litlas
ログインアカウント作成

Daniele Merico

2006–2025 年に発表

67
論文数
21,116
被引用数
47
h 指数
61
i10 指数

被引用数

Daniele Merico の年別被引用数1943 年: 被引用 1 件1955 年: 被引用 1 件1972 年: 被引用 1 件1976 年: 被引用 1 件1996 年: 被引用 2 件2000 年: 被引用 1 件2001 年: 被引用 1 件2003 年: 被引用 1 件2007 年: 被引用 4 件2008 年: 被引用 8 件2009 年: 被引用 11 件2010 年: 被引用 34 件2011 年: 被引用 109 件2012 年: 被引用 131 件2013 年: 被引用 136 件2014 年: 被引用 176 件2015 年: 被引用 262 件2016 年: 被引用 287 件2017 年: 被引用 387 件2018 年: 被引用 420 件2019 年: 被引用 1,065 件2020 年: 被引用 1,079 件2021 年: 被引用 1,118 件2022 年: 被引用 887 件2023 年: 被引用 524 件2024 年: 被引用 809 件2025 年: 被引用 363 件2026 年: 被引用 17 件1944〜1954 年は被引用が無いため表示していません1956〜1971 年は被引用が無いため表示していません1973〜1975 年は被引用が無いため表示していません1977〜1995 年は被引用が無いため表示していません1997〜1999 年は被引用が無いため表示していません2002 年は被引用が無いため表示していません2004〜2006 年は被引用が無いため表示していません

引用元

国・地域

この著者を引用した国・地域の世界地図アメリカ合衆国: 引用元論文 3,199 件、この内訳の 24.2%中国: 引用元論文 1,060 件、この内訳の 8%カナダ: 引用元論文 981 件、この内訳の 7.4%イギリス: 引用元論文 980 件、この内訳の 7.4%ドイツ: 引用元論文 720 件、この内訳の 5.4%フランス: 引用元論文 500 件、この内訳の 3.8%イタリア: 引用元論文 476 件、この内訳の 3.6%オーストラリア: 引用元論文 441 件、この内訳の 3.3%オランダ: 引用元論文 407 件、この内訳の 3.1%スペイン: 引用元論文 357 件、この内訳の 2.7%スイス: 引用元論文 285 件、この内訳の 2.1%スウェーデン: 引用元論文 272 件、この内訳の 2.1%
0%24.2%その他 26.9%

機関

分野

  • Biochemistry, Genetics and Molecular Biology50.8%
  • Medicine23.4%
  • Neuroscience13.6%
  • Computer Science3.9%
  • Immunology and Microbiology3%
  • Agricultural and Biological Sciences1.3%
  • その他4%

トピック

  • Genetics and Neurodevelopmental Disorders5.3%
  • Genomic variations and chromosomal abnormalities4.6%
  • Autism Spectrum Disorder Research4.5%
  • Genomics and Rare Diseases4.4%
  • RNA Research and Splicing2.3%
  • RNA modifications and cancer2.3%
  • その他76.6%

共著者

全論文

検索で開く
  1. Pathway enrichment analysis and visualization of omics data using g:Profiler, GSEA, Cytoscape and EnrichmentMap

    著者: Jüri Reimand, Ruth Isserlin, Véronique Voisin, Mike Kucera, Christian Tannus-Lopes, Asha Rostamianfar, Lina Wadi, Mona Meyer, J. D. Wong, Changjiang Xu, Daniele Merico, Gary D. Bader - Nature Protocols 2019 被引用: 2,143

  2. Enrichment Map: A Network-Based Method for Gene-Set Enrichment Visualization and Interpretation

    著者: Daniele Merico, Ruth Isserlin, Oliver Stueker, Andrew Emili, Gary D. Bader - PLoS ONE 2010 被引用: 2,441

  3. Deep learning in biomedicine

    著者: Michael Wainberg, Daniele Merico, Andrew Delong, Brendan J. Frey - Nature Biotechnology 2018 被引用: 604

