| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
An emerging role for microRNAs in NF1 tumorigenesis
|
Sedani, Ashni
|
|
2012
|
6 |
1 |
|
artikel
|
| 2 |
A new era in the discovery of de novo mutations underlying human genetic disease
|
Ku, Chee-Seng
|
|
2012
|
6 |
1 |
|
artikel
|
| 3 |
A new home for Human Genomics
|
Vasiliou, Vasilis
|
|
2012
|
6 |
1 |
|
artikel
|
| 4 |
Association of genome variations in the renin-angiotensin system with physical performance
|
Sgourou, Argyro
|
|
2012
|
6 |
1 |
|
artikel
|
| 5 |
Collaborative software for traditional and translational research
|
Berman, Ari E
|
|
2012
|
6 |
1 |
|
artikel
|
| 6 |
Conservation of the three-dimensional structure in non-homologous or unrelated proteins
|
Sousounis, Konstantinos
|
|
2012
|
6 |
1 |
|
artikel
|
| 7 |
CXCL5 polymorphisms are associated with variable blood pressure in cardiovascular disease-free adults
|
Beitelshees, Amber L
|
|
2012
|
6 |
1 |
|
artikel
|
| 8 |
Estimating ancestral proportions in a multi-ethnic US sample: implications for studies of admixed populations
|
Levran, Orna
|
|
2012
|
6 |
1 |
|
artikel
|
| 9 |
Gene family matters: expanding the HGNC resource
|
Daugherty, Louise C
|
|
2012
|
6 |
1 |
|
artikel
|
| 10 |
Genetic mechanisms and age-related macular degeneration: common variants, rare variants, copy number variations, epigenetics, and mitochondrial genetics
|
Liu, Melissa M
|
|
2012
|
6 |
1 |
|
artikel
|
| 11 |
Genotype-phenotype associations in neurofibromatosis type 1 (NF1): an increased risk of tumor complications in patients with NF1 splice-site mutations?
|
Alkindy, Adila
|
|
2012
|
6 |
1 |
|
artikel
|
| 12 |
GWIDD: a comprehensive resource for genome-wide structural modeling of protein-protein interactions
|
Kundrotas, Petras J
|
|
2012
|
6 |
1 |
|
artikel
|
| 13 |
Identification of functional DNA variants in the constitutive promoter region of MDM2
|
Lalonde, Marie-Eve
|
|
2012
|
6 |
1 |
|
artikel
|
| 14 |
Local sequence determinants of two in-frame triplet deletion/duplication hotspots in the RHD/RHCE genes
|
Chen, Jian-Min
|
|
2012
|
6 |
1 |
|
artikel
|
| 15 |
Mitochondrial and nuclear genomics and the emergence of personalized medicine
|
Parr, Ryan L
|
|
2012
|
6 |
1 |
|
artikel
|
| 16 |
Molecular heterogeneity in malignant peripheral nerve sheath tumors associated with neurofibromatosis type 1
|
Thomas, Laura
|
|
2012
|
6 |
1 |
|
artikel
|
| 17 |
Patterns of gene expression in microarrays and expressed sequence tags from normal and cataractous lenses
|
Sousounis, Konstantinos
|
|
2012
|
6 |
1 |
|
artikel
|
| 18 |
Pseudoexfoliation syndrome, a systemic disorder with ocular manifestations
|
Elhawy, Eman
|
|
2012
|
6 |
1 |
|
artikel
|
| 19 |
Review of “Molecules that Changed the World” by KC Nikolaou and T Montagnon
|
Tsonis, Panagiotis A
|
|
2012
|
6 |
1 |
|
artikel
|
| 20 |
‘Sifting the significance from the data’ - the impact of high-throughput genomic technologies on human genetics and health care
|
Clarke, Angus J
|
|
2012
|
6 |
1 |
|
artikel
|
| 21 |
SNPTrackTM : an integrated bioinformatics system for genetic association studies
|
Xu, Joshua
|
|
2012
|
6 |
1 |
|
artikel
|
| 22 |
Strong interaction between T allele of endothelial nitric oxide synthase with B1 allele of cholesteryl ester transfer protein TaqIB highly elevates the risk of coronary artery disease and type 2 diabetes mellitus
|
Rahimi, Zohreh
|
|
2012
|
6 |
1 |
|
artikel
|
| 23 |
16th Carbonyl Metabolism Meeting: from enzymology to genomics
|
Maser, Edmund
|
|
2012
|
6 |
1 |
|
artikel
|
| 24 |
The human crystallin gene families
|
Wistow, Graeme
|
|
2012
|
6 |
1 |
|
artikel
|
| 25 |
The human protein disulfide isomerase gene family
|
Galligan, James J
|
|
2012
|
6 |
1 |
|
artikel
|
| 26 |
6th Golden Helix Pharmacogenomics Day: pharmacogenomics and individualized therapy
|
Stojiljkovic, Maja
|
|
2012
|
6 |
1 |
|
artikel
|
| 27 |
Usability survey of biomedical question answering systems
|
Bauer, Michael A
|
|
2012
|
6 |
1 |
|
artikel
|
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