Deborah L. Renaud

1.3k total citations
41 papers, 470 citations indexed

About

Deborah L. Renaud is a scholar working on Molecular Biology, Neurology and Clinical Biochemistry. According to data from OpenAlex, Deborah L. Renaud has authored 41 papers receiving a total of 470 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 9 papers in Neurology and 7 papers in Clinical Biochemistry. Recurrent topics in Deborah L. Renaud's work include RNA regulation and disease (10 papers), Metabolism and Genetic Disorders (7 papers) and Mitochondrial Function and Pathology (6 papers). Deborah L. Renaud is often cited by papers focused on RNA regulation and disease (10 papers), Metabolism and Genetic Disorders (7 papers) and Mitochondrial Function and Pathology (6 papers). Deborah L. Renaud collaborates with scholars based in United States, Canada and Italy. Deborah L. Renaud's co-authors include Ann M. Reed, Farid H. Mahmud, Aida Lteif, Chad K. Brands, Andrew McKeon, Vanda A. Lennon, Sean J. Pittock, Michael C. Brodsky, Joseph Y. Matsumoto and Stacey Clardy and has published in prestigious journals such as SHILAP Revista de lepidopterología, PEDIATRICS and Ophthalmology.

In The Last Decade

Deborah L. Renaud

35 papers receiving 459 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Deborah L. Renaud United States 11 233 180 88 79 53 41 470
Geetha Anand United Kingdom 13 303 1.3× 98 0.5× 77 0.9× 105 1.3× 34 0.6× 34 565
Sietske H. Kevelam Netherlands 10 283 1.2× 100 0.6× 86 1.0× 83 1.1× 19 0.4× 11 473
Michaela Brunner‐Krainz Austria 10 147 0.6× 146 0.8× 129 1.5× 56 0.7× 62 1.2× 22 393
Michela Ripolone Italy 13 349 1.5× 72 0.4× 67 0.8× 63 0.8× 74 1.4× 40 526
S Vlaho Germany 10 200 0.9× 90 0.5× 103 1.2× 40 0.5× 49 0.9× 24 513
Marwan Nashabat Saudi Arabia 13 229 1.0× 53 0.3× 130 1.5× 105 1.3× 28 0.5× 25 422
Patrick Verloo Belgium 11 273 1.2× 41 0.2× 108 1.2× 56 0.7× 48 0.9× 25 434
Carlos Casasnovas Spain 14 270 1.2× 179 1.0× 27 0.3× 42 0.5× 43 0.8× 40 567
Jutta Gärtner Germany 14 366 1.6× 53 0.3× 56 0.6× 109 1.4× 60 1.1× 19 650
Rabab Debs France 12 114 0.5× 237 1.3× 46 0.5× 24 0.3× 84 1.6× 25 486

Countries citing papers authored by Deborah L. Renaud

Since Specialization
Citations

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

Fields of papers citing papers by Deborah L. Renaud

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Deborah L. Renaud. 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 Deborah L. Renaud. The network helps show where Deborah L. Renaud may publish in the future.

Co-authorship network of co-authors of Deborah L. Renaud

This figure shows the co-authorship network connecting the top 25 collaborators of Deborah L. Renaud. A scholar is included among the top collaborators of Deborah L. Renaud 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 Deborah L. Renaud. Deborah L. Renaud 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.
Bertini, Enrico, Francesco Nicita, Daniela Pohl, et al.. (2025). POLR3-Related Leukodystrophy: A Qualitative Study on Parents’ Experiences With the Health Care System. Pediatric Neurology. 166. 81–87.
2.
Flamini, Robert, Andrea Rossi, Enrico Bertini, et al.. (2024). Stress and Quality of Life of Parents of Children With POLR3-Related Leukodystrophy: A Cross-Sectional Pilot Study. Journal of Child Neurology. 40(1). 26–38.
3.
4.
Kirsch, Alexandra C., et al.. (2021). Neuropsychological Functioning in Alexander Disease: A Case Series. SHILAP Revista de lepidopterología. 8. 2329048X211048614–2329048X211048614. 4 indexed citations
5.
Boczek, Nicole J., Erica L. Macke, Jennifer L. Kemppainen, et al.. (2020). Expansion of PURA-Related Phenotypes and Discovery of a Novel PURA Variant: A Case Report. SHILAP Revista de lepidopterología. 7. 2329048X2095500–2329048X2095500. 4 indexed citations
6.
Blackburn, Patrick R., Matthew Schultz, Dong Li, et al.. (2020). Expanding the clinical and phenotypic heterogeneity associated with biallelic variants in ACO2. Annals of Clinical and Translational Neurology. 7(6). 1013–1028. 5 indexed citations
7.
Lund, Troy C., Weston P. Miller, Julie B. Eisengart, et al.. (2019). Biochemical and clinical response after umbilical cord blood transplant in a boy with early childhood‐onset beta‐mannosidosis. Molecular Genetics & Genomic Medicine. 7(7). e00712–e00712. 5 indexed citations
8.
Mauermann, Michelle L., Zhiyv Niu, Deborah L. Renaud, et al.. (2018). Targeted gene approach with biochemical assay confirms ABCD1 mutation of X-linked adrenoleukodystrophy in a 62-year-old man with gait imbalance. Neuromuscular Disorders. 29(2). 146–149. 2 indexed citations
9.
Agosta, Guillermo, William Benko, Jens C. Eickhoff, et al.. (2015). CSF and Blood Levels of GFAP in Alexander Disease. eNeuro. 2(5). ENEURO.0080–15.2015. 31 indexed citations
10.
Renaud, Deborah L. & Michael C. Brodsky. (2015). GM2-Gangliosidosis, AB Variant: Clinical, Ophthalmological, MRI, and Molecular Findings. JIMD Reports. 25. 83–86. 14 indexed citations
11.
Wang, Jing, Guoli Wang, Soledad Kleppe, et al.. (2013). Biochemical, molecular, and clinical diagnoses of patients with cerebral creatine deficiency syndromes. Molecular Genetics and Metabolism. 109(3). 260–268. 29 indexed citations
12.
Tillema, Jan‐Mendelt, Deborah L. Renaud, & B. Mark Keegan. (2013). A CNS multifocal disease: Important diagnostic considerations regarding multiple sclerosis. Multiple Sclerosis and Related Disorders. 3(3). 402–407. 1 indexed citations
13.
Renaud, Deborah L.. (2012). Lysosomal Disorders Associated with Leukoencephalopathy. Seminars in Neurology. 32(1). 51–54. 18 indexed citations
14.
Dhamija, Radhika, Deborah L. Renaud, Sean J. Pittock, et al.. (2011). Neuronal Voltage-Gated Potassium Channel Complex Autoimmunity in Children. Pediatric Neurology. 44(4). 275–281. 43 indexed citations
15.
Barger, Andrew V., Norbert G. Campeau, John D. Port, & Deborah L. Renaud. (2009). MRS is the Test of Choice for Detecting and Monitoring Disorders of Creatine Metabolism. Pediatric Neurology. 40(5). 408–410. 3 indexed citations
16.
Renaud, Deborah L., et al.. (2008). Magnetic Resonance Imaging Findings in Alexander Disease. Pediatric Neurology. 38(5). 373–374. 6 indexed citations
17.
Renaud, Deborah L., et al.. (2006). Spondyloarthropathy presenting at a young age: case report and review. Skeletal Radiology. 36(2). 161–164. 5 indexed citations
18.
Laird, Philip W., Brian G. Mohney, & Deborah L. Renaud. (2006). Bull’s-Eye Maculopathy in an Infant With Leigh Disease. American Journal of Ophthalmology. 142(1). 186–187. 4 indexed citations
19.
Renaud, Deborah L. & Suresh Kotagal. (2006). Pantothenate-Kinase Associated Neurodegeneration (PKAN) “Eye of the Tiger” Sign. Pediatric Neurology. 36(1). 70–71. 5 indexed citations
20.
Mahmud, Farid H., Aida Lteif, Deborah L. Renaud, Ann M. Reed, & Chad K. Brands. (2003). Steroid-Responsive Encephalopathy Associated With Hashimoto’s Thyroiditis in an Adolescent With Chronic Hallucinations and Depression: Case Report and Review. PEDIATRICS. 112(3). 686–690. 57 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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