Human Genome Epidemiology Literature Finder
Records 1 - 27 (of 27 Records) |
Query Trace: CALHM1[original query] |
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A polymorphism in CALHM1 influences Ca2+ homeostasis, Abeta levels, and Alzheimer's disease risk. Cell 2008 Jun 133 (7): 1149-61. Dreses-Werringloer Ute, Lambert Jean-Charles, Vingtdeux Valérie, Zhao Haitian, Vais Horia, Siebert Adam, Jain Ankit, Koppel Jeremy, Rovelet-Lecrux Anne, Hannequin Didier, Pasquier Florence, Galimberti Daniela, Scarpini Elio, Mann David, Lendon Corinne, Campion Dominique, Amouyel Philippe, Davies Peter, Foskett J Kevin, Campagne Fabien, Marambaud Philip |
The P86L common allele of CALHM1 does not influence risk for Alzheimer disease in Japanese cohorts. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2010 Mar 153B (2): 532-5. Inoue Ken, Tanaka Noriko, Yamashita Fumio, Sawano Yoshie, Asada Takashi, Goto Yu-ic |
CALHM1 variant is not associated with Alzheimer's disease among Asians. Neurobiology of aging 2011 Mar 32 (3): 546.e11-2. Tan E K, Ho P, Cheng S Y, Yih Yuen, Li H H, Fook-Chong S, Lee W L, Zhao |
CALHM1 polymorphism is not associated with late-onset Alzheimer disease. Annals of human genetics 2009 May 73 (Pt 3): 379-81. Beecham Gary W, Schnetz-Boutaud Nathalie, Haines Jonathan L, Pericak-Vance Margaret |
No association between CALHM1 and risk for Alzheimer dementia in a Belgian population. Human mutation 2009 Apr 30 (4): E570-4. Sleegers Kristel, Brouwers Nathalie, Bettens Karolien, Engelborghs Sebastiaan, van Miegroet Helen, De Deyn Peter P, Van Broeckhoven Christi |
No association between CALHM1 variation and risk of Alzheimer disease. Human mutation 2009 Apr 30 (4): E566-9. Minster Ryan L, Demirci F Yesim, DeKosky Steven T, Kamboh M Ily |
CALHM1 P86L polymorphism does not alter amyloid-beta or tau in cerebrospinal fluid. Neuroscience letters 2010 Jan 469 (2): 265-7. Giedraitis Vilmantas, Glaser Anna, Sarajärvi Timo, Brundin RoseMarie, Gunnarsson Malin Degerman, Schjeide Brit-Maren, Tanzi Rudolph E, Helisalmi Seppo, Pirttilä Tuula, Kilander Lena, Lannfelt Lars, Soininen Hilkka, Bertram Lars, Ingelsson Martin, Hiltunen Mik |
The CALHM1 P86L polymorphism is a genetic modifier of age at onset in Alzheimer's disease: a meta-analysis study. Journal of Alzheimer's disease : JAD 2010 22 (1): 247-55. Lambert Jean-Charles, Sleegers Kristel, González-Pérez Antonio, Ingelsson Martin, Beecham Gary W, Hiltunen Mikko, Combarros Onofre, Bullido Maria J, Brouwers Nathalie, Bettens Karolien, Berr Claudine, Pasquier Florence, Richard Florence, Dekosky Steven T, Hannequin Didier, Haines Jonathan L, Tognoni Gloria, Fiévet Nathalie, Dartigues Jean-François, Tzourio Christophe, Engelborghs Sebastiaan, Arosio Beatrice, Coto Elicer, De Deyn Peter, Del Zompo Maria, Mateo Ignacio, Boada Merce, Antunez Carmen, Lopez-Arrieta Jesus, Epelbaum Jacques, Schjeide Brit-Maren Michaud, Frank-Garcia Ana, Giedraitis Vilmentas, Helisalmi Seppo, Porcellini Elisa, Pilotto Alberto, Forti Paola, Ferri Raffaele, Delepine Marc, Zelenika Diana, Lathrop Mark, Scarpini Elio, Siciliano Gabriele, Solfrizzi Vincenzo, Sorbi Sandro, Spalletta Gianfranco, Ravaglia Giovanni, Valdivieso Fernando, Vepsäläinen Saila, Alvarez Victoria, Bosco Paolo, Mancuso Michelangelo, Panza Francesco, Nacmias Benedetta, Bossù Paola, Hanon Olivier, Piccardi Paola, Annoni Giorgio, Mann David, Marambaud Philippe, Seripa Davide, Galimberti Daniela, Tanzi Rudolph E, Bertram Lars, Lendon Corinne, Lannfelt Lars, Licastro Federico, Campion Dominique, Pericak-Vance Margaret A, Soininen Hilkka, Van Broeckhoven Christine, Alpérovitch Annick, Ruiz Agustin, Kamboh M Ilyas, Amouyel Philip |
