Colleen Muraresku

752 total citations
19 papers, 313 citations indexed

About

Colleen Muraresku is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Colleen Muraresku has authored 19 papers receiving a total of 313 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 13 papers in Clinical Biochemistry and 7 papers in Genetics. Recurrent topics in Colleen Muraresku's work include Metabolism and Genetic Disorders (13 papers), Mitochondrial Function and Pathology (12 papers) and Genomics and Rare Diseases (4 papers). Colleen Muraresku is often cited by papers focused on Metabolism and Genetic Disorders (13 papers), Mitochondrial Function and Pathology (12 papers) and Genomics and Rare Diseases (4 papers). Colleen Muraresku collaborates with scholars based in United States, Türkiye and Italy. Colleen Muraresku's co-authors include Marni J. Falk, Elizabeth M. McCormick, Amy Goldstein, Rebecca Ganetzky, Zarazuela Zolkipli‐Cunningham, Shana E. McCormack, K. Taylor Wild, Giulio Zuccoli, Arastoo Vossough and Fabrício Guimarães Gonçalves and has published in prestigious journals such as Journal of Biological Chemistry, Neurology and Annals of Neurology.

In The Last Decade

Colleen Muraresku

15 papers receiving 305 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Colleen Muraresku United States 10 263 175 41 30 30 19 313
Joyeeta Rahman United Kingdom 6 389 1.5× 226 1.3× 57 1.4× 26 0.9× 38 1.3× 7 458
Magdalena Pajdowska Poland 11 316 1.2× 209 1.2× 76 1.9× 15 0.5× 27 0.9× 22 422
Silvio Ferraris Italy 12 262 1.0× 198 1.1× 42 1.0× 34 1.1× 43 1.4× 12 370
Magalie Barth France 12 274 1.0× 171 1.0× 35 0.9× 25 0.8× 92 3.1× 32 378
Lisa Worgan Australia 9 281 1.1× 189 1.1× 65 1.6× 20 0.7× 35 1.2× 14 376
Heiko Brennenstuhl Germany 11 180 0.7× 99 0.6× 74 1.8× 47 1.6× 30 1.0× 25 315
Sara Scapolan Italy 10 271 1.0× 70 0.4× 49 1.2× 43 1.4× 34 1.1× 11 348
Jack J. Collier United Kingdom 5 248 0.9× 93 0.5× 23 0.6× 30 1.0× 37 1.2× 6 344
Takuya Fushimi Japan 9 259 1.0× 143 0.8× 30 0.7× 12 0.4× 13 0.4× 23 299

