Human Genome Epidemiology Literature Finder
Records 1 - 16 (of 16 Records) |
Query Trace: HCN1[original query] |
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Association study for genes at chromosome 5p13-q11 in attention deficit hyperactivity disorder. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2008 Jul 147B (5): 600-5. Laurin Nancy, Lee Jonghun, Ickowicz Abel, Pathare Tejaswee, Malone Molly, Tannock Rosemary, Kennedy James L, Schachar Russell J, Barr Cathy |
Mutation analysis of the hyperpolarization-activated cyclic nucleotide-gated channels HCN1 and HCN2 in idiopathic generalized epilepsy. Neurobiology of disease 2008 Jan 29 (1): 59-70. Tang Bin, Sander Thomas, Craven Kimberley B, Hempelmann Anne, Escayg Andr |
Chromosome 5 and Gilles de la Tourette syndrome: Linkage in a large pedigree and association study of six candidates in the region. American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics 2009 Jan 150B (1): 95-103. Laurin Nancy, Wigg Karen G, Feng Yu, Sandor Paul, Barr Cathy |
Association between breast cancer susceptibility loci and mammographic density: the Multiethnic Cohort. Breast cancer research : BCR 2009 11 (1): R10. Woolcott Christy G, Maskarinec Gertraud, Haiman Christopher A, Verheus Martijn, Pagano Ian S, Le Marchand Loïc, Henderson Brian E, Kolonel Laurence |
Combined effect of low-penetrant SNPs on breast cancer risk. British journal of cancer 2012 Jan 106 (2): 389-96. Harlid S, Ivarsson M I L, Butt S, Grzybowska E, Eyfjörd J E, Lenner P, Försti A, Hemminki K, Manjer J, Dillner J, Carlson |
Genetic variation in Hyperpolarization-activated cyclic nucleotide-gated channels and its relationship with neuroticism, cognition and risk of depression. Frontiers in genetics 2012 3 116. McIntosh Andrew M, Simen Arthur A, Evans Kathryn L, Hall Jeremy, Macintyre Donald J, Blackwood Douglas, Morris Andrew D, Smith Blair H, Dominiczak Anna, Porteous David, Deary Hb Ian J, Thomson Pippa |
GENOME-WIDE INTERACTION WITH SELECTED TYPE 2 DIABETES LOCI REVEALS NOVEL LOCI FOR TYPE 2 DIABETES IN AFRICAN AMERICANS. Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing 2016 22 242-253. Keaton Jacob M, Hellwege Jacklyn N, Ng Maggie C Y, Palmer Nicholette D, Pankow James S, Fornage Myriam, Wilson James G, Correa Adolfo, Rasmussen-Torvik Laura J, Rotter Jerome I, Chen Yii-DER I, Taylor Kent D, Rich Stephen S, Wagenknecht Lynne E, Freedman Barry I, Bowden Donald |
Polymorphisms of ESR1, UGT1A1, HCN1, MAP3K1 and CYP2B6 are associated with the prognosis of hormone receptor-positive early breast cancer. Oncotarget 2017 Feb . Kuo Sung-Hsin, Yang Shi-Yi, You San-Lin, Lien Huang-Chun, Lin Ching-Hung, Lin Po-Han, Huang Chiun-She |
A polygenic risk score for breast cancer risk in a Taiwanese population. Breast cancer research and treatment 2017 Feb . Hsieh Yi-Chen, Tu Shih-Hsin, Su Chien-Tien, Cho Er-Chieh, Wu Chih-Hsiung, Hsieh Mao-Chih, Lin Shiyng-Yu, Liu Yun-Ru, Hung Chin-Sheng, Chiou Hung- |
Case-control pharmacogenetic study of HCN1/HCN2 variants and genetic generalized epilepsies. Clinical and experimental pharmacology & physiology 2017 Oct . Wu Shu-Zhi, Ye Hua, Yang Xiao-Guo, Lu Zhi-Li, Qu Qiang, Qu Ji |
Gene mutational analysis in a cohort of Chinese children with unexplained epilepsy: Identification of a new KCND3 phenotype and novel genes causing Dravet syndrome. Seizure 2019 2 66 26-30. Wang Jiaping, Wen Yongxin, Zhang Qingping, Yu Shujie, Chen Yan, Wu Xiru, Zhang YueHua, Bao Xinh |
Genome-wide Association of Endophenotypes for Schizophrenia From the Consortium on the Genetics of Schizophrenia (COGS) Study.
JAMA psychiatry 2019 Oct . Greenwood Tiffany A, Lazzeroni Laura C, Maihofer Adam X, Swerdlow Neal R, Calkins Monica E, Freedman Robert, Green Michael F, Light Gregory A, Nievergelt Caroline M, Nuechterlein Keith H, Radant Allen D, Siever Larry J, Silverman Jeremy M, Stone William S, Sugar Catherine A, Tsuang Debby W, Tsuang Ming T, Turetsky Bruce I, Gur Ruben C, Gur Raquel E, Braff David |
A common variation in HCN1 is associated with heart rate variability in schizophrenia. Schizophrenia research 2020 Nov . Refisch Alexander, Chung Ha-Yeun, Komatsuzaki Shoko, Schumann Andy, Mühleisen Thomas W, Nöthen Markus M, Hübner Christian A, Bär Karl-Jürg |
Evidence for the contribution of HCN1 gene polymorphism (rs1501357) to working memory at both behavioral and neural levels in schizophrenia patients and healthy controls. Schizophrenia (Heidelberg, Germany) 2022 Aug 8 (1): 66. Chen Xiongying, Zhang Qiumei, Su Yanyan, Zhao Wan, Li Yang, Du Boqi, Deng Xiaoxiang, Ji Feng, Dong Qi, Chen Chuansheng, Li J |
Peripheral Ion Channel Genes Screening in Painful Small Fiber Neuropathy. International journal of molecular sciences 2022 11 23 (22): . ?l?czkowska Milena, Almomani Rowida, Marchi Margherita, Salvi Erika, de Greef Bianca T A, Sopacua Maurice, Hoeijmakers Janneke G J, Lindsey Patrick, Waxman Stephen G, Lauria Giuseppe, Faber Catharina G, Smeets Hubert J M, Gerrits Monique |
The HCN1 p.Ser399Pro variant causes epileptic encephalopathy with super-refractory status epilepticus. Human genome variation 2023 6 10 (1): 20. Yu Kobayashi, Jun Tohyama, Noriyuki Akasaka, Kei Yamada, Moemi Hojo, Eijun Seki, Masaki Miura, Noriko Soma, Takeshi Ono, Mitsuhiro Kato, Mitsuko Nakashima, Hirotomo Saitsu, Naomichi Matsumo |
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- Page last updated:Apr 22, 2024
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