nava Caroline, Héron Delphine, Keren Boris, Depienne Christel, Benoit Valérie, Maystadt Isabelle, Lederer Damien, Amsallem Daniel, Piard Juliet |
Disruptive de novo mutations of DYRK1A lead to a syndromic form of autism and ID. Molecular psychiatry 2015 Feb . van Bon B W M, Coe B P, Bernier R, Green C, Gerdts J, Witherspoon K, Kleefstra T, Willemsen M H, Kumar R, Bosco P, Fichera M, Li D, Amaral D, Cristofoli F, Peeters H, Haan E, Romano C, Mefford H C, Scheffer I, Gecz J, de Vries B B A, Eichler E |
Association of DYRK1A polymorphisms with sporadic Parkinson's disease in Chinese Han population. Neuroscience letters 2016 Oct 632 39-43. Cen Luan, Xiao Yousheng, Wei Lei, Mo Mingshu, Chen Xiang, Li Shaomin, Yang Xingling, Huang Qinghui, Qu Shaogang, Pei Zhong, Xu Ping |
The GBA, DYRK1A and MS4A6A polymorphisms influence the age at onset of Chinese Parkinson patients. Neuroscience letters 2016 Apr 621 133-136. Fan Kuan, Tang Bei-Sha, Wang Ya-Qin, Kang Ji-Feng, Li Kai, Liu Zhen-Hua, Sun Qi-Ying, Xu Qian, Yan Xin-Xiang, Guo Ji-Fe |
Association of the Single Nucleotide Polymorphisms in RUNX1, DYRK1A, and KCNJ15 with Blood Related Traits in Pigs. Asian-Australasian journal of animal sciences 2016 Dec 29 (12): 1675-1681. Lee Jae-Bong, Yoo Chae-Kyoung, Park Hee-Bok, Cho In-Cheol, Lim Hyun-T |
Autism-associated Dyrk1a truncation mutants impair neuronal dendritic and spine growth and interfere with postnatal cortical development. Molecular psychiatry 2018 03 23 (3): 747-758. Dang T, Duan W Y, Yu B, Tong D L, Cheng C, Zhang Y F, Wu W, Ye K, Zhang W X, Wu M, Wu B B, An Y, Qiu Z L, Wu B |
DYRK1A-haploinsufficiency in mice causes autistic-like features and febrile seizures. Neurobiology of disease 2017 12 110 180-191. Raveau Matthieu, Shimohata Atsushi, Amano Kenji, Miyamoto Hiroyuki, Yamakawa Kazuhi |
Alzheimer's disease susceptibility genes modify the risk of Parkinson disease and Parkinson's disease-associated cognitive impairment. Neuroscience letters 2018 Apr 677 55-59. Fang Lu, Tang Bei-Sha, Fan Kuan, Wan Chang-Min, Yan Xin-Xiang, Guo Ji-Fe |
Genome-wide meta-analysis identifies 3 novel loci associated with stroke.
Annals of neurology 2018 Dec 84 (6): 934-939. Malik Rainer, Rannikmäe Kristiina, Traylor Matthew, Georgakis Marios K, Sargurupremraj Muralidharan, Markus Hugh S, Hopewell Jemma C, Debette Stephanie, Sudlow Cathie L M, Dichgans Martin, |
De novo damaging variants associated with congenital heart diseases contribute to the connectome. Scientific reports 2020 Apr 10 (1): 7046. Ji Weizhen, Ferdman Dina, Copel Joshua, Scheinost Dustin, Shabanova Veronika, Brueckner Martina, Khokha Mustafa K, Ment Laura |
Genetic landscape of autism spectrum disorder in Vietnamese children. Scientific reports 2020 3 10 (1): 5034. Tran Kien Trung, Le Vinh Sy, Bui Hoa Thi Phuong, Do Duong Huy, Ly Ha Thi Thanh, Nguyen Hieu Thi, Dao Lan Thi Mai, Nguyen Thanh Hong, Vu Duc Minh, Ha Lien Thi, Le Huong Thi Thanh, Mukhopadhyay Arijit, Nguyen Liem Tha |
Association analysis and polygenic risk score evaluation of 38 GWAS-identified Loci in a Chinese population with Parkinson's disease. Neuroscience letters 2021 Aug 762 136150. Zheng Ran, Qiao Song, Chen Ying, Jin Chongyao, Fang Yi, Lin Zhihao, Xue Naijia, Yan Yiqun, Gu Luyan, Gao Ting, Tian Jun, Yan Yaping, Yin Xinzhen, Pu Jiali, Zhang Baoro |
Whole genome sequencing of 45 Japanese patients with intellectual disability. American journal of medical genetics. Part A 2021 2 185 (5): 1468-1480. Abe-Hatano Chihiro, Iida Aritoshi, Kosugi Shunichi, Momozawa Yukihide, Terao Chikashi, Ishikawa Keiko, Okubo Mariko, Hachiya Yasuo, Nishida Hiroya, Nakamura Kazuyuki, Miyata Rie, Murakami Chie, Takahashi Kan, Hoshino Kyoko, Sakamoto Haruko, Ohta Sayaka, Kubota Masaya, Takeshita Eri, Ishiyama Akihiko, Nakagawa Eiji, Sasaki Masayuki, Kato Mitsuhiro, Matsumoto Naomichi, Kamatani Yoichiro, Kubo Michiaki, Takahashi Yoshiyuki, Natsume Jun, Inoue Ken, Goto Yu-Ic |
[Clinical and genetic analysis of a child with mental retardation autosomal dominant 7]. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2022 5 39 (5): 530-533. Zhuo Zhihong, Wang Yao, Fu Tianjiao, Fang Xiao, Xu Xiaoli, Wang Yue, Kong Huimin, Wang Huai |
A Bioinformatics Evaluation of the Role of Dual-Specificity Tyrosine-Regulated Kinases in Colorectal Cancer. Cancers 2022 4 14 (8): . Laham Amina Jamal, El-Awady Raafat, Lebrun Jean-Jacques, Ayad Maha Sab |
Rare copy number variation analysis identifies disease-related variants in atrioventricular septal defect patients. Frontiers in genetics 2023 2 14 1075349. Hu Huan, Geng Zilong, Zhang Shasha, Xu Yuejuan, Wang Qingjie, Chen Sun, Zhang Bing, Sun Kun, Lu Yan |
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