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Gillian Rice

14PUBLICATIONS
219CO-AUTHORS
AllergySensory systemsNeurogeneticsEpigenetics (incl. genome methylation and epigenomics)Innate immunity
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Journal

Publications (14)

Sort by Publication Date:
|Mar 10, 2026
The STING HAQ haplotype and clinical non-penetrance in COPA syndrome.

Clémence David, Tifenn Wauquier, Alix de Becdelièvre

|Jan 09, 2026
De novo and inherited dominant variants in U4 and U6 snRNA genes cause retinitis pigmentosa.

Mathieu Quinodoz, Kim Rodenburg, Zuzana Cvackova

|Jun 24, 2025
Publisher Correction: Analysis of R-loop forming regions identifies RNU2-2 and RNU5B-1 as neurodevelopmental disorder genes.

Adam Jackson, Nishi Thaker, Alexander Blakes

|May 29, 2025
Analysis of R-loop forming regions identifies RNU2-2 and RNU5B-1 as neurodevelopmental disorder genes.

Adam Jackson, Nishi Thaker, Alexander Blakes

|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 25, 2024
Type I interferon regulates interleukin-1beta and IL-18 production and secretion in human macrophages.

Rodrigo Díaz-Pino, Gillian I Rice, Diego San Felipe

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Frequent Collaborators

5 joint publications

Yanick J Crow

4 joint publications

Marie-Louise Frémond

4 joint publications

Luis Seabra

4 joint publications

Alice Lepelley

3 joint publications

Jamie M Ellingford

3 joint publications

Brigitte Bader-Meunier

3 joint publications

John H Livingston

3 joint publications

Raymond T O'Keefe

3 joint publications

Erika Della Mina

3 joint publications

Sam Griffiths-Jones

Frequent Collaborators

5 joint publications

Yanick J Crow

4 joint publications

Marie-Louise Frémond

4 joint publications

Luis Seabra

4 joint publications

Alice Lepelley

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