Journal of Human Genetics - Table of Contents alert Volume 56 Issue 12

TABLE OF CONTENTS Volume 56, Issue 12 (December 2011) In this issue Commentary Original Articles Short Communications Also new AOP Sign up for e-alerts Recommend to your library Web feed Subscribe Advertisement Medical Genetics Web Focus Series Journal of Human Genetics is proud to present the Medical Genetics Web Focus, a collection of the latest original and review articles on medical genetics. The first collection represents some of the most downloaded, highly cited articles published to date in the journal in a wide scope of medical genetics. Access the Medical Genetics Web Focus today!   Commentary Top Male lineages in the Himalayan foothills: A commentary on Y-chromosome haplogroup diversity in the sub-Himalayan Terai and Duars populations of East India Qasim Ayub J Hum Genet 2011 56: 813-814; advance online publication, October 6, 2011; 10.1038/jhg.2011.114 Full Text Original Articles Top Genetic characteristics and migration history of a bronze culture population in the West Liao-River valley revealed by ancient DNA Hongjie Li, Xin Zhao, Yongbin Zhao, Chunxiang Li, Dayong Si, Hui Zhou and Yinqiu Cui J Hum Genet 2011 56: 815-822; advance online publication, September 22, 2011; 10.1038/jhg.2011.102 Abstract | Full Text Single-nucleotide polymorphisms at five loci are associated with C-reactive protein levels in a cohort of Filipino young adults Ghenadie Curocichin, Ying Wu, Thomas W McDade, Christopher W Kuzawa, Judith B Borja, Li Qin, Ethan M Lange, Linda S Adair, Leslie A Lange and Karen L Mohlke J Hum Genet 2011 56: 823-827; advance online publication, September 22, 2011; 10.1038/jhg.2011.106 Abstract | Full Text High prevalence of an anti-hypertriglyceridemic variant of the MLXIPL gene in Central Asia Kazuhiro Nakayama, Yoshiko Yanagisawa, Ayumi Ogawa, Yuumi Ishizuka, Lkhagvasuren Munkhtulga, Phitaya Charupoonphol, Somjit Supannnatas, Stevenson Kuartei, Ulziiburen Chimedregzen, Yoshiro Koda, Takafumi Ishida, Yasuo Kagawa and Sadahiko Iwamoto J Hum Genet 2011 56: 828-833; advance online publication, September 22, 2011; 10.1038/jhg.2011.109 Abstract | Full Text Detection of uniparental isodisomy in autosomal recessive mitochondrial DNA depletion syndrome by high-density SNP array analysis Ganka V Douglas, Joanna Wiszniewska, Mark H Lipson, David R Witt, Taryn McDowell, Mara Sifry-Platt, Michio Hirano, William J Craigen and Lee-Jun C Wong J Hum Genet 2011 56: 834-839; advance online publication, October 20, 2011; 10.1038/jhg.2011.112 Abstract | Full Text Polymorphisms of transforming growth factor-β signaling pathway and Kawasaki disease in the Taiwanese population Ho-Chang Kuo, Yoshihiro Onouchi, Yu-Wen Hsu, Wei-Chiao Chen, Jin-Ding Huang, Ying-Hsien Huang, Ya-Ling Yang, Mei-Chyn Chao, Hong-Ren Yu, Yung-Shun Juan, Chiu-Ming Kuo, Kuender D Yang, Jung-San Huang and Wei-Chiao Chang J Hum Genet 2011 56: 840-845; advance online publication, October 20, 2011; 10.1038/jhg.2011.113 Abstract | Full Text SLC2A1 gene analysis of Japanese patients with glucose transporter 1 deficiency syndrome Natsuko Hashimoto, Kuriko Kagitani-Shimono, Norio Sakai, Takanobu Otomo, Koji Tominaga, Shin Nabatame, Yukiko Mogami, Yukitoshi Takahashi, Katsumi Imai, Keiko Yanagihara, Takeshi Okinaga, Toshisaburo Nagai, Masako Taniike and Keiichi Ozono J Hum Genet 2011 56: 846-851; advance online publication, October 20, 2011; 10.1038/jhg.2011.115 Abstract | Full Text A genome-wide CNV association study on panic disorder in a Japanese population Yoshiya Kawamura, Takeshi Otowa, Asako Koike, Nagisa Sugaya, Eiji Yoshida, Shin Yasuda, Ken Inoue, Kunio Takei, Yoshiaki Konishi, Hisashi Tanii, Takafumi Shimada, Mamoru Tochigi, Chihiro Kakiuchi, Tadashi Umekage, Xiaoxi Liu, Nao Nishida, Katsushi Tokunaga, Ryozo Kuwano, Yuji Okazaki, Hisanobu Kaiya and Tsukasa Sasaki J Hum Genet 2011 56: 852-856; advance online publication, October 20, 2011; 10.1038/jhg.2011.117 Abstract | Full Text Association of fucosyltransferase 8 (FUT8) polymorphism Thr267Lys with pulmonary emphysema Miki Yamada, Takeo Ishii, Shinobu Ikeda, Makiko Naka-Mieno, Noriko Tanaka, Tomio Arai, Toshio Kumasaka, Akihiko Gemma, Kozui Kida, Masaaki Muramatsu and Motoji Sawabe J Hum Genet 2011 56: 857-860; advance online publication, October 20, 2011; 10.1038/jhg.2011.118 Abstract | Full Text Mutational analysis for biotinidase deficiency of a Greek patients’ cohort ascertained through expanded newborn screening Georgia Thodi, Elina Molou, Vassiliki Georgiou, Yannis L Loukas, Yannis Dotsikas, Sofia Biti, Konstantinos Papadopoulos, Dimitris Konstantinou, Marina Antoniadi and Emmanuel Doulgerakis J Hum Genet 2011 56: 861-865; advance online publication, October 20, 2011; 10.1038/jhg.2011.119 Abstract | Full Text Short Communications Top A new autosomal recessive nonsyndromic hearing impairment locus DFNB96 on chromosome 1p36.31–p36.13 Muhammad Ansar, Kwanghyuk Lee, Syed Kamran-ul-Hassan Naqvi, Paula B Andrade, Sulman Basit, Regie Lyn P Santos-Cortez, Wasim Ahmad and Suzanne M Leal J Hum Genet 2011 56: 866-868; advance online publication, September 22, 2011; 10.1038/jhg.2011.110 Abstract | Full Text Analysis of complete mitochondrial genomes of patients with schizophrenia and bipolar disorder Cinzia Bertolin, Chiara Magri, Sergio Barlati, Andrea Vettori, Giulia Ida Perini, Pio Peruzzi, Maria Luisa Mostacciuolo and Giovanni Vazza J Hum Genet 2011 56: 869-872; advance online publication, October 13, 2011; 10.1038/jhg.2011.111 Abstract | Full Text Advertisement Looking to publish your next paper? 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