Journal of Human Genetics - Table of Contents alert Volume 60 Issue 2

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TABLE OF CONTENTS Volume 60, Issue 2 (February 2015) In this issue Original Articles Short Communications Corrigendum Also new AOP Sign up for e-alerts Recommend to your library Web feed Subscribe Advertisement Nature Genetics, Central South University, and Anhui Medical University present: Genome Variation in Precision Medicine 2015 May 17-19, 2015 | Changsha, China  Register Now!  Original Articles Top Downregulation of the microRNA-1/133a cluster enhances cancer cell migration and invasion in lung-squamous cell carcinoma via regulation of Coronin1C Hiroko Mataki, Hideki Enokida, Takeshi Chiyomaru, Keiko Mizuno, Ryosuke Matsushita, Yusuke Goto, Rika Nishikawa, Ikkou Higashimoto, Takuya Samukawa, Masayuki Nakagawa, Hiromasa Inoue and Naohiko Seki J Hum Genet 2015 60: 53-61; advance online publication, December 18, 2014; 10.1038/jhg.2014.111 Abstract | Full Text Deep sequencing of RYR3 gene identifies rare and common variants associated with increased carotid intima-media thickness (cIMT) in HIV-infected individuals Degui Zhi, Aditi Shendre, Rebecca Scherzer, Marguerite R Irvin, Rodney T Perry, Shawn Levy, Donna K Arnett, Carl Grunfeld and Sadeep Shrestha J Hum Genet 2015 60: 63-67; advance online publication, December 11, 2014; 10.1038/jhg.2014.104 Abstract | Full Text Genetic structure among Fijian island populations Gerhard P Shipley, Diana A Taylor, Anand Tyagi, Geetanjali Tiwari and Alan J Redd J Hum Genet 2015 60: 69-75; advance online publication, January 8, 2015; 10.1038/jhg.2014.105 Abstract | Full Text A powerful association test for qualitative traits incorporating imprinting effects using general pedigree data Ji-Yuan Zhou, Hai-Qiang He, Xiao-Ping You, Shao-Zhan Li, Ping-Yan Chen and Wing Kam Fung J Hum Genet 2015 60: 77-83; advance online publication, December 18, 2014; 10.1038/jhg.2014.109 Abstract | Full Text Mutations in the glucocerebrosidase gene are responsible for Chinese patients with Parkinson’s disease Zhe Yu, Ting Wang, Jun Xu, Wei Wang, Guifang Wang, Chao Chen, Lili Zheng, Li Pan, Dianrong Gong, Xueli Li, Huaiqian Qu, Fang Li, Bin Zhang, Weidong Le and Fabin Han J Hum Genet 2015 60: 85-90; advance online publication, December 18, 2014; 10.1038/jhg.2014.110 Abstract | Full Text Short Communications Top Silver–Russell syndrome without body asymmetry in three patients with duplications of maternally derived chromosome 11p15 involving CDKN1C Shinichi Nakashima, Fumiko Kato, Tomoki Kosho, Keisuke Nagasaki, Toru Kikuchi, Masayo Kagami, Maki Fukami and Tsutomu Ogata J Hum Genet 2015 60: 91-95; advance online publication, November 27, 2014; 10.1038/jhg.2014.100 Abstract | Full Text Mutations in the glutaminyl-tRNA synthetase gene cause early-onset epileptic encephalopathy Hirofumi Kodera, Hitoshi Osaka, Mizue Iai, Noriko Aida, Akio Yamashita, Yoshinori Tsurusaki, Mitsuko Nakashima, Noriko Miyake, Hirotomo Saitsu and Naomichi Matsumoto J Hum Genet 2015 60: 97-101; advance online publication, December 4, 2014; 10.1038/jhg.2014.103 Abstract | Full Text Severe phenotypes in a Charcot–Marie–Tooth 1A patient with PMP22 triplication Sung Min Kim, Jinho Lee, Bo Ram Yoon, Ye Jin Kim, Byung-Ok Choi and Ki Wha Chung J Hum Genet 2015 60: 103-106; advance online publication, December 11, 2014; 10.1038/jhg.2014.102 Abstract | Full Text Corrigendum Top An A/C germline single-nucleotide polymorphism in the TNFAIP3 gene is associated with advanced disease stage and survival in only surgically treated esophageal cancer Tarik Ghadban, Magdalena Schmidt-Yang, Faik G Uzunoglu, Daniel R Perez, Tung Y Tsui, Alexander T El Gammal, Peter J Erbes, Veacheslav Zilbermints, Ulrich Wellner, Klaus Pantel, Jakob R Izbicki and Yogesh K Vashist J Hum Genet 2015 60: 107; 10.1038/jhg.2014.106 Full Text Natureevents is a fully searchable, multi-disciplinary database designed to maximise exposure for events organisers. 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