Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 46 Records) |
Query Trace: CACNB2[original query] |
---|
Physical, behavioural and genetic predictors of adult hypertension: the findings of the Kaunas Cardiovascular Risk Cohort study. PloS one 2014 9 (10): e109974. Petkeviciene Janina, Klumbiene Jurate, Simonyte Sandrita, Ceponiene Indre, Jureniene Kristina, Kriaucioniene Vilma, Raskiliene Asta, Smalinskiene Alina, Lesauskaite Vai |
Genetic Analysis of Arrhythmogenic Diseases in the Era of NGS: The Complexity of Clinical Decision-Making in Brugada Syndrome. PloS one 2015 10 (7): e0133037. Allegue Catarina, Coll Mònica, Mates Jesus, Campuzano Oscar, Iglesias Anna, Sobrino Beatriz, Brion Maria, Amigo Jorge, Carracedo Angel, Brugada Pedro, Brugada Josep, Brugada Ram |
Germline mutations causing familial lung cancer. Journal of human genetics 2015 Jul . Tomoshige Koichi, Matsumoto Keitaro, Tsuchiya Tomoshi, Oikawa Masahiro, Miyazaki Takuro, Yamasaki Naoya, Mishima Hiroyuki, Kinoshita Akira, Kubo Toru, Fukushima Kiyoyasu, Yoshiura Koh-Ichiro, Nagayasu Takes |
Genome-wide analysis implicates microRNAs and their target genes in the development of bipolar disorder. Translational psychiatry 2015 5 e678. Forstner A J, Hofmann A, Maaser A, Sumer S, Khudayberdiev S, Mühleisen T W, Leber M, Schulze T G, Strohmaier J, Degenhardt F, Treutlein J, Mattheisen M, Schumacher J, Breuer R, Meier S, Herms S, Hoffmann P, Lacour A, Witt S H, Reif A, Müller-Myhsok B, Lucae S, Maier W, Schwarz M, Vedder H, Kammerer-Ciernioch J, Pfennig A, Bauer M, Hautzinger M, Moebus S, Priebe L, Sivalingam S, Verhaert A, Schulz H, Czerski P M, Hauser J, Lissowska J, Szeszenia-Dabrowska N, Brennan P, McKay J D, Wright A, Mitchell P B, Fullerton J M, Schofield P R, Montgomery G W, Medland S E, Gordon S D, Martin N G, Krasnov V, Chuchalin A, Babadjanova G, Pantelejeva G, Abramova L I, Tiganov A S, Polonikov A, Khusnutdinova E, Alda M, Cruceanu C, Rouleau G A, Turecki G, Laprise C, Rivas F, Mayoral F, Kogevinas M, Grigoroiu-Serbanescu M, Propping P, Becker T, Rietschel M, Cichon S, Schratt G, Nöthen M |
Genome-wide association study of antidepressant response: involvement of the inorganic cation transmembrane transporter activity pathway. BMC psychiatry 2016 16 (1): 106. Cocchi Enrico, Fabbri Chiara, Han Changsu, Lee Soo-Jung, Patkar Ashwin A, Masand Prakash S, Pae Chi-Un, Serretti Alessand |
Does Sudden Unexplained Nocturnal Death Syndrome Remain the Autopsy-Negative Disorder: A Gross, Microscopic, and Molecular Autopsy Investigation in Southern China. Mayo Clinic proceedings 2016 Oct . Zhang Liyong, Tester David J, Lang Di, Chen Yili, Zheng Jinxiang, Gao Rui, Corliss Robert F, Tang Shuangbo, Kyle John W, Liu Chao, Ackerman Michael J, Makielski Jonathan C, Cheng Jiandi |
Pathway analysis of bladder cancer genome-wide association study identifies novel pathways involved in bladder cancer development. Genes & cancer 2016 Jul 7 (7-8): 229-239. Chen Meng, Rothman Nathaniel, Ye Yuanqing, Gu Jian, Scheet Paul A, Huang Maosheng, Chang David W, Dinney Colin P, Silverman Debra T, Figueroa Jonine D, Chanock Stephen J, Wu Xife |
Genetic findings are challenging the symptom-based diagnostic classification system of mental disorders. Shanghai archives of psychiatry 2016 Feb 28 (1): 42-7. Zhang Ch |
DNA methylation in a Scottish family multiply affected by bipolar disorder and major depressive disorder. Clinical epigenetics 2016 8 5. Walker Rosie May, Christoforou Andrea Nikie, McCartney Daniel L, Morris Stewart W, Kennedy Nicholas A, Morten Peter, Anderson Susan Maguire, Torrance Helen Scott, Macdonald Alix, Sussmann Jessika Elizabeth, Whalley Heather Clare, Blackwood Douglas H R, McIntosh Andrew Mark, Porteous David John, Evans Kathryn Loui |
