Journal of Human Genetics - Table of Contents alert Volume 56 Issue 10

TABLE OF CONTENTS Volume 56, Issue 10 (October 2011) In this issue Review Original Articles Short Communication Corrigenda Erratum Also new AOP Advertisement The Next Generation Sequencing (NGS) Collection for Pipeline Pilot The Next Generation Sequencing (NGS) Collection for Pipeline Pilot Accelrys, the company that pioneered graphical data pipelining, introduces the new NGS Collection for Pipeline Pilot, a uniquely agile and scalable platform for the dynamic next generation sequencing domain. Check out the unparalleled power and flexibility of the recently launched NGS Collection in our on-demand Overview Webinar. Sign up for e-alerts Recommend to your library Web feed Subscribe Advertisement Need Access to the Journal of Human Genetics? Recommend the Journal of Human Genetics to your librarian to ensure your access. For more information about the Journal of Human Genetics visit www.nature.com/jhg.   Review Top The generation of mitochondrial DNA large-scale deletions in human cells Tao Chen, Jing He, Yushan Huang and Weiwei Zhao J Hum Genet 2011 56: 689-694; advance online publication, August 25, 2011; 10.1038/jhg.2011.97 Abstract | Full Text Original Articles Top Association of variants in genes involved in pancreatic β-cell development and function with type 2 diabetes in North Indians Sreenivas Chavali, Anubha Mahajan, Rubina Tabassum, Om Prakash Dwivedi, Ganesh Chauhan, Saurabh Ghosh, Nikhil Tandon and Dwaipayan Bharadwaj J Hum Genet 2011 56: 695-700; advance online publication, August 4, 2011; 10.1038/jhg.2011.83 Abstract | Full Text A nonsense mutation in the HOXD13 gene underlies synpolydactyly with incomplete penetrance Mazen Kurban, Muhammad Wajid, Lynn Petukhova, Yutaka Shimomura and Angela M Christiano J Hum Genet 2011 56: 701-706; advance online publication, August 4, 2011; 10.1038/jhg.2011.84 Abstract | Full Text HRAS mutants identified in Costello syndrome patients can induce cellular senescence: possible implications for the pathogenesis of Costello syndrome Tetsuya Niihori, Yoko Aoki, Nobuhiko Okamoto, Kenji Kurosawa, Hirofumi Ohashi, Seiji Mizuno, Hiroshi Kawame, Johji Inazawa, Toshihiro Ohura, Hiroshi Arai, Shin Nabatame, Kiyoshi Kikuchi, Yoshikazu Kuroki, Masaru Miura, Toju Tanaka, Akira Ohtake, Isaku Omori, Kenji Ihara, Hiroyo Mabe, Kyoko Watanabe, Shinichi Niijima, Erika Okano, Hironao Numabe and Yoichi Matsubara J Hum Genet 2011 56: 707-715; advance online publication, August 18, 2011; 10.1038/jhg.2011.85 Abstract | Full Text Computed tomography analysis of the association between the SH2B1 rs7498665 single-nucleotide polymorphism and visceral fat area Kikuko Hotta, Takuya Kitamoto, Aya Kitamoto, Seiho Mizusawa, Tomoaki Matsuo, Yoshio Nakata, Hideyuki Hyogo, Hidenori Ochi, Seika Kamohara, Nobuyuki Miyatake, Kazuaki Kotani, Ryoya Komatsu, Naoto Itoh, Ikuo Mineo, Jun Wada, Masato Yoneda, Atsushi Nakajima, Tohru Funahashi, Shigeru Miyazaki, Katsuto Tokunaga, Hiroaki Masuzaki, Takato Ueno, Kazuaki Chayama, Kazuyuki Hamaguchi, Kentaro