Human Genome Epidemiology Literature Finder
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Records 1 - 14 (of 14 Records) |
| Query Trace: Disease and HAP1[original query] |
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| Association of angiotensinogen haplotypes with angiotensinogen levels but not with blood pressure or coronary artery disease: the Ludwigshafen Risk and Cardiovascular Health Study. Journal of molecular medicine (Berlin, Germany) 2005 Mar 83 (3): 235-9. Renner Wilfried, Nauck Markus, Winkelmann Bernhard R, Hoffmann Michael M, Scharnagl Hubert, Mayer Volker, Boehm Bernhard O, März Winfried, |
| A polymorphism in the protease-like domain of apolipoprotein(a) is associated with severe coronary artery disease. Arteriosclerosis, thrombosis, and vascular biology 2007 Sep 27 (9): 2030-6. Luke May M, Kane John P, Liu Dongming M, Rowland Charles M, Shiffman Dov, Cassano June, Catanese Joseph J, Pullinger Clive R, Leong Diane U, Arellano Andre R, Tong Carmen H, Movsesyan Irina, Naya-Vigne Josephina, Noordhof Curtis, Feric Nicole T, Malloy Mary J, Topol Eric J, Koschinsky Marlys L, Devlin James J, Ellis Stephen |
| A common interleukin 18 haplotype is associated with higher body mass index in subjects with diabetes and coronary heart disease. Metabolism: clinical and experimental 2007 May 56 (5): 662-9. Thompson Simon R, Sanders Julie, Stephens Jeffrey W, Miller George J, Humphries Steve |
| The INSIG1 gene, not the INSIG2 gene, associated with coronary heart disease: tagSNPs and haplotype-based association study. The Beijing Atherosclerosis Study. Thrombosis and haemostasis 2008 Nov 100 (5): 886-92. Liu Xiaoli, Li Yun, Wang Laiyuan, Zhao Qi, Lu Xiangfeng, Huang Jianfeng, Fan Zhongjie, Gu Dongfe |
| Huntingtin-associated protein-1 is a modifier of the age-at-onset of Huntington's disease. Human molecular genetics 2008 Apr 17 (8): 1137-46. Metzger Silke, Rong Juan, Nguyen Huu-Phuc, Cape Austin, Tomiuk Juergen, Soehn Anne S, Propping Peter, Freudenberg-Hua Yun, Freudenberg Jan, Tong Liang, Li Shi-Hua, Li Xiao-Jiang, Riess Ol |
| Strong evidence of a combination polymorphism of the tyrosine kinase 2 gene and the signal transducer and activator of transcription 3 gene as a DNA-based biomarker for susceptibility to Crohn's disease in the Japanese population. Journal of clinical immunology 2009 Nov 29 (6): 815-25. Sato Kayoko, Shiota Mizuho, Fukuda Sayaka, Iwamoto Eiko, Machida Haruhisa, Inamine Tatsuo, Kondo Shinji, Yanagihara Katsunori, Isomoto Hajime, Mizuta Yohei, Kohno Shigeru, Tsukamoto Kazuhi |
| Vitamin D binding protein genotype and osteoporosis. Calcified tissue international 2009 Aug 85 (2): 85-93. Fang Yue, van Meurs Joyce B J, Arp Pascal, van Leeuwen Johannes P T, Hofman Albert, Pols Huibert A P, Uitterlinden André |
| Haplotype-tagging single nucleotide polymorphisms in the GSTP1 gene promoter and susceptibility to lung cancer. Cancer detection and prevention 2009 32 (5-6): 403-15. Tan Xiang-Lin, Moslehi Roxana, Han WeiGuo, Spivack Simon |
| Age at onset in Huntington's disease: replication study on the associations of ADORA2A, HAP1 and OGG1. Neurogenetics 2010 Oct 11 (4): 435-9. Taherzadeh-Fard Elahe, Saft Carsten, Wieczorek Stefan, Epplen Jörg T, Arning Laris |
| Age at onset in Huntington's disease: replication study on the association of HAP1. Parkinsonism & related disorders 2012 Nov 18 (9): 1027-8. Karadima Georgia, Dimovasili Christina, Koutsis Georgios, Vassilopoulos Demetris, Panas Mari |
| Long-standing balancing selection in the THBS4 gene: influence on sex-specific brain expression and gray matter volumes in Alzheimer disease. Human mutation 2013 May 34 (5): 743-53. Cagliani Rachele, Guerini Franca R, Rubio-Acero Raquel, Baglio Francesca, Forni Diego, Agliardi Cristina, Griffanti Ludovica, Fumagalli Matteo, Pozzoli Uberto, Riva Stefania, Calabrese Elena, Sikora Martin, Casals Ferran, Comi Giacomo P, Bresolin Nereo, Cáceres Mario, Clerici Mario, Sironi Manue |
| Molecular characterization of genes modifying the age at onset in Huntington's disease in Uruguayan patients. The International journal of neuroscience 2015 May 1-17. Vital Marcelo, Bidegain Estela, Raggio Victor, Esperon Patric |
| Population genetics of IFITM3 in Portugal and Central Africa reveals a potential modifier of influenza severity. Immunogenetics 2017 Aug . David Susana, Correia Vanessa, Antunes Liliana, Faria Ricardo, Ferrão José, Faustino Paula, Nunes Baltazar, Maltez Fernando, Lavinha João, Rebelo de Andrade Hele |
| The longevity SNP rs2802292 uncovered: HSF1 activates stress-dependent expression of FOXO3 through an intronic enhancer. Nucleic acids research 2018 5 46 (11): 5587-5600. Grossi Valentina, Forte Giovanna, Sanese Paola, Peserico Alessia, Tezil Tugsan, Lepore Signorile Martina, Fasano Candida, Lovaglio Rosaura, Bagnulo Rosanna, Loconte Daria C, Susca Francesco C, Resta Nicoletta, Simone Cristia |
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