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Elise Robinson

Active 2011–2025

67
Papers
20,354
Citations
46
h-index
62
i10-index

Citations

Citations per year for Elise Robinson1992: 3 citations1995: 1 citations2003: 1 citations2004: 1 citations2008: 1 citations2009: 1 citations2011: 3 citations2012: 10 citations2013: 26 citations2014: 38 citations2015: 104 citations2016: 203 citations2017: 308 citations2018: 409 citations2019: 1,050 citations2020: 1,139 citations2021: 1,203 citations2022: 1,093 citations2023: 845 citations2024: 1,174 citations2025: 553 citations2026: 22 citations1993–1994: no citations, so these years are not shown1996–2002: no citations, so these years are not shown2005–2007: no citations, so these years are not shown2010: no citations, so this year is not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 3,572 citing papers, 22.1% of this breakdownUnited Kingdom: 1,674 citing papers, 10.4% of this breakdownChina: 1,124 citing papers, 6.9% of this breakdownNetherlands: 801 citing papers, 5% of this breakdownAustralia: 771 citing papers, 4.8% of this breakdownGermany: 765 citing papers, 4.7% of this breakdownCanada: 676 citing papers, 4.2% of this breakdownSweden: 598 citing papers, 3.7% of this breakdownDenmark: 442 citing papers, 2.7% of this breakdownFrance: 434 citing papers, 2.7% of this breakdownItaly: 428 citing papers, 2.6% of this breakdownNorway: 386 citing papers, 2.4% of this breakdown
0%22.1%Other 27.8%

Institutions

Fields

  • Biochemistry, Genetics and Molecular Biology47.4%
  • Medicine22.6%
  • Neuroscience20.3%
  • Psychology4%
  • Engineering1.5%
  • Immunology and Microbiology1.1%
  • Other3.1%

Topics

  • Genetic Associations and Epidemiology10%
  • Autism Spectrum Disorder Research6.7%
  • Genetics and Neurodevelopmental Disorders5.9%
  • Genomics and Rare Diseases3.1%
  • Attention Deficit Hyperactivity Disorder2.6%
  • Genomic variations and chromosomal abnormalities2.5%
  • Other69.2%

Coauthors

All papers

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  1. An atlas of genetic correlations across human diseases and traits

    Authors: Brendan Bulik‐Sullivan, Hilary K. Finucane, Verneri Anttila, Alexander Gusev, Felix R. Day, Po‐Ru Loh, Laramie E. Duncan, John R. B. Perry, Nick Patterson, Elise Robinson, Mark J. Daly, Alkes L. Price, Benjamin M. Neale - Nature Genetics 2015 cited by 4,690

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

    Authors: Jakob Grove, BUPGEN, Stephan Ripke, Thomas D. Als, Manuel Mattheisen, Raymond K. Walters, Hyejung Won, Jonatan Pallesen, Esben Agerbo, Ole A. Andreassen, Richard Anney, Swapnil Awashti, Rich Belliveau, Francesco Bettella, Joseph D. Buxbaum, Jonas Bybjerg‐Grauholm, Marie Bækvad‐Hansen, Felecia Cerrato, Kimberly Chambert, Jane Christensen, Claire Churchhouse, Karin Dellenvall, Ditte Demontis, Silvia De Rubeis, Bernie Devlin, Srdjan Djurovic, Ashley Dumont, Jacqueline I. Goldstein, Christine Søholm Hansen, Mads E. Hauberg, 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

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

    Authors: Ditte Demontis, Raymond K. Walters, Joanna Martin, Manuel Mattheisen, Thomas D. Als, Esben Agerbo, Gísli Baldursson, Rich Belliveau, Jonas Bybjerg‐Grauholm, Marie Bækvad‐Hansen, Felecia Cerrato, Kimberly Chambert, Claire Churchhouse, Ashley Dumont, Nicholas Eriksson, Michael J. Gandal, Jacqueline I. Goldstein, Katrina L. Grasby, Jakob Grove, Ólafur Ó. Guðmundsson, Christine Søholm Hansen, Mads E. Hauberg, Mads V. Hollegaard, Daniel P. Howrigan, Hailiang Huang, Julian Maller, Alicia R. Martin, Nicholas G. Martin, Jennifer L. Moran, Jonatan Pallesen, 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

