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Genetic variation in the human interleukin 4 (IL4) gene is associated with gallstone susceptibility
Tönjes, A, Tönjes, A, Strauch, T, Ruffert, C, Mössner, J, Stumvoll, M, Kovacs, P, Wittenburg, H
Published in Zeitschrift für Gastroenterologie (13.01.2011)
Published in Zeitschrift für Gastroenterologie (13.01.2011)
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Prioritizing genes responsible for host resistance to influenza using network approaches
Bao, Suying, Zhou, Xueya, Zhang, Liangcai, Zhou, Jie, To, Kelvin Kai-Wang, Wang, Binbin, Wang, Liqiu, Zhang, Xuegong, Song, You-Qiang
Published in BMC genomics (21.11.2013)
Published in BMC genomics (21.11.2013)
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Genome-Wide Analysis Reveals Four Novel Loci for Attention-Deficit Hyperactivity Disorder in Korean Youths
Kweon, Kukju, Shin, Eun-Soon, Park, Kee Jeong, Lee, Jong-Keuk, Joo, Yeonho, Kim, Hyo-Won
Published in Soa--chʻŏngsonyŏn chŏngsin ŭihak = Journal of child & adolescent psychiatry (2018)
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Published in Soa--chʻŏngsonyŏn chŏngsin ŭihak = Journal of child & adolescent psychiatry (2018)
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Variability of hemoglobin F expression in hemoglobin EE disease: Hematological and molecular analysis
Pakdee, Naruwat, Yamsri, Supawadee, Fucharoen, Goonnapa, Sanchaisuriya, Kanokwan, Pissard, Serge, Fucharoen, Supan
Published in Blood cells, molecules, & diseases (01.06.2014)
Published in Blood cells, molecules, & diseases (01.06.2014)
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Association between variants in the gene encoding myosin light chain kinase (MLCK) and asthma and atopy
Munoz, M., Zambelli-Weiner, A., Grant, A., Lorenzo, M., Ehrlich, E., Burki, M., Gao, L., Ye, S., Beaty, T.H., Garcia, J.G., Barnes, K.C.
Published in Journal of allergy and clinical immunology (2004)
Published in Journal of allergy and clinical immunology (2004)
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The effect of phenotype variation on detection of linkage in the COGA data
Birznieks, Gunther, Ghosh, Soumitra, Watanabe, Richard M., Mitchell, Braxton D.
Published in Genetic epidemiology (1999)
Published in Genetic epidemiology (1999)
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Collagen type XVIII alpha 1 chain (COL18A1) variants affect the risk of anti‐tuberculosis drug‐induced hepatotoxicity: A prospective study
Cheng, Yuhui, Jiao, Lin, Li, Weixiu, Wang, Jialing, Lin, Zhangyu, Lai, Hongli, Ying, Binwu
Published in Journal of clinical laboratory analysis (01.02.2021)
Published in Journal of clinical laboratory analysis (01.02.2021)
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A Three-Single-Nucleotide Polymorphism Haplotype in Intron 1 of 0CA2 Explains Most Human Eye-Color Variation
Duffy, D L, Montgomery, G W, Chen, W, Zhao, Z Z, Le, L, James, M R, Hayward, N K, Martin, NG, Sturm, R A
Published in American journal of human genetics (01.02.2007)
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Published in American journal of human genetics (01.02.2007)
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Neuropeptide Y Receptor Genes Are Associated With Alcohol Dependence, Alcohol Withdrawal Phenotypes, and Cocaine Dependence
Wetherill, Leah, Schuckit, Marc A., Hesselbrock, Victor, Xuei, Xiaoling, Liang, Tiebing, Dick, Danielle M., Kramer, John, Nurnberger Jr, John I., Tischfield, Jay A., Porjesz, Bernice, Edenberg, Howard J., Foroud, Tatiana
Published in Alcoholism, clinical and experimental research (01.12.2008)
Published in Alcoholism, clinical and experimental research (01.12.2008)
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Identification of Genetic Loci Underlying the Phenotypic Constructs of Autism Spectrum Disorders
Liu, Xiao-Qing, Georgiades, Stelios, Duku, Eric, Thompson, Ann, Devlin, Bernie, Cook, Edwin H., Wijsman, Ellen M., Paterson, Andrew D., Szatmari, Peter
Published in Journal of the American Academy of Child and Adolescent Psychiatry (01.07.2011)
Published in Journal of the American Academy of Child and Adolescent Psychiatry (01.07.2011)
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Study design for the investigation of likely aetiological factors of juvenile osteochondral conditions (JOCC) in foals and yearlings
Robert, Céline, Valette, Jean-Paul, Jacquet, Sandrine, Lepeule, Johanna, Denoix, Jean-Marie
Published in The veterinary journal (1997) (01.07.2013)
Published in The veterinary journal (1997) (01.07.2013)
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A Whole-Genome Scan for Obstructive Sleep Apnea and Obesity
Palmer, Lyle J., Buxbaum, Sarah G., Larkin, Emma, Patel, Sanjay R., Elston, Robert C., Tishler, Peter V., Redline, Susan
Published in American journal of human genetics (01.02.2003)
Published in American journal of human genetics (01.02.2003)
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Genome-Wide Linkage Scan for the Metabolic Syndrome in the HERITAGE Family Study
Loos, Ruth J. F., Katzmarzyk, Peter T., Rao, D. C., Rice, Treva, Leon, Arthur S., Skinner, James S., Wilmore, Jack H., Rankinen, Tuomo, Bouchard, Claude
Published in The journal of clinical endocrinology and metabolism (01.12.2003)
Published in The journal of clinical endocrinology and metabolism (01.12.2003)
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Genetic Variants Within the LPIN1 Gene, Encoding Lipin, Are Influencing Phenotypes of the Metabolic Syndrome in Humans
Wiedmann, Silke, Fischer, Marcus, Koehler, Martina, Neureuther, Katharina, Riegger, Guenter, Doering, Angela, Schunkert, Heribert, Hengstenberg, Christian, Baessler, Andrea
Published in Diabetes (New York, N.Y.) (01.01.2008)
Published in Diabetes (New York, N.Y.) (01.01.2008)
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Genetic loci for blood lipid levels identified by linkage and association analyses in Caribbean Hispanics[S]
Dong, Chuanhui, Beecham, Ashley, Wang, Liyong, Slifer, Susan, Wright, Clinton B., Blanton, Susan H., Rundek, Tatjana, Sacco, Ralph L.
Published in Journal of lipid research (01.07.2011)
Published in Journal of lipid research (01.07.2011)
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