TABLE OF CONTENTS
Volume 52, Issue 10 (October 2007)
Original Articles
SNPs in the KCNJ11-ABCC8 gene locus are associated with type 2 diabetes and blood pressure levels in the Japanese population
Yukiko Sakamoto, Hiroshi Inoue, Parvaneh Keshavarz, Katsuyuki Miyawaki, Yuka Yamaguchi, Maki Moritani, Kiyoshi Kunika, Naoto Nakamura, Toshikazu Yoshikawa, Natsuo Yasui, Hiroshi Shiota, Toshihito Tanahashi and Mitsuo Itakura
J Hum Genet 52: 781-793; advance online publication, September 6, 2007; doi:10.1007/s10038-007-0190-x
Association analysis of HSP90B1 with bipolar disorder
Chihiro Kakiuchi, Mizuho Ishiwata, Shinichiro Nanko, Hiroshi Kunugi, Yoshio Minabe, Kazuhiko Nakamura, Norio Mori, Kumiko Fujii, Tadashi Umekage, Mamoru Tochigi, Kazuhisa Kohda, Tsukasa Sasaki, Kazuo Yamada, Takeo Yoshikawa and Tadafumi Kato
J Hum Genet 52: 794-803; advance online publication, September 4, 2007; doi:10.1007/s10038-007-0188-4
Genetic variations and haplotype structures of the DPYD gene encoding dihydropyrimidine dehydrogenase in Japanese and their ethnic differences
Keiko Maekawa, Mayumi Saeki, Yoshiro Saito, Shogo Ozawa, Kouichi Kurose, Nahoko Kaniwa, Manabu Kawamoto, Naoyuki Kamatani, Ken Kato, Tetsuya Hamaguchi, Yasuhide Yamada, Kuniaki Shirao, Yasuhiro Shimada, Manabu Muto, Toshihiko Doi, Atsushi Ohtsu, Teruhiko Yoshida, Yasuhiro Matsumura, Nagahiro Saijo and Jun-ichi Sawada
J Hum Genet 52: 804-819; advance online publication, September 9, 2007; doi:10.1007/s10038-007-0186-6
Analysis of ENG and ACVRL1 genes in 137 HHT Italian families identifies 76 different mutations (24 novel). Comparison with other European studies
Carla Olivieri, Fabio Pagella, Lucia Semino, Luca Lanzarini, Cristina Valacca, Andrea Pilotto, Sabrina Corno, Susi Scappaticci, Guido Manfredi, Elisabetta Buscarini and Cesare Danesino
J Hum Genet 52: 820-829; advance online publication, September 5, 2007; doi:10.1007/s10038-007-0187-5
Danon disease presenting with dilated cardiomyopathy and a complex phenotype
Matthew R G Taylor, Lisa Ku, Dobromir Slavov, Jean Cavanaugh, Mark Boucek, Xiao Zhu, Sharon Graw, Elisa Carniel, Carl Barnes, Dianna Quan, Ryan Prall, Mark A Lovell, Gary Mierau, Patsy Ruegg, Naresh Mandava, Michael R Bristow, Jeffrey A Towbin and Luisa Mestroni
J Hum Genet 52: 830-835; advance online publication, September 26, 2007; doi:10.1007/s10038-007-0184-8
Role of genetic polymorphisms in ACE and TNF-
gene in sarcoidosis: a meta-analysis
Igor Medica, Andrej Kastrin, Ales Maver and Borut Peterlin
J Hum Genet 52: 836-847; advance online publication, September 4, 2007; doi:10.1007/s10038-007-0185-7
Spectrum and prevalence of autosomal dominant spinocerebellar ataxia in Hokkaido, the northern island of Japan: a study of 113 Japanese families
Rehana Basri, Ichiro Yabe, Hiroyuki Soma and Hidenao Sasaki
J Hum Genet 52: 848-855; advance online publication, September 5, 2007; doi:10.1007/s10038-007-0182-x
High-resolution SNP and haplotype maps of the human gamma-glutamyl carboxylase gene (GGCX) and association study between polymorphisms in GGCX and the warfarin maintenance dose requirement of the Japanese population
Pei-Chieng Cha, Taisei Mushiroda, Atsushi Takahashi, Shigeru Saito, Hideki Shimomura, Takao Suzuki, Naoyuki Kamatani and Yusuke Nakamura
J Hum Genet 52: 856-864; advance online publication, September 5, 2007; doi:10.1007/s10038-007-0183-9
Short Communications
Novel and recurrent ALDH3A2 mutations in Italian patients with Sjögren-Larsson syndrome
Biagio Didona, Andrea Codispoti, Enrico Bertini, Wiliam B Rizzo, Gael Carney, Giovanna Zambruno, Carlo Dionisi-Vici, Mauro Paradisi, Cristina Pedicelli, Gerry Melino and Alessandro Terrinoni
J Hum Genet 52: 865-870; advance online publication, September 28, 2007; doi:10.1007/s10038-007-0180-z
