Michel Massaad

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Talal ChatilaHarvard Medical School; Boston Children's HospitalAdresse e-mail validée de childrens.harvard.edu
Ghassan DbaiboProfessor of Pediatrics and Biochemistry, American University of BeirutAdresse e-mail validée de aub.edu.lb
Silvia GilianiUniversity of BresciaAdresse e-mail validée de unibs.it
Abdulrahman AlsultanProfessor, King Saud UniversityAdresse e-mail validée de ksu.edu.sa
Abdullah A. AlangariProfessor of Pediatrics, King Saud UniversityAdresse e-mail validée de ksu.edu.sa
Francis LuscinskasProfessor of Pathology, Harvard Medical School and Brigham and Women's HospitalAdresse e-mail validée de partners.org
Andre MegarbaneLebanese American University, School of MedicineAdresse e-mail validée de lau.edu.lb
Louis-Marie CharbonnierBoston Children's Hospital, Harvard Medical SchoolAdresse e-mail validée de childrens.harvard.edu
Fowzan S Alkuraya, MDProfessor of Human Genetics, Alfaisal University and KFSHRC, Riyadh, Saudi ArabiaAdresse e-mail validée de kfshrc.edu.sa
Emad RaddaouiProfessor and consultant pathologist, Alfaisal UniversityAdresse e-mail validée de alfaisal.edu
Lalit KumarBoston Children's Hospital and Harvard Medical SchoolAdresse e-mail validée de childrens.harvard.edu
Craig D. PlattBoston Children's HospitalAdresse e-mail validée de childrens.harvard.edu
Ali SobhMansoura University Children's Hospital, Faculty of Medicine, Mansoura UniversityAdresse e-mail validée de mans.edu.eg
Nima RezaeiTehran University of Medical Sciences; Universal Scientific Education and Research Network (USERN)Adresse e-mail validée de tums.ac.ir
Hassan AbolhassaniKarolinska InstitutetAdresse e-mail validée de ki.se
Mingyan Fang (方明艳)BGIAdresse e-mail validée de genomics.cn
Alessandro PlebaniUniversità di BresciaAdresse e-mail validée de unibs.it
Antonella CianferoniThe University of Pennsylvania, Children's Hospital of PhiladelphiaAdresse e-mail validée de email.chop.edu
Patrick RevyImagine Institute, "Genome Dynamics in Human Diseases" Laboratory, Paris, FranceAdresse e-mail validée de inserm.fr
ahmet ozenMarmara UniversityAdresse e-mail validée de marmara.edu.tr

Suivre

Michel Massaad

Assistant Professor of Immunology, Faculty of Medicine, American University of Beirut, Beirut

