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Yanick J. Crow

Active 2000–2025

Also published as
Yanick J Crow
152
Papers
28,117
Citations
91
h-index
146
i10-index

Citations

Citations per year for Yanick J. Crow2000: 1 citations2001: 5 citations2002: 6 citations2003: 14 citations2004: 33 citations2005: 36 citations2006: 33 citations2007: 54 citations2008: 71 citations2009: 96 citations2010: 123 citations2011: 139 citations2012: 223 citations2013: 251 citations2014: 279 citations2015: 395 citations2016: 417 citations2017: 380 citations2018: 372 citations2019: 1,259 citations2020: 1,308 citations2021: 1,455 citations2022: 1,260 citations2023: 927 citations2024: 1,401 citations2025: 590 citations2026: 16 citations

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 3,015 citing papers, 25.1% of this breakdownUnited Kingdom: 1,043 citing papers, 8.7% of this breakdownChina: 905 citing papers, 7.5% of this breakdownFrance: 836 citing papers, 6.9% of this breakdownGermany: 766 citing papers, 6.4% of this breakdownItaly: 512 citing papers, 4.3% of this breakdownCanada: 406 citing papers, 3.4% of this breakdownAustralia: 367 citing papers, 3% of this breakdownNetherlands: 359 citing papers, 3% of this breakdownJapan: 316 citing papers, 2.6% of this breakdownSpain: 266 citing papers, 2.2% of this breakdownSwitzerland: 230 citing papers, 1.9% of this breakdown
0%25.1%Other 25%

Institutions

Fields

  • Biochemistry, Genetics and Molecular Biology33.2%
  • Immunology and Microbiology31.7%
  • Medicine28.8%
  • Neuroscience4%
  • Agricultural and Biological Sciences1.4%
  • Nursing0.2%
  • Other0.7%

Topics

  • interferon and immune responses9%
  • Inflammasome and immune disorders3.7%
  • Immunodeficiency and Autoimmune Disorders3.1%
  • RNA regulation and disease3.1%
  • RNA Research and Splicing2.7%
  • Immune Response and Inflammation2.3%
  • Other76.1%

Coauthors

All papers

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  1. The type I interferonopathies: 10 years on

    Authors: Yanick J. Crow, Daniel B. Stetson - Nature reviews. Immunology 2021 cited by 465

  2. Mitochondrial double-stranded RNA triggers antiviral signalling in humans

    Authors: Ashish Dhir, Somdutta Dhir, Lukasz S. Borowski, Laura Jiménez, Michael A. Teitell, Agnès Rötig, Yanick J. Crow, Gillian Rice, Darragh Duffy, Christelle Tamby, Takayuki Nojima, Arnold Münnich, Manuel Schiff, Claudia Ribeiro de Almeida, Jan Rehwinkel, Andrzej Dziembowski, Roman J. Szczęsny, Nicholas Proudfoot - Nature 2018 cited by 649

  3. Mutations in ADAR1 cause Aicardi-Goutières syndrome associated with a type I interferon signature

    Authors: Gillian Rice, Paul R. Kasher, Gabriella Forte, Niamh Mannion, Sam M. Greenwood, Marcin Szynkiewicz, Jonathan E. Dickerson, Sanjeev S. Bhaskar, Massimiliano Zampini, Tracy A. Briggs, Emma M. Jenkinson, Carlos A. Bacino, Roberta Battini, Enrico Bertini, Paul Brogan, Louise Brueton, Marialuisa Carpanelli, Corinne De Laet, Pascale de Lonlay, Mireia del Toro, Isabelle Desguerre, Elisa Fazzi, Àngels García‐Cazorla, Arvid Heiberg, Masakazu Kawaguchi, Ram Kumar, Jean‐Pierre Lin, Charles Marques Lourenço, Alison Male, Wilson Marques, Cyril Mignot, Ivana Olivieri, Simona Orcesi, Prab Prabhakar, Magnhild Rasmussen, Robert A. Robinson, Flore Rozenberg, Johanna Schmidt, Katharina Steindl, Tiong Yang Tan, William G van der Merwe, Adeline Vanderver, Grace Vassallo, Emma Wakeling, Evangeline Wassmer, Elizabeth Whittaker, John H. Livingston, Pierre Lebon, Tamio Suzuki, Paul McLaughlin, Liam P. Keegan, Mary A. O’Connell, Simon C. Lovell, Yanick J. Crow - Nature Genetics 2012 cited by 943

