Sean McGrath

18.4k total citations · 3 hit papers
37 papers, 3.9k citations indexed

About

Sean McGrath is a scholar working on Molecular Biology, Genetics and Plant Science. According to data from OpenAlex, Sean McGrath has authored 37 papers receiving a total of 3.9k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 11 papers in Genetics and 9 papers in Plant Science. Recurrent topics in Sean McGrath's work include Genomics and Phylogenetic Studies (9 papers), Chromosomal and Genetic Variations (8 papers) and Genomic variations and chromosomal abnormalities (6 papers). Sean McGrath is often cited by papers focused on Genomics and Phylogenetic Studies (9 papers), Chromosomal and Genetic Variations (8 papers) and Genomic variations and chromosomal abnormalities (6 papers). Sean McGrath collaborates with scholars based in United States, Australia and United Kingdom. Sean McGrath's co-authors include Devin P. Locke, Elaine R. Mardis, Evan E. Eichler, Richard K. Wilson, Robert S. Fulton, Ze Cheng, Daniel Pinkel, Andrew J. Sharp, Donna G. Albertson and Stuart Schwartz and has published in prestigious journals such as Nature, Cell and Proceedings of the National Academy of Sciences.

In The Last Decade

Sean McGrath

37 papers receiving 3.8k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

BreakDancer: an algorithm for high-resolution mapping of genomic structural variation

2009 997 citations Ken Chen, John W. Wallis et al. Nature Methods profile →
Segmental Duplications and Copy-Number Variation in the Human Genome

2005 678 citations Andrew J. Sharp, Devin P. Locke et al. The American Journal of Human Genetics profile →
Characterizing the Major Structural Variant Alleles of the Human Genome

2019 269 citations Peter A. Audano, Arvis Sulovari et al. Cell profile →

Peers

Sean McGrath

GENET

PPCH

Norman A. Doggett United States

Christine Bird United Kingdom

Jürg Müller Germany

Catherine Ingle United Kingdom

Rafael Jiménez Spain

P. J. Hastings United States

Donna Karolchik United States

Ann‐Christine Syvänen Sweden

Simon J. McGowan United Kingdom

Ye Zhan United States

Norman A. Doggett United States

Sean McGrath

2.5k ×1.1

1.1k ×0.5

GENET

441 ×0.4

233 ×0.5

92 ×0.4

PPCH

Citations per year, relative to Sean McGrath Sean McGrath (= 1×) peers Norman A. Doggett

Countries citing papers authored by Sean McGrath

Since Specialization

Citations

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

Fields of papers citing papers by Sean McGrath

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sean McGrath

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

Kautto, Esko A., Kathleen M. Schieffer, Sean McGrath, et al.. (2022). Expanding the Clinical Phenotype of FGFR1 Internal Tandem Duplication. Molecular Case Studies. 8(2). mcs.a006174–mcs.a006174. 5 indexed citations

Miller, Anthony R., Saranga Wijeratne, Sean McGrath, et al.. (2022). Pacific Biosciences Fusion and Long Isoform Pipeline for Cancer Transcriptome–Based Resolution of Isoform Complexity. Journal of Molecular Diagnostics. 24(12). 1292–1306. 6 indexed citations

Wang, Huanyu, Sophonie Jean, Sarah A. Wilson, et al.. (2021). A deletion in the N gene of SARS-CoV-2 may reduce test sensitivity for detection of SARS-CoV-2. Diagnostic Microbiology and Infectious Disease. 102(4). 115631–115631. 12 indexed citations

McGrath, Sean, Alex Spurling, Peter Lock, et al.. (2021). A switch in mechanism of action prevents doxorubicin-mediated cardiac damage. Biochemical Pharmacology. 185. 114410–114410. 7 indexed citations

Singh, Anirudh K., Shireen A. Woodiga, Seon‐Sook An, et al.. (2021). A novel sialic acid-binding adhesin present in multiple species contributes to the pathogenesis of Infective endocarditis. PLoS Pathogens. 17(1). e1009222–e1009222. 12 indexed citations

