Journal of Human Genetics - Table of Contents alert Volume 56 Issue 7

TABLE OF CONTENTS Volume 56, Issue 7 (July 2011) In this issue Commentaries Original Articles Short Communications Also new AOP Advertisement SureSelect Target Enrichment for DNA and RNA - The most complete solution for NGS Target Enrichment The only provider of Targeted RNA-seq with SureSelect RNA Capture. Easily customize to your regions of interest with the most published and trusted platform. Learn more: www.agilent.com/genomics/nextgen Sign up for e-alerts Recommend to your library Web feed Subscribe Advertisement Now Live - a new multidisciplinary research journal from the publishers of Nature Online and open access, Scientific Reports provides rapid publication and high visibility of research - for all areas of science. All papers accepted for publication are technically sound, without any requirement for impact. Submit your next paper to Scientific Reports   Commentaries Top Congenital factor XIII deficiency: A commentary on ‘Homozygous intronic mutation leading to inefficient transcription combined with a novel frame-shift mutation in F13A1 gene causes FXIII deficiency’ Keiko Shinozawa J Hum Genet 2011 56: 475-476; advance online publication, June 2, 2011; 10.1038/jhg.2011.53 Abstract | Full Text A Commentary on Identification of an autosomal dominant locus for intracranial aneurysm through a model-based family collection in a geographically limited area Akio Koizumi J Hum Genet 2011 56: 477; advance online publication, June 2, 2011; 10.1038/jhg.2011.57 Abstract | Full Text Original Articles Top Dysbindin-1 and NRG-1 gene expression in immortalized lymphocytes from patients with schizophrenia Hidenaga Yamamori, Ryota Hashimoto, Louise Verrall, Yuka Yasuda, Kazutaka Ohi, Motoyuki Fukumoto, Satomi Umeda-Yano, Akira Ito and Masatoshi Takeda J Hum Genet 2011 56: 478-483; advance online publication, April 21, 2011; 10.1038/jhg.2011.40 Abstract | Full Text Novel USH2A mutations in Japanese Usher syndrome type 2 patients: marked differences in the mutation spectrum between the Japanese and other populations Hiroshi Nakanishi, Masafumi Ohtsubo, Satoshi Iwasaki, Yoshihiro Hotta, Shin-ichi Usami, Kunihiro Mizuta, Hiroyuki Mineta and Shinsei Minoshima J Hum Genet 2011 56: 484-490; advance online publication, May 19, 2011; 10.1038/jhg.2011.45 Abstract | Full Text Pleiotropy of type 2 diabetes with obesity Sandra J Hasstedt, Craig L Hanis, Swapan K Das and Steven C Elbein the American Diabetes Association GENNID Study Group J Hum Genet 2011 56: 491-495; advance online publication, April 28, 2011; 10.1038/jhg.2011.46 Abstract | Full Text Germ-line sequence variants of PTEN do not have an important role in hereditary and non-hereditary prostate cancer susceptibility Chunmei C Xie, Lingyi Lu, Jielin Sun, S Lilly Zheng, William B Isaacs, Henrik Gronberg and Jianfeng Xu J Hum Genet 2011 56: 496-502; advance online publication, June 2, 2011; 10.1038/jhg.2011.48 Abstract | Full Text Cumulative association of eight susceptibility genes with systemic lupus erythematosus in a Japanese female population Minori Koga, Aya Kawasaki, Ikue Ito, Takumi Furuya, Jun Ohashi, Chieko Kyogoku, Satoshi Ito, Taichi Hayashi, Isao Matsumoto, Makio Kusaoi, Yoshinari Takasaki, Hiroshi Hashimoto, Takayuki Sumida and Naoyuki Tsuchiya J Hum Genet 2011 56: 503-507; advance online publication, May 12, 2011; 10.1038/jhg.2011.49 Abstract | Full Text Investigation of modifier genes within copy number variations in Rett syndrome Rosangela Artuso, Filomena T Papa, Elisa Grillo, Mafalda Mucciolo, Dag H Yasui, Keith W Dunaway, Vittoria Disciglio, Maria A Mencarelli, Marzia Pollazzon, Michele Zappella, Giuseppe Hayek, Francesca Mari, Alessandra Renieri, Janine M LaSalle and Francesca Ariani J Hum Genet 2011 56: 508-515; advance online publication, May 19, 2011; 