  4. Aicardi–Goutières syndrome and the type I interferonopathies

    Authors: Yanick J. Crow, Nicolas Manel - Nature reviews. Immunology 2015 cited by 913

  5. Characterization of human disease phenotypes associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, ADAR, and IFIH1

    Authors: Yanick J. Crow, Diana Chase, Johanna L. Schmidt, Marcin Szynkiewicz, Gabriella Forte, Hannah Gornall, Anthony Oojageer, Beverley Anderson, Amy Pizzino, Guy Helman, Mohamed S. Abdel‐Hamid, Ghada M. H. Abdel‐Salam, Sam Ackroyd, Alec Aeby, Guillermo Agosta, Catherine S. W. Albin, Stavit A. Shalev, Montse Arellano, Giada Ariaudo, Vijay Aswani, Riyana Babul‐Hirji, Eileen Baildam, Nadia Bahi‐Buisson, Kathryn Bailey, Christine Barnérias, Magalie Barth, Roberta Battini, Michael W. Beresford, Geneviève Bernard, Marika Bianchi, Thierry Billette de Villemeur, Edward Blair, Miriam Bloom, Alberto Burlina, Maria Luisa Carpanelli, Daniel R. Carvalho, Manuel Castro‐Gago, Anna Cavallini, Cristina Cereda, Kate Chandler, David Chitayat, Abigail E. Collins, Concepción Sierra Córcoles, Nuno Cordeiro, Giovanni Crichiutti, Lyvia Dabydeen, Russell C. Dale, Stefano D’Arrigo, Christian G E L De Goede, Corinne De Laet, Liesbeth M. H. De Waele, Inés María Denzler, Isabelle Desguerre, Koenraad Devriendt, Maja Di Rocco, Michael Fahey, Elisa Fazzi, Colin D. Ferrie, António Figueiredo, Blanca Gener, Cyril Goizet, Nirmala Gowrinathan, Kalpana Gowrishankar, Donncha Hanrahan, Bertrand Isidor, Bülent Kara, Naz Khan, Mary D. King, Edwin P. Kirk, Ram Kumar, Lieven Lagae, P. Landrieu, Heinz Lauffer, Vincent Laugel, Roberta La Piana, Ming Lim, Jean‐Pierre Lin, Tarja Linnankivi, Mark T. Mackay, Daphna Marom, Charles Marques Lourenço, Shane McKee, Isabella Moroni, Jenny E.V. Morton, Marie‐Laure Moutard, Kevin Murray, Rima Nabbout, Sheela Nampoothiri, Noemí Núñez‐Enamorado, P.J. Oades, Ivana Olivieri, John R. Østergaard, Belén Pérez‐Dueñas, Julie Prendiville, Venkateswaran Ramesh, Magnhild Rasmussen, Luc Régal, Federica Ricci, Marlène Rio, Diana Rodriguez and 36 more - American Journal of Medical Genetics Part A 2015 cited by 613

  6. Mutations in the gene encoding the 3′-5′ DNA exonuclease TREX1 cause Aicardi-Goutières syndrome at the AGS1 locus

    Authors: Yanick J. Crow, Bruce E. Hayward, Rekha Parmar, Peter Robins, Andrea Leitch, Manir Ali, Deborah N. Black, Hans van Bokhoven, Han G. Brunner, Ben C.J. Hamel, Peter Corry, Frances M. Cowan, Suzanna G.M. Frints, Joerg Klepper, John H. Livingston, Sally Ann Lynch, R. Massey, Jean François Meritet, Jacques L. Michaud, G Ponsot, Thomas Voït, Pierre Lebon, David T. Bonthron, Andrew P. Jackson, Deborah E. Barnes, Tomas Lindahl - Nature Genetics 2006 cited by 892

