| | Title | Authors / Editors | Date |
|
unige:159327 |
Genetic Predictors for Sinusoidal Obstruction Syndrome - A Systematic Review |
Waespe, Nicolas; Strebel, Sven; Mlakar, Simona; Krajinovic, Maja; ... Ansari Djaberi, Marc Georges |
2021 |
|
unige:159449 |
Usefulness of current candidate genetic markers to identify childhood cancer patients at risk for platinum-induced ototoxicity: Results of the European PanCareLIFE cohort study |
Langer, Thorsten; Clemens, Eva; Broer, Linda; Maier, Lara; ... Zolk, Oliver |
2020 |
|
unige:138509 |
Next Generation Sequencing Analysis in Early Onset Dementia Patients |
Bonvicini, Cristian; Scassellati, Catia; Benussi, Luisa; Di Maria, Emilio; ... Gennarelli, Massimo |
2019 |
|
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:138252 |
Gene-diet interactions associated with complex trait variation in an advanced intercross outbred mouse line |
Vorobyev, Artem; Gupta, Yask; Sezin, Tanya; Koga, Hiroshi; ... Ludwig, Ralf J |
2019 |
|
unige:116068 |
Rare nonsynonymous variants in SORT1 are associated with increased risk for frontotemporal dementia |
BELNEU Consortium, EU EOD Consortium |
2018 |
|
unige:116553 |
Genome-wide and candidate gene approaches of clopidogrel efficacy using pharmacodynamic and clinical end points-Rationale and design of the International Clopidogrel Pharmacogenomics Consortium (ICPC) |
International Clopidogrel Pharmacogenomics Consortium |
2018 |
|
unige:107726 |
Clinical spectrum and genotype-phenotype associations of KCNA2-related encephalopathies |
Masnada, Silvia; Hedrich, Ulrike B S; Gardella, Elena; Korff, Christian; ... Rubboli, Guido |
2017 |
|
unige:111388 |
Pharmacogenetics of antidepressant response: A polygenic approach |
Major Depressive DisorderWorking Group of the Psychiatric Genomic Consortium1 |
2017 |
|
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:88476 |
Excess maternal transmission of variants in the THADA gene to offspring with type 2 diabetes |
Prasad, Rashmi B; Lessmark, Anna; Almgren, Peter; Kovacs, Györgyi; ... Groop, Leif |
2016 |
|
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:161988 |
Novel carboxypeptidase A6 (CPA6) mutations identified in patients with juvenile myoclonic and generalized epilepsy |
Sapio, Matthew R; Vessaz, Monique; Thomas, Pierre; Genton, Pierre; ... Salzmann, Annick |
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:90264 |
Allelic mapping bias in RNA-sequencing is not a major confounder in eQTL studies |
Panousis, Nikolaos; Gutierrez Arcelus, Maria; Dermitzakis, Emmanouil; Lappalainen, Tuuli Emilia |
2014 |
|
unige:90266 |
Cis and trans effects of human genomic variants on gene expression |
Bryois, Julien; Buil Demur, Alfonso Alberto; Evans, David M; Kemp, John P; ... Dermitzakis, Emmanouil |
2014 |
|
unige:55178 |
EXOSC3 mutations in pontocerebellar hypoplasia type 1: novel mutations and genotype-phenotype correlations |
Eggens, Veerle Rc; Barth, Peter G; Niermeijer, Jikke-Mien F; Berg, Jonathan N; ... Baas, Frank |
2014 |
|
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:32170 |
Analysis of case-control association studies with known risk variants |
Zaitlen, Noah; Pasaniuc, Bogdan; Patterson, Nick; Pollack, Samuela; ... Price, Alkes L |
2012 |
Genetic association studies
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