Glenda Hendson

2.3k total citations · 1 hit paper
45 papers, 1.3k citations indexed

About

Glenda Hendson is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Glenda Hendson has authored 45 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 14 papers in Genetics and 13 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Glenda Hendson's work include Glioma Diagnosis and Treatment (11 papers), Fetal and Pediatric Neurological Disorders (11 papers) and Neonatal and fetal brain pathology (7 papers). Glenda Hendson is often cited by papers focused on Glioma Diagnosis and Treatment (11 papers), Fetal and Pediatric Neurological Disorders (11 papers) and Neonatal and fetal brain pathology (7 papers). Glenda Hendson collaborates with scholars based in Canada, United States and Germany. Glenda Hendson's co-authors include Paul Steinbok, Mary Connolly, Vann Chau, Steven P. Miller, Ning Luo, Jaime Struve, Stephen A. Back, Joshua R. Buser, Thuan Nguyen and Jennifer Maire and has published in prestigious journals such as Neurology, Cancer and Annals of Neurology.

In The Last Decade

Glenda Hendson

43 papers receiving 1.2k citations

Hit Papers

Arrested preoligodendrocyte maturation contributes to mye... 2011 2026 2016 2021 2011 100 200 300

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Glenda Hendson Canada 19 497 288 242 184 178 45 1.3k
Jennifer M. Plane United States 14 326 0.7× 278 1.0× 135 0.6× 81 0.4× 41 0.2× 16 1.1k
Yukiko Kasahara Japan 19 155 0.3× 231 0.8× 142 0.6× 223 1.2× 42 0.2× 25 852
Zoltán Patay United States 25 336 0.7× 462 1.6× 200 0.8× 740 4.0× 76 0.4× 105 2.0k
Roy D. Elterman United States 15 695 1.4× 280 1.0× 150 0.6× 492 2.7× 801 4.5× 22 1.5k
Ryosuke Hanaya Japan 19 303 0.6× 268 0.9× 138 0.6× 560 3.0× 393 2.2× 130 1.7k
Francesco Nicita Italy 23 188 0.4× 412 1.4× 73 0.3× 66 0.4× 288 1.6× 94 1.3k
T. Masaryk United States 13 144 0.3× 499 1.7× 165 0.7× 80 0.4× 265 1.5× 24 1.4k
Michael A. Nigro United States 21 139 0.3× 618 2.1× 108 0.4× 318 1.7× 180 1.0× 36 1.4k
Andreas Hahn Germany 21 90 0.2× 680 2.4× 150 0.6× 224 1.2× 198 1.1× 93 1.3k
Kari Skullerud Norway 21 167 0.3× 302 1.0× 247 1.0× 582 3.2× 110 0.6× 52 1.4k

Countries citing papers authored by Glenda Hendson

Since Specialization
Citations

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

Fields of papers citing papers by Glenda Hendson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Glenda Hendson

This figure shows the co-authorship network connecting the top 25 collaborators of Glenda Hendson. A scholar is included among the top collaborators of Glenda Hendson 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 Glenda Hendson. Glenda Hendson 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.
Dunham, Christopher, et al.. (2023). Are CUL3 variants an underreported cause of congenital heart disease?. American Journal of Medical Genetics Part A. 191(12). 2903–2907.
2.
Dixon, Katherine, Kathryn Selby, Yaoqing Shen, et al.. (2021). An infant with congenital respiratory insufficiency and diaphragmatic paralysis: A novel BICD2 phenotype?. American Journal of Medical Genetics Part A. 188(3). 926–930. 3 indexed citations
3.
Rakić, Bojana, Catherine Brunel‐Guitton, Glenda Hendson, et al.. (2019). Congenital lactic acidosis, cerebral cysts and pulmonary hypertension in an infant with FOXRED1 related complex I deficiency. Molecular Genetics and Metabolism Reports. 18. 32–38. 7 indexed citations
4.
Thibodeau, My Linh, Colin H. Peters, Katelin N. Townsend, et al.. (2017). Compound heterozygous TRPV4 mutations in two siblings with a complex phenotype including severe intellectual disability and neuropathy. American Journal of Medical Genetics Part A. 173(11). 3087–3092. 14 indexed citations
5.
Morimoto, Marie, Zhongxin Yu, Andrew K. Gormley, et al.. (2015). Transcriptional and posttranscriptional mechanisms contribute to the dysregulation of elastogenesis in Schimke immuno-osseous dysplasia. Pediatric Research. 78(6). 609–617. 5 indexed citations
6.
Chau, Vann, Kenneth J. Poskitt, Christopher Dunham, Glenda Hendson, & Steven P. Miller. (2014). Magnetic Resonance Imaging in the Encephalopathic Term Newborn. Current Pediatric Reviews. 10(1). 28–36. 25 indexed citations
7.
Ailon, Tamir, Christopher Dunham, Anne‐Sophie Carret, et al.. (2014). The role of resection alone in select children with intracranial ependymoma: the Canadian Pediatric Brain Tumour Consortium experience. Child s Nervous System. 31(1). 57–65. 15 indexed citations
8.
Walton, Cheryl, et al.. (2013). Expression profile and mitochondrial colocalization of Tdp1 in peripheral human tissues. Journal of Molecular Histology. 44(4). 481–494. 18 indexed citations
9.
Alfadhel, Majid, Yolanda Lillquist, Paula J. Waters, et al.. (2011). Infantile cardioencephalopathy due to a COX15 gene defect: Report and review. American Journal of Medical Genetics Part A. 155(4). 840–844. 26 indexed citations
10.
Brunetti‐Pierri, Nicola, Kathryn Selby, Maureen J. O’Sullivan, et al.. (2008). Rapidly Progressive Neurological Deterioration in a Child with Alpers Syndrome Exhibiting a Previously Unremarkable Brain MRI. Neuropediatrics. 39(3). 179–183. 11 indexed citations
11.
Agrawal, Deepak, Ash Singhal, Glenda Hendson, & Felix Durity. (2007). Gyriform Differentiation in Medulloblastoma – A Radiological Predictor of Histology. Pediatric Neurosurgery. 43(2). 142–145. 2 indexed citations
12.
Hendson, Glenda, et al.. (2007). Successful treatment of a child with a primary intracranial rhabdomyosarcoma with chemotherapy and radiation therapy. Journal of Neuro-Oncology. 86(1). 79–82. 20 indexed citations
13.
Steinbok, Paul, Ken Poskitt, & Glenda Hendson. (2006). Spontaneous regression of cerebellar astrocytoma after subtotal resection. Child s Nervous System. 22(6). 572–576. 17 indexed citations
14.
Basheer, Sheikh, et al.. (2006). Hemispheric Surgery in Children with Refractory Epilepsy: Seizure Outcome, Complications, and Adaptive Function. Epilepsia. 48(1). 133–140. 127 indexed citations
15.
Connolly, Mary, Glenda Hendson, & Paul Steinbok. (2006). Tuberous sclerosis complex: a review of the management of epilepsy with emphasis on surgical aspects. Child s Nervous System. 22(8). 896–908. 43 indexed citations
16.
Sadleir, Lynette G., Mary Connolly, Derek A. Applegarth, et al.. (2004). Spasms in children with definite and probable mitochondrial disease*. European Journal of Neurology. 11(2). 103–110. 13 indexed citations
17.
Rajcan‐Separovic, Evica, Glenda Hendson, Steven Tang, et al.. (2002). Interphase fluorescence in situ hybridization and DNA flow cytometry analysis of medulloblastomas with a normal karyotype. Cancer Genetics and Cytogenetics. 133(1). 94–97. 3 indexed citations
18.
Hader, Walter, Paul Steinbok, Ken Poskitt, & Glenda Hendson. (1999). Intramedullary Spinal Teratoma and Diastematomyelia. Pediatric Neurosurgery. 30(3). 140–145. 38 indexed citations
19.
Knezevich, Stevan R., Glenda Hendson, Joan Mathers, et al.. (1998). Absence of detectable EWS/FLI1 expression after therapy-induced neural differentiation in ewing sarcoma. Human Pathology. 29(3). 289–294. 25 indexed citations
20.
Hendson, Glenda, et al.. (1998). Murine MPS I: insights into the pathogenesis of Hurler syndrome. Clinical Genetics. 53(5). 349–361. 86 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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