Berenice Y Gitomer
Overview
Explore the profile of Berenice Y Gitomer including associated specialties, affiliations and a list of published articles.
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Articles
19
Citations
211
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Recent Articles
1.
Jawaid T, Elbarougy D, Lavu S, Buia G, Senum S, Olinger E, et al.
J Am Soc Nephrol
. 2025 Feb;
PMID: 39899384
Background: Autosomal dominant polycystic kidney disease (ADPKD) is a common, inherited nephropathy often resulting in kidney failure. It is genetically heterogeneous; along with the major genes, PKD1 and PKD2, at...
2.
Gitomer B, Chonchol M, Zhou X, Garbinsky D, Wang J, Nunna S, et al.
Kidney360
. 2025 Jan;
5(9):1364-1366.
PMID: 39752236
No abstract available.
3.
Gitomer B, Wang W, George D, Coleman E, Nowak K, Struemph T, et al.
Contemp Clin Trials
. 2023 Dec;
137:107423.
PMID: 38151173
Background: Autosomal dominant polycystic kidney disease (ADPKD) is characterized by the development and continued growth of multiple cysts in the kidneys leading to ultimate loss of kidney function in most...
4.
Kleczko E, Nguyen D, Marsh K, Bauer C, Li A, Monaghan M, et al.
JCI Insight
. 2023 Jun;
8(12).
PMID: 37345660
Innate and adaptive immune cells modulate the severity of autosomal dominant polycystic kidney disease (ADPKD), a common kidney disease with inadequate treatment options. ADPKD has parallels with cancer, in which...
5.
Steele C, Oh E, Wang W, Farmer-Bailey H, Gitomer B, Chonchol M, et al.
Am J Nephrol
. 2023 May;
54(5-6):165-174.
PMID: 37231790
Introduction: Cerebrovascular dysfunction, characterized by increased brain pulsatile flow, reduced cerebrovascular reactivity, and cerebral hypoperfusion precedes the onset of dementia and is linked to cognitive dysfunction. Autosomal dominant polycystic kidney...
6.
Perrone R, Oberdhan D, Ouyang J, Bichet D, Budde K, Chapman A, et al.
Kidney Int Rep
. 2023 May;
8(5):989-1001.
PMID: 37180499
Introduction: The course of autosomal dominant polycystic kidney disease (ADPKD) varies greatly among affected individuals, necessitating natural history studies to characterize the determinants and effects of disease progression. Therefore, we...
7.
Nguyen D, Kleczko E, Dwivedi N, Monaghan M, Gitomer B, Chonchol M, et al.
JCI Insight
. 2022 Nov;
8(1).
PMID: 36422996
Autosomal dominant polycystic kidney disease (ADPKD), the most common monogenic nephropathy, is characterized by phenotypic variability that exceeds genic effects. Dysregulated metabolism and immune cell function are key disease modifiers....
8.
Klawitter J, Jackson M, Smith P, Hopp K, Chonchol M, Gitomer B, et al.
J Nephrol
. 2022 Jul;
36(1):83-91.
PMID: 35867237
Background: Autosomal dominant polycystic kidney disease (ADPKD) is a common hereditary disorder, characterized by kidney cyst formation. A major pathological feature of ADPKD is the development of interstitial inflammation. Due...
9.
Klawitter J, Sempio C, Jackson M, Smith P, Hopp K, Chonchol M, et al.
Am J Nephrol
. 2022 Mar;
53(4):264-272.
PMID: 35263737
Introduction: Autosomal dominant polycystic kidney disease (ADPKD) is a commonly inherited disorder characterized by renal cyst formation. A major pathological feature of ADPKD is the development of interstitial inflammation. The...
10.
Hopp K, Kleczko E, Gitomer B, Chonchol M, Klawitter J, Christians U, et al.
Am J Physiol Renal Physiol
. 2022 Jan;
322(3):F258-F267.
PMID: 35037466
Autosomal dominant polycystic kidney disease (ADPKD) is the most common inherited kidney disease and affects 1 in 1,000 individuals. There is accumulating evidence suggesting that there are shared cellular mechanisms...