Countries citing papers authored by Colleen Muraresku

Since Specialization
Citations

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

Fields of papers citing papers by Colleen Muraresku

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Colleen Muraresku

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

All Works

19 of 19 papers shown
1.
Alves, Cesar, Maria Camilla Rossi‐Espagnet, Francisco A. Perez, et al.. (2025). Single Large-Scale Mitochondrial Deletion Syndromes: Neuroimaging Phenotypes and Longitudinal Progression in Pediatric Patients. American Journal of Neuroradiology. 46(6). 1272–1281. 1 indexed citations
2.
Shen, Li, Marie T. Lott, Elizabeth M. McCormick, et al.. (2025). P704: A virtual registry of 9K Leigh syndrome and primary mitochondrial disease cases constructed through semi-automated literature mining and expert curation. Genetics in Medicine Open. 3. 103073–103073.
3.
Nomakuchi, Tomoki, Dong Li, Holly Dubbs, et al.. (2024). Utility of genome sequencing in exome‐negative pediatric patients with neurodevelopmental phenotypes. American Journal of Medical Genetics Part A. 194(12). e63817–e63817.
4.
Stanley, K., Elizabeth M. McCormick, Colleen Muraresku, et al.. (2024). Bridging the clinical-research gap: Harnessing an electronic data capture, integration, and visualization platform to systematically assess prospective patient-reported outcomes in mitochondrial medicine. Molecular Genetics and Metabolism. 142(1). 108348–108348. 2 indexed citations
5.
Christian, Thomas, Isao Masuda, Fenglin Li, et al.. (2024). A kinetic model for compound heterozygous pathogenic variants in Tyrosyl-tRNA synthetase gene YARS2-Associated neonatal phenotype. Journal of Biological Chemistry. 301(1). 108092–108092.
6.
Wang, Jing, Jorune Balciuniene, Maria Alejandra Diaz‐Miranda, et al.. (2021). Advanced approach for comprehensive mtDNA genome testing in mitochondrial disease. Molecular Genetics and Metabolism. 135(1). 93–101. 9 indexed citations
7.
Muraresku, Colleen, et al.. (2021). COXPD9 in an individual from Puerto Rico and literature review. American Journal of Medical Genetics Part A. 185(8). 2519–2525.
8.
Gonçalves, Fabrício Guimarães, Colleen Muraresku, Elizabeth M. McCormick, et al.. (2020). The Perirolandic Sign: A Unique Imaging Finding Observed in Association with Polymerase γ-Related Disorders. American Journal of Neuroradiology. 41(5). 917–922. 8 indexed citations
9.
Madsen, Karen L., Bruce H. Cohen, Marni J. Falk, et al.. (2020). Safety and efficacy of omaveloxolone in patients with mitochondrial myopathy. Neurology. 94(7). e687–e698. 43 indexed citations
10.
Shen, Li, Elizabeth M. McCormick, Colleen Muraresku, Marni J. Falk, & Xiaowu Gai. (2020). Clinical Bioinformatics in Precise Diagnosis of Mitochondrial Disease. Clinics in Laboratory Medicine. 40(2). 149–161. 8 indexed citations
11.
12.
Alves, Cesar, Sara Reis Teixeira, Juan Sebastián Martín-Saavedra, et al.. (2020). Pediatric Leigh Syndrome: Neuroimaging Features and Genetic Correlations. Annals of Neurology. 88(2). 218–232. 51 indexed citations
13.
Wild, K. Taylor, Amy Goldstein, Colleen Muraresku, & Rebecca Ganetzky. (2019). Broadening the phenotypic spectrum of Pearson syndrome: Five new cases and a review of the literature. American Journal of Medical Genetics Part A. 182(2). 365–373. 23 indexed citations
14.
McCormick, Elizabeth M., Colleen Muraresku, & Marni J. Falk. (2018). Mitochondrial Genomics: A Complex Field Now Coming of Age. PubMed. 6(2). 52–61. 36 indexed citations
15.
Muraresku, Colleen, Elizabeth M. McCormick, & Marni J. Falk. (2018). Mitochondrial Disease: Advances in Clinical Diagnosis, Management, Therapeutic Development, and Preventative Strategies. PubMed. 6(2). 62–72. 43 indexed citations
16.
Muraresku, Colleen, et al.. (2017). Risk factors for poor bone health in primary mitochondrial disease. Journal of Inherited Metabolic Disease. 40(5). 673–683. 28 indexed citations
17.
Shen, Li, Maria Angela Diroma, Michael Gonzalez, et al.. (2016). MSeqDR: A Centralized Knowledge Repository and Bioinformatics Web Resource to Facilitate Genomic Investigations in Mitochondrial Disease. Human Mutation. 37(6). 540–548. 31 indexed citations
18.
Ganetzky, Rebecca, Kosuke Izumi, Andrew C. Edmondson, et al.. (2015). Fetal akinesia deformation sequence due to a congenital disorder of glycosylation. American Journal of Medical Genetics Part A. 167(10). 2411–2417. 11 indexed citations
19.
Ahrens‐Nicklas, Rebecca C., et al.. (2015). Cobalamin C Disease Missed by Newborn Screening in a Patient with Low Carnitine Level. JIMD Reports. 23. 71–75. 11 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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2026