Association between the polymorphisms of CALHM1 and GOLPH2 genes and Alzheimer's disease. Psychiatric genetics 2010 Aug 20 (4): 190. Lin Kangguang, Tang Muni, Han Haiying, Guo Yangbo, Lin Yuhua, Ma C |
Validating predicted biological effects of Alzheimer's disease associated SNPs using CSF biomarker levels. Journal of Alzheimer's disease : JAD 2010 21 (3): 833-42. Kauwe John S K, Cruchaga Carlos, Bertelsen Sarah, Mayo Kevin, Latu Wayne, Nowotny Petra, Hinrichs Anthony L, Fagan Anne M, Holtzman David M, , Goate Alison |
Lack of implication for CALHM1 P86L common variation in Italian patients with early and late onset Alzheimer's disease. Journal of Alzheimer's disease : JAD 2010 20 (1): 37-41. Nacmias Benedetta, Tedde Andrea, Bagnoli Silvia, Lucenteforte Ersilia, Cellini Elena, Piaceri Irene, Guarnieri Bianca Maria, Bessi Valentina, Bracco Laura, Sorbi Sand |
CALHM1 P86L polymorphism is associated with late-onset Alzheimer's disease in a recessive model. Journal of Alzheimer's disease : JAD 2010 20 (1): 247-51. Boada Mercè, Antúnez Carmen, López-Arrieta Jesús, Galán José Jorge, Morón Francisco J, Hernández Isabel, Marín Juan, Martínez-Lage Pablo, Alegret Montserrat, Carrasco Jose M, Moreno Concha, Real Luis M, González-Pérez Antonio, Tárraga Lluís, Ruiz Agust |
Genetic association between CALHM1, 2, and 3 polymorphisms and Alzheimer's disease in a Japanese population. Journal of Alzheimer's disease : JAD 2010 20 (2): 417-21. Shibata Nobuto, Kuerban Bolati, Komatsu Miwa, Ohnuma Tohru, Baba Hajime, Arai He |
CALHM1 P86L polymorphism is a risk factor for Alzheimer's disease in the Chinese population. Journal of Alzheimer's disease : JAD 2010 19 (1): 31-5. Cui Pei-Jing, Zheng Lan, Cao Li, Wang Ying, Deng Yu-Lei, Wang Gang, Xu Wei, Tang Hui-Dong, Ma Jian-Fang, Zhang Ting, Ding Jian-Qing, Cheng Qi, Chen Sheng- |
CALHM1 P86L polymorphism modulates CSF Aß levels in cognitively healthy individuals at risk for Alzheimer's disease. Molecular medicine (Cambridge, Mass.) 0 17 (9-10): 974-9. Koppel Jeremy, Campagne Fabien, Vingtdeux Valérie, Dreses-Werringloer Ute, Ewers Michael, Rujescu Dan, Hampel Harald, Gordon Marc L, Christen Erica, Chapuis Julien, Greenwald Blaine S, Davies Peter, Marambaud Philip |
No association between CALHM1 polymorphism and Alzheimer's disease risk in a Hungarian population. Psychiatric genetics 2011 Oct 21 (5): 249-52. Fehér Agnes, Juhász Anna, Rimanóczy Agnes, Pákáski Magdolna, Kálmán János, Janka Zolt |
A polymorphism in CALHM1 is associated with temporal lobe epilepsy. Epilepsy & behavior : E&B 2011 Apr 20 (4): 681-5. Lv Rui-juan, He Jin-sheng, Fu Yuan-hui, Shao Xiao-qiu, Wu Li-wen, Lu Qiang, Jin Li-ri, Liu H |
