Mette T. Christiansen

Palle Juul Jensens Boulevard 99
Arhus, 8200, Denmark

Last Updated: 09/26/2026

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Found 50 publications

From Validation to Clinical Interpretation: A Flow Cytometric Th17-Cell Assay for STAT1- and STAT3-Related Inborn Errors of Immunity.

From Validation to Clinical Interpretation: A Flow Cytometric Th17-Cell Assay for STAT1- and STAT3-Related Inborn Errors of Immunity.

Journal: Scandinavian journal of immunology

Published: March 06, 2026

Constitutional methylation of the MLH1 promoter: a case series including tumors not typically caused by Lynch Syndrome.

Constitutional methylation of the MLH1 promoter: a case series including tumors not typically caused by Lynch Syndrome.

Journal: European journal of human genetics : EJHG

Published: January 24, 2026

Short-read genome sequencing at population scale: diagnostic insights from 2317 patients.

Short-read genome sequencing at population scale: diagnostic insights from 2317 patients.

Journal: European journal of human genetics : EJHG

Published: August 22, 2025

Staphylococci in high resolution: Capturing diversity within the human nasal microbiota.

Staphylococci in high resolution: Capturing diversity within the human nasal microbiota.

Journal: Cell reports

Published: January 21, 2025

Diagnostic and Monitoring Strategies for VEXAS Syndrome: Evaluating Sanger Sequencing, NGS, and the SWIM-Score.

Diagnostic and Monitoring Strategies for VEXAS Syndrome: Evaluating Sanger Sequencing, NGS, and the SWIM-Score.

Journal: Journal of clinical immunology

Published: December 08, 2024

Bi-allelic variants in POPDC2 cause an autosomal recessive syndrome presenting with cardiac conduction defects and hypertrophic cardiomyopathy.

Bi-allelic variants in POPDC2 cause an autosomal recessive syndrome presenting with cardiac conduction defects and hypertrophic cardiomyopathy.

Journal: American journal of human genetics

Published: August 18, 2024

Biallelic variants in POPDC2 cause a novel autosomal recessive syndrome presenting with cardiac conduction defects and variable hypertrophic cardiomyopathy.

Biallelic variants in POPDC2 cause a novel autosomal recessive syndrome presenting with cardiac conduction defects and variable hypertrophic cardiomyopathy.

Journal: medRxiv : the preprint server for health sciences

Published: July 15, 2024

"Developing the tool SDM:KOMPASS. Supporting shared decision making implementation processes".

"Developing the tool SDM:KOMPASS. Supporting shared decision making implementation processes".

Journal: PloS one

Published: January 17, 2024

An IKBKE variant conferring functional cGAS/STING pathway deficiency and susceptibility to recurrent HSV-2 meningitis.

An IKBKE variant conferring functional cGAS/STING pathway deficiency and susceptibility to recurrent HSV-2 meningitis.

Journal: JCI insight

Published: June 13, 2023

Kinetics of Torque Teno virus in heart transplant patients.

Kinetics of Torque Teno virus in heart transplant patients.

Journal: Human immunology

Published: May 22, 2023

Congenital pure red cell anemia and idiopathic very early onset of severe colitis cured by allogeneic hematopoetic stem cell transplantation.

Congenital pure red cell anemia and idiopathic very early onset of severe colitis cured by allogeneic hematopoetic stem cell transplantation.

Journal: Pediatric blood & cancer

Published: January 23, 2023

Low levels of the innate immune system proteins MASP-2 and MAp44 in patients with common variable immunodeficiency.

Low levels of the innate immune system proteins MASP-2 and MAp44 in patients with common variable immunodeficiency.

Journal: Scandinavian journal of immunology

Published: January 12, 2022

Showing 1-12 of 50

Last Updated: 09/26/2026