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ESMO Open|December 24, 2021
Integrative molecular analysis of combined small-cell lung carcinomas identifies major subtypes with different therapeutic opportunitiesM Simbolo, G Centonze, G Ali, et al.
European Journal of Surgical Oncology : the Journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology|June 7, 2016
Gastric GISTs: Analysis of c-Kit, PDGFRA and BRAF mutations in relation to prognosis and clinical pathological characteristics of patients - A GIRCG studyL Capelli, E Petracci, V Quagliuolo, et al.
Diabetes & Metabolism|November 27, 2018
Type A competitiveness traits correlate with downregulation of c-Fos expression in patients with type 1 diabetesJ-C Chauvet-Gélinier, A-L Mosca-Boidron, C Lemogne, et al.
JIMD Reports|January 29, 2015
Homozygous Truncating Intragenic Duplication in TUSC3 Responsible for Rare Autosomal Recessive Nonsyndromic Intellectual Disability with No Clinical or Biochemical Metabolic MarkersS El Chehadeh, C Bonnet, P Callier, et al.
Science Translational Medicine|April 2, 2025
Mavoglurant reduces cocaine use in patients with cocaine use disorder in a phase 2 clinical trialBaltazar Gomez-Mancilla, Kenneth M Dürsteler, Marc Vogel, et al.
Clinical Genetics|July 5, 2011
What can we learn from old microdeletion syndromes using array-CGH screening?A L Mosca-Boidron, S Bouquillon, L Faivre, et al.
Gut|July 18, 2000
The Vienna classification of gastrointestinal epithelial neoplasiaR J Schlemper, R H Riddell, Y Kato, et al.
Molecular Psychiatry|May 12, 2016
CNTN6 mutations are risk factors for abnormal auditory sensory perception in autism spectrum disordersO Mercati, G Huguet, A Danckaert, et al.
Clinical Genetics|March 16, 2013
Molecular characterization of 39 de novo sSMC: contribution to prognosis and genetic counselling, a prospective studyN Marle, D Martinet, A Aboura, et al.
Clinical Genetics|October 21, 2016
Xq28 duplication including MECP2 in six unreported affected females: what can we learn for diagnosis and genetic counselling?S El Chehadeh, R Touraine, F Prieur, et al.
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