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Fawaz Awad

Impact of human monocyte and macrophage polarization on NLR expression and NLRP3 inflammasome activation
2017 · Fawaz Awad, Eman Assrawi, et al. · PLoS ONE · 192
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Inflammasome biology, molecular pathology and therapeutic implications
2018 · Fawaz Awad, Eman Assrawi, et al. · Pharmacology & Therapeutics · 138
Photoaging and skin cancer: Is the inflammasome the missing link?
2018 · Fawaz Awad, Eman Assrawi, et al. · Mechanisms of Ageing and Development · 101
Expression of SAA1, SAA2 and SAA4 genes in human primary monocytes and monocyte-derived macrophages
2019 · Claire Jumeau, Fawaz Awad, et al. · PLoS ONE · 70
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NLRP3-associated autoinflammatory diseases: Phenotypic and molecular characteristics of germline versus somatic mutations
2019 · Camille Louvrier, Eman Assrawi, et al. · Journal of Allergy and Clinical Immunology · 67
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Proteasomal degradation of NOD2 by NLRP12 in monocytes promotes bacterial tolerance and colonization by enteropathogens
2018 · Sylvain Normand, Nadine Waldschmitt, et al. · Nature Communications · 50
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Somatic Mosaic NLRP3 Mutations and Inflammasome Activation in Late-Onset Chronic Urticaria
2019 · Eman Assrawi, Camille Louvrier, et al. · Journal of Investigative Dermatology · 32
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Association of hidradenitis suppurativa and familial Mediterranean fever: A case series of 6 patients
2016 · Salam Abbara, Sophie Georgin-Lavialle, et al. · Joint Bone Spine · 31
Absence of NLRP3 somatic mutations and VEXAS ‐related UBA1 mutations in a large cohort of patients with Schnitzler syndrome
2022 · Camille Louvrier, Fawaz Awad, et al. · Allergy · 18
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RNF213-associated urticarial lesions with hypercytokinemia
2022 · Camille Louvrier, Fawaz Awad, et al. · Journal of Allergy and Clinical Immunology · 14
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Spondyloarthritis associated with familial Mediterranean fever: successful treatment with anakinra
2016 · Sophie Georgin-Lavialle, Katia Stankovic Stojanovic, et al. · Rheumatology · 14
Chronic myelomonocytic leukemia as a cause of fatal uncontrolled inflammation in familial Mediterranean fever
2015 · Fawaz Awad, Sophie Georgin-Lavialle, et al. · Orphanet Journal of Rare Diseases · 10
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The NLRP3 p.A441V Mutation in NLRP3‐AID Pathogenesis: Functional Consequences, Phenotype‐Genotype Correlations and Evidence for a Recurrent Mutational Event
2019 · Fawaz Awad, Eman Assrawi, et al. · ACR Open Rheumatology · 9
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遅発性慢性じん麻疹における体細胞モザイクnlrp3変異とインフラマソーム活性化【jst・京大機械翻訳】
2020 · Assrawi Eman, Louvrier Camille, et al. · Journal of Investigative Dermatology · 2
Expanding the phenotypic spectrum associated with CFAP43 mutations: a case report of familial male infertility with respiratory manifestations
2025 · Fawaz Awad, Razan Abukhaizaran, et al. · Frontiers in Reproductive Health · 1
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P-588 A novel homozygous TUBB8 variant in a patient with oocyte maturation defects: A case report
2025 · R Abukhaizaran, Z Nasser, et al. · Human Reproduction · 1
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Adult presentation of SLC29A3-related disorder spectrum with marked hypogammaglobulinemia due to a recurrent homozygous pathogenic variant (G437R): a case report
2026 · Mohammad Ameen Ishqair, Abbas K. H. Masalma, et al. · Frontiers in Genetics
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Expansion of the Clinical Spectrum of Autosomal Recessive Fatty Acyl‐ CoA Reductase 1 ( FAR1 ) Deficiency: A Previously Unreported Association With Imperforate Anus—A Case Report
2026 · Mostafa Ibraheem Abo Alrob, Fawaz Awad, et al. · American Journal of Medical Genetics Part A
L26/O-337 Monogenic causes of recurrent euploid pregnancy loss identified by whole-exome sequencing of products of conception: a retrospective cohort study
2026 · F. Awad, H. Kassem, et al. · Human Reproduction
Clinical heterogeneity, genotype, and neurological outcomes in six Palestinian patients with ornithine transcarbamylase deficiency
2026 · Imad Dweikat, Hanin Kassem, et al. · BMC Pediatrics
Lésions urticariennes chroniques associées à une hypercytokinémie massive : une nouvelle maladie mendélienne
2021 · Camille Louvrier, Fawaz Awad, et al. · Annales de Dermatologie et de Vénéréologie - FMC
Mutation en mosaïque de NLRP3 dans des urticaires neutrophiliques avec fièvre: une nouvelle entité
2019 · E. Assrawi, C. Louvrier, et al. · Annales de Dermatologie et de Vénéréologie
L’infection à Clostridium difficile comme déclencheur de crise de fièvre méditerranéenne familiale chez l’homme : étude clinique et physiopathologique
2018 · S. Georgin Lavialle, F. Awad, et al. · La Revue de Médecine Interne
Association d’une maladie de Verneuil à une fièvre méditerranéenne familiale : 6 cas
2017 · Salam Abbara, Sophie Georgin-Lavialle, et al. · Revue du Rhumatisme
Chronic myelomonocytic leukemia as a cause of fatal uncontrolled inflammation in familial Mediterranean fever
2015 · F Awad, S Georgin-Lavialle, et al. · Pediatric Rheumatology
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Works count: 29
Citation count: 750
H-index: 11
I10-index: 12
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