Human Genome Epidemiology Literature Finder
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Records 1 - 30 (of 92 Records) |
| Query Trace: CA2[original query] |
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| Association Study of Sequence Variants in Voltage-gated Ca2+ Channel Subunit Alpha-1C and Autism Spectrum Disorders. Reports of biochemistry & molecular biology 2019 Apr 8 (1): 56-62. Sayad Arezou, Ghafouri-Fard Soudeh, Noroozi Rezvan, Omrani Mir Davood, Ganji Maziar, Dastmalchi Romina, Glassy Mark, Taheri Mohamm |
| COMT polymorphism regulates the hippocampal subfield volumes in first-episode, drug-naive patients with major depressive disorder. Neuropsychiatric disease and treatment 2019 6 15 1537-1545. Otsuka Yuka, Kakeda Shingo, Sugimoto Koichiro, Katsuki Asuka, Nguyen Le Hoa, Igata Ryohei, Watanabe Keita, Ueda Issei, Kishi Taro, Iwata Nakao, Korogi Yukunori, Yoshimura Rei |
| Recessive gene disruptions in autism spectrum disorder. Nature genetics 2019 6 51 (7): 1092-1098. Doan Ryan N, Lim Elaine T, De Rubeis Silvia, Betancur Catalina, Cutler David J, Chiocchetti Andreas G, Overman Lynne M, Soucy Aubrie, Goetze Susanne, , Freitag Christine M, Daly Mark J, Walsh Christopher A, Buxbaum Joseph D, Yu Timothy |
| Increased prevalence of granulovacuolar degeneration in C9orf72 mutation. Acta neuropathologica 2019 5 138 (5): 783-793. Riku Yuichi, Duyckaerts Charles, Boluda Susana, Plu Isabelle, Le Ber Isabelle, Millecamps Stéphanie, Salachas François, , Yoshida Mari, Ando Takashi, Katsuno Masahisa, Sobue Gen, Seilhean Daniel |
| Ser96Ala genetic variant of the human histidine-rich calcium-binding protein is a genetic predictor of recurrence after catheter ablation in patients with paroxysmal atrial fibrillation. PloS one 2019 14 (3): e0213208. Amioka Michitaka, Nakano Yukiko, Ochi Hidenori, Onohara Yuko, Sairaku Akinori, Tokuyama Takehito, Motoda Chikaaki, Matsumura Hiroya, Tomomori Shunsuke, Hironobe Naoya, Okubo Yousaku, Okamura Sho, Chayama Kazuaki, Kihara Yasu |
| Association of ATP2B1 gene polymorphism with incidence of eclampsia. European review for medical and pharmacological sciences 2019 Dec 23 (24): 10609-10616. Sun X-M, Yang M, Jiang C |
| Neural mechanisms of AVPR1A RS3-RS1 haplotypes that impact verbal learning and memory. NeuroImage 2020 Aug 222 117283. Zhang Yan, Zhu Dan, Zhang Peng, Li Wei, Qin Wen, Liu Feng, Xu Jiayuan, Xu Qiang, Wang Junping, Ye Zhaoxiang, Yu Chunsh |
| Mitochondrial Energetics and Ca2-Activated ATPase in Obstructive Hypertrophic Cardiomyopathy. Journal of clinical medicine 2020 6 9 (6): . Lombardi Maria, Lazzeroni Davide, Pisano Annalinda, Girolami Francesca, Alfieri Ottavio, La Canna Giovanni, d'Amati Giulia, Olivotto Iacopo, Rimoldi Ornella E, Foglieni Chiara, Camici Paolo |
| A TREML2 missense variant influences specific hippocampal subfield volumes in cognitively normal elderly subjects. Brain and behavior 2020 Feb e01573. Wang Si-Yu, Xue Xiao, Duan Rui, Gong Peng-Yu, E Yan, Jiang Teng, Zhang Ying-Dong, |
