| | Title | Authors / Editors | Date |
|
unige:160626 |
APOE2, E3, and E4 differentially modulate cellular homeostasis, cholesterol metabolism, and inflammatory response in isogenic iPSC-derived astrocytes |
de Leeuw, Sherida M; Kirschner, Aron W T; Lindner, Karina; Rust, Ruslan; ... Tackenberg, Christian |
2022 |
|
unige:156394 |
Analysis of biological models to predict clinical outcomes based on HLA-DPB1 disparities in unrelated transplantation |
Buhler, Stéphane; Baldomero, Helen; Ferrari-Lacraz, Sylvie; Mamez, Anne-Claire; ... Villard, Jean |
2021 |
|
unige:156393 |
Characterization of the novel HLA-B*15:514 allele in a French hematopoietic stem cell donor |
Dard, Céline; Senoussi, Ornella; Buhler, Stéphane; Bardy, Béatrice; Masson, Dominique |
2020 |
|
unige:150378 |
Determinants of mesial temporal lobe volume loss in older individuals with preserved cognition: a longitudinal PET amyloid study |
Montandon Zaidi, Marie-Louise; Herrmann, François; Garibotto, Valentina; Rodriguez, Cristelle; ... Giannakopoulos, Panteleimon |
2020 |
|
unige:144661 |
Expression estimation and eQTL mapping for HLA genes with a personalized pipeline |
Aguiar, Vitor; César, Jônatas; Delaneau, Olivier; Dermitzakis, Emmanouil; Meyer, Diogo |
2019 |
|
unige:145465 |
RINT1 Bi-allelic variations cause infantile-onset recurrent acute liver failure and skeletal abnormalities |
Cousin, Margot A; Conboy, Erin; Wang, Jian-She; Lenz, Dominic; ... Klee, Eric W |
2019 |
|
unige:143934 |
Clinical and biological features of PTPN2-deleted adult and pediatric T-cell acute lymphoblastic leukemia |
Alcantara, Marion; Simonin, Mathieu; Lhermitte, Ludovic; Touzart, Aurore; ... Asnafi, Vahid |
2019 |
|
unige:138509 |
Next Generation Sequencing Analysis in Early Onset Dementia Patients |
Bonvicini, Cristian; Scassellati, Catia; Benussi, Luisa; Di Maria, Emilio; ... Gennarelli, Massimo |
2019 |
|
unige:146823 |
Duration of preclinical, prodromal, and dementia stages of Alzheimer's disease in relation to age, sex, and APOE genotype |
Vermunt, Lisa; Sikkes, Sietske A M; van den Hout, Ardo; Handels, Ron; ... Visser, Pieter Jelle |
2019 |
|
unige:128592 |
A new mutation in the C-terminal end of TTC37 leading to a mild form of syndromic diarrhea/tricho-hepato-enteric syndrome in seven patients from two families |
Fabre, Alexandre; Petit, Laëtitia Marie; Hansen, Lars F; Wewer, Anne V; ... Paerregaard, Anders |
2018 |
|
unige:145582 |
Identification of seven novel HLA class I and II alleles |
Ferrari-Lacraz, Sylvie; Masson, Dominique; Villard, Jean; Buhler, Stéphane |
2018 |
|
unige:128591 |
Genetic polymorphisms associated with smoking behaviour predict the risk of surgery in patients with Crohn's disease |
Lang, B M; Biedermann, L; van Haaften, W T; de Vallière, C; ... Misselwitz, B |
2018 |
|
unige:115121 |
Mutational epidemiology of congenital fibrinogen disorders |
Casini, Alessandro; Blondon, Marc; Tintillier, Veronique; Goodyer, Matthew; ... Neerman Arbez, Marguerite |
2018 |
|
unige:124464 |
Molecular characterization of Treponema pallidum subsp. pallidum in Switzerland and France with a new multilocus sequence typing scheme |
Grillová, Linda; Bawa, Tanika; Mikalová, Lenka; Gayet-Ageron, Angèle; ... Bosshard, Philipp P |
2018 |
|
unige:160563 |
Cas9-mediated allelic exchange repairs compound heterozygous recessive mutations in mice |
Wang, Dan; Li, Jia; Song, Chun-Qing; Tran, Karen; ... Gao, Guangping |
2018 |
|
unige:112784 |
Genetic effects on gene expression across human tissues |
GTEx Consortium |
2017 |
|
unige:111193 |
The forensic use of behavioral genetics in criminal proceedings: Case of the MAOA-L genotype |
McSwiggan, Sally; Elger, Bernice Simone; Appelbaum, Paul S |
2017 |
|
unige:107719 |
Inborn errors in RNA polymerase III underlie severe varicella zoster virus infections |
Ogunjimi, Benson; Zhang, Shen-Ying; Sørensen, Katrine B; Fluss, Joel Victor; ... Mogensen, Trine H |
2017 |
|
unige:144215 |
Precision and prognostic value of clone-specific minimal residual disease in acute myeloid leukemia |
Hirsch, Pierre; Tang, Ruoping; Abermil, Nassera; Flandrin, Pascale; ... Delhommeau, François |
2017 |
|
unige:128976 |
Genetic invalidation of Lp-PLA2 as a therapeutic target: Large-scale study of five functional Lp-PLA2-lowering alleles |
EPIC-CVD consortium and the CHD Exome+ consortium |
2017 |
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