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Sean McGrath

Active 1992–2026

110
Papers
20,384
Citations
39
h-index
67
i10-index

Citations

Citations per year for Sean McGrath1983: 1 citations1993: 1 citations1996: 1 citations1998: 1 citations1999: 2 citations2000: 7 citations2001: 7 citations2002: 13 citations2003: 19 citations2004: 10 citations2005: 38 citations2006: 101 citations2007: 89 citations2008: 121 citations2009: 174 citations2010: 300 citations2011: 415 citations2012: 427 citations2013: 456 citations2014: 456 citations2015: 363 citations2016: 353 citations2017: 309 citations2018: 299 citations2019: 717 citations2020: 664 citations2021: 630 citations2022: 498 citations2023: 376 citations2024: 528 citations2025: 226 citations2026: 12 citations1984–1992: no citations, so these years are not shown1994–1995: no citations, so these years are not shown1997: no citations, so this year is not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 3,639 citing papers, 31.8% of this breakdownUnited Kingdom: 992 citing papers, 8.7% of this breakdownChina: 788 citing papers, 6.9% of this breakdownGermany: 715 citing papers, 6.3% of this breakdownCanada: 450 citing papers, 3.9% of this breakdownItaly: 413 citing papers, 3.6% of this breakdownFrance: 394 citing papers, 3.4% of this breakdownNetherlands: 358 citing papers, 3.1% of this breakdownSpain: 330 citing papers, 2.9% of this breakdownAustralia: 284 citing papers, 2.5% of this breakdownJapan: 282 citing papers, 2.5% of this breakdownSwitzerland: 220 citing papers, 1.9% of this breakdown
0%31.8%Other 22.5%

Institutions

Fields

  • Biochemistry, Genetics and Molecular Biology53.9%
  • Medicine31.2%
  • Computer Science4.3%
  • Agricultural and Biological Sciences2.9%
  • Neuroscience1.7%
  • Immunology and Microbiology1.6%
  • Other4.4%

Topics

  • Cancer Genomics and Diagnostics6.4%
  • Acute Myeloid Leukemia Research6%
  • Genomics and Phylogenetic Studies4.6%
  • Epigenetics and DNA Methylation4%
  • Genomic variations and chromosomal abnormalities3.6%
  • Genomics and Rare Diseases3%
  • Other72.4%

Coauthors

All papers

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  1. Evaluation of GRCh38 and de novo haploid genome assemblies demonstrates the enduring quality of the reference assembly

    Authors: Valérie Schneider, Tina A. Graves-Lindsay, Kerstin Howe, Nathan Bouk, Hsiu-Chuan Chen, Paul Kitts, Terence D. Murphy, Kim D. Pruitt, Françoise Thibaud‐Nissen, Derek Albracht, Robert S. Fulton, Milinn Kremitzki, Vincent Magrini, Chris Markovic, Sean McGrath, Karyn Meltz Steinberg, Kate Auger, William Chow, Joanna Collins, Glenn Harden, Tim Hubbard, Sarah Pelan, Jared T. Simpson, Glen Threadgold, James Torrance, Jonathan Wood, Laura Clarke, Sergey Koren, Matthew Boitano, Paul Peluso, Heng Li, Chen-Shan Chin, Adam M. Phillippy, Richard Durbin, Richard K. Wilson, Paul Flicek, Evan E. Eichler, Deanna M. Church - Genome Research 2017 cited by 1,294

  2. Directly Reprogrammed Human Neurons Retain Aging-Associated Transcriptomic Signatures and Reveal Age-Related Nucleocytoplasmic Defects

    Authors: Jérôme Mertens, Apuã C.M. Paquola, Manching Ku, Emily M. Hatch, Lena Böhnke, Shauheen Ladjevardi, Sean McGrath, Benjamin C. Campbell, Hyungjun Lee, Joseph R. Herdy, J. Tiago Gonçalves, Tomohisa Toda, Yongsung Kim, Jürgen Winkler, Jun Yao, Martin W. Hetzer, Fred H. Gage - Cell stem cell 2015 cited by 757

