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Capucine Pïcard
الانتماء : Hôpital Necker-Enfants Malades · Inserm · Université Paris Cité · Institut Necker Enfants Malades · Centre de Référence Déficits Immunitaires Héréditaires · Assistance Publique – Hôpitaux de Paris · Institut des Maladies Génétiques Imagine · Université Paris Descartes
- 41منشورات (انتماء فرنسي)
- 657مجموع المنشورات
- 57478الاستشهادات
- 129مؤشر h
الملف البحثي
لدى Capucine Pïcard 41 منشور(ات) مفهرسة (2006–2025). تُنشر أعماله أساسًا في «Journal of Clinical Immunology»، «The Journal of Experimental Medicine» و«Annales de Dermatologie et de Vénéréologie». أكثر مقالاته استشهادًا هو «Human Inborn Errors of Immunity: 2019 Update on the Classification from the International Union of Immunological Societies Expert Committee» (2020)، وقد استُشهد به 1213 مرة. 3 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، المملكة المتحدة، الجزائر، تونس.
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إنشاء ملفي المجاني إضافة منشوراتيمجالات البحث
- Immunodeficiency and Autoimmune Disorders
- T-cell and B-cell Immunology
- Blood disorders and treatments
- Immune Response and Inflammation
- Autoimmune and Inflammatory Disorders Research
المنشورات (41)
- Human inborn errors of immunity: 2024 update on the classification from the International Union of Immunological Societies Expert Committee
- The 2024 update of IUIS phenotypic classification of human inborn errors of immunity
- Characterization of novel mutations in the TEL-patch domain of the telomeric factor TPP1 associated with telomere biology disorders
- Human Inborn Errors of Immunity: 2022 Update on the Classification from the International Union of Immunological Societies Expert Committee
- The 2022 Update of IUIS Phenotypical Classification for Human Inborn Errors of Immunity
- The Ever-Increasing Array of Novel Inborn Errors of Immunity: an Interim Update by the IUIS Committee
- Human STAT3 variants underlie autosomal dominant hyper-IgE syndrome by negative dominance
- Human Inborn Errors of Immunity: 2019 Update on the Classification from the International Union of Immunological Societies Expert Committee
- Human Inborn Errors of Immunity: 2019 Update of the IUIS Phenotypical Classification
- Correction to: Human Inborn Errors of Immunity: 2019 Update on the Classification from the International Union of Immunological Societies Expert Committee
- Corrigendum to: Diagnostic Yield of Next-Generation Sequencing in Very Early-Onset Inflammatory Bowel Diseases: A Multicenter Study
- Érythrodermie ichtyosiforme révélant un déficit immunitaire combiné sévère
- Hemophagocytic Lymphohistiocytosis and Diagnostic Difficulties
- 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
- Diagnostic Yield of Next-generation Sequencing in Very Early-onset Inflammatory Bowel Diseases: A Multicentre Study
- Incomplete penetrance for isolated congenital asplenia in humans with mutations in translated and untranslated RPSA exons
- First homozygous large deletion in EDARADD gene associated with a severe form of anhidrotic ectodermal dysplasia
- International Union of Immunological Societies: 2017 Primary Immunodeficiency Diseases Committee Report on Inborn Errors of Immunity
- The 2017 IUIS Phenotypic Classification for Primary Immunodeficiencies
- Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype
- 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
- Unique and shared signaling pathways cooperate to regulate the differentiation of human CD4+ T cells into distinct effector subsets
- Whole-exome sequencing to analyze population structure, parental inbreeding, and familial linkage
- Successful Haploidentical Stem Cell Transplantation with Post-Transplant Cyclophosphamide in a Severe Combined Immune Deficiency Patient: a First Report
- Primary Immunodeficiency Diseases: an Update on the Classification from the International Union of Immunological Societies Expert Committee for Primary Immunodeficiency 2015
- Human TYK2 deficiency: Mycobacterial and viral infections without hyper-IgE syndrome
- The 2015 IUIS Phenotypic Classification for Primary Immunodeficiencies
- Inherited CARD9 deficiency in otherwise healthy children and adults with Candida species–induced meningoencephalitis, colitis, or both
- Monogenic mutations differentially affect the quantity and quality of T follicular helper cells in patients with human primary immunodeficiencies
- Primary Immunodeficiency Diseases: An Update on the Classification from the International Union of Immunological Societies Expert Committee for Primary Immunodeficiency
- Corrigendum: Primary Immunodeficiency Diseases: An Update on the Classification from the International Union of Immunological Societies Expert Committee for Primary Immunodeficiency
- Péricardite purulente et infiltration colique à Salmonella enteritidis compliquée d’invagination intestinale aiguë dans un cas de déficit en IL-12Rβ1
- Le déficit en DOCK8 (dedicator of cytokinesis 8 gene) : à propos d’un nouveau cas
- Le déficit en dedicator of cytokinesis 8 gene (DOCK8) : à propos d’un nouveau cas
- Deep Dermatophytosis and Inherited CARD9 Deficiency
- Clinical Features of Candidiasis in Patients With Inherited Interleukin 12 Receptor β1 Deficiency
- 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
مجلات النشر
- Journal of Clinical Immunology × 11
- The Journal of Experimental Medicine × 5
- Annales de Dermatologie et de Vénéréologie × 3
- Journal of Allergy and Clinical Immunology × 3
- Journal of Human Immunity × 2
- Journal of Crohn s and Colitis × 2
المنشورات حسب السنة
- 20252
- 20241
- 20222
- 20212
- 20205
- 20191
- 20185
- 20172
- 20166
- 20155
التعاون العلمي
المؤسسات الشريكة : Sorbonne Paris Cité · Rockefeller University · Human Genetic of Infectious Diseases · Howard Hughes Medical Institute · Hôpital Saint-Louis
بلدان المؤلفين المشاركين : الولايات المتحدة · المملكة المتحدة · الجزائر · تونس
المؤلفون المشاركون
- Jean‐Laurent Casanova
- Anne Puel
- Laurent Abel
- Jacinta C. Bustamante
- Stéphanie Boisson‐Dupuis
- Éric Oksenhendler
- Mélanie Migaud
- Emmanuelle Jouanguy
- Quentin B. Vincent
- Alain Fischer
- Caroline Deswarte
- Bertrand Boisson
البيانات البيبليوغرافية مصدرها OpenAlex (قاعدة مفتوحة).
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