Eric Olinger

2.4k total citations
43 papers, 1.1k citations indexed

About

Eric Olinger is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Eric Olinger has authored 43 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 15 papers in Genetics and 14 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Eric Olinger's work include Pediatric Urology and Nephrology Studies (13 papers), Genetic and Kidney Cyst Diseases (11 papers) and Renal and related cancers (10 papers). Eric Olinger is often cited by papers focused on Pediatric Urology and Nephrology Studies (13 papers), Genetic and Kidney Cyst Diseases (11 papers) and Renal and related cancers (10 papers). Eric Olinger collaborates with scholars based in Switzerland, United Kingdom and Belgium. Eric Olinger's co-authors include Olivier Devuyst, Luca Rampoldi, John A. Sayer, Natsuko Tokonami, Johannes Loffing, Kai‐Uwe Eckardt, Stefanie Weber, Anthony J. Bleyer, Stanislav Kmoch and Tomoaki Takata and has published in prestigious journals such as SHILAP Revista de lepidopterología, Scientific Reports and Journal of Cell Science.

In The Last Decade

Eric Olinger

41 papers receiving 1.1k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Eric Olinger Switzerland 18 456 397 288 230 210 43 1.1k
Judith Blaine United States 18 433 0.9× 763 1.9× 179 0.6× 67 0.3× 228 1.1× 41 1.4k
Naziha Bakouh France 13 312 0.7× 320 0.8× 202 0.7× 74 0.3× 172 0.8× 21 852
Rojesh Shrestha United States 9 1.0k 2.3× 394 1.0× 205 0.7× 98 0.4× 135 0.6× 13 1.6k
Roman‐Ulrich Müller Germany 22 903 2.0× 304 0.8× 149 0.5× 124 0.5× 358 1.7× 96 1.7k
Sally A. Hulton United Kingdom 14 932 2.0× 255 0.6× 498 1.7× 306 1.3× 91 0.4× 28 1.3k
Arezoo Daryadel Switzerland 16 388 0.9× 352 0.9× 118 0.4× 35 0.2× 147 0.7× 32 940
Liping Yu United States 13 656 1.4× 519 1.3× 104 0.4× 64 0.3× 116 0.6× 20 1.3k
Hanna Shalev Israel 18 475 1.0× 249 0.6× 231 0.8× 71 0.3× 120 0.6× 43 1.5k
Neera K. Dahl United States 15 473 1.0× 198 0.5× 191 0.7× 169 0.7× 508 2.4× 58 939
Li-Wen Lai United States 15 401 0.9× 201 0.5× 89 0.3× 54 0.2× 136 0.6× 30 916

Countries citing papers authored by Eric Olinger

Since Specialization
Citations

This map shows the geographic impact of Eric Olinger's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Eric Olinger with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Eric Olinger more than expected).

Fields of papers citing papers by Eric Olinger

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Eric Olinger. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Eric Olinger. The network helps show where Eric Olinger may publish in the future.

Co-authorship network of co-authors of Eric Olinger

This figure shows the co-authorship network connecting the top 25 collaborators of Eric Olinger. A scholar is included among the top collaborators of Eric Olinger based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Eric Olinger. Eric Olinger is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
2.
Olinger, Eric, Ian Wilson, Catharina M. C. Mels, et al.. (2024). UMOD Genotype and Determinants of Urinary Uromodulin in African Populations. Kidney International Reports. 9(12). 3477–3489.
3.
Anderegg, Manuel, Eric Olinger, Matteo Bargagli, et al.. (2024). Prevalence and characteristics of genetic disease in adult kidney stone formers. Nephrology Dialysis Transplantation. 39(9). 1426–1441. 19 indexed citations
4.
Gillion, Valentine, Arnaud Devresse, Eric Olinger, et al.. (2023). Monogenic Kidney Diseases in Kidney Transplantation. Kidney International Reports. 9(3). 549–568. 1 indexed citations
5.
Geraghty, Robert, et al.. (2023). Use of whole genome sequencing to determine the genetic basis of visceral myopathies including Prune Belly syndrome. PubMed. 2(1). 9–9. 2 indexed citations
6.
7.
Mabillard, Holly, Eric Olinger, & John A. Sayer. (2022). UMOD and you! Explaining a rare disease diagnosis. PubMed. 1(1). 4–4. 1 indexed citations
8.
Devuyst, Olivier, Murielle Bochud, & Eric Olinger. (2022). UMOD and the architecture of kidney disease. Pflügers Archiv - European Journal of Physiology. 474(8). 771–781. 12 indexed citations
9.
10.
Olinger, Eric, Issa Al Salmi, Elisa Molinari, et al.. (2021). A discarded synonymous variant in NPHP3 explains nephronophthisis and congenital hepatic fibrosis in several families. Human Mutation. 42(10). 1221–1228. 9 indexed citations
11.
Ponte, Belén, Marie C. Sadler, Eric Olinger, et al.. (2021). Mendelian randomization to assess causality between uromodulin, blood pressure and chronic kidney disease. Kidney International. 100(6). 1282–1291. 27 indexed citations
12.
Zyla, Dawid, Pavel Afanasyev, Jingwei Xu, et al.. (2020). The cryo-EM structure of the human uromodulin filament core reveals a unique assembly mechanism. eLife. 9. 30 indexed citations
13.
Olinger, Eric, Susan Sheehan, Tomoaki Takata, et al.. (2019). Hepsin-mediated Processing of Uromodulin is Crucial for Salt-sensitivity and Thick Ascending Limb Homeostasis. Scientific Reports. 9(1). 12287–12287. 42 indexed citations
14.
Devuyst, Olivier, Eric Olinger, & Luca Rampoldi. (2017). Uromodulin: from physiology to rare and complex kidney disorders. Nature Reviews Nephrology. 13(9). 525–544. 208 indexed citations
15.
Hadj‐Rabia, S., Gaëlle Brideau, Yasser Al‐Sarraj, et al.. (2017). Multiplex epithelium dysfunction due to CLDN10 mutation: the HELIX syndrome. Genetics in Medicine. 20(2). 190–201. 68 indexed citations
16.
Huynh‐Do, Uyen, Urs Widmer, Huguette Debaix, et al.. (2017). Impact of cardio-renal syndrome on adverse outcomes in patients with Fabry disease in a long-term follow-up. International Journal of Cardiology. 249. 261–267. 21 indexed citations
17.
Terryn, Sara, Karo Tanaka, Jean‐Philippe Lengelé, et al.. (2016). Tubular proteinuria in patients with HNF1α mutations: HNF1α drives endocytosis in the proximal tubule. Kidney International. 89(5). 1075–1089. 30 indexed citations
18.
Gailly, Philippe, et al.. (2014). P2Y2 receptor activation inhibits the expression of the sodium-chloride cotransporter NCC in distal convoluted tubule cells. Pflügers Archiv - European Journal of Physiology. 466(11). 2035–2047. 8 indexed citations
19.
Labriola, Laura, Eric Olinger, Hendrica Belge, et al.. (2014). Paradoxical response to furosemide in uromodulin-associated kidney disease. Nephrology Dialysis Transplantation. 30(2). 330–335. 15 indexed citations
20.
Olinger, Eric, Beat Schwaller, Johannes Loffing, Philippe Gailly, & Olivier Devuyst. (2012). Parvalbumin: calcium and magnesium buffering in the distal nephron. Nephrology Dialysis Transplantation. 27(11). 3988–3994. 33 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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