Miguel Verbitsky
Overview
Explore the profile of Miguel Verbitsky including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
40
Citations
1911
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Zanoni F, Marasa M, Carlassara L, Verbitsky M, Khan A, Wang C, et al.
J Am Soc Nephrol
. 2025 Mar;
PMID: 40067412
Background: A family history of health conditions may reflect shared genetic and/or environmental risk. It is not well known to what extent family history impacts outcomes among patients with chronic...
2.
Motelow J, Malakar A, Krishna Murthy S, Verbitsky M, Kahn A, Estrella E, et al.
medRxiv
. 2025 Mar;
PMID: 40034785
Interstitial cystitis/bladder pain syndrome (IC/BPS) is a poorly understood and underdiagnosed syndrome of chronic bladder/pelvic pain with urinary frequency and urgency. Though IC/BPS can be hereditary, little is known of...
3.
Elliott M, Vena N, Marasa M, Cocchi E, Bheda S, Bogyo K, et al.
J Clin Invest
. 2024 Sep;
134(17).
PMID: 39225089
BACKGROUNDIt is unknown whether the risk of kidney disease progression and failure differs between patients with and without genetic kidney disorders.METHODSThree cohorts were evaluated: the prospective Cure Glomerulonephropathy Network (CureGN)...
4.
Gupta Y, Friedman D, McNulty M, Khan A, Lane B, Wang C, et al.
Nat Commun
. 2023 Nov;
14(1):7836.
PMID: 38036523
African Americans have a significantly higher risk of developing chronic kidney disease, especially focal segmental glomerulosclerosis -, than European Americans. Two coding variants (G1 and G2) in the APOL1 gene...
5.
Gupta Y, Friedman D, McNulty M, Khan A, Lane B, Wang C, et al.
medRxiv
. 2023 Aug;
PMID: 37577628
Black Americans have a significantly higher risk of developing chronic kidney disease (CKD), especially focal segmental glomerulosclerosis (FSGS), than European Americans. Two coding variants (G1 and G2) in the gene...
6.
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...
7.
Lim T, Verbitsky M, Sanna-Cherchi S
Eur J Hum Genet
. 2023 Jan;
31(3):275-277.
PMID: 36631543
No abstract available.
8.
Verbitsky M, Krishnamurthy S, Krithivasan P, Hughes D, Khan A, Marasa M, et al.
J Am Soc Nephrol
. 2022 Oct;
34(4):607-618.
PMID: 36302597
Significance Statement: Pathogenic structural genetic variants, also known as genomic disorders, have been associated with pediatric CKD. This study extends those results across the lifespan, with genomic disorders enriched in...
9.
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...
10.
Petukhova L, Patel A, Rigo R, Bian L, Verbitsky M, Sanna-Cherchi S, et al.
Exp Dermatol
. 2019 Jun;
29(3):243-253.
PMID: 31169925
Alopecia areata (AA) is a highly prevalent autoimmune disease that attacks the hair follicle and leads to hair loss that can range from small patches to complete loss of scalp...