  4. Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci

    Authors: Stephan Sanders, Xin He, A. Jeremy Willsey, A. Gulhan Ercan‐Sencicek, Kaitlin E. Samocha, A. Ercüment Çiçek, Michael T. Murtha, Vanessa H. Bal, Somer Bishop, Shan Dong, Arthur P. Goldberg, Jinlu Cai, John F. Keaney, Lambertus Klei, Jeffrey D. Mandell, Daniel Moreno‐De‐Luca, Christopher S. Poultney, Elise Robinson, Louw Smith, Tor Solli-Nowlan, Mack Y. Su, Nicole A. Teran, Michael F. Walker, Donna M. Werling, Arthur L. Beaudet, Rita M. Cantor, Éric Fombonne, Daniel H. Geschwind, Dorothy E. Grice, Catherine Lord, Jennifer K. Lowe, Shrikant Mane, Donna M. Martin, Eric M. Morrow, Michael E. Talkowski, James S. Sutcliffe, Christopher A. Walsh, Timothy W. Yu, David H. Ledbetter, Christa Lese Martin, Edwin H. Cook, Joseph D. Buxbaum, Mark J. Daly, Bernie Devlin, Kathryn Roeder, Matthew W. State - Neuron 2015 cited by 1,547

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

    Authors: Michael J. Gandal, Jillian R. Haney, Neelroop Parikshak, Virpi Leppä, Gokul Ramaswami, Christopher Hartl, Andrew J. Schork, Vivek Appadurai, Alfonso Buil, Thomas Werge, Chunyu Liu, Kevin P. White, iPSYCH-BROAD Working Group, Steve Horvath, Daniel H. Geschwind, Nenad Šestan, Flora M. Vaccarino, Mark Gerstein, Sherman M. Weissman, Sirisha Pochareddy, Matthew W. State, James A. Knowles, Peggy Farnham, Schahram Akbarian, Dalila Pinto, Harm Van Baekl, Stella Dracheva, Andrew E. Jaffe, Thomas M. Hyde, Peter P. Zandi, 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

  6. In vivo Perturb-Seq reveals neuronal and glial abnormalities associated with autism risk genes

    Authors: Xin Jin, Sean Simmons, Amy X. Guo, Ashwin S. Shetty, Michelle Ko, Lan Nguyễn, Vahbiz Jokhi, Elise Robinson, Paul Oyler, Nathan Curry, Giulio Deangeli, Simona Lodato, Joshua Z. Levin, Aviv Regev, Feng Zhang, Paola Arlotta - Science 2020 cited by 328

  7. In situ T-cell transfection by anti-CD3-conjugated lipid nanoparticles leads to T-cell activation, migration, and phenotypic shift

    Authors: Azadeh Kheirolomoom, Aris J. Kare, Elizabeth S. Ingham, Ramasamy Paulmurugan, Elise Robinson, Mo Baikoghli, Mohammed Inayathullah, Jai Woong Seo, James Wang, Brett Z. Fite, Bo Wu, Spencer K. Tumbale, Marina N. Raie, R. Holland Cheng, Lisa Nichols, Alexander D. Borowsky, Katherine W. Ferrara - Biomaterials 2021 cited by 146

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

    Authors: Danny Antaki, James P. Guevara, Adam X. Maihofer, Marieke Klein, Madhusudan Gujral, Jakob Grove, Caitlin E. Carey, Oanh Hong, María J. Arranz, Amaia Hervás, Christina Corsello, Keith K. Vaux, Alysson R. Muotri, Lilia M. Iakoucheva, Eric Courchesne, Karen Pierce, Joseph G. Gleeson, Elise Robinson, Caroline M. Nievergelt, Jonathan Sebat - Nature Genetics 2022 cited by 199

