Andrea Martin-Nalda (Andrea Martín-Nalda)

Publication Activity (10 Years)

Years Active: 2019-2021
Publications (10 Years): 4

Top Topics

Pluripotent Stem Cells

Inflammatory Response

Ejection Fraction

Smoking Cessation

Top Venues

Molecular genetics & genomic medicine

Science (New York, N.Y.)

The Journal of experimental medicine

Journal of immunology (Baltimore, Md. : 1950)

This page only lists publications with an associated author ORCID identifier.

Publications

Jie Chen, Huie Jing, Andrea Martin-Nalda, Paul Bastard, Jacques G Riviere, Zhiyong Liu, Roger Colobran, Danyel Lee, Wesley Tung, Jérémy Manry, Mary L Hasek, Soraya Boucherit, Lazaro Lorenzo, Flore Rozenberg, Mélodie Aubart, Laurent Abel, Helen C Su, Pere Soler-Palacin, Jean Laurent Casanova, Shen-Ying Zhang
Inborn errors of TLR3- or MDA5-dependent type I IFN immunity in children with enterovirus rhombencephalitis. The Journal of experimental medicine 218 (12) (2021)
Nieves Diaz, Maria Juarez, Caterina Cancrini, Maximilian Heeg, Pere Soler-Palacin, Andrew Payne, Geoffrey I Johnston, Eric Helmer, Dionne Cain, Joanne Mann, Daisy Yuill, Francesca Conti, Silvia Di Cesare, Stephan Ehl, Marina Garcia-Prat, Maria Elena Maccari, Andrea Martin-Nalda, Mónica Martínez-Gallo, Despina Moshous, Veronica Santilli, Michaela Semeraro, Alessandra Simonetti, Felipe Suarez, Marina Cavazzana, Sven Kracker
Seletalisib for Activated PI3Kδ Syndromes: Open-Label Phase 1b and Extension Studies. Journal of immunology (Baltimore, Md. : 1950) 205 (11) (2020)
Qian Zhang, Paul Bastard, Zhiyong Liu, Jérémie Le Pen, Marcela Moncada-Velez, Jie Chen, Masato Ogishi, Ira K D Sabli, Stephanie Hodeib, Cecilia Korol, Jérémie Rosain, Kaya Bilguvar, Junqiang Ye, Alexandre Bolze, Benedetta Bigio, Jean-Laurent Casanova, Andrés Augusto Arias, Qinhua Zhou, Yu Zhang, Fanny Onodi, Sarantis Korniotis, Léa Karpf, Quentin Philippot, Marwa Chbihi, Lucie Bonnet-Madin, Karim Dorgham, Nikaïa Smith, William M Schneider, Brandon S Razooky, Hans-Heinrich Hoffmann, Eleftherios Michailidis, Leen Moens, Ji Eun Han, Lazaro Lorenzo, Lucy Bizien, Philip Meade, Anna-Lena Neehus, Aileen Camille Ugurbil, Aurélien Corneau, Gaspard Kerner, Peng Zhang, Franck Rapaport, Yoann Seeleuthner, Jérémy Manry, Cecile Masson, Yohann Schmitt, Agatha Schlüter, Tom Le Voyer, Taushif Khan, Juan Li, Jacques Fellay, Lucie Roussel, Mohammad Shahrooei, Mohammed F Alosaimi, Davood Mansouri, Haya Al-Saud, Fahd Al-Mulla, Feras Almourfi, Saleh Zaid Al-Muhsen, Fahad Alsohime, Saeed H Al Turki, Rana Hasanato, Diederik van de Beek, Andrea Biondi, Laura Rachele Bettini, Mariella D'Angio', Bonfanti Paolo, Luisa Imberti, Alessandra Sottini, Simone Paghera, Eugenia Quiros-Roldan, Camillo Rossi, Andrew J Oler, Miranda F Tompkins, Camille Alba, Isabelle Vandernoot, Jean-Christophe Goffard, Guillaume Smits, Isabelle Migeotte, Filomeen Haerynck, Pere Soler-Palacin, Andrea Martin-Nalda, Roger Colobran, Pierre-Emmanuel Morange, Sevgi Keles, Fatma Çölkesen, Tayfun Ozcelik, Kadriye Kart Yasar, Sevtap Şenoğlu, Semsi Nur Karabela, Carlos Flores, Giuseppe Novelli, Sami Hraiech, Yacine Tandjaoui-Lambiotte, Xavier Duval, Cédric Laouénan, null null, null null, null null, null null, null null, null null, null null, null null, Andrew L Snow, Clifford L Dalgard, Joshua D Milner, Donald C Vinh, Trine Hyrup Mogensen, Nico Marr, András N Spaan, Bertrand Boisson, Stéphanie Boisson-Dupuis, Jacinta Bustamante, Anne Puel, Michael J Ciancanelli, Isabelle Meyts, Tom Maniatis, Vassili Soumelis, Ali Amara, Michel C Nussenzweig, Adolfo García-Sastre, Florian Krammer, Aurora Pujol, Darragh Duffy, Richard P Lifton, Shen-Ying Zhang, Guy Gorochov, Vivien Béziat, Emmanuelle Jouanguy, Sancho-Shimizu Vanessa, Charles M Rice, Laurent Abel, Luigi Daniele Notarangelo, Aurélie Cobat, Helen C Su, Jean Laurent Casanova
Inborn errors of type I IFN immunity in patients with life-threatening COVID-19. Science (New York, N.Y.) 370 (6515) (2020)
Andrea Martin-Nalda, Anna M Cueto-González, Ana Argudo-Ramírez, Jose L Marin-Soria, Monica Martinez-Gallo, Roger Colobran, Albert Plaja, Neus Castells, Jacques Riviere, Eduardo F Tizzano, Pere Soler-Palacin
Identification of 22q11.2 deletion syndrome via newborn screening for severe combined immunodeficiency. Two years' experience in Catalonia (Spain). Molecular genetics & genomic medicine 7 (12) (2019)