Saunder Bernes

1.8k total citations
16 papers, 500 citations indexed

About

Saunder Bernes is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Saunder Bernes has authored 16 papers receiving a total of 500 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 3 papers in Genetics and 3 papers in Cellular and Molecular Neuroscience. Recurrent topics in Saunder Bernes's work include Muscle Physiology and Disorders (4 papers), Mitochondrial Function and Pathology (3 papers) and Neurogenetic and Muscular Disorders Research (3 papers). Saunder Bernes is often cited by papers focused on Muscle Physiology and Disorders (4 papers), Mitochondrial Function and Pathology (3 papers) and Neurogenetic and Muscular Disorders Research (3 papers). Saunder Bernes collaborates with scholars based in United States, Canada and Switzerland. Saunder Bernes's co-authors include Allen M. Kaplan, Margaret A. Pearson, Nathan Fischel‐Ghodsian, Toni R. Prezant, Carlos A. Bacino, Neil Kulkarni, Theresa A. Grebe, Sha Tang, Ratan D. Bhardwaj and Vinod Sahgal and has published in prestigious journals such as Neurology, The Journal of Pediatrics and Acta Neuropathologica.

In The Last Decade

Saunder Bernes

16 papers receiving 486 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Saunder Bernes United States	14	316	109	107	79	75	16	500
Amal Y. Kentab Saudi Arabia	13	443 1.4×	53 0.5×	196 1.8×	30 0.4×	127 1.7×	44	780
Rebecca McClellan United States	12	224 0.7×	40 0.4×	205 1.9×	33 0.4×	48 0.6×	21	485
Veronika Karcagi Hungary	13	461 1.5×	79 0.7×	101 0.9×	43 0.5×	100 1.3×	32	616
Ardinger Hh United States	6	192 0.6×	37 0.3×	124 1.2×	27 0.3×	56 0.7×	287	402
Adam Mp	6	180 0.6×	37 0.3×	113 1.1×	27 0.3×	56 0.7×	286	388
Bean Ljh	6	180 0.6×	37 0.3×	113 1.1×	26 0.3×	56 0.7×	285	386
Tena Varvil United States	9	198 0.6×	217 2.0×	174 1.6×	89 1.1×	24 0.3×	10	586
Sharan Goobie Canada	15	162 0.5×	55 0.5×	281 2.6×	88 1.1×	20 0.3×	29	504
Cristina da Silva United States	12	225 0.7×	81 0.7×	218 2.0×	63 0.8×	16 0.2×	19	528
Sara Hardy United States	13	521 1.6×	113 1.0×	67 0.6×	81 1.0×	12 0.2×	36	794

Countries citing papers authored by Saunder Bernes

Since Specialization

Citations

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

Fields of papers citing papers by Saunder Bernes

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Saunder Bernes

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

All Works

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16 of 16 papers shown

Tiwari, Nishant, Jennifer Vaughn, Saunder Bernes, et al.. (2023). Epithelioid neoplasm of the spinal cord in a child with spinal muscular atrophy treated with onasemnogene abeparvovec. Molecular Therapy. 31(10). 2991–2998. 18 indexed citations

Ghosh, Rajarshi, Saunder Bernes, Pranoot Tanpaiboon, et al.. (2020). GARS‐related disease in infantile spinal muscular atrophy: Implications for diagnosis and treatment. American Journal of Medical Genetics Part A. 182(5). 1167–1176. 18 indexed citations

Wang, Julia, Emily Kim, Hannes Vogel, et al.. (2018). Clinical and molecular spectrum of thymidine kinase 2-related mtDNA maintenance defect. Molecular Genetics and Metabolism. 124(2). 124–130. 26 indexed citations

Kaye, Robin, et al.. (2018). A comprehensive institutional overview of intrathecal nusinersen injections for spinal muscular atrophy. Pediatric Radiology. 48(12). 1797–1805. 33 indexed citations

Bernes, Saunder, et al.. (2016). Outcomes of thoracoscopic thymectomy in patients with juvenile myasthenia gravis. Journal of Pediatric Surgery. 51(7). 1078–1083. 12 indexed citations

Hunter, Jesse M., Mary Ellen Ahearn, Winnie S. Liang, et al.. (2015). Novel pathogenic variants and genes for myopathies identified by whole exome sequencing. Molecular Genetics & Genomic Medicine. 3(4). 283–301. 35 indexed citations

Kulkarni, Neil, Sha Tang, Ratan D. Bhardwaj, Saunder Bernes, & Theresa A. Grebe. (2015). Progressive Movement Disorder in Brothers Carrying a GNAO1 Mutation Responsive to Deep Brain Stimulation. Journal of Child Neurology. 31(2). 211–214. 49 indexed citations

Schrauwen, Isabelle, Szabolcs Szelinger, Ashley L. Siniard, et al.. (2015). A De Novo Mutation inTEAD1Causes Non–X-Linked Aicardi Syndrome. Investigative Ophthalmology & Visual Science. 56(6). 3896–3896. 14 indexed citations

Siskind, Carly E., Shawna Feely, Saunder Bernes, Michael E. Shy, & James Garbern. (2009). Persistent CNS dysfunction in a boy with CMT1X. Journal of the Neurological Sciences. 279(1-2). 109–113. 31 indexed citations

10.

Pegoraro, Elena, R. Neil Schimke, H. Stern, et al.. (1995). Genetic and biochemical normalization in female carriers of Duchenne muscular dystrophy. Neurology. 45(4). 677–690. 66 indexed citations

11.

Kaplan, Allen M., et al.. (1995). Hemolytic uremic syndrome with particular involvement of basal ganglia and favorable outcome. Pediatric Neurology. 12(2). 155–158. 21 indexed citations

12.

Bernes, Saunder & Allen M. Kaplan. (1994). Evolution of Neonatal Seizures. Pediatric Clinics of North America. 41(5). 1069–1104. 32 indexed citations

13.

Bernes, Saunder, et al.. (1993). Identical mitochondrial DNA deletion in mother with progressive external ophthalmoplegia and son with Pearson marrow-pancreas syndrome. The Journal of Pediatrics. 123(4). 598–602. 82 indexed citations

14.

Kaler, Stephen G., Judith A. Westman, Saunder Bernes, et al.. (1993). Gastrointestinal hemorrhage associated with gastric polyps in Menkes disease. The Journal of Pediatrics. 122(1). 93–95. 33 indexed citations

15.

Sahgal, Vinod, et al.. (1983). Ultrastructure of muscle spindle in congenital myotonic dystrophy. Acta Neuropathologica. 61(3-4). 207–213. 5 indexed citations

16.

Sahgal, Vinod, et al.. (1983). Skeletal muscle in preterm infants with congenital myotonic dystrophy. Journal of the Neurological Sciences. 59(1). 47–55. 25 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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