Works matching IS 03406717 AND DT 2012 AND VI 131 AND IP 7

Results: 28

Randall H. Morse (ed.): Chromatin remodelling: methods and protocols.

Published in:

2012

By:

Waters, Raymond

Publication type:

Book Review

Erratum to: Association between gout and polymorphisms in GCKR in male Han Chinese.

Published in:

2012

By:

Wang, Jing;
Liu, Shiguo;
Wang, Binbin;
Miao, Zhimin;
Han, Lin;
Chu, Nan;
Zhang, Kun;
Meng, Dongmei;
Li, Changgui;
Ma, Xu

Publication type:

Correction Notice

Loss-of-function mutations in filaggrin gene associate with psoriasis vulgaris in Chinese population.

Published in:

Human Genetics, 2012, v. 131, n. 7, p. 1269, doi. 10.1007/s00439-012-1155-5

By:

Hu, Zhengmao;
Xiong, Zhimin;
Xu, Xiaojuan;
Li, Fangfang;
Lu, Lina;
Li, Wei;
Su, Juan;
Liu, Yalan;
Liu, Deyuan;
Xie, Zhiguo;
Peng, Yu;
Kuang, Yehong;
Wu, Lisha;
Zhang, Jianglin;
Pan, Qian;
Tang, Beisha;
Chen, Xiang;
Xia, Kun

Publication type:

Article

Association between gout and polymorphisms in GCKR in male Han Chinese.

Published in:

Human Genetics, 2012, v. 131, n. 7, p. 1261, doi. 10.1007/s00439-012-1151-9

By:

Wang, Jing;
Liu, Shiguo;
Wang, Binbin;
Miao, Zhimin;
Han, Lin;
Chu, Nan;
Zhang, Kun;
Meng, Dongmei;
Li, Changgui;
Ma, Xu

Publication type:

Article

Genetic variants of the MRC1 gene and the IFNG gene are associated with leprosy in Han Chinese from Southwest China.

Published in:

Human Genetics, 2012, v. 131, n. 7, p. 1251, doi. 10.1007/s00439-012-1153-7

By:

Wang, Dong;
Feng, Jia-Qi;
Li, Yu-Ye;
Zhang, Deng-Feng;
Li, Xiao-An;
Li, Qing-Wei;
Yao, Yong-Gang

Publication type:

Article

The prevalence of CD33 and MS4A6A variant in Chinese Han population with Alzheimer's disease.

Published in:

Human Genetics, 2012, v. 131, n. 7, p. 1245, doi. 10.1007/s00439-012-1154-6

By:

Deng, Yu-Lei;
Liu, Li-Hua;
Wang, Ying;
Tang, Hui-Dong;
Ren, Ru-Jing;
Xu, Wei;
Ma, Jian-Fang;
Wang, Li-Ling;
Zhuang, Jun-Peng;
Wang, Gang;
Chen, Sheng-Di

Publication type:

Article

Polymorphisms in the XPG gene and risk of gastric cancer in Chinese populations.

Published in:

Human Genetics, 2012, v. 131, n. 7, p. 1235, doi. 10.1007/s00439-012-1152-8

By:

He, Jing;
Qiu, Li-Xin;
Wang, Meng-Yun;
Hua, Rui-Xi;
Zhang, Ruo-Xin;
Yu, Hong-Ping;
Wang, Ya-Nong;
Sun, Meng-Hong;
Zhou, Xiao-Yan;
Yang, Ya-Jun;
Wang, Jiu-Cun;
Jin, Li;
Wei, Qing-Yi;
Li, Jin

Publication type:

Article

Genome-wide two-locus epistasis scans in prostate cancer using two European populations.

Published in:

Human Genetics, 2012, v. 131, n. 7, p. 1225, doi. 10.1007/s00439-012-1148-4

By:

Tao, Sha;
Feng, Junjie;
Webster, Timothy;
Jin, Guangfu;
Hsu, Fang-Chi;
Chen, Shyh-Huei;
Kim, Seong-Tae;
Wang, Zhong;
Zhang, Zheng;
Zheng, Siqun;
Isaacs, William;
Xu, Jianfeng;
Sun, Jielin

Publication type:

Article

NIPA2 located in 15q11.2 is mutated in patients with childhood absence epilepsy.

Published in:

Human Genetics, 2012, v. 131, n. 7, p. 1217, doi. 10.1007/s00439-012-1149-3

By:

Jiang, Yuwu;
Zhang, Yuehua;
Zhang, Pingping;
Sang, Tian;
Zhang, Feng;
Ji, Taoyun;
Huang, Qionghui;
Xie, Han;
Du, Renqian;
Cai, Bin;
Zhao, Haijuan;
Wang, Jingmin;
Wu, Ye;
Wu, Husheng;
Xu, Keming;
Liu, Xiaoyan;
Chan, Piu;
Wu, Xiru

Publication type:

Article

Evolutionary genetics of the human Rh blood group system.

Published in:

Human Genetics, 2012, v. 131, n. 7, p. 1205, doi. 10.1007/s00439-012-1147-5

By:

Perry, George;
Xue, Yali;
Smith, Richard;
Meyer, Wynn;
Çalışkan, Minal;
Yanez-Cuna, Omar;
Lee, Arthur;
Gutiérrez-Arcelus, María;
Ober, Carole;
Hollox, Edward;
Tyler-Smith, Chris;
Lee, Charles

Publication type:

Article

Genetic variant in TP63 on locus 3q28 is associated with risk of lung adenocarcinoma among never-smoking females in Asia.

Published in:

Human Genetics, 2012, v. 131, n. 7, p. 1197, doi. 10.1007/s00439-012-1144-8

By:

Hosgood, H.;
Wang, Wen-Chang;
Hong, Yun-Chul;
Wang, Jiu-Cun;
Chen, Kexin;
Chang, I-Shou;
Chen, Chien-Jen;
Lu, Daru;
Yin, Zhihua;
Wu, Chen;
Zheng, Wei;
Qian, Biyun;
Park, Jae;
Kim, Yeul;
Chatterjee, Nilanjan;
Chen, Ying;
Chang, Gee-Chen;
Hsiao, Chin-Fu;
Yeager, Meredith;
Tsai, Ying-Huang

Publication type:

Article

Cognitive and serum BDNF correlates of BDNF Val66Met gene polymorphism in patients with schizophrenia and normal controls.

Published in:

Human Genetics, 2012, v. 131, n. 7, p. 1187, doi. 10.1007/s00439-012-1150-x

By:

Zhang, Xiang;
Chen, Da;
Xiu, Mei;
Haile, Colin;
Luo, Xingguang;
Xu, Ke;
Zhang, Hui;
Zuo, Lingjun;
Zhang, Zhijun;
Zhang, Xiangrong;
Kosten, Therese;
Kosten, Thomas

Publication type:

Article

Y chromosome haplogroups and prostate cancer in populations of European and Ashkenazi Jewish ancestry.

Published in:

Human Genetics, 2012, v. 131, n. 7, p. 1173, doi. 10.1007/s00439-012-1139-5

By:

Wang, Zhaoming;
Parikh, Hemang;
Jia, Jinping;
Myers, Timothy;
Yeager, Meredith;
Jacobs, Kevin;
Hutchinson, Amy;
Burdett, Laurie;
Ghosh, Arpita;
Thun, Michael;
Gapstur, Susan;
Ryan Diver, W.;
Virtamo, Jarmo;
Albanes, Demetrius;
Cancel-Tassin, Geraldine;
Valeri, Antoine;
Cussenot, Olivier;
Offit, Kenneth;
Giovannucci, Ed;
Ma, Jing

Publication type:

Article

Interaction between genetic and epigenetic variation defines gene expression patterns at the asthma-associated locus 17q12-q21 in lymphoblastoid cell lines.

Published in:

Human Genetics, 2012, v. 131, n. 7, p. 1161, doi. 10.1007/s00439-012-1142-x

By:

Berlivet, Soizik;
Moussette, Sanny;
Ouimet, Manon;
Verlaan, Dominique;
Koka, Vonda;
Al Tuwaijri, Abeer;
Kwan, Tony;
Sinnett, Daniel;
Pastinen, Tomi;
Naumova, Anna

Publication type:

Article

The human lactase persistence-associated SNP −13910*T enables in vivo functional persistence of lactase promoter-reporter transgene expression.

Published in:

Human Genetics, 2012, v. 131, n. 7, p. 1153, doi. 10.1007/s00439-012-1140-z

By:

Fang, Lin;
Ahn, Jong;
Wodziak, Dariusz;
Sibley, Eric

Publication type:

Article

A multi-ethnic study of a PNPLA3 gene variant and its association with disease severity in non-alcoholic fatty liver disease.

Published in:

Human Genetics, 2012, v. 131, n. 7, p. 1145, doi. 10.1007/s00439-012-1141-y

By:

Zain, Shamsul;
Mohamed, Rosmawati;
Mahadeva, Sanjiv;
Cheah, Phaik;
Rampal, Sanjay;
Basu, Roma;
Mohamed, Zahurin

Publication type:

Article

A functional variant of the collagen type III alpha1 gene modify risk of sporadic intracranial aneurysms.

Published in:

Human Genetics, 2012, v. 131, n. 7, p. 1137, doi. 10.1007/s00439-012-1138-6

By:

Chen, Jingzhou;
Zhu, Yufang;
Jiang, Yuhua;
Yu, Hui;
Sun, Kai;
Song, Weihua;
Luan, Liming;
Lou, Kejia;
Li, Youxiang;
Jiang, Peng;
Pang, Qi;
Hui, Rutai

Publication type:

Article

Unraveling the genetic component of systemic sclerosis.

Published in:

Human Genetics, 2012, v. 131, n. 7, p. 1023, doi. 10.1007/s00439-011-1137-z

By:

Martín, José;
Bossini-Castillo, Lara;
Martín, Javier

Publication type:

Article

LG2 agrin mutation causing severe congenital myasthenic syndrome mimics functional characteristics of non-neural (z−) agrin.

Published in:

Human Genetics, 2012, v. 131, n. 7, p. 1123, doi. 10.1007/s00439-011-1132-4

By:

Maselli, Ricardo;
Fernandez, Jose;
Arredondo, Juan;
Navarro, Carmen;
Ngo, Maian;
Beeson, David;
Cagney, Órla;
Williams, D.;
Wollmann, Robert;
Yarov-Yarovoy, Vladimir;
Ferns, Michael

Publication type:

Article

Mutation risk associated with paternal and maternal age in a cohort of retinoblastoma survivors.

Published in:

Human Genetics, 2012, v. 131, n. 7, p. 1115, doi. 10.1007/s00439-011-1126-2

By:

Mills, Melissa;
Hudgins, Louanne;
Balise, Raymond;
Abramson, David;
Kleinerman, Ruth

Publication type:

Article

Genetic association between human chitinases and lung function in COPD.

Published in:

Human Genetics, 2012, v. 131, n. 7, p. 1105, doi. 10.1007/s00439-011-1127-1

By:

Aminuddin, F.;
Akhabir, L.;
Stefanowicz, D.;
Paré, P.;
Connett, J.;
Anthonisen, N.;
Fahy, J.;
Seibold, M.;
Burchard, E.;
Eng, C.;
Gulsvik, A.;
Bakke, P.;
Cho, M.;
Litonjua, A.;
Lomas, D.;
Anderson, W.;
Beaty, T.;
Crapo, J.;
Silverman, E.;
Sandford, A.

Publication type:

Article

Validation of prostate cancer risk-related loci identified from genome-wide association studies using family-based association analysis: evidence from the International Consortium for Prostate Cancer Genetics (ICPCG).

Published in:

Human Genetics, 2012, v. 131, n. 7, p. 1095, doi. 10.1007/s00439-011-1136-0

By:

Jin, Guangfu;
Lu, Lingyi;
Cooney, Kathleen;
Ray, Anna;
Zuhlke, Kimberly;
Lange, Ethan;
Cannon-Albright, Lisa;
Camp, Nicola;
Teerlink, Craig;
FitzGerald, Liesel;
Stanford, Janet;
Wiley, Kathleen;
Isaacs, Sarah;
Walsh, Patrick;
Foulkes, William;
Giles, Graham;
Hopper, John;
Severi, Gianluca;
Eeles, Ros;
Easton, Doug

Publication type:

Article

GWAS-linked GAK locus in Parkinson's disease in Han Chinese and meta-analysis.

Published in:

Human Genetics, 2012, v. 131, n. 7, p. 1089, doi. 10.1007/s00439-011-1133-3

By:

Li, Nan-Nan;
Chang, Xue-Li;
Mao, Xue-Ye;
Zhang, Jin-Hong;
Zhao, Dong-Mei;
Tan, Eng-King;
Peng, Rong

Publication type:

Article

Effects of MAOA promoter methylation on susceptibility to paranoid schizophrenia.

Published in:

Human Genetics, 2012, v. 131, n. 7, p. 1081, doi. 10.1007/s00439-011-1131-5

By:

Chen, Yanbo;
Zhang, Jiexu;
Zhang, Li;
Shen, Yan;
Xu, Qi

Publication type:

Article

OPRM1 and EGFR contribute to skin pigmentation differences between Indigenous Americans and Europeans.

Published in:

Human Genetics, 2012, v. 131, n. 7, p. 1073, doi. 10.1007/s00439-011-1135-1

By:

Quillen, Ellen;
Bauchet, Marc;
Bigham, Abigail;
Delgado-Burbano, Miguel;
Faust, Franz;
Klimentidis, Yann;
Mao, Xianyun;
Stoneking, Mark;
Shriver, Mark

Publication type:

Article

Consistency of genome-wide associations across major ancestral groups.

Published in:

Human Genetics, 2012, v. 131, n. 7, p. 1057, doi. 10.1007/s00439-011-1124-4

By:

Ntzani, Evangelia;
Liberopoulos, George;
Manolio, Teri;
Ioannidis, John

Publication type:

Article

Association of PDE4B polymorphisms and schizophrenia in Northwestern Han Chinese.

Published in:

Human Genetics, 2012, v. 131, n. 7, p. 1047, doi. 10.1007/s00439-011-1120-8

By:

Guan, Fanglin;
Zhang, Chen;
Wei, Shuguang;
Zhang, Hongbo;
Gong, Xiaomin;
Feng, Jiali;
Gao, Chengge;
Su, Rong;
Yang, Huanming;
Li, Shengbin

Publication type:

Article

Altered patterns of multiple recombinant events are associated with nondisjunction of chromosome 21.

Published in:

Human Genetics, 2012, v. 131, n. 7, p. 1039, doi. 10.1007/s00439-011-1121-7

By:

Oliver, Tiffany;
Tinker, Stuart;
Allen, Emily;
Hollis, Natasha;
Locke, Adam;
Bean, Lora;
Chowdhury, Reshmi;
Begum, Ferdouse;
Marazita, Mary;
Cheung, Vivian;
Feingold, Eleanor;
Sherman, Stephanie

Publication type:

Article