10.1038/jhg.2011.50 Abstract | Full Text LCR-initiated rearrangements at the IDS locus, completed with Alu-mediated recombination or non-homologous end joining Junko Oshima, Jennifer A Lee, Amy M Breman, Priscilla H Fernandes, Dusica Babovic-Vuksanovic, Patricia A Ward, Lynne A Wolfe, Christine M Eng and Daniela del Gaudio J Hum Genet 2011 56: 516-523; advance online publication, May 19, 2011; 10.1038/jhg.2011.51 Abstract | Full Text A population-based study of copy number variants and regions of homozygosity in healthy Swedish individuals Shu-Mei Teo, Chee-Seng Ku, Nasheen Naidoo, Per Hall, Kee-Seng Chia, Agus Salim and Yudi Pawitan J Hum Genet 2011 56: 524-533; advance online publication, June 2, 2011; 10.1038/jhg.2011.52 Abstract | 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: 534-540; advance online publication, June 2, 2011; 10.1038/jhg.2011.55 Abstract | Full Text Short Communications Top 16p13.11 duplication is a risk factor for a wide spectrum of neuropsychiatric disorders Arivudainambi Ramalingam, Xin-Gang Zhou, Stephanie D Fiedler, Sarah J Brawner, Julie M Joyce, Hong-Yu Liu and Shihui Yu J Hum Genet 2011 56: 541-544; advance online publication, May 26, 2011; 10.1038/jhg.2011.42 Abstract | Full Text A single nucleotide polymorphism in the 3′-untranslated region of MyD88 gene is associated with Buerger disease but not with Takayasu arteritis in Japanese Zhiyong Chen, Toshiaki Nakajima, Yoshinori Inoue, Toshifumi Kudo, Masatoshi Jibiki, Takehisa Iwai and Akinori Kimura J Hum Genet 2011 56: 545-547; advance online publication, April 28, 2011; 10.1038/jhg.2011.44 Abstract | Full Text   Advertisement Looking to publish your next paper? Submit to the Journal of Human Genetics today. The Journal of Human Genetics is a great outlet in which to publish your next paper in a timely manner. This journal covers all aspects of human genetics with a focus on medical genetics and genomics. The Journal of Human Genetics accepts papers related to: - medical genetics - human genome analysis - gene cloning and mapping - mutational analysis - gene therapy - cancer genetics. Review the Guide to Authors and Submit today.   Natureevents is a fully searchable, multi-disciplinary database designed to maximise exposure for events organisers. The contents of the Natureevents Directory are now live. The digital version is available here. Find the latest scientific conferences, courses, meetings and symposia on natureevents.com. For event advertising opportunities across the Nature Publishing Group portfolio please contact natureevents@nature.com More Nature Events Please note that you need to be a subscriber or site-licence holder to enjoy full-text access to Journal of Human Genetics. In order to do so, please purchase a subscription. You have been sent this Table of Contents Alert because you have opted in to receive it. You can change or discontinue your e-mail alerts at any time, by modifying your preferences on your nature.com account at: www.nature.com/nams/svc/myaccount (You will need to log in to be recognised as a nature.com registrant). For further technical assistance, please contact our registration department. For print subscription enquiries, please contact our subscription department. For other enquiries, please contact our customer feedback department. Nature Publishing Group | 75 Varick Street, 9th Floor | New York | NY 10013-1917 | USA Nature Publishing Group's worldwide offices: London - Paris - Munich - New Delhi - Tokyo - Melbourne San Diego - San Francisco - Washington - New York - Boston Macmillan Publishers Limited is a company incorporated in England and Wales under company number 785998 and whose registered office is located at Brunel Road, Houndmills, Basingstoke, Hampshire RG21 6XS. © 2011 Nature Publishing Group, a division of Macmillan Publishers Limited. All Rights Reserved.