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BMJ Case Reports|May 30, 2013
Atypical clinical presentation of a WT1-related syndrome associated with a novel exon 6 gene mutationPietro Dattolo, Marco Allinovi, Paraskevas Iatropoulos, et al.
Pediatric Nephrology (Berlin, Germany)|June 5, 2012
Discordant phenotype in monozygotic twins with renal coloboma syndrome and a PAX2 mutationParaskevas Iatropoulos, Erica Daina, Caterina Mele, et al.
Frontiers in Immunology|November 30, 2018
Unraveling the Molecular Mechanisms Underlying Complement Dysregulation by Nephritic Factors in C3G and IC-MPGNRoberta Donadelli, Patrizia Pulieri, Rossella Piras, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|March 10, 2006
Glutamate AMPA receptor subunit 1 gene (GRIA1) and DSM-IV-TR schizophrenia: a pilot case-control association study in an Italian sampleChiara Magri, Rita Gardella, Stefano Davide Barlati, et al.
Psychiatric Genetics|July 31, 2009
Association study and mutational screening of SYNGR1 as a candidate susceptibility gene for schizophreniaParaskevas Iatropoulos, Rita Gardella, Paolo Valsecchi, et al.
Frontiers in Medicine|November 23, 2020
Molecular Studies and an <i>ex vivo</i> Complement Assay on Endothelium Highlight the Genetic Complexity of Atypical Hemolytic Uremic Syndrome: The Case of a Pedigree With a Null CD46 VariantRossella Piras, Paraskevas Iatropoulos, Elena Bresin, et al.
Frontiers in Genetics|July 2, 2021
<i>CFH</i> and <i>CFHR</i> Copy Number Variations in C3 Glomerulopathy and Immune Complex-Mediated Membranoproliferative GlomerulonephritisRossella Piras, Matteo Breno, Elisabetta Valoti, et al.
Frontiers in Immunology|May 24, 2019
Rare Functional Variants in Complement Genes and Anti-FH Autoantibodies-Associated aHUSElisabetta Valoti, Marta Alberti, Paraskevas Iatropoulos, et al.
Age (Dordrecht, Netherlands)|May 10, 2012
Variations of the angiotensin II type 1 receptor gene are associated with extreme human longevityAriela Benigni, Silvia Orisio, Marina Noris, et al.
American Journal of Human Genetics|July 5, 2011
Disruption of PTPRO causes childhood-onset nephrotic syndromeFatih Ozaltin, Tulin Ibsirlioglu, Ekim Z Taskiran, et al.
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