  4. The human splicing code reveals new insights into the genetic determinants of disease

    著者: Hui Xiong, Babak Alipanahi, Leo J. Lee, Hannes Bretschneider, Daniele Merico, Ryan K. C. Yuen, Yimin Hua, Serge Gueroussov, Hamed S. Najafabadi, Timothy Hughes, Quaid Morris, Yoseph Barash, Adrian R. Krainer, Nebojša Jojić, Stephen W. Scherer, Benjamin J. Blencowe, Brendan J. Frey - Science 2014 被引用: 1,318

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

    著者: Christian R. Marshall, Daniel P. Howrigan, Daniele Merico, Bhooma Thiruvahindrapuram, Wenting Wu, Douglas S. Greer, Danny Antaki, Aniket Shetty, Peter Holmans, Dalila Pinto, Madhusudan Gujral, William M. Brandler, Dheeraj Malhotra, Zhouzhi Wang, Karin V. Fuentes Fajarado, Michelle S. Maile, Stephan Ripke, Ingrid Agartz, Margot Albus, Madeline Alexander, Farooq Amin, Joshua Atkins, Silviu‐Alin Bacanu, Richard A. Belliveau, Sarah E. Bergen, Marcelo Bertalan, Elizabeth Bevilacqua, Tim B. Bigdeli, Donald W. Black, Richard Bruggeman, 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 ほか 163 名 - Nature Genetics 2016 被引用: 1,142

  6. Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder

    著者: Ryan K. C. Yuen, Daniele Merico, Matt Bookman, Jennifer Howe, Bhooma Thiruvahindrapuram, Rohan Patel, J. Andrew Whitney, Nicole Deflaux, Jonathan Bingham, Zhuozhi Wang, Giovanna Pellecchia, Janet A. Buchanan, Susan Walker, Christian R. Marshall, Mohammed Uddin, Mehdi Zarrei, Éric Deneault, Lia D’Abate, Ada J. S. Chan, Stephanie Koyanagi, Tara Paton, Sérgio L. Pereira, Ny Hoang, Worrawat Engchuan, Edward J. Higginbotham, Karen Ho, Sylvia Lamoureux, Weili Li, Jeffrey R. MacDonald, Thomas Nalpathamkalam, Wilson W. L. Sung, Fiona J. Tsoi, John Wei, Lizhen Xu, Anne-Marie Tasse, Emily Kirby, William Van Etten, Simon Twigger, Wendy Roberts, Irene Drmic, Sanne Jilderda, Bonnie MacKinnon Modi, Barbara Kellam, Michael J. Szego, Cheryl Cytrynbaum, Rosanna Weksberg, Lonnie Zwaigenbaum, Marc Woodbury‐Smith, Jessica Brian, Lili Senman, Alana Iaboni, Krissy A.R. Doyle‐Thomas, Ann Thompson, Christina Chrysler, Jonathan Leef, Tal Savion‐Lemieux, Isabel M. Smith, Xudong Liu, Rob Nicolson, Vicki Seifer, Angie Fedele, Edwin H. Cook, Stephen R. Dager, Annette Estes, Louise Gallagher, Beth A. Malow, Jeremy Parr, Sarah Spence, Jacob Vorstman, Brendan J. Frey, James Robinson, Lisa J. Strug, Bridget A. Fernandez, Mayada Elsabbagh, Melissa T. Carter, Joachim Hallmayer, Bartha Maria Knoppers, Evdokia Anagnostou, Péter Szatmári, Robert H. Ring, David Glazer, Mathew T. Pletcher, Stephen W. Scherer - Nature Neuroscience 2017 被引用: 936

