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Genetics|June 22, 2023
Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variantsJonah Einson, Dafni Glinos, Eric Boerwinkle, et al.
British Journal of Cancer|December 8, 2011
Segmental chromosomal alterations lead to a higher risk of relapse in infants with MYCN-non-amplified localised unresectable/disseminated neuroblastoma (a SIOPEN collaborative study)G Schleiermacher, J Michon, A Ribeiro, et al.
Biorxiv : the Preprint Server for Biology|February 13, 2023
Genetic control of mRNA splicing as a potential mechanism for incomplete penetrance of rare coding variantsJonah Einson, Dafni Glinos, Eric Boerwinkle, et al.
Revista Espanola De Cardiologia (English Ed.)|September 2, 2022
Durable ventricular assist device in Spain (2007-2020). First report of the REGALAD registryManuel Gómez-Bueno, Enrique Pérez de la Sota, Alberto Forteza Gil, et al.
Nature Medicine|April 24, 2026
Targeted therapies plus radiotherapy for diffuse intrinsic pontine glioma: the randomized phase 2 BIOMEDE trialMarie-Anne Debily, Gwenael Le Teuff, Thomas Kergrohen, et al.
ESMO Real World Data and Digital Oncology|February 6, 2026
The impact of targeted therapies on molecular alterations identified by an institutional molecular tumor board: an approach based on ESCAT classificationK Rahmani Narj Abadi, C Dupain, I Guillou, et al.
International Journal of Biological Sciences|November 24, 2025
Extracellular matrix dysregulation in aging, calcification, and cancer diseases: insights into cellular senescence, inflammation, and novel therapeutic strategiesDiego Liviu Boaru, Diego De Leon-Oliva, Patricia De Castro-Martinez, et al.
The British Journal of Dermatology|October 4, 2023
Omalizumab in the treatment of bullous pemphigoid resistant to first-line therapy: a French national multicentre retrospective study of 100 patientsRéda Chebani, Florian Lombart, Guillaume Chaby, et al.
Acta Neuropathologica Communications|November 19, 2024
Diffuse pediatric high-grade glioma of methylation-based RTK2A and RTK2B subclasses present distinct radiological and histomolecular features including Gliomatosis cerebri phenotypeArnault Tauziède-Espariat, Lea L Friker, Gunther Nussbaumer, et al.
Science (New York, N.Y.)|September 11, 2020
Cell type-specific genetic regulation of gene expression across human tissuesSarah Kim-Hellmuth, François Aguet, Meritxell Oliva, et al.
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