Publications by authors named "Adele Mitrotti"

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Author Correction: Exome analysis links kidney malformations to developmental disorders and reveals causal genes.
Hila Milo Rasouly, Sarath Babu Krishna Murthy, Natalie Vena, Gundula Povysil, Andrew Beenken, Adele Mitrotti

Nat Commun· October 2025

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Exome analysis links kidney malformations to developmental disorders and reveals causal genes.
Hila Milo Rasouly, Sarath Babu Krishna Murthy, Natalie Vena, Gundula Povysil, Andrew Beenken, Adele Mitrotti

Nat Commun· August 2025

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Natural History and Clinicopathological Associations of TRPC6-Associated Podocytopathy.
Benjamin Wooden, Andrew Beenken, Elena Martinelli, Ken Saida, Andrea L Knob, Adele Mitrotti

J Am Soc Nephrol· February 2025

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Autoantibodies Targeting Nephrin in Podocytopathies.
Felicitas E Hengel, Silke Dehde, Moritz Lassé, Gunther Zahner, Larissa Seifert, Adele Mitrotti

N Engl J Med· August 2024

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Hidden genetics behind glomerular scars: an opportunity to understand the heterogeneity of focal segmental glomerulosclerosis?
Adele Mitrotti, Marica Giliberti, Vincenzo Di Leo, Ighli di Bari, Paola Pontrelli

Pediatr Nephrol· June 2024

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The complement system in the pathogenesis and progression of kidney diseases: What doesn't kill you makes you older.
Emma Diletta Stea, Giuseppina D'Ettorre, Adele Mitrotti, Loreto Gesualdo

Eur J Intern Med· June 2024

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What Is Hidden in Patients with Unknown Nephropathy? Genetic Screening Could Be the Missing Link in Kidney Transplantation Diagnosis and Management.
Adele Mitrotti, Ighli Di Bari, Marica Giliberti, Rossana Franzin, Francesca Conserva

Int J Mol Sci· January 2024

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Effect of music therapy intervention on anxiety and pain during percutaneous renal biopsy: a randomized controlled trial.
Filippo Giordano, Adele Mitrotti, Antonia Losurdo, Flavia Esposito, Antonio Granata

Clin Kidney J· December 2023

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Strong protective effect of the APOL1 p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease.
Yask Gupta, David J Friedman, Michelle T McNulty, Atlas Khan, Brandon Lane, Adele Mitrotti

Nat Commun· November 2023

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Implementation and Feasibility of Clinical Genome Sequencing Embedded Into the Outpatient Nephrology Care for Patients With Proteinuric Kidney Disease.
Maddalena Marasa, Dina F Ahram, Atteeq U Rehman, Adele Mitrotti, Avinash Abhyankar

Kidney Int Rep· August 2023

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Strong protective effect of the p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease.
Yask Gupta, David J Friedman, Michelle McNulty, Atlas Khan, Brandon Lane, Adele Mitrotti

medRxiv· August 2023

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Genome-wide association analyses define pathogenic signaling pathways and prioritize drug targets for IgA nephropathy.
Krzysztof Kiryluk, Elena Sanchez-Rodriguez, Xu-Jie Zhou, Francesca Zanoni, Lili Liu, Adele Mitrotti

Nat Genet· July 2023

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Rare Single Nucleotide and Copy Number Variants and the Etiology of Congenital Obstructive Uropathy: Implications for Genetic Diagnosis.
Dina F Ahram, Tze Y Lim, Juntao Ke, Gina Jin, Miguel Verbitsky, Adele Mitrotti

J Am Soc Nephrol· June 2023

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Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome.
Alexandra Barry, Michelle T McNulty, Xiaoyuan Jia, Yask Gupta, Hanna Debiec, Adele Mitrotti

Nat Commun· April 2023

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The frequency of rare and monogenic diseases in pediatric organ transplant recipients in Italy.
Tiziana Vaisitti, Daniela Peritore, Paola Magistroni, Andrea Ricci, Letizia Lombardini, Adele Mitrotti

Orphanet J Rare Dis· September 2021

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Copy Number Variant Analysis and Genome-wide Association Study Identify Loci with Large Effect for Vesicoureteral Reflux.
Miguel Verbitsky, Priya Krithivasan, Ekaterina Batourina, Atlas Khan, Sarah E Graham, Adele Mitrotti

J Am Soc Nephrol· April 2021

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De novo TRIM8 variants impair its protein localization to nuclear bodies and cause developmental delay, epilepsy, and focal segmental glomerulosclerosis.
Patricia L Weng, Amar J Majmundar, Kamal Khan, Tze Y Lim, Shirlee Shril, Adele Mitrotti

Am J Hum Genet· February 2021

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Podocytes: The Role of Lysosomes in the Development of Nephrotic Syndrome.
Marica Giliberti, Adele Mitrotti, Loreto Gesualdo

Am J Pathol· June 2020

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Author Correction: The copy number variation landscape of congenital anomalies of the kidney and urinary tract.
Miguel Verbitsky, Rik Westland, Alejandra Perez, Krzysztof Kiryluk, Qingxue Liu, Adele Mitrotti

Nat Genet· April 2019

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The Burden of Candidate Pathogenic Variants for Kidney and Genitourinary Disorders Emerging From Exome Sequencing.
Hila Milo Rasouly, Emily E Groopman, Reuben Heyman-Kantor, David A Fasel, Adele Mitrotti

Ann Intern Med· January 2019

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The copy number variation landscape of congenital anomalies of the kidney and urinary tract.
Miguel Verbitsky, Rik Westland, Alejandra Perez, Krzysztof Kiryluk, Qingxue Liu, Adele Mitrotti

Nat Genet· January 2019

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Diagnostic Utility of Exome Sequencing for Kidney Disease.
Emily E Groopman, Maddalena Marasa, Sophia Cameron-Christie, Slavé Petrovski, Vimla S Aggarwal, Adele Mitrotti

N Engl J Med· January 2019

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[Medicine and Nephrology from Social Networks].
Vincenzo Montinaro, Emanuela Cataldo, Francesca Cianciotta, Vincenza Colucci, Giuseppina D'Ettorre, Adele Mitrotti

G Ital Nefrol· February 2018

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Whole-Exome Sequencing in Adults With Chronic Kidney Disease: A Pilot Study.
Sneh Lata, Maddalena Marasa, Yifu Li, David A Fasel, Emily Groopman, Adele Mitrotti

Ann Intern Med· January 2018

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Exome-wide Association Study Identifies GREB1L Mutations in Congenital Kidney Malformations.
Simone Sanna-Cherchi, Kamal Khan, Rik Westland, Priya Krithivasan, Lorraine Fievet, Adele Mitrotti

Am J Hum Genet· December 2017

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