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Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|December 26, 2014
Paradoxical response to furosemide in uromodulin-associated kidney diseaseLaura Labriola, Eric Olinger, Hendrica Belge, et al.
Clinical & Translational Oncology : Official Publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico|February 11, 2026
Inherited cancer syndromes in adult oncology: a referral guide based on malignant tumor and polyp featuresAudrey Guilmot, Magali Belpaire, Eric Olinger, et al.
Annals of Human Genetics|December 10, 2021
Pseudodominant Alport syndrome caused by pathogenic homozygous and compound heterozygous COL4A3 splicing variantsMaha Mohamed, James Tellez, Carsten Bergmann, et al.
Nature Reviews. Disease Primers|September 7, 2019
Autosomal dominant tubulointerstitial kidney diseaseOlivier Devuyst, Eric Olinger, Stefanie Weber, et al.
Molecular Genetics & Genomic Medicine|January 24, 2021
Update of genetic variants in CEP120 and CC2D2A-With an emphasis on genotype-phenotype correlations, tissue specific transcripts and exploring mutation specific exon skipping therapiesMiguel Barroso-Gil, Eric Olinger, Simon A Ramsbottom, et al.
EMBO Molecular Medicine|October 27, 2023
Allelic effects on uromodulin aggregates drive autosomal dominant tubulointerstitial kidney diseaseGuglielmo Schiano, Jennifer Lake, Marta Mariniello, et al.
Genetics in Medicine Open|December 13, 2024
Copy-number analysis from genome sequencing data of 11,754 rare-disease parent-child trios: A model for identifying autosomal recessive human gene knockouts including a novel gene for autosomal recessive retinopathyEric Olinger, Ian J Wilson, Sarah Orr, et al.
Annals of Human Genetics|April 12, 2023
Molecular genetic diagnosis of kidney ciliopathies: Lessons from interpreting genomic sequencing data and the requirement for accurate phenotypic dataSarah Orr, Eric Olinger, Sotia Iosifidou, et al.
Kidney International Reports|March 14, 2024
Monogenic Kidney Diseases in Kidney TransplantationValentine Gillion, Arnaud Devresse, Eric Olinger, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|March 15, 2022
Biallelic variants in TTC21B as a rare cause of early-onset arterial hypertension and tubuloglomerular kidney diseaseEric Olinger, Pran Phakdeekitcharoen, Yasar Caliskan, et al.
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