| NOS1AP polymorphisms reduce NOS1 activity and interact with prolonged repolarization in arrhythmogenesis. Cardiovascular research 2020 2 117 (2): 472-483. Ronchi Carlotta, Bernardi Joyce, Mura Manuela, Stefanello Manuela, Badone Beatrice, Rocchetti Marcella, Crotti Lia, Brink Paul, Schwartz Peter J, Gnecchi Massimiliano, Zaza Anton |
| Novel mutations in PLCZ1 cause male infertility due to fertilization failure or poor fertilization. Human reproduction (Oxford, England) 2020 2 35 (2): 472-481. Yan Zheng, Fan Yong, Wang Fei, Yan Zhiguang, Li Menghui, Ouyang Jie, Wu Ling, Yin Mingru, Zhao Jilang, Kuang Yanping, Li Bin, Lyu Qife |
| Genetic Polymorphisms of RGS14 and Renal Stone Disease. Archives of medical research 2020 Dec . Guan Fanglin, Han Wei, Ni Tong, Zhao Longrui, Li Xiaoming, Zhang Bo, Zhang Tianxi |
| Polymorphism rs7214723 in CAMKK1: a new genetic variant associated with cardiovascular diseases. Bioscience reports 2021 6 41 (7): . Beghi Sofia, Cavaliere Francesca, Manfredini Matteo, Ferrarese Sandro, Corazzari Claudio, Beghi Cesare, Buschini Annamar |
| The Drosophila ortholog of the schizophrenia-associated CACNA1A and CACNA1B voltage-gated calcium channels regulate memory, sleep and circadian rhythms. Neurobiology of disease 2021 May 155 105394. Hidalgo Sergio, Campusano Jorge M, Hodge James J |
| CACNA1C rs1006737 SNP increases the risk of essential hypertension in both Chinese Han and ethnic Russian people of Northeast Asia. Medicine 2021 Feb 100 (8): e24825. Zhang Hao, Pushkarev Boris, Zhou Jiexin, Mu Yuyuan, Bolshakova Olga, Shrestha Sandeep, Wang Ningning, Jian Baiyu, Jin Ming, Zhang Keyong, Cong Mingyu, Liu Jicheng, Vitkovsky Yuri, Qiu Changch |
| INPP5E controls ciliary localization of phospholipids and the odor response in olfactory sensory neurons. Journal of cell science 2021 (5): . Ukhanov Kirill, Uytingco Cedric, Green Warren, Zhang Lian, Schurmans Stephane, Martens Jeffrey |
| Genome-Wide Association Study for Idiopathic Ventricular Tachyarrhythmias Identifies Key Role of CCR7 and PKN2 in Calcium Homeostasis and Cardiac Rhythm Maintenance. Circulation. Genomic and precision medicine 2022 Jul 101161CIRCGEN121003603. Fang Chen, Wang Pengxia, Yu Dong, Zhang Xiaoyu, Gou Dongzhi, Liang Lina, Bai Xuemei, Xie Wen, Li Hui, Pu Jielin, Yao Yufeng, Wang Binbin, Ren Xiang, Ke Tie, Tu Xin, Xu Chengqi, Wang Qing |
| Genome-Wide Association Studies and Haplotype-Sharing Analysis Targeting the Egg Production Traits in Shaoxing Duck. Frontiers in genetics 2022 4 13 828884. Xu Wenwu, Wang Zhenzhen, Qu Yuanqi, Li Qingyi, Tian Yong, Chen Li, Tang Jianhong, Li Chengfeng, Li Guoqin, Shen Junda, Tao Zhengrong, Cao Yongqing, Zeng Tao, Lu Liz |
| Whole-Exome Sequencing Implicates Neuronal Calcium Channel with Familial Atrial Fibrillation. Frontiers in genetics 2022 2 13 806429. Vad Oliver Bundgaard, Yan Yannan, Denti Federico, Ahlberg Gustav, Refsgaard Lena, Bomholtz Sofia Hammami, Santos Joana Larupa, Rasmussen Simon, Haunsø Stig, Svendsen Jesper Hastrup, Christophersen Ingrid Elizabeth, Schmitt Nicole, Olesen Morten Salling, Bentzen Bo Hjor |
| APOE alleles are associated with sex-specific structural differences in brain regions affected in Alzheimer's disease and related dementia. PLoS biology 2022 12 20 (12): e3001863. Savignac Chloé, Villeneuve Sylvia, Badhwar AmanPreet, Saltoun Karin, Shafighi Kimia, Zajner Chris, Sharma Vaibhav, Gagliano Taliun Sarah A, Farhan Sali, Poirier Judes, Bzdok Dani |