Genetic variability of the gene cluster CALHM 1-3 in sporadic Creutzfeldt-Jakob disease. Prion 0 6 (4): 407-12. Calero Olga, Bullido María J, Clarimón Jordi, Hortigüela Rafael, Frank-García Ana, Martínez-Martín Pablo, Lleó Alberto, Rey María Jesús, Sastre Isabel, Rábano Alberto, de Pedro-Cuesta Jesús, Ferrer Isidro, Calero Migu |
Rare variants in calcium homeostasis modulator 1 (CALHM1) found in early onset Alzheimer's disease patients alter calcium homeostasis. PloS one 2013 8 (9): e74203. Rubio-Moscardo Fanny, Setó-Salvia Núria, Pera Marta, Bosch-Morató Mònica, Plata Cristina, Belbin Olivia, Gené Gemma, Dols-Icardo Oriol, Ingelsson Martin, Helisalmi Seppo, Soininen Hilkka, Hiltunen Mikko, Giedraitis Vilmantas, Lannfelt Lars, Frank Ana, Bullido Ma Jesús, Combarros Onofre, Sánchez-Juan Pascual, Boada Mercè, Tárraga Lluís, Pastor Pau, Pérez-Tur Jordi, Baquero Miquel, Molinuevo José L, Sánchez-Valle Raquel, Fuentes-Prior Pablo, Fortea Juan, Blesa Rafael, Muñoz Francisco J, Lleó Alberto, Valverde Miguel A, Clarimón Jor |
No association between polymorphisms in the calcium homeostasis modulator 1 gene and mesial temporal lobe epilepsy risk in a Chinese population. Seizure 2014 Mar 23 (3): 231-3. Li Xiang, Wang Yongcai, Gu Jia, Meng Qingming, Gao Yong, Zhao Hongyu, Yin Zhongm |
Lack of association between CALHM1 p.P86L variation and Alzheimer's disease in the Han Chinese population. Neurobiology of aging 2014 Aug 35 (8): 1956.e13-4. Tao Qing-Qing, Sun Yi-Min, Liu Zhi-Jun, Yang Ping, Li Hong-Lei, Lu Shen-Ji, Wu Zhi-Yi |
Genetic association of CALHM1 rs2986017 polymorphism with risk of Alzheimer's disease: a meta-analysis. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2015 Dec . Lu Yanjun, Liu Wei, Tan Kun, Peng Jing, Zhu Yaowu, Wang Xio |
Two-stage replication of previous genome-wide association studies of AS3MT-CNNM2-NT5C2 gene cluster region in a large schizophrenia case-control sample from Han Chinese population. Schizophrenia research 2016 Jul . Guan Fanglin, Zhang Tianxiao, Li Lu, Fu Dongke, Lin Huali, Chen Gang, Chen Te |
Calcium homeostasis modulator 1 gene P86L polymorphism and the risk for alzheimer's disease: A meta-analysis. Neuroscience letters 2016 Mar . Mun Myung-Jin, Kim Jin-Ho, Choi Ji-Young, Jang Won-Cheo |
Validation of a priori candidate Alzheimer's disease SNPs with brain amyloid-beta deposition. Scientific reports 2019 Nov 9 (1): 17069. Vacher Michael, Porter Tenielle, Villemagne Victor L, Milicic Lidija, Peretti Madeline, Fowler Christopher, Martins Ralph, Rainey-Smith Stephanie, Ames David, Masters Colin L, Rowe Christopher C, Doecke James D, Laws Simon |
Genetic and molecular features of seizure-freedom following surgical resections for focal epilepsy: A pilot study. Frontiers in neurology 2022 10 13 942643. Louis Shreya, Busch Robyn M, Lal Dennis, Hockings Jennifer, Hogue Olivia, Morita-Sherman Marcia, Vegh Deborah, Najm Imad, Ghosh Chaitali, Bazeley Peter, Eng Charis, Jehi Lara, Rotroff Daniel |
A higher dysregulation burden of brain DNA methylation in female patients implicated in the sex bias of Schizophrenia. Molecular psychiatry 2023 9 . Jiaqi Zhou, Yan Xia, Miao Li, Yu Chen, Jiacheng Dai, Chunyu Liu, Chao Ch |
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