Works matching IS 14345161 AND DT 2011 AND VI 56 AND IP 11

Results: 10

Identification of independent risk loci for Graves' disease within the MHC in the Japanese population.

Published in:

Journal of Human Genetics, 2011, v. 56, n. 11, p. 772, doi. 10.1038/jhg.2011.99

By:

Nakabayashi, Kazuhiko;
Tajima, Atsushi;
Yamamoto, Ken;
Takahashi, Atsushi;
Hata, Kenichiro;
Takashima, Yasuo;
Koyanagi, Midori;
Nakaoka, Hirofumi;
Akamizu, Takashi;
Ishikawa, Naofumi;
Kubota, Sumihisa;
Maeda, Shiro;
Tsunoda, Tatsuhiko;
Kubo, Michiaki;
Kamatani, Naoyuki;
Nakamura, Yusuke;
Sasazuki, Takehiko;
Shirasawa, Senji

Publication type:

Article

Support for association between the Ser205Leu polymorphism of p75<sup>NTR</sup> and major depressive disorder.

Published in:

Journal of Human Genetics, 2011, v. 56, n. 11, p. 806, doi. 10.1038/jhg.2011.107

By:

Fujii, Takashi;
Yamamoto, Noriko;
Hori, Hiroaki;
Hattori, Kotaro;
Sasayama, Daimei;
Teraishi, Toshiya;
Hashikura, Miyako;
Tatsumi, Masahiko;
Okamoto, Nagahisa;
Higuchi, Teruhiko;
Kunugi, Hiroshi

Publication type:

Article

Y-chromosome haplogroup diversity in the sub-Himalayan Terai and Duars populations of East India.

Published in:

Journal of Human Genetics, 2011, v. 56, n. 11, p. 765, doi. 10.1038/jhg.2011.98

By:

Debnath, Monojit;
Palanichamy, Malliya G;
Mitra, Bikash;
Jin, Jie-Qiong;
Chaudhuri, Tapas K;
Zhang, Ya-Ping

Publication type:

Article

Contribution of MSX1 variants to the risk of non-syndromic cleft lip and palate in a Malay population.

Published in:

Journal of Human Genetics, 2011, v. 56, n. 11, p. 755, doi. 10.1038/jhg.2011.95

By:

Salahshourifar, Iman;
Halim, Ahmad Sukari;
Wan Sulaiman, Wan Azman;
Zilfalil, Bin Alwi

Publication type:

Article

Gene expression analysis in lymphoblastoid cells as a potential biomarker of bipolar disorder.

Published in:

Journal of Human Genetics, 2011, v. 56, n. 11, p. 779, doi. 10.1038/jhg.2011.101

By:

Kato, Tadafumi;
Hayashi-Takagi, Akiko;
Toyota, Tomoko;
Yoshikawa, Takeo;
Iwamoto, Kazuya

Publication type:

Article

Tandem configurations of variably duplicated segments of 22q11.2 confirmed by fiber-FISH analysis.

Published in:

Journal of Human Genetics, 2011, v. 56, n. 11, p. 810, doi. 10.1038/jhg.2011.100

By:

Shimojima, Keiko;
Okamoto, Nobuhiko;
Inazu, Tetsuya;
Yamamoto, Toshiyuki

Publication type:

Article

Mutations in mitochondrially encoded complex I enzyme as the second common cause in a cohort of Chinese patients with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes.

Published in:

Journal of Human Genetics, 2011, v. 56, n. 11, p. 759, doi. 10.1038/jhg.2011.96

By:

Zhao, Danhua;
Hong, Daojun;
Zhang, Wei;
Yao, Sheng;
Qi, Xiaokun;
Lv, He;
Zheng, Riliang;
Feng, Liqun;
Huang, Yining;
Yuan, Yun;
Wang, Zhaoxia

Publication type:

Article

HVS-I polymorphism screening of ancient human mitochondrial DNA provides evidence for N9a discontinuity and East Asian haplogroups in the Neolithic Hungary.

Published in:

Journal of Human Genetics, 2011, v. 56, n. 11, p. 784, doi. 10.1038/jhg.2011.103

By:

Guba, Zsuzsanna;
Hadadi, Éva;
Major, Ágnes;
Furka, Tünde;
Juhász, Emese;
Koós, Judit;
Nagy, Károly;
Zeke, Tamás

Publication type:

Article

Genome-wide association study identifies genetic variants in GOT1 determining serum aspartate aminotransferase levels.

Published in:

Journal of Human Genetics, 2011, v. 56, n. 11, p. 801, doi. 10.1038/jhg.2011.105

By:

Shen, Haiqing;
Damcott, Coleen;
Shuldiner, Scott R;
Chai, Sumbul;
Yang, Rongze;
Hu, Hong;
Gibson, Quince;
Ryan, Kathleen A;
Mitchell, Braxton D;
Gong, Da-Wei

Publication type:

Article

UBE3C genetic variations as potent markers of nasal polyps in Korean asthma patients.

Published in:

Journal of Human Genetics, 2011, v. 56, n. 11, p. 797, doi. 10.1038/jhg.2011.104

By:

Pasaje, Charisse Flerida A;
Kim, Jeong-Hyun;
Park, Byung-Lae;
Park, Jong-Sook;
Uh, Soo-Taek;
Kim, Mi-Kyeong;
Park, Choon-Sik;
Shin, Hyoung Doo

Publication type:

Article