Works matching IS 14345161 AND DT 2010 AND VI 55 AND IP 9

Results: 14

Homozygosity for constitutional chromosomal rearrangements: a systematic review with reference to origin, ascertainment and phenotype.

Published in:

Journal of Human Genetics, 2010, v. 55, n. 9, p. 559, doi. 10.1038/jhg.2010.80

By:

O'Neill, Iain D

Publication type:

Article

An association study between the dymeclin gene and schizophrenia in the Japanese population.

Published in:

Journal of Human Genetics, 2010, v. 55, n. 9, p. 631, doi. 10.1038/jhg.2010.72

By:

Yazaki, Saori;
Koga, Minori;
Ishiguro, Hiroki;
Inada, Toshiya;
Ujike, Hiroshi;
Itokawa, Masanari;
Otowa, Takeshi;
Watanabe, Yuichiro;
Someya, Toshiyuki;
Iwata, Nakao;
Kunugi, Hiroshi;
Ozaki, Norio;
Arinami, Tadao

Publication type:

Article

Combined effect of longevity-associated mitochondrial DNA 5178 C/A polymorphism and coffee consumption on the risk of hyper-LDL cholesterolemia in middle-aged Japanese men.

Published in:

Journal of Human Genetics, 2010, v. 55, n. 9, p. 577, doi. 10.1038/jhg.2010.71

By:

Kokaze, Akatsuki;
Ishikawa, Mamoru;
Matsunaga, Naomi;
Karita, Kanae;
Yoshida, Masao;
Shimada, Naoki;
Ohtsu, Tadahiro;
Shirasawa, Takako;
Ochiai, Hirotaka;
Kawamoto, Teruyoshi;
Ito, Taku;
Hoshino, Hiromi;
Takashima, Yutaka

Publication type:

Article

Glutathione-S-transferase gene polymorphisms (GSTM1, GSTT1, GSTP1) and idiopathic male infertility: novel perspectives versus facts.

Published in:

2010

By:

Economopoulos, Konstantinos P.;
Sergentanis, Theodoros N.;
Choussein, Souzana

Publication type:

Opinion

The pattern of natural selection in somatic cancer mutations of human mtDNA.

Published in:

Journal of Human Genetics, 2010, v. 55, n. 9, p. 605, doi. 10.1038/jhg.2010.76

By:

Stafford, Pete;
Chen-Quin, Estella B.

Publication type:

Article

Mutation spectrum of MMACHC in Chinese patients with combined methylmalonic aciduria and homocystinuria.

Published in:

Journal of Human Genetics, 2010, v. 55, n. 9, p. 621, doi. 10.1038/jhg.2010.81

By:

Mei-Ying Liu;
Yan-Ling Yang;
Ying-Chen Chang;
Szu-Hui Chiang;
Shuan-Pei Lin;
Lian-Shu Han;
Yu Qi;
Kwang-Jen Hsiao;
Tze-Tze Liu

Publication type:

Article

The GCKR rs780094 polymorphism is associated with susceptibility of type 2 diabetes, reduced fasting plasma glucose levels, increased triglycerides levels and lower HOMA-IR in Japanese population.

Published in:

Journal of Human Genetics, 2010, v. 55, n. 9, p. 600, doi. 10.1038/jhg.2010.75

By:

Onuma, Hiroshi;
Tabara, Yasuharu;
Kawamoto, Ryuichi;
Shimizu, Ikki;
Kawamura, Ryoichi;
Takata, Yasunori;
Nishida, Wataru;
Ohashi, Jun;
Miki, Tetsuro;
Kohara, Katsuhiko;
Makino, Hideichi;
Osawa, Haruhiko

Publication type:

Article

Worldwide allele frequency distribution of four polymorphisms associated with warfarin dose requirements.

Published in:

Journal of Human Genetics, 2010, v. 55, n. 9, p. 582, doi. 10.1038/jhg.2010.73

By:

Ross, Kendra A.;
Bigham, Abbigail W.;
Edwards, Melissa;
Gozdzik, Agnes;
Suarez-Kurtz, Guilherme;
Parra, Esteban J.

Publication type:

Article

Copy-number variations on the X chromosome in Japanese patients with mental retardation detected by array-based comparative genomic hybridization analysis.

Published in:

Journal of Human Genetics, 2010, v. 55, n. 9, p. 590, doi. 10.1038/jhg.2010.74

By:

Honda, Shozo;
Hayashi, Shin;
Imoto, Issei;
Toyama, Jun;
Okazawa, Hitoshi;
Nakagawa, Eiji;
Goto, Yu-ichi;
Inazawa, Johji

Publication type:

Article

Commentary on 'Mutation spectrum of the dystrophin gene in 442 Duchenne/Becker muscular dystrophy cases from one Japanese referral center'.

Published in:

2010

By:

Kondo-Iida, Eri

Publication type:

Opinion

Linkage analysis and mutation screening of the rhodopsin gene in a Chinese Bai family with autosomal dominant retinitis pigmentosa.

Published in:

Journal of Human Genetics, 2010, v. 55, n. 9, p. 571, doi. 10.1038/jhg.2010.68

By:

Haike Guo;
Yongjie Qin;
Qianli Meng;
Hongyang Zhang;
Haiying Jin;
Yanlei Chen

Publication type:

Article

A genome-wide analysis of loss of heterozygosity and chromosomal copy number variation in Proteus syndrome using high-density SNP microarrays.

Published in:

Journal of Human Genetics, 2010, v. 55, n. 9, p. 627, doi. 10.1038/jhg.2010.70

By:

Yilmaz, Ahmet;
Hamel, Nancy;
Schwartz, Charles E;
Houlston, Richard S;
Harper, John I;
Foulkes, William D

Publication type:

Article

The association of glutathione-S-transferase gene polymorphisms (GSTM1, GSTT1, GSTP1) with idiopathic male infertility.

Published in:

Journal of Human Genetics, 2010, v. 55, n. 9, p. 565, doi. 10.1038/jhg.2010.59

By:

Safarinejad, Mohammad Reza;
Shafiei, Nayyer;
Safarinejad, Shiva

Publication type:

Article

Examination of disease-based selection, demographic history and population structure in European Y-chromosome haplogroup I.

Published in:

Journal of Human Genetics, 2010, v. 55, n. 9, p. 613, doi. 10.1038/jhg.2010.77

By:

Sezgin, Efe;
Drosdak, Alyssa;
McIntosh, Carl;
Kessing, Bailey;
Lautenberger, James A.;
Goedert, James J.;
Phair, John P.;
Troyer, Jennifer L.;
Smith, Michael W.;
O'Brien, Stephen J.

Publication type:

Article