Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 41 Records) |
Query Trace: HAP1[original query] |
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Increasing the number of SNP loci does not necessarily improve prediction power at least in the comparison of MTHFR SNP and haplotypes. Journal of epidemiology / Japan Epidemiological Association 2008 18 (6): 243-50. Miyaki Koichi, Takahashi Yoshimitsu, Song Yixuan, Zhang Ling, Muramatsu Masaaki, Nakayama Tak |
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 |
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 |
Genetic interaction of Hsp70 family genes polymorphisms with high-altitude pulmonary edema among Chinese railway constructors at altitudes exceeding 4000 meters. Clinica chimica acta; international journal of clinical chemistry 2009 Jul 405 (1-2): 17-22. Qi Yue, Niu Wen-Quan, Zhu Tong-Chun, Liu Jing-Liang, Dong Wei-Ya, Xu Ying, Ding Shou-Quan, Cui Cheng-Bing, Pan Yun-Jun, Yu Guo-Shu, Zhou Wen-Yu, Qiu Chang-Ch |
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 |
Functional variant in complement C3 gene promoter and genetic susceptibility to temporal lobe epilepsy and febrile seizures. PloS one 2010 5 (9): 9. Jamali Sarah, Salzmann Annick, Perroud Nader, Ponsole-Lenfant Magali, Cillario Jennifer, Roll Patrice, Roeckel-Trevisiol Nathalie, Crespel Ariel, Balzar Jorg, Schlachter Kurt, Gruber-Sedlmayr Ursula, Pataraia Ekaterina, Baumgartner Christoph, Zimprich Alexander, Zimprich Fritz, Malafosse Alain, Szepetowski Pier |
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 |
Genetic variation within IL18 is associated with insulin levels, insulin resistance and postprandial measures. Nutrition, metabolism, and cardiovascular diseases : NMCD 2011 Jul 21 (7): 476-84. Smart M C, Dedoussis G, Yiannakouris N, Grisoni M L, Dror G K, Yannakoulia M, Papoutsakis C, Louizou E, Mantzoros C S, Melistas L, Kontogianni M D, Cooper J A, Humphries S E, Talmud P J, |
Analysis of 6 single-nucleotide polymorphisms in the androgen receptor gene in Chilean patients with primary spermatogenic failure. Journal of andrology 0 33 (1): 88-95. Parada-Bustamante Alexis, Lardone María Cecilia, Valdevenito Raúl, Ebensperger Mauricio, López Patricia V, Madariaga Marcia, Piottante Antonio, Castro Andr |
Novel genetic variation in exon 28 of FBN1 gene is associated with essential hypertension. American journal of hypertension 2011 Jun 24 (6): 687-93. Shen Chong, Lu Xiangfeng, Wang Laiyuan, Chen Shufeng, Li Yun, Liu Xiaoli, Li Jianxin, Huang Jianfeng, Gu Dongfe |
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 |
MAP2K3 is associated with body mass index in American Indians and Caucasians and may mediate hypothalamic inflammation. Human molecular genetics 2013 Nov 22 (21): 4438-49. Bian Li, Traurig Michael, Hanson Robert L, Marinelarena Alejandra, Kobes Sayuko, Muller Yunhua L, Malhotra Alka, Huang Ke, Perez Jessica, Gale Alex, Knowler William C, Bogardus Clifton, Baier Leslie |
Progression of lumbar spinal stenosis is influenced by polymorphism of thrombospondin 2 gene in the Korean population. European spine journal : official publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society 2014 Jan 23 (1): 57-63. Hyun Seung-Jae, Park Borae G, Rhim Seung-Chul, Jang Jun-Won, Jeon Sang-Ryong, Roh Sung-W |
Genetic variation and haplotype structure of the gene Vitamin K epoxide reductase complex, subunit 1 in the Tamilian population. Journal of pharmacology & pharmacotherapeutics 2013 Jan 4 (1): 53-8. Kumar Dhakchinamoorthi Krishna, Shewade Deepak Gopal, Surendiran Adithan, Adithan Chandrasekar |
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 |