| A functional population-specific variant rs77416373 in the Ca2.1 gene is associated with antidepressant treatment response in Han Chinese subjects with major depressive disorder. Asian journal of psychiatry 2022 10 77 103272. Zhang Yan, Zhang Chu-Yi, Li Shi-Wu, Yuan Jing, Xu Li, Wei Yu-Jun, Zhou Fang, Wang Jun-Yang, Huo Jin-Hua, Wang Lu, Feng Li-Mei, Kang Chuan-Yuan, Yang Jian-Zho |
| Genomic Alterations as Independent Prognostic Factors to Predict the Type of Lung Cancer Recurrence. Gene 2023 8 147690. A Valter, L Luhari, H Pisarev, B Truumees, A Planken, O P Smolander, K Osel |
| Rare variants in ANO1, encoding a calcium-activated chloride channel, predispose to moyamoya disease. Brain : a journal of neurology 2023 5 . Amélie Pinard, Wenlei Ye, Stuart M Fraser, Jill A Rosenfeld, Pavel Pichurin, Scott E Hickey, Dongchuan Guo, Alana C Cecchi, Maura L Boerio, Stéphanie Guey, Chaker Aloui, Kwanghyuk Lee, Markus Kraemer, Saleh Omar Alyemni, , Michael J Bamshad, Deborah A Nickerson, Elisabeth Tournier-Lasserve, Shozeb Haider, Sheng Chih Jin, Edward R Smith, Kristopher T Kahle, Lily Yeh Jan, Mu He, Dianna M Milewi |
| Construction and validation of a fatty acid metabolism-related gene signature for predicting prognosis and therapeutic response in patients with prostate cancer. PeerJ 2023 2 11 e14854. Zhao Hongjun, Wu Tong, Luo Zehao, Huang Qinyao, Zhu Sihua, Li Chunling, Zhang Zubing, Zhang Jiahao, Zeng Jianwen, Zhang Yuyi |
| A genome-wide and candidate gene association study of preterm birth in Korean pregnant women. PloS one 2023 11 18 (11): e0294948. Young Min Hur, Jae Young Yoo, Young Ah You, Sunwha Park, Soo Min Kim, Gain Lee, Young Ju K |
| Hailey-Hailey Disease is Associated with Diabetes: A Population-based Cohort Study, Clinical Cohort Study, and Pedigree Analysis. Acta dermato-venereologica 2023 11 103 adv10436. Philip Curman, William Jebril, Carmella Evans-Molina, Etty Bachar-Wikstrom, Henrik Larsson, Martin Cederlöf, Jakob D Wikstr |
| Lymphocyte disturbance and functional assessment of the [Asp521Asn] ZAP70 mutation. Clinical immunology (Orlando, Fla.) 2023 1 247 109236. Lin Yung-Feng, Lee Wen-I, Ho Ching-Huang, Chen Shih-Hsiang, Hsu Mei-Hsin, Wu Ren-Chin, Lee Wan-Fang, Jaing Tang-Her, Huang Jing-Long, Tsai Shih-Fe |
| Expression of Concern: Association between Genetic Polymorphisms in Cav2.3 (R-type) Ca2+ Channels and Fentanyl Sensitivity in Patients Undergoing Painful Cosmetic Surgery. PloS one 2023 1 18 (1): e0278809. Authors are not available |
| Progressive Ataxia due to de novo Missense Variants in the CACNA1A Gene. Cerebellum (London, England) 2024 6 . Chen-Hao Zhu, Jin-Yang Yu, Yin Ma, Yi Dong, Zhi-Ying |
| KRAP regulates mitochondrial Ca2+ uptake by licensing IP3 receptor activity and stabilizing ER-mitochondrial junctions. Journal of cell science 2024 5 . Peace Atakpa-Adaji, Adelina Ivanova, Karolina Kujawa, Colin W Tayl |
- Page last reviewed:Feb 1, 2024
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