Adele Mitrotti
Overview
Explore the profile of Adele Mitrotti including associated specialties, affiliations and a list of published articles.
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25
Citations
768
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Recent Articles
11.
Barry A, McNulty M, Jia X, Gupta Y, Debiec H, Luo Y, et al.
Nat Commun
. 2023 Apr;
14(1):2481.
PMID: 37120605
Pediatric steroid-sensitive nephrotic syndrome (pSSNS) is the most common childhood glomerular disease. Previous genome-wide association studies (GWAS) identified a risk locus in the HLA Class II region and three additional...
12.
Ahram D, Lim T, Ke J, Jin G, Verbitsky M, Bodria M, et al.
J Am Soc Nephrol
. 2023 Mar;
34(6):1105-1119.
PMID: 36995132
Significance Statement: Congenital obstructive uropathy (COU) is a prevalent human developmental defect with highly heterogeneous clinical presentations and outcomes. Genetics may refine diagnosis, prognosis, and treatment, but the genomic architecture...
13.
Vaisitti T, Peritore D, Magistroni P, Ricci A, Lombardini L, Gringeri E, et al.
Orphanet J Rare Dis
. 2021 Sep;
16(1):374.
PMID: 34481500
Background: Rare diseases are chronic and life-threatening disorders affecting < 1 person every 2,000. For most of them, clinical symptoms and signs can be observed at birth or childhood. Approximately...
14.
Verbitsky M, Krithivasan P, Batourina E, Khan A, Graham S, Marasa M, et al.
J Am Soc Nephrol
. 2021 Feb;
32(4):805-820.
PMID: 33597122
Background: Vesicoureteral reflux (VUR) is a common, familial genitourinary disorder, and a major cause of pediatric urinary tract infection (UTI) and kidney failure. The genetic basis of VUR is not...
15.
Weng P, Majmundar A, Khan K, Lim T, Shril S, Jin G, et al.
Am J Hum Genet
. 2021 Jan;
108(2):357-367.
PMID: 33508234
Focal segmental glomerulosclerosis (FSGS) is the main pathology underlying steroid-resistant nephrotic syndrome (SRNS) and a leading cause of chronic kidney disease. Monogenic forms of pediatric SRNS are predominantly caused by...
16.
Giliberti M, Mitrotti A, Gesualdo L
Am J Pathol
. 2020 Apr;
190(6):1172-1174.
PMID: 32305354
This commentary highlights the article by Li et al that links ceramide accumulation in podocytes to cellular damage and nephrotic syndrome.
17.
Verbitsky M, Westland R, Perez A, Kiryluk K, Liu Q, Krithivasan P, et al.
Nat Genet
. 2019 Mar;
51(4):764.
PMID: 30816350
In the version of this article initially published, affiliation 38 incorrectly read "ICNU-Nephrology and Urology Department, Barcelona, Spain"; "Renal Division, Hospital Clinic, IDIBAPS, University of Barcelona, Barcelona, Spain" is the...
18.
Groopman E, Marasa M, Cameron-Christie S, Petrovski S, Aggarwal V, Milo-Rasouly H, et al.
N Engl J Med
. 2018 Dec;
380(2):142-151.
PMID: 30586318
Background: Exome sequencing is emerging as a first-line diagnostic method in some clinical disciplines, but its usefulness has yet to be examined for most constitutional disorders in adults, including chronic...
19.
Verbitsky M, Westland R, Perez A, Kiryluk K, Liu Q, Krithivasan P, et al.
Nat Genet
. 2018 Dec;
51(1):117-127.
PMID: 30578417
Congenital anomalies of the kidney and urinary tract (CAKUT) are a major cause of pediatric kidney failure. We performed a genome-wide analysis of copy number variants (CNVs) in 2,824 cases...
20.
Rasouly H, Groopman E, Heyman-Kantor R, Fasel D, Mitrotti A, Westland R, et al.
Ann Intern Med
. 2018 Nov;
170(1):11-21.
PMID: 30476936
Background: Exome sequencing is increasingly being used for clinical diagnostics, with an impetus to expand reporting of incidental findings across a wide range of disorders. Analysis of population cohorts can...