Works matching IS 14345161 AND DT 2013 AND VI 58 AND IP 4

Results: 13

Follow-up study of 22 Chinese children with Alexander disease and analysis of parental origin of de novo GFAP mutations.

Published in:

Journal of Human Genetics, 2013, v. 58, n. 4, p. 183, doi. 10.1038/jhg.2012.152

By:

Zang, Lili;
Wang, Jingmin;
Jiang, Yuwu;
Gu, Qiang;
Gao, Zhijie;
Yang, Yanling;
Xiao, Jiangxi;
Wu, Ye

Publication type:

Article

DRD2 haplotype associated with negative symptoms and sustained attention deficits in Han Chinese with schizophrenia in Taiwan.

Published in:

Journal of Human Genetics, 2013, v. 58, n. 4, p. 229, doi. 10.1038/jhg.2012.157

By:

Chien, Yi-Ling;
Hwu, Hai-Gwo;
Fann, Cathy S-J;
Chang, Chien-Ching;
Tsuang, Ming-T;
Liu, Chih-Min

Publication type:

Article

Recapitulation of previous genome-wide association studies with two distinct pathophysiological entities of gastric cancer in the Korean population.

Published in:

Journal of Human Genetics, 2013, v. 58, n. 4, p. 233, doi. 10.1038/jhg.2012.158

By:

Hwang, Joo-Yeon;
Kim, Duk-Hwan;
Ji, Yong-Ick;
Jin Go, Min;
Heo, Lyong;
Jin Kim, Young;
Sung Sohn, Tae;
Hyung Noh, Jae;
Kim, Sung;
Lee, Yeon-Su;
Kim, Sook-Young;
Kim, Young-Woo;
Won Ryu, Keun;
Choi, Il Ju;
Lee, Juyoung;
Kim, Bong-Jo;
Han, Bok-Ghee;
Park, Joobae;
Lee, Jong-Young

Publication type:

Article

Confirmation of two novel loci for infantile hypertrophic pyloric stenosis on chromosomes 3 and 5.

Published in:

Journal of Human Genetics, 2013, v. 58, n. 4, p. 236, doi. 10.1038/jhg.2013.10

By:

Everett, Kate V;
Chung, Eddie M K

Publication type:

Article

A commentary on assignment of Y-chromosomal SNPs found in Japanese population to Y-chromosomal haplogroup tree.

Published in:

Journal of Human Genetics, 2013, v. 58, n. 4, p. 181, doi. 10.1038/jhg.2013.11

By:

Yuasa, Isao

Publication type:

Article

Assignment of Y-chromosomal SNPs found in Japanese population to Y-chromosomal haplogroup tree.

Published in:

Journal of Human Genetics, 2013, v. 58, n. 4, p. 195, doi. 10.1038/jhg.2012.159

By:

Naitoh, Sae;
Kasahara-Nonaka, Iku;
Minaguchi, Kiyoshi;
Nambiar, Phrabhakaran

Publication type:

Article

3′-UTR variations and G6PD deficiency.

Published in:

Journal of Human Genetics, 2013, v. 58, n. 4, p. 189, doi. 10.1038/jhg.2012.155

By:

Amini, Farahnaz;
Ismail, Endom

Publication type:

Article

Exome sequencing identifies novel rheumatoid arthritis-susceptible variants in the BTNL2.

Published in:

Journal of Human Genetics, 2013, v. 58, n. 4, p. 210, doi. 10.1038/jhg.2013.2

By:

Mitsunaga, Shigeki;
Hosomichi, Kazuyoshi;
Okudaira, Yuko;
Nakaoka, Hirofumi;
Kunii, Nanae;
Suzuki, Yasuo;
Kuwana, Masataka;
Sato, Shinji;
Kaneko, Yuko;
Homma, Yasuhiko;
Kashiwase, Koichi;
Azuma, Fumihiro;
Kulski, Jerzy K;
Inoue, Ituro;
Inoko, Hidetoshi

Publication type:

Article

Ancient DNA of Emperor CAO Cao's granduncle matches those of his present descendants: a commentary on present Y chromosomes reveal the ancestry of Emperor CAO Cao of 1800 years ago.

Published in:

Journal of Human Genetics, 2013, v. 58, n. 4, p. 238, doi. 10.1038/jhg.2013.5

By:

Wang, Chuan-Chao;
Yan, Shi;
Yao, Can;
Huang, Xiu-Yuan;
Ao, Xue;
Wang, Zhanfeng;
Han, Sheng;
Jin, Li;
Li, Hui

Publication type:

Article

Mutational analysis of TSC1 and TSC2 in Japanese patients with tuberous sclerosis complex revealed higher incidence of TSC1 patients than previously reported.

Published in:

Journal of Human Genetics, 2013, v. 58, n. 4, p. 216, doi. 10.1038/jhg.2013.3

By:

Niida, Yo;
Wakisaka, Akiko;
Tsuji, Takanori;
Yamada, Hiroshi;
Kuroda, Mondo;
Mitani, Yusuke;
Okumura, Akiko;
Yokoi, Ayano

Publication type:

Article

A microRNA-520 mirSNP at the MMP2 gene influences susceptibility to endometriosis in Chinese women.

Published in:

Journal of Human Genetics, 2013, v. 58, n. 4, p. 202, doi. 10.1038/jhg.2013.1

By:

Tsai, Eing-Mei;
Wang, Yung-Song;
Lin, Chang-Shen;
Lin, Wen-Yin;
Hsi, Edward;
Wu, Ming-Tsang;
Juo, Suh-Hang H

Publication type:

Article

Exome sequencing reveals SCO2 mutations in a family presented with fatal infantile hyperthermia.

Published in:

Journal of Human Genetics, 2013, v. 58, n. 4, p. 226, doi. 10.1038/jhg.2012.156

By:

Sambuughin, Nyamkhishig;
Liu, Xinyue;
Bijarnia, Sunita;
Wallace, Tarina;
Verma, Ishwar C;
Hamilton, Susan;
Muldoon, Sheila;
Tallon, Luke J;
Wang, Shuishu

Publication type:

Article

A commentary on DRD2 haplotype associated with negative symptoms and sustained attention deficits in Han Chinese with schizophrenia in Taiwan.

Published in:

Journal of Human Genetics, 2013, v. 58, n. 4, p. 182, doi. 10.1038/jhg.2013.13

By:

Wang, Yu-Mei

Publication type:

Article