Luis Seabra

9PUBLICATIONS
174CO-AUTHORS
Industrial molecular engineering of nucleic acids and proteinsEpigenetics (incl. genome methylation and epigenomics)AutoimmunityAllergyNeurology and neuromuscular diseases
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Publications (9)

|Sep 16, 2026
NAP1 switches from an activator to a limiter of interferon induction by trapping TBK1 in condensates.

|Jul 09, 2026
ADAR1 loss-of-function variants altering RNA editing define a new interferon-dependent psoriasis subtype.

|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 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

|Mar 14, 2024
Biallelic NAA60 variants with impaired n-terminal acetylation capacity cause autosomal recessive primary familial brain calcifications.

Viorica Chelban, Henriette Aksnes, Reza Maroofian

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Frequent Collaborators

8 joint publications

Yanick J Crow

6 joint publications

Alice Lepelley

6 joint publications

Marie-Louise Frémond

5 joint publications

Gillian I Rice