Sandra T. Cooper

7.1k total citations
95 papers, 3.6k citations indexed

About

Sandra T. Cooper is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Cell Biology. According to data from OpenAlex, Sandra T. Cooper has authored 95 papers receiving a total of 3.6k indexed citations (citations by other indexed papers that have themselves been cited), including 79 papers in Molecular Biology, 23 papers in Cardiology and Cardiovascular Medicine and 20 papers in Cell Biology. Recurrent topics in Sandra T. Cooper's work include Muscle Physiology and Disorders (40 papers), RNA Research and Splicing (22 papers) and Cardiomyopathy and Myosin Studies (21 papers). Sandra T. Cooper is often cited by papers focused on Muscle Physiology and Disorders (40 papers), RNA Research and Splicing (22 papers) and Cardiomyopathy and Myosin Studies (21 papers). Sandra T. Cooper collaborates with scholars based in Australia, United States and United Kingdom. Sandra T. Cooper's co-authors include Kathryn N. North, Paul L. McNeil, Neil S. Millar, Frances J. Evesson, Angela Lek, Harriet P. Lo, Biljana Ilkovski, Nigel F. Clarke, Nigel G. Laing and Alison G. Compton and has published in prestigious journals such as Journal of Biological Chemistry, Nature Communications and Nature Genetics.

In The Last Decade

Sandra T. Cooper

92 papers receiving 3.6k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Sandra T. Cooper Australia	38	2.7k	801	650	445	401	95	3.6k
Yassemi Capetanaki United States	38	3.4k 1.3×	1.1k 1.4×	2.0k 3.1×	395 0.9×	209 0.5×	71	4.6k
Katsuya Miyake United States	31	2.5k 0.9×	415 0.5×	1.0k 1.6×	384 0.9×	143 0.4×	50	3.8k
Teruo Shimizu Japan	33	2.0k 0.7×	459 0.6×	543 0.8×	999 2.2×	168 0.4×	129	3.7k
Stephan Lange United States	30	2.3k 0.8×	1.7k 2.2×	703 1.1×	371 0.8×	143 0.4×	71	3.5k
Philippe Chafey France	28	2.4k 0.9×	260 0.3×	414 0.6×	540 1.2×	201 0.5×	60	3.8k
Ryuichi Tatsumi Japan	28	2.3k 0.8×	310 0.4×	700 1.1×	312 0.7×	421 1.0×	88	3.3k
Peter F. M. van der Ven Germany	39	3.2k 1.2×	2.3k 2.9×	1.2k 1.8×	948 2.1×	332 0.8×	106	4.5k
E. Bonilla United States	40	4.8k 1.8×	325 0.4×	271 0.4×	771 1.7×	193 0.5×	76	5.4k
James E. Sylvester United States	30	2.4k 0.9×	289 0.4×	252 0.4×	322 0.7×	275 0.7×	53	3.5k
Marianne Schwartz Denmark	40	3.2k 1.2×	279 0.3×	323 0.5×	478 1.1×	219 0.5×	116	4.9k

Countries citing papers authored by Sandra T. Cooper

Since Specialization

Citations

This map shows the geographic impact of Sandra T. Cooper'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 Sandra T. Cooper with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sandra T. Cooper more than expected).

Fields of papers citing papers by Sandra T. Cooper

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sandra T. Cooper. 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 Sandra T. Cooper. The network helps show where Sandra T. Cooper may publish in the future.

Co-authorship network of co-authors of Sandra T. Cooper

This figure shows the co-authorship network connecting the top 25 collaborators of Sandra T. Cooper. A scholar is included among the top collaborators of Sandra T. Cooper 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 Sandra T. Cooper. Sandra T. Cooper 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

Jones, Dina M., Jing Jin, Katherine Donald, et al.. (2025). Evidence-based practices are effective in increasing smoke-free home rules among Black women who smoke. JNCI Monographs. 2025(70). 224–234.

Bournazos, Adam, Vanessa Sarkozy, John A. Lawson, et al.. (2024). Deep Sequencing and Phenotyping in an Australian Tuberous Sclerosis Complex “No Mutations Identified” Cohort. Molecular Genetics & Genomic Medicine. 12(10). e70017–e70017. 1 indexed citations

Riley, Lisa G., Subrata Sabui, Hamid M. Said, et al.. (2024). Genome sequencing enables diagnosis and treatment of SLC5A6 neuropathy. European Journal of Human Genetics. 32(8). 947–953.

Dawes, Ruebena, et al.. (2023). SpliceVault predicts the precise nature of variant-associated mis-splicing. Nature Genetics. 55(2). 324–332. 34 indexed citations

Riley, Lisa G., Purvi M. Kakadia, Stefan K. Bohlander, et al.. (2023). Biallelic ATP2B1 variants as a likely cause of a novel neurodevelopmental malformation syndrome with primary hypoparathyroidism. European Journal of Human Genetics. 32(1). 125–129. 3 indexed citations

Akesson, Lauren, Adam Bournazos, Andrew Fennell, et al.. (2020). Rapid exome sequencing and adjunct RNA studies confirm the pathogenicity of a novel homozygous ASNS splicing variant in a critically ill neonate. Human Mutation. 41(11). 1884–1891. 8 indexed citations

Jones, Hannah, Samantha J. Bryen, Leigh B. Waddell, et al.. (2019). Importance of muscle biopsy to establish pathogenicity of DMD missense and splice variants. Neuromuscular Disorders. 29(12). 913–919. 11 indexed citations

Summers, Matthew A., Thusitha Rupasinghe, Frances J. Evesson, et al.. (2017). Dietary intervention rescues myopathy associated with neurofibromatosis type 1. Human Molecular Genetics. 27(4). 577–588. 19 indexed citations

Menezes, Minal, Yiran Guo, Jianguo Zhang, et al.. (2015). Mutation in mitochondrial ribosomal protein S7 (MRPS7) causes congenital sensorineural deafness, progressive hepatic and renal failure and lactic acidemia. Human Molecular Genetics. 24(8). 2297–2307. 58 indexed citations

10.

Riley, Lisa G., Joëlle Rudinger‐Thirion, Klaus Schmitz‐Abe, et al.. (2015). LARS2 Variants Associated with Hydrops, Lactic Acidosis, Sideroblastic Anemia, and Multisystem Failure. JIMD Reports. 28. 49–57. 39 indexed citations

11.

Miller, David K., Minal Menezes, Cas Simons, et al.. (2014). Rapid Identification of a Novel Complex I MT-ND3 m.10134C>A Mutation in a Leigh Syndrome Patient. PLoS ONE. 9(8). e104879–e104879. 9 indexed citations

12.

Redpath, Gregory, Frances A. Lemckert, Angela Lek, et al.. (2014). Calpain cleavage within dysferlin exon 40a releases a synaptotagmin-like module for membrane repair. Molecular Biology of the Cell. 25(19). 3037–3048. 63 indexed citations

13.

Lo, Harriet P., Enrico Bertini, Massimiliano Mirabella, et al.. (2011). Mosaic caveolin-3 expression in acquired rippling muscle disease without evidence of myasthenia gravis or acetylcholine receptor autoantibodies. Neuromuscular Disorders. 21(3). 194–203. 11 indexed citations

14.

Egan, Jonathan R., Tanya L. Butler, Andrew D. Cole, et al.. (2009). Myocardial membrane injury in pediatric cardiac surgery: An animal model. Journal of Thoracic and Cardiovascular Surgery. 137(5). 1154–1162. 7 indexed citations

15.

Au, Carol G., Tanya L. Butler, Jonathan R. Egan, et al.. (2008). Changes in skeletal muscle expression of AQP1 and AQP4 in dystrophinopathy and dysferlinopathy patients. Acta Neuropathologica. 116(3). 235–246. 24 indexed citations

16.

Cooper, Sandra T., Eddy Kizana, Harriet P. Lo, et al.. (2007). Dystrophinopathy carrier determination and detection of protein deficiencies in muscular dystrophy using lentiviral MyoD-forced myogenesis. Neuromuscular Disorders. 17(4). 276–284. 27 indexed citations

17.

Corbett, Mark, P. Anthony Akkari, Ana Domazetovska, et al.. (2004). An αtropomyosin mutation alters dimer preference in nemaline myopathy. Annals of Neurology. 57(1). 42–49. 44 indexed citations

18.

Latiff, Haifa Abdul, Gary F. Sholler, & Sandra T. Cooper. (2003). Balloon Dilatation of Aortic Stenosis in Infants Younger than 6 Months of Age: Intermediate Outcome. Pediatric Cardiology. 24(1). 17–26. 19 indexed citations

19.

Ilkovski, Biljana, Sandra T. Cooper, Kristen L. Nowak, et al.. (2001). Nemaline Myopathy Caused by Mutations in the Muscle α-Skeletal-Actin Gene. The American Journal of Human Genetics. 68(6). 1333–1343. 119 indexed citations

20.

Cooper, Sandra T. & Neil S. Millar. (1998). Host Cell‐Specific Folding of the Neuronal Nicotinic Receptor α8 Subunit. Journal of Neurochemistry. 70(6). 2585–2593. 36 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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