Hyejung Won

Active 2009–2025

64
Papers
20,612
Citations
42
h-index
59
i10-index

Citations

Citations per year for Hyejung Won1965: 1 citations1992: 5 citations1994: 1 citations1995: 1 citations2002: 1 citations2005: 1 citations2009: 2 citations2010: 4 citations2011: 10 citations2012: 13 citations2013: 25 citations2014: 65 citations2015: 81 citations2016: 104 citations2017: 141 citations2018: 258 citations2019: 1,023 citations2020: 1,360 citations2021: 1,482 citations2022: 1,224 citations2023: 858 citations2024: 1,204 citations2025: 544 citations2026: 29 citations1966–1991: no citations, so these years are not shown1993: no citations, so this year is not shown1996–2001: no citations, so these years are not shown2003–2004: no citations, so these years are not shown2006–2008: no citations, so these years are not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 3,210 citing papers, 25.1% of this breakdownUnited Kingdom: 1,184 citing papers, 9.3% of this breakdownChina: 897 citing papers, 7% of this breakdownGermany: 661 citing papers, 5.2% of this breakdownCanada: 598 citing papers, 4.7% of this breakdownNetherlands: 588 citing papers, 4.6% of this breakdownAustralia: 499 citing papers, 3.9% of this breakdownItaly: 417 citing papers, 3.3% of this breakdownSweden: 398 citing papers, 3.1% of this breakdownFrance: 329 citing papers, 2.6% of this breakdownSpain: 324 citing papers, 2.5% of this breakdownDenmark: 317 citing papers, 2.5% of this breakdown
0%25.1%Other 26.2%

Fields

  • Biochemistry, Genetics and Molecular Biology48.5%
  • Neuroscience25.9%
  • Medicine18.2%
  • Psychology3.9%
  • Immunology and Microbiology0.7%
  • Environmental Science0.6%
  • Other2.2%

Topics

  • Genetic Associations and Epidemiology7.9%
  • Genetics and Neurodevelopmental Disorders7.1%
  • Autism Spectrum Disorder Research6.9%
  • Epigenetics and DNA Methylation3.1%
  • Attention Deficit Hyperactivity Disorder2.7%
  • Bioinformatics and Genomic Networks2.5%
  • Other69.8%

Coauthors

All papers

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  1. Identification of common genetic risk variants for autism spectrum disorder

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Mads V. Hollegaard, Sigrun Hope, Daniel P. Howrigan, Hailiang Huang, Christina M. Hultman, Lambertus Klei, Julian Maller, Joanna Martin, Alicia R. Martin, Jennifer L. Moran, Mette Nyegaard, Terje Nærland, Duncan S. Palmer, Aarno Palotie, Carsten Bøcker Pedersen, Marianne Giørtz Pedersen, Timothy dPoterba, Jesper Buchhave Poulsen, Beaté St Pourcain, Per Qvist, Karola Rehnström, Abraham Reichenberg, Jennifer Reichert, Elise Robinson, Kathryn Roeder, Panos Roussos, Evald Sæmundsen, Sven Sandin, F. Kyle Satterstrom, George Davey Smith, Hreinn Stefánsson, Stacy Steinberg, Christine Stevens, Patrick F. Sullivan, Patrick Turley, G. Bragi Walters, Xinyi Xu, Kāri Stefánsson, Daniel H. Geschwind, Merete Nordentoft, David M. Hougaard, Thomas Werge, Ole Mors, Preben Bo Mortensen, Benjamin M. Neale, Mark J. Daly, Anders D. Børglum - Nature Genetics 2019 cited by 2,632

  2. Discovery of the first genome-wide significant risk loci for attention deficit/hyperactivity disorder

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Duncan S. Palmer, Carsten Bøcker Pedersen, Marianne Giørtz Pedersen, Timothy Poterba, Jesper Buchhave Poulsen, Stephan Ripke, Elise Robinson, F. Kyle Satterstrom, Hreinn Stefánsson, Christine Stevens, Patrick Turley, G. Bragi Walters, Hyejung Won, Margaret J. Wright, Ole A. Andreassen, Philip Asherson, Christie L. Burton, Dorret I. Boomsma, Bru Cormand, Søren Dalsgaard, Barbara Franke, Joel Gelernter, Daniel H. Geschwind, Håkon Håkonarson, Jan Haavik, Henry R. Kranzler, Jonna Kuntsi, K. Langley, Klaus‐Peter Lesch, Christel M. Middeldorp, Andreas Reif, Luís Augusto Rohde, Panos Roussos, Russell Schachar, Pamela Sklar, Edmund Sonuga‐Barke, Patrick F. Sullivan, Anita Thapar, Joyce Y. Tung, Irwin D. Waldman, Sarah E. Medland, Kāri Stefánsson, Merete Nordentoft, David M. Hougaard, Thomas Werge, Ole Mors, Preben Bo Mortensen, Mark J. Daly, Stephen V. Faraone, Anders D. Børglum, Benjamin M. Neale - Nature Genetics 2018 cited by 2,320

  3. Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Clement C. Zai, Esben Agerbo, María J. Arranz, Philip Asherson, Marie Bækvad‐Hansen, Gísli Baldursson, Mark A. Bellgrove, Richard A. Belliveau, Jan K. Buitelaar, Christie L. Burton, Jonas Bybjerg‐Grauholm, Miguel Casas, Felecia Cerrato, Kimberly Chambert, Claire Churchhouse, Bru Cormand, Jennifer Crosbie, Søren Dalsgaard, Ditte Demontis, Alysa E. Doyle, Ashley Dumont, Josephine Elia, Jakob Grove, Ólafur Ó. Guðmundsson, Jan Haavik, Håkon Håkonarson, Christine Søholm Hansen, Catharina A. Hartman, Ziarih Hawi, Amaia Hervás, David M. Hougaard, Daniel P. Howrigan, Hailiang Huang, Jonna Kuntsi, K. Langley, Klaus‐Peter Lesch, Patrick W. L. Leung, Sandra K. Loo, Joanna Martin, Alicia R. Martin, James J. McGough, Sarah E. Medland, Jennifer L. Moran, Ole Mors, Preben Bo Mortensen, Robert D. Oades, Duncan S. Palmer, Carsten Bøcker Pedersen, Marianne G. Pedersen, Triinu Peters, Timothy Poterba, Jesper Buchhave Poulsen, Josep Antoni Ramos‐Quiroga, Andreas Reif, Marta Ribasés, Aribert Rothenberger, Paula Rovira, Cristina Sánchez‐Mora, F. Kyle Satterstrom, Russell Schachar, María Soler Artigas, Stacy Steinberg, Hreinn Stefánsson, Patrick Turley, G. Bragi Walters, Thomas Werge, Tetyana Zayats, Dan E. Arking, Francesco Bettella, Joseph D. Buxbaum and 506 more - Cell 2019 cited by 1,516

  4. Transcriptome-wide isoform-level dysregulation in ASD, schizophrenia, and bipolar disorder

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Mark Gerstein, Chunyu Liu, Lilia M. Iakoucheva, Dalila Pinto, Daniel H. Geschwind, Allison E. Ashley‐Koch, Gregory E. Crawford, Melanie E. Garrett, Lingyun Song, Alexias Safi, Graham D. Johnson, Gregory A. Wray, Timothy E. Reddy, Fernando S. Goes, Peter P. Zandi, Julien Bryois, Andrew E. Jaffe, Amanda J. Price, Nikolay A. Ivanov, Leonardo Collado‐Torres, Thomas M. Hyde, Emily E. Burke, Joel E. Kleiman, Ran Tao, Joo Heon Shin, Schahram Akbarian, Kiran Girdhar, Yan Jiang, Marija Kundaković, Leanne Brown, Bibi Kassim, Royce Park, Jennifer Wiseman, Elizabeth Zharovsky, Rivka Jacobov, Olivia Devillers, Elie Flatow, Gabriel E. Hoffman, Barbara K. Lipska, David A. Lewis, Vahram Haroutunian, Chang-Gyu Hahn, Alexander W. Charney, Stella Dracheva, Alexey Kozlenkov, Judson Belmont, Diane M. Del Valle, Nancy Francoeur, Evi Hadjimichael, Dalila Pinto, Harm van Bakel, Panos Roussos, John F. Fullard, Jaroslav Bendl, Mads E. Hauberg, Lara M. Mangravite, Mette A. Peters, Yooree Chae, Junmin Peng, Mingming Niu, Xusheng Wang, Maree J. Webster, Thomas G. Beach, Chao Chen, Yi Jiang, Rujia Dai, Annie W. Shieh, Chunyu Liu, Kay Grennan, Yan Xia and 88 more - Science 2018 cited by 1,370

  5. Comprehensive functional genomic resource and integrative model for the human brain

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Gregory E. Crawford, Panos Roussos, Schahram Akbarian, Andrew E. Jaffe, Kevin P. White, Zhiping Weng, Nenad Šestan, Daniel H. Geschwind, James A. Knowles, Mark Gerstein, Allison E. Ashley‐Koch, Gregory E. Crawford, Melanie E. Garrett, Lingyun Song, Alexias Safi, Graham D. Johnson, Gregory A. Wray, Timothy E. Reddy, Fernando S. Goes, Peter P. Zandi, Julien Bryois, Andrew E. Jaffe, Amanda J. Price, Nikolay A. Ivanov, Leonardo Collado‐Torres, Thomas M. Hyde, Emily E. Burke, Joel E. Kleiman, Ran Tao, Joo Heon Shin, Schahram Akbarian, Kiran Girdhar, Yan Jiang, Marija Kundaković, Leanne Brown, Bibi Kassim, Royce Park, Jennifer Wiseman, Elizabeth Zharovsky, Rivka Jacobov, Olivia Devillers, Elie Flatow, Gabriel E. Hoffman, Barbara K. Lipska, David A. Lewis, Vahram Haroutunian, Chang-Gyu Hahn, Alexander W. Charney, Stella Dracheva, Alexey Kozlenkov, Judson Belmont, Diane M. Del Valle, Nancy Francoeur, Evi Hadjimichael, Dalila Pinto, Harm van Bakel, Panos Roussos, John F. Fullard, Jaroslav Bendl, Mads E. Hauberg, Lara M. Mangravite, Mette A. Peters, Yooree Chae, Junmin Peng, Mingming Niu, Xusheng Wang, Maree J. Webster, Thomas G. Beach, Chao Chen, Yi Jiang and 93 more - Science 2018 cited by 1,102

  6. Integrative functional genomic analysis of human brain development and neuropsychiatric risks

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Michael O‘Donovan, James Walters, Daniëlle Posthuma, Mark A. Reimers, Pat Levitt, Daniel R. Weinberger, Thomas M. Hyde, Joel E. Kleinman, Daniel H. Geschwind, Michael Hawrylycz, Matthew W. State, Stephan Sanders, Patrick F. Sullivan, Mark Gerstein, Ed S. Lein, James A. Knowles, Nenad Šestan, A. Jeremy Willsey, Aaron Oldre, Aaron Szafer, Adrian Camarena, Adriana Cherskov, Alexander W. Charney, Alexej Abyzov, Alexey Kozlenkov, Alexias Safi, Allan R. Jones, Allison E. Ashley‐Koch, Amanda Ebbert, Amanda J. Price, Amanda Sekijima, Amira Kefi, Amy Bernard, Anahita Amiri, Andrea Sboner, Andrew E. Clark, Andrew E. Jaffe, Andrew T.N. Tebbenkamp, Andy J. Sodt, Angie Guillozet‐Bongaarts, Angus C. Nairn, Anita Carey, Anita Hüttner, Ann Chervenak, Anna Szekely, Annie W. Shieh, Arif Harmanci, Barbara K. Lipska, Becky C. Carlyle, Ben W. Gregor, Bibi Kassim, Brooke Sheppard, Candace Bichsel, Chang-Gyu Hahn, Chang-Kyu Lee, Chao Chen, Chihchau L. Kuan, Chinh Dang, Chris Lau, Christine Cuhaciyan, Christoper Armoskus, Christopher E. Mason, Chunyu Liu, Cliff Slaughterbeck, Crissa Bennet, Dalila Pinto, Damon Polioudakis, Daniel Franjic, Daniel J. Miller, Darren Bertagnolli and 187 more - Science 2018 cited by 901

  7. Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Laura M. Huckins, Douglas M. Ruderfer, Enrique Santiago, Pamela Sklar, Eli A. Stahl, Hyejung Won, Esben Agerbo, Thomas D. Als, Ole A. Andreassen, Marie Bækvad‐Hansen, Preben Bo Mortensen, Carsten Bøcker Pedersen, Anders D. Børglum, Jonas Bybjerg‐Grauholm, Srdjan Djurovic, Naser Durmishi, Marianne Giørtz Pedersen, В. Е. Голимбет, Jakob Grove, David M. Hougaard, Manuel Mattheisen, Espen Molden, Ole Mors, Merete Nordentoft, Milica Pejović-Milovančević, Engilbert Sigurðsson, Teimuraz Silagadze, Christine Søholm Hansen, Kāri Stefánsson, Hreinn Stefánsson, Stacy Steinberg, Sarah Tosato, Thomas Werge, David Collier, Dan Rujescu, George Kirov, Michael J. Owen, Michael O‘Donovan, James Walters - Nature Genetics 2018 cited by 1,728

  8. Integrative Functional Genomic Analyses Implicate Specific Molecular Pathways and Circuits in Autism

    Authors: , , , , , , , - Cell 2013 cited by 1,132

  9. A computational tool (H-MAGMA) for improved prediction of brain-disorder risk genes by incorporating brain chromatin interaction profiles

    Authors: , , , , , , , , - Nature Neuroscience 2020 cited by 323

  10. Advancing the understanding of autism disease mechanisms through genetics

    Authors: , , , - Nature Medicine 2016 cited by 856

  11. Single-cell genomics and regulatory networks for 388 human brains

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Diego Garrido-Martín, Sophia C. Gaynor-Gillett, Jennifer Grundman, Natalie Hawken, Ella Henry, Gabriel E. Hoffman, Ao Huang, Yunzhe Jiang, Ting Jin, Nikolas L. Jorstad, Riki Kawaguchi, Saniya Khullar, Jianyin Liu, Jianyin Liu, Junhao Liu, Junhao Liu, Shuang Liu, Shaojie Ma, Michael Margolis, Samantha Mazariegos, Jill E. Moore, Jennifer Moran, Éric Nguyen, Nishigandha Phalke, Milos Pjanic, Henry Pratt, Diana Quintero, Ananya S. Rajagopalan, Tiernon R. Riesenmy, Nicole Shedd, Manman Shi, Megan Spector, Rosemarie Terwilliger, Kyle J. Travaglini, Brie Wamsley, Gaoyuan Wang, Yan Xia, Shaohua Xiao, Andrew C. Yang, Suchen Zheng, Michael J. Gandal, Donghoon Lee, Ed S. Lein, Panos Roussos, Nenad Šestan, Zhiping Weng, Kevin P. White, Hyejung Won, Matthew J. Girgenti, Jing Zhang, Daifeng Wang, Daniel H. Geschwind, Mark Gerstein, Schahram Akbarian, Alexej Abyzov, Nadav Ahituv, Dhivya Arasappan, José Juan Almagro Armenteros, Brian J. Beliveau, Sabina Berretta, Rahul Bharadwaj, Arjun Bhattacharya, Kristen Brennand, Davide Capauto, Frances A. Champagne, Chris Chatzinakos, H. Isaac Chen, Lijun Cheng, Andrew Chess, Jo-fan Chien and 140 more - Science 2024 cited by 149

  12. Chromosome conformation elucidates regulatory relationships in developing human brain

    Authors: , , , , , , , , , , , , , , - Nature 2016 cited by 651

  13. The PsychENCODE project

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Nancy Francoeur, Menachem Fromer, Robert Gao, Kay Grennan, Jennifer Herstein, David H. Kavanagh, Nikolay A. Ivanov, Yan Jiang, Robert R. Kitchen, Alexey Kozlenkov, Marija Kundaković, Mingfeng Li, Zhen Li, Shuang Liu, Lara M. Mangravite, Eugenio Mattei, Eirene Markenscoff-Papadimitriou, Fábio C. P. Navarro, Nicole North, Larsson Omberg, David M. Panchision, Neelroop Parikshak, Jérémie Poschmann, Amanda J. Price, Michael Purcaro, Timothy E. Reddy, Panos Roussos, Shannon Schreiner, Soraya Scuderi, Robert Sebra, Mikihito Shibata, Annie W. Shieh, Mario Škarica, Wenjie Sun, Vivek Swarup, Amber Thomas, Junko Tsuji, Harm van Bakel, Daifeng Wang, Yongjun Wang, Kai Wang, Donna M. Werling, A. Jeremy Willsey, Heather Witt, Hyejung Won, Chloe C. Y. Wong, Gregory A. Wray, Emily Wu, Xuming Xu, Lijing Yao, Geetha Senthil, Thomas Lehner, Pamela Sklar, Nenad Šestan - Nature Neuroscience 2015 cited by 488

  14. Transcriptome-wide association study of schizophrenia and chromatin activity yields mechanistic disease insights

    Authors: , , , , , , , , , , , , , , , , , - Nature Genetics 2018 cited by 560

  15. The Dynamic Landscape of Open Chromatin during Human Cortical Neurogenesis

    Authors: , , , , , , - Cell 2018 cited by 392

  16. Neuronal and glial 3D chromatin architecture informs the cellular etiology of brain disorders

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Yan Jiang, Marija Kundaković, Leanne Brown, Jennifer Wiseman, Elizabeth Zharovsky, Rivka Jacobov, Olivia Devillers, Elie Flatow, Gabriel E. Hoffman, Judson Belmont, Diane M. Del Valle, Nancy Francoeur, Evi Hadjimichael, Dalila Pinto, Harm van Bakel, Panos Roussos, John F. Fullard, Jaroslav Bendl, Mads E. Hauberg, Alexander W. Charney, Vahram Haroutunian, Barbara K. Lipska, David A. Lewis, Chang-Gyu Hahn, Lara M. Mangravite, Mette A. Peters, Yooree Chae, Junmin Peng, Mingming Niu, Xusheng Wang, Maree J. Webster, Thomas G. Beach, Chao Chen, Yi Jiang, Rujia Dai, Yongjun Wang, Yan Xia, Annie W. Shieh, Chunyu Liu, Kay Grennan, Ramu Vadukapuram, Gina Giase, Dominic Fitzgerald, Lijun Cheng, Miguel Brown, Mimi Brown, Tonya M. Brunetti, Thomas Goodman, Majd Alsayed, Kevin P. White, Mohana Ray, Damon Polioudakis, Brie Wamsley, Jiani Yin, Luis de la Torre-Ubieta, Michael J. Gandal, Vivek Swarup, Stephan Sanders, Matthew W. State, Donna M. Werling, Joon‐Yong An, Brooke Sheppard, A. Jeremy Willsey, Amira Kefi, Eugenio Mattei, Michael Purcaro, Zhiping Weng, J. Russell Moore, Henry Pratt, Jack Huey and 56 more - Nature Communications 2021 cited by 107

  17. Genetic insights into human cortical organization and development through genome-wide analyses of 2,347 neuroimaging phenotypes

    Authors: , , , , , , , , , , , , , , , , , , , , - Nature Genetics 2023 cited by 79

  18. Autistic-like social behaviour in Shank2-mutant mice improved by restoring NMDA receptor function

    Authors: , , , , , , , , , , , , , , , , , - Nature 2012 cited by 722

  19. Neuron-specific signatures in the chromosomal connectome associated with schizophrenia risk

    Authors: , , , , , , , , , , , , , , , , , , , , , , , - Science 2018 cited by 234

  20. A genome-wide association study of shared risk across psychiatric disorders implicates gene regulation during fetal neurodevelopment

    Authors: , , , , , , , , , , , , , , , , , , , , , , , - Nature Neuroscience 2019 cited by 226

  21. Human evolved regulatory elements modulate genes involved in cortical expansion and neurodevelopmental disease susceptibility

    Authors: , , , , - Nature Communications 2019 cited by 160

  22. Integrative genomics identifies a convergent molecular subtype that links epigenomic with transcriptomic differences in autism

    Authors: , , , , , , , , , - Nature Communications 2020 cited by 115

  23. Common genetic risk variants identified in the SPARK cohort support DDHD2 as a candidate risk gene for autism

    Authors: , , , , , , , , , , , , - Translational Psychiatry 2020 cited by 108

  24. Systematic investigation of allelic regulatory activity of schizophrenia-associated common variants

    Authors: , , , , , , , , , , , , , , , , - Cell Genomics 2023 cited by 45