Broadening the Spectrum of Diseases Related to Podocin Mutations

Gianluca Caridi, Roberta Bertelli, Marco Di Duca, +12

Journal of the American Society of Nephrology

Rivaroxaban or aspirin for patent foramen ovale and embolic stroke of undetermined source: a prespecified subgroup analysis from the NAVIGATE ESUS trial

Scott E. Kasner, Balakumar Swaminathan, Pablo M. Lavados, +1294

The Lancet Neurology

Recurrence of focal segmental glomerulosclerosis after renal transplantation in patients with mutations of podocin

Roberta Bertelli, Fabrizio Ginevri, Gianluca Caridi, +13

American Journal of Kidney Diseases

Glomerular DiseaseGlomerulonephritisTransplantation SurgeryUrologyRenal Function +9

Exome sequencing identified MYO1E and NEIL1 as candidate genes for human autosomal recessive steroid-resistant nephrotic syndrome

Simone Sanna‐Cherchi, Katelyn E. Burgess, Shannon N. Nees, +21

Kidney International

Candidate GenesMendelian DisorderGenetic DisorderMedicineGenetics +6

Discrete Changes in Glucose Metabolism Define Aging

Silvia Ravera, Marina Podestà, Federica Sabatini, +5

Scientific Reports

Mutations in SOX17 are associated with congenital anomalies of the kidney and the urinary tract

Stefania Gimelli, Gianluca Caridi, Silvana Beri, +12

Human Mutation

Clinical Features and Long-Term Outcome of Nephrotic Syndrome Associated with Heterozygous NPHS1 and NPHS2 Mutations

Gianluca Caridi, Maddalena Gigante, Pietro Ravani, +15

Clinical Journal of the American Society of Nephrology

Nephronophthisis type 1 deletion syndrome with neurological symptoms: Prevalence and significance of the association

Gianluca Caridi, Monica Dagnino, Andrea Rossi, +7

Kidney International

Neurological DisorderNeurological SymptomsNeurologyEncephalitisNeuropathology +2

A Novel WT1 Gene Mutation in a Three-Generation Family with Progressive Isolated Focal Segmental Glomerulosclerosis

Elisa Benetti, Gianluca Caridi, Cristina Malaventura, +6

Clinical Journal of the American Society of Nephrology

Localization of a Gene for Nonsyndromic Renal Hypodysplasia to Chromosome 1p32-33

Simone Sanna‐Cherchi, Gianluca Caridi, Patricia L. Weng, +14

The American Journal of Human Genetics

ChromatinMendelian DisorderCytogeneticsGenetic DisorderGenetics +7