Works matching IS 03406717 AND DT 2014 AND VI 133 AND IP 5

Results: 20

A genome-wide association study of prostate cancer in West African men.

Published in:

Human Genetics, 2014, v. 133, n. 5, p. 509, doi. 10.1007/s00439-013-1387-z

By:

Cook, Michael;
Wang, Zhaoming;
Yeboah, Edward;
Tettey, Yao;
Biritwum, Richard;
Adjei, Andrew;
Tay, Evelyn;
Truelove, Ann;
Niwa, Shelley;
Chung, Charles;
Chokkalingam, Annand;
Chu, Lisa;
Yeager, Meredith;
Hutchinson, Amy;
Yu, Kai;
Rand, Kristin;
Haiman, Christopher;
Hoover, Robert;
Hsing, Ann;
Chanock, Stephen

Publication type:

Article

Significant associations of CHRNA2 and CHRNA6 with nicotine dependence in European American and African American populations.

Published in:

Human Genetics, 2014, v. 133, n. 5, p. 575, doi. 10.1007/s00439-013-1398-9

By:

Wang, Shaolin;
van der Vaart, Andrew;
Xu, Qing;
Seneviratne, Chamindi;
Pomerleau, Ovide;
Pomerleau, Cynthia;
Payne, Thomas;
Ma, Jennie;
Li, Ming

Publication type:

Article

Identification of BACH2 as a susceptibility gene for Graves' disease in the Chinese Han population based on a three-stage genome-wide association study.

Published in:

Human Genetics, 2014, v. 133, n. 5, p. 661, doi. 10.1007/s00439-013-1404-2

By:

Liu, Wei;
Wang, Hai-Ning;
Gu, Zhao-Hui;
Yang, Shao-Ying;
Ye, Xiao-Ping;
Pan, Chun-Ming;
Zhao, Shuang-Xia;
Xue, Li-Qiong;
Xie, Hui-Jun;
Yu, Sha-Sha;
Guo, Cui-Cui;
Du, Wen-Hua;
Liang, Jun;
Zhang, Xiao-Mei;
Yuan, Guo-Yue;
Li, Chang-Gui;
Su, Qing;
Gao, Guan-Qi;
Song, Huai-Dong

Publication type:

Article

Does variation in NIPA2 contribute to genetic generalized epilepsy?

Published in:

2014

By:

Hildebrand, Michael;
Damiano, John;
Mullen, Saul;
Bellows, Susannah;
Scheffer, Ingrid;
Berkovic, Samuel

Publication type:

Letter

Exploring the genetic architecture of alcohol dependence in African-Americans via analysis of a genomewide set of common variants.

Published in:

Human Genetics, 2014, v. 133, n. 5, p. 617, doi. 10.1007/s00439-013-1399-8

By:

Yang, Can;
Li, Cong;
Kranzler, Henry;
Farrer, Lindsay;
Zhao, Hongyu;
Gelernter, Joel

Publication type:

Article

Natural and orthogonal model for estimating gene-gene interactions applied to cutaneous melanoma.

Published in:

Human Genetics, 2014, v. 133, n. 5, p. 559, doi. 10.1007/s00439-013-1392-2

By:

Xiao, Feifei;
Ma, Jianzhong;
Cai, Guoshuai;
Fang, Shenying;
Lee, Jeffrey;
Wei, Qingyi;
Amos, Christopher

Publication type:

Article

Improving genetic risk prediction by leveraging pleiotropy.

Published in:

Human Genetics, 2014, v. 133, n. 5, p. 639, doi. 10.1007/s00439-013-1401-5

By:

Li, Cong;
Yang, Can;
Gelernter, Joel;
Zhao, Hongyu

Publication type:

Article

COOH-terminal collagen Q ( COLQ) mutants causing human deficiency of endplate acetylcholinesterase impair the interaction of ColQ with proteins of the basal lamina.

Published in:

Human Genetics, 2014, v. 133, n. 5, p. 599, doi. 10.1007/s00439-013-1391-3

By:

Arredondo, Juan;
Lara, Marian;
Ng, Fiona;
Gochez, Danielle;
Lee, Diana;
Logia, Stephanie;
Nguyen, Joanna;
Maselli, Ricardo

Publication type:

Article

A genome-wide association study on copy-number variation identifies a 11q11 loss as a candidate susceptibility variant for colorectal cancer.

Published in:

Human Genetics, 2014, v. 133, n. 5, p. 525, doi. 10.1007/s00439-013-1390-4

By:

Fernandez-Rozadilla, C.;
Cazier, J.;
Tomlinson, I.;
Brea-Fernández, A.;
Lamas, M.;
Baiget, M.;
López-Fernández, L.;
Clofent, J.;
Bujanda, L.;
Gonzalez, D.;
Castro, L.;
Hemminki, K.;
Bessa, X.;
Andreu, M.;
Jover, R.;
Xicola, R.;
Llor, X.;
Moreno, V.;
Castells, A.;
Castellví-Bel, S.

Publication type:

Article

Erratum to: RET and NRG1 interplay in Hirschsprung disease.

Published in:

2014

By:

Gui, Hongsheng;
Tang, Wai-Kiu;
So, Man-Ting;
Proitsi, Petroola;
Sham, Pak;
Tam, Paul;
Ngan, Elly;
Cherny, Stacey;
Garcia-Barceló, Maria-Mercè

Publication type:

Erratum

Genome-wide association study of subtype-specific epithelial ovarian cancer risk alleles using pooled DNA.

Published in:

Human Genetics, 2014, v. 133, n. 5, p. 481, doi. 10.1007/s00439-013-1383-3

By:

Earp, Madalene;
Kelemen, Linda;
Magliocco, Anthony;
Swenerton, Kenneth;
Chenevix-Trench, Georgia;
Lu, Yi;
Hein, Alexander;
Ekici, Arif;
Beckmann, Matthias;
Fasching, Peter;
Lambrechts, Diether;
Despierre, Evelyn;
Vergote, Ignace;
Lambrechts, Sandrina;
Doherty, Jennifer;
Rossing, Mary;
Chang-Claude, Jenny;
Rudolph, Anja;
Friel, Grace;
Moysich, Kirsten

Publication type:

Article

Case-control association study of polymorphisms in the voltage-gated sodium channel genes SCN1A, SCN2A, SCN3A, SCN1B, and SCN2B and epilepsy.

Published in:

Human Genetics, 2014, v. 133, n. 5, p. 651, doi. 10.1007/s00439-013-1405-1

By:

Baum, Larry;
Haerian, Batoul;
Ng, Ho-Keung;
Wong, Virginia;
Ng, Ping;
Lui, Colin;
Sin, Ngai;
Zhang, Chunbo;
Tomlinson, Brian;
Wong, Gary;
Tan, Hui;
Raymond, Azman;
Mohamed, Zahurin;
Kwan, Patrick

Publication type:

Article

Gene-gene and gene-environment interactions in ulcerative colitis.

Published in:

Human Genetics, 2014, v. 133, n. 5, p. 547, doi. 10.1007/s00439-013-1395-z

By:

Wang, Ming-Hsi;
Fiocchi, Claudio;
Zhu, Xiaofeng;
Ripke, Stephan;
Kamboh, M.;
Rebert, Nancy;
Duerr, Richard;
Achkar, Jean-Paul

Publication type:

Article

Comparative-high resolution melting: a novel method of simultaneous screening for small mutations and copy number variations.

Published in:

Human Genetics, 2014, v. 133, n. 5, p. 535, doi. 10.1007/s00439-013-1393-1

By:

Borun, Pawel;
Kubaszewski, Lukasz;
Banasiewicz, Tomasz;
Walkowiak, Jaroslaw;
Skrzypczak-Zielinska, Marzena;
Kaczmarek-Rys, Marta;
Plawski, Andrzej

Publication type:

Article

Common DNA variants predict tall stature in Europeans.

Published in:

Human Genetics, 2014, v. 133, n. 5, p. 587, doi. 10.1007/s00439-013-1394-0

By:

Liu, Fan;
Hendriks, A.;
Ralf, Arwin;
Boot, Annemieke;
Benyi, Emelie;
Sävendahl, Lars;
Oostra, Ben;
Duijn, Cornelia;
Hofman, Albert;
Rivadeneira, Fernando;
Uitterlinden, André;
Drop, Stenvert;
Kayser, Manfred

Publication type:

Article

X-linked congenital ptosis and associated intellectual disability, short stature, microcephaly, cleft palate, digital and genital abnormalities define novel Xq25q26 duplication syndrome.

Published in:

Human Genetics, 2014, v. 133, n. 5, p. 625, doi. 10.1007/s00439-013-1403-3

By:

Møller, R.;
Jensen, L.;
Maas, S.;
Filmus, J.;
Capurro, M.;
Hansen, C.;
Marcelis, C.;
Ravn, K.;
Andrieux, J.;
Mathieu, M.;
Kirchhoff, M.;
Rødningen, O.;
Leeuw, N.;
Yntema, H.;
Froyen, G.;
Vandewalle, J.;
Ballon, K.;
Klopocki, E.;
Joss, S.;
Tolmie, J.

Publication type:

Article

Erratum to: A genome-wide association study of prostate cancer in West African men.

Published in:

2014

By:

Cook, Michael;
Wang, Zhaoming;
Yeboah, Edward;
Tettey, Yao;
Biritwum, Richard;
Adjei, Andrew;
Tay, Evelyn;
Truelove, Ann;
Niwa, Shelley;
Chung, Charles;
Chokkalingam, Annand;
Chu, Lisa;
Yeager, Meredith;
Hutchinson, Amy;
Yu, Kai;
Rand, Kristin;
Haiman, Christopher;
Hoover, Robert;
Hsing, Ann;
Chanock, Stephen

Publication type:

Erratum

NIPA2 mutations are correlative with childhood absence epilepsy in the Han Chinese population.

Published in:

2014

By:

Jiang, Yuwu;
Zhang, Yuehua;
Zhang, Pingping;
Zhang, Feng;
Xie, Han;
Chan, Piu;
Wu, Xiru

Publication type:

Letter

BRG1 variant rs1122608 on chromosome 19p13.2 confers protection against stroke and regulates expression of pre-mRNA-splicing factor SFRS3.

Published in:

Human Genetics, 2014, v. 133, n. 5, p. 499, doi. 10.1007/s00439-013-1389-x

By:

Xiong, Xin;
Xu, Chengqi;
Zhang, Yuting;
Li, Xiuchun;
Wang, Binbin;
Wang, Fan;
Yang, Qin;
Wang, Dan;
Wang, Xiaojing;
Li, Sisi;
Chen, Shanshan;
Zhao, Yuanyuan;
Yin, Dan;
Huang, Yufeng;
Zhu, Xuan;
Wang, Li;
Wang, Longfei;
Chang, Le;
Xu, Chaoping;
Li, Hui

Publication type:

Article

The genetic basis of pulmonary arterial hypertension.

Published in:

Human Genetics, 2014, v. 133, n. 5, p. 471, doi. 10.1007/s00439-014-1419-3

By:

Ma, Lijiang;
Chung, Wendy

Publication type:

Article