| Title | Authors / Editors | Date |
unige:7534 |
Genetic variation in IL28B is associated with chronic hepatitis C and treatment failure: a genome-wide association study |
Rauch, Andri; Kutalik, Zoltan; Descombes, Patrick; Cai, Tao; ... Bochud, Pierre-Yves |
2010 |
unige:9214 |
In vitro whole-genome analysis identifies a susceptibility locus for HIV-1 |
Loeuillet, Corinne; Deutsch, Samuel; Ciuffi, Angela; Robyr, Daniel; ... Telenti, Amalio |
2008 |
unige:8630 |
CNVs and genetic medicine (excitement and consequences of a rediscovery) |
Beckmann, J. S.; Sharp, A. J.; Antonarakis, Stylianos |
2008 |
unige:8884 |
Subtelomeric 6p deletion: clinical and array-CGH characterization in two patients |
Martinet, Danielle; Filges, Isabel; Besuchet Schmutz, Nathalie; Morris, Michael Andréw; ... Bena, Frédérique |
2008 |
unige:7088 |
Contribution of 20 single nucleotide polymorphisms of 13 genes to dyslipidemia associated with antiretroviral therapy |
Arnedo, Mireia; Taffe, Patrick; Sahli, Roland; Furrer, Hansjakob; ... Tarr, P. E. |
2007 |
unige:8629 |
Copy number variants and genetic traits: closer to the resolution of phenotypic to genotypic variability |
Beckmann, J. S.; Estivill, Xavier; Antonarakis, Stylianos |
2007 |
unige:8864 |
Promoter polymorphisms and allelic imbalance in ABCB1 expression |
Loeuillet, Corinne; Weale, Michael; Deutsch, Samuel; Rotger, Margalida; ... Telenti, Amalio |
2007 |
unige:8604 |
Mendelian disorders deserve more attention |
Antonarakis, Stylianos; Beckmann, J. S. |
2006 |