Kimberly Jett

898 total citations
15 papers, 605 citations indexed

About

Kimberly Jett is a scholar working on Neurology, Epidemiology and Molecular Biology. According to data from OpenAlex, Kimberly Jett has authored 15 papers receiving a total of 605 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Neurology, 4 papers in Epidemiology and 3 papers in Molecular Biology. Recurrent topics in Kimberly Jett's work include Neurofibromatosis and Schwannoma Cases (9 papers), Meningioma and schwannoma management (4 papers) and Mitochondrial Function and Pathology (3 papers). Kimberly Jett is often cited by papers focused on Neurofibromatosis and Schwannoma Cases (9 papers), Meningioma and schwannoma management (4 papers) and Mitochondrial Function and Pathology (3 papers). Kimberly Jett collaborates with scholars based in Canada, United States and Germany. Kimberly Jett's co-authors include Jan M. Friedman, Scot C. Leary, Rosa Nguyen, Victor‐Felix Mautner, Cornelis van Breemen, Mitra Esfandiarei, Pascal Bernatchez, Wenli Cai, Gordon J. Harris and Jason Z. Cui and has published in prestigious journals such as Journal of Biological Chemistry, PLoS ONE and Scientific Reports.

In The Last Decade

Kimberly Jett

14 papers receiving 589 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Kimberly Jett Canada	10	411	156	150	122	101	15	605
Claudia Mischung Germany	6	205 0.5×	51 0.3×	133 0.9×	82 0.7×	234 2.3×	6	565
Nobuo Ito Japan	11	174 0.4×	36 0.2×	103 0.7×	97 0.8×	229 2.3×	30	555
Muhammad S. Ali United States	13	770 1.9×	110 0.7×	246 1.6×	369 3.0×	129 1.3×	24	986
Takayuki Sugawara Japan	17	511 1.2×	147 0.9×	54 0.4×	173 1.4×	110 1.1×	77	841
Peter Jun United States	15	207 0.5×	144 0.9×	28 0.2×	69 0.6×	301 3.0×	20	741
Jungho Ahn South Korea	14	133 0.3×	82 0.5×	221 1.5×	65 0.5×	93 0.9×	29	540
Roope A. Kallionpää Finland	14	551 1.3×	196 1.3×	187 1.2×	154 1.3×	103 1.0×	38	737
Zhongxue Wu China	15	434 1.1×	85 0.5×	75 0.5×	118 1.0×	112 1.1×	57	622
M Zavanone Italy	15	109 0.3×	88 0.6×	38 0.3×	55 0.5×	131 1.3×	33	582
Miyuki Kanematsu Japan	7	399 1.0×	27 0.2×	142 0.9×	213 1.7×	102 1.0×	14	662

Countries citing papers authored by Kimberly Jett

Since Specialization

Citations

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

Fields of papers citing papers by Kimberly Jett

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kimberly Jett

This figure shows the co-authorship network connecting the top 25 collaborators of Kimberly Jett. A scholar is included among the top collaborators of Kimberly Jett 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 Kimberly Jett. Kimberly Jett is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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15 of 15 papers shown

Jett, Kimberly, Aren Boulet, Stanley A. Moore, et al.. (2025). Heart is the most susceptible organ in an isogenic background to loss of function mutations in the mitochondrial metallochaperone SCO1. Human Molecular Genetics. 34(19). 1599–1609. 1 indexed citations

Allan, Nick, Jacob M. Hooker, Wendy Bernhard, et al.. (2025). Olfactory Drug Delivery in Rodents: Deposition and Pharmacokinetics. ACS Pharmacology & Translational Science. 8(7). 2167–2179.

Bernhard, Wendy, Kris Barreto, Ayman El‐Sayed, et al.. (2023). Evaluation of nimotuzumab Fab2 as an optical imaging agent in EGFR positive cancers. Scientific Reports. 13(1). 10990–10990. 2 indexed citations

Esfandiarei, Mitra, et al.. (2018). Neurofibromin haploinsufficiency results in altered spermatogenesis in a mouse model of neurofibromatosis type 1. PLoS ONE. 13(12). e0208835–e0208835. 8 indexed citations

Jett, Kimberly, Aren Boulet, Paul A. Cobine, et al.. (2017). The mitochondrial metallochaperone SCO1 maintains CTR1 at the plasma membrane to preserve copper homeostasis in the murine heart. Human Molecular Genetics. 26(23). 4617–4628. 27 indexed citations

Jett, Kimberly & Scot C. Leary. (2017). Building the CuA site of cytochrome c oxidase: A complicated, redox-dependent process driven by a surprisingly large complement of accessory proteins. Journal of Biological Chemistry. 293(13). 4644–4652. 39 indexed citations

Jett, Kimberly, Rosa Nguyen, Patricia Birch, et al.. (2015). Quantitative associations of scalp and body subcutaneous neurofibromas with internal plexiform tumors in neurofibromatosis 1. American Journal of Medical Genetics Part A. 167(7). 1518–1524. 5 indexed citations

Cui, Jason Z., et al.. (2014). Quantification of aortic and cutaneous elastin and collagen morphology in Marfan syndrome by multiphoton microscopy. Journal of Structural Biology. 187(3). 242–253. 45 indexed citations

Armstrong, Linlea, Kimberly Jett, Patricia Birch, et al.. (2013). The generalized bone phenotype in children with neurofibromatosis 1: A sibling matched case–control study. American Journal of Medical Genetics Part A. 161(7). 1654–1661. 22 indexed citations

10.

Nguyen, Rosa, Kimberly Jett, Gordon J. Harris, et al.. (2013). Benign whole body tumor volume is a risk factor for malignant peripheral nerve sheath tumors in neurofibromatosis type 1. Journal of Neuro-Oncology. 116(2). 307–313. 50 indexed citations

11.

Kluwe, Lan, Rosa Nguyen, J. Vogt, et al.. (2012). Internal tumor burden in neurofibromatosis Type I patients with large NF1 deletions. Genes Chromosomes and Cancer. 51(5). 447–451. 28 indexed citations

12.

Schnabel, Claudia, Kimberly Jett, Jan M. Friedman, et al.. (2012). Effect of vitamin D3 treatment on bone density in neurofibromatosis 1 patients: A retrospective clinical study. Joint Bone Spine. 80(3). 315–319. 16 indexed citations

13.

Nguyen, Rosa, Lan Kluwe, Kimberly Jett, et al.. (2012). Cardiac characterization of 16 patients with large NF1 gene deletions. Clinical Genetics. 84(4). 344–349. 24 indexed citations

14.

Heran, Manraj K.S., Mary Connolly, Jan M. Friedman, et al.. (2010). Cerebrovasculopathy in NF1 associated with ocular and scalp defects. American Journal of Medical Genetics Part A. 155(2). 380–385. 12 indexed citations

15.

Jett, Kimberly & Jan M. Friedman. (2010). Clinical and genetic aspects of neurofibromatosis 1. Genetics in Medicine. 12(1). 1–11. 326 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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