TABLE OF CONTENTS
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Volume 60, Issue 2 (February 2015)
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 | In this issue
 Original Articles
Short Communications
Corrigendum
Also new
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ORIGINAL ARTICLES
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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
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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
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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
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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
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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
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SHORT COMMUNICATIONS
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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
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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
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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
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CORRIGENDUM
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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
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