Testing of candidate single nucleotide variants associated with paclitaxel neuropathy in the trial NCCTG N08C1 (Alliance). Cancer medicine 2016 Jan . Boora Ganesh K, Kanwar Rahul, Kulkarni Amit A, Abyzov Alexej, Sloan Jeff, Ruddy Kathryn J, Banck Michaela S, Loprinzi Charles L, Beutler Andreas |
Risk-Conferring Glutamatergic Genes and Brain Glutamate Plus Glutamine in Schizophrenia. Frontiers in psychiatry 2017 8 79. Bustillo Juan R, Patel Veena, Jones Thomas, Jung Rex, Payaknait Nattida, Qualls Clifford, Canive Jose M, Liu Jingyu, Perrone-Bizzozero Nora Irma, Calhoun Vince D, Turner Jessica A, Gasparovic Charl |
Pleiotropic genes in psychiatry: Calcium channels and the stress-related FKBP5 gene in antidepressant resistance. Progress in neuro-psychopharmacology & biological psychiatry 2017 Oct . Fabbri Chiara, Corponi Filippo, Albani Diego, Raimondi Ilaria, Forloni Gianluigi, Schruers Koen, Kasper Siegfried, Kautzky Alexander, Zohar Joseph, Souery Daniel, Montgomery Stuart, Cristalli Carlotta Pia, Mantovani Vilma, Mendlewicz Julien, Serretti Alessand |
The genetic overlap between mood disorders and cardiometabolic diseases: a systematic review of genome wide and candidate gene studies. Translational psychiatry 2017 Jan 7 (1): e1007. Amare A T, Schubert K O, Klingler-Hoffmann M, Cohen-Woods S, Baune B |
Association between ATP2B1 and CACNB2 polymorphisms and high blood pressure in a population of Lithuanian children and adolescents: a cross-sectional study. BMJ open 2018 Jul 8 (7): e019902. Simonyte Sandrita, Kuciene Renata, Dulskiene Virginija, Lesauskaite Vai |
Bifid T waves on the ECG and genetic variation in calcium channel voltage-dependent beta 2 subunit gene (CACNB2) in acute Kawasaki disease. Congenital heart disease 2019 Mar 14 (2): 213-220. Oyamada Jun, Shimizu Chisato, Kim Jihoon, Williams Matthew R, Png Eileen, Hibberd Martin L, Tremoulet Adriana H, Perry James C, Burns Jane |
An African loss-of-function CACNA1C variant p.T1787M associated with a risk of ventricular fibrillation. Scientific reports 2018 10 8 (1): 14619. Blancard Malorie, Debbiche Amal, Kato Koichi, Cardin Christelle, Sabrina Guichard, Gandjbakhch Estelle, Probst Vincent, Haissaguerre Michel, Extramiana Fabrice, Hocini Mélèze, Olivier Geoffroy, Leenhardt Antoine, Guicheney Pascale, Rougier Jean-Sébasti |
Voltage-gated calcium channel activity and complex related genes and schizophrenia: A systematic investigation based on Han Chinese population. Journal of psychiatric research 2018 10 106 99-105. Zhang Tianxiao, Zhu Li, Ni Tong, Liu Dan, Chen Gang, Yan Zhilan, Lin Huali, Guan Fanglin, Rice John |
Further evidence for the genetic association between CACNA1I and schizophrenia. Hereditas 2018 155 16. Xie Yijun, Huang Di, Wei Li, Luo Xiong-Ji |
CACNB2 Is a Novel Susceptibility Gene for Diabetic Retinopathy in Type 1 Diabetes. Diabetes 2019 8 68 (11): 2165-2174. Vuori Nadja, Sandholm Niina, Kumar Anmol, Hietala Kustaa, Syreeni Anna, Forsblom Carol, Juuti-Uusitalo Kati, Skottman Heli, Imamura Minako, Maeda Shiro, Summanen Paula A, Lehto Markku, Groop Per-Henrik, |
Influence of genetic factors on long-term treatment related neurocognitive complications, and on anxiety and depression in survivors of childhood acute lymphoblastic leukemia: The Petale study. PloS one 2019 14 (6): e0217314. Petrykey Kateryna, Lippé Sarah, Robaey Philippe, Sultan Serge, Laniel Julie, Drouin Simon, Bertout Laurence, Beaulieu Patrick, St-Onge Pascal, Boulet-Craig Aubrée, Rezgui Aziz, Yasui Yutaka, Sapkota Yadav, Krull Kevin R, Hudson Melissa M, Laverdière Caroline, Sinnett Daniel, Krajinovic Ma |
