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FEBS Letters|September 3, 2013
Endoplasmic reticulum stress reduces COPII vesicle formation and modifies Sec23a cycling at ERESsGiuseppina Amodio, Rossella Venditti, Maria Antonietta De Matteis, et al.European Journal of Medical Genetics|February 12, 2020
Two cases of 16q12.1q21 deletions and refinement of the critical regionDiletta Apuzzo, Gerarda Cappuccio, Taneli Vaisanen, et al.Journal of Cardiovascular Translational Research|June 23, 2017
Association Study Between Coronary Artery Disease and rs1333049 Polymorphism at 9p21.3 Locus in Italian PopulationPiero Pignataro, Lucia Pezone, Giuseppe Di Gioia, et al.Plos One|November 9, 2013
Impact of interleukin-6 -174 G>C gene promoter polymorphism on neuroblastomaFrancesca Totaro, Flora Cimmino, Piero Pignataro, et al.Medical Sciences (Basel, Switzerland)|March 2, 2019
Chromosomal Microarray Analysis versus Karyotyping in Fetuses with Increased Nuchal TranslucencyRita Cicatiello, Piero Pignataro, Antonella Izzo, et al.Oncotarget|June 29, 2016
A comprehensive characterization of rare mitochondrial DNA variants in neuroblastomaFrancesco Maria Calabrese, Rosanna Clima, Piero Pignataro, et al.Diabetes/Metabolism Research and Reviews|August 13, 2020
The Pro12Ala polymorphism of PPARγ2 modulates beta cell function and failure to oral glucose-lowering drugs in patients with type 2 diabetesMaria Masulli, Giuseppe Della Pepa, Sara Cocozza, et al.Journal of Translational Medicine|May 19, 2016
An 18 gene expression-based score classifier predicts the clinical outcome in stage 4 neuroblastomaDaniela Formicola, Giuseppe Petrosino, Vito Alessandro Lasorsa, et al.Clinical Genetics|July 7, 2019
Germline mutations and new copy number variants among 40 pediatric cancer patients suspected for genetic predispositionAntonella Gambale, Roberta Russo, Immacolata Andolfo, et al.American Journal of Hematology|February 4, 2018
Multi-gene panel testing improves diagnosis and management of patients with hereditary anemiasRoberta Russo, Immacolata Andolfo, Francesco Manna, et al.Pageof 2