All papers authored by Kerry Dobbs
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2022
Javiera de la Cruz,
Carmelo Carmona-Rivera 
,
Tovah E. Markowitz,
Clifton L. Dalgard ,
Yu Zhang ,
Andrew J. Oler ,
Dillon R. Claybaugh,
Kerry Dobbs ,
Ottavia M. Delmonte ,
Nicoletta Crescenzio,
Luisa Imberti,
Alessandra Sottini,
Virginia Quaresima ,
Markowitz Te,
Chiara Fiorini
and 44 other authors
,
Tovah E. Markowitz,
Clifton L. Dalgard ,
Yu Zhang ,
Andrew J. Oler ,
Dillon R. Claybaugh,
Kerry Dobbs ,
Ottavia M. Delmonte ,
Nicoletta Crescenzio,
Luisa Imberti,
Alessandra Sottini,
Virginia Quaresima ,
Markowitz Te,
Chiara Fiorini
and 44 other authors
Multicenter analysis of neutrophil extracellular trap dysregulation in adult and pediatric COVID-19
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András N. Spaan ,
Anna-Lena Neehus ,
Emmanuel Laplantine ,
Frederik Staels ,
Masato Ogishi ,
Yoann Seeleuthner,
Franck Rapaport ,
Keenan A. Lacey ,
Erika Van Nieuwenhove ,
Maya Chrabieh,
David Hum ,
Mélanie Migaud ,
Araksya Izmiryan ,
Lazaro Lorenzo ,
Tatiana Kochetkov
and 47 other authors
,
Anna-Lena Neehus ,
Emmanuel Laplantine ,
Frederik Staels ,
Masato Ogishi ,
Yoann Seeleuthner,
Franck Rapaport ,
Keenan A. Lacey ,
Erika Van Nieuwenhove ,
Maya Chrabieh,
David Hum ,
Mélanie Migaud ,
Araksya Izmiryan ,
Lazaro Lorenzo ,
Tatiana Kochetkov
and 47 other authors
Human OTULIN haploinsufficiency impairs cell-intrinsic immunity to staphylococcal α-toxin
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2020
Michael S. Abers ,
Ottavia M. Delmonte ,
Emily E. Ricotta ,
Jonathan Fintzi,
Danielle L. Fink,
Adriana A. Almeida de Jesus ,
Kol A. Zarember ,
Sara Alehashemi ,
Vasileios Oikonomou ,
Jigar V. Desai ,
Scott W. Canna ,
Bita Shakoory ,
Kerry Dobbs ,
Luisa Imberti,
Alessandra Sottini
and 31 other authors
,
Ottavia M. Delmonte ,
Emily E. Ricotta ,
Jonathan Fintzi,
Danielle L. Fink,
Adriana A. Almeida de Jesus ,
Kol A. Zarember ,
Sara Alehashemi ,
Vasileios Oikonomou ,
Jigar V. Desai ,
Scott W. Canna ,
Bita Shakoory ,
Kerry Dobbs ,
Luisa Imberti,
Alessandra Sottini
and 31 other authors
An immune-based biomarker signature is associated with mortality in COVID-19 patients
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Rushika C. Wirasinha ,
Ainsley R. Davies ,
Monika Srivastava ,
Julie M. Sheridan ,
Xavier Y. X. Sng ,
Ottavia M. Delmonte ,
Kerry Dobbs ,
Khai L. Loh ,
Lisa A. Miosge ,
Cindy Eunhee Lee ,
Rochna Chand ,
Anna Chan ,
Jin Yan Yap ,
Michael D. Keller ,
Karin Chen
and 10 other authors
,
Ainsley R. Davies ,
Monika Srivastava ,
Julie M. Sheridan ,
Xavier Y. X. Sng ,
Ottavia M. Delmonte ,
Kerry Dobbs ,
Khai L. Loh ,
Lisa A. Miosge ,
Cindy Eunhee Lee ,
Rochna Chand ,
Anna Chan ,
Jin Yan Yap ,
Michael D. Keller ,
Karin Chen
and 10 other authors
Nfkb2 variants reveal a p100-degradation threshold that defines autoimmune susceptibility
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2019
Fabien G. Lafaille,
Oliver Harschnitz ,
Yoon Seung Lee,
Peng Zhang,
Mary L. Hasek,
Gaspard Kerner,
Yuval Itan,
Osefame Ewaleifoh,
Franck Rapaport,
Thomas M. Carlile,
Madalina E. Carter-Timofte,
Dominik Paquet,
Kerry Dobbs ,
Bastian Zimmer,
Daxing Gao
and 28 other authors
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,
Yoon Seung Lee,
Peng Zhang,
Mary L. Hasek,
Gaspard Kerner,
Yuval Itan,
Osefame Ewaleifoh,
Franck Rapaport,
Thomas M. Carlile,
Madalina E. Carter-Timofte,
Dominik Paquet,
Kerry Dobbs ,
Bastian Zimmer,