Evaluating the association of polymorphisms in the HAP1 gene with lung cancer risk: a meta-analysis. Tumour biology : the journal of the International Society for Oncodevelopmental Biology and Medicine 2014 Nov 35 (11): 10825-31. Wang Wei, Yan Haicheng, Zhang Qiang, Song Wei, Li Haina, Xu J |
Association between secreted phosphoprotein-1 (SPP1) polymorphisms and low bone mineral density in women. PloS one 2014 9 (5): e97428. Chen Jen-Hau, Chen Yen-Ching, Mao Chien-Lin, Chiou Jeng-Min, Tsao Chwen Keng, Tsai Keh-Su |
Exome array analysis identifies CAV1/CAV2 as a susceptibility locus for intraocular pressure. Investigative ophthalmology & visual science 2015 Jan 56 (1): 544-51. Chen Fei, Klein Alison P, Klein Barbara E K, Lee Kristine E, Truitt Barbara, Klein Ronald, Iyengar Sudha K, Duggal Pri |
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 |
Association of MMP-9 Haplotypes and TIMP-1 Polymorphism with Spontaneous Deep Intracerebral Hemorrhage in the Taiwan Population. PloS one 2015 10 (5): e0125397. Ho Wei-Min, Chen Chiung-Mei, Lee Yun-Shien, Chang Kuo-Hsuan, Chen Huei-Wen, Chen Sien-Tsong, Chen Yi-Ch |
Multiple microRNA regulation of lipoprotein lipase gene abolished by 3'UTR polymorphisms in a triglyceride-lowering haplotype harboring p.Ser474Ter. Atherosclerosis 2016 Jan 246 280-286. Caussy Cyrielle, Charrière Sybil, Meirhaeghe Aline, Dallongeville Jean, Lefai Etienne, Rome Sophie, Cuerq Charlotte, Euthine Vanessa, Delay Mireille, Marmontel Oriane, Di Filippo Mathilde, Lagarde Michel, Moulin Philippe, Marçais Christop |
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 |
Potential Minor Haplotypes of CYP2D6 in the Japanese Population. Drug metabolism letters 2017 Jun . Masuda Masatoshi, Fujiwara Tsutomu, Matsunaga Masayuki, Matsumaru Takehi |
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 |
Myelodysplastic syndromes with 20q deletion: incidence, prognostic value and impact on response to azacitidine of ASXL1 chromosomal deletion and genetic mutations. British journal of haematology 2021 7 194 (4): 708-717. Martín Iván, Villamón Eva, Abellán Rosario, Calasanz Maria José, Irigoyen Aroa, Sanz Guillermo, Such Esperanza, Mora Elvira, Gutiérrez Míriam, Collado Rosa, García-Serra Rocío, Vara Míriam, Blanco Mª Laura, Oiartzabal Itziar, Álvarez Sara, Bernal Teresa, Granada Isabel, Xicoy Blanca, Jerez Andrés, Calabuig Marisa, Diez Rosana, Gil Ángela, Díez-Campelo María, Solano Carlos, Tormo Mar, |
A common Matrix metalloproteinase 8 promoter haplotype enhances the risk for hypertension via diminished interactions with nuclear factor kappa B. Journal of hypertension 2022 Jul . Maghajothi Sakthisree, Subramanian Lakshmi, Mani Preethi, Singh Mrityunjay, Iyer Dhanya R, Sharma Saurabh, Khullar Madhu, Victor Suma M, Asthana Shailendra, Mullasari Ajit S, Mahapatra Nitish |
Uncovering a Genetic Polymorphism Located in Huntingtin Associated Protein 1 in Modulation of Central Pain Sensitization Signaling Pathways.
Frontiers in neuroscience 2022 7 16 807773. Gloor Yvonne, Matthey Alain, Sobo Komla, Mouterde Médéric, Kosek Eva, Pickering Gisèle, Poloni Estella S, Cedraschi Christine, Ehret Georg, Desmeules Jules |
Candidate loci for leaf angle in maize revealed by a combination of genome-wide association study and meta-analysis. Frontiers in genetics 2022 11 13 1004211. Duan Haiyang, Li Jianxin, Sun Yan, Xiong Xuehang, Sun Li, Li Wenlong, Gao Jionghao, Li Na, Zhang Junli, Cui Jiangkuan, Fu Zhiyuan, Zhang Xuehai, Tang Jih |
Identification of mutations in porcine STAT5A that contributes to the transcription of CISH. Frontiers in veterinary science 2023 2 9 1090833. Yao Diwen, Guo Dongchun, Zhang Yingkun, Chen Zhihua, Gao Xiaowen, Xing Guiling, Yang Xiuqin, Wang Xibiao, Di Shengwei, Cai Jiancheng, Niu Buy |
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