Lynn E. DeLisi

Active 1981–2026

105
Papers
25,232
Citations
83
h-index
104
i10-index

Citations

Citations per year for Lynn E. DeLisi1940: 2 citations1980: 1 citations1982: 4 citations1983: 8 citations1984: 3 citations1985: 5 citations1986: 2 citations1987: 26 citations1988: 29 citations1989: 22 citations1990: 41 citations1991: 41 citations1992: 81 citations1993: 83 citations1994: 92 citations1995: 95 citations1996: 76 citations1997: 124 citations1998: 149 citations1999: 171 citations2000: 163 citations2001: 153 citations2002: 158 citations2003: 180 citations2004: 141 citations2005: 170 citations2006: 162 citations2007: 148 citations2008: 178 citations2009: 153 citations2010: 193 citations2011: 235 citations2012: 198 citations2013: 211 citations2014: 135 citations2015: 173 citations2016: 164 citations2017: 184 citations2018: 192 citations2019: 475 citations2020: 602 citations2021: 538 citations2022: 549 citations2023: 505 citations2024: 863 citations2025: 364 citations2026: 10 citations1941–1979: no citations, so these years are not shown1981: no citations, so this year is not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 3,770 citing papers, 28.1% of this breakdownUnited Kingdom: 1,331 citing papers, 9.9% of this breakdownCanada: 704 citing papers, 5.2% of this breakdownGermany: 670 citing papers, 5% of this breakdownChina: 614 citing papers, 4.6% of this breakdownAustralia: 554 citing papers, 4.1% of this breakdownNetherlands: 519 citing papers, 3.9% of this breakdownItaly: 430 citing papers, 3.2% of this breakdownFrance: 356 citing papers, 2.6% of this breakdownSweden: 333 citing papers, 2.5% of this breakdownDenmark: 304 citing papers, 2.3% of this breakdownSpain: 294 citing papers, 2.2% of this breakdown
0%28.1%Other 26.4%

Fields

  • Biochemistry, Genetics and Molecular Biology41.3%
  • Medicine31.6%
  • Neuroscience19.2%
  • Psychology4.2%
  • Computer Science0.9%
  • Pharmacology, Toxicology and Pharmaceutics0.5%
  • Other2.3%

Topics

  • Genetic Associations and Epidemiology7.8%
  • Schizophrenia research and treatment7.5%
  • Genetics and Neurodevelopmental Disorders4.3%
  • Functional Brain Connectivity Studies4%
  • Genomic variations and chromosomal abnormalities3.7%
  • Genomics and Rare Diseases2.6%
  • Other70.1%

Coauthors

All papers

Open in search
  1. Mapping genomic loci implicates genes and synaptic biology in schizophrenia

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Mariam Al Eissa, Margot Albus, Madeline Alexander, Behrooz Z. Alizadeh, Köksal Alptekın, Thomas D. Als, Farooq Amin, Volker Arolt, Manuel Arrojo, Lavinia Athanasiu, M.H. Azevedo, Silviu‐Alin Bacanu, Nicholas Bass, Martin Begemann, Richard A. Belliveau, Judit Bene, Beben Benyamin, Sarah E. Bergen, Giuseppe Blasi, Julio Bobes, Stefano Bonassi, Alice Braun, Rodrigo A. Bressan, Evelyn J. Bromet, Richard Bruggeman, P.F. Buckley, Randy L. Buckner, Jonas Bybjerg‐Grauholm, Wiepke Cahn, Murray J. Cairns, Monica E. Calkins, Vaughan J. Carr, David Castle, Stanley V. Catts, Kimberley D. Chambert, Raymond Chan, Boris Chaumette, Wei Cheng, Eric F.C. Cheung, Siow Ann Chong, David Cohen, Angèle Consoli, Quirino Cordeiro, Javier Costas, Charles Curtis, Michael Davidson, Kenneth L. Davis, Lieuwe de Haan, Franziska Degenhardt, Lynn E. DeLisi, Ditte Demontis, Faith Dickerson, Dimitris Dikeos, Timothy G. Dinan, Srdjan Djurovic, Jubao Duan, Giuseppe Ducci, Frank Dudbridge, Johan G. Eriksson, Lourdes Fañanás, Stephen V. Faraone, Alessia Fiorentino, Andreas J. Forstner, Josef Frank, Nelson B. Freimer, Menachem Fromer, Alessandra Frustaci, Ary Gadelha, Giulio Genovese, Elliot S. Gershon and 513 more - Nature 2022 cited by 2,857

  2. Rare coding variants in ten genes confer substantial risk for schizophrenia

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Andrea Ganna, Giulio Genovese, David C. Glahn, Jakob Grove, Mei‐Hua Hall, Eija Hämäläinen, Henrike Heyne, Matti Holi, David M. Hougaard, Daniel P. Howrigan, Hailiang Huang, Hai‐Gwo Hwu, René S. Kahn, Hyun Min Kang, Konrad J. Karczewski, George Kirov, James A. Knowles, Francis S. Lee, Douglas S. Lehrer, Francesco Lescai, Dolores Malaspina, Stephen R. Marder, Steven A. McCarroll, Andrew M. McIntosh, Helena Medeiros, Lili Milani, Christopher P. Morley, Derek W. Morris, Preben Bo Mortensen, R Myers, Merete Nordentoft, Niamh L. O’Brien, Ana Maria Olivares, Döst Öngür, Willem H. Ouwehand, Duncan S. Palmer, Tiina Paunio, Digby Quested, Mark Hyman Rapaport, Elliott Rees, Brandi Rollins, F. Kyle Satterstrom, Alan F. Schatzberg, Edward M. Scolnick, Laura J. Scott, Sally I. Sharp, Pamela Sklar, Jordan W. Smoller, Janet L. Sobell, Matthew Solomonson, Eli A. Stahl, Christine Stevens, Jaana Suvisaari, Grace Tiao, Stanley J. Watson, Nicholas A. Watts, Douglas Blackwood, Anders D. Børglum, Bruce M. Cohen, Aiden Corvin, Tõnu Esko, Nelson B. Freimer, Stephen J. Glatt, Christina M. Hultman, Andrew McQuillin, Aarno Palotie, Carlos N. Pato, Michele T. Pato, Ann E. Pulver, David St Clair and 11 more - Nature 2022 cited by 916

  3. Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Peter M. Visscher, Peter Kraft, Nick Patterson, Alkes L. Price, Stephan Ripke, Benjamin M. Neale, Aiden Corvin, James Walters, Kai-How Farh, Peter Holmans, Phil Lee, Brendan Bulik‐Sullivan, David Collier, Hailiang Huang, Tune H. Pers, Ingrid Agartz, Esben Agerbo, Margot Albus, Madeline Alexander, Farooq Amin, Silviu‐Alin Bacanu, Martin Begemann, Richard A. Belliveau, Judit Bene, Sarah E. Bergen, Elizabeth Bevilacqua, Tim B. Bigdeli, Donald W. Black, Richard Bruggeman, Nancy G. Buccola, Randy L. Buckner, William Byerley, Wiepke Cahn, Guiqing Cai, Dominique Campion, Rita M. Cantor, Vaughan J. Carr, Noa Carrera, Stanley V. Catts, Kimberly D. Chambert, Raymond Chan, Ronald Y.L. Chen, Eric Chen, Wei Cheng, Eric F.C. Cheung, Siow Ann Chong, C. Robert Cloninger, David Cohen, Nadine Cohen, Paul Cormican, Nick Craddock, James J. Crowley, David Curtis, Michael Davidson, Kenneth L. Davis, Franziska Degenhardt, Jurgen Del‐Favero, Lynn E. DeLisi, Ditte Demontis, Dimitris Dikeos, Timothy G. Dinan, Srdjan Djurovic, Gary Donohoe, Elodie Drapeau, Jubao Duan, Frank Dudbridge, Naser Durmishi, Peter Eichhammer, Johan G. Eriksson, Valentina Escott‐Price and 302 more - The American Journal of Human Genetics 2015 cited by 1,489

  4. Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Nancy G. Buccola, Randy L. Buckner, Brendan Bulik‐Sullivan, William Byerley, Wiepke Cahn, Guiqing Cai, Murray J. Cairns, Dominique Campion, Rita M. Cantor, Vaughan J. Carr, Noa Carrera, Stanley V. Catts, Kimberley D. Chambert, Wei Cheng, C. Robert Cloninger, David Cohen, Paul Cormican, Nick Craddock, Benedicto Crespo‐Facorro, James J Crowley, David Curtis, Michael Davidson, Kenneth L. Davis, Franziska Degenhardt, Jurgen Del‐Favero, Lynn E. DeLisi, Dimitris Dikeos, Timothy G. Dinan, Srdjan Djurovic, Gary Donohoe, Elodie Drapeau, Jubao Duan, Frank Dudbridge, Peter Eichhammer, Johan G. Eriksson, Valentina Escott‐Price, Laurent Essioux, Ayman H. Fanous, Kai-How Farh, Martilias S. Farrell, Josef Frank, Lude Franke, Robert Freedman, Nelson B. Freimer, Joseph I. Friedman, Andreas J. Forstner, Menachem Fromer, Giulio Genovese, Lyudmila Georgieva, Elliot S. Gershon, Ina Giegling, Paola Giusti‐Rodríguez, Stephanie Godard, Jacqueline I. Goldstein, Jacob Gratten, Lieuwe de Haan, Marian L. Hamshere, Mark Hansen, Thomas Folkmann Hansen, Vahram Haroutunian, Annette M. Hartmann, Frans A. Henskens, Stefan Herms, Joel N. Hirschhorn, Per Hoffmann, Andrea Hofman, Hailiang Huang, Masashi Ikeda, Inge Joa, Anna K. Kähler and 163 more - Nature Genetics 2016 cited by 1,142

  5. Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common Diseases

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Hailiang Huang, Tune H. Pers, Ingrid Agartz, Esben Agerbo, Margot Albus, Madeline Alexander, Farooq Amin, Silviu‐Alin Bacanu, Martin Begemann, Richard A. Belliveau, Judit Bene, Sarah E. Bergen, Elizabeth Bevilacqua, Tim B. Bigdeli, Donald W. Black, Anders D. Børglum, Richard Bruggeman, Nancy G. Buccola, Randy L. Buckner, William Byerley, Wiepke Cahn, Guiqing Cai, Dominique Campion, Rita M. Cantor, Vaughan J. Carr, Noa Carrera, Stanley V. Catts, Kimberly D. Chambert, Raymond Chan, Ronald Y.L. Chen, Eric Chen, Wei Cheng, Eric Cheung, Siow Ann Chong, C. Robert Cloninger, David Cohen, Nadine Cohen, Paul Cormican, Nick Craddock, James J. Crowley, David Curtis, Michael H. Davidson, Kenneth L. Davis, Franziska Degenhardt, Jurgen Del‐Favero, Lynn E. DeLisi, Ditte Demontis, Dimitris Dikeos, Timothy G. Dinan, Srdjan Djurovic, Gary Donohoe, Elodie Drapeau, Jubao Duan, Frank Dudbridge, Naser Durmishi, Peter Eichhammer, Johan G. Eriksson, Valentina Escott‐Price, Laurent Essioux, Ayman H. Fanous, Martilias S. Farrell, Josef Frank, Lude Franke, Robert Freedman, Nelson B. Freimer, Marion Friedl, Joseph I. Friedman, Menachem Fromer, Giulio Genovese, Lyudmila Georgieva and 245 more - The American Journal of Human Genetics 2014 cited by 654

  6. The schizophrenia syndrome, circa 2024: What we know and how that informs its nature

    Authors: , , , , , , , , , , , , , , , , - Schizophrenia Research 2023 cited by 171

  7. Effects of Cannabis Use on Human Behavior, Including Cognition, Motivation, and Psychosis: A Review

    Authors: , , , , , , , , - JAMA Psychiatry 2016 cited by 861

  8. Mutations in SYNGAP1 in Autosomal Nonsyndromic Mental Retardation

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , - New England Journal of Medicine 2009 cited by 351

  9. Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants With Treatment Resistance in Schizophrenia

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Michael J. Owen, James H. MacCabe, Michael O‘Donovan, James Walters, Stephan Ripke, Benjamin M. Neale, Kai-How Farh, Phil Lee, Brendan Bulik‐Sullivan, David Collier, Hailiang Huang, Tune H. Pers, Ingrid Agartz, Esben Agerbo, Margot Albus, Madeline Alexander, Farooq Amin, Silviu‐Alin Bacanu, Martin Begemann, Richard A. Belliveau, Judit Bene, Sarah E. Bergen, Elizabeth Bevilacqua, Donald W. Black, Richard Bruggeman, Nancy G. Buccola, Randy L. Buckner, William Byerley, Wiepke Cahn, Guiqing Cai, Dominique Campion, Rita M. Cantor, Vaughan J. Carr, Noa Carrera, Stanley V. Catts, Kimberly D. Chambert, Raymond C. Chan, Ronald Y.L. Chen, Eric Chen, Wei Cheng, Eric F.C. Cheung, Siow Ann Chong, C. Robert Cloninger, David Cohen, Nadine Cohen, Paul Cormican, Nick Craddock, James J. Crowley, David Curtis, Michael Davidson, Kenneth L. Davis, Franziska Degenhardt, Jurgen Del‐Favero, Lynn E. DeLisi, Ditte Demontis, Dimitris Dikeos, Timothy G. Dinan, Srdjan Djurovic, Gary Donohoe, Elodie Drapeau, Jubao Duan, Frank Dudbridge, Naser Durmishi, Peter Eichhammer, Johan G. Eriksson, Valentina Escott‐Price, Laurent Essioux, Martilias S. Farrell, Lude Franke, Robert Freedman and 261 more - JAMA Psychiatry 2022 cited by 106

  10. Review and Consensus on Pharmacogenomic Testing in Psychiatry

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Daniel J. Müller - Pharmacopsychiatry 2020 cited by 211

  11. Truncating mutations in NRXN2 and NRXN1 in autism spectrum disorders and schizophrenia

    Authors: , , , , , , , , , , , , , , , , , , , , - Human Genetics 2011 cited by 281

  12. Contributions of common genetic variants to risk of schizophrenia among individuals of African and Latino ancestry

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Mantosh Dewan, James Nemesh, Diana O. Perkins, Shaun Purcell, Jeffrey J. Rakofsky, Edward M. Scolnick, Brooke M. Sklar, Pamela Sklar, Jordan W. Smoller, Patrick F. Sullivan, Fabìo Macciardi, Stephen R. Marder, Ruben C. Gur, Raquel E. Gur, David Braff, Monica E. Calkins, Robert R. Freedman, Michael F. Green, Tiffany A. Greenwood, Laura C. Lazzeroni, Gregory A. Light, Keith H. Nuechterlein, Allen D. Radant, Larry J. Seidman, Larry J. Siever, Jeremy M. Silverman, William S. Stone, Catherine A. Sugar, Neal R. Swerdlow, Debby W. Tsuang, Ming T. Tsuang, Bruce I. Turetsky, Humberto Nicolini, Michael Escamilla, Marquis P. Vawter, Janet L. Sobell, Dolores Malaspina, Douglas S. Lehrer, P.F. Buckley, Mark Hyman Rapaport, James A. Knowles, Ayman H. Fanous, Michele T. Pato, Steven A. McCarroll, Carlos N. Pato - Molecular Psychiatry 2019 cited by 141

  13. Microduplications of 16p11.2 are associated with schizophrenia

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Timothy J. Crow, Susan L. Christian, Jeffrey A. Lieberman, T. Scott Stroup, Terho Lehtimäki, Kaija Puura, Chad Haldeman‐Englert, Justin Pearl, Meredith Goodell, Virginia L. Willour, Pamela DeRosse, Jo Steele, Layla Kassem, Jessica Wolff, Nisha Chitkara, Francis J. McMahon, Anil K. Malhotra, James B. Potash, Thomas G. Schulze, Markus M. Nöthen, Sven Cichon, Marcella Rietschel, Ellen Leibenluft, Vlad Kustanovich, Clara Lajonchere, James S. Sutcliffe, David Skuse, Michael Gill, Louise Gallagher, Nancy R. Mendell, Nick Craddock, Michael J. Owen, Michael O‘Donovan, Tamim H. Shaikh, Ezra Susser, Lynn E. DeLisi, Patrick F. Sullivan, Curtis K. Deutsch, Judith L. Rapoport, Deborah L. Levy, Mary‐Claire King, Jonathan Sebat - Nature Genetics 2009 cited by 736

  14. De novo mutations in the gene encoding the synaptic scaffolding protein SHANK3 in patients ascertained for schizophrenia

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Kathleen Daignault, Ousmane Diallo, Joannie Duguay, Marina Drits, Édouard Henrion, Philippe Jolivet, Frédéric Kuku, Karine Lachapelle, Guy Laliberté, Sandra B. Laurent, Meijiang Liao, Carlos Marino, Amélie Piton, A Raymond, Annie Reynolds, Daniel Rochefort, Judith St‐Onge, Pascale Thibodeau, Kazuya Tsurudome, Yanlian Yang, Sophie Leroy, Katia Ossian, Mélanie Chayet, David Gourion - National Academy of Sciences, Proceedings of the National Academy of Sciences 2010 cited by 380

  15. Lithium Treatment in the Prevention of Repeat Suicide-Related Outcomes in Veterans With Major Depression or Bipolar Disorder

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , David A. Cory, Dena Davidson, Patrica Dickmann, Erica Duncan, Ronald Fernando, Karen Floyd, Steven D. Forman, Phillip Gale, Jayant Geete, Michael Ignatowski, Kari Jones, Timothy Juergens, George Jurjus, Gauri Khatkhate, Eric P. Konicki, Dean D. Krahn, Gunnar Larson, Susan G. Leckband, Joel Mack, Scott C. Matthews, L. Fernández Mayo, Erin McGlade, James P. Michalets, Elizabeth Miller, E. Chris Muly, Alexander B. Niculescu, Michael J. Ostacher, Prasad R. Padala, Kalpana P. Padala, Peggy J. Pazzaglia, Murray A. Raskind, Perry F. Renshaw, Geetha Shivakumar, Julia C. Smith, Dennis H. Sullivan, Patricia Suppes, Alan C. Swann, Lia Thomas, Shabnam I. Thompson, Erick H. Turner, Maria A. Umbert, Joseph Westermeyer, A. E. Wood, Hal S. Wortzel, Deborah Yurgelun‐Todd - JAMA Psychiatry 2021 cited by 84

  16. Speech Disorder in Schizophrenia: Review of the Literature and Exploration of Its Relation to the Uniquely Human Capacity for Language

    Authors: - Schizophrenia Bulletin 2001 cited by 329

  17. A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Marie McDonald, Joe J. Hoo, Beatrice N. French, Cindy Hudson, John P. Johnson, Jillian R. Ozmore, John B. Moeschler, Urvashi Surti, Luis Escobar, Dima El‐Khechen, Jerome L. Gorski, Jennifer Kussmann, Bonnie Anne Salbert, Yves Lacassie, Alisha Biser, Donna M. McDonald‐McGinn, Elaine H. Zackai, Matthew A. Deardorff, Tamim H. Shaikh, Eric Haan, Kathryn Friend, Marco Fichera, Corrado Romano, Jozef Gécz, Lynn E. DeLisi, Jonathan Sebat, Mary‐Claire King, Lisa G. Shaffer, Evan E. Eichler - Nature Genetics 2010 cited by 674

  18. An international research agenda for clozapine-resistant schizophrenia

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , - The Lancet Psychiatry 2023 cited by 33

  19. An automated method to analyze language use in patients with schizophrenia and their first-degree relatives

    Authors: , , , - Journal of Neurolinguistics 2009 cited by 135

  20. Rare mutations in N-methyl-D-aspartate glutamate receptors in autism spectrum disorders and schizophrenia

    Authors: , , , , , , , , , , , , , , , , , , , , , , - Translational Psychiatry 2011 cited by 227

  21. Duplications of the neuropeptide receptor gene VIPR2 confer significant risk for schizophrenia

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , - Nature 2011 cited by 332

  22. A Rare Functional Noncoding Variant at the GWAS-Implicated MIR137/MIR2682 Locus Might Confer Risk to Schizophrenia and Bipolar Disorder

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Colony Abbott, Brooke Skar, P.F. Buckley, Evelyn J. Bromet, Michael A. Escamilla, Ayman H. Fanous, Douglas S. Lehrer, Fabìo Macciardi, Dolores Malaspina, Steve McCarroll, Stephen R. Marder, Jennifer L. Moran, Christopher P. Morley, Humberto Nicolini, Diana O. Perkins, Shaun Purcell, Mark Hyman Rapaport, Pamela Sklar, Jordan W. Smoller, James A. Knowles, Carlos N. Pato, Andrew McQuillin, Alan R. Sanders, Elliot S. Gershon, Lynn E. DeLisi, A. R. Bishop, Hugh Gurling, Michele T. Pato, Douglas F. Levinson, Kenneth S. Kendler, Carlos N. Pato, Pablo V. Gejman - The American Journal of Human Genetics 2014 cited by 109

  23. Systematic resequencing of X-chromosome synaptic genes in autism spectrum disorder and schizophrenia

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Laurent Mottron, Ridha Joober, Éric Fombonne, Pierre Drapeau, Guy A. Rouleau - Molecular Psychiatry 2010 cited by 320

  24. A Comprehensive Family-Based Replication Study of Schizophrenia Genes

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , - JAMA Psychiatry 2013 cited by 159