Lindsay C. Swanson

2.5k total citations
26 papers, 990 citations indexed

About

Lindsay C. Swanson is a scholar working on Genetics, Molecular Biology and Cell Biology. According to data from OpenAlex, Lindsay C. Swanson has authored 26 papers receiving a total of 990 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 12 papers in Molecular Biology and 4 papers in Cell Biology. Recurrent topics in Lindsay C. Swanson's work include Genetics and Neurodevelopmental Disorders (19 papers), Genomic variations and chromosomal abnormalities (6 papers) and Muscle Physiology and Disorders (5 papers). Lindsay C. Swanson is often cited by papers focused on Genetics and Neurodevelopmental Disorders (19 papers), Genomic variations and chromosomal abnormalities (6 papers) and Muscle Physiology and Disorders (5 papers). Lindsay C. Swanson collaborates with scholars based in United States, Australia and United Kingdom. Lindsay C. Swanson's co-authors include Tim A. Benke, Heather E. Olson, Scott Demarest, Helen Leonard, Alan H. Beggs, Elia Pestana‐Knight, Dennis Lal, Michael W. Lawlor, Henk Granzier and Orrin Devinsky and has published in prestigious journals such as Neurology, Annals of Neurology and The Lancet Neurology.

In The Last Decade

Lindsay C. Swanson

25 papers receiving 974 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Lindsay C. Swanson United States 15 537 497 207 148 127 26 990
Katherine L. Helbig United States 20 641 1.2× 1.1k 2.1× 58 0.3× 105 0.7× 411 3.2× 42 1.6k
Alex R. Paciorkowski United States 21 630 1.2× 669 1.3× 36 0.2× 151 1.0× 270 2.1× 49 1.4k
Giulia Barcia France 17 583 1.1× 501 1.0× 90 0.4× 160 1.1× 539 4.2× 56 1.3k
Joon‐Yong An South Korea 15 541 1.0× 397 0.8× 32 0.2× 279 1.9× 91 0.7× 49 982
Heather E. Olson United States 21 513 1.0× 861 1.7× 47 0.2× 162 1.1× 753 5.9× 58 1.8k
Rose Tobias Canada 15 303 0.6× 523 1.1× 28 0.1× 77 0.5× 68 0.5× 19 979
Gemma L. Carvill United States 19 560 1.0× 671 1.4× 46 0.2× 58 0.4× 402 3.2× 41 1.2k
Kimberly Chambert United States 10 509 0.9× 704 1.4× 22 0.1× 104 0.7× 64 0.5× 10 1.1k
Mercédes Pineda Spain 18 499 0.9× 278 0.6× 13 0.1× 84 0.6× 94 0.7× 29 1.0k
Mina Ohadi Iran 18 525 1.0× 270 0.5× 26 0.1× 46 0.3× 97 0.8× 73 1.0k

Countries citing papers authored by Lindsay C. Swanson

Since Specialization
Citations

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

Fields of papers citing papers by Lindsay C. Swanson

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lindsay C. Swanson. 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 Lindsay C. Swanson. The network helps show where Lindsay C. Swanson may publish in the future.

