Eric Olinger

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 16

Top Topics

Arterial Hypertension

Top Venues

Clinical journal of the American Society of Nephrology : CJASN

Hypertension (Dallas, Tex. : 1979)

Annals of human genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Florian J Wopperer, Eric Olinger, Antje Wiesener, Katharina A-E Broeker, Karl X Knaup, Jan T Schaefer, Matthias Galiano, Karen Schneider, Mario Schiffer, null null, Frederick Pfister, André Reis, Roland Erich Schmieder, Francesca Pasutto, Karl F Hilgers, Marko Poglitsch, Christine Ziegler, Robin Shoemaker, John A Sayer, Michael S Wiesener
Progressive Kidney Failure by Angiotensinogen Inactivation in the Germline. Hypertension (Dallas, Tex. : 1979) 81 (9) (2024)
Florian J Wopperer, Eric Olinger, Antje Wiesener, Katharina A-E Broeker, Karl X Knaup, Jan T Schaefer, Matthias Galiano, Karen Schneider, Mario Schiffer, null null, Frederick Pfister, André Reis, Roland Erich Schmieder, Francesca Pasutto, Karl F Hilgers, Marko Poglitsch, Christine Ziegler, Robin Shoemaker, John A Sayer, Michael S Wiesener
Progressive Kidney Failure by Angiotensinogen Inactivation in the Germline. Hypertension (Dallas, Tex. : 1979) (2024)
Sarah Orr, Eric Olinger, Sotia Iosifidou, Miguel Barroso-Gil, Ruxandra Neatu, Katrina Wood, Ian Wilson, null null, John Andrew Sayer
Molecular genetic diagnosis of kidney ciliopathies: Lessons from interpreting genomic sequencing data and the requirement for accurate phenotypic data. Annals of human genetics (2023)
Guglielmo Schiano, Jennifer Lake, Marta Mariniello, Céline Schaeffer, Marianne Harvent, Luca Rampoldi, Eric Olinger, Olivier Devuyst
Allelic effects on uromodulin aggregates drive autosomal dominant tubulointerstitial kidney disease. EMBO molecular medicine (2023)
Eric Olinger, Pran Phakdeekitcharoen, Yasar K Caliskan, Sarah Orr, Holly Mabillard, Charles Pickles, Yincent Tse, Katrina Wood, null null, John Andrew Sayer
Biallelic variants in TTC21B as a rare cause of early-onset arterial hypertension and tubuloglomerular kidney disease. American journal of medical genetics. Part C, Seminars in medical genetics 190 (1) (2022)
Miguel Barroso-Gil, Eric Olinger, John Andrew Sayer
Molecular genetics of renal ciliopathies. Biochemical Society transactions 49 (3) (2022)
Eric Olinger, Céline Schaeffer, Kendrah Kidd, Elhussein A E Elhassan, Yurong Cheng, Inès Dufour, Guglielmo Schiano, Holly Mabillard, Elena Pasqualetto, Patrick Hofmann, Daniel G Fuster, Andreas David Kistler, Ian J Wilson, Stanislav Kmoch, Laure Raymond, Thomas Robert, null null, Kai Uwe Eckardt, Anthony J Bleyer, Anna Köttgen, Peter J Conlon, Michael S Wiesener, John Andrew Sayer, Luca Rampoldi, Olivier Devuyst
An intermediate-effect size variant in UMOD confers risk for chronic kidney disease. Proceedings of the National Academy of Sciences of the United States of America 119 (33) (2022)
Laura A Devlin, Janice Coles, Claire L Jackson, Miguel Barroso-Gil, Ben Green, Woolf T Walker, N Simon Thomas, James Thompson, Simon A Rock, Ruxandra Neatu, Laura Powell, Elisa Molinari, null null, Ian J Wilson, Heather J Cordell, Eric Olinger, Colin G Miles, John Andrew Sayer, Gabrielle Wheway, Jane S A Lucas
Biallelic variants in CEP164 cause a motile ciliopathy-like syndrome. Clinical genetics (2022)
Christina B Joseph, Marta Mariniello, Ayumi Yoshifuji, Guglielmo Schiano, Jennifer Lake, Jonathan Marten, Anne Richmond, Jennifer E Huffman, Archie Campbell, Sarah E Harris, Stephan Troyanov, Massimiliano Cocca, Antonietta Robino, Sébastien Thériault, Kai Uwe Eckardt, Matthias Wuttke, Yurong Cheng, Tanguy Corre, Ivana Kolcic, Corrinda Black, Vanessa Bruat, Maria Pina Concas, Cinzia Sala, Stefanie Aeschbacher, Franz Schaefer, Sven Bergmann, Harry Campbell, Matthias Olden, Ozren Polasek, David J Porteous, Ian J Deary, Francois Madore, Philip Awadalla, Giorgia Girotto, Sheila Ulivi, David Conen, Elke Wuehl, Eric Olinger, James F Wilson, Murielle Bochud, Anna Kottgen, Caroline Hayward, Olivier Devuyst
Meta-GWAS Reveals Novel Genetic Variants Associated with Urinary Excretion of Uromodulin. Journal of the American Society of Nephrology : JASN 33 (3) (2022)
Belén Ponte, Menno Pruijm, Daniel Ackermann, Eric Olinger, Sonia Youhanna, Bruno Vogt, Michel Burnier, Antoinette Pechere-Bertschi, Murielle Bochud, Olivier Devuyst
Uromodulin, Salt, and 24-Hour Blood Pressure in the General Population. Clinical journal of the American Society of Nephrology : CJASN 16 (5) (2021)
Intisar Al Alawi, Mohamed S Al Riyami, Miguel Barroso-Gil, Laura Powell, Eric Olinger, Isa Al Salmi, John Andrew Sayer
The diagnostic yield of whole exome sequencing as a first approach in consanguineous Omani renal ciliopathy syndrome patients. F1000Research 10 (2021)
Miguel Barroso-Gil, Eric Olinger, Simon A Rock, Elisa Molinari, Colin G Miles, John Andrew Sayer
Update of genetic variants in CEP120 and CC2D2A-With an emphasis on genotype-phenotype correlations, tissue specific transcripts and exploring mutation specific exon skipping therapies. Molecular genetics & genomic medicine (2021)
Eric Olinger, Intisar Al Alawi, Mohammed S Al Riyami, Isa Al Salmi, Elisa Molinari, Eissa Ali Faqeih, Mohamed H Al-Hamed, Miguel Barroso-Gil, Laura Powell, Abdulrahman A Al-Hussaini, Khawla A Rahim, Naif A M Almontashiri, Colin Miles, Shirlee Shril, Friedhelm Hildebrandt, Genomics England Research Consortium, Ian J Wilson, John Andrew Sayer
A discarded synonymous variant in NPHP3 explains nephronophthisis and congenital hepatic fibrosis in several families. Human mutation 42 (10) (2021)
Maha Mohamed, James Tellez, Carsten Bergmann, Daniel P Gale, John Andrew Sayer, Eric Olinger
Pseudodominant Alport syndrome caused by pathogenic homozygous and compound heterozygous COL4A3 splicing variants. Annals of human genetics (2021)
Anne Kipp, Eric Olinger
What Does Uromodulin Do? Clinical journal of the American Society of Nephrology : CJASN 16 (1) (2020)
Jessica J Stanisich, Dawid S Żyła, Pavel Afanasyev, Jingwei Xu, Anne Kipp, Eric Olinger, Olivier Devuyst, Martin Pilhofer, Daniel Boehringer, Rudi Glockshuber
The cryo-EM structure of the human uromodulin filament core reveals a unique assembly mechanism. eLife 9 (2020)