Kendrah Kidd

1.2k total citations
23 papers, 265 citations indexed

About

Kendrah Kidd is a scholar working on Nephrology, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Kendrah Kidd has authored 23 papers receiving a total of 265 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Nephrology, 10 papers in Molecular Biology and 10 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Kendrah Kidd's work include Renal Diseases and Glomerulopathies (11 papers), Kidney Stones and Urolithiasis Treatments (7 papers) and Ion Transport and Channel Regulation (6 papers). Kendrah Kidd is often cited by papers focused on Renal Diseases and Glomerulopathies (11 papers), Kidney Stones and Urolithiasis Treatments (7 papers) and Ion Transport and Channel Regulation (6 papers). Kendrah Kidd collaborates with scholars based in United States, Czechia and Ireland. Kendrah Kidd's co-authors include Anthony J. Bleyer, Stanislav Kmoch, Martina Živná, Yeawon Kim, Ying Maggie Chen, Rebecca Perry, Eric K. Peden, Rick Mishler, Samuel E. Wilson and Timmy Lee and has published in prestigious journals such as Journal of Biological Chemistry, Nature Communications and Journal of the American Society of Nephrology.

In The Last Decade

Kendrah Kidd

21 papers receiving 260 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Kendrah Kidd United States 8 122 109 64 55 47 23 265
Eduardo Machuca Chile 8 341 2.8× 180 1.7× 26 0.4× 57 1.0× 81 1.7× 10 401
Shiho Makabe Japan 10 92 0.8× 59 0.5× 51 0.8× 107 1.9× 32 0.7× 33 218
Shinya Ogasawara Japan 8 249 2.0× 116 1.1× 42 0.7× 46 0.8× 33 0.7× 10 388
Prabha Senguttuvan India 7 167 1.4× 88 0.8× 35 0.5× 32 0.6× 53 1.1× 15 263
Matthew J. Seasock United States 5 155 1.3× 192 1.8× 31 0.5× 64 1.2× 17 0.4× 8 358
Linda Xu United States 5 222 1.8× 207 1.9× 146 2.3× 87 1.6× 49 1.0× 10 422
Daniel Rodríguez Switzerland 8 95 0.8× 151 1.4× 38 0.6× 181 3.3× 57 1.2× 25 349
Stéphanie De Rechter Belgium 10 70 0.6× 132 1.2× 36 0.6× 129 2.3× 32 0.7× 16 264
Ke Song China 7 26 0.2× 103 0.9× 28 0.4× 16 0.3× 10 0.2× 13 237
Hiroko Togawa Japan 10 260 2.1× 76 0.7× 39 0.6× 37 0.7× 111 2.4× 15 324

Countries citing papers authored by Kendrah Kidd

Since Specialization
Citations

This map shows the geographic impact of Kendrah Kidd'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 Kendrah Kidd with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Kendrah Kidd more than expected).

Fields of papers citing papers by Kendrah Kidd

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Kendrah Kidd. 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 Kendrah Kidd. The network helps show where Kendrah Kidd may publish in the future.

