Works matching IS 14345161 AND DT 2015 AND VI 60 AND IP 2

Results: 9

A powerful association test for qualitative traits incorporating imprinting effects using general pedigree data.

Published in:

Journal of Human Genetics, 2015, v. 60, n. 2, p. 77, doi. 10.1038/jhg.2014.109

By:

Zhou, Ji-Yuan;
He, Hai-Qiang;
You, Xiao-Ping;
Li, Shao-Zhan;
Chen, Ping-Yan;
Fung, Wing Kam

Publication type:

Article

An A/C germline single-nucleotide polymorphism in the TNFAIP3 gene is associated with advanced disease stage and survival in only surgically treated esophageal cancer.

Published in:

Journal of Human Genetics, 2015, v. 60, n. 2, p. 107, doi. 10.1038/jhg.2014.106

By:

Ghadban, Tarik;
Schmidt-Yang, Magdalena;
Uzunoglu, Faik G;
Perez, Daniel R;
Tsui, Tung Y;
El Gammal, Alexander T;
Erbes, Peter J;
Zilbermints, Veacheslav;
Wellner, Ulrich;
Pantel, Klaus;
Izbicki, Jakob R;
Vashist, Yogesh K

Publication type:

Article

Downregulation of the microRNA-1/133a cluster enhances cancer cell migration and invasion in lung-squamous cell carcinoma via regulation of Coronin1C.

Published in:

Journal of Human Genetics, 2015, v. 60, n. 2, p. 53, doi. 10.1038/jhg.2014.111

By:

Mataki, Hiroko;
Enokida, Hideki;
Chiyomaru, Takeshi;
Mizuno, Keiko;
Matsushita, Ryosuke;
Goto, Yusuke;
Nishikawa, Rika;
Higashimoto, Ikkou;
Samukawa, Takuya;
Nakagawa, Masayuki;
Inoue, Hiromasa;
Seki, Naohiko

Publication type:

Article

Genetic structure among Fijian island populations.

Published in:

Journal of Human Genetics, 2015, v. 60, n. 2, p. 69, doi. 10.1038/jhg.2014.105

By:

Shipley, Gerhard P;
Taylor, Diana A;
Tyagi, Anand;
Tiwari, Geetanjali;
Redd, Alan J

Publication type:

Article

Deep sequencing of RYR3 gene identifies rare and common variants associated with increased carotid intima-media thickness (cIMT) in HIV-infected individuals.

Published in:

Journal of Human Genetics, 2015, v. 60, n. 2, p. 63, doi. 10.1038/jhg.2014.104

By:

Zhi, Degui;
Shendre, Aditi;
Scherzer, Rebecca;
Irvin, Marguerite R;
Perry, Rodney T;
Levy, Shawn;
Arnett, Donna K;
Grunfeld, Carl;
Shrestha, Sadeep

Publication type:

Article

Mutations in the glutaminyl-tRNA synthetase gene cause early-onset epileptic encephalopathy.

Published in:

Journal of Human Genetics, 2015, v. 60, n. 2, p. 97, doi. 10.1038/jhg.2014.103

By:

Kodera, Hirofumi;
Osaka, Hitoshi;
Iai, Mizue;
Aida, Noriko;
Yamashita, Akio;
Tsurusaki, Yoshinori;
Nakashima, Mitsuko;
Miyake, Noriko;
Saitsu, Hirotomo;
Matsumoto, Naomichi

Publication type:

Article

Silver-Russell syndrome without body asymmetry in three patients with duplications of maternally derived chromosome 11p15 involving CDKN1C.

Published in:

Journal of Human Genetics, 2015, v. 60, n. 2, p. 91, doi. 10.1038/jhg.2014.100

By:

Nakashima, Shinichi;
Kato, Fumiko;
Kosho, Tomoki;
Nagasaki, Keisuke;
Kikuchi, Toru;
Kagami, Masayo;
Fukami, Maki;
Ogata, Tsutomu

Publication type:

Article

Severe phenotypes in a Charcot-Marie-Tooth 1A patient with PMP22 triplication.

Published in:

Journal of Human Genetics, 2015, v. 60, n. 2, p. 103, doi. 10.1038/jhg.2014.102

By:

Kim, Sung Min;
Lee, Jinho;
Yoon, Bo Ram;
Kim, Ye Jin;
Choi, Byung-Ok;
Chung, Ki Wha

Publication type:

Article

Mutations in the glucocerebrosidase gene are responsible for Chinese patients with Parkinson's disease.

Published in:

Journal of Human Genetics, 2015, v. 60, n. 2, p. 85, doi. 10.1038/jhg.2014.110

By:

Yu, Zhe;
Wang, Ting;
Xu, Jun;
Wang, Wei;
Wang, Guifang;
Chen, Chao;
Zheng, Lili;
Pan, Li;
Gong, Dianrong;
Li, Xueli;
Qu, Huaiqian;
Li, Fang;
Zhang, Bin;
Le, Weidong;
Han, Fabin

Publication type:

Article