Nadja Lucas

Dresden, SN, Germany

Last Updated: 09/26/2026

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Found 13 publications

Truncating RELA variants drive autoinflammation and autoimmunity by impairing the negative feedback control of NF-κB.

Truncating RELA variants drive autoinflammation and autoimmunity by impairing the negative feedback control of NF-κB.

Journal: JCI insight

Published: August 11, 2026

A rare manifestation of STING-associated vasculopathy with onset in infancy: a case report.

A rare manifestation of STING-associated vasculopathy with onset in infancy: a case report.

Journal: Pediatric rheumatology online journal

Published: October 03, 2023

C-terminal variants in CDC42 drive type I interferon-dependent autoinflammation in NOCARH syndrome reversible by ruxolitinib.

C-terminal variants in CDC42 drive type I interferon-dependent autoinflammation in NOCARH syndrome reversible by ruxolitinib.

Journal: Clinical immunology (Orlando, Fla.)

Published: June 21, 2023

Phenotypic spectrum in recessive STING-associated vasculopathy with onset in infancy: Four novel cases and analysis of previously reported cases.

Phenotypic spectrum in recessive STING-associated vasculopathy with onset in infancy: Four novel cases and analysis of previously reported cases.

Journal: Frontiers in immunology

Published: August 27, 2022

Novel mutation and expanding phenotype in IRF2BP2 deficiency.

Novel mutation and expanding phenotype in IRF2BP2 deficiency.

Journal: Rheumatology (Oxford, England)

Published: January 18, 2022

SAMHD1 controls innate immunity by regulating condensation of immunogenic self RNA.

SAMHD1 controls innate immunity by regulating condensation of immunogenic self RNA.

Journal: Molecular cell

Published: December 14, 2021

Curative Treatment of POMP-Related Autoinflammation and Immune Dysregulation (PRAID) by Hematopoietic Stem Cell Transplantation.

Curative Treatment of POMP-Related Autoinflammation and Immune Dysregulation (PRAID) by Hematopoietic Stem Cell Transplantation.

Journal: Journal of clinical immunology

Published: March 11, 2021

Interferon signature guiding therapeutic decision making: ruxolitinib as first-line therapy for severe juvenile dermatomyositis?

Interferon signature guiding therapeutic decision making: ruxolitinib as first-line therapy for severe juvenile dermatomyositis?

Journal: Rheumatology (Oxford, England)

Published: June 16, 2020

PNPT1 mutations may cause Aicardi-Goutières-Syndrome.

PNPT1 mutations may cause Aicardi-Goutières-Syndrome.

Journal: Brain & development

Published: May 25, 2020

Severe Bleeding Diathesis in Siblings with Platelet Dysfunction due to a Novel Nonsense RASGRP2 Mutation.

Severe Bleeding Diathesis in Siblings with Platelet Dysfunction due to a Novel Nonsense RASGRP2 Mutation.

Journal: TH open : companion journal to thrombosis and haemostasis

Published: March 25, 2020

Aicardi-Goutières syndrome due to a paternal mosaic IFIH1 mutation.

Aicardi-Goutières syndrome due to a paternal mosaic IFIH1 mutation.

Journal: Neurology. Genetics

Published: June 07, 2019

Variable clinical phenotype in two siblings with Aicardi-Goutières syndrome type 6 and a novel mutation in the ADAR gene.

Variable clinical phenotype in two siblings with Aicardi-Goutières syndrome type 6 and a novel mutation in the ADAR gene.

Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society

Published: June 27, 2017

Showing 1-12 of 13

Last Updated: 09/26/2026