Co-authorship network of co-authors of Lindsay C. Swanson

This figure shows the co-authorship network connecting the top 25 collaborators of Lindsay C. Swanson. A scholar is included among the top collaborators of Lindsay C. Swanson 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 Lindsay C. Swanson. Lindsay C. Swanson 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.
Srivastava, Siddharth, Lindsay C. Swanson, Boris Keren, et al.. (2024). Cohort Expansion and Genotype-Phenotype Analysis of RAB11A-Associated Neurodevelopmental Disorder. Pediatric Neurology. 160. 45–53.
2.
Saby, Joni N., Sarika U. Peters, Tim A. Benke, et al.. (2023). Comparison of evoked potentials across four related developmental encephalopathies. Journal of Neurodevelopmental Disorders. 15(1). 10–10. 11 indexed citations
3.
Leonard, Helen, Jenny Downs, Tim A. Benke, et al.. (2022). CDKL5 deficiency disorder: clinical features, diagnosis, and management. The Lancet Neurology. 21(6). 563–576. 80 indexed citations
4.
Drew, Jacqueline M., Jamie Love‐Nichols, Lindsay C. Swanson, et al.. (2022). Genetic Diagnosis Impacts Medical Management for Pediatric Epilepsies. Pediatric Neurology. 138. 71–80. 14 indexed citations
5.
Delépine, Chloé, Lindsay C. Swanson, Mustafa Şahin, et al.. (2022). Molecular Signatures of Response to Mecasermin in Children With Rett Syndrome. Frontiers in Neuroscience. 16. 868008–868008. 2 indexed citations
6.
Zlatic, Stephanie A., Duc M. Duong, Kamal K.E. Gadalla, et al.. (2022). Convergent cerebrospinal fluid proteomes and metabolic ontologies in humans and animal models of Rett syndrome. iScience. 25(9). 104966–104966. 4 indexed citations
7.
Olson, Heather E., Lindsay C. Swanson, Scott Demarest, et al.. (2021). Current neurologic treatment and emerging therapies in CDKL5 deficiency disorder. Journal of Neurodevelopmental Disorders. 13(1). 40–40. 32 indexed citations
8.
Braden, Ruth, David J. Amor, Simon E. Fisher, et al.. (2021). Severe speech impairment is a distinguishing feature of FOXP1‐related disorder. Developmental Medicine & Child Neurology. 63(12). 1417–1426. 27 indexed citations
9.
Srivastava, Siddharth, Erica L. Macke, Lindsay C. Swanson, et al.. (2021). Expansion of the Genotypic and Phenotypic Spectrum of WASF1-Related Neurodevelopmental Disorder. Brain Sciences. 11(7). 931–931. 9 indexed citations
10.
Chen, Teresa C., Elizabeth D. Buttermore, Robin J. Kleiman, et al.. (2021). Generation and characterization of human induced pluripotent stem cells (iPSCs) from three male and three female patients with CDKL5 Deficiency Disorder (CDD). Stem Cell Research. 53. 102276–102276. 7 indexed citations
11.
Srivastava, Siddharth, Angelica D’Amore, Julie S. Cohen, et al.. (2020). Expansion of the genetic landscape of ERLIN2‐related disorders. Annals of Clinical and Translational Neurology. 7(4). 573–578. 13 indexed citations
12.
Olson, Heather E., Scott Demarest, Elia Pestana‐Knight, et al.. (2019). Cyclin-Dependent Kinase-Like 5 Deficiency Disorder: Clinical Review. Pediatric Neurology. 97. 18–25. 150 indexed citations
13.
Demarest, Scott, Heather E. Olson, Angela Moss, et al.. (2019). CDKL5 deficiency disorder: Relationship between genotype, epilepsy, cortical visual impairment, and development. Epilepsia. 60(8). 1733–1742. 98 indexed citations
14.
O’Leary, Heather M., Walter E. Kaufmann, Kush Kapur, et al.. (2018). Placebo‐controlled crossover assessment of mecasermin for the treatment of Rett syndrome. Annals of Clinical and Translational Neurology. 5(3). 323–332. 58 indexed citations
15.
Beggs, Alan H., B. Byrne, Tmirah Haselkorn, et al.. (2017). A multicenter, retrospective medical record review of patients with X-Linked Myotubular myopathy (XLMTM): the RECENSUS study. Neuromuscular Disorders. 27. S172–S172. 1 indexed citations
16.
Ceyhan‐Birsoy, Ozge, Beril Talim, Lindsay C. Swanson, et al.. (2015). Whole Exome Sequencing Reveals DYSF, FKTN, and ISPD Mutations in Congenital Muscular Dystrophy Without Brain or Eye Involvement. Journal of Neuromuscular Diseases. 2(1). 87–92. 10 indexed citations
17.
Janssen, Paul M.L., Robert W. Grange, Lin Yang, et al.. (2014). Tissue Triage and Freezing for Models of Skeletal Muscle Disease. Journal of Visualized Experiments. 28 indexed citations
18.
Meng, Hui, Paul M.L. Janssen, Robert W. Grange, et al.. (2014). Tissue Triage and Freezing for Models of Skeletal Muscle Disease. Journal of Visualized Experiments. 71 indexed citations
19.
Agrawal, Pankaj B., Christopher R. Pierson, Mugdha Joshi, et al.. (2014). SPEG Interacts with Myotubularin, and Its Deficiency Causes Centronuclear Myopathy with Dilated Cardiomyopathy. The American Journal of Human Genetics. 95(2). 218–226. 115 indexed citations
20.
McEliece, Robert J. & Lindsay C. Swanson. (1994). Reed-Solomon Codes and the Exploration of the Solar System. NASA Technical Reports Server (NASA). 14 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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