الرئيسية › دليل الباحثين › Laurent Abel
Laurent Abel
الانتماء : Hôpital Necker-Enfants Malades · Inserm · Université Paris Cité · Human Genetic of Infectious Diseases · Institut des Maladies Génétiques Imagine · Université Paris Descartes
- 49منشورات (انتماء فرنسي)
- 731مجموع المنشورات
- 69210الاستشهادات
- 135مؤشر h
الملف البحثي
لدى Laurent Abel 49 منشور(ات) مفهرسة (2004–2026). تُنشر أعماله أساسًا في «The Journal of Experimental Medicine»، «Journal of Clinical Immunology» و«Science Immunology». أكثر مقالاته استشهادًا هو «Deep Dermatophytosis and Inherited CARD9 Deficiency» (2013)، وقد استُشهد به 392 مرة. 8 من هذه المنشورات تعود إلى آخر ثلاث سنوات من النشاط. شارك في تأليف أعماله 12 باحثًا على الأقل، منهم باحثون من مؤسسات في الولايات المتحدة، إيطاليا، إسبانيا، بلجيكا.
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إنشاء ملفي المجاني إضافة منشوراتيمجالات البحث
- Immunodeficiency and Autoimmune Disorders
- Genetic Associations and Epidemiology
- interferon and immune responses
- Tuberculosis Research and Epidemiology
- COVID-19 Clinical Research Studies
المنشورات (49)
- Human LFA-1 governs T cell immune surveillance of the skin
- Humans homozygous for rare or common hypomorphic IL23R variants are prone to tuberculosis
- Auto-antibodies neutralizing type I interferons in ~10% of Moroccan patients with life-threatening COVID-19
- High risk of hypoxemic COVID-19 pneumonia in myasthenia gravis patients with type I IFN autoantibodies
- High risk of hypoxemic COVID-19 pneumonia in myasthenia gravis patients with type I IFN autoantibodies
- Human LY9 governs CD4 + T cell IFN-γ immunity to Mycobacterium tuberculosis
- Deleterious variants in the autophagy-related gene RB1CC1/FIP200 impair immunity to SARS-CoV-2
- A human YEATS4 variant confers resistance to TST and IGRA conversion despite Mycobacterium tuberculosis exposure
- Humans with inherited MyD88 and IRAK-4 deficiencies are predisposed to hypoxemic COVID-19 pneumonia
- Autoantibodies Neutralizing Type I IFNs in the Bronchoalveolar Lavage of at Least 10% of Patients During Life-Threatening COVID-19 Pneumonia
- Mendelian Susceptibility to Mycobacterial Disease (MSMD): Clinical, Immunological, and Genetic Features of 22 Patients from 15 Moroccan Kindreds
- Mendelian susceptibility to mycobacterial disease: an overview
- Studying severe long COVID to understand post-infectious disorders beyond COVID-19
- Human T-bet governs the generation of a distinct subset of CD11c high CD21 low B cells
- Impaired IL-23–dependent induction of IFN-γ underlies mycobacterial disease in patients with inherited TYK2 deficiency
- Decoding the Human Genetic and Immunological Basis of COVID-19 mRNA Vaccine-Induced Myocarditis
- Human STAT3 variants underlie autosomal dominant hyper-IgE syndrome by negative dominance
- Inherited GATA2 Deficiency Is Dominant by Haploinsufficiency and Displays Incomplete Clinical Penetrance
- High Th2 cytokine levels and upper airway inflammation in human inherited T-bet deficiency
- Inherited human c-Rel deficiency disrupts myeloid and lymphoid immunity to multiple infectious agents
- Human T-bet Governs Innate and Innate-like Adaptive IFN-γ Immunity against Mycobacteria
- Human SNORA31 variations impair cortical neuron-intrinsic immunity to HSV-1 and underlie herpes simplex encephalitis
- Prevalence and risk factors for latent tuberculosis infection among healthcare workers in Morocco
