Variant rs9939609 in the <it>FTO </it>gene is associated with body mass index among Chinese children

by Liu Ailing, Zhang Qian, Hu Xiaoqi, Du Songming, Li Yanping, Fang Hongyun, Ma Guansheng
Published 2010-09-01

EEG alpha phenotypes: linkage analyses and relation to alcohol dependence in an American Indian community study

by Phillips Evelyn, Gizer Ian R, Ehlers Cindy L, Wilhelmsen Kirk C
Published 2010-03-01

Meta-analysis of associations between <it>TCF7L2</it> polymorphisms and risk of type 2 diabetes mellitus in the Chinese population

by Wang Jinjin, Hu Fulan, Feng Tianping, Zhao Jingzhi, Yin Lei, Li Linlin, Wang Yan, Wang Qian, Hu Dongsheng
Published 2013-01-01

Living kidney transplantation between brothers with unrecognized renal amyloidosis as the first manifestation of familial Mediterranean fever: a case report

by Ramón Peces, Sara Afonso, Carlos Peces, Julián Nevado, Rafael Selgas
Published 2017-08-01

Mutation analysis of SDHB and SDHC: novel germline mutations in sporadic head and neck paraganglioma and familial paraganglioma and/or pheochromocytoma

by Wong Nora, Ferrando Barbara, Pasini Barbara, Menko Fred H, Oomen Peter HN, Jansen Jeroen C, Weiss Marjan M, van Minderhout Ivonne, Bayley Jean-Pierre, Alpert Lesley C, Williams Rosie, Blair Edward, Devilee Peter, Taschner Peter EM
Published 2006-01-01

<it>MFN2 </it>point mutations occur in 3.4% of Charcot-Marie-Tooth families. An investigation of 232 Norwegian CMT families

by Lobato Ana, Sand Jette C, Braathen Geir J, Høyer Helle, Russell Michael B
Published 2010-03-01

Association of glucocorticoid receptor gene polymorphism and occupational stress with hypertension in desert petroleum workers in Xinjiang, China

by Ning Tao, Hua Ge, Wenfeng Wu, Hengqing An, Jiwen Liu, Xinjuan Xu
Published 2018-12-01

Investigating the relationship between <it>UMODL1</it> gene polymorphisms and high myopia: a case–control study in Chinese

by Zhu Miao-miao, Yap Maurice KH, Ho Daniel WH, Fung Wai Yan, Ng Po Wah, Gu Yang-shun, Yip Shea Ping
Published 2012-08-01

Dominant inhibition of Fas ligand-mediated apoptosis due to a heterozygous mutation associated with autoimmune lymphoproliferative syndrome (ALPS) Type Ib

by McDonald Jay M, Reddy Vishnu, Makris Christopher, Dale Janet K, Zheng Lixin, Atkinson T Prescott, Pan George, Bi Lilia L, Siegel Richard M, Puck Jennifer M, Lenardo Michael J, Straus Stephen E
Published 2007-07-01

A novel compound heterozygous variant of the SLC12A3 gene in Gitelman syndrome pedigree

by Yixin Chen, Ziyi Zhang, Xihua Lin, Qianqian Pan, Fenping Zheng, Hong Li
Published 2018-01-01

De novo mutations in SCN1A are associated with classic Rett syndrome: a case report

by Mari Wold Henriksen, Kirstine Ravn, Benedicte Paus, Stephen von Tetzchner, Ola H Skjeldal
Published 2018-10-01

Effect of GRM7 polymorphisms on the development of noise-induced hearing loss in Chinese Han workers: a nested case-control study

by Peipei Yu, Jie Jiao, Guoshun Chen, Wenhui Zhou, Huanling Zhang, Hui Wu, Yanhong Li, Guizhen Gu, Yuxin Zheng, Yue Yu, Shanfa Yu
Published 2018-01-01

A pooling-based genome-wide analysis identifies new potential candidate genes for atopy in the European Community Respiratory Health Survey (ECRHS)

by Kogevinas Manolis, Ramon González Juan, Bustamante Mariona, Castro-Giner Francesc, Jarvis Deborah, Heinrich Joachim, Antó Josep-Maria, Wjst Matthias, Estivill Xavier, de Cid Rafael
Published 2009-12-01

Estrogen Receptor-Beta Gene Polymorphism in women with Breast Cancer at the Imam Khomeini Hospital Complex, Iran

by Abbasi Sakineh
Published 2010-07-01

DNA methylation and mRNA expression of <it>SYN III</it>, a candidate gene for schizophrenia

by Singh Shiva M, O'Reilly Richard L, Murphy Brenda C
Published 2008-12-01

COPA syndrome in an Icelandic family caused by a recurrent missense mutation in COPA

by Brynjar O. Jensson, Sif Hansdottir, Gudny A. Arnadottir, Gerald Sulem, Ragnar P. Kristjansson, Asmundur Oddsson, Stefania Benonisdottir, Hakon Jonsson, Agnar Helgason, Jona Saemundsdottir, Olafur T. Magnusson, Gisli Masson, Gudmundur A. Thorisson, Adalbjorg Jonasdottir, Aslaug Jonasdottir, Asgeir Sigurdsson, Ingileif Jonsdottir, Vigdis Petursdottir, Jon R. Kristinsson, Daniel F. Gudbjartsson, Unnur Thorsteinsdottir, Reynir Arngrimsson, Patrick Sulem, Gunnar Gudmundsson, Kari Stefansson
Published 2017-11-01

<it>FTO </it>variant rs9939609 is associated with body mass index and waist circumference, but not with energy intake or physical activity in European- and African-American youth

by Dong Yanbin, Treiber Frank A, Stallmann-Jorgensen Inger S, Gutin Bernard, Lagou Vasiliki, Zhu Haidong, Liu Gaifen, Snieder Harold
Published 2010-04-01

Assessment of risk based on variant pathways and establishment of an artificial neural network model of thyroid cancer

by Yinlong Zhao, Lingzhi Zhao, Tiezhu Mao, Lili Zhong
Published 2019-05-01

Association of preeclampsia with infant APOL1 genotype in African Americans

by Anna K. Miller, Timur Azhibekov, John F. O’Toole, John R. Sedor, Scott M. Williams, Raymond W. Redline, Leslie A. Bruggeman
Published 2020-05-01

Association between paraoxonase gene and stroke in the Han Chinese population

by Zhang Guojun, Li Wenjin, Li Zhiqiang, Lv Hong, Ren Yonghong, Ma Ruimin, Li Xiaohong, Kang Xixiong, Shi Yongyong, Sun Yimin
Published 2013-01-01