Piero Pignataro

Federico II University Hospital — Italy

Medicine · Health Sciences

11h-index544citations27works0.02yr avg
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Research Topics

Neuroblastoma Research and Treatments(6), Cancer, Hypoxia, and Metabolism(5), Childhood Cancer Survivors' Quality of Life(4), BRCA gene mutations in cancer(3), Acute Lymphoblastic Leukemia research(3)

Publications27 total

Peculiar footprints in a child with agenesis of corpus callosum
Journal of Paediatrics and Child Health·2022
Peculiar footprints in a child with agenesis of corpus callosum
Journal of Paediatrics and Child Health·2021
P.185 The role for rare structural variants in the genetics of treatment resistant schizophrenia: preliminary data
European Neuropsychopharmacology·2020
The <scp>Pro12Ala</scp> polymorphism of <scp>PPARγ2</scp> modulates beta cell function and failure to oral glucose‐lowering drugs in patients with type 2 diabetes
Diabetes/Metabolism Research and Reviews·2020· 3 cited
Apparent recessive inheritance of sideroblastic anemia type 2 due to uniparental isodisomy at the SLC25A38 locus
Haematologica·2020· 9 citedOpen Access
A small 7q11.23 microduplication involving <scp> <i>GTF2I</i> </scp> in a family with intellectual disability
Clinical Genetics·2020· 13 citedOpen Access
M170. GENETIC CHARACTERIZATION OF A COHORT OF PATIENTS AFFECTED BY SCHIZOPHRENIA. THE ROLE FOR RARE STRUCTURAL VARIANTS IN MODULATING TREATMENT RESISTANT ENDOPHENOTYPES: PRELIMINARY DATA
Schizophrenia Bulletin·2020Open Access
M169. HIPPOCAMPAL GLUTAMATE AND HIPPOCAMPUS SUBFIELD VOLUMES IN ANTIPSYCHOTIC-NAIVE FIRST EPISODE PSYCHOSIS SUBJECTS AND RELATIONSHIPS TO DURATION OF UNTREATED PSYCHOSIS
Schizophrenia Bulletin·2020Open Access
Author response for "A small 7q11.23 microduplication involving &lt;i&gt;GTF2I&lt;/i&gt; in a family with intellectual disability"
2020
Two cases of 16q12.1q21 deletions and refinement of the critical region
European Journal of Medical Genetics·2020· 5 cited
Germline mutations and new copy number variants among 40 pediatric cancer patients suspected for genetic predisposition
Clinical Genetics·2019· 20 cited
Author response for "Germline mutations and new copy number variants among 40 pediatric cancer patients suspected for genetic predisposition"
2019
Author response for "Germline mutations and new copy number variants among 40 pediatric cancer patients suspected for genetic predisposition"
2019
Author response for "Germline mutations and new copy number variants among 40 pediatric cancer patients suspected for genetic predisposition"
2019
Chromosomal Microarray Analysis versus Karyotyping in Fetuses with Increased Nuchal Translucency
Medical Sciences·2019· 19 citedOpen Access
P27. The smallest 7Q11.23 duplication encompassing GTF2I and GTF2IRD1 genes in an individual with intellectual disability
Università degli Studi di Salerno·2019Open Access
Incidence of fatigue and low-dose corticosteroid use in prostate cancer patients receiving systemic treatment: a meta-analysis of randomized controlled trials
World Journal of Urology·2018· 6 cited
Fine mapping of 2q35 high‐risk neuroblastoma locus reveals independent functional risk variants and suggests full‐length BARD1 as tumor‐suppressor
International Journal of Cancer·2018· 55 citedOpen Access
Multi‐gene panel testing improves diagnosis and management of patients with hereditary anemias
American Journal of Hematology·2018· 155 cited
Erratum to: Association Study between Coronary Artery Disease and rs1333049 Polymorphism at 9p21.3 Locus in Italian Population
Journal of Cardiovascular Translational Research·2017· 7 cited
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Frequent Co-authors

Achille Iolascon(16), Mario Capasso(15), Rita Genesio(15), Immacolata Andolfo(9), Antonella Gambale(9), Roberta Russo(6), Gerarda Cappuccio(6), Nicola Brunetti‐Pierri(6), Flora Cimmino(4), Gian Paolo Tonini(4), Lucia Quaglietta(4), Gianluca De Rosa(4), Valentina Contestabile(4), Lucia De Martino(4), Sabrina Giglio(4), Rosanna Parasole(4), Barbara Pasini(4), Lucio Nitsch(4), Vito Alessandro Lasorsa(3), Daniela Formicola(3)