Journal of Human Genetics

Letter from the new Editor-in-Chief
pp. 103-103(1)
Author: Tokunaga, Katsushi

Developmental dyslexia: an update
pp. 104-109(6)
Author: Shastry, Barkur

Human CHIT1 gene distribution: new data from Mediterranean and European populations
pp. 110-116(7)
Authors: Piras, Ignazio; Melis, Alessandra; Ghiani, Maria; Falchi, Alessandra; Luiselli, Donata; Moral, Pedro; Varesi, Laurent; Calò, Carla; Vona, Giuseppe

Human organic cation transporter (OCT1 and OCT2) gene polymorphisms and therapeutic effects of metformin
pp. 117-122(6)
Authors: Shikata, Eriko; Yamamoto, Rei; Takane, Hiroshi; Shigemasa, Chiaki; Ikeda, Tadasu; Otsubo, Kenji; Ieiri, Ichiro

Patients with primary cataract as a genetic pool of DMPK protomutation
pp. 123-128(6)
Authors: Medica, Igor; Teran, Natasa; Volk, Marija; Pfeifer, Vladimir; Ladavac, Edi; Peterlin, Borut

Polymorphic Alu insertions among Mayan populations
pp. 129-142(14)
Authors: Herrera, R.; Rojas, D.; Terreros, M.

Combinational effect of genes for the renin-angiotensin system in conferring susceptibility to diabetic nephropathy
pp. 143-151(9)
Authors: Osawa, Norihisa; Koya, Daisuke; Araki, Shin-ichi; Uzu, Takashi; Tsunoda, Tatsuhiko; Kashiwagi, Atsunori; Nakamura, Yusuke; Maeda, Shiro

Interleukin-18 and its three gene polymorphisms relating to allergic rhinitis
pp. 152-158(7)
Authors: Sebelova, Sarka; Izakovicova-Holla, Lydie; Stejskalova, Andrea; Schüller, Marcel; Znojil, Vladimir; Vasku, Anna

CYP17 gene polymorphism and its association with high-risk north Indian breast cancer patients
pp. 159-165(7)
Authors: Chakraborty, Anurupa; Murthy, N.; Chintamani, Chintamani; Bhatnagar, D.; Mohil, R.; Sharma, P.; Saxena, Sunita

Genetic polymorphisms associated with adverse events and elimination of methotrexate in childhood acute lymphoblastic leukemia and malignant lymphoma
pp. 166-171(6)
Authors: Imanishi, Hiroyuki; Okamura, Noboru; Yagi, Mariko; Noro, Yukari; Moriya, Yuka; Nakamura, Tsutomu; Hayakawa, Akira; Takeshima, Yasuhiro; Sakaeda, Toshiyuki; Matsuo, Masafumi; Okumura, Katsuhiko

Glucocorticoid-induced alternative promoter usage for a novel 5′ variant of granzyme A
pp. 172-178(7)
Authors: Ruike, Yoshinao; Katsuma, Susumu; Hirasawa, Akira; Tsujimoto, Gozoh

A genomewide linkage analysis of Kawasaki disease: evidence for linkage to chromosome 12
pp. 179-190(12)
Authors: Onouchi, Yoshihiro; Tamari, Mayumi; Takahashi, Atsushi; Tsunoda, Tatsuhiko; Yashiro, Mayumi; Nakamura, Yoshikazu; Yanagawa, Hiroshi; Wakui, Keiko; Fukushima, Yoshimitsu; Kawasaki, Tomisaku; Nakamura, Yusuke; Hata, Akira

Haplotype analysis at the alcohol dehydrogenase gene region in New Zealand Māori
pp. 191-194(4)
Authors: Hall, David; Chambers, Geoffrey; Lea, Rodney

A novel intronic mutation that may affect genotyping result of CYP2C8 by polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) is strongly associated with CYP2C8*3 in a South American population
pp. 195-199(5)
Authors: Bravo-Villalta, Heydy; Yamamoto, Koujirou; Nakamura, Katsunori; Bayá, Ana; Horiuchi, Ryuya