Kether Guerrero

1.1k total citations
15 papers, 221 citations indexed

About

Kether Guerrero is a scholar working on Molecular Biology, Cell Biology and Cellular and Molecular Neuroscience. According to data from OpenAlex, Kether Guerrero has authored 15 papers receiving a total of 221 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 2 papers in Cell Biology and 1 paper in Cellular and Molecular Neuroscience. Recurrent topics in Kether Guerrero's work include RNA regulation and disease (13 papers), RNA and protein synthesis mechanisms (6 papers) and RNA modifications and cancer (5 papers). Kether Guerrero is often cited by papers focused on RNA regulation and disease (13 papers), RNA and protein synthesis mechanisms (6 papers) and RNA modifications and cancer (5 papers). Kether Guerrero collaborates with scholars based in Canada, United States and Netherlands. Kether Guerrero's co-authors include Geneviève Bernard, Luan T. Tran, Adeline Vanderver, Bernard Brais, Marjo S. van der Knaap, Cathy A. Stevens, Martine Tétreault, William T. Gibson, Ana S.A. Cohen and Sakkubai Naidu and has published in prestigious journals such as SHILAP Revista de lepidopterología, Neurology and Journal of Medical Genetics.

In The Last Decade

Kether Guerrero

14 papers receiving 219 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Kether Guerrero Canada	9	195	25	23	20	19	15	221
K. Wong United States	5	186 1.0×	18 0.7×	53 2.3×	44 2.2×	19 1.0×	10	242
Eline M. Hamilton Netherlands	6	173 0.9×	16 0.6×	25 1.1×	40 2.0×	35 1.8×	9	216
Martha A. Cady United States	9	210 1.1×	17 0.7×	48 2.1×	45 2.3×	12 0.6×	11	262
Andrea Dal Mas Italy	6	257 1.3×	14 0.6×	22 1.0×	31 1.6×	7 0.4×	7	310
Jana Key Germany	10	154 0.8×	13 0.5×	17 0.7×	39 1.9×	18 0.9×	22	238
Katherine R. Chao United States	8	120 0.6×	6 0.2×	45 2.0×	14 0.7×	14 0.7×	16	177
Ivana Spiga Italy	7	94 0.5×	5 0.2×	21 0.9×	13 0.7×	13 0.7×	10	163
Mark Martin United States	7	196 1.0×	26 1.0×	15 0.7×	15 0.8×	3 0.2×	11	242
Alexander P. Runko United States	6	195 1.0×	19 0.8×	24 1.0×	36 1.8×	4 0.2×	8	254
Matteo Gorza Germany	5	129 0.7×	12 0.5×	29 1.3×	62 3.1×	30 1.6×	6	199

Countries citing papers authored by Kether Guerrero

Since Specialization

Citations

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

Fields of papers citing papers by Kether Guerrero

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Kether Guerrero

This figure shows the co-authorship network connecting the top 25 collaborators of Kether Guerrero. A scholar is included among the top collaborators of Kether Guerrero 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 Kether Guerrero. Kether Guerrero 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

Guerrero, Kether, Luan T. Tran, Christoph W. Müller, et al.. (2024). Novel Pathogenic Variants in POLR3K Cause POLR3‐Related Leukodystrophy. Human Mutation. 2024(1). 8807171–8807171.

Pinard, Maxime, Luan T. Tran, Kether Guerrero, et al.. (2023). Biallelic pathogenic variants in POLR3D alter tRNA transcription and cause a hypomyelinating leukodystrophy: A case report. Frontiers in Neurology. 14. 1254140–1254140. 4 indexed citations

Guerrero, Kether, Luan T. Tran, Mackenzie A. Michell‐Robinson, et al.. (2023). Solving inherited white matter disorder etiologies in the neurology clinic: Challenges and lessons learned using next-generation sequencing. Frontiers in Neurology. 14. 1148377–1148377. 3 indexed citations

Shih, Hung‐Yu, Diane Forget, Luan T. Tran, et al.. (2021). Variants in LSM7 impair LSM complexes assembly, neurodevelopment in zebrafish and may be associated with an ultra-rare neurological disease. SHILAP Revista de lepidopterología. 2(3). 100034–100034. 8 indexed citations

Accogli, Andrea, Kether Guerrero, Daniela D’Agostino, et al.. (2018). Biallelic Loss-of-Function Variants in AIMP1 Cause a Rare Neurodegenerative Disease. Journal of Child Neurology. 34(2). 74–80. 8 indexed citations

Tran, Luan T., Kether Guerrero, Adeline Vanderver, et al.. (2018). Dystonia in RNA Polymerase III‐Related Leukodystrophy. Movement Disorders Clinical Practice. 6(2). 155–159. 18 indexed citations

Gutiérrez, Mariana, Isabelle Thiffault, Kether Guerrero, et al.. (2015). Large exonic deletions in POLRB gene cause POLR3-related leukodystrophy. Orphanet Journal of Rare Diseases. 10(1). 69–69. 17 indexed citations

Jurkiewicz, Elżbieta, Dorota Dunin-Wąsowicz, Dorota Gieruszczak‐Białek, et al.. (2015). Recessive Mutations in POLR3B Encoding RNA Polymerase III Subunit Causing Diffuse Hypomyelination in Patients with 4H Leukodystrophy with Polymicrogyria and Cataracts. Clinical Neuroradiology. 27(2). 213–220. 12 indexed citations

Spaendonk, Rosalina van, Miriam Nickel, Annette Bley, et al.. (2015). POLR3A and POLR3B Mutations in Unclassified Hypomyelination. Neuropediatrics. 46(3). 221–228. 6 indexed citations

10.

Popović, Vera, Jelena Ostojić, Sandra Pekić, et al.. (2015). Neurogenic bladder and neuroendocrine abnormalities in Pol III-related leukodystrophy. BMC Neurology. 15(1). 22–22. 4 indexed citations

11.

Kashani, Alireza, Isabelle Thiffault, Marie-Emmanuelle Dilenge, et al.. (2014). A homozygous mutation in the NDUFS1 gene presents with a mild cavitating leukoencephalopathy. Neurogenetics. 15(3). 161–164. 13 indexed citations

12.

Pizzino, Amy, Tyler Mark Pierson, Yiran Guo, et al.. (2014). TUBB4A de novo mutations cause isolated hypomyelination. Neurology. 83(10). 898–902. 39 indexed citations

13.

Tran, Luan T., Kether Guerrero, Bernard Brais, et al.. (2014). Spastic Paraparesis and Marked Improvement of Leukoencephalopathy in Aicardi–Goutières Syndrome. Neuropediatrics. 45(6). 406–410. 8 indexed citations

14.

Daoud, Hussein, Martine Tétreault, William T. Gibson, et al.. (2013). Mutations in POLR3A and POLR3B are a major cause of hypomyelinating leukodystrophies with or without dental abnormalities and/or hypogonadotropic hypogonadism. Journal of Medical Genetics. 50(3). 194–197. 70 indexed citations

15.

Guerrero, Kether, Magdalena Bachvarova, Jean‐Pierre Grégoire, et al.. (2012). A novel genome-based approach correlates TMPRSS3 overexpression in ovarian cancer with DNA hypomethylation. Gynecologic Oncology. 125(3). 720–726. 11 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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