Human Genome Epidemiology Literature Finder
Records 1 - 25 (of 25 Records) |
Query Trace: CELSR1[original query] |
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Mutational analysis of the neuronal cadherin gene CELSR1 and exclusion as a candidate for catatonic schizophrenia in a large family. Psychiatric genetics 2002 1 11 (4): 197-200. Gross J, Grimm O, Ortega G, Teuber I, Lesch K P, Meyer |
Genetic variation in the seven-pass transmembrane cadherin CELSR1: lack of association with schizophrenia. Psychiatric genetics 2003 Jun 13 (2): 103-6. Georgieva Lyudmila, Nikolov Ivan, Poriazova Nadezhda, Jones Gaynor, Toncheva Draga, Kirov George, Owen Michael |
Identification of CELSR1 as a susceptibility gene for ischemic stroke in Japanese individuals by a genome-wide association study. Atherosclerosis 2009 Nov 207 (1): 144-9. Yamada Yoshiji, Fuku Noriyuki, Tanaka Masashi, Aoyagi Yukitoshi, Sawabe Motoji, Metoki Norifumi, Yoshida Hidemi, Satoh Kei, Kato Kimihiko, Watanabe Sachiro, Nozawa Yoshinori, Hasegawa Aki, Kojima Tosh |
Replication of the CELSR1 association with ischemic stroke in a Portuguese case-control cohort. Atherosclerosis 2011 Jul 217 (1): 260-2. Gouveia Liliana O, Sobral João, Vicente Astrid M, Ferro José M, Oliveira Sofia |
Role of the planar cell polarity gene CELSR1 in neural tube defects and caudal agenesis. Birth defects research. Part A, Clinical and molecular teratology 2012 Mar 94 (3): 176-81. Allache Redouane, De Marco Patrizia, Merello Elisa, Capra Valeria, Kibar Zo |
The CELSR1 polymorphisms rs6007897 and rs4044210 are associated with ischaemic stroke in Chinese Han population. Annals of human biology 2015 Jan 42 (1): 26-30. Zhan Yi-Hong, Lin Yi, Tong Sui-Jun, Ma Qi-Lin, Lu Cong-Xia, Fang Ling, Wei Wei, Cai Bin, Wang Ni |
Association of genetic variants of CELSR1 and 3q28 with hypertension in community-dwelling individuals. Biomedical reports 2013 Nov 1 (6): 840-844. Ueyama Chikara, Horibe Hideki, Fujimaki Tetsuo, Oguri Mitsutoshi, Kato Kimihiko, Yamada Yoshi |
Identification of novel CELSR1 mutations in spina bifida. PloS one 2014 9 (3): e92207. Lei Yunping, Zhu Huiping, Yang Wei, Ross M Elizabeth, Shaw Gary M, Finnell Richard |
Pooled genetic analysis reveals an association of SNPs of only a few genes with risk predisposition to ischemic stroke in a Chinese population. IUBMB life 2015 Mar 67 (3): 170-4. Zhang Zhenchang, Su Gang, Guo Jia, Li Jiong, Wu Hua, Wang Manxia, Xie Xiaodo |
[Association Between SNP rs6007897 of CELSR1 and Acute Ischemic Stroke in Western China Han Population: a Case-control Study]. Sichuan da xue xue bao. Yi xue ban = Journal of Sichuan University. Medical science edition 2015 Jul 46 (4): 578-80. Qin Feng-qin, Yu Li-hua, Hu Wen-ting, Guo Jian, Chen Ning, Guo Jiang, Fang Jing-huan, He |
Sex-Based Genetic Association Study Identifies CELSR1 as a Possible Chronic Obstructive Pulmonary Disease Risk Locus among Women. American journal of respiratory cell and molecular biology 2017 03 56 (3): 332-341. Hardin Megan, Cho Michael H, Sharma Sunita, Glass Kimberly, Castaldi Peter J, McDonald Merry-Lynn, Aschard Hugues, Senter-Sylvia Jody, Tantisira Kelan, Weiss Scott T, Hersh Craig P, Morrow Jarrett D, Lomas David, Agusti Alvar, Bakke Per, Gulsvik Amund, O'Connor George T, Dupuis Josée, Hokanson John, Crapo James D, Beaty Terri H, Laird Nan, Silverman Edwin K, DeMeo Dawn L, |
CELSR2 is a candidate susceptibility gene in idiopathic scoliosis. PloS one 2017 12 (12): e0189591. Einarsdottir Elisabet, Grauers Anna, Wang Jingwen, Jiao Hong, Escher Stefan A, Danielsson Aina, Simony Ane, Andersen Mikkel, Christensen Steen Bach, Åkesson Kristina, Kou Ikuyo, Khanshour Anas M, Ohlin Acke, Wise Carol, Ikegawa Shiro, Kere Juha, Gerdhem Pa |
Digenic variants of planar cell polarity genes in human neural tube defect patients. Molecular genetics and metabolism 2018 3 124 (1): 94-100. Wang Linlin, Xiao Yanhui, Tian Tian, Jin Lei, Lei Yunping, Finnell Richard H, Ren Aig |
Genetics of heart rate in heart failure patients (GenHRate).