  9. Polygenic architecture of rare coding variation across 394,783 exomes

    Authors: Daniel J. Weiner, Ajay Nadig, Karthik A. Jagadeesh, Kushal K. Dey, Benjamin M. Neale, Elise Robinson, Konrad J. Karczewski, Luke J. O’Connor - Nature 2023 cited by 168

  10. A framework for the interpretation of de novo mutation in human disease

    Authors: Kaitlin E. Samocha, Elise Robinson, Stephan Sanders, Christine Stevens, Aniko Sabo, Lauren M. McGrath, Jack A. Kosmicki, Karola Rehnström, Swapan Mallick, Andrew Kirby, Dennis P. Wall, Daniel G. MacArthur, Stacey Gabriel, Mark A. DePristo, Shaun Purcell, Aarno Palotie, Eric Boerwinkle, Joseph D. Buxbaum, Edwin H. Cook, Richard A. Gibbs, Gerard D. Schellenberg, James S. Sutcliffe, Bernie Devlin, Kathryn Roeder, Benjamin M. Neale, Mark J. Daly - Nature Genetics 2014 cited by 1,123

  11. Genetic correlates of phenotypic heterogeneity in autism

    Authors: Varun Warrier, Xinhe Zhang, Patrick Reed, Alexandra Havdahl, Tyler M. Moore, Freddy Cliquet, Claire S. Leblond, Thomas Rolland, Anders Rosengren, EU-AIMS LEAP, Antonia San José Cáceres, Hannah Hayward, Daisy Crawley, Jessica Faulkner, Jessica Sabet, Claire L. Ellis, Bethany Oakley, Eva Loth, Tony Charman, Declan Murphy, Rosemary Holt, Jack Waldman, Jessica Upadhyay, Nicola Gunby, Meng‐Chuan Lai, Gwilym Renouf, Amber Ruigrok, Emily Taylor, Hisham Ziauddeen, Julia Deakin, Sara Ambrosino di Bruttopilo, Sarai van Dijk, Yvonne Rijks, Tabitha Koops, Miriam Douma, Alyssia Spaan, Iris Selten, Maarten Steffers, Anna Ver Loren van Themaat, Nico Bast, Sarah Baumeister, Larry O’Dwyer, Carsten Bours, Annika Rausch, Daniel von Rhein, Ineke Cornelissen, Yvette de Bruin, Maartje J. Graauwmans, Elżbieta Kostrzewa, Élodie Cauvet, Kristiina Tammimies, Rouslan Sitnikow, Guillaume Dumas, Yang-Min Kim, Thomas Bourgeron, iPSYCH-Autism Working Group, David M. Hougaard, Jonas Bybjerg‐Grauholm, Thomas Werge, Preben Bo Mortensen, Ole Mors, Merete Nordentoft, Spectrum 10K and APEX Consortia, Dwaipayan Adhya, Armandina Alamanza, Carrie Allison, Isabelle Garvey, Tracey Parsons, Paula Smith, Alex Tsompanidis, Graham J. Burton, Alexander Heazell, Lidia V. Gabis, Tal Biron-Shental, Madeline A. Lancaster, Deepak P. Srivastava, Jonathan Mill, David H. Rowitch, Matthew E. Hurles, Daniel H. Geschwind, Anders D. Børglum, Elise Robinson, Jakob Grove, Hilary C. Martin, Thomas Bourgeron, Simon Baron‐Cohen - Nature Genetics 2022 cited by 146

  12. Intranasal delivery of targeted polyfunctional gold–iron oxide nanoparticles loaded with therapeutic microRNAs for combined theranostic multimodality imaging and presensitization of glioblastoma to temozolomide