  7. Inherited STING-activating mutation underlies a familial inflammatory syndrome with lupus-like manifestations

    Authors: Nadia Jeremiah, Bénédicte Neven, Matteo Gentili, Isabelle Callebaut, Sophia Maschalidi, Marie‐Claude Stolzenberg, Nicolas Goudin, Marie-Louis Frémond, Patrick Nitschké, Thierry Jo Molina, Stéphane Blanche, Capucine Pïcard, Gillian Rice, Yanick J. Crow, Nicolas Manel, Alain Fischer, Brigitte Bader‐Meunier, Frédéric Rieux‐Laucat - Journal of Clinical Investigation 2014 cited by 546

  8. Detection of interferon alpha protein reveals differential levels and cellular sources in disease

    Authors: Mathieu P. Rodero, Jérémie Decalf, Vincent Bondet, David Hunt, Gillian Rice, Scott Werneke, Sarah McGlasson, Marie‐Alexandra Alyanakian, Brigitte Bader‐Meunier, Christine Barnérias, N. Bellon, Alexandre Bélot, Christine Bodemer, Tracy A. Briggs, Isabelle Desguerre, Marie‐Louise Frémond, Marie Hully, Arn M. J. M. van den Maagdenberg, Isabelle Melki, Isabelle Meyts, Lucile Musset, Nadine Pelzer, Pierre Quartier, Gisela M. Terwindt, Joanna M. Wardlaw, Stewart Wiseman, Frédéric Rieux‐Laucat, Y Rose, Bénédicte Neven, Christina Hertel, Adrian Hayday, Matthew L. Albert, Flore Rozenberg, Yanick J. Crow, Darragh Duffy - The Journal of Experimental Medicine 2017 cited by 376

  9. Gain-of-function mutations in IFIH1 cause a spectrum of human disease phenotypes associated with upregulated type I interferon signaling

    Authors: Gillian Rice, Yoandris del Toro Duany, Emma M. Jenkinson, Gabriella Forte, Beverley Anderson, Giada Ariaudo, Brigitte Bader‐Meunier, Eileen Baildam, Roberta Battini, Michael W. Beresford, Manuela Casarano, Mondher Chouchane, Rolando Cimaz, Abigail E. Collins, Nuno Cordeiro, Russell C. Dale, Joyce Davidson, Liesbeth De Waele, Isabelle Desguerre, Laurence Faivre, Elisa Fazzi, Bertrand Isidor, Lieven Lagae, Andrew Latchman, Pierre Lebon, Chumei Li, John H. Livingston, Charles Marques Lourenço, Maria Margherita Mancardi, Alice Masurel‐Paulet, Iain B. McInnes, Manoj P. Menezes, Cyril Mignot, James O’Sullivan, Simona Orcesi, Paolo Picco, Enrica Riva, Robert A. Robinson, Diana Rodriguez, E. Salvatici, Christiaan Scott, Marta Szybowska, John Tolmie, Adeline Vanderver, Catherine Vanhulle, José Pedro Vieira, Kate Webb, Robyn Whitney, Simon G. Williams, Lynne A. Wolfe, Sameer M. Zuberi, Sun Hur, Yanick J. Crow - Nature Genetics 2014 cited by 591

  10. Mutations in COPA lead to abnormal trafficking of STING to the Golgi and interferon signaling

    Authors: Alice Lepelley, Maria José Martin-Niclós, Melvin Le Bihan, Joseph A. Marsh, Carolina Uggenti, Gillian Rice, Vincent Bondet, Darragh Duffy, Jonny Hertzog, Jan Rehwinkel, Serge Amselem, Siham Boulisfane-El Khalifi, Mary Brennan, Edwin Carter, Lucienne Chatenoud, Stéphanie Chhun, Aurore Coulomb L’Herminé, Marine Depp, Marie Legendre, Karen J. Mackenzie, Jonathan Marey, Catherine M. McDougall, Kathryn J. McKenzie, Thierry Jo Molina, Bénédicte Neven, Luís Seabra, C. Thumerelle, Marie Wislez, Nadia Nathan, Nicolas Manel, Yanick J. Crow, Marie‐Louise Frémond - The Journal of Experimental Medicine 2020 cited by 216