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

    著者: Dalila Pinto, Alistair T. Pagnamenta, Lambertus Klei, Richard Anney, Daniele Merico, Regina Regan, Judith Conroy, Tiago R. Magalhães, Catarina Correia, Brett S. Abrahams, Joana Almeida, Elena Bacchelli, Gary D. Bader, Anthony Bailey, Gillian Baird, Agatino Battaglia, T. P. Berney, Nadia Bolshakova, Sven Bölte, Patrick Bolton, Thomas Bourgeron, S. Brennan, Jessica Brian, Susan E. Bryson, Andrew R. Carson, Guillermo Casallo, Jillian P. Casey, Brian Hon‐Yin Chung, Lynne Cochrane, Christina Corsello, 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 ほか 77 名 - Nature 2010 被引用: 2,066

  8. Immune Checkpoint Inhibition for Hypermutant Glioblastoma Multiforme Resulting From Germline Biallelic Mismatch Repair Deficiency

    著者: Éric Bouffet, Valérie Larouche, Brittany Campbell, Daniele Merico, Richard de Borja, Melyssa Aronson, Carol Durno, Joerg Krueger, Vanja Cabric, Vijay Ramaswamy, Nataliya Zhukova, Gary Mason, Roula Farah, Samina Afzal, Michal Yalon, Gideon Rechavi, Vanan Magimairajan, Michael F. Walsh, Shlomi Constantini, Rina Dvir, Ronit Elhasid, Alyssa Reddy, Michael Osborn, Michael Sullivan, Jordan R. Hansford, Andrew Dodgshun, Nancy Klauber‐DeMore, Lindsay L. Peterson, Sunil J. Patel, Scott Lindhorst, Jeffrey Atkinson, Zane Cohen, Rachel Laframboise, Peter B. Dirks, Michael D. Taylor, David Malkin, Steffen Albrecht, Roy Dudley, Nada Jabado, Cynthia Hawkins, Adam Shlien, Uri Tabori - Journal of Clinical Oncology 2016 被引用: 869

  9. Improved diagnostic yield compared with targeted gene sequencing panels suggests a role for whole-genome sequencing as a first-tier genetic test

    著者: Anath C. Lionel, Gregory Costain, Nasim Monfared, Susan Walker, Miriam S. Reuter, S. Mohsen Hosseini, Bhooma Thiruvahindrapuram, Daniele Merico, Rebekah Jobling, Thomas Nalpathamkalam, Giovanna Pellecchia, Wilson W. L. Sung, Zhuozhi Wang, Peter Bikangaga, Cyrus Boelman, Melissa T. Carter, Dawn Cordeiro, Cheryl Cytrynbaum, Sharon Dell, Priya Dhir, James J. Dowling, Elise Héon, Stacy Hewson, Linda T. Hiraki, Michal Inbar‐Feigenberg, Regan Klatt, Jonathan B. Kronick, Ronald M. Laxer, Christoph Licht, H. Robson MacDonald, Saadet Mercimek‐Andrews, Roberto Mendoza‐Londono, Tino D. Piscione, Rayfel Schneider, Andreas Schulze, Earl D. Silverman, Komudi Siriwardena, O. Carter Snead, Neal Sondheimer, Joanne Sutherland, Ajoy Vincent, Jonathan D. Wasserman, Rosanna Weksberg, Cheryl Shuman, Chris Carew, Michael J. Szego, Robin Z. Hayeems, Raveen Basran, Dimitri J. Stavropoulos, Peter N. Ray, Sarah Bowdin, M. Stephen Meyn, Ronald D. Cohn, Stephen W. Scherer, Christian R. Marshall - Genetics in Medicine 2017 被引用: 565

  10. A copy number variation map of the human genome

    著者: Mehdi Zarrei, Jeffrey R. MacDonald, Daniele Merico, Stephen W. Scherer - Nature Reviews Genetics 2015 被引用: 987

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

    著者: Dalila Pinto, Elsa Delaby, Daniele Merico, Mafalda Barbosa, Alison Merikangas, Lambertus Klei, Bhooma Thiruvahindrapuram, Xiao Xu, Robert Ziman, Zhuozhi Wang, Jacob Vorstman, Ann Thompson, Regina Regan, Marion Pilorge, Giovanna Pellecchia, Alistair T. Pagnamenta, Bárbara Oliveira, Christian R. Marshall, Tiago R. Magalhães, Jennifer K. Lowe, Jennifer Howe, Anthony J. Griswold, John R. Gilbert, Eftichia Duketis, Beth A. Dombroski, Maretha Jonge, Michael L. Cuccaro, Emily L. Crawford, Catarina Correia, Judith Conroy, 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 ほか 12 名 - The American Journal of Human Genetics 2014 被引用: 1,028

  12. Integration of Genomic and Transcriptional Features in Pancreatic Cancer Reveals Increased Cell Cycle Progression in Metastases

    著者: Ashton A. Connor, Robert E. Denroche, Gun Ho Jang, Mathieu Lemire, Amy Zhang, Michelle Chan‐Seng‐Yue, Gavin W. Wilson, Robert C. Grant, Daniele Merico, Ilinca M. Lungu, John M.S. Bartlett, Dianne Chadwick, Sheng-Ben Liang, Jenna Eagles, Faridah Mbabaali, Jessica K. Miller, Paul M. Krzyzanowski, Heather Armstrong, Xuemei Luo, Lars Jorgensen, Joan Miguel Romero, Prashant Bavi, Sandra E. Fischer, Stefano Serra, Sara Hafezi‐Bakhtiari, Derin Çağlar, Michael H. A. Roehrl, Sean P. Cleary, Michael A. Hollingsworth, Gloria M. Petersen, Sarah P. Thayer, Calvin Law, Sulaiman Nanji, Talia Golan, Alyssa Smith, Ayelet Borgida, Anna Dodd, David W. Hedley, Bradly G. Wouters, Grainne M. O’Kane, Julie M. Wilson, George Zogopoulos, Faiyaz Notta, Jennifer J. Knox, Steven Gallinger - Cancer Cell 2019 被引用: 247

  13. Combined hereditary and somatic mutations of replication error repair genes result in rapid onset of ultra-hypermutated cancers

    著者: Adam Shlien, Brittany Campbell, Richard de Borja, Ludmil B. Alexandrov, Daniele Merico, David C. Wedge, Peter Van Loo, Patrick Tarpey, Paul Coupland, Sam Behjati, Aaron Pollett, Tatiana Lipman, Abolfazl Heidari, Shriya Deshmukh, N. Avitzur, Bettina Meier, Moritz Gerstung, Ye Hong, Diana M. Merino, Manasa Ramakrishna, Marc Remke, Roland Arnold, Gagan B. Panigrahi, Neha Thakkar, Karl P. Hodel, Erin E. Henninger, A. Yasemin Göksenin, Doua Bakry, George S. Charames, Harriet Druker, Jordan Lerner‐Ellis, Matthew Mistry, Rina Dvir, Ronald Grant, Ronit Elhasid, Roula Farah, Glenn Taylor, Paul C. Nathan, Sarah Alexander, Shay Ben‐Shachar, Simon C. Ling, Steven Gallinger, Shlomi Constantini, Peter B. Dirks, Annie Huang, Stephen W. Scherer, Richard G. Grundy, Carol Durno, Melyssa Aronson, Anton Gartner, M. Stephen Meyn, Michael D. Taylor, Zachary F. Pursell, Christopher E. Pearson, David Malkin, P. Andrew Futreal, Michael R. Stratton, Éric Bouffet, Cynthia Hawkins, Peter J. Campbell, Uri Tabori - Nature Genetics 2015 被引用: 381

