| Title | Authors / Editors | Date |
unige:45219 |
A map of human genome variation from population-scale sequencing |
1000 Genomes Project Consortium |
2010 |
unige:32728 |
A novel frameshift mutation in FGA (c.1846 del A) leading to congenital afibrinogenemia in a consanguineous Syrian family |
Levrat, Emmanuel; Aboukhamis, Imad; De Moerloose, Philippe; Farho, Jaafar; ... Neerman Arbez, Marguerite |
2011 |
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:21098 |
ADME pharmacogenetics: investigation of the pharmacokinetics of the antiretroviral agent lopinavir coformulated with ritonavir |
Lubomirov, Rubin; di Iulio, J.; Fayet, A.; Colombo, Sara; ... Telenti, A. |
2010 |
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:32170 |
Analysis of case-control association studies with known risk variants |
Zaitlen, Noah; Pasaniuc, Bogdan; Patterson, Nick; Pollack, Samuela; ... Price, Alkes L |
2012 |
unige:25737 |
Association of a common vitamin D-binding protein polymorphism with inflammatory bowel disease |
Eloranta, Jyrki J; Wenger, Christa; Mwinyi, Jessica; Hiller, Christian; ... Kullak-Ublick, Gerd A |
2011 |
unige:21036 |
Association of AKT1 gene variants and protein expression in both schizophrenia and bipolar disorder |
Karege, Félicien; Perroud, Nader Ali; Schurhoff, F.; Meary, A.; ... Malafosse, Alain |
2010 |
unige:21005 |
Association of STR polymorphisms in CMA1 and IL-4 with asthma and atopy: the SAPALDIA cohort |
Hersberger, Martin; Thun, Gian-Andri; Imboden, Medea; Brandstatter, Anita; ... Probst-Hensch, Nicole |
2010 |
unige:21077 |
BRD2 and TAP-1 genes and juvenile myoclonic epilepsy |
Layouni, Samia; Buresi, Catherine; Thomas, Pierre; Malafosse, Alain; Dogui, Mohamed |
2010 |
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:24045 |
Clinical and genetic correlates of suicidal ideation during antidepressant treatment in a depressed outpatient sample |
Perroud, Nader Ali; Bondolfi, Guido; Uher, Rudolf; Gex-Fabry, Marianne; ... Kosel, Markus Mathaus |
2011 |
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:34655 |
Duplications of BHLHA9 are associated with ectrodactyly and tibia hemimelia inherited in non-Mendelian fashion |
Klopocki, Eva; Lohan, Silke; Doelken, Sandra C; Stricker, Sigmar; ... Mundlos, Stefan |
2012 |
unige:32175 |
Epigenome-wide scans identify differentially methylated regions for age and age-related phenotypes in a healthy ageing population |
Bell, Jordana T; Tsai, Pei-Chien; Yang, Tsun-Po; Pidsley, Ruth; ... Deloukas, Panos |
2012 |
unige:21124 |
European collaborative study of early-onset bipolar disorder: Evidence for genetic heterogeneity on 2q14 according to age at onset |
Mathieu, Flavie; Dizier, Marie-Helene; Etain, Bruno; Jamain, Stephane; ... Bellivier, Frank |
2010 |
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: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: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:159327 |
Genetic Predictors for Sinusoidal Obstruction Syndrome - A Systematic Review |
Waespe, Nicolas; Strebel, Sven; Mlakar, Simona; Krajinovic, Maja; ... Ansari Djaberi, Marc Georges |
2021 |