Luis Seabra

8PUBLICATIONS
166CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)AutoimmunityAllergyNeurology and neuromuscular diseasesGene expression (incl. microarray and other genome-wide approaches)
Featured researcher

Get your video featured.

JoVEPublish with JoVE
Journal

Publications (8)

|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

|Mar 13, 2024
NOTCH1-Related Leukoencephalopathy: A Novel Variant and Literature Review.

Stefania Della Vecchia, Alessandra Tessa, Rosa Pasquariello

Pageof 2

Frequent Collaborators

7 joint publications

Yanick J Crow

5 joint publications

Alice Lepelley

5 joint publications

Marie-Louise Frémond

4 joint publications

Gillian I Rice