TABLE OF CONTENTS
Volume 52, Issue 8 (August 2007)
Original Articles
Redefining the disease locus of 16q22.1-linked autosomal dominant cerebellar ataxia
Takeshi Amino, Kinya Ishikawa, Shuta Toru, Taro Ishiguro, Nozomu Sato, Taiji Tsunemi, Miho Murata, Kazuhiro Kobayashi, Johji Inazawa, Tatsushi Toda and Hidehiro Mizusawa
J Hum Genet 52: 643-649; advance online publication, July 5, 2007; doi:10.1007/s10038-007-0154-1
A grid-search algorithm for optimal allocation of sample size in two-stage association studies
S H Wen and C K Hsiao
J Hum Genet 52: 650-658; advance online publication, June 30, 2007; doi:10.1007/s10038-007-0159-9
The association of Y chromosome haplogroups with spermatogenic failure in the Han Chinese
Chuncheng Lu, Feng Zhang, Yankai Xia, Bin Wu, Aihua Gu, Ningxia Lu, Shoulin Wang, Hongbing Shen, Li Jin and Xinru Wang
J Hum Genet 52: 659-663; advance online publication, June 9, 2007; doi:10.1007/s10038-007-0160-3
Association of the aspartic acid-repeat polymorphism in the asporin gene with age at onset of knee osteoarthritis in Han Chinese Population
Dongquan Shi, Takahiro Nakamura, Jin Dai, Long Yi, Jianghui Qin, Dongyang Chen, Zhihong Xu, Yong Wang, Shiro Ikegawa and Qing Jiang
J Hum Genet 52: 664-667; advance online publication, June 30, 2007; doi:10.1007/s10038-007-0166-x
Lack of association of fragile histidine triad (FHIT) polymorphisms with lung cancer in the Korean population
Hae-Yun Jung, Jae Sook Sung, Young Mi Whang, Hyoung Doo Shin, Byung Lae Park, Jun Suk Kim, Sang Won Shin, Hee Yun Seo, Hwa Jung Sung, In Keun Choi, Sang Cheul Oh, Jae Hong Seo and Yeul Hong Kim
J Hum Genet 52: 668-674; advance online publication, July 4, 2007; doi:10.1007/s10038-007-0169-7
Nationwide survey on predictive genetic testing for late-onset, incurable neurological diseases in Japan
Kunihiro Yoshida, Takahito Wada, Akihiro Sakurai, Keiko Wakui, Shu-ichi Ikeda and Yoshimitsu Fukushima
J Hum Genet 52: 675-679; advance online publication, July 5, 2007; doi:10.1007/s10038-007-0170-1
Longevity-associated mitochondrial DNA 5178 C/A polymorphism and its interaction with cigarette consumption are associated with pulmonary function in middle-aged Japanese men
Akatsuki Kokaze, Mamoru Ishikawa, Naomi Matsunaga, Masao Yoshida, Masao Satoh, Koji Teruya, Rie Honmyo, Takako Shirasawa, Hiromi Hoshino and Yutaka Takashima
J Hum Genet 52: 680-685; advance online publication, July 17, 2007; doi:10.1007/s10038-007-0171-0
Short Communications
A Japanese patient with a mild Lenz-Majewski syndrome
Sumito Dateki, Tatsuro Kondoh, Gen Nishimura, Katsuaki Motomura, Koh-ichiro Yoshiura, Akira Kinoshita, Hideo Kuniba, Yoshiyuki Koga and Hiroyuki Moriuchi
J Hum Genet 52: 686-689; advance online publication, June 26, 2007; doi:10.1007/s10038-007-0165-y
OCA2*481Thr, a hypofunctional allele in pigmentation, is characteristic of northeastern Asian populations
Isao Yuasa, Kazuo Umetsu, Shinji Harihara, Aya Miyoshi, Naruya Saitou, Kyung Sook Park, Bumbein Dashnyam, Feng Jin, Gérard Lucotte, Prasanta K Chattopadhyay, Lotte Henke and Jürgen Henke
J Hum Genet 52: 690-693; advance online publication, June 14, 2007; doi:10.1007/s10038-007-0167-9
TP53 codon 72 polymorphism in 12 populations of insular Southeast Asia and Oceania
Taeko Kashima, Kumiko Makino, Augustinua Soemantri and Takafumi Ishida
J Hum Genet 52: 694-697; advance online publication, July 3, 2007; doi:10.1007/s10038-007-0168-8
Clinical and genetic analysis of HLXB9 gene in Korean patients with Currarino syndrome
In-Suk Kim, Soo-young Oh, Suk-Joo Choi, Jong-Hwa Kim, Kwan Hyun Park, Hyun-Kyung Park, Jong-Won Kim and Chang-Seok Ki
J Hum Genet 52: 698-701; advance online publication, July 6, 2007; doi:10.1007/s10038-007-0173-y