  3. DNMT3A Mutations in Acute Myeloid Leukemia

    Authors: Timothy J. Ley, Li Ding, Matthew J. Walter, Michael D. McLellan, Tamara Lamprecht, David E. Larson, Cyriac Kandoth, Jacqueline E. Payton, Jack Baty, John S. Welch, Christopher Harris, Cheryl F. Lichti, R. Reid Townsend, Robert S. Fulton, David J. Dooling, Daniel C. Koboldt, Heather K. Schmidt, Qunyuan Zhang, John R. Osborne, Ling Lin, Michelle D. O’Laughlin, Joshua F. McMichael, Kim D. Delehaunty, Sean McGrath, Lucinda A. Fulton, Vincent Magrini, Tammi L. Vickery, Jasreet Hundal, Lisa L. Cook, Joshua J. Conyers, Gary W. Swift, Jerry P. Reed, Patricia A. Alldredge, Todd Wylie, Jason Walker, Joelle Kalicki, Mark A. Watson, Sharon E. Heath, William D. Shannon, Nobish Varghese, Rakesh Nagarajan, Peter Westervelt, Michael H. Tomasson, Daniel C. Link, Timothy A. Graubert, John F. DiPersio, Elaine R. Mardis, Richard K. Wilson - New England Journal of Medicine 2010 cited by 1,980

  4. Clonal evolution in relapsed acute myeloid leukaemia revealed by whole-genome sequencing

    Authors: Li Ding, Timothy J. Ley, David E. Larson, Christopher A. Miller, Daniel C. Koboldt, John S. Welch, Julie Ritchey, Margaret A. Young, Tamara Lamprecht, Michael D. McLellan, Joshua F. McMichael, John W. Wallis, Charles Lu, Dong Shen, Christopher Harris, David J. Dooling, Robert S. Fulton, Lucinda Fulton, Ken Chen, Heather K. Schmidt, Joelle Kalicki-Veizer, Vincent Magrini, Lisa Cook, Sean McGrath, Tammi L. Vickery, Michael C. Wendl, Sharon E. Heath, Mark A. Watson, Daniel C. Link, Michael H. Tomasson, William D. Shannon, Jacqueline E. Payton, Shashikant Kulkarni, Peter Westervelt, Matthew J. Walter, Timothy A. Graubert, Elaine R. Mardis, Richard K. Wilson, John F. DiPersio - Nature 2012 cited by 2,027

  5. Recurring Mutations Found by Sequencing an Acute Myeloid Leukemia Genome

    Authors: Elaine R. Mardis, Li Ding, David J. Dooling, David E. Larson, Michael D. McLellan, Ken Chen, Daniel C. Koboldt, Robert S. Fulton, Kim D. Delehaunty, Sean McGrath, Lucinda A. Fulton, Devin P. Locke, Vincent Magrini, Rachel M. Abbott, Tammi L. Vickery, Jerry S. Reed, Jody S. Robinson, Todd Wylie, Scott M. Smith, Lynn K. Carmichael, James M. Eldred, Christopher Harris, Jason Walker, Joshua B. Peck, Feiyu Du, Adam F. Dukes, Gabriel E. Sanderson, Anthony M. Brummett, Eric M. Clark, Joshua F. McMichael, Rick Meyer, Jonathan K. Schindler, Craig Pohl, John W. Wallis, Xiaoqi Shi, Ling Lin, Heather K. Schmidt, Yuzhu Tang, Carrie A. Haipek, Madeline E. Wiechert, Jolynda V. Ivy, Joelle Kalicki, Glendoria Elliott, Rhonda E. Ries, Jacqueline E. Payton, Peter Westervelt, Michael H. Tomasson, Mark A. Watson, Jack Baty, Sharon E. Heath, William D. Shannon, Rakesh Nagarajan, Daniel C. Link, Matthew J. Walter, Timothy A. Graubert, John F. DiPersio, Richard K. Wilson, Timothy J. Ley - New England Journal of Medicine 2009 cited by 2,226

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

    Authors: Ken Chen, John W. Wallis, Michael D. McLellan, David E. Larson, Joelle Kalicki, Craig Pohl, Sean McGrath, Michael C. Wendl, Qunyuan Zhang, Devin P. Locke, Xiaoqi Shi, Robert S. Fulton, Timothy J. Ley, Richard K. Wilson, Li Ding, Elaine R. Mardis - Nature Methods 2009 cited by 1,585

  7. Characterizing the Major Structural Variant Alleles of the Human Genome

    Authors: Peter A. Audano, Arvis Sulovari, Tina A. Graves-Lindsay, Stuart Cantsilieris, Melanie Sorensen, AnneMarie E. Welch, Max L. Dougherty, Bradley J. Nelson, Ankeeta Shah, Susan K. Dutcher, Wesley C. Warren, Vincent Magrini, Sean McGrath, Yang Li, Richard K. Wilson, Evan E. Eichler - Cell 2019 cited by 582

  8. Meta‐analysis of the difference of medians

    Authors: Sean McGrath, Hojoon Sohn, Russell Steele, Andrea Benedetti - Biometrical Journal 2019 cited by 212

  9. The Origin and Evolution of Mutations in Acute Myeloid Leukemia

    Authors: John S. Welch, Timothy J. Ley, Daniel C. Link, Christopher A. Miller, David E. Larson, Daniel C. Koboldt, Lukas D. Wartman, Tamara Lamprecht, Fulu Liu, Jun Xia, Cyriac Kandoth, Robert S. Fulton, Michael D. McLellan, David J. Dooling, John W. Wallis, Ken Chen, Christopher Harris, Heather K. Schmidt, Joelle Kalicki-Veizer, Charles Lu, Qunyuan Zhang, Ling Lin, Michelle D. O’Laughlin, Joshua F. McMichael, Kim D. Delehaunty, Lucinda A. Fulton, Vincent Magrini, Sean McGrath, Ryan Demeter, Tammi L. Vickery, Jasreet Hundal, Lisa L. Cook, Gary W. Swift, Jerry P. Reed, Patricia A. Alldredge, Todd Wylie, Jason Walker, Mark A. Watson, Sharon E. Heath, William D. Shannon, Nobish Varghese, Rakesh Nagarajan, Jacqueline E. Payton, Jack Baty, Shashikant Kulkarni, Jeffery M. Klco, Michael H. Tomasson, Peter Westervelt, Matthew J. Walter, Timothy A. Graubert, John F. DiPersio, Li Ding, Elaine R. Mardis, Richard K. Wilson - Cell 2012 cited by 1,576

  10. DNA sequencing of a cytogenetically normal acute myeloid leukaemia genome

    Authors: Timothy J. Ley, Elaine R. Mardis, Li Ding, Bob Fulton, Michael D. McLellan, Ken Chen, David J. Dooling, Brian H. Dunford-Shore, Sean McGrath, Matthew T. Hickenbotham, Lisa L. Cook, Rachel M. Abbott, David E. Larson, Dan Koboldt, Craig Pohl, Scott M. Smith, Amy Hawkins, Scott Abbott, Devin P. Locke, LaDeana Hillier, Tracie L. Miner, Lucinda Fulton, Vincent Magrini, Todd Wylie, Jarret Glasscock, Joshua J. Conyers, Nathan Sander, Xiaoqi Shi, John R. Osborne, Patrick Minx, David Gordon, Asif Chinwalla, Yu Zhao, Rhonda E. Ries, Jacqueline E. Payton, Peter Westervelt, Michael H. Tomasson, Mark A. Watson, Jack Baty, Jennifer Ivanovich, Sharon E. Heath, William D. Shannon, Rakesh Nagarajan, Matthew J. Walter, Daniel C. Link, Timothy A. Graubert, John F. DiPersio, Richard K. Wilson - Nature 2008 cited by 1,440

  11. Segmental Duplications and Copy-Number Variation in the Human Genome

    Authors: Andrew J. Sharp, Devin P. Locke, Sean McGrath, Ze Cheng, Jeffrey A. Bailey, Rhea U. Vallente, L.M. Pertz, Royden A. Clark, Stuart Schwartz, Rick Segraves, Vanessa V. Oseroff, Donna G. Albertson, Daniel Pinkel, Evan E. Eichler - The American Journal of Human Genetics 2005 cited by 977

  12. Genome remodelling in a basal-like breast cancer metastasis and xenograft

    Authors: Li Ding, Matthew J. Ellis, Shunqiang Li, David E. Larson, Ken Chen, John W. Wallis, Christopher Harris, Michael D. McLellan, Robert S. Fulton, Lucinda Fulton, Rachel M. Abbott, Jeremy Hoog, David J. Dooling, Daniel C. Koboldt, Heather K. Schmidt, Joelle Kalicki, Qunyuan Zhang, Lei Chen, Ling Lin, Michael C. Wendl, Joshua F. McMichael, Vincent Magrini, Lisa Cook, Sean McGrath, Tammi L. Vickery, Elizabeth L. Appelbaum, Katherine DeSchryver, Sherri R. Davies, Therese Guintoli, Lin Li, Robert J. Crowder, Tao Yu, Jacqueline Snider, Scott M. Smith, Adam F. Dukes, Gabriel E. Sanderson, Craig Pohl, Kim D. Delehaunty, Catrina C. Fronick, Kimberley A. Pape, Jerry S. Reed, Jody S. Robinson, Jennifer S. Hodges, William Schierding, Nathan D. Dees, Dong Shen, Devin P. Locke, Madeline E. Wiechert, James M. Eldred, Josh B. Peck, Benjamin J. Oberkfell, Justin T. Lolofie, Feiyu Du, Amy Hawkins, Michelle D. O’Laughlin, Kelly E. Bernard, Mark Cunningham, Glendoria Elliott, Mark Mason, Dominic M. Thompson, Jennifer Ivanovich, Paul J. Goodfellow, Charles M. Perou, George M. Weinstock, Rebecca Aft, Mark A. Watson, Timothy J. Ley, Richard K. Wilson, Elaine R. Mardis - Nature 2010 cited by 1,172

  13. Detection of brain somatic variation in epilepsy‐associated developmental lesions

    Authors: Tracy A. Bedrosian, Katherine E. Miller, Olivia Grischow, Kathleen M. Schieffer, Stephanie LaHaye, Hyojung Yoon, Anthony R. Miller, Jason B. Navarro, Jesse J. Westfall, Kristen Leraas, Samantha Choi, Rachel Williamson, James Fitch, Benjamin Kelly, Peter White, Kristy Lee, Sean McGrath, Catherine E. Cottrell, Vincent Magrini, Jeffrey R. Leonard, Jonathan Pindrik, Ammar Shaikhouni, Daniel R. Boué, Diana Thomas, Christopher R. Pierson, Richard K. Wilson, Adam P. Ostendorf, Elaine R. Mardis, Daniel C. Koboldt - Epilepsia 2022 cited by 53

  14. Mutant U2AF1 Expression Alters Hematopoiesis and Pre-mRNA Splicing In Vivo

    Authors: Cara Lunn Shirai, James N. Ley, Brian S. White, Sanghyun P. Kim, Justin Tibbitts, Jin Shao, Matthew Ndonwi, Brian A. Wadugu, Eric J. Duncavage, Theresa Okeyo-Owuor, Tuoen Liu, Malachi Griffith, Sean McGrath, Vincent Magrini, Robert S. Fulton, Catrina C. Fronick, Michelle D. O’Laughlin, Timothy A. Graubert, Matthew J. Walter - Cancer Cell 2015 cited by 284

  15. Evaluation of GRCh38 and de novo haploid genome assemblies demonstrates the enduring quality of the reference assembly

    Authors: Valérie Schneider, Tina Graves-Lindsay, Kerstin Howe, Nathan Bouk, Hsiu-Chuan Chen, Paul Kitts, Terence D. Murphy, Kim D. Pruitt, Françoise Thibaud‐Nissen, Derek Albracht, Robert S. Fulton, Milinn Kremitzki, Vincent Magrini, Chris Markovic, Sean McGrath, Karyn Meltz Steinberg, Kate Auger, William Chow, Joanna Collins, Glenn Harden, Tim Hubbard, Sarah Pelan, Jared T. Simpson, Glen Threadgold, James Torrance, Jonathan Wood, Laura Clarke, Sergey Koren, Matthew Boitano, Heng Li, Chen-Shan Chin, Adam M. Phillippy, Richard Durbin, Richard K. Wilson, Paul Flicek, Deanna M. Church - 2016 cited by 116

  16. gfoRmula: An R Package for Estimating the Effects of Sustained Treatment Strategies via the Parametric g-formula

    Authors: Sean McGrath, Victoria Lin, Zilu Zhang, Lucia C. Petito, Roger W. Logan, Miguel A. Hernán, Jessica G. Young - Patterns 2020 cited by 90

  17. Accuracy of rapid point-of-care antigen-based diagnostics for SARS-CoV-2: An updated systematic review and meta-analysis with meta-regression analyzing influencing factors

    Authors: Lukas E. Brümmer, Stephan Katzenschlager, Sean McGrath, Stephani Schmitz, Mary Gaeddert, Christian Erdmann, Marc Bota, Maurizio Grilli, Jan Larmann, Markus Weigand, Nira R. Pollock, Aurélien Macé, Berra Erkoşar, Sergio Carmona, Jilian A. Sacks, Stefano Ongarello, Claudia M. Denkinger - PLoS Medicine 2022 cited by 75

  18. Optimizing Cancer Genome Sequencing and Analysis

    Authors: Malachi Griffith, Christopher A. Miller, Obi L. Griffith, Kilannin Krysiak, Zachary L. Skidmore, Avinash Ramu, Jason Walker, Ha X. Dang, Lee Trani, David E. Larson, Ryan Demeter, Michael C. Wendl, Joshua F. McMichael, Rachel Austin, Vincent Magrini, Sean McGrath, Amy Ly, Shashikant Kulkarni, Matthew G. Cordes, Catrina C. Fronick, Robert S. Fulton, Christopher A. Maher, Li Ding, Jeffery M. Klco, Elaine R. Mardis, Timothy J. Ley, Richard K. Wilson - Cell Systems 2015 cited by 206

  19. Impact of molecular diagnostic tests on diagnostic and treatment delays in tuberculosis: a systematic review and meta-analysis

    Authors: Jae Hyoung Lee, Tushar Garg, Jungsil Lee, Sean McGrath, Lori Rosman, Samuel G. Schumacher, Andrea Benedetti, Zhi Zhen Qin, Geneviève Gore, Madhukar Pai, Hojoon Sohn - BMC Infectious Diseases 2022 cited by 35

  20. PTEN somatic mutations contribute to spectrum of cerebral overgrowth

    Authors: Daniel C. Koboldt, Katherine E. Miller, Anthony R. Miller, Jocelyn Bush, Sean McGrath, Kristen Leraas, Erin Crist, Summer Fair, Wesley N. Schwind, Saranga Wijeratne, James Fitch, Jeffrey R. Leonard, Ammar Shaikhouni, Mark E. Hester, Vincent Magrini, Mai‐Lan Ho, Christopher R. Pierson, Richard K. Wilson, Adam P. Ostendorf, Elaine R. Mardis, Tracy A Bedrosian - Brain 2021 cited by 44

  21. A Sequence Motif within Chromatin Entry Sites Directs MSL Establishment on the Drosophila X Chromosome

    Authors: Artyom A. Alekseyenko, Shouyong Peng, Erica Larschan, Andrey A. Gorchakov, Ok-Kyung Lee, Peter V. Kharchenko, Sean McGrath, Charlotte I. Wang, Elaine R. Mardis, Peter J. Park, Mitzi I. Kuroda - Cell 2008 cited by 303

  22. Biomarkers That Correlate with Active Pulmonary Tuberculosis Treatment Response: a Systematic Review and Meta-analysis

    Authors: Alexandra J. Zimmer, Federica Lainati, Nathaly Aguilera Vasquez, Carole Chedid, Sean McGrath, Andrea Benedetti, Emily MacLean, Morten Ruhwald, Claudia M. Denkinger, Mikashmi Kohli - Journal of Clinical Microbiology 2021 cited by 60

  23. Clonally expanded mtDNA point mutations are abundant in individual cells of human tissues

    Authors: Ekaterina Nekhaeva, Natalya D. Bodyak, Yevgenya Kraytsberg, Sean McGrath, Nathalie J. van Orsouw, Anna Pluzhnikov, Jeanne Y. Wei, Jan Vijg, Konstantin Khrapko - National Academy of Sciences, Proceedings of the National Academy of Sciences 2002 cited by 212

  24. Chimpanzee and human Y chromosomes are remarkably divergent in structure and gene content

    Authors: Jennifer F. Hughes, Helen Skaletsky, Tatyana Pyntikova, Tina Graves, Saskia K.M. van Daalen, Patrick Minx, Robert S. Fulton, Sean McGrath, Devin P. Locke, Cynthia Friedman, Barbara J. Trask, Elaine R. Mardis, Wesley C. Warren, Sjoerd Repping, Steve Rozen, Richard K. Wilson, David C. Page - Nature 2010 cited by 437