Yamada, Toshiaki Hanafusa, Shinichi Oikawa, Hironobu Yoshimatsu, Toshiie Sakata, Kiyoji Tanaka, Yuji Matsuzawa, Kazuwa Nakao and Akihiro Sekine J Hum Genet 2011 56: 716-719; advance online publication, July 28, 2011; 10.1038/jhg.2011.86 Abstract | Full Text Common variants of FTO and the risk of obesity and type 2 diabetes in Indians Ganesh Chauhan, Rubina Tabassum, Anubha Mahajan, Om Prakash Dwivedi, Yuvaraj Mahendran, Ismeet Kaur, Shubhanchi Nigam, Himanshu Dubey, Binuja Varma, Sri Venkata Madhu, Sandeep K Mathur, Saurabh Ghosh, Nikhil Tandon and Dwaipayan Bharadwaj J Hum Genet 2011 56: 720-726; advance online publication, August 4, 2011; 10.1038/jhg.2011.87 Abstract | Full Text Integration-free and stable expression of FVIII using a human artificial chromosome Hajime Kurosaki, Masaharu Hiratsuka, Natsuko Imaoka, Yuichi Iida, Narumi Uno, Yasuhiro Kazuki, Chie Ishihara, Yuwna Yakura, Jun Mimuro, Youichi Sakata, Hiroyuki Takeya and Mitsuo Oshimura J Hum Genet 2011 56: 727-733; advance online publication, August 11, 2011; 10.1038/jhg.2011.88 Abstract | Full Text Mitochondrial DNA and Y-chromosome microstructure in Tunisia Hajer Ennafaa, Rosa Fregel, Houssein Khodjet-el-khil, Ana M González, Hejer Abdallah El Mahmoudi, Vicente M Cabrera, José M Larruga and Amel Benammar-Elgaaïed J Hum Genet 2011 56: 734-741; advance online publication, August 11, 2011; 10.1038/jhg.2011.92 Abstract | Full Text Remapping and mutation analysis of benign adult familial myoclonic epilepsy in a Japanese pedigree Satsuki Mori, Masayuki Nakamura, Takeshi Yasuda, Shu-ichi Ueno, Sunao Kaneko and Akira Sano J Hum Genet 2011 56: 742-747; advance online publication, August 18, 2011; 10.1038/jhg.2011.93 Abstract | Full Text Short Communication Top An association analysis of Per2 with panic disorder in the Japanese population Takeshi Otowa, Mamoru Tochigi, Yoshiya Kawamura, Nagisa Sugaya, Eiji Yoshida, Ken Inoue, Shin Yasuda, Tadashi Umekage, Takashi Ebisawa, Hisashi Tanii, Hisanobu Kaiya, Yuji Okazaki, Nobumasa Kato and Tsukasa Sasaki J Hum Genet 2011 56: 748-750; advance online publication, August 4, 2011; 10.1038/jhg.2011.94 Abstract | Full Text Corrigenda Top Molecular diagnosis and clinical onset of Charcot–Marie–Tooth disease in Japan Akiko Abe, Chikahiko Numakura, Kazuki Kijima, Makiko Hayashi, Taeko Hashimoto and Kiyoshi Hayasaka J Hum Genet 2011 56: 751; 10.1038/jhg.2011.81 Full Text Molecular and clinical studies of X-linked deafness among Pakistani families Ali M Waryah, Zubair M Ahmed, Munir A Binder, Daniel I Choo, Robert A Sisk, Mohsin Shahzad, Shaheen N Khan, Thomas B Friedman, Sheikh Riazuddin and Saima Riazuddin J Hum Genet 2011 56: 752; 10.1038/jhg.2011.89 Full Text Erratum Top Identification of a novel recombinant mutation in Korean patients with Gaucher disease using a long-range PCR approach Seon-Yong Jeong, Seo-Jin Kim, Jeong-A Yang, Ji-Hee Hong, Su-Jin Lee and Hyon J Kim J Hum Genet 2011 56: 753-754; 10.1038/jhg.2011.90 Full Text Advertisement Looking to publish your next paper? 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