Journal of Human Genetics - Table of Contents alert Volume 57 Issue 12

TABLE OF CONTENTS Volume 57, Issue 12 (December 2012) In this issue Commentaries Original Articles Short Communications Corrigendum Erratum Also new AOP 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.   Commentaries Top A commentary on the history of human populations in the Japanese Archipelago inferred from genome-wide SNP data with a special reference to the Ainu and the Ryukyuan populations Jun Gojobori J Hum Genet 2012 57: 753-754; advance online publication, November 15, 2012; 10.1038/jhg.2012.121 Full Text A Commentary on Confirmation and refinement of an autosomal dominant congenital motor nystagmus locus in chromosome 1q31.3–q32.1 Kinya Ishikawa J Hum Genet 2012 57: 755; advance online publication, November 15, 2012; 10.1038/jhg.2012.122 Full Text Original Articles Top Confirmation and refinement of an autosomal dominant congenital motor nystagmus locus in chromosome 1q31.3–q32.1 Lin Li, Xueshan Xiao, Changxian Yi, Xiaodong Jiao, Xiangming Guo, James Fielding Hejtmancik and Qingjiong Zhang J Hum Genet 2012 57: 756-759; advance online publication, August 23, 2012; 10.1038/jhg.2012.103 Abstract | Full Text Tandem repeat sequences evolutionarily related to SVA-type retrotransposons are expanded in the centromere region of the western hoolock gibbon, a small ape Toru Hara, Yuriko Hirai, Israt Jahan, Hirohisa Hirai and Akihiko Koga J Hum Genet 2012 57: 760-765; advance online publication, August 30, 2012; 10.1038/jhg.2012.107 Abstract | Full Text A genome-wide association study identifies a genetic variant in the SIAH2 locus associated with hormonal receptor-positive breast cancer in Japanese Seham Elgazzar, Hitoshi Zembutsu, Atsushi Takahashi, Michiaki Kubo, Fuminori Aki, Koichi Hirata, Yuichi Takatsuka, Minoru Okazaki, Shozo Ohsumi, Takashi Yamakawa, Mitsunori Sasa, Toyomasa Katagiri, Yoshio Miki and Yusuke Nakamura J Hum Genet 2012 57: 766-771; advance online publication, September 6, 2012; 10.1038/jhg.2012.108 Abstract | Full Text Extended screening for major mitochondrial DNA point mutations in patients with hereditary hearing loss Tomofumi Kato, Yutaka Nishigaki, Yoshihiro Noguchi, Noriyuki Fuku, Taku Ito, Eri Mikami, Ken Kitamura and Masashi Tanaka J Hum Genet 2012 57: 772-775; advance online publication, September 13, 2012; 10.1038/jhg.2012.109 Abstract | Full Text Variations with modest effects have an important role in the genetic background of type 2 diabetes and diabetes-related traits Hayato Fujita, Kazuo Hara, Nobuhiro Shojima, Momoko Horikoshi, Minoru Iwata, Yushi Hirota, Kazuyuki Tobe, Susumu Seino and Takashi Kadowaki J Hum Genet 2012 57: 776-779; advance online publication, September 20, 2012; 10.1038/jhg.2012.110 Abstract | Full Text Is the prevalence of MTHFR C677T polymorphism associated with ultraviolet radiation in Eurasia? Wang Yafei, Pei Lijun, Wang Jinfeng and Zheng Xiaoying J Hum Genet 2012 57: 780-786; advance online publication, September 20, 2012; 10.1038/jhg.2012.113 Abstract | Full Text The history of human populations in the Japanese Archipelago inferred from genome-wide SNP data with a special reference to the Ainu and the Ryukyuan populations Japanese Archipelago Human Population Genetics Consortium:  Timothy Jinam, Nao Nishida, Momoki Hirai, Shoji Kawamura, Hiroki Oota, Kazuo Umetsu, Ryosuke Kimura, Jun Ohashi, Atsushi Tajima, Toshimichi Yamamoto, Hideyuki Tanabe, Shuhei Mano, Yumiko Suto, Tadashi Kaname, Kenji Naritomi, Kumiko Yanagi, Norio Niikawa, Keiichi Omoto, Katsushi Tokunaga and Naruya Saitou J Hum Genet 2012 57: 787-795; advance online publication, November 8, 2012; 10.1038/jhg.2012.114 Abstract | Full Text Haplotype analysis of the CAG and CCG repeats in 21 Brazilian families with Huntington’s disease Luciana de A Agostinho, Catielly F Rocha, Enrique Medina-Acosta, Hazel N Barboza, Antônio F Alves da Silva, Simão P F Pereira, Iane dos Santos da Silva, Eduardo R Paradela, André L dos S Figueiredo, Eduardo de M Nogueira, Regina M P Alvarenga, Pedro Hernan Cabello, Suely R dos Santos and Carmen L A Paiva J Hum Genet 2012 57: 796-803; advance online publication, October 11, 2012; 10.1038/jhg.2012.120 Abstract | Full Text Short Communications Top Sibling cases of moyamoya disease having homozygous and heterozygous c.14576G>A variant in RNF213 showed varying clinical course and severity Satoko Miyatake, Hajime Touho, Noriko Miyake, Chihiro Ohba, Hiroshi Doi, Hirotomo Saitsu, Masataka Taguri, Satoshi Morita and Naomichi Matsumoto J Hum Genet 2012 57: 804-806; advance online publication, August 30, 2012; 10.1038/jhg.2012.105 Abstract | Full Text Pentanucleotide repeat-primed PCR for genetic diagnosis of spinocerebellar ataxia type 31 Takayuki Ishige, Setsu Sawai, Sakae Itoga, Kenichi Sato, Emi Utsuno, Minako Beppu, Kazuaki Kanai, Motoi Nishimura, Kazuyuki Matsushita, Satoshi Kuwabara and Fumio Nomura J Hum Genet 2012 57: 807-808; advance online publication, September 20, 2012; 10.1038/jhg.2012.112 Abstract | Full Text Corrigendum Top Variations with modest effects have an important role in the genetic background of type 2 diabetes and diabetes-related traits Hayato Fujita, Kazuo Hara, Nobuhiro Shojima, Momoko Horikoshi, Minoru Iwata, Yushi Hirota, Kazuyuki Tobe, Susumu Seino and Takashi Kadowaki J Hum Genet 2012 57: 809; 10.1038/jhg.2012.132 Full Text Erratum Top Haplotype analysis of the CAG and CCG repeats in 21 Brazilian families with Huntington’s disease Luciana de A Agostinho, Catielly F Rocha, Enrique Medina-Acosta, Hazel N Barboza, Antônio F Alves da Silva, Simão P F Pereira, Iane dos Santos da Silva, Eduardo R Paradela, André L dos S Figueiredo, Eduardo de M Nogueira, Regina M P Alvarenga, Pedro Hernan Cabello, Suely R dos Santos and Carmen L A Paiva J Hum Genet 2012 57: 810; 10.1038/jhg.2012.125 Full Text Advertisement Looking to publish your next paper? 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