Monica Bodria

Istituto Giannina Gaslini — Italy

Medicine · Health Sciences

27h-index4.1kcitations57works3.32yr avg
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Research Topics

Renal Diseases and Glomerulopathies(28), Renal and related cancers(17), Pediatric Urology and Nephrology Studies(12), Urological Disorders and Treatments(9), Autoimmune Bullous Skin Diseases(8)

Publications57 total

APOL1 kidney risk variants and outcomes in children with congenital anomalies of the kidney and urinary tract
Pediatric Nephrology·2026
Author Correction: Exome analysis links kidney malformations to developmental disorders and reveals causal genes
Nature Communications·2025Open Access
Exome analysis links kidney malformations to developmental disorders and reveals causal genes
Nature Communications·2025· 6 citedOpen Access
Efficacy of Calcineurin Inhibition in Children With Steroid-Resistant Nephrotic Syndrome
Kidney International Reports·2025· 3 citedOpen Access
Loss of GalNAc-T14 links O-glycosylation defects to alterations in B cell homing in IgA nephropathy
Journal of Clinical Investigation·2025· 10 citedOpen Access
Diffusion-weighted MRI in the identification of renal parenchymal involvement in children with a first episode of febrile urinary tract infection
Frontiers in Radiology·2024· 3 citedOpen Access
Exome-wide analysis of congenital kidney anomalies reveals new genes and shared architecture with developmental disorders
2024· 1 citedOpen Access
Genome-wide studies define new genetic mechanisms of IgA vasculitis
2024· 4 citedOpen Access
Brain and spine malformations and neurodevelopmental disorders in a cohort of children with CAKUT
Pediatric Nephrology·2024· 3 cited
Strong protective effect of the APOL1 p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease
Nature Communications·2023· 59 citedOpen Access
Mouse and human studies support DSTYK loss of function as a low-penetrance and variable expressivity risk factor for congenital urinary tract anomalies
Genetics in Medicine·2023· 4 citedOpen Access
Strong protective effect of the <i>APOL1</i> p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease
2023· 3 citedOpen Access
Genome-wide association analyses define pathogenic signaling pathways and prioritize drug targets for IgA nephropathy
Nature Genetics·2023· 156 citedOpen Access
Multi-population genome-wide association study implicates immune and non-immune factors in pediatric steroid-sensitive nephrotic syndrome
Nature Communications·2023· 42 citedOpen Access
Rare Single Nucleotide and Copy Number Variants and the Etiology of Congenital Obstructive Uropathy: Implications for Genetic Diagnosis
Journal of the American Society of Nephrology·2023· 15 citedOpen Access
Multi-population genome-wide association study implicates both immune and non-immune factors in the etiology of pediatric steroid sensitive nephrotic syndrome
2022· 1 citedOpen Access
Management of the congenital solitary kidney: consensus recommendations of the Italian Society of Pediatric Nephrology
Pediatric Nephrology·2022· 46 citedOpen Access
Functional Magnetic Resonance Urography in Ureteropelvic Junction Obstruction: Proposal for a Pediatric Quantitative Score
Frontiers in Pediatrics·2022· 2 citedOpen Access
GWAS defines pathogenic signaling pathways and prioritizes drug targets for IgA nephropathy
2021· 5 citedOpen Access
Prognostic Factors and Long-Term Outcome with ANCA-Associated Kidney Vasculitis in Childhood
Clinical Journal of the American Society of Nephrology·2021· 39 citedOpen Access
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Frequent Co-authors

Gian Marco Ghiggeri(34), Simone Sanna‐Cherchi(23), Ali G. Gharavi(20), Loreto Gesualdo(20), Francesco Scolari(18), Krzysztof Kiryluk(16), Claudia Izzi(16), Miguel Verbitsky(14), Adele Mitrotti(14), Isabella Pisani(14), Rik Westland(13), Maddalena Marasà(13), Landino Allegri(12), Marijan Saraga(12), Velibor Tasić(12), Gianluca Caridi(11), Marcin Zaniew(11), Matthew G. Sampson(11), Patricia L. Weng(11), Anna Materna‐Kiryluk(11)