Variation in the CACNB2 gene is associated with functional connectivity of the Hippocampus in bipolar disorder. BMC psychiatry 2019 Feb 19 (1): 62. Liu Fang, Gong Xiaohong, Yao Xudong, Cui Lingling, Yin Zhiyang, Li Chao, Tang Yanqing, Wang F |
Association between CANCA1C gene rs1034936 polymorphism and alcohol dependence in bipolar disorder. Journal of affective disorders 2019 Oct 261 181-186. Mosheva Mariela, Serretti Alessandro, Stukalin Yelena, Fabbri Chiara, Hagin Michal, Horev Sagi, Mantovani Vilma, Bin Sofia, Mattiaccio Alessandro, Nivoli Alessandra, Vieta Eduard, Popovic Di |
The genetic risk for hypertension is lower among the Hungarian Roma population compared to the general population. PloS one 2020 6 15 (6): e0234547. Soltész Beáta, Pikó Péter, Sándor János, Kósa Zsigmond, Ádány Róza, Fiatal Szilv |
CACNB2 rs11013860 polymorphism correlates of prefrontal cortex thickness in bipolar patients with first-episode mania. Journal of affective disorders 2020 3 268 82-87. Chen Jianshan, Tan Jiuwei, Greenshaw Andrew J, Sawalha Jeff, Liu Yang, Zhang Xiaofei, Zou Wenjin, Cheng Xiaofang, Deng Wenhao, Zhang Yizhi, Cui Liqian, Liu Chuihong, Sun Jiaqi, Cheng Xiongchao, Wu Qiuxia, Li Suyi, Mai Siming, Lan Xiaofeng, Chen Yingmei, Cai Yinglian, Zheng Chaodun, Cheng Daomeng, Zhang Bin, Yang Chanjuan, Li Xuan, Li Xinmin, Ye Biyu, Yousefnezhad Muhammad, Zhang Yamin, Zhao Liansheng, Soares Jair C, Zhang Xiangyang, Li Tao, Cao Bo, Cao Lipi |
Association between gene polymorphisms of voltage-dependent Ca channels and hypertension in the Dai people of China: a case-control study. BMC medical genetics 2020 Feb 21 (1): 44. Huang Lifan, Chu Yan, Huang Xiaoqin, Ma Shaohui, Lin Keqin, Huang Kai, Sun Hao, Yang Zhaoqi |
Genetic variants associated with psychotic symptoms across psychiatric disorders. Neuroscience letters 2020 Jan 134754. Calabrò Marco, Porcelli Stefano, Crisafulli Concetta, Albani Diego, Kasper Siegfried, Zohar Joseph, Souery Daniel, Montgomery Stuart, Mantovani Vilma, Mendlewicz Julien, Bonassi Stefano, Vieta Eduard, Frustaci Alessandra, Ducci Giuseppe, Landi Stefano, Boccia Stefania, Bellomo Antonello, Di Nicola Marco, Janiri Luigi, Colombo Roberto, Benedetti Francesco, Mandelli Laura, Fabbri Chiara, Serretti Alessand |
Interactions between PDA-associated polymorphisms and genetic ancestry alter ductus arteriosus gene expression. Pediatric research 2021 4 91 (4): 903-911. Clyman Ronald I, Hills Nancy K, Dagle John M, Murray Jeffrey C, Kelsey Keeg |
AS3MT Polymorphism: A Risk Factor for Epilepsy Susceptibility and Adverse Drug Reactions to Valproic Acid and Oxcarbazepine Treatment in Children From South China. Frontiers in neuroscience 2021 12 15 705297. Fan Xiaomei, Chen Yuna, Lu Jieluan, Li Wenzhou, Li Xi, Guo Huijuan, Chen Qing, Yang Yanxia, Xia Hanbi |
Association study of hypertension susceptibility genes ITGA9, MOV10, and CACNB2 with preeclampsia in Chinese Han population. The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians 2021 Jan 1-9. Xin Qian, Xin Gang, Li Li, Sun Wenjuan, Jiang Wen, Wang Jue, Luan Yun, Zhang Ying, Cheng Ling, Duan Shuhong, Hong Fanzhen, Ji Qinghong, Ma Weiho |
A Post-GWAS Functional Analysis Confirming Effects of Three BTA13 Genes CACNB2, SLC39A12, and ZEB1 on Dairy Cattle Reproduction. Frontiers in genetics 2022 6 13 882951. Sammad Abdul, Zhang Hailiang, Shi Rui, Dong Yixin, Luo Hanpeng, Chen Ziwei, Liu Lin, Guo Gang, Liu Aoxing, Wang Yach |
- Page last reviewed:Feb 1, 2024
- Page last updated:Apr 22, 2024
- Content source: