Works matching IS 03406717 AND DT 2013 AND VI 132 AND IP 1

Results: 12

Association between TNFRSF11B gene polymorphisms and history of ischemic stroke in Italian diabetic patients.

Published in:

Human Genetics, 2013, v. 132, n. 1, p. 49, doi. 10.1007/s00439-012-1224-9

By:

Biscetti, Federico;
Straface, Giuseppe;
Giovannini, Silvia;
Santoliquido, Angelo;
Angelini, Flavia;
Santoro, Luca;
Porreca, Carlo;
Pecorini, Giovanni;
Ghirlanda, Giovanni;
Flex, Andrea

Publication type:

Article

HOXB13 is a susceptibility gene for prostate cancer: results from the International Consortium for Prostate Cancer Genetics (ICPCG).

Published in:

Human Genetics, 2013, v. 132, n. 1, p. 5, doi. 10.1007/s00439-012-1229-4

By:

Xu, Jianfeng;
Lange, Ethan;
Lu, Lingyi;
Zheng, Siqun;
Wang, Zhong;
Thibodeau, Stephen;
Cannon-Albright, Lisa;
Teerlink, Craig;
Camp, Nicola;
Johnson, Anna;
Zuhlke, Kimberly;
Stanford, Janet;
Ostrander, Elaine;
Wiley, Kathleen;
Isaacs, Sarah;
Walsh, Patrick;
Maier, Christiane;
Luedeke, Manuel;
Vogel, Walther;
Schleutker, Johanna

Publication type:

Article

Leon E. Rosenberg and Diane Drobnis Rosenberg: Human Genes and Genomes: Science, Health, Society.

Published in:

2013

By:

Kamath, Arveen

Publication type:

Book Review

Novel association of a PROC variant with ischemic stroke in a Chinese Han population.

Published in:

Human Genetics, 2013, v. 132, n. 1, p. 69, doi. 10.1007/s00439-012-1225-8

By:

Lu, Xuan;
Tang, Liang;
Xu, Kang;
Ma, Jie;
Guo, Tao;
Mei, Heng;
Yang, Rui;
Yu, Jianming;
Wang, Qingyun;
Yang, Yan;
Jian, Xiaorong;
Hu, Yu

Publication type:

Article

A Bayesian ensemble approach with a disease gene network predicts damaging effects of missense variants of human cancers.

Published in:

Human Genetics, 2013, v. 132, n. 1, p. 15, doi. 10.1007/s00439-012-1218-7

By:

Won, Hong-Hee;
Kim, Jong-Won;
Lee, Doheon

Publication type:

Article

VKORC1 rs2359612C allele is associated with increased risk of coronary artery disease in the presence of coronary calcification.

Published in:

Human Genetics, 2013, v. 132, n. 1, p. 29, doi. 10.1007/s00439-012-1222-y

By:

Wang, Yibo;
Chen, Jinxing;
Zhang, Yu;
Bin, Lv;
Sun, Kai;
Yu, Weifeng;
Liu, Jibin;
Zhang, Channa;
Shen, Haiqing;
Hou, Zhihui;
Yu, Fangfang;
Hui, Rutai

Publication type:

Article

Linkage disequilibrium pattern and age-at-diagnosis are critical for replicating genetic associations across ethnic groups in leprosy.

Published in:

Human Genetics, 2013, v. 132, n. 1, p. 107, doi. 10.1007/s00439-012-1227-6

By:

Alter, Andrea;
Fava, Vinicius;
Huong, Nguyen;
Singh, Meenakshi;
Orlova, Marianna;
Thuc, Nguyen;
Katoch, Kiran;
Thai, Vu;
Ba, Nguyen;
Abel, Laurent;
Mehra, Narinder;
Alcaïs, Alexandre;
Schurr, Erwin

Publication type:

Article

A genome-wide association study of breast cancer in women of African ancestry.

Published in:

Human Genetics, 2013, v. 132, n. 1, p. 39, doi. 10.1007/s00439-012-1214-y

By:

Chen, Fang;
Chen, Gary;
Stram, Daniel;
Millikan, Robert;
Ambrosone, Christine;
John, Esther;
Bernstein, Leslie;
Zheng, Wei;
Palmer, Julie;
Hu, Jennifer;
Rebbeck, Tim;
Ziegler, Regina;
Nyante, Sarah;
Bandera, Elisa;
Ingles, Sue;
Press, Michael;
Ruiz-Narvaez, Edward;
Deming, Sandra;
Rodriguez-Gil, Jorge;
DeMichele, Angela

Publication type:

Article

Characterization of CCDC28B reveals its role in ciliogenesis and provides insight to understand its modifier effect on Bardet-Biedl syndrome.

Published in:

Human Genetics, 2013, v. 132, n. 1, p. 91, doi. 10.1007/s00439-012-1228-5

By:

Cardenas-Rodriguez, Magdalena;
Osborn, Daniel;
Irigoín, Florencia;
Graña, Martín;
Romero, Héctor;
Beales, Philip;
Badano, Jose

Publication type:

Article

Genome-wide study identifies two loci associated with lung function decline in mild to moderate COPD.

Published in:

Human Genetics, 2013, v. 132, n. 1, p. 79, doi. 10.1007/s00439-012-1219-6

By:

Hansel, Nadia;
Ruczinski, Ingo;
Rafaels, Nicholas;
Sin, Don;
Daley, Denise;
Malinina, Alla;
Huang, Lili;
Sandford, Andrew;
Murray, Tanda;
Kim, Yoonhee;
Vergara, Candelaria;
Heckbert, Susan;
Psaty, Bruce;
Li, Guo;
Elliott, W.;
Aminuddin, Farzian;
Dupuis, Josée;
O'Connor, George;
Doheny, Kimberly;
Scott, Alan

Publication type:

Article

Familial prostate cancer and HOXB13 founder mutations: geographic and racial/ethnic variations.

Published in:

2013

By:

Lynch, Henry;
Shaw, Trudy

Publication type:

Letter

Investigation of genetic risk factors for chronic adult diseases for association with preterm birth.

Published in:

Human Genetics, 2013, v. 132, n. 1, p. 57, doi. 10.1007/s00439-012-1223-x

By:

Falah, Nadia;
McElroy, Jude;
Snegovskikh, Victoria;
Lockwood, Charles;
Norwitz, Errol;
Murray, Jeffey;
Kuczynski, Edward;
Menon, Ramkumar;
Teramo, Kari;
Muglia, Louis;
Morgan, Thomas

Publication type:

Article