  11. Human intracellular ISG15 prevents interferon-α/β over-amplification and auto-inflammation

    Authors: Xianqin Zhang, Dusan Bogunovic, Béatrice Payelle‐Brogard, Véronique François-Newton, Scott D. Speer, Chao Yuan, Stefano Volpi, Zhi Li, Özden Sanal, Davood Mansouri, İlhan Tezcan, Gillian Rice, Chun‐Yuan Chen, Nahal Mansouri, Seyed Alireza Mahdaviani, Yuval Itan, Bertrand Boisson, Satoshi Okada, Lu Zeng, Xing Wang, Hui Jiang, Wenqiang Liu, Tiantian Han, Delin Liu, Tao Ma, Bo Wang, Mugen Liu, Jing-Yu Liu, Qing K. Wang, Dilek Yalnızoğlu, Lilliana Radoshevich, Gilles Uzé, Philippe Gros, Flore Rozenberg, Shen‐Ying Zhang, Emmanuelle Jouanguy, Jacinta Bustamante, Adolfo García‐Sastre, Laurent Abel, Pierre Lebon, Luigi D. Notarangelo, Yanick J. Crow, Stéphanie Boisson‐Dupuis, Jean‐Laurent Casanova, Sandra Pellegrini - Nature 2014 cited by 566

  12. Assessment of interferon-related biomarkers in Aicardi-Goutières syndrome associated with mutations in TREX1, RNASEH2A, RNASEH2B, RNASEH2C, SAMHD1, and ADAR: a case-control study

    Authors: Gillian Rice, Gabriella Forte, Marcin Szynkiewicz, Diana Chase, Alec Aeby, Mohamed S. Abdel‐Hamid, Sam Ackroyd, Rebecca Allcock, Kathryn Bailey, Umberto Balottin, Christine Barnérias, Geneviève Bernard, Christine Bodemer, M.P. Botella, Cristina Cereda, Kate Chandler, Lyvia Dabydeen, Russell C. Dale, Corinne De Laet, Christian G E L De Goede, Mireia del Toro, Laila K. Effat, Noemí Núñez Enamorado, Elisa Fazzi, Blanca Gener, Madli Haldre, Jean‐Pierre Lin, John H. Livingston, Charles Marques Lourenço, Wilson Marques, P.J. Oades, Pärt Peterson, Magnhild Rasmussen, Agathe Roubertie, Johanna Schmidt, Stavit A. Shalev, Rogelio Simón, Ronen Spiegel, Kathryn J. Swoboda, Samia A. Temtamy, Grace Vassallo, Catheline Vilain, Julie Vogt, Vanessa Wermenbol, William Whitehouse, Doriette Soler, Ivana Olivieri, Simona Orcesi, Mona Aglan, Maha S. Zaki, Ghada M. H. Abdel‐Salam, Adeline Vanderver, Kai Kisand, Flore Rozenberg, Pierre Lebon, Yanick J. Crow - The Lancet Neurology 2013 cited by 438

  13. Modeling of TREX1-Dependent Autoimmune Disease using Human Stem Cells Highlights L1 Accumulation as a Source of Neuroinflammation

    Authors: Charles A. Thomas, Leon Tejwani, Cleber A. Trujillo, Priscilla D. Negraes, Roberto H. Herai, Pinar Mesci, Ángela Macia, Yanick J. Crow, Alysson R. Muotri - Cell stem cell 2017 cited by 342

