Show items per page
Elements: 35
Page 2 on 2
 TitleAuthors / EditorsDate
add to browser selection
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
add to browser selection
Identification of regulatory variants associated with genetic susceptibility to meningococcal disease Borghini, Lisa; Png, Eileen; Binder, Alexander; Wright, Victoria J; ... Davila, Sonia 2019
add to browser selection
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
add to browser selection
Inferior vena cava agenesis: Association with bilateral lower-limb deep vein thrombosis in young males Guanella, Raphaël; Glauser, Frédéric; Bounameaux, Henri; Mazzolai, Lucia 2009
add to browser selection
Next Generation Sequencing Analysis in Early Onset Dementia Patients Bonvicini, Cristian; Scassellati, Catia; Benussi, Luisa; Di Maria, Emilio; ... Gennarelli, Massimo 2019
add to browser selection
Pharmacogenetics of antidepressant response: A polygenic approach Major Depressive DisorderWorking Group of the Psychiatric Genomic Consortium1 2017
add to browser selection
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
add to browser selection
Rare nonsynonymous variants in SORT1 are associated with increased risk for frontotemporal dementia BELNEU Consortium, EU EOD Consortium 2018
add to browser selection
Replication of association between a SCN1A splice variant and febrile seizures Le Gal, François; Trachsler-Salzmann, Annick; Crespel, Arielle; Malafosse, Alain 2011
add to browser selection
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
add to browser selection
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
add to browser selection
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
add to browser selection
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
add to browser selection
The relevance of HLA sequencing in population genetics studies Sanchez-Mazas, Alicia; Meyer, Diogo 2014
add to browser selection
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
| 1 | 2 | next >>