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Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|November 25, 2010
Extent and patterns of MGMT promoter methylation in glioblastoma- and respective glioblastoma-derived spheresDavide Sciuscio, Annie-Claire Diserens, Kristof van Dommelen, et al.
Pediatric Critical Care Medicine : a Journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies|May 17, 2011
16q24.1 microdeletion in a premature newborn: usefulness of array-based comparative genomic hybridization in persistent pulmonary hypertension of the newbornFlore Zufferey, Danielle Martinet, Maria-Chiara Osterheld, et al.
EMBO Molecular Medicine|March 1, 2015
A single epidermal stem cell strategy for safe ex vivo gene therapyStéphanie Droz-Georget Lathion, Ariane Rochat, Graham Knott, et al.
American Journal of Human Genetics|October 22, 2013
SCRIB and PUF60 are primary drivers of the multisystemic phenotypes of the 8q24.3 copy-number variantAndrew Dauber, Christelle Golzio, Cécile Guenot, et al.
Plos One|April 16, 2011
Network-guided analysis of genes with altered somatic copy number and gene expression reveals pathways commonly perturbed in metastatic melanomaArmand Valsesia, Donata Rimoldi, Danielle Martinet, et al.
American Journal of Human Genetics|June 2, 2009
Mutations in the heparan-sulfate proteoglycan glypican 6 (GPC6) impair endochondral ossification and cause recessive omodysplasiaAna Belinda Campos-Xavier, Danielle Martinet, John Bateman, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|April 17, 2015
A new CRB1 rat mutation links Müller glial cells to retinal telangiectasiaMin Zhao, Charlotte Andrieu-Soler, Laura Kowalczuk, et al.
The Journal of Allergy and Clinical Immunology|November 27, 2015
IL-17 receptor A and adenosine deaminase 2 deficiency in siblings with recurrent infections and chronic inflammationFlorence Fellmann, Federica Angelini, Jacqueline Wassenberg, et al.
Acta Neuropathologica|January 18, 2012
Presence of an oligodendroglioma-like component in newly diagnosed glioblastoma identifies a pathogenetically heterogeneous subgroup and lacks prognostic value: central pathology review of the EORTC_26981/NCIC_CE.3 trialMonika E Hegi, Robert-Charles Janzer, Wanyu L Lambiv, et al.
Science Translational Medicine|January 7, 2011
Epigenetic modification of the FMR1 gene in fragile X syndrome is associated with differential response to the mGluR5 antagonist AFQ056Sébastien Jacquemont, Aurore Curie, Vincent des Portes, et al.
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