Eric Olinger
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Explore the profile of Eric Olinger including associated specialties, affiliations and a list of published articles.
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55
Citations
842
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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.
Zagorec N, Calamel A, Delaporte M, Olinger E, Orr S, Sayer J, et al.
Am J Kidney Dis
. 2024 Dec;
PMID: 39732359
Rationale & Objective: Monoallelic predicted loss-of-function (pLoF) variants in IFT140 have recently been associated with an autosomal dominant polycystic kidney disease (ADPKD)-like phenotype. This study enhanced the characterization of this...
3.
Strauss-Kruger M, Olinger E, Hofmann P, Wilson I, Mels C, Kruger R, et al.
Kidney Int Rep
. 2024 Dec;
9(12):3477-3489.
PMID: 39698369
Introduction: Single-nucleotide polymorphisms (SNPs) in the genetic locus are associated with chronic kidney disease (CKD) in European populations, through their effect on urinary uromodulin (uUMOD) levels. The genetic and nongenetic...
4.
Kidd K, Williams A, Taylor A, Martin L, Robins V, Sayer J, et al.
BMC Nephrol
. 2024 Dec;
25(1):449.
PMID: 39696072
Background: MUC1 and UMOD pathogenic variants cause autosomal dominant tubulointerstitial kidney disease (ADTKD). MUC1 is expressed in kidney, nasal mucosa and respiratory tract, while UMOD is expressed only in kidney....
5.
Olinger E, Wilson I, Orr S, Barroso-Gil M, Neatu R, Atan D, et al.
Genet Med Open
. 2024 Dec;
2:101834.
PMID: 39669628
Purpose: In parent-child trios with genome sequencing data, we investigated inherited biallelic deletions to identify known and novel genetic disorders. Methods: We developed a copy-number variations analysis pipeline based on...
6.
Kidd K, Williams A, Taylor A, Martin L, Robins V, Sayer J, et al.
medRxiv
. 2024 Jul;
PMID: 39006416
Background: and pathogenic variants cause autosomal dominant tubulointerstitial kidney disease (ADTKD). is expressed in kidney, nasal mucosa and respiratory tract, while is expressed only in kidney. Due to haplo-insufficiency ADTKD-...
7.
Wopperer F, Olinger E, Wiesener A, Broeker K, Knaup K, Schaefer J, et al.
Hypertension
. 2024 Jul;
81(9):1857-1868.
PMID: 39005223
Background: Autosomal recessive renal tubular dysgenesis is a rare, usually fatal inherited disorder of the renin-angiotensis system (RAS). Herein, we report an adolescent individual experiencing an unknown chronic kidney disease...
8.
Lesmann H, Hustinx A, Moosa S, Klinkhammer H, Marchi E, Caro P, et al.
Res Sq
. 2024 Jun;
PMID: 38903062
The most important factor that complicates the work of dysmorphologists is the significant phenotypic variability of the human face. Next-Generation Phenotyping (NGP) tools that assist clinicians with recognizing characteristic syndromic...
9.
Gillion V, Devresse A, Olinger E, Dahlqvist G, Demoulin N, Godefroid N, et al.
Kidney Int Rep
. 2024 Mar;
9(3):549-568.
PMID: 38481491
Monogenic kidney diseases are involved in up to 15% of end-stage kidney diseases (ESKDs) in adults, and in 70 % of pediatric patients. When these disorders lead to kidney failure...
10.
Schiano G, Lake J, Mariniello M, Schaeffer C, Harvent M, Rampoldi L, et al.
EMBO Mol Med
. 2023 Oct;
15(12):e18242.
PMID: 37885358
Missense mutations in the uromodulin (UMOD) gene cause autosomal dominant tubulointerstitial kidney disease (ADTKD), one of the most common monogenic kidney diseases. The unknown impact of the allelic and gene...