  14. Tahoe-100M : A Giga-Scale Single-Cell Perturbation Atlas for Context-Dependent Gene Function and Cellular Modeling

    著者: Jesse Zhang, Airol A Ubas, Richard de Borja, Valentine Svensson, Nicole Thomas, Neha Thakar, Ian Lai, Aidan Winters, Umair Khan, Matthew G. Jones, John D. Thompson, Vuong Tran, Joseph Pangallo, Efthymia Papalexi, Ajay Sapre, Hoai Nguyen, Oliver Sanderson, Maria Nigos, Olivia Kaplan, Sarah Schroeder, Bryan Hariadi, Simone Marrujo, Crina Curca Alec Salvino, Guillermo Gallareta Olivares, Ryan Koehler, Gary Geiss, Alexander Rosenberg, Charles Roco, Daniele Merico, Nima Alidoust, Hani Goodarzi, Johnny Yu - 2025 被引用: 82

  15. Whole-genome sequencing of quartet families with autism spectrum disorder

    著者: Ryan K. C. Yuen, Bhooma Thiruvahindrapuram, Daniele Merico, Susan Walker, Kristiina Tammimies, Ny Hoang, Christina Chrysler, Thomas Nalpathamkalam, Giovanna Pellecchia, Yi Liu, Matthew J. Gazzellone, Lia D’Abate, Éric Deneault, Jennifer Howe, Richard S C Liu, Ann Thompson, Mehdi Zarrei, Mohammed Uddin, Christian R. Marshall, Robert H. Ring, Lonnie Zwaigenbaum, Peter N. Ray, Rosanna Weksberg, Melissa T. Carter, Bridget A. Fernandez, Wendy Roberts, Péter Szatmári, Stephen W. Scherer - Nature Medicine 2015 被引用: 541

  16. Molecular Diagnostic Yield of Chromosomal Microarray Analysis and Whole-Exome Sequencing in Children With Autism Spectrum Disorder

    著者: Kristiina Tammimies, Christian R. Marshall, Susan Walker, Gaganjot Kaur, Bhooma Thiruvahindrapuram, Anath C. Lionel, Ryan K. C. Yuen, Mohammed Uddin, Wendy Roberts, Rosanna Weksberg, Marc Woodbury‐Smith, Lonnie Zwaigenbaum, Evdokia Anagnostou, Zhuozhi Wang, John Wei, Jennifer Howe, Matthew J. Gazzellone, Lynette Lau, Wilson W. L. Sung, Kathy Whitten, Cathy Vardy, Victoria Crosbie, Brian Tsang, Lia D’Abate, Winnie W. L. Tong, Sandra Luscombe, Tyna Doyle, Melissa T. Carter, Péter Szatmári, Susan Stuckless, Daniele Merico, Dimitri J. Stavropoulos, Stephen W. Scherer, Bridget A. Fernandez - JAMA 2015 被引用: 439

  17. Whole-genome sequencing expands diagnostic utility and improves clinical management in paediatric medicine

    著者: Dimitri J. Stavropoulos, Daniele Merico, Rebekah Jobling, Sarah Bowdin, Nasim Monfared, Bhooma Thiruvahindrapuram, Thomas Nalpathamkalam, Giovanna Pellecchia, Ryan K. C. Yuen, Michael J. Szego, Robin Z. Hayeems, Randi Zlotnik Shaul, Michael Brudno, Marta Gîrdea, Brendan J. Frey, Babak Alipanahi, Sohnee Ahmed, Riyana Babul‐Hirji, Ramses Badilla Porras, Melissa T. Carter, Lauren Chad, Ayeshah Chaudhry, David Chitayat, Soghra Jougheh Doust, Cheryl Cytrynbaum, Lucie Dupuis, Resham Ejaz, Leona Fishman, Andrea Guerin, Bita Hashemi, Mayada Helal, Stacy Hewson, Michal Inbar‐Feigenberg, Pekka Kannus, Natalya Karp, Raymond H. Kim, Jonathan B. Kronick, Eriskay Liston, H. Robson MacDonald, Saadet Mercimek‐Mahmutoglu, Roberto Mendoza‐Londono, Enas Nasr, Graeme Nimmo, Nicole Parkinson, Nada Quercia, Julian Raiman, Maian Roifman, Andreas Schulze, Andrea Shugar, Cheryl Shuman, Pierre Sinajon, Komudi Siriwardena, Rosanna Weksberg, Grace Yoon, Chris Carew, Raith Erickson, Richard A. Leach, Robert J. Klein, Peter N. Ray, M. Stephen Meyn, Stephen W. Scherer, Ronald D. Cohn, Christian R. Marshall - npj Genomic Medicine 2016 被引用: 377

  18. Compound heterozygous mutations in the noncoding RNU4ATAC cause Roifman Syndrome by disrupting minor intron splicing

    著者: Daniele Merico, Maian Roifman, Ulrich Braunschweig, Ryan K. C. Yuen, Roumiana Alexandrova, Andrea Bates, Brenda Reid, Thomas Nalpathamkalam, Zhuozhi Wang, Bhooma Thiruvahindrapuram, Paul Gray, Alyson Kakakios, Jane Peake, Stephanie Hogarth, David Manson, Raymond Buncic, Sérgio L. Pereira, Jo-Anne Herbrick, Benjamin J. Blencowe, Chaim M. Roifman, Stephen W. Scherer - Nature Communications 2015 被引用: 145

  19. Transcriptome-Wide Off-Target Effects of Steric-Blocking Oligonucleotides

    著者: Erle M. Holgersen, Shreshth Gandhi, Yongchao Zhou, Jin‐Kuk Kim, Brandon Vaz, Jovanka Bogojeski, Magdalena Bugno, Zvi Shalev, Kahlin Cheung-Ong, João Gonçalves, Matthew O’Hara, Ken J. Kron, Marta Verby, Mark Sun, Boyko Kakaradov, Andrew Delong, Daniele Merico, Amit G. Deshwar - Nucleic Acid Therapeutics 2021 被引用: 90

  20. BRAF Mutation and CDKN2A Deletion Define a Clinically Distinct Subgroup of Childhood Secondary High-Grade Glioma

    著者: Matthew Mistry, Nataliya Zhukova, Daniele Merico, Patricia Rakopoulos, Rahul Krishnatry, Mary Shago, James Stavropoulos, Noa Alon, Jason D. Pole, Peter N. Ray, Vilma Navickiene, Joshua Mangerel, Marc Remke, Pawel Buczkowicz, Vijay Ramaswamy, Ana Guerreiro Stücklin, Martin Li, Edwin J. Young, Cindy Zhang, Pedro Castelo‐Branco, Doua Bakry, Suzanne Laughlin, Adam Shlien, Jennifer A. Chan, Keith L. Ligon, James T. Rutka, Peter B. Dirks, Michael D. Taylor, Mark Greenberg, David Malkin, Annie Huang, Éric Bouffet, Cynthia Hawkins, Uri Tabori - Journal of Clinical Oncology 2015 被引用: 285

  21. A large data resource of genomic copy number variation across neurodevelopmental disorders

    著者: Mehdi Zarrei, Christie L. Burton, Worrawat Engchuan, Edwin J. Young, Edward J. Higginbotham, Jeffrey R. MacDonald, Brett Trost, Ada J. S. Chan, Susan Walker, Sylvia Lamoureux, Tracy Heung, Bahareh A. Mojarad, Barbara Kellam, Tara Paton, Muhammad Faheem, Karin Miron, Chao Lu, Ting Wang, Kozue Samler, Xiaolin Wang, Gregory Costain, Ny Hoang, Giovanna Pellecchia, John Wei, Rohan Patel, Bhooma Thiruvahindrapuram, Maian Roifman, Daniele Merico, Tara Goodale, Irene Drmic, Marsha Speevak, Jennifer Howe, Ryan K. C. Yuen, Janet A. Buchanan, Jacob Vorstman, Christian R. Marshall, Richard F. Wintle, David R. Rosenberg, Gregory L. Hanna, Marc Woodbury‐Smith, Cheryl Cytrynbaum, Lonnie Zwaigenbaum, Mayada Elsabbagh, Janine Flanagan, Bridget A. Fernandez, Melissa T. Carter, Péter Szatmári, Wendy Roberts, Jason P. Lerch, Xudong Liu, Rob Nicolson, Stelios Georgiades, Rosanna Weksberg, Paul Arnold, Anne S. Bassett, Jennifer Crosbie, Russell Schachar, Dimitri J. Stavropoulos, Evdokia Anagnostou, Stephen W. Scherer - npj Genomic Medicine 2019 被引用: 201

  22. WordCloud: a Cytoscape plugin to create a visual semantic summary of networks

    著者: Layla Oesper, Daniele Merico, Ruth Isserlin, Gary D. Bader - Source Code for Biology and Medicine, Source Code Biol. Medicine 2011 被引用: 185

  23. Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypes

    著者: A. C. Lionel, Kristiina Tammimies, Andrea K. Vaags, Jill A. Rosenfeld, Joo Wook Ahn, Daniele Merico, Abdul Noor, Cassandra Runke, Vamsee Pillalamarri, M. T. Carter, Matthew J. Gazzellone, Bhooma Thiruvahindrapuram, Christina Fagerberg, Lone Walentin Laulund, Giovanna Pellecchia, Sylvia Lamoureux, Charu Deshpande, Jill Clayton‐Smith, A. Clinton White, Susan Leather, J Q Trounce, H. Melanie Bedford, Eli Hatchwell, Peggy S. Eis, Ryan K. C. Yuen, Susan Walker, Mohammed Uddin, Michael T. Geraghty, Sarah M. Nikkel, Eva Tomiak, Bridget A. Fernandez, Noam Soreni, Jennifer Crosbie, Paul Arnold, Russell Schachar, Wendy Roberts, Andrew D. Paterson, Jonathan So, Péter Szatmári, Christina Chrysler, Marc Woodbury‐Smith, R. Brian Lowry, Lonnie Zwaigenbaum, D. Mandyam, John Wei, Jeffrey R. MacDonald, Jennifer Howe, Thomas Nalpathamkalam, Z. Wang, Debbie Tolson, Donna Cobb, Timothy Wilks, Merete Juul Sørensen, Patricia I. Bader, Yu An, Bai-Lin Wu, S Musumeci, Corrado Romano, Diana Postorivo, A. Nardone, Matteo Della Monica, Gioacchino Scarano, Leonardo Zoccante, Francesca Novara, Orsetta Zuffardi, Roberto Ciccone, Vincenzo Antona, Massimo Carella, Leopoldo Zelante, Pietro Cavalli, Carlo Poggiani, Ugo Cavallari, Bob Argiropoulos, Judy Chernos, Charlotte Brasch‐Andersen, Marsha Speevak, Marco Fichera, Caroline Mackie Ogilvie, Ya Shen, JM Hodge, Michael E. Talkowski, Dimitri J. Stavropoulos, Christian R. Marshall, Stephen W. Scherer - Human Molecular Genetics 2013 被引用: 175

  24. Genome-wide rare variant score associates with morphological subtypes of autism spectrum disorder

    著者: Ada J. S. Chan, Worrawat Engchuan, Miriam S. Reuter, Zhuozhi Wang, Bhooma Thiruvahindrapuram, Brett Trost, Thomas Nalpathamkalam, Carol Negrijn, Sylvia Lamoureux, Giovanna Pellecchia, Rohan Patel, Wilson W. L. Sung, Jeffrey R. MacDonald, Jennifer Howe, Jacob Vorstman, Neal Sondheimer, Nicole Takahashi, Judith H. Miles, Evdokia Anagnostou, Kristiina Tammimies, Mehdi Zarrei, Daniele Merico, Dimitri J. Stavropoulos, Ryan K. C. Yuen, Bridget A. Fernandez, Stephen W. Scherer - Nature Communications 2022 被引用: 28