Clémence David

5PUBLICATIONS
75CO-AUTHORS
AutoimmunityGene expression (incl. microarray and other genome-wide approaches)AllergyEpigenetics (incl. genome methylation and epigenomics)Haematology
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Publications (5)

|Mar 30, 2026
Familial lupus associated with a P2RY8 variant: Navigating the boundary between monogenic disease and genetic susceptibility to lupus.

Clémence David, Anne Welfringer-Morin, Luis Seabra

|Mar 18, 2026
Novel TLR7 gain-of-function variant and review of the associated disease spectrum.

Maud Tusseau, Claire Desvignes, Guilaine Boursier

|Mar 10, 2026
The STING HAQ haplotype and clinical non-penetrance in COPA syndrome.

Clémence David, Tifenn Wauquier, Alix de Becdelièvre

|Jun 13, 2024
Gain-of-function human UNC93B1 variants cause systemic lupus erythematosus and chilblain lupus.

Clémence David, Carlos A Arango-Franco, Mihaly Badonyi

|Feb 17, 2022
Clonal haematopoiesis of indeterminate potential and cardiovascular events in systemic lupus erythematosus (HEMATOPLUS study).

Clémence David, Nicolas Duployez, Philippine Eloy

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