Adresse e-mail validée de aub.edu.lb

Pediatric Primary Immunodeficiency Disorders


Titre Trier par citations Trier par année Trier par titre	Citée par Citée par	Année
Wiskott‐Aldrich syndrome: a comprehensive review MJ Massaad, N Ramesh, RS Geha Annals of the New York Academy of Sciences 1285 (1), 26-43, 2013	442	2013
LPS-responsive beige-like anchor (LRBA) gene mutation in a family with inflammatory bowel disease and combined immunodeficiency A Alangari, A Alsultan, N Adly, MJ Massaad, IS Kiani, A Aljebreen, ... Journal of Allergy and Clinical Immunology 130 (2), 481-488. e2, 2012	287	2012
Regulatory T-cell deficiency and immune dysregulation, polyendocrinopathy, enteropathy, X-linked–like disorder caused by loss-of-function mutations in LRBA LM Charbonnier, E Janssen, J Chou, TK Ohsumi, S Keles, JT Hsu, ... Journal of Allergy and Clinical Immunology 135 (1), 217-227. e9, 2015	283	2015
A missense mutation in TFRC, encoding transferrin receptor 1, causes combined immunodeficiency HH Jabara, SE Boyden, J Chou, N Ramesh, MJ Massaad, H Benson, ... Nature genetics 48 (1), 74-78, 2016	252	2016
DOCK8 functions as an adaptor that links TLR-MyD88 signaling to B cell activation HH Jabara, DR McDonald, E Janssen, MJ Massaad, N Ramesh, ... Nature immunology 13 (6), 612-620, 2012	249	2012
Spectrum of Phenotypes Associated with Mutations in LRBA OK Alkhairy, H Abolhassani, N Rezaei, M Fang, KK Andersen, ... Journal of clinical immunology 36, 33-45, 2016	226	2016
The extended clinical phenotype of 64 patients with dedicator of cytokinesis 8 deficiency KR Engelhardt, ME Gertz, S Keles, AA Schäffer, EC Sigmund, C Glocker, ... Journal of Allergy and Clinical Immunology 136 (2), 402-412, 2015	218	2015
A novel primary human immunodeficiency due to deficiency in the WASP-interacting protein WIP G Lanzi, D Moratto, D Vairo, S Masneri, O Delmonte, T Paganini, ... Journal of Experimental Medicine 209 (1), 29-34, 2012	209	2012
Inherited DOCK2 deficiency in patients with early-onset invasive infections K Dobbs, C Domínguez Conde, SY Zhang, S Parolini, M Audry, J Chou, ... New England Journal of Medicine 372 (25), 2409-2422, 2015	196	2015
A homozygous mucosa-associated lymphoid tissue 1 (MALT1) mutation in a family with combined immunodeficiency HH Jabara, T Ohsumi, J Chou, MJ Massaad, H Benson, A Megarbane, ... Journal of allergy and clinical immunology 132 (1), 151-158, 2013	159	2013
A systematic analysis of recombination activity and genotype-phenotype correlation in human recombination-activating gene 1 deficiency YN Lee, F Frugoni, K Dobbs, JE Walter, S Giliani, AR Gennery, W Al-Herz, ... Journal of allergy and clinical immunology 133 (4), 1099-1108. e12, 2014	153	2014
B cell–intrinsic deficiency of the Wiskott-Aldrich syndrome protein (WASp) causes severe abnormalities of the peripheral B-cell compartment in mice M Recher, SO Burns, MA de la Fuente, S Volpi, C Dahlberg, JE Walter, ... Blood, The Journal of the American Society of Hematology 119 (12), 2819-2828, 2012	135	2012
Inherited human IFN-γ deficiency underlies mycobacterial disease G Kerner, J Rosain, A Guérin, A Al-Khabaz, C Oleaga-Quintas, ... The Journal of clinical investigation 130 (6), 3158-3171, 2020	127	2020
A DOCK8-WIP-WASp complex links T cell receptors to the actin cytoskeleton E Janssen, M Tohme, M Hedayat, M Leick, S Kumari, N Ramesh, ... The Journal of clinical investigation 126 (10), 3837-3851, 2016	116	2016
Clinical, immunologic, and genetic spectrum of 696 patients with combined immunodeficiency H Abolhassani, J Chou, W Bainter, CD Platt, M Tavassoli, T Momen, ... Journal of Allergy and Clinical Immunology 141 (4), 1450-1458, 2018	108	2018
Deficiency of base excision repair enzyme NEIL3 drives increased predisposition to autoimmunity MJ Massaad, J Zhou, D Tsuchimoto, J Chou, H Jabara, E Janssen, ... The Journal of Clinical Investigation 126 (11), 4219-4236, 2016	83	2016
Clinical, immunologic and genetic profiles of DOCK8-deficient patients in Kuwait W Al-Herz, R Ragupathy, MJ Massaad, A Nanda, KR Engelhardt, ... Clinical immunology 143 (3), 266-272, 2012	77	2012
Defective nuclear translocation of nuclear factor of activated T cells and extracellular signal-regulated kinase underlies deficient IL-2 gene expression in Wiskott-Aldrich … A Cianferoni, M Massaad, S Feske, MA de la Fuente, L Gallego, ... Journal of allergy and clinical immunology 116 (6), 1364-1371, 2005	77	2005
Successful engraftment of donor marrow following allogeneic hematopoietic cell transplantation in autosomal recessive Hyper IgE syndrome due to DOCK8 deficiency DR McDonald, MJ Massaad, A Johnston, S Keles, T Chatila, RS Geha, ... The Journal of allergy and clinical immunology 126 (6), 1304, 2010	76	2010
The yeast split-ubiquitin membrane protein two-hybrid screen identifies BAP31 as a regulator of the turnover of endoplasmic reticulum-associated protein tyrosine phosphatase-like B B Wang, J Pelletier, MJ Massaad, A Herscovics, GC Shore Molecular and cellular biology, 2004	76	2004

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