Get started
Author

Alessandra Meloni

Observed names: A Meloni, A. Meloni, ALESSANDRA MELONI, Allesandra Meloni, MELONI, A, Meloni, A, Meloni, Alessandra
Observed institutions: Università Cattolica del Sacro Cuore, Roma Tre University, Azerbaijan National Academy of Sciences, University of Cagliari, University of Milan, IRCCS Materno Infantile Burlo Garofolo, Ospedale San Paolo, Institute of Genetic and Biomedical Research, Azienda Ospedaliero-Universitaria Cagliari, Ospedale Microcitemico, Ospedale di Parma, National Research Council, Azienda Ospedaliera G. Brotzu, University of Bari Aldo Moro
ORCID: 0000-0002-6475-4691
Observed ORCID: 0000-0002-6475-4691
OpenAlex ID: A5081582419
Overexpression of the Cytokine BAFF and Autoimmunity Risk
2017 · Maristella Steri, Valeria Orrù, et al. · New England Journal of Medicine · 383
PDF
A common mutation in Sardinian autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy patients
1998 · M. C. Rosatelli, Alessandra Meloni, et al. · Human Genetics · 246
Molecular characterization of beta-thalassemia in the Sardinian population.
1992 · M C Rosatelli, A Dozy, et al. · PubMed · 96
Crisponi Syndrome Is Caused by Mutations in the CRLF1 Gene and Is Allelic to Cold-Induced Sweating Syndrome Type 1
2007 · Laura Crisponi, Giangiorgio Crisponi, et al. · The American Journal of Human Genetics · 89
Delineation of the Molecular Defects in the AIRE Gene in Autoimmune Polyendocrinopathy-Candidiasis-Ectodermal Dystrophy Patients from Southern Italy
2002 · Alessandra Meloni, Roberto Perniola, et al. · The Journal of Clinical Endocrinology & Metabolism · 86
Molecular screening and fetal diagnosis of ?-thalassemia in the Italian population
1992 · Maria Cristina Rosatelli, Teresa Tuveri, et al. · Human Genetics · 64
Characterization of a Disease-associated Mutation Affecting a Putative Splicing Regulatory Element in Intron 6b of the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) Gene
2009 · Valeria Faà, Federica Incani, et al. · Journal of Biological Chemistry · 45
PDF
Differential secretion of the mutated protein is a major component affecting phenotypic severity in CRLF1-associated disorders
2011 · Jana Herholz, Alessandra Meloni, et al. · European Journal of Human Genetics · 43
PDF
Vitamin D Responsive Elements within the HLA-DRB1 Promoter Region in Sardinian Multiple Sclerosis Associated Alleles
2012 · Eleonora Cocco, Alessandra Meloni, et al. · PLoS ONE · 41
PDF
Role of PHD fingers and COOH-terminal 30 amino acids in AIRE transactivation activity
2007 · Alessandra Meloni, Federica Incani, et al. · Molecular Immunology · 39
Electrophysiological and pharmacological characteristics of nigral dopaminergic neurons in the conscious, head‐restrained rat
2003 · Mauro Fà, Giampaolo Mereu, et al. · Synapse · 39
Two novel mutations of the AIRE protein affecting its homodimerization properties
2005 · A. Meloni, E. Fiorillo, et al. · Human Mutation · 33
PDF
Promoter mutations producing mild β‐thalassaemia in the Italian population
1992 · Alessandra Meloni, M. Cristina Rosatelli, et al. · British Journal of Haematology · 29
Thalassaemia in Azerbaijan.
1994 · A M Kuliev, I M Rasulov, et al. · Journal of Medical Genetics · 28
PDF
The Forkhead Transcription Factor Foxl2 Is Sumoylated in Both Human and Mouse: Sumoylation Affects Its Stability, Localization, and Activity
2010 · Mara Marongiu, Manila Deiana, et al. · PLoS ONE · 26
PDF
DAXX Is a New AIRE-interacting Protein
2010 · Allesandra Meloni, Edoardo Fiorillo, et al. · Journal of Biological Chemistry · 24
PDF
Features and Functions of Human Microglia Cells
1997 · Fulvia Gremo, Valeria Sogos, et al. · Advances in experimental medicine and biology · 24
AIRE acetylation and deacetylation: effect on protein stability and transactivation activity
2014 · Federica Incani, Maria Luisa Serra, et al. · Journal of Biomedical Science · 23
PDF
Crigler-Najjar syndrome type II resulting from three different mutations in the bilirubin uridine 5′-diphosphate-glucuronosyltransferase (UGT1A1) gene
2000 · ACHILLE IOLASCON, ALESSANDRA MELONI, et al. · Journal of Medical Genetics · 23
PDF
A novel splicing defect (IVS6+1G>T) in a patient with pseudovitamin D deficiency rickets
2002 · L. Porcu, A. Meloni, et al. · Journal of Endocrinological Investigation · 21
A simple electrophoretic procedure for fetal diagnosis of β‐thalassaemia due to short deletions
1992 · V. Faà, M. C. Rosatelli, et al. · Prenatal Diagnosis · 21
Amniocentesis and chorionic villus sampling in HIV‐infected pregnant women: a multicentre case series
2016 · M Floridia, G Masuelli, et al. · BJOG An International Journal of Obstetrics & Gynaecology · 20
PDF
Molecular analysis of patients of Sardinian descent with Crigler-Najjar syndrome type I.
1997 · M C Rosatelli, A Meloni, et al. · Journal of Medical Genetics · 20
PDF
Voluntary pregnancy termination among women with HIV in the HAART era (2002–2008): a case series from a national study
2009 · Marco Floridia, Enrica Tamburrini, et al. · AIDS Care · 19
PDF
A promoter mutation, C → T at position ‐92, leading to silent /3‐thalassaemia
1995 · MARIA CRISTINA ROSATELLI, VALERIA FAA, et al. · British Journal of Haematology · 18
Works count: 125
Citation count: 1,844
H-index: 21
I10-index: 41
Year
Topic
Type