CD
Clémence David
Institut des Maladies Génétiques Imagine
Research areas: Medicine · Critical Care and Intensive Care Medicine · Clinical Nutrition and Gastroenterology · Eating Disorders and Behaviors · Central Venous Catheters and Hemodialysis
0000-0001-6455-3251
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Publications (24)
- Familial lupus associated with a P2RY8 variant: Navigating the boundary between monogenic disease and genetic susceptibility to lupus Save
- The STING HAQ haplotype and clinical non-penetrance in COPA syndrome Save
- Novel TLR7 gain-of-function variant and review of the associated disease spectrum Save
- Insights from a novel monogenic autoinflammatory disease: overview of a multicentric European cohort of 38 patients with COPA syndrome Save
- TLR mediated inflammatory disease and other type I interferonopathies Save
- Gain-of-function human UNC93B1 variants cause systemic lupus erythematosus and chilblain lupus Save
- Functional Validation of a COPA Mutation Broadens the Spectrum of COPA Syndrome Save
- Interface Gain-of-Function Mutations in TLR7 Cause Systemic and Neuro-inflammatory Disease Save
- Identification of EPX Variants in Human Eosinophilic Granulomatosis With Polyangiitis (Churg-Strauss) Save
- Clinical Non-penetrance Associated with Biallelic Mutations in the RNase H2 Complex Save
- Un cow-boy est passé par là Save
- Clonal haematopoiesis of indeterminate potential and cardiovascular events in systemic lupus erythematosus (HEMATOPLUS study) Save
- Soluble CD163 and incident cardiovascular events in patients with systemic lupus erythematosus: An observational cohort study Save
- Quand penser à une interféronopathie de type I chez l’adulte ? Save
- Susac syndrome: A scoping review Save
- Lung Inflammation in STING-Associated Vasculopathy with Onset in Infancy (SAVI) Save
- Actualités dans le syndrome de Susac Save
- Hunting for the genetic basis of Susac syndrome Save
- Primary biliary cholangitis and systemic sclerosis (Reynolds syndrome): A case–control study Save
- Chronic obstructive pulmonary disease associated with hypocomplementemic urticarial vasculitis Save