Olivia Balderes
Overview
Explore the profile of Olivia Balderes including associated specialties, affiliations and a list of published articles.
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Articles
8
Citations
473
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Recent Articles
1.
Fernandez H, Lipton M, Balderes O, Lin F, Marasa M, Rasouly H, et al.
Pediatr Nephrol
. 2024 Oct;
40(3):755-763.
PMID: 39382664
Background: While genetic testing is now more accessible in pediatric nephrology, little is known about the views of pediatric nephrologists regarding genetic testing in clinical settings. Methods: An online 41-item...
2.
Kiryluk K, Sanchez-Rodriguez E, Zhou X, Zanoni F, Liu L, Mladkova N, et al.
Nat Genet
. 2023 Jun;
55(7):1091-1105.
PMID: 37337107
IgA nephropathy (IgAN) is a progressive form of kidney disease defined by glomerular deposition of IgA. Here we performed a genome-wide association study of 10,146 kidney-biopsy-diagnosed IgAN cases and 28,751...
3.
Rasouly H, Balderes O, Marasa M, Fernandez H, Lipton M, Lin F, et al.
Genet Med
. 2023 Feb;
25(5):100814.
PMID: 36789889
Purpose: The success of genomic medicine hinges on the implementation of genetic knowledge in clinical settings. In novel subspecialties, it requires that clinicians refer patients to genetic evaluation or testing,...
4.
Liu L, Khan A, Sanchez-Rodriguez E, Zanoni F, Li Y, Steers N, et al.
Nat Commun
. 2023 Feb;
14(1):655.
PMID: 36746961
No abstract available.
5.
Liu L, Khan A, Sanchez-Rodriguez E, Zanoni F, Li Y, Steers N, et al.
Nat Commun
. 2022 Nov;
13(1):6859.
PMID: 36369178
Immunoglobulin A (IgA) mediates mucosal responses to food antigens and the intestinal microbiome and is involved in susceptibility to mucosal pathogens, celiac disease, inflammatory bowel disease, and IgA nephropathy. We...
6.
Xie J, Liu L, Mladkova N, Li Y, Ren H, Wang W, et al.
Nat Commun
. 2020 Apr;
11(1):1600.
PMID: 32231244
Membranous Nephropathy (MN) is a rare autoimmune cause of kidney failure. Here we report a genome-wide association study (GWAS) for primary MN in 3,782 cases and 9,038 controls of East...
7.
Steers N, Li Y, Drace Z, DAddario J, Fischman C, Liu L, et al.
N Engl J Med
. 2019 May;
380(20):1918-1928.
PMID: 31091373
Background: In the context of kidney transplantation, genomic incompatibilities between donor and recipient may lead to allosensitization against new antigens. We hypothesized that recessive inheritance of gene-disrupting variants may represent...
8.
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...