| | Title | Authors / Editors | Date |
|
unige:34666 |
Rapid detection of genetic variants in hypertrophic cardiomyopathy by custom DNA resequencing array in clinical practice |
Fokstuen, Siv; Munoz, Analia; Melacini, Paola; Iliceto, Sabino; ... Blouin, Jean-Louis |
2011 |
|
unige:45209 |
A two-stage meta-analysis identifies several new loci for Parkinson's disease |
French Parkinson's Disease Genetics Study Group |
2011 |
|
unige:45211 |
Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies |
Nalls, Michael A; Plagnol, Vincent; Hernandez, Dena G; Sharma, Manu; ... Wood, Nicholas W |
2011 |
|
unige:45235 |
Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case-control study |
Ross, Owen A |
2011 |
|
unige:45244 |
A large-scale genetic association study to evaluate the contribution of Omi/HtrA2 (PARK13) to Parkinson's disease |
Krüger, Rejko; Sharma, Manu |
2011 |
|
unige:28410 |
Consistency between cross-sectional and longitudinal SNP: blood lipid associations |
Costanza, Michael C; Beer-Borst, Sigrid; James, Richard William; Gaspoz, Jean-Michel; Morabia, Alfredo |
2012 |
|
unige:31211 |
Polymorphism in multidrug resistance-associated protein gene 3 is associated with outcomes in childhood acute lymphoblastic leukemia |
Ansari Djaberi, Marc Georges; Sauty, G; Labuda, M; Gagné, V; ... Krajinovic, M |
2012 |
|
unige:27166 |
A genetic validation study reveals a role of vitamin D metabolism in the response to interferon-alfa-based therapy of chronic hepatitis C. |
Lange, Christian M; Bibert, Stéphanie; Kutalik, Zoltan; Burgisser, Philippe; ... Moradpour, Darius |
2012 |
|
unige:26871 |
A predictive clinical-genetic model of tissue plasminogen activator response in acute ischemic stroke |
del Río-Espínola, Alberto; Fernández-Cadenas, Israel; Giralt, Dolors; Quiroga, Adoracion; ... Montaner, Joan |
2012 |
|
unige:45205 |
Identification of VPS35 mutations replicated in French families with Parkinson disease |
Lesage, S; Condroyer, C; Klebe, S; Honoré, A; ... Brice, A |
2012 |
|
unige:45216 |
An integrated map of genetic variation from 1,092 human genomes |
1000 Genomes Project Consortium |
2012 |
|
unige:37818 |
An integrated encyclopedia of DNA elements in the human genome |
ENCODE Project Consortium |
2012 |
|
unige:33603 |
The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphism |
Klebe, Stephan; Golmard, Jean-Louis; Nalls, Michael A; Saad, Mohamad; ... Corvol, Jean-Christophe |
2013 |
|
unige:35220 |
First evidence of a polygenic susceptibility to pain in a pediatric cohort |
Mamie, Chantal; Rebsamen, Michela; Morris, Michael Andréw; Morabia, Alfredo |
2013 |
|
unige:34328 |
Transcriptome and genome sequencing uncovers functional variation in humans |
Lappalainen, Tuuli Emilia; Giger, Thomas; Padioleau, Ismael; Ongen, Halit; ... Dermitzakis, Emmanouil |
2013 |
|
unige:90281 |
Gene expression changes with age in skin, adipose tissue, blood and brain |
Glass, Daniel; Viñuela, Ana; Davies, Matthew N; Ramasamy, Adaikalavan; ... Spector, Tim D |
2013 |
|
unige:34640 |
Genetic characterization of northeastern Italian population isolates in the context of broader European genetic diversity |
Esko, Tõnu; Mezzavilla, Massimo; Nelis, Mari; Borel, Christelle; Antonarakis, Stylianos |
2013 |
|
unige:40637 |
Genome-wide association analysis of blood-pressure traits in African-ancestry individuals reveals common associated genes in African and non-African populations |
Franceschini, Nora |
2013 |
|
unige:43643 |
Hierarchical modeling identifies novel lung cancer susceptibility variants in inflammation pathways among 10,140 cases and 11,012 controls |
Brenner, Darren R; Brennan, Paul; Boffetta, Paolo; Amos, Christopher I; ... Hung, Rayjean J |
2013 |
|
unige:89750 |
Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration |
van der Zee, Julie |
2014 |
Polymorphism, single nucleotide/genetics
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