Audano, Peter A., Arvis Sulovari, Tina A. Graves-Lindsay, et al.. (2019). Characterizing the Major Structural Variant Alleles of the Human Genome. Cell. 176(3). 663–675.e19. 269 indexed citations breakdown →

McGrath, Sean, Belinda S. Parker, Alex Spurling, et al.. (2017). Encapsulation of Mitoxantrone within Cucurbit[8]uril Decreases Toxicity and Enhances Survival in a Mouse Model of Cancer. ACS Medicinal Chemistry Letters. 8(5). 538–542. 28 indexed citations

Gasser, Robin B., et al.. (2016). Assessing the performance of multiplexed tandem PCR for the diagnosis of pathogenic genotypes of Theileria orientalis using pooled blood samples from cattle. Molecular and Cellular Probes. 31. 70–75. 9 indexed citations

Shirai, Cara Lunn, James N. Ley, Brian S. White, et al.. (2015). Mutant U2AF1 Expression Alters Hematopoiesis and Pre-mRNA Splicing In Vivo. Cancer Cell. 27(5). 631–643. 211 indexed citations

10.

Cabanski, Christopher R., Vincent Magrini, Malachi Griffith, et al.. (2014). cDNA Hybrid Capture Improves Transcriptome Analysis on Low-Input and Archived Samples. Journal of Molecular Diagnostics. 16(4). 440–451. 30 indexed citations

11.

Romanov, Michael N, Elaina M. Tuttle, Marlys L. Houck, et al.. (2009). The value of avian genomics to the conservation of wildlife. BMC Genomics. 10(Suppl 2). S10–S10. 105 indexed citations

12.

Chen, Ken, John W. Wallis, Michael D. McLellan, et al.. (2009). BreakDancer: an algorithm for high-resolution mapping of genomic structural variation. Nature Methods. 6(9). 677–681. 997 indexed citations breakdown →

13.

Alekseyenko, Artyom A., Shouyong Peng, Erica Larschan, et al.. (2008). A Sequence Motif within Chromatin Entry Sites Directs MSL Establishment on the Drosophila X Chromosome. Cell. 134(4). 599–609. 208 indexed citations

14.

Locke, Devin P., Andrew J. Sharp, Steven A. McCarroll, et al.. (2006). Linkage Disequilibrium and Heritability of Copy-Number Polymorphisms within Duplicated Regions of the Human Genome. The American Journal of Human Genetics. 79(2). 275–290. 231 indexed citations

15.

Newman, Tera L., Eray Tüzün, Victoria Morrison, et al.. (2005). A genome-wide survey of structural variation between human and chimpanzee. Genome Research. 15(10). 1344–1356. 141 indexed citations

16.

Sharp, Andrew J., Devin P. Locke, Sean McGrath, et al.. (2005). Segmental Duplications and Copy-Number Variation in the Human Genome. The American Journal of Human Genetics. 77(1). 78–88. 678 indexed citations breakdown →

17.

Jiang, Zhaoshi, Sean McGrath, Karen Hayden, et al.. (2005). Lineage-Specific Expansions of Retroviral Insertions within the Genomes of African Great Apes but Not Humans and Orangutans. PLoS Biology. 3(4). e110–e110. 76 indexed citations

18.

Tabrizi, Arash Rafii, Barbara A. Zehnbauer, Ingrid B. Borecki, et al.. (2002). The Frequency and Effects of Cytochrome P450 (CYP) 2C9 Polymorphisms in Patients Receiving Warfarin. Journal of the American College of Surgeons. 194(3). 267–273. 70 indexed citations

19.

Tabrizi, Arash Rafii, Sean McGrath, Morey A. Blinder, et al.. (2001). Extreme warfarin sensitivity in siblings associated with multiple cytochrome P450 polymorphisms. American Journal of Hematology. 67(2). 144–146. 12 indexed citations

20.

Freeman, Bradley D., Barbara A. Zehnbauer, Sean McGrath, Ingrid B. Borecki, & Timothy G. Buchman. (2000). Cytochrome P450 polymorphisms are associated with reduced warfarin dose. Surgery. 128(2). 281–285. 62 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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