nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Genetic determinants of mortality. Can findings from genome-wide association studies explain variation in human mortality?
|
Ganna, Andrea |
|
2013 |
132 |
5 |
p. 553-561 |
artikel |
2 |
Genetic variants associated with breast cancer risk for Ashkenazi Jewish women with strong family histories but no identifiable BRCA1/2 mutation
|
Rinella, Erica S. |
|
2013 |
132 |
5 |
p. 523-536 |
artikel |
3 |
Haploinsufficiency of KDM6A is associated with severe psychomotor retardation, global growth restriction, seizures and cleft palate
|
Lindgren, Amelia M. |
|
|
132 |
5 |
p. 537-552 |
artikel |
4 |
Haploinsufficiency of KDM6A is associated with severe psychomotor retardation, global growth restriction, seizures and cleft palate
|
Lindgren, Amelia M. |
|
2013 |
132 |
5 |
p. 537-552 |
artikel |
5 |
Hierarchical modeling identifies novel lung cancer susceptibility variants in inflammation pathways among 10,140 cases and 11,012 controls
|
Brenner, Darren R. |
|
2013 |
132 |
5 |
p. 579-589 |
artikel |
6 |
Human loci involved in drug biotransformation: worldwide genetic variation, population structure, and pharmacogenetic implications
|
Maisano Delser, Pierpaolo |
|
2013 |
132 |
5 |
p. 563-577 |
artikel |
7 |
Imputation across genotyping arrays for genome-wide association studies: assessment of bias and a correction strategy
|
Johnson, Eric O. |
|
2013 |
132 |
5 |
p. 509-522 |
artikel |
8 |
RET and NRG1 interplay in Hirschsprung disease
|
Gui, Hongsheng |
|
2013 |
132 |
5 |
p. 591-600 |
artikel |
9 |
Silencing human genetic diseases with oligonucleotide-based therapies
|
MartÃnez, Tamara |
|
2013 |
132 |
5 |
p. 481-493 |
artikel |
10 |
Systematic identification of interaction effects between genome- and environment-wide associations in type 2 diabetes mellitus
|
Patel, Chirag J. |
|
2013 |
132 |
5 |
p. 495-508 |
artikel |
11 |
Telling genes: the story of genetic counseling in America
|
Skirton, Heather |
|
2013 |
132 |
5 |
p. 601 |
artikel |