Dalila Pinto

Active 2004–2025

55
Papers
23,426
Citations
44
h-index
54
i10-index

Citations

Citations per year for Dalila Pinto1965: 1 citations1985: 1 citations1995: 2 citations2000: 1 citations2002: 1 citations2003: 1 citations2004: 1 citations2005: 6 citations2006: 4 citations2008: 79 citations2009: 122 citations2010: 240 citations2011: 372 citations2012: 385 citations2013: 381 citations2014: 331 citations2015: 354 citations2016: 274 citations2017: 272 citations2018: 325 citations2019: 1,010 citations2020: 1,055 citations2021: 1,031 citations2022: 823 citations2023: 576 citations2024: 773 citations2025: 332 citations2026: 15 citations1966–1984: no citations, so these years are not shown1986–1994: no citations, so these years are not shown1996–1999: no citations, so these years are not shown2001: no citations, so this year is not shown2007: no citations, so this year is not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 3,546 citing papers, 27.2% of this breakdownUnited Kingdom: 1,116 citing papers, 8.6% of this breakdownChina: 906 citing papers, 6.9% of this breakdownCanada: 688 citing papers, 5.3% of this breakdownGermany: 661 citing papers, 5.1% of this breakdownItaly: 505 citing papers, 3.9% of this breakdownNetherlands: 484 citing papers, 3.7% of this breakdownAustralia: 446 citing papers, 3.4% of this breakdownFrance: 443 citing papers, 3.4% of this breakdownSweden: 311 citing papers, 2.4% of this breakdownSpain: 282 citing papers, 2.2% of this breakdownJapan: 255 citing papers, 2% of this breakdown
0%27.2%Other 25.9%

Fields

  • Biochemistry, Genetics and Molecular Biology58.8%
  • Neuroscience23.9%
  • Medicine11.6%
  • Psychology2.2%
  • Agricultural and Biological Sciences0.8%
  • Immunology and Microbiology0.7%
  • Other2%

Topics

  • Genetics and Neurodevelopmental Disorders8.1%
  • Autism Spectrum Disorder Research7.1%
  • Genomic variations and chromosomal abnormalities7%
  • Genetic Associations and Epidemiology5%
  • Genomics and Rare Diseases4%
  • Congenital heart defects research3%
  • Other65.8%

Coauthors

All papers

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  1. 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

  2. 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

  3. 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

  4. Shared molecular neuropathology across major psychiatric disorders parallels polygenic overlap

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Gregory E. Crawford, Pat Sullivan, Wesley K. Thompson, Preben Bo Mortensen, Esben Agerbo, Marianne Giørtz Pedersen, Carsten Bøcker Pedersen, Ole Mors, Anders D. Børglum, Merete Nordentoft, David M. Hougaard, Jonas Bybjerg‐Grauholm, Marie Bækvad‐Hansen, Alicia R. Martin, Ashley Dumont, Christine Stevens, Claire Churchhouse, Daniel P. Howrigan, Duncan S. Palmer, Elise Robinson, Kyle Satterstrom, Felecia Cerrato, Hailiang Huang, Jacqueline I. Goldstein, Jennifer L. Moran, Joanna Martin Julian, M. Alonge Kimberly, C. Seed Patrick, Patrick Turley, Raymond K. Walters, Rich Belliveau, Stephan Ripke, Timothy Poterba, Mark J. Daly, Benjamin M. Neale, Menachem Fromer, Panos Roussos, Jessica Johnson, Hardik Shah, Milind Mahajan, Eric E. Schadt, Vahram Haroutunian, Douglas M. Ruderfer, Joseph D. Buxbaum, Solveig K. Sieberts, Kristen K. Dang, Ben Logsdon, Lara M. Mangravite, Mette A. Peters, Raquel E. Gur, Chang-Gyu Hahn, Bernie Devlin, Lambertus Klei, David A. Lewis, Barbara K. Lipska, Keisuke Hirai, Hiroyoshi Toyoshiba, Enrico Domenici - Science 2018 cited by 1,177

  5. Gene expression elucidates functional impact of polygenic risk for schizophrenia

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Benjamin A. Logsdon, Konrad Talbot, Towfique Raj, David A. Bennett, Philip L. De Jager, Jun Zhu, Bin Zhang, Patrick F. Sullivan, Andrew Chess, Shaun Purcell, Leslie A. Shinobu, Lara M. Mangravite, Hiroyoshi Toyoshiba, Raquel E. Gur, Chang-Gyu Hahn, David A. Lewis, Vahram Haroutunian, Mette A. Peters, Barbara K. Lipska, Joseph D. Buxbaum, Eric E. Schadt, Keisuke Hirai, Kathryn Roeder, Kristen Brennand, Nicholas Katsanis, Enrico Domenici, Bernie Devlin, Pamela Sklar - Nature Neuroscience 2016 cited by 1,217

  6. 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

  7. Functional impact of global rare copy number variation in autism spectrum disorders

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Emily L. Crawford, Andrew Crossett, Cheryl Cytrynbaum, Géraldine Dawson, Maretha Jonge, Richard Delorme, Irene Drmic, Eftichia Duketis, Frederico Duque, Annette Estes, Penny Farrar, Bridget A. Fernandez, Susan E. Folstein, Éric Fombonne, Christine M. Freitag, John R. Gilbert, Christopher Gillberg, Joseph Glessner, Jeremy Goldberg, Andrew Green, Jonathan Green, Stephen J. Guter, Håkon Håkonarson, Elizabeth A. Heron, Matthew Hill, Richard Holt, Jennifer Howe, Gillian Hughes, Vanessa Hus, Roberta Igliozzi, Cecilia Kim, Sabine M. Klauck, A lexander Kolevzon, Olena Korvatska, Vlad Kustanovich, Clara Lajonchere, Janine A. Lamb, Magdalena Laskawiec, Marion Leboyer, Ann Le Couteur, Bennett Leventhal, Anath C. Lionel, Xiao-Qing Liu, Catherine Lord, Linda Lotspeich, Sabata C. Lund, Elena Maestrini, William J. Mahoney, Carine Mantoulan, Christian R. Marshall, Helen McConachie, Christopher J. McDougle, Jane McGrath, William M. McMahon, Alison Merikangas, Ohsuke Migita, Nancy J. Minshew, Ghazala Mirza, Jeff Munson, Stanley F. Nelson, Carolyn Noakes, Abdul Noor, Gudrun Nygren, Guiomar Oliveira, Κaterina Papanikolaou, Jeremy Parr, Barbara Parrini, Tara Paton, Andrew Pickles, Marion Pilorge and 77 more - Nature 2010 cited by 2,066

  8. 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

  9. Structural Variation of Chromosomes in Autism Spectrum Disorder

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Lonnie Zwaigenbaum, Wendy Roberts, Bridget A. Fernandez, Péter Szatmári, Stephen W. Scherer - The American Journal of Human Genetics 2008 cited by 1,843

  10. Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: A Gradient of Severity in Cognitive Impairments

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Agnès Rastetter, Alexis Brice, Françoise Devillard, Brigitte Assouline, Fanny Laffargue, James Lespinasse, Jean Chiésa, François Rivier, Dominique Bonneau, Béatrice Regnault, Diana Zélénika, Marc Délepine, Mark Lathrop, Damien Sanlaville, Caroline Schluth‐Bolard, Patrick Edery, Laurence Perrin, Anne Claude Tabet, Michael J. Schmeißer, Tobias M. Boeckers, Mary Coleman, Daisuke Sato, Péter Szatmári, Stephen W. Scherer, Guy A. Rouleau, Catalina Betancur, Marion Leboyer, Christopher Gillberg, Richard Delorme, Thomas Bourgeron - PLoS Genetics 2014 cited by 664

  11. Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Inês C. Conceição, Andreas G. Chiocchetti, Jillian P. Casey, Guiqing Cai, Christelle Cabrol, Nadia Bolshakova, Elena Bacchelli, Richard Anney, Steven Gallinger, Michelle Cotterchio, Graham Casey, Lonnie Zwaigenbaum, Kerstin Wittemeyer, Kirsty Wing, Simon Wallace, Hermán van Engeland, Ana Tryfon, Susanne Thomson, Latha Soorya, Bernadette Rogé, Wendy Roberts, Fritz Poustka, Susana Mouga, Nancy J. Minshew, L. Alison McInnes, Susan G. McGrew, Catherine Lord, Marion Leboyer, Ann S. Couteur, A lexander Kolevzon, Patricia González, Suma Jacob, Richard Holt, Stephen J. Guter, Jonathan Green, Andrew Green, Christopher Gillberg, Bridget A. Fernandez, Frederico Duque, Richard Delorme, Géraldine Dawson, Pauline Chaste, Cátia Café, S. Brennan, Thomas Bourgeron, Patrick Bolton, Sven Bölte, Raphael Bernier, Gillian Baird, Anthony Bailey, Evdokia Anagnostou, Joana Almeida, Ellen M. Wijsman, Veronica J. Vieland, Astrid M. Vicente, Gerard D. Schellenberg, Margaret A. Pericak‐Vance, Andrew D. Paterson, Jeremy Parr, Guiomar Oliveira, John I. Nürnberger, Anthony P. Monaco, Elena Maestrini, Sabine M. Klauck, Håkon Håkonarson, Jonathan L. Haines, Daniel H. Geschwind, Christine M. Freitag, Susan E. Folstein, Sean Ennis and 12 more - The American Journal of Human Genetics 2014 cited by 1,028

  12. Transcriptome and epigenome landscape of human cortical development modeled in organoids

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Emily E. Burke, Adrian Camarena, Becky C. Carlyle, Yooree Chae, Alexander W. Charney, Chao Chen, Lijun Cheng, Adriana Cherskov, Jinmyung Choi, Declan Clarke, Leonardo Collado‐Torres, Rujia Dai, Luis de la Torre-Ubieta, Diane M. Del Valle, Olivia Devillers, Stella Dracheva, Prashant S. Emani, Oleg V. Evgrafov, Peggy Farnham, Dominic Fitzgerald, Elie Flatow, Nancy Francoeur, John F. Fullard, Michael J. Gandal, Tianliuyun Gao, Melanie E. Garrett, Daniel H. Geschwind, Gina Giase, Kiran Girdhar, Paola Giusti‐Rodríguez, Fernando S. Goes, Thomas Goodman, Kay Grennan, Mengting Gu, Gamze Gürsoy, Evi Hadjimichael, Chang-Gyu Hahn, Vahram Haroutunian, Mads E. Hauberg, Gabriel E. Hoffman, Jack Huey, Thomas M. Hyde, Nikolay A. Ivanov, Rivka Jacobov, Andrew E. Jaffe, Yan Jiang, Yi Jiang, Graham D. Johnson, Bibi Kassim, Amira Kefi, Yunjung Kim, Robert R. Kitchen, Joel E. Kleiman, James A. Knowles, Alexey Kozlenkov, Mingfeng Li, Zhen Li, Barbara K. Lipska, Chunyu Liu, Shuang Liu, Lara M. Mangravite, Jessica Mariani, Eugenio Mattei, Daniel J. Miller, J. Russell Moore, Angus C. Nairn, Fábio C. P. Navarro, Royce Park, Mette A. Peters, Dalila Pinto and 47 more - Science 2018 cited by 315

  13. Dissecting the Shared Genetic Architecture of Suicide Attempt, Psychiatric Disorders, and Known Risk Factors

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Scott J. Crow, Emily DiBlasi, Philibert Duriez, Fernando Fernández‐Aranda, Manfred M. Fichter, Steven Gallinger, Stephen J. Glatt, Philip Gorwood, Yiran Guo, Hakon Hakonarson, Katherine A. Halmi, Hai‐Gwo Hwu, Sonia Jain, Stéphane Jamain, Susana Jiménez-Murcia, Craig Johnson, Allan S. Kaplan, Walter H. Kaye, Pamela K. Keel, James L. Kennedy, Kelly L. Klump, Dong Li, Shih‐Cheng Liao, Klaus Lieb, Lisa Lilenfeld, Chih‐Min Liu, Pierre J. Magistretti, Christian R. Marshall, James E. Mitchell, Eric T. Monson, Richard M. Myers, Dalila Pinto, Abigail Powers, Nicolas Ramoz, Stefan Roepke, Vsevolod Rozanov, Stephen W. Scherer, Christian Schmahl, Marcus Sokolowski, Michael Strober, Laura M. Thornton, Janet Treasure, Ming T. Tsuang, Stephanie H. Witt, D. Blake Woodside, Zeynep Yılmaz, Lea Zillich, Rolf Adolfsson, Ingrid Agartz, Tracy Air, Martin Alda, Lars Alfredsson, Ole A. Andreassen, Adebayo Anjorin, Vivek Appadurai, María Soler Artigas, Sandra Van der Auwera, M.H. Azevedo, Nicholas Bass, Claiton H.D. Bau, Bernhard T. Baune, Frank Bellivier, Klaus Peter Berger, Joanna M. Biernacka, Tim B. Bigdeli, Elisabeth B. Binder, Michael Boehnke, Marco P. Boks, Rosa Bosch, David Braff and 1,023 more - Biological Psychiatry 2021 cited by 247

  14. Origins and functional impact of copy number variation in the human genome

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , - Nature 2009 cited by 2,062

  15. GWAS Meta-Analysis of Suicide Attempt: Identification of 12 Genome-Wide Significant Loci and Implication of Genetic Risks for Specific Health Factors

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Melanie E. Garrett, Lauren P. Hair, Philip D. Harvey, Elizabeth R. Hauser, Michael A. Hauser, Jennifer E. Huffman, Daniel Jacobson, Ravi Madduri, Benjamin H. McMahon, David W. Oslin, Jodie Trafton, Swapnil Awasthi, Wade H. Berrettini, Martin Bohus, Xiao Chang, Hsi‐Chung Chen, Wei J. Chen, Erik D. Christensen, Scott J. Crow, Philibert Duriez, Alexis C. Edwards, Fernando Fernández‐Aranda, Hanga Galfalvy, Michael J. Gandal, Philip Gorwood, Yiran Guo, Jonathan D. Hafferty, Håkon Håkonarson, Katherine A. Halmi, Akitoyo Hishimoto, Sonia Jain, Stéphane Jamain, Susana Jiménez‐Múrcia, Craig Johnson, Allan S. Kaplan, Walter H. Kaye, Pamela K. Keel, James L. Kennedy, Minsoo Kim, Kelly L. Klump, Daniel F. Levey, Dong Li, Shih‐Cheng Liao, Klaus Lieb, Lisa Lilenfeld, Christian R. Marshall, James E. Mitchell, Satoshi Okazaki, Ikuo Otsuka, Dalila Pinto, Abigail Powers, Nicolás Ramoz, Stephan Ripke, Stefan Roepke, Vsevolod Rozanov, Stephen W. Scherer, Christian Schmahl, Marcus Sokolowski, Anna Starnawska, Michael Strober, Mei‐Hsin Su, Laura M. Thornton, Janet Treasure, Erin B. Ware, Hunna J. Watson, Stephanie H. Witt, D. Blake Woodside, Zeynep Yılmaz, Lea Zillich, Rolf Adolfsson and 150 more - American Journal of Psychiatry 2023 cited by 150

  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. Contribution of SHANK3 Mutations to Autism Spectrum Disorder

    Authors: , , , , , , , , , , - The American Journal of Human Genetics 2007 cited by 691

  18. Towards a comprehensive structural variation map of an individual human genome

    Authors: , , , , , , , , , , , , , - Genome biology 2010 cited by 359

  19. Identification of novel genetic causes of Rett syndrome-like phenotypes

    Authors: , , , , , , , , , , , , , , , , , , , - Journal of Medical Genetics 2016 cited by 194

  20. Landscape of Conditional eQTL in Dorsolateral Prefrontal Cortex and Co-localization with Schizophrenia GWAS

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Kathryn Roeder, Lu Xie, Konrad Talbot, Scott E. Hemby, Laurent Essioux, Andrew Browne, Andrew Chess, Aaron Topol, Alexander W. Charney, Amanda Dobbyn, Ben Readhead, Bin Zhang, Dalila Pinto, David A. Bennett, David H. Kavanagh, Douglas M. Ruderfer, Eli A. Stahl, Eric E. Schadt, Gabriel E. Hoffman, Hardik Shah, Jun Zhu, Jessica Johnson, John F. Fullard, Joel T. Dudley, Kiran Girdhar, Kristen Brennand, Laura G. Sloofman, Laura M. Huckins, Menachem Fromer, Milind Mahajan, Panos Roussos, Schahram Akbarian, Shaun Purcell, Tymor Hamamsy, Towfique Raj, Vahram Haroutunian, Ying‐Chih Wang, Zeynep H. Gümüş, Geetha Senthil, Robin S. S. Kramer, Benjamin A. Logsdon, Jonathan M.J. Derry, Kristen K. Dang, Solveig K. Sieberts, Thanneer M. Perumal, Roberto Visintainer, Leslie A. Shinobu, Patrick F. Sullivan, Lambertus Klei, Schahram Akbarian, Panos Roussos, Enrico Domenici, Bernie Devlin, Pamela Sklar, Eli A. Stahl, Solveig K. Sieberts - The American Journal of Human Genetics 2018 cited by 172

  21. Identifying Signatures of Natural Selection in Tibetan and Andean Populations Using Dense Genome Scan Data

    Authors: , , , , , , , , , , , , , - PLoS Genetics 2010 cited by 611

  22. HLA-DRB1*11 and variants of the MHC class II locus are strong risk factors for systemic juvenile idiopathic arthritis

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Sara Signa, Richard H. Duerr, J ACHKAR, M. Ilyas Kamboh, Kenneth M. Kaufman, Leah C. Kottyan, Dalila Pinto, Stephen W. Scherer, Marta E. Alarcón‐Riquelme, Elisa Docampo, Xavier Estivill, Ahmet Gül, British Society of Pediatric and Adolescent Rheumatology (BSPAR) Study Group, Childhood Arthritis Prospective Study (CAPS) Group, Randomized Placebo Phase Study of Rilonacept in sJIA (RAPPORT) Investigators, Sparks-Childhood Arthritis Response to Medication Study (CHARMS) Group, Biologically Based Outcome Predictors in JIA (BBOP) Group, Paul I. W. de Bakker, Soumya Raychaudhuri, Carl D. Langefeld, Susan Thompson, Eleftheria Zeggini, Wendy Thomson, Daniel L. Kastner, Patricia Woo, J ACHKAR, Marta E. Alarcón‐Riquelme, Roger C. Allen, Jordi Antón, Elizabeth Baskin, Stefan Berg, Bianca Bica, Yelda Bilginer, John F. Bohnsack, André Cavalcanti, Jeffrey Chaitow, Joanna Cobb, Rubin Cuttica, Paul I. W. de Bakker, Elisa Docampo, Richard H. Duerr, Justine A. Ellis, Xavier Estivill, Terri H. Finkel, Dirk Foell, Marco Gattorno, Alexei A. Grom, Ahmet Gül, Johannes‐Peter Haas, Håkon Håkonarson, Buhm Han, Maria Odete Esteves Hilário, Anne Hinks, Norman T. Ilowite, M. Ilyas Kamboh, Daniel L. Kastner, Kenneth M. Kaufman, Leah C. Kottyan, Carl Langefeld, Cláudio Arnaldo Len, Alberto Martini, Elizabeth Mellins, Kirstin Minden, Kevin Murray, Sheila Oliveira, Michael J. Ombrello, Seza Özen, Jane Park, Dalila Pinto, Sampath Prahalad and 165 more - National Academy of Sciences, Proceedings of the National Academy of Sciences 2015 cited by 185

  23. Genetic and Functional Analyses of SHANK2 Mutations Suggest a Multiple Hit Model of Autism Spectrum Disorders

    Authors: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Sabine M. Klauck, Fritz Poustka, Christine M. Freitag, Regina Waltes, Marnie Kopp, Eftichia Duketis, Elena Bacchelli, Fiorella Minopoli, Liliana Ruta, Agatino Battaglia, Luigi Mazzone, Elena Maestrini, Ana Filipa Sequeira, Bárbara Oliveira, Astrid M. Vicente, Guiomar Oliveira, Dalila Pinto, Stephen W. Scherer, Diana Zélénika, Marc Délepine, Mark Lathrop, Dominique Bonneau, Vincent Guinchat, Françoise Devillard, Brigitte Assouline, Marie–Christine Mouren, Marion Leboyer, Christopher Gillberg, Tobias M. Boeckers, Thomas Bourgeron - PLoS Genetics 2012 cited by 443

  24. Direct reprogramming induces vascular regeneration post muscle ischemic injury

    Authors: , , , , , , , , , , , , , , , , , , , , , , , - Molecular Therapy 2021 cited by 41