Human Genome Epidemiology Literature Finder
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Records 1 - 8 (of 8 Records) |
| Query Trace: Disease and 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 |
| 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 |
| 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, |
| 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 |
| 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 |
| 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, |
| 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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