- A recessive form of hyper-IgE syndrome by disruption of ZNF341-dependent STAT3 transcription and activity
- Disruption of an antimycobacterial circuit between dendritic and helper T cells in human SPPL2a deficiency
- Incomplete penetrance for isolated congenital asplenia in humans with mutations in translated and untranslated RPSA exons
- Human Genetics of Tuberculosis of the Nervous System
- Genetic, immunological, and clinical features of patients with bacterial and fungal infections due to inherited IL-17RA deficiency
- Mycobacterial disease in patients with chronic granulomatous disease: A retrospective analysis of 71 cases
- Dual T cell– and B cell–intrinsic deficiency in humans with biallelic RLTPR mutations
- Whole-exome sequencing to analyze population structure, parental inbreeding, and familial linkage
- A genome-wide association study of pulmonary tuberculosis in Morocco
- Utility of the QuantiFERON®-TB Gold In-Tube assay for the diagnosis of tuberculosis in Moroccan children
- Human TYK2 deficiency: Mycobacterial and viral infections without hyper-IgE syndrome
- Inherited and acquired immunodeficiencies underlying tuberculosis in childhood
- Inherited CARD9 deficiency in otherwise healthy children and adults with Candida species–induced meningoencephalitis, colitis, or both
- Pott's disease in Moroccan children: clinical features and investigation of the interleukin-12/interferon-γ pathway
- Human genetics of tuberculosis: a long and winding road
- Association Study of Genes Controlling IL-12-dependent IFN-γ Immunity: STAT4 Alleles Increase Risk of Pulmonary Tuberculosis in Morocco
- Chronic Granulomatous Disease in Morocco: Genetic, Immunological, and Clinical Features of 12 Patients from 10 Kindreds
- Deep Dermatophytosis and Inherited CARD9 Deficiency
- Clinical Features of Candidiasis in Patients With Inherited Interleukin 12 Receptor β1 Deficiency
- Primary Immunodeficiency Diseases Worldwide: More Common than Generally Thought
- IL-12Rβ1 Deficiency in Two of Fifty Children with Severe Tuberculosis from Iran, Morocco, and Turkey
- Major histocompatibility complex class II expression deficiency caused by a RFXANK founder mutation: a survey of 35 patients
- Primary immunodeficiencies of protective immunity to primary infections
- X-linked susceptibility to mycobacteria is caused by mutations in NEMO impairing CD40-dependent IL-12 production
- An autosomal dominant major gene confers predisposition to pulmonary tuberculosis in adults
- Association ofIL12RB1Polymorphisms with Pulmonary Tuberculosis in Adults in Morocco
مجلات النشر
- The Journal of Experimental Medicine × 9
- Journal of Clinical Immunology × 6
- Science Immunology × 4
- Proceedings of the National Academy of Sciences × 4
- Nature Medicine × 2
- PLoS ONE × 2
المنشورات حسب السنة
- 20265
- 20253
- 20234
- 20224
- 20214
- 20201
- 20192
- 20183
- 20171
- 20166
التعاون العلمي
المؤسسات الشريكة : Rockefeller University · Assistance Publique – Hôpitaux de Paris · Howard Hughes Medical Institute · Sorbonne Paris Cité · Institut Necker Enfants Malades
بلدان المؤلفين المشاركين : الولايات المتحدة · إيطاليا · إسبانيا · بلجيكا
المؤلفون المشاركون
- Jean‐Laurent Casanova
- Stéphanie Boisson‐Dupuis
- Jacinta C. Bustamante
- Anne Puel
- Capucine Pïcard
- Aurélie Cobat
- Emmanuelle Jouanguy
- Caroline Deswarte
- Mélanie Migaud
- Jérémie Rosain
- Vivien Béziat
- Bertrand Boisson
البيانات البيبليوغرافية مصدرها OpenAlex (قاعدة مفتوحة).
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