Works matching IS 03406717 AND DT 2013 AND VI 132 AND IP 5

Results: 10

Hierarchical modeling identifies novel lung cancer susceptibility variants in inflammation pathways among 10,140 cases and 11,012 controls.
Published in:
Human Genetics, 2013, v. 132, n. 5, p. 579, doi. 10.1007/s00439-013-1270-y
By:
- Brenner, Darren;
- Brennan, Paul;
- Boffetta, Paolo;
- Amos, Christopher;
- Spitz, Margaret;
- Chen, Chu;
- Goodman, Gary;
- Heinrich, Joachim;
- Bickeböller, Heike;
- Rosenberger, Albert;
- Risch, Angela;
- Muley, Thomas;
- McLaughlin, John;
- Benhamou, Simone;
- Bouchardy, Christine;
- Lewinger, Juan;
- Witte, John;
- Chen, Gary;
- Bull, Shelley;
- Hung, Rayjean
Publication type:
Article
Genetic variants associated with breast cancer risk for Ashkenazi Jewish women with strong family histories but no identifiable BRCA1/2 mutation.
Published in:
Human Genetics, 2013, v. 132, n. 5, p. 523, doi. 10.1007/s00439-013-1269-4
By:
- Rinella, Erica;
- Shao, Yongzhao;
- Yackowski, Lauren;
- Pramanik, Sreemanta;
- Oratz, Ruth;
- Schnabel, Freya;
- Guha, Saurav;
- LeDuc, Charles;
- Campbell, Christopher;
- Klugman, Susan;
- Terry, Mary;
- Senie, Ruby;
- Andrulis, Irene;
- Daly, Mary;
- John, Esther;
- Roses, Daniel;
- Chung, Wendy;
- Ostrer, Harry
Publication type:
Article
Telling genes: the story of genetic counseling in America.
Published in:
2013
By:
- Skirton, Heather
Publication type:
Book Review
Haploinsufficiency of KDM6A is associated with severe psychomotor retardation, global growth restriction, seizures and cleft palate.
Published in:
Human Genetics, 2013, v. 132, n. 5, p. 537, doi. 10.1007/s00439-013-1263-x
By:
- Lindgren, Amelia;
- Hoyos, Tatiana;
- Talkowski, Michael;
- Hanscom, Carrie;
- Blumenthal, Ian;
- Chiang, Colby;
- Ernst, Carl;
- Pereira, Shahrin;
- Ordulu, Zehra;
- Clericuzio, Carol;
- Drautz, Joanne;
- Rosenfeld, Jill;
- Shaffer, Lisa;
- Velsher, Lea;
- Pynn, Tania;
- Vermeesch, Joris;
- Harris, David;
- Gusella, James;
- Liao, Eric;
- Morton, Cynthia
Publication type:
Article
Genetic determinants of mortality. Can findings from genome-wide association studies explain variation in human mortality?
Published in:
Human Genetics, 2013, v. 132, n. 5, p. 553, doi. 10.1007/s00439-013-1267-6
By:
- Ganna, Andrea;
- Rivadeneira, Fernando;
- Hofman, Albert;
- Uitterlinden, André;
- Magnusson, Patrik;
- Pedersen, Nancy;
- Ingelsson, Erik;
- Tiemeier, Henning
Publication type:
Article
Human loci involved in drug biotransformation: worldwide genetic variation, population structure, and pharmacogenetic implications.
Published in:
Human Genetics, 2013, v. 132, n. 5, p. 563, doi. 10.1007/s00439-013-1268-5
By:
- Maisano Delser, Pierpaolo;
- Fuselli, Silvia
Publication type:
Article
Silencing human genetic diseases with oligonucleotide-based therapies.
Published in:
Human Genetics, 2013, v. 132, n. 5, p. 481, doi. 10.1007/s00439-013-1288-1
By:
- Martínez, Tamara;
- Wright, Natalia;
- López-Fraga, Marta;
- Jiménez, Ana;
- Pañeda, Covadonga
Publication type:
Article
Imputation across genotyping arrays for genome-wide association studies: assessment of bias and a correction strategy.
Published in:
Human Genetics, 2013, v. 132, n. 5, p. 509, doi. 10.1007/s00439-013-1266-7
By:
- Johnson, Eric;
- Hancock, Dana;
- Levy, Joshua;
- Gaddis, Nathan;
- Saccone, Nancy;
- Bierut, Laura;
- Page, Grier
Publication type:
Article
RET and NRG1 interplay in Hirschsprung disease.
Published in:
Human Genetics, 2013, v. 132, n. 5, p. 591, doi. 10.1007/s00439-013-1272-9
By:
- Gui, Hongsheng;
- Tang, Wai-Kiu;
- So, Man-Ting;
- Proitsi, Petroola;
- Sham, Pak;
- Tam, Paul;
- Sau-Wai Ngan, Elly;
- Cherny, Stacey;
- Garcia-Barceló, Maria-Mercè
Publication type:
Article
Systematic identification of interaction effects between genome- and environment-wide associations in type 2 diabetes mellitus.
Published in:
Human Genetics, 2013, v. 132, n. 5, p. 495, doi. 10.1007/s00439-012-1258-z
By:
- Patel, Chirag;
- Chen, Rong;
- Kodama, Keiichi;
- Ioannidis, John;
- Butte, Atul
Publication type:
Article