  14. Preexisting autoantibodies to type I IFNs underlie critical COVID-19 pneumonia in patients with APS-1

    Authors: Paul Bastard, Elizaveta Orlova, Leila Sozaeva, Romain Lévy, Alyssa James, Monica M. Schmitt, Sebastian Ochoa, Maria Kareva, Yulia Rodina, Adrian Gervais, Tom Le Voyer, Jérémie Rosain, Quentin Philippot, Anna‐Lena Neehus, Elana Shaw, Mélanie Migaud, Lucy Bizien, Olov Ekwall, Stefan Berg, Guglielmo Beccuti, Lucia Ghizzoni, G. Thiriez, Arthur Pavot, Cécile Goujard, Marie‐Louise Frémond, Edwin Carter, Anya Rothenbühler, Agnès Linglart, B Mignot, Aurélie Comte, Nathalie Cheikh, Olivier Hermine, Lars Breivik, Eystein S. Husebye, S. Humbert, Pierre‐Simon Rohrlich, A. Coaquette, F. Vuoto, Karine Faure, Nizar Mahlaoui, Primož Kotnik, Tadej Battelino, Katarina Trebušak Podkrajšek, Kai Kisand, Elise M. N. Ferré, Thomas DiMaggio, Lindsey B. Rosen, Peter D. Burbelo, Martin McIntyre, Nelli Y. Kann, Anna Shcherbina, Maria G. Pavlova, Anna Kolodkina, Steven M. Holland, Shen‐Ying Zhang, Yanick J. Crow, Luigi D. Notarangelo, Helen C. Su, Laurent Abel, Mark S. Anderson, Emmanuelle Jouanguy, Bénédicte Neven, Anne Puel, Jean‐Laurent Casanova, Michail S. Lionakis - The Journal of Experimental Medicine 2021 cited by 306

  15. Overview of STING-Associated Vasculopathy with Onset in Infancy (SAVI) Among 21 Patients

    Authors: Marie‐Louise Frémond, Alice Hadchouel, Laureline Berteloot, Isabelle Melki, Violaine Bresson, Laura Barnabei, Nadia Jeremiah, Alexandre Bélot, Vincent Bondet, Olivier Brocq, Damien Chan, Rawane Dagher, J.‐C. Dubus, Darragh Duffy, Séverine Feuillet-Soummer, Mathieu Fusaro, Marco Gattorno, Antonella Insalaco, Éric Jeziorski, Naoki Kitabayashi, Mireia López-Corbeto, Françoise Mazingue, Marie‐Anne Morren, Gillian Rice, Jacques G. Rivière, Luís Seabra, Jérôme Sirvente, Pere Soler‐Palacín, Nathalie Stremler-Le Bel, Guillaume Thouvenin, C. Thumerelle, Eline van Aerde, Stefano Volpi, Sophie Willcocks, Carine Wouters, Sylvain Breton, Thierry Jo Molina, Brigitte Bader‐Meunier, Despina Moshous, Alain Fischer, Stéphane Blanche, Frédéric Rieux‐Laucat, Yanick J. Crow, Bénédicte Neven - The Journal of Allergy and Clinical Immunology In Practice 2020 cited by 207

  16. HIV-1 restriction factor SAMHD1 is a deoxynucleoside triphosphate triphosphohydrolase

    Authors: David C. Goldstone, Valerie Ennis-Adeniran, Joseph J. Hedden, Harriet C. T. Groom, Gillian Rice, Evangelos Christodoulou, P.A. Walker, Geoff Kelly, L.F. Haire, Melvyn W. Yap, Luiz Pedro S. de Carvalho, Jonathan P. Stoye, Yanick J. Crow, Ian A. Taylor, Michelle Webb - Nature 2011 cited by 831

  17. ARF1 prevents aberrant type I interferon induction by regulating STING activation and recycling

    Authors: Maximilian Hirschenberger, Alice Lepelley, Ulrich Rupp, Susanne Klute, Victoria Hunszinger, Lennart Koepke, Veronika Merold, Blaise Didry‐Barca, Fanny Wondany, Tim Bergner, Tatiana Moreau, Mathieu P. Rodero, R. Rosler, Sebastian Wiese, Stefano Volpi, Marco Gattorno, Riccardo Papa, Sally Ann Lynch, Marte G. Haug, Gunnar Houge, Kristen Wigby, Jessica Sprague, Jerica Lenberg, Clarissa Read, Paul Walther, Jens Michaelis, Frank Kirchhoff, Carina C. de Oliveira Mann, Yanick J. Crow, Konstantin M. J. Sparrer - Nature Communications 2023 cited by 49