Human genomics 2019 May 13 (1): 22. Evans Kaleigh L, Wirtz Heidi S, Li Jia, She Ruicong, Maya Juan, Gui Hongsheng, Hamer Andrew, Depre Christophe, Lanfear David |
Human exome and mouse embryonic expression data implicate ZFHX3, TRPS1, and CHD7 in human esophageal atresia. PloS one 2020 6 15 (6): e0234246. Zhang Rong, Gehlen Jan, Kawalia Amit, Melissari Maria-Theodora, Dakal Tikam Chand, Menon Athira M, Höfele Julia, Riedhammer Korbinian, Waffenschmidt Lea, Fabian Julia, Breuer Katinka, Kalanithy Jeshurun, Hilger Alina Christine, Sharma Amit, Hölscher Alice, Boemers Thomas M, Pauly Markus, Leutner Andreas, Fuchs Jörg, Seitz Guido, Ludwikowski Barbara M, Gomez Barbara, Hubertus Jochen, Heydweiller Andreas, Kurz Ralf, Leonhardt Johannes, Kosch Ferdinand, Holland-Cunz Stefan, Münsterer Oliver, Ure Beno, Schmiedeke Eberhard, Neser Jörg, Degenhardt Petra, Märzheuser Stefanie, Kleine Katharina, Schäfer Mattias, Spychalski Nicole, Deffaa Oliver J, Gosemann Jan-Hendrik, Lacher Martin, Heilmann-Heimbach Stefanie, Zwink Nadine, Jenetzky Ekkehart, Ludwig Michael, Grote Phillip, Schumacher Johannes, Thiele Holger, Reutter Hei |
Rare copy number variations of planar cell polarity genes are associated with human neural tube defects. Neurogenetics 2020 May . Tian Tian, Lei Yunping, Chen Yongyan, Guo Yinnan, Jin Lei, Finnell Richard H, Wang Linlin, Ren Aig |
Identification of Possible Risk Variants of Familial Strabismus Using Exome Sequencing Analysis. Genes 2021 1 12 (1): . An Joon-Yong, Jung Jae Ho, Choi Leejee, Wieben Eric D, Mohney Brian |
Identification of candidate genes encoding tumor-specific neoantigens in early- and late-stage colon adenocarcinoma. Aging 2021 Jan 12 . Wang Chong, Xue Wenhua, Zhang Haohao, Fu Ya |
Clinical staging and genetic profiling of Korean patients with primary lymphedema using targeted gene sequencing. Scientific reports 2022 8 12 (1): 13591. Seo Soo Hyun, Lee Seungjun, Park Joseph Kyu-Hyung, Yang Eun Joo, Kim Boram, Lee Jee-Soo, Kim Man Jin, Park Sung Sup, Seong Moon-Woo, Nam Sun-Young, Heo Chan-Yeong, Myung Yuj |
Associations of HER2 Mutation With Immune-Related Features and Immunotherapy Outcomes in Solid Tumors. Frontiers in immunology 2022 3 13 799988. Wang Deqiang, Chen Xiaofeng, Du Yian, Li Xiaoqin, Ying Leqian, Lu Yi, Shen Bo, Gao Xuan, Yi Xin, Xia Xuefeng, Sui Xinbing, Shu Yongqi |
CELSR1 Risk Alleles in Familial Bicuspid Aortic Valve and Hypoplastic Left Heart Syndrome. Circulation. Genomic and precision medicine 2022 2 15 (2): e003523. Theis Jeanne L, Niaz Talha, Sundsbak Rhianna S, Fogarty Zachary C, Bamlet William R, Hagler Donald J, Olson Timothy |
Whole-exome sequencing of transforming oral lichen planus reveals mutations in DNA damage repair and apoptosis pathway genes. Journal of oral pathology & medicine : official publication of the International Association of Oral Pathologists and the American Academy of Oral Pathology 2022 Feb . Xie Fangyi, Gleue Casey A, Deschaine Maria, Dasari Surendra, Lau Julie S, Sartori-Valinotti Julio C, Meves Alexander, Lehman Julia |
CELSR1 variants are associated with partial epilepsy of childhood. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2022 12 189 (7-8): 247-256. Chen Zheng, Luo Sheng, Liu Zhi-Gang, Deng Yan-Chun, He Su-Li, Liu Xiao-Rong, Yi Yong-Hong, Wang Jie, Gao Liang-Di, Li Bing-Mei, Wu Zhi-Jun, Ye Zi-Long, Liang De-Hai, Bian Wen-Jun, Liao Wei-Ping, |
Whole-genome resequencing reveals new mutations in candidate genes for Beichuan-white goat prolificacya. Animal biotechnology 2023 9 1-12. Aimin Zhou, Yi Ding, Xiaohui Zhang, Yugang Zhou, Yadong Liu, Tingjian Li, Long Xi |
Ureteropelvic junction obstruction with primary lymphoedema associated with CELSR1 variants. Journal of medical genetics 2023 5 . Murat Alpaslan, Sandrine Mestré-Godin, Aurélie Lay, Guido Giacalone, Raphaël Helaers, Salma Adham, Hélène Kovacsik, Sophie Guillemard, Erick Mercier, Laurence Boon, Nicole Revencu, Pascal Brouillard, Isabelle Quere, Miikka Vikku |
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- Page last updated:Apr 22, 2024
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