Joseph G. Gleeson

Active 1988–2025

200
Papers
29,923
Citations
99
h-index
194
i10-index

Citations

Citations per year for Joseph G. Gleeson1966: 2 citations1990: 1 citations1992: 3 citations1993: 1 citations1995: 2 citations1996: 3 citations1997: 1 citations1998: 13 citations1999: 37 citations2000: 69 citations2001: 81 citations2002: 87 citations2003: 91 citations2004: 111 citations2005: 163 citations2006: 198 citations2007: 262 citations2008: 192 citations2009: 259 citations2010: 318 citations2011: 316 citations2012: 360 citations2013: 403 citations2014: 352 citations2015: 362 citations2016: 363 citations2017: 386 citations2018: 430 citations2019: 953 citations2020: 1,090 citations2021: 1,139 citations2022: 839 citations2023: 653 citations2024: 1,010 citations2025: 475 citations2026: 17 citations1967–1989: no citations, so these years are not shown1991: no citations, so this year is not shown1994: no citations, so this year is not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 3,895 citing papers, 26.3% of this breakdownUnited Kingdom: 1,099 citing papers, 7.4% of this breakdownGermany: 1,014 citing papers, 6.9% of this breakdownChina: 1,008 citing papers, 6.8% of this breakdownFrance: 829 citing papers, 5.6% of this breakdownItaly: 595 citing papers, 4% of this breakdownCanada: 563 citing papers, 3.8% of this breakdownJapan: 489 citing papers, 3.3% of this breakdownNetherlands: 477 citing papers, 3.2% of this breakdownAustralia: 384 citing papers, 2.6% of this breakdownSpain: 361 citing papers, 2.4% of this breakdownSwitzerland: 313 citing papers, 2.1% of this breakdown
0%26.3%Other 25.6%

Fields

  • Biochemistry, Genetics and Molecular Biology62.2%
  • Medicine18.2%
  • Neuroscience14.6%
  • Immunology and Microbiology2.2%
  • Agricultural and Biological Sciences0.7%
  • Engineering0.5%
  • Other1.6%

Topics

  • Genetic and Kidney Cyst Diseases5%
  • RNA modifications and cancer3.9%
  • Genetics and Neurodevelopmental Disorders3.4%
  • Microtubule and mitosis dynamics3.4%
  • Neurogenesis and neuroplasticity mechanisms3.3%
  • Genomics and Rare Diseases2.9%
  • Other78.1%

Coauthors

All papers

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  1. Aberrant methylation of tRNAs links cellular stress to neuro‐developmental disorders

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , - The EMBO Journal 2014 cited by 634

  2. A phenotypic spectrum of autism is attributable to the combined effects of rare variants, polygenic risk and sex

    Authors: , , , , , , , , , , , , , , , , , , , - Nature Genetics 2022 cited by 199

  3. NSun2-Mediated Cytosine-5 Methylation of Vault Noncoding RNA Determines Its Processing into Regulatory Small RNAs

    Authors: , , , , , , , , , , - Cell Reports 2013 cited by 606

  4. Impaired Amino Acid Transport at the Blood Brain Barrier Is a Cause of Autism Spectrum Disorder

    Authors: , , , , , , , , , , , , , , , , , , , , , , , - Cell 2016 cited by 370

  5. Genome Sequencing for Diagnosing Rare Diseases

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Denny Popp, Tilman Polster, Konrad Platzer, Eric A. Pierce, Emily Place, Sander Pajusalu, Lynn Pais, Katrin Õunap, Ikeoluwa Osei‐Owusu, Henry Opperman, Volkan Okur, Kaisa Teele Oja, Melanie O’Leary, Emily O’Heir, Chantal F. Morel, Andreas Merkenschlager, Rhett G. Marchant, Brian Mangilog, Jill A. Madden, Daniel G. MacArthur, Alysia Kern Lovgren, Jordan Lerner‐Ellis, Jasmine Lin, Nigel G. Laing, Friedhelm Hildebrandt, Julia Hentschel, Emily Groopman, Julia K. Goodrich, Joseph G. Gleeson, Roula Ghaoui, Casie A. Genetti, Janina Gburek‐Augustat, Hanna T. Gazda, Vijay Ganesh, Mythily Ganapathi, Lyndon Gallacher, Jack Fu, Emily Evangelista, Eleina England, Sandra Donkervoort, Stephanie DiTroia, Sandra T. Cooper, Wendy K. Chung, John Christodoulou, Katherine R. Chao, Liam D. Cato, Kinga M. Bujakowska, Samantha J. Bryen, Harrison Brand, Carsten G. Bönnemann, Alan H. Beggs, Samantha Baxter, Tobias Bartolomaeus, Pankaj B. Agrawal, Michael E. Talkowski, Christina Austin‐Tse, Rami Abou Jamra, Heidi L. Rehm, Anne O’Donnell‐Luria - New England Journal of Medicine 2024 cited by 184

  6. NSUN2 introduces 5-methylcytosines in mammalian mitochondrial tRNAs

    Authors: , , , , , , , , , , , , , - Nucleic Acids Research 2019 cited by 174

  7. Heteromeric clusters of ubiquitinated ER-shaping proteins drive ER-phagy

    Authors: , , , , , , , , , , , , , , , , , , , , , , - Nature 2023 cited by 86

  8. Characterization of Greater Middle Eastern genetic variation for enhanced disease gene discovery

    Authors: , , , , , , , , , , , , , - Nature Genetics 2016 cited by 390

  9. Diagnosis of genetic diseases in seriously ill children by rapid whole-genome sequencing and automated phenotyping and interpretation

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , M. Janes, Kejia Lin, Paul McDonagh, Kyle McBride, Patrick Mulrooney, Shareef Nahas, Daeheon Oh, Albert Oriol, Laura Puckett, Zia Rady, Martin G. Reese, Julie Ryu, Lisa Salz, Erica Sanford Kobayashi, Lawrence Stewart, Nathaly M. Sweeney, Mari Tokita, Luca Van Der Kraan, Sarah White, Kristen Wigby, Brett Williams, Terence C. Wong, Meredith S. Wright, Catherine Yamada, Peter Schols, John Reynders, Kevin P. Hall, David Dimmock, Narayanan Veeraraghavan, Thomas Defay, Stephen F. Kingsmore - Science Translational Medicine 2019 cited by 295

  10. Doublecortin Is a Microtubule-Associated Protein and Is Expressed Widely by Migrating Neurons

    Authors: , , , - Neuron 1999 cited by 1,350

  11. The mutation significance cutoff: gene-level thresholds for variant predictions

    Authors: , , , , , , , , , , , , , , - Nature Methods 2016 cited by 327

  12. A human three-dimensional neural-perivascular ‘assembloid’ promotes astrocytic development and enables modeling of SARS-CoV-2 neuropathology

    Authors: , , , , , , , , , - Nature Medicine 2021 cited by 147

  13. Comprehensive multi-omic profiling of somatic mutations in malformations of cortical development

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Marco Prinz, David D. Limbrick, Christina A. Gurnett, Matthew D. Smyth, Shifteh Sattar, Mark Nespeca, David D. Gonda, Katsumi Imai, Yukitoshi Takahashi, Hsin-Hung Chen, Jin‐Wu Tsai, Valerio Conti, Renzo Guerrini, Orrin Devinsky, Wilson A. Silva, Hélio Rubens Machado, Gary W. Mathern, Alexej Abyzov, Sara Baldassari, Stéphanie Baulac, Joseph G. Gleeson, Marilyn C. Jones, Diane Masser‐Frye, Shifteh Sattar, Mark Nespeca, David D. Gonda, Katsumi Imai, Yukitoshi Takahashi, Hsin-Hung Chen, Jin‐Wu Tsai, Valerio Conti, Renzo Guerrini, Orrin Devinsky, Hélio Rubens Machado, Camila Araújo Bernardino Garcia, Wilson A. Silva, Se Hoon Kim, Hoon‐Chul Kang, Yasemin Alanay, Seema Kapoor, Carola A. Haas, Georgia Ramantani, Thomas J. Feuerstein, Ingmar Blümcke, Robyn M. Busch, Zhong Ying, Vadym Biloshytsky, Kostiantyn Kostiuk, Pedachenko Eg, Gary W. Mathern, Christina A. Gurnett, Matthew D. Smyth, Ingo Helbig, Benjamin C. Kennedy, Judy Liu, Felix Chan, Darcy A. Krueger, Richard E. Frye, Angus A. Wilfong, David L. Adelson, William D. Gaillard, Chima Oluigbo, Anne E. Anderson, Brain Somatic Mosaicism Network, Alice Lee, August Yue Huang, Alissa M. D’Gama, Caroline Dias, Christopher A. Walsh, Eduardo Maury and 105 more - Nature Genetics 2023 cited by 111

  14. The landscape of somatic mutation in cerebral cortex of autistic and neurotypical individuals revealed by ultra-deep whole-genome sequencing

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Isidro Cortes, Lovelace J. Luquette, Maxwell A. Sherman, Michael E. Coulter, Michael A. Lodato, Peter J. Park, Rebeca B. Monroy, Sonia N. Kim, Yanmei Dou, Andrew Chess, Attila Gulyás-Kovács, Chaggai Rosenbluh, Schahram Akbarian, Ben Langmead, Jeremy Thorpe, Jonathan Pevsner, Soonweng Cho, Andrew E. Jaffe, Apuã C.M. Paquola, Daniel R. Weinberger, Jennifer A. Erwin, Jooheon Shin, Richard E. Straub, Rujuta Narurkar, Alexej Abyzov, Taejeong Bae, Anjené Addington, David M. Panchision, Doug Meinecke, Geetha Senthil, Lora Bingaman, Tara Dutka, Thomas Lehner, Laura Saucedo-Cuevas, Tara Conniff, Kenneth Daily, Mette A. Peters, Fred H. Gage, Meiyan Wang, Patrick Reed, Sara B. Linker, Alex E. Urban, Bo Zhou, Xiaowei Zhu, Aitor Serres, David Juan, Inna Povolotskaya, Irene Lobón, Manuel Solís-Moruno, Raquel García-Pérez, Tomàs Marquès‐Bonet, Gary W. Mathern, Jing Gu, Joseph G. Gleeson, Laurel Ball, Renee D. George, Tiziano Pramparo, Diane A. Flasch, Trenton J. Frisbie, Jeffrey M. Kidd, John B. Moldovan, John V. Moran, Kenneth Y. Kwan, Ryan E. Mills, Sarah B. Emery, Weichen Zhou, Yifan Wang, Aakrosh Ratan, Michael J. McConnell, Flora M. Vaccarino and 7 more - Nature Neuroscience 2021 cited by 135

  15. The human gene damage index as a gene-level approach to prioritizing exome variants

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , - National Academy of Sciences, Proceedings of the National Academy of Sciences 2015 cited by 279

  16. Cell-type-resolved mosaicism reveals clonal dynamics of the human forebrain

    Authors: , , , , , , , , , , , , , , , , - Nature 2024 cited by 52

  17. De novo somatic mutations in components of the PI3K-AKT3-mTOR pathway cause hemimegalencephaly

    Authors: , , , , , , , , , , , , , , - Nature Genetics 2012 cited by 696

  18. Exome Sequencing Links Corticospinal Motor Neuron Disease to Common Neurodegenerative Disorders

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Nasir Al‐Allawi, Parayil Sankaran Bindu, Matloob Azam, Murat Günel, Ahmet Okay Çağlayan, Kaya Bilgüvar, Aslıhan Tolun, Mahmoud Y. Issa, Jana Schroth, Emily Spencer, Rasim Özgür Rosti, Naiara Akizu, Keith K. Vaux, Anide Johansen, Alice A. Koh, Hisham Megahed, Alexandra Dürr, Alexis Brice, Giovanni Stévanin, Stacy Gabriel, Trey Ideker, Joseph G. Gleeson - Science 2014 cited by 548

  19. Primary Cilia in the Developing and Mature Brain

    Authors: , , - Neuron 2014 cited by 295

  20. CLP1 Founder Mutation Links tRNA Splicing and Maturation to Cerebellar Development and Neurodegeneration

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Murat Günel, Frank Baas, Joseph G. Gleeson - Cell 2014 cited by 284

  21. Defining the phenotypic spectrum of SLC6A1 mutations

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Yvonne Weber, Caroline Nava, Boris Keren, Diane Doummar, Élise Schaefer, Sarah Hopkins, Holly Dubbs, Jessica Shaw, Laura Rosa Pisani, Candace T. Myers, Sha Tang, Shan Tang, Deb K. Pal, J Gordon Millichap, Gemma L. Carvill, Kathrine L. Helbig, Oriano Mecarelli, Pasquale Striano, Ingo Helbig, Guido Rubboli, Heather C. Mefford, Rikke S. Møller - Epilepsia 2018 cited by 152

  22. Cytosine-5 RNA methylation links protein synthesis to cell metabolism

    Authors: , , , , , , , , , , , , , , - PLoS Biology 2019 cited by 135

  23. Negative selection on human genes underlying inborn errors depends on disease outcome and both the mode and mechanism of inheritance

    Authors: , , , , , , , , , , , , , , , - National Academy of Sciences, Proceedings of the National Academy of Sciences 2021 cited by 79

  24. Analysis of somatic mutations in 131 human brains reveals aging-associated hypermutability

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Daniel R. Weinberger, John V. Moran, Fred H. Gage, Flora M. Vaccarino, Joseph G. Gleeson, Gary W. Mathern, Eric Courchesne, Subhojit Roy, Andrew Chess, Schahram Akbarian, Sara Bizzotto, Michael E. Coulter, Caroline Dias, Alissa M. D’Gama, Javier Ganz, Robert Hill, August Yue Huang, Sattar Khoshkhoo, Sonia Kim, Alice Lee, Michael A. Lodato, Eduardo A. Maury, Michael Miller, Rebeca Borges-Monroy, Rachel E. Rodin, Zinan Zhou, Craig L. Bohrson, Chong Chu, Isidro Cortés‐Ciriano, Yanmei Dou, Alon Galor, D. Gulhan, Min‐Seok Kwon, Joe Luquette, Maxwell A. Sherman, Vinay Viswanadham, Attila Jones, Chaggai Rosenbluh, Sean Cho, Ben Langmead, Jeremy Thorpe, Jennifer A. Erwin, Andrew E. Jaffe, Michael J. McConnell, Rujuta Narurkar, Apuã C.M. Paquola, Jooheon Shin, Richard E. Straub, Alexej Abyzov, Taejeong Bae, Yeongjun Jang, Yifan Wang, Cindy Molitor, Mette A. Peters, Sara B. Linker, Patrick Reed, Meiyan Wang, Alexander E. Urban, Bo Zhou, Xiaowei Zhu, Reenal Pattni, Aitor Serres Amero, David Juan, Irene Lobón, Tomàs Marquès‐Bonet, Manuel Solis Moruno, Raquel García Pérez, Inna Povolotskaya, Eduardo Soriano, Danny Antaki and 21 more - Science 2022 cited by 72