Daxing Gao
and 28 other authors
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Hye Kyung Lim ,
Sarah X. L. Huang,
Jie Chen ,
Priya Luthra,
Gaspard Kerner ,
Olivier Gilliaux ,
Paul Bastard ,
Flore Rozenberg,
Kerry Dobbs ,
Catherine Vedrinne,
Nicholas Hernandez,
Nicolas Goudin ,
Mary L. Hasek,
Jordan S. Orange,
Eduardo Javier García Reino
and 17 other authors
,
Sarah X. L. Huang,
Jie Chen ,
Priya Luthra,
Gaspard Kerner ,
Olivier Gilliaux ,
Paul Bastard ,
Flore Rozenberg,
Kerry Dobbs ,
Catherine Vedrinne,
Nicholas Hernandez,
Nicolas Goudin ,
Mary L. Hasek,
Jordan S. Orange,
Eduardo Javier García Reino
and 17 other authors
Severe influenza pneumonitis in children with inherited TLR3 deficiency
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Elise M. N. Ferré ,
Timothy J. Break,
Peter D. Burbelo ,
Michael Allgäuer ,
David E. Kleiner ,
Dakai Jin ,
Ziyue Xu ,
Les R. Folio ,
Daniel J. Mollura,
Muthulekha Swamydas ,
Wenjuan Gu,
Sally Hunsberger,
Chyi-Chia R. Lee ,
Anamaria Bondici,
Kevin W. Hoffman
and 22 other authors
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,
Timothy J. Break,
Peter D. Burbelo ,
Michael Allgäuer ,
David E. Kleiner ,
Dakai Jin ,
Ziyue Xu ,
Les R. Folio ,
Daniel J. Mollura,
Muthulekha Swamydas ,
Wenjuan Gu,
Sally Hunsberger,
Chyi-Chia R. Lee ,
Anamaria Bondici,
Kevin W. Hoffman
and 22 other authors
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2018
Immacolata Brigida ,
Matteo Zoccolillo,
Maria Pia Cicalese,
Laurène Pfajfer,
Federica Barzaghi,
Serena Scala,
Carmen Oleaga-Quintas,
Jesus A. Álvarez-Álvarez,
Lucia Sereni,
Stefania Giannelli,
Claudia Sartirana,
Francesca Dionisio,
Luca Pavesi,
Marta Benavides-Nieto,
Luca Basso-Ricci
and 31 other authors
,
Matteo Zoccolillo,
Maria Pia Cicalese,
Laurène Pfajfer,
Federica Barzaghi,
Serena Scala,
Carmen Oleaga-Quintas,
Jesus A. Álvarez-Álvarez,
Lucia Sereni,
Stefania Giannelli,
Claudia Sartirana,
Francesca Dionisio,
Luca Pavesi,
Marta Benavides-Nieto,
Luca Basso-Ricci
and 31 other authors
T-cell defects in patients with ARPC1B germline mutations account for combined immunodeficiency
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Silvia Preite ,
Jennifer L. Cannons,
Andrea J. Radtke,
Ivan Vujkovic-Cvijin ,
Julio Gomez-Rodriguez,
Stefano Volpi ,
Bonnie Huang,
Jun Cheng,
Nicholas Collins,
Julie Reilley,
Robin Handon,
Kerry Dobbs ,
Lutfi Huq,
Indu Raman,
Chengsong Zhu
and 8 other authors
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,
Jennifer L. Cannons,
Andrea J. Radtke,
Ivan Vujkovic-Cvijin ,
Julio Gomez-Rodriguez,
Stefano Volpi ,
Bonnie Huang,
Jun Cheng,
Nicholas Collins,
Julie Reilley,
Robin Handon,
Kerry Dobbs ,
Lutfi Huq,
Indu Raman,
Chengsong Zhu
and 8 other authors
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2017
Stefano Volpi ,
Yasuhiro Yamazaki,
Patrick M. Brauer,
Ellen van Rooijen,
Atsuko Hayashida,
Anne Slavotinek,
Hye Sun Kuehn,
Maja Di Rocco,
Carlo Rivolta ,
Ileana Bortolomai,
Likun Du,
Kerstin Felgentreff,
Lisa Ott de Bruin,
Kazutaka Hayashida,
George Freedman
and 24 other authors
,
Yasuhiro Yamazaki,
Patrick M. Brauer,
Ellen van Rooijen,
Atsuko Hayashida,
Anne Slavotinek,
Hye Sun Kuehn,
Maja Di Rocco,
Carlo Rivolta ,
Ileana Bortolomai,
Likun Du,
Kerstin Felgentreff,
Lisa Ott de Bruin,
Kazutaka Hayashida,
George Freedman
and 24 other authors
EXTL3 mutations cause skeletal dysplasia, immune deficiency, and developmental delay
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