Adrian G. Todd

555 total citations
20 papers, 449 citations indexed

About

Adrian G. Todd is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, Adrian G. Todd has authored 20 papers receiving a total of 449 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 9 papers in Genetics and 7 papers in Physiology. Recurrent topics in Adrian G. Todd's work include Neurogenetic and Muscular Disorders Research (9 papers), RNA modifications and cancer (7 papers) and Lysosomal Storage Disorders Research (6 papers). Adrian G. Todd is often cited by papers focused on Neurogenetic and Muscular Disorders Research (9 papers), RNA modifications and cancer (7 papers) and Lysosomal Storage Disorders Research (6 papers). Adrian G. Todd collaborates with scholars based in United States, United Kingdom and France. Adrian G. Todd's co-authors include Darin J. Falk, Barry J. Byrne, David D. Fuller, Elliot J. Androphy, Philip J. Young, Robert Morse, Meghan S. Soustek, Howard Stebbings, Lucia Notterpek and Sara K. Custer and has published in prestigious journals such as PLoS ONE, Journal of Molecular Biology and Annals of Neurology.

In The Last Decade

Adrian G. Todd

19 papers receiving 446 citations

Peers

Adrian G. Todd

PHYSI

GENET

RHEUM

Denise Griffiths United States

Kerry O. Cresawn United States

Johan Deniaud France

Rachel Flomen United Kingdom

Atze J. Bergsma Netherlands

Rose-Mary Boustany United States

Sara Marcó Spain

Robert L. Conway United States

Darren Murrey United States

Daniel K. Borger United States

Denise Griffiths United States

Adrian G. Todd

146 ×0.5

157 ×1.0

PHYSI

73 ×0.5

GENET

73 ×1.0

GENET

26 ×0.4

RHEUM

Citations per year, relative to Adrian G. Todd Adrian G. Todd (= 1×) peers Denise Griffiths

Countries citing papers authored by Adrian G. Todd

Since Specialization

Citations

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

Fields of papers citing papers by Adrian G. Todd

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Adrian G. Todd. 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 Adrian G. Todd. The network helps show where Adrian G. Todd may publish in the future.

Co-authorship network of co-authors of Adrian G. Todd

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

All Works

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20 of 20 papers shown

Fuller, David D., Sabhya Rana, Adrian G. Todd, et al.. (2025). Neonatal systemic gene therapy restores cardiorespiratory function in a rat model of Pompe disease. Molecular Therapy. 33(9). 4276–4289.

Todd, Adrian G., Darin J. Falk, Kathryn H. Morelli, et al.. (2019). HSP90 Inhibitor, NVP-AUY922, Improves Myelination in Vitro and Supports the Maintenance of Myelinated Axons in Neuropathic Mice. ACS Chemical Neuroscience. 10(6). 2890–2902. 10 indexed citations

Baligand, Céline, Adrian G. Todd, Brittany Lee‐McMullen, et al.. (2017). 13C/31P MRS Metabolic Biomarkers of Disease Progression and Response to AAV Delivery of hGAA in a Mouse Model of Pompe Disease. Molecular Therapy — Methods & Clinical Development. 7. 42–49. 9 indexed citations

Falk, Darin J., et al.. (2017). Locomotor and skeletal muscle abnormalities in trembler J neuropathic mice. Muscle & Nerve. 57(4). 664–671. 4 indexed citations

Custer, Sara K., et al.. (2016). Altered mRNA Splicing in SMN-Depleted Motor Neuron-Like Cells. PLoS ONE. 11(10). e0163954–e0163954. 16 indexed citations

Falk, Darin J., Meghan S. Soustek, Adrian G. Todd, et al.. (2015). Comparative impact of AAV and enzyme replacement therapy on respiratory and cardiac function in adult Pompe mice. Molecular Therapy — Methods & Clinical Development. 2. 15007–15007. 47 indexed citations

Doerfler, Phillip A., Adrian G. Todd, Nathalie Clément, et al.. (2015). Copackaged AAV9 Vectors Promote Simultaneous Immune Tolerance and Phenotypic Correction of Pompe Disease. Human Gene Therapy. 27(1). 43–59. 43 indexed citations

Todd, Adrian G., Robert W. Grange, David D. Fuller, et al.. (2015). Correcting Neuromuscular Deficits With Gene Therapy in Pompe Disease. Annals of Neurology. 78(2). 222–234. 44 indexed citations

Lee, Sooyeon, Andrew B. Harris, Darin J. Falk, et al.. (2014). Rapamycin improves peripheral nerve myelination while it fails to benefit neuromuscular performance in neuropathic mice. Neurobiology of Disease. 70. 224–236. 29 indexed citations

10.

Falk, Darin J., Adrian G. Todd, Meghan S. Soustek, et al.. (2014). Peripheral nerve and neuromuscular junction pathology in Pompe disease. Human Molecular Genetics. 24(3). 625–636. 67 indexed citations

11.

Custer, Sara K., Adrian G. Todd, Natalia N. Singh, & Elliot J. Androphy. (2013). Dilysine motifs in exon 2b of SMN protein mediate binding to the COPI vesicle protein α-COP and neurite outgrowth in a cell culture model of spinal muscular atrophy. Human Molecular Genetics. 22(20). 4043–4052. 34 indexed citations

12.

Mah, Cathryn, Meghan S. Soustek, Adrian G. Todd, et al.. (2013). Adeno-Associated Virus–Mediated Gene Therapy for Metabolic Myopathy. Human Gene Therapy. 24(11). 928–936. 8 indexed citations

13.

Todd, Adrian G., Hai Lin, Allison D. Ebert, Yunlong Liu, & Elliot J. Androphy. (2012). COPI transport complexes bind to specific RNAs in neuronal cells. Human Molecular Genetics. 22(4). 729–736. 40 indexed citations

14.

Morse, Robert, Adrian G. Todd, & Philip J. Young. (2012). Using Mini-genes to Identify Factors That Modulate Alternative Splicing. Methods in molecular biology. 867. 349–362. 3 indexed citations

15.

Todd, Adrian G., et al.. (2010). Analysis of SMN-neurite granules: Core Cajal body components are absent from SMN-cytoplasmic complexes. Biochemical and Biophysical Research Communications. 397(3). 479–485. 24 indexed citations

16.

Morse, Robert, et al.. (2010). Mutations in the Survival Motor Neuron (SMN) Protein Alter the Dynamic Nature of Nuclear Bodies. NeuroMolecular Medicine. 13(1). 77–87. 1 indexed citations

17.

Todd, Adrian G., et al.. (2010). SMN and the Gemin proteins form sub-complexes that localise to both stationary and dynamic neurite granules. Biochemical and Biophysical Research Communications. 394(1). 211–216. 23 indexed citations

18.

Todd, Adrian G., et al.. (2010). SMN, Gemin2 and Gemin3 Associate with β-Actin mRNA in the Cytoplasm of Neuronal Cells In Vitro. Journal of Molecular Biology. 401(5). 681–689. 29 indexed citations

19.

Morse, Robert, et al.. (2009). Identification of a tripartite import signal in the Ewing Sarcoma protein (EWS). Biochemical and Biophysical Research Communications. 390(4). 1197–1201. 11 indexed citations

20.

Lorson, Monique A., Alexa Dickson, Adrian G. Todd, et al.. (2008). Identification and characterisation of a nuclear localisation signal in the SMN associated protein, Gemin4. Biochemical and Biophysical Research Communications. 375(1). 33–37. 7 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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