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JAMA Dermatology|December 18, 2014
Familial chilblain lupus due to a novel mutation in the exonuclease III domain of 3' repair exonuclease 1 (TREX1)Claudia Günther, Nicole Berndt, Christine Wolf, et al.
Seminars in Immunopathology|May 23, 2015
Type I interferonopathies--an expanding disease spectrum of immunodysregulationMin Ae Lee-Kirsch, Christine Wolf, Stefanie Kretschmer, et al.
Molecular and Cellular Pediatrics|September 12, 2024
Monogenic lupus - from gene to targeted therapyKatharina Menzel, Kateryna Novotna, Nivya Jeyakumar, et al.
Pediatric Rheumatology Online Journal|September 9, 2015
Severe immune dysregulation with neurological impairment and minor bone changes in a child with spondyloenchondrodysplasia due to two novel mutations in the ACP5 geneHermann Girschick, Christine Wolf, Henner Morbach, et al.
Pediatric Rheumatology Online Journal|January 4, 2024
A rare manifestation of STING-associated vasculopathy with onset in infancy: a case reportSophia Weidler, Sarah Koss, Christine Wolf, et al.
Annual Review of Medicine|November 5, 2016
The Type I InterferonopathiesMin Ae Lee-Kirsch
The Journal of Clinical Investigation|January 18, 2022
Sensing of RNA stress by mTORC1 drives autoinflammationMin Ae Lee-Kirsch
Methods in Molecular Biology (Clifton, N.J.)|October 19, 2017
Single Cell Gel Electrophoresis for the Detection of Genomic RibonucleotidesBarbara Kind, Christine Wolf, Kerstin Engel, et al.
Stem Cell Research|August 26, 2022
Generation of induced pluripotent stem cell lines from two patients with Aicardi-Goutières syndrome type 1 due to biallelic TREX1 mutationsVanessa Hänchen, Stefanie Kretschmer, Christine Wolf, et al.
Stem Cell Research|September 17, 2022
Generation of induced pluripotent stem cell lines from three patients with Aicardi-Goutières syndrome type 5 due to biallelic SAMDH1 mutationsVanessa Hänchen, Stefanie Kretschmer, Christine Wolf, et al.
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