| | Title | Authors / Editors | Date |
|
unige:154099 |
Unmasking viral sequences by metagenomic next-generation sequencing in adult human blood samples during steroid-refractory/dependent graft-versus-host disease |
Zanella, Marie-Céline; Cordey, Samuel; Laubscher, Florian; Docquier, Mylene; ... Vu Cantero, Diem-Lan |
2021 |
|
unige:155090 |
Orthohantavirus Isolated in Reservoir Host Cells Displays Minimal Genetic Changes and Retains Wild-Type Infection Properties |
Strandin, Tomas; Smura, Teemu; Ahola, Paula; Aaltonen, Kirsi; ... Forbes, Kristian M |
2020 |
|
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:149432 |
Unbiased metagenomic next-generation sequencing of blood from hospitalized febrile children in Gabon |
Fernandes, José Francisco; Laubscher, Florian; Held, Jana; Eckerle, Isabella Anne; ... Cordey, Samuel |
2020 |
|
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:132957 |
High-throughput sequencing for the aetiologic identification of viral encephalitis, meningoencephalitis, and meningitis. A narrative review and clinical appraisal |
Zanella, Marie-Céline; Lenggenhager, Lauriane; Schrenzel, Jacques; Cordey, Samuel; Kaiser, Laurent |
2019 |
|
unige:146004 |
The spectrum of intermediate SCN8A-related epilepsy |
Johannesen, Katrine M; Gardella, Elena; Encinas, Alejandra C; Lehesjoki, Anna-Elina; ... Møller, Rikke S |
2019 |
|
unige:146396 |
Are we approaching the end of pediatric culture-negative osteoarticular infections? |
Ceroni, Dimitri; Dayer, Romain Olivier Pierre; Steiger, Christina |
2019 |
|
unige:157595 |
Sequencing and analysis of globally obtained human parainfluenza viruses 1 and 3 genomes |
Bose, Michael E; Shrivastava, Susmita; He, Jie; Nelson, Martha I; ... Henrickson, Kelly J |
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:144668 |
Accurate, scalable and integrative haplotype estimation |
Delaneau, Olivier; Zagury, Jean-François; Robinson, Matthew R; Marchini, Jonathan L; Dermitzakis, Emmanouil |
2019 |
|
unige:126802 |
Handicap intellectuel : apport de la génétique pour le diagnostic étiologique |
Jouan, Chrystel; Kosel, Markus Mathaus; Abramowicz, Marc; Giacobino, Ariane |
2018 |
|
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:116900 |
Integration of Shh and Fgf signaling in controlling Hox gene expression in cultured limb cells |
Rodrigues, Alan R; Yakushiji-Kaminatsui, Nayuta; Atsuta, Yuji; Andrey, Guillaume; ... Tabin, Clifford J |
2017 |
|
unige:92439 |
Maladies génétiques rénales : perspectives diagnostiques |
Bouatou, Yassine; Giacobino, Ariane; Parvex, Paloma Maria; De Seigneux Matthey, Sophie |
2016 |
|
unige:107492 |
Advances in venomics |
Oldrati, Vera; Arrell, Miriam; Violette, Aude; Perret, Frédéric; ... Stöcklin, Reto |
2016 |
|
unige:94499 |
Astrovirus VA1 identified by next-generation sequencing in a nasopharyngeal specimen of a febrile Tanzanian child with acute respiratory disease of unknown etiology |
Cordey, Samuel; Brito, Francisco; Vu Cantero, Diem-Lan; Turin, Lara; ... Kaiser, Laurent |
2016 |
|
unige:111930 |
Novel fusion genes and chimeric transcripts in ependymal tumors |
Olsen, Thale Kristin; Panagopoulos, Ioannis; Gorunova, Ludmila; Micci, Francesca; ... Brandal, Petter |
2016 |
|
unige:99531 |
Clinical metagenomics for the management of hospital- and healthcare-acquired pneumonia |
Ruppe, Etienne; Baud, Damien; Schicklin, Stéphane; Guigon, Ghislaine; Schrenzel, Jacques |
2016 |
|
unige:96551 |
Next-generation personalised medicine for high-risk paediatric cancer patients - The INFORM pilot study |
Worst, Barbara C; van Tilburg, Cornelis M; Balasubramanian, Gnana Prakash; Fiesel, Petra; Von Bueren, André |
2016 |
High-throughput nucleotide sequencing
add all
remove all