  18. cGAS-mediated induction of type I interferon due to inborn errors of histone pre-mRNA processing

    Authors: Carolina Uggenti, Alice Lepelley, Marine Depp, Andrew P. Badrock, Mathieu P. Rodero, Marie‐Thérèse El‐Daher, Gillian Rice, Somdutta Dhir, Ann P. Wheeler, Ashish Dhir, Waad Albawardi, Marie‐Louise Frémond, Luís Seabra, Jennifer Doig, Natalie Blair, Maria José Martin-Niclós, Erika Della Mina, Alejandro Rubio-Roldán, José L. García-Pérez, Duncan Sproul, Jan Rehwinkel, Jonny Hertzog, Anne Boland, Robert Olaso, Jean‐François Deleuze, Julien Baruteau, Karine Brochard, Jonathan D. Buckley, Vanessa Cavallera, Cristina Cereda, Liesbeth M. H. De Waele, Angus Dobbie, Diane Doummar, Frances Elmslie, Margarete Koch‐Hogrebe, Ram Kumar, Kate Lamb, John H. Livingston, Anirban Majumdar, Charles Marques Lorenço, Simona Orcesi, Sylviane Peudenier, Kevin Rostásy, Caroline A. Salmon, Christiaan Scott, Davide Tonduti, Guy Touati, Marialuisa Valente, Hélio van der Linden, Hilde Van Esch, Marie Vermelle, Kate Webb, Andrew P. Jackson, Martin A.M. Reijns, Nick Gilbert, Yanick J. Crow - Nature Genetics 2020 cited by 197

  19. Assessment of Type I Interferon Signaling in Pediatric Inflammatory Disease

    Authors: Gillian Rice, Isabelle Melki, Marie‐Louise Frémond, Tracy A. Briggs, Mathieu P. Rodero, Naoki Kitabayashi, Anthony Oojageer, Brigitte Bader‐Meunier, Alexandre Bélot, Christine Bodemer, Pierre Quartier, Yanick J. Crow - Journal of Clinical Immunology 2016 cited by 206

  20. Mutations in genes encoding ribonuclease H2 subunits cause Aicardi-Goutières syndrome and mimic congenital viral brain infection

    Authors: Yanick J. Crow, Andrea Leitch, Bruce E. Hayward, Anna Garner, Rekha Parmar, Elen Griffith, Manir Ali, Colin A. Semple, Jean Aicardi, Riyana Babul‐Hirji, Clarisse Baumann, Peter Baxter, Enrico Bertini, Kate Chandler, David Chitayat, D. Cau, Catherine Déry, Elisa Fazzi, Cyril Goizet, Mary D. King, Joerg Klepper, Didier Lacombe, Giovanni Lanzi, Hermione Lyall, María Luisa Martínez‐Frías, Michèle Mathieu, C McKeown, Anne Monier, Yvette Oade, Oliver Quarrell, Christopher Rittey, R. Curtis Rogers, Amparo Sanchís, John B.P. Stephenson, Uta Tacke, Marianne Till, John Tolmie, Pam Tomlin, Thomas Voït, Bernhard Weschke, C. Geoffrey Woods, Pierre Lebon, David T. Bonthron, Chris P. Ponting, Andrew P. Jackson - Nature Genetics 2006 cited by 673

