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
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
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
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