Human Genome Epidemiology Literature Finder
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Records 1 - 5 (of 5 Records) |
| Query Trace: Disease and MEGF10[original query] |
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| MEGF10 association with schizophrenia. Biological psychiatry 2008 Mar 63 (5): 441-8. Chen Xiangning, Wang Xu, Chen Qi, Williamson Vernell, van den Oord Edwin, Maher Brion S, O'Neill F Anthony, Walsh Dermot, Kendler Kenneth |
| Apoptotic engulfment pathway and schizophrenia. PloS one 2009 4 (9): e6875. Chen Xiangning, Sun Cuie, Chen Qi, O'Neill F Anthony, Walsh Dermot, Fanous Ayman H, Chowdari Kodavali V, Nimgaonkar Vishwajit L, Scott Adrian, Schwab Sibylle G, Wildenauer Dieter B, Che Ronglin, Tang Wei, Shi Yongyong, He Lin, Luo Xiong-Jian, Su Bing, Edwards Todd L, Zhao Zhongming, Kendler Kenneth |
| Mutations in the satellite cell gene MEGF10 cause a recessive congenital myopathy with minicores. Neurogenetics 2012 May 13 (2): 115-24. Boyden Steven E, Mahoney Lane J, Kawahara Genri, Myers Jennifer A, Mitsuhashi Satomi, Estrella Elicia A, Duncan Anna R, Dey Friederike, DeChene Elizabeth T, Blasko-Goehringer Jessica M, Bönnemann Carsten G, Darras Basil T, Mendell Jerry R, Lidov Hart G W, Nishino Ichizo, Beggs Alan H, Kunkel Louis M, Kang Peter |
| Genetic variants in the transcription regulatory region of MEGF10 are associated with autism in Chinese Han population. Scientific reports 2017 May 7 (1): 2292. Wu Zhiliu, Qin Jian, You Yang, Ma Yuanlin, Jia Meixiang, Wang Linyan, Lu Tianlan, Yue Weihua, Ruan Yanyan, Zhang Dai, Li Jun, Wang Lifa |
| Novel caries loci in children and adults implicated by genome-wide analysis of families. BMC oral health 2018 6 18 (1): 98. Govil Manika, Mukhopadhyay Nandita, Weeks Daniel E, Feingold Eleanor, Shaffer John R, Levy Steven M, Vieira Alexandre R, Slayton Rebecca L, McNeil Daniel W, Weyant Robert J, Crout Richard J, Marazita Mary |
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