Works matching IS 14345161 AND DT 2012 AND VI 57 AND IP 10

Results: 14

Genetic variants at 5p12 and risk of breast cancer in Han Chinese.

Published in:

Journal of Human Genetics, 2012, v. 57, n. 10, p. 638, doi. 10.1038/jhg.2012.83

By:

Liu, Xiao'an;
Qin, Zhenzhen;
Shen, Hao;
Xue, Jialei;
Jiang, Yue;
Hu, Zhibin;
Shen, Hongbing;
Wang, Shui

Publication type:

Article

NDesign: software for study design for the detection of rare variants from next-generation sequencing data.

Published in:

Journal of Human Genetics, 2012, v. 57, n. 10, p. 676, doi. 10.1038/jhg.2012.81

By:

Sugaya, Yuki;
Akazawa, Yasuaki;
Saito, Akira;
Kamitsuji, Shigeo

Publication type:

Article

Warfarin pharmacogenetics: development of a dosing algorithm for Omani patients.

Published in:

Journal of Human Genetics, 2012, v. 57, n. 10, p. 665, doi. 10.1038/jhg.2012.94

By:

Pathare, Anil;
Al Khabori, Murtadha;
Alkindi, Salam;
Al Zadjali, Shoaib;
Misquith, Rhea;
Khan, Hammad;
Lapoumeroulie, Claudine;
Paldi, Andras;
Krishnamoorthy, Rajagopal

Publication type:

Article

Association of common PAX9 variants with permanent tooth size variation in non-syndromic East Asian populations.

Published in:

Journal of Human Genetics, 2012, v. 57, n. 10, p. 654, doi. 10.1038/jhg.2012.90

By:

Lee, Won-Chul;
Yamaguchi, Tetsutaro;
Watanabe, Chiaki;
Kawaguchi, Akira;
Takeda, Mayako;
Kim, Yong-Il;
Haga, Shugo;
Tomoyasu, Yoko;
Ishida, Hajime;
Maki, Koutaro;
Park, Soo-Byung;
Kimura, Ryosuke

Publication type:

Article

Paternal uniparental isodisomy of chromosome 22 in a patient with metachromatic leukodystrophy.

Published in:

Journal of Human Genetics, 2012, v. 57, n. 10, p. 687, doi. 10.1038/jhg.2012.97

By:

Niida, Yo;
Kuroda, Mondo;
Mitani, Yusuke;
Yokoi, Ayano;
Ozaki, Mamoru

Publication type:

Article

USH1K, a novel locus for type I Usher syndrome, maps to chromosome 10p11.21-q21.1.

Published in:

Journal of Human Genetics, 2012, v. 57, n. 10, p. 633, doi. 10.1038/jhg.2012.79

By:

Jaworek, Thomas J;
Bhatti, Rashid;
Latief, Noreen;
Khan, Shaheen N;
Riazuddin, Saima;
Ahmed, Zubair M

Publication type:

Article

Genome-wide association study identifies GYS2 as a novel genetic factor for polycystic ovary syndrome through obesity-related condition.

Published in:

Journal of Human Genetics, 2012, v. 57, n. 10, p. 660, doi. 10.1038/jhg.2012.92

By:

Hwang, Joo-Yeon;
Lee, Eun-Ju;
Jin Go, Min;
Sung, Yeon-Ah;
Lee, Hye Jin;
Heon Kwak, Soo;
Jang, Hak C;
Soo Park, Kyung;
Lee, Hye-Ja;
Byul Jang, Han;
Song, Jihyun;
Park, Kyung-Hee;
Kim, Hyung-Lae;
Cho, Myeong-Chan;
Lee, Jong-Young

Publication type:

Article

DBGSA: a novel method of distance-based gene set analysis.

Published in:

Journal of Human Genetics, 2012, v. 57, n. 10, p. 642, doi. 10.1038/jhg.2012.86

By:

Li, Jin;
Wang, Limei;
Xu, Liangde;
Zhang, Ruijie;
Huang, Meilin;
Wang, Ke;
Xu, Jiankai;
Lv, Hongchao;
Shang, Zhenwei;
Zhang, Mingming;
Jiang, Yongshuai;
Guo, Maozu;
Li, Xia

Publication type:

Article

On the Y-chromosome haplogroup C3c classification.

Published in:

Journal of Human Genetics, 2012, v. 57, n. 10, p. 685, doi. 10.1038/jhg.2012.93

By:

Malyarchuk, Boris A;
Derenko, Miroslava;
Denisova, Galina

Publication type:

Article

A commentary on 'TECTA mutations in Japanese with mid-frequency hearing loss affected by Zona Pellucida domain protein secretion'.

Published in:

Journal of Human Genetics, 2012, v. 57, n. 10, p. 619, doi. 10.1038/jhg.2012.89

By:

Maeda, Yukihide;
Fukushima, Kunihiro

Publication type:

Article

Identification of ALK germline mutation (3605delG) in pediatric anaplastic medulloblastoma.

Published in:

Journal of Human Genetics, 2012, v. 57, n. 10, p. 682, doi. 10.1038/jhg.2012.87

By:

Coco, Simona;
De Mariano, Marilena;
Valdora, Francesca;
Servidei, Tiziana;
Ridola, Vita;
Andolfo, Immacolata;
Oberthuer, André;
Tonini, Gian Paolo;
Longo, Luca

Publication type:

Article

Hypermethylation of OPRM1 promoter region in European Americans with alcohol dependence.

Published in:

Journal of Human Genetics, 2012, v. 57, n. 10, p. 670, doi. 10.1038/jhg.2012.98

By:

Zhang, Huiping;
Herman, Aryeh I;
Kranzler, Henry R;
Anton, Raymond F;
Simen, Arthur A;
Gelernter, Joel

Publication type:

Article

Novel PNPLA2 gene mutations in Chinese Han patients causing neutral lipid storage disease with myopathy.

Published in:

Journal of Human Genetics, 2012, v. 57, n. 10, p. 679, doi. 10.1038/jhg.2012.84

By:

Lin, Pengfei;
Li, Wei;
Wen, Bing;
Zhao, Yuying;
Fenster, Danielle S;
Wang, Yongxiang;
Gong, Yaoqin;
Yan, Chuanzhu

Publication type:

Article

Next-generation sequencing: impact of exome sequencing in characterizing Mendelian disorders.

Published in:

Journal of Human Genetics, 2012, v. 57, n. 10, p. 621, doi. 10.1038/jhg.2012.91

By:

Rabbani, Bahareh;
Mahdieh, Nejat;
Hosomichi, Kazuyoshi;
Nakaoka, Hirofumi;
Inoue, Ituro

Publication type:

Article