    Authors: Uday Kumar Sukumar, Rajendran JC Bose, Meenakshi Malhotra, Husam Babikir, Rayhaneh Afjei, Elise Robinson, Yitian Zeng, Edwin Chang, Frezghi Habte, Robert Sinclair, Sanjiv S. Gambhir, Tarik F. Massoud, Ramasamy Paulmurugan - Biomaterials 2019 cited by 251

  13. Tumor Cell-Derived Extracellular Vesicle-Coated Nanocarriers: An Efficient Theranostic Platform for the Cancer-Specific Delivery of Anti-miR-21 and Imaging Agents

    Authors: Rajendran JC Bose, Uday Kumar Sukumar, Yitian Zeng, Rayhaneh Afjei, Elise Robinson, Kenneth Lau, Abel Bermudez, Frezghi Habte, Sharon J. Pitteri, Robert Sinclair, Jürgen K. Willmann, Tarik F. Massoud, Sanjiv S. Gambhir, Ramasamy Paulmurugan - ACS Nano 2018 cited by 226

  14. Identification of shared and differentiating genetic architecture for autism spectrum disorder, attention-deficit hyperactivity disorder and case subgroups

    Authors: Manuel Mattheisen, Jakob Grove, Thomas D. Als, Joanna Martin, Georgios Voloudakis, Sandra Meier, Ditte Demontis, Jaroslav Bendl, Raymond K. Walters, Caitlin E. Carey, Anders Rosengren, Nora I. Strom, Mads E. Hauberg, Biao Zeng, Gabriel E. Hoffman, Wen Zhang, Jonas Bybjerg‐Grauholm, Marie Bækvad‐Hansen, Esben Agerbo, Bru Cormand, Merete Nordentoft, Thomas Werge, Ole Mors, David M. Hougaard, Joseph D. Buxbaum, Stephen V. Faraone, Barbara Franke, Søren Dalsgaard, Preben Bo Mortensen, Elise Robinson, Panos Roussos, Benjamin M. Neale, Mark J. Daly, Anders D. Børglum - Nature Genetics 2022 cited by 76

  15. Examining and interpreting the female protective effect against autistic behavior

    Authors: Elise Robinson, Paul Lichtenstein, Henrik Anckarsäter, Francesca Happé, Angelica Ronald - National Academy of Sciences, Proceedings of the National Academy of Sciences 2013 cited by 551

  16. Engineered immune cells as highly sensitive cancer diagnostics

    Authors: Amin Aalipour, Hui-Yen Chuang, Surya Murty, Aloma D’Souza, Seung Min Park, Gunsagar S. Gulati, Chirag B. Patel, Corinne Beinat, Federico Simonetta, I. Martinić, Gayatri Gowrishankar, Elise Robinson, Eamon Aalipour, Zahra Zhian, Sanjiv S. Gambhir - Nature Biotechnology 2019 cited by 146

  17. The female protective effect against autism spectrum disorder

    Authors: Emilie M. Wigdor, Daniel J. Weiner, Jakob Grove, Jack Fu, Wesley K. Thompson, Caitlin E. Carey, Nikolas Baya, Celia van der Merwe, Raymond K. Walters, F. Kyle Satterstrom, Duncan S. Palmer, Anders Rosengren, Jonas Bybjerg‐Grauholm, David M. Hougaard, Preben Bo Mortensen, Mark J. Daly, Michael E. Talkowski, Stephan Sanders, Somer Bishop, Anders D. Børglum, Elise Robinson - Cell Genomics 2022 cited by 112

  18. Immune modulation resulting from MR-guided high intensity focused ultrasound in a model of murine breast cancer

    Authors: Brett Z. Fite, James Wang, Aris J. Kare, Asaf Ilovitsh, Michael Chavez, Tali Ilovitsh, Nisi Zhang, Weiyu Chen, Elise Robinson, Hua Zhang, Azadeh Kheirolomoom, Matthew T. Silvestrini, Elizabeth S. Ingham, Lisa M. Mahakian, Sarah Tam, Ryan R. Davis, Clifford G. Tepper, Alexander D. Borowsky, Katherine W. Ferrara - Scientific Reports 2021 cited by 89

  19. Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples

    Authors: Jack A. Kosmicki, Kaitlin E. Samocha, Daniel P. Howrigan, Stephan Sanders, Kamil Slowikowski, Monkol Lek, Konrad J. Karczewski, David J. Cutler, Bernie Devlin, Kathryn Roeder, Joseph D. Buxbaum, Benjamin M. Neale, Daniel G. MacArthur, Dennis P. Wall, Elise Robinson, Mark J. Daly - Nature Genetics 2017 cited by 367

  20. Genes To Mental Health (G2MH): A Framework to Map the Combined Effects of Rare and Common Variants on Dimensions of Cognition and Psychopathology

    Authors: Sébastien Jacquemont, Guillaume Huguet, Marieke Klein, Samuel J. R. A. Chawner, Kirsten A. Donald, Marianne B. M. van den Bree, Jonathan Sebat, David H. Ledbetter, John N. Constantino, Rachel K. Earl, Donna M. McDonald‐McGinn, Thérèse van Amelsvoort, Ann Swillen, Anne O’Donnell‐Luria, David C. Glahn, Laura Almasy, Evan E. Eichler, Stephen W. Scherer, Elise Robinson, Anne S. Bassett, Christa Lese Martin, Brenda Finucane, Jacob Vorstman, Carrie E. Bearden, Raquel E. Gur, and the Genes to Mental Health Network - American Journal of Psychiatry 2022 cited by 65

  21. Predicting Polygenic Risk of Psychiatric Disorders

    Authors: Alicia R. Martin, Mark J. Daly, Elise Robinson, Steven E. Hyman, Benjamin M. Neale - Biological Psychiatry 2018 cited by 316

  22. Examining Sex-Differentiated Genetic Effects Across Neuropsychiatric and Behavioral Traits

    Authors: Joanna Martin, Ekaterina Khramtsova, Slavina B. Goleva, Gabriëlla A.M. Blokland, Michela Traglia, Raymond K. Walters, Christopher Hübel, Jonathan R. I. Coleman, Gerome Breen, Anders D. Børglum, Ditte Demontis, Jakob Grove, Thomas Werge, Janita Bralten, Cynthia M. Bulik, Phil H. Lee, Carol A. Mathews, Roseann E. Peterson, Stacey J. Winham, Naomi R. Wray, Howard J. Edenberg, Wei Guo, Yin Yao Shugart, Benjamin M. Neale, Stephen V. Faraone, Tracey L. Petryshen, Lauren A. Weiss, Laramie E. Duncan, Jill M. Goldstein, Jordan W. Smoller, Barbara E. Stranger, Lea K. Davis, Martin Alda, Marco Bortolato, Christie L. Burton, Enda M. Byrne, Caitlin E. Carey, Lauren Erdman, Laura M. Huckins, Manuel Mattheisen, Elise Robinson, Eli Stahl - Biological Psychiatry 2021 cited by 87

  23. Reconstructed Apoptotic Bodies as Targeted “Nano Decoys” to Treat Intracellular Bacterial Infections within Macrophages and Cancer Cells

    Authors: Rajendran JC Bose, Nagendran Tharmalingam, Fernando Jose Garcia-Marques, Uday Kumar Sukumar, Arutselvan Natarajan, Yitian Zeng, Elise Robinson, Abel Bermudez, Edwin Chang, Frezghi Habte, Sharon J. Pitteri, Jason R. McCarthy, Sanjiv S. Gambhir, Tarik F. Massoud, Eleftherios Mylonakis, Ramasamy Paulmurugan - ACS Nano 2020 cited by 84

  24. Evidence That Autistic Traits Show the Same Etiology in the General Population and at the Quantitative Extremes (5%, 2.5%, and 1%)

    Authors: Elise Robinson - Archives of General Psychiatry 2011 cited by 325