Co-authorship network of co-authors of Kendrah Kidd

This figure shows the co-authorship network connecting the top 25 collaborators of Kendrah Kidd. A scholar is included among the top collaborators of Kendrah Kidd 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 Kendrah Kidd. Kendrah Kidd 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.
Bleyer, Anthony J., Kendrah Kidd, Martina Živná, & Stanislav Kmoch. (2025). Autosomal Dominant Tubulointerstitial Kidney Disease: A Review. American Journal of Kidney Diseases. 86(5). 677–689. 1 indexed citations
2.
Wenzel, Andrea, Jean‐Baptiste Gibier, Claire‐Marie Dhaenens, et al.. (2024). Description of a New Simple and Cost-Effective Molecular Testing That Could Simplify MUC1 Variant Detection. Kidney International Reports. 9(5). 1451–1457. 6 indexed citations
3.
Kidd, Kendrah, et al.. (2024). 426 Healthcare priorities and needs for LGBTQIA+ people with CF: a concept mapping study. Journal of Cystic Fibrosis. 23. S227–S228.
4.
Jorge, Sofía, Kendrah Kidd, Petr Vyleťal, et al.. (2023). Bi-allelic REN Mutations and Undetectable Plasma Renin Activity in a Patient With Progressive CKD. Kidney International Reports. 8(5). 1112–1116. 1 indexed citations
5.
Airik, Merlin, Chi‐Wei Chen, Katherine M. Aird, et al.. (2023). Mitochondrial ROS Triggers KIN Pathogenesis in FAN1-Deficient Kidneys. Antioxidants. 12(4). 900–900. 5 indexed citations
6.
Kim, Yeawon, Chuang Li, Chenjian Gu, et al.. (2023). MANF stimulates autophagy and restores mitochondrial homeostasis to treat autosomal dominant tubulointerstitial kidney disease in mice. Nature Communications. 14(1). 6493–6493. 30 indexed citations
7.
Al‐bataineh, Mohammad M., Carol L. Kinlough, Allison L. Marciszyn, et al.. (2023). Influence of glycoprotein MUC1 on trafficking of the Ca2+-selective ion channels, TRPV5 and TRPV6, and on in vivo calcium homeostasis. Journal of Biological Chemistry. 299(3). 102925–102925. 4 indexed citations
8.
Bleyer, Anthony J., Kendrah Kidd, Adrienne H. Williams, et al.. (2022). Maternal health and pregnancy outcomes in autosomal dominant tubulointerstitial kidney disease. Obstetric Medicine. 16(3). 162–169.
9.
Živná, Martina, Kendrah Kidd, Veronika Barešová, et al.. (2022). Autosomal dominant tubulointerstitial kidney disease: A review. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 190(3). 309–324. 12 indexed citations
10.
Buglioni, Alessia, Linda Hasadsri, Samih H. Nasr, et al.. (2021). Mitochondriopathy Manifesting as Inherited Tubulointerstitial Nephropathy Without Symptomatic Other Organ Involvement. Kidney International Reports. 6(9). 2514–2518. 3 indexed citations
11.
Bleyer, Anthony J., Matthias T. F. Wolf, Kendrah Kidd, Martina Živná, & Stanislav Kmoch. (2021). Autosomal dominant tubulointerstitial kidney disease: more than just HNF1β. Pediatric Nephrology. 37(5). 933–946. 7 indexed citations
12.
Bleyer, Anthony J., Kendrah Kidd, Hannah C. Ainsworth, et al.. (2021). A Cohort Study of Patients with Autosomal Dominant Tubulointerstitial Kidney Disease (ADTKD) Started on SGLT-2 Inhibitors. Journal of the American Society of Nephrology. 32(10S). 419–419. 1 indexed citations
13.
Kim, Yeawon, Zheyu Wang, Chuang Li, et al.. (2021). Ultrabright plasmonic fluor nanolabel-enabled detection of a urinary ER stress biomarker in autosomal dominant tubulointerstitial kidney disease. American Journal of Physiology-Renal Physiology. 321(2). F236–F244. 6 indexed citations
14.
Murray, Susan, Anthony Dorman, Katherine A. Benson, et al.. (2019). Utility of Genomic Testing after Renal Biopsy. American Journal of Nephrology. 51(1). 43–53. 19 indexed citations
15.
Bleyer, Anthony J., Vincent Scavo, Samuel E. Wilson, et al.. (2019). A randomized trial of vonapanitase (PATENCY-1) to promote radiocephalic fistula patency and use for hemodialysis. Journal of Vascular Surgery. 69(2). 507–515. 35 indexed citations
16.
Cormican, Sarah, Dervla M. Connaughton, Claire Kennedy, et al.. (2019). Autosomal dominant tubulointerstitial kidney disease (ADTKD) in Ireland. Renal Failure. 41(1). 832–841. 14 indexed citations
17.
Hnı́zda, Aleš, Irène Ceballos-Picot, Amret Hawfield, et al.. (2018). Chronic tubulointerstitial kidney disease in untreated adenine phosphoribosyl transferase (APRT) deficiency: A case report. Clinical Nephrology. 90(4). 296–301. 6 indexed citations
18.
Kim, Yeawon, Scott R. Manson, Carlos A. Molina, et al.. (2017). Elevated urinary CRELD2 is associated with endoplasmic reticulum stress–mediated kidney disease. JCI Insight. 2(23). 33 indexed citations
19.
Bleyer, Anthony J., Kendrah Kidd, Martina Živná, & Stanislav Kmoch. (2017). Autosomal Dominant Tubulointerstitial Kidney Disease. Advances in Chronic Kidney Disease. 24(2). 86–93. 49 indexed citations
20.
Blumenstiel, Brendan, Matthew DeFelice, Ozge Ceyhan‐Birsoy, et al.. (2016). Development and Validation of a Mass Spectrometry–Based Assay for the Molecular Diagnosis of Mucin-1 Kidney Disease. Journal of Molecular Diagnostics. 18(4). 566–571. 23 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026