  21. Enhanced cGAS-STING–dependent interferon signaling associated with mutations in ATAD3A

    Authors: Alice Lepelley, Erika Della Mina, Erika Van Nieuwenhove, Lise Waumans, Sylvie Fraïtag, Gillian Rice, Ashish Dhir, Marie‐Louise Frémond, Mathieu P. Rodero, Luís Seabra, Edwin Carter, Christine Bodemer, Daniela Buhaş, Bert Callewaert, Pascale de Lonlay, Lien De Somer, David A. Dyment, Fran Faes, Lucy Grove, Simon Holden, Marie Hully, Manju A. Kurian, Hugh J. McMillan, Kristin Suetens, Henna Tyynismaa, Stéphanie Chhun, Timothy Wai, Carine Wouters, Brigitte Bader‐Meunier, Yanick J. Crow - The Journal of Experimental Medicine 2021 cited by 90

  22. Type I interferon-mediated autoinflammation due to DNase II deficiency

    Authors: Mathieu P. Rodero, Alessandra Tesser, Eva Bartok, Gillian Rice, Erika Della Mina, Marine Depp, Benoît Beitz, Vincent Bondet, Nicolas Cagnard, Darragh Duffy, Michaël Dussiot, Marie‐Louise Frémond, Marco Gattorno, Flavia Guillem, Naoki Kitabayashi, Fabrice Porcheray, Frédéric Rieux‐Laucat, Luís Seabra, Carolina Uggenti, Stefano Volpi, Leo Zeef, Marie‐Alexandra Alyanakian, Jacques Beltrand, Anna Monica Bianco, Nathalie Boddaert, Chantal Brouzes, Sophie Candon, Roberta Caorsi, Marina Charbit, Monique Fabrè, Flavio Faletra, M Girard, Annie Harroche, Evelyn Hartmann, Dominique Lasne, Annalisa Marcuzzi, Bénédicte Neven, Patrick Nitschké, Tiffany Pascreau, Serena Pastore, Capucine Pïcard, Paolo Picco, Elisa Piscianz, Michel Polak, Pierre Quartier, Marion Rabant, Gabriele Stocco, Andrea Taddio, Florence Uettwiller, Erica Valencic, Diego Vozzi, Gunther Hartmann, Winfried Barchet, Olivier Hermine, Brigitte Bader‐Meunier, Alberto Tommasini, Yanick J. Crow - Nature Communications 2017 cited by 228

  23. Life-threatening influenza pneumonitis in a child with inherited IRF9 deficiency

    Authors: Nicholas Hernandez, Isabelle Melki, Huie Jing, Tanwir Habib, Susie S.Y. Huang, Jeffrey J. Danielson, Tomasz Kula, Scott Drutman, Serkan Belkaya, Vimel Rattina, Lazaro Lorenzo, Anaïs Boulai, Y Rose, Naoki Kitabayashi, Mathieu P. Rodero, Cécile Dumaine, Stéphane Blanche, Marie‐Noëlle Lebras, Man C. Leung, Lisa Sara Mathew, Bertrand Boisson, Shen‐Ying Zhang, Stéphanie Boisson‐Dupuis, Silvia Giliani, Damien Chaussabel, Luigi D. Notarangelo, Stephen J. Elledge, Michael J. Ciancanelli, Laurent Abel, Qian Zhang, Nico Marr, Yanick J. Crow, Helen C. Su, Jean‐Laurent Casanova - The Journal of Experimental Medicine 2018 cited by 198

  24. Human USP18 deficiency underlies type 1 interferonopathy leading to severe pseudo-TORCH syndrome

    Authors: Marije Meuwissen, Rachel Schot, Sofija Buta, Grétel Oudesluijs, Sigrid Tinschert, Scott D. Speer, Zhi Li, Leontine van Unen, Daphne Heijsman, Tobias Goldmann, Maarten H. Lequin, Johan M. Kros, Wendy Stam, Mark Hermann, Rob Willemsen, Rutger W. W. Brouwer, Wilfred F. J. van IJcken, Marta Martín-Fernández, I.F.M. de Coo, Jeroen Dudink, Femke A.T. de Vries, Aida Bertoli Avella, Marco Prinz, Yanick J. Crow, Frans W. Verheijen, Sandra Pellegrini, Dusan Bogunovic, Grazia M.S. Mancini - The Journal of Experimental Medicine 2016 cited by 290