TABLE OF CONTENTS
|  |  |  | Volume 56, Issue 7 (July 2011) |  | In this issue Commentaries Original Articles Short Communications
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| | |  |  |  | Advertisement |  | |  | | 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 areaAkio 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 schizophreniaHidenaga 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 populationsHiroshi 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 obesitySandra 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 susceptibilityChunmei 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 populationMinori 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 syndromeRosangela 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 joiningJunko 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 individualsShu-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 familiesAli 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 disordersArivudainambi 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 JapaneseZhiyong 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 |  | |  | |  |  |  |  |  |  |  | Natureevents is a fully searchable, multi-disciplinary database designed to maximise exposure for events organisers. 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