Rebecca McClellan

919 total citations
21 papers, 485 citations indexed

About

Rebecca McClellan is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Genetics. According to data from OpenAlex, Rebecca McClellan has authored 21 papers receiving a total of 485 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 5 papers in Cardiology and Cardiovascular Medicine and 5 papers in Genetics. Recurrent topics in Rebecca McClellan's work include Mitochondrial Function and Pathology (5 papers), Cardiac electrophysiology and arrhythmias (4 papers) and Genetics and Neurodevelopmental Disorders (3 papers). Rebecca McClellan is often cited by papers focused on Mitochondrial Function and Pathology (5 papers), Cardiac electrophysiology and arrhythmias (4 papers) and Genetics and Neurodevelopmental Disorders (3 papers). Rebecca McClellan collaborates with scholars based in United States, Qatar and India. Rebecca McClellan's co-authors include Hilary J. Vernon, SakkuBai Naidu, Siddharth Srivastava, Leila Jamal, Ali Fatemi, Kristin Barañano, Julie S. Cohen, Richard I. Kelley, Ronald L. Eisenberg and Yana Sandlers and has published in prestigious journals such as Circulation, Annals of Neurology and Radiology.

In The Last Decade

Rebecca McClellan

18 papers receiving 474 citations

Peers

Rebecca McClellan

GENET

CCM

PMH

Amal Y. Kentab Saudi Arabia

Joy B. Redman United States

S. Ghariani Belgium

Mondher Chouchane France

J E Wraith United Kingdom

Cláudia Suemi Kamoi Kay Brazil

Morteza Heidari Iran

Marie Hully France

Jean‐Michel Pedespan France

Juan F. Calderón Chile

Amal Y. Kentab Saudi Arabia

Rebecca McClellan

443 ×2.0

196 ×1.0

GENET

127 ×2.6

63 ×1.4

CCM

76 ×1.8

PMH

Citations per year, relative to Rebecca McClellan Rebecca McClellan (= 1×) peers Amal Y. Kentab

Countries citing papers authored by Rebecca McClellan

Since Specialization

Citations

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

Fields of papers citing papers by Rebecca McClellan

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rebecca McClellan

This figure shows the co-authorship network connecting the top 25 collaborators of Rebecca McClellan. A scholar is included among the top collaborators of Rebecca McClellan 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 Rebecca McClellan. Rebecca McClellan 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

Miller, Marcus J., Adam D. Kennedy, Rebecca McClellan, et al.. (2025). The emerging role of metabolomics analysis in genetic and genomic testing: A points to consider statement of the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine. 27(10). 101493–101493.

Fetterman, Jessica L., Patrick F. Chinnery, Rebecca McClellan, et al.. (2025). Mitochondrial Genetics in Cardiovascular Health and Disease: A Scientific Statement From the American Heart Association. Circulation. 153(5). e42–e68.

Asatryan, Babken, Brittney Murray, Alessio Gasperetti, Rebecca McClellan, & Andreas S. Barth. (2024). Unraveling Complexities in Genetically Elusive Long QT Syndrome. Circulation Arrhythmia and Electrophysiology. 17(2). e012356–e012356. 5 indexed citations

Isakadze, Nino, Marc C. Engels, Dominik Beer, et al.. (2022). C-reactive Protein Elevation Is Associated With QTc Interval Prolongation in Patients Hospitalized With COVID-19. Frontiers in Cardiovascular Medicine. 9. 866146–866146. 6 indexed citations

Beer, Dominik, Nino Isakadze, Rebecca McClellan, Hugh Calkins, & Andreas S. Barth. (2021). Acquired Long QT and Ventricular Arrhythmias in the Setting of Acute Inflammation. JACC Case Reports. 3(8). 1103–1107. 3 indexed citations

Murray, Brittney, et al.. (2021). Anxiety and depression in inherited channelopathy patients with implantable cardioverter-defibrillators. Heart Rhythm O2. 2(4). 388–393. 14 indexed citations

Brown, Emily, Kathleen Byrne, Dorothy M. Davis, et al.. (2020). Incorporation of genetic testing significantly increases the number of individuals diagnosed with familial hypercholesterolemia. Journal of clinical lipidology. 14(3). 331–338. 4 indexed citations

McClellan, Rebecca, et al.. (2019). Functional exercise capacity, strength, balance and motion reaction time in Barth syndrome. Orphanet Journal of Rare Diseases. 14(1). 37–37. 25 indexed citations

Shukla, Anju, et al.. (2019). Variants in the transcriptional corepressor BCORL1 are associated with an X‐linked disorder of intellectual disability, dysmorphic features, and behavioral abnormalities. American Journal of Medical Genetics Part A. 179(5). 870–874. 15 indexed citations

10.

Gipson, Tanjala, Andrea Poretti, Rebecca McClellan, & Michael V. Johnston. (2017). Tuberous Sclerosis Complex. Oxford University Press eBooks. 2 indexed citations

11.

Thompson, William, et al.. (2016). New targets for monitoring and therapy in Barth syndrome. Genetics in Medicine. 18(10). 1001–1010. 31 indexed citations

12.

Ye, Yizhou, Megan T. Cho, Kyle Retterer, et al.. (2015). De novo POGZ mutations are associated with neurodevelopmental disorders and microcephaly. Molecular Case Studies. 1(1). a000455–a000455. 39 indexed citations

13.

Vernon, Hilary J., Yana Sandlers, Rebecca McClellan, & Richard I. Kelley. (2014). Clinical laboratory studies in Barth Syndrome. Molecular Genetics and Metabolism. 112(2). 143–147. 35 indexed citations

14.

Srivastava, Siddharth, Julie S. Cohen, Hilary J. Vernon, et al.. (2014). Clinical whole exome sequencing in child neurology practice. Annals of Neurology. 76(4). 473–483. 181 indexed citations

15.

Roh, Jeffrey, et al.. (2013). Allogeneic morphogenetic protein vs. recombinant human bone morphogenetic protein-2 in lumbar interbody fusion procedures: a radiographic and economic analysis. Journal of Orthopaedic Surgery and Research. 8(1). 49–49. 20 indexed citations

16.

Parker, Katrina, et al.. (1996). MR features of an intracerebellar chloroma.. PubMed. 17(8). 1592–4. 29 indexed citations

17.

McClellan, Rebecca, Taher El Gammal, & Lanning B. Kline. (1995). Early bilateral radiation-induced optic neuropathy with follow-up MRI. Neuroradiology. 37(2). 131–133. 15 indexed citations

18.

McClellan, Rebecca, Taher El Gammal, & Lanning B. Kline. (1995). Early bilateral radiation-induced optic neuropathy with follow-up MRI. Neuroradiology. 37(2). 131–133.

19.

McClellan, Rebecca, et al.. (1992). Persistent infantile odontoid process: a variant of abnormal atlantoaxial segmentation.. American Journal of Roentgenology. 158(6). 1305–1307. 1 indexed citations

20.

McClellan, Rebecca, et al.. (1988). Routine CT screening of psychiatry inpatients.. Radiology. 169(1). 99–100. 28 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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