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Rapid Whole-Genome Sequencing of Mycobacterium tuberculosis Isolates Directly from Clinical Samples

Journal of clinical microbiology, 2015-07, Vol.53 (7), p.2230-2237

2015

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Comparison of Next-Generation Sequencing Technologies for Comprehensive Assessment of Full-Length Hepatitis C Viral Genomes

Journal of clinical microbiology, 2016-10, Vol.54 (10), p.2470-2484

2016

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Whole-Genome Sequencing of Chlamydia trachomatis Directly from Human Samples

Methods in molecular biology (Clifton, N.J.), 2019, Vol.2042, p.45

2019

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The genetic component of preeclampsia: A whole-exome sequencing study

PloS one, 2018-05, Vol.13 (5), p.e0197217-e0197217

2018

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EMG-normalised kinase activation during exercise is higher in human gastrocnemius compared to soleus muscle

PloS one, 2012-02, Vol.7 (2), p.e31054-e31054

2012

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Whole-Genome Enrichment Using RNA Probes and Sequencing of Chlamydia trachomatis Directly from Clinical Samples

Methods in molecular biology (Clifton, N.J.), 2017, Vol.1616, p.1

2017

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5′‐AMP activated protein kinase α2 controls substrate metabolism during post‐exercise recovery via regulation of pyruvate dehydrogenase kinase 4

The Journal of physiology, 2015-11, Vol.593 (21), p.4765-4780

2015

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Whole-genome sequencing of Chlamydia trachomatis isolates from persistently infected patients

International journal of STD & AIDS, 2022-04, Vol.33 (5), p.442-446

2022

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Genome-wide high-throughput screening to investigate essential genes involved in methicillin-resistant Staphylococcus aureus Sequence Type 398 survival

PloS one, 2014-02, Vol.9 (2), p.e89018-e89018

2014

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Identification of Novel Genetic Variants in CVID Patients With Autoimmunity, Autoinflammation, or Malignancy

Frontiers in immunology, 2020-01, Vol.10, p.3022-3022

2020

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Whole-genome enrichment and sequencing of Chlamydia trachomatis directly from clinical samples

BMC infectious diseases, 2014-11, Vol.14 (1), p.591-591

2014

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Idiopathic hypereosinophilic syndrome: A rare diagnosis in children

Clinical case reports, 2020-10, Vol.8 (10), p.2013-2016

2020

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Host Genetics, Innate Immune Responses, and Cellular Death Pathways in Poliomyelitis Patients

Frontiers in microbiology, 2019-07, Vol.10, p.1495-1495

2019

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Ectodermal dysplasia with immunodeficiency caused by a branch-point mutation in IKBKG/NEMO

Journal of allergy and clinical immunology, 2016-12, Vol.138 (6), p.1706-1709.e4

2016

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Interview with Mette Christiansen (September 2021)

Sociální pedagogika, 2021-11, Vol.9 (2), p.78-83

Christiansen, Mette

2021

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

JCI insight, 2023-11, Vol.8 (21)

2023

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Cooperation of the Cockayne Syndrome Group B Protein and Poly(ADP-Ribose) Polymerase 1 in the Response to Oxidative Stress

Molecular and Cellular Biology, 2005-09, Vol.25 (17), p.7625-7636

2005

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Islands of linkage in an ocean of pervasive recombination reveals two-speed evolution of human cytomegalovirus genomes

Virus evolution, 2016-01, Vol.2 (1), p.vew017-vew017

2016

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Cockayne syndrome group B protein is engaged in processing of DNA adducts of lipid peroxidation product trans-4-hydroxy-2-nonenal

Mutation research, 2009-06, Vol.666 (1-2), p.23

2009

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Functional crosstalk between hOgg1 and the helicase domain of Cockayne syndrome group B protein

DNA repair, 2002-11, Vol.1 (11), p.913-927

2002

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Refined Method for Droplet Microfluidics-Enabled Detection of Plasmodium falciparum Encoded Topoisomerase I in Blood from Malaria Patients

Micromachines (Basel), 2015-10, Vol.6 (10), p.1505-1513

2015

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Increased transmissibility of SARS-CoV-2 lineage B.1.1.7 by age and viral load

Nature communications, 2021-12, Vol.12 (1), p.7251-7251, Article 7251

2021

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

Pediatric blood & cancer, 2023-11, Vol.70 (11), p.e30525-e30525

2023

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Detecting mismatched donor HLA types from allograft biopsies – An easily applicable tool for improved individualized risk assessment

Human immunology, 2020-07, Vol.81 (7), p.337-341

2020

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Functional IRF3 deficiency in a patient with herpes simplex encephalitis

The Journal of experimental medicine, 2015-08, Vol.212 (9), p.1371-1379

2015

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Rapid Whole-Genome Sequencing of Mycobacterium tuberculosis Isolates Directly from Clinical Samples

Comparison of Next-Generation Sequencing Technologies for Comprehensive Assessment of Full-Length Hepatitis C Viral Genomes

Whole-Genome Sequencing of Chlamydia trachomatis Directly from Human Samples

The genetic component of preeclampsia: A whole-exome sequencing study

EMG-normalised kinase activation during exercise is higher in human gastrocnemius compared to soleus muscle

Whole-Genome Enrichment Using RNA Probes and Sequencing of Chlamydia trachomatis Directly from Clinical Samples

5′‐AMP activated protein kinase α2 controls substrate metabolism during post‐exercise recovery via regulation of pyruvate dehydrogenase kinase 4

Whole-genome sequencing of Chlamydia trachomatis isolates from persistently infected patients

Genome-wide high-throughput screening to investigate essential genes involved in methicillin-resistant Staphylococcus aureus Sequence Type 398 survival

Identification of Novel Genetic Variants in CVID Patients With Autoimmunity, Autoinflammation, or Malignancy

Whole-genome enrichment and sequencing of Chlamydia trachomatis directly from clinical samