| | Title | Authors / Editors | Date |
|
unige:26176 |
GSTP1 hypermethylation is associated with reduced protein expression, aggressive disease and prognosis in neuroblastoma |
Gumy-Pause, Fabienne; Pardo, Bruno; Khoshbeen-Boudal, Mary; Ansari, Marc; ... Ozsahin, Ayse Hulya |
2012 |
|
unige:145129 |
Identification of regulatory variants associated with genetic susceptibility to meningococcal disease |
Borghini, Lisa; Png, Eileen; Binder, Alexander; Wright, Victoria J; ... Davila, Sonia |
2019 |
|
unige:108546 |
Impact of CD14 Polymorphisms on Anti-Apolipoprotein A-1 IgG-Related Coronary Artery Disease Prediction in the General Population |
Antiochos, Panagiotis; Marques-Vidal, Pedro; Virzi, Julien; Pagano, Sabrina; ... Vuilleumier, Nicolas |
2017 |
|
unige:19536 |
Inferior vena cava agenesis: Association with bilateral lower-limb deep vein thrombosis in young males |
Guanella, Raphaël; Glauser, Frédéric; Bounameaux, Henri; Mazzolai, Lucia |
2009 |
|
unige:138509 |
Next Generation Sequencing Analysis in Early Onset Dementia Patients |
Bonvicini, Cristian; Scassellati, Catia; Benussi, Luisa; Di Maria, Emilio; ... Gennarelli, Massimo |
2019 |
|
unige:111388 |
Pharmacogenetics of antidepressant response: A polygenic approach |
Major Depressive DisorderWorking Group of the Psychiatric Genomic Consortium1 |
2017 |
|
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:116068 |
Rare nonsynonymous variants in SORT1 are associated with increased risk for frontotemporal dementia |
BELNEU Consortium, EU EOD Consortium |
2018 |
|
unige:25698 |
Replication of association between a SCN1A splice variant and febrile seizures |
Le Gal, François; Trachsler-Salzmann, Annick; Crespel, Arielle; Malafosse, Alain |
2011 |
|
unige:45252 |
Serum iron levels and the risk of Parkinson disease: a Mendelian randomization study |
Pichler, Irene; Del Greco M, Fabiola; Gögele, Martin; Lill, Christina M; ... Pramstaller, Peter |
2013 |
|
unige:32743 |
SNPs and other features as they predispose to complex disease: genome-wide predictive analysis of a quantitative phenotype for hypertension |
Won, Joong-Ho; Ehret, Georg Benedikt; Chakravarti, Aravinda; Olshen, Richard A |
2011 |
|
unige:89654 |
Synchronized age-related gene expression changes across multiple tissues in human and the link to complex diseases |
Yang, Jialiang; Huang, Tao; Petralia, Francesca; Long, Quan; ... Mobbs, Charles V |
2015 |
|
unige:74422 |
The IFNL3/4 ΔG variant increases susceptibility to cytomegalovirus retinitis among HIV-infected patients |
Bibert, Stéphanie; Wojtowicz, Agnieszka; Taffe, Patrick; Manuel, Oriol; ... Bochud, Pierre-Yves |
2014 |
|
unige:102919 |
The relevance of HLA sequencing in population genetics studies |
Sanchez-Mazas, Alicia; Meyer, Diogo |
2014 |
|
unige:32729 |
Two different fibrinogen gene mutations associated with bleeding in the same family (A αGly13Glu and γGly16Ser) and their impact on fibrin clot properties: fibrinogen Krakow II and Krakow III. |
Pietrys, Danuta; Balwierz, Walentyna; Iwaniec, Teresa; Vorjohann, Silja; ... Undas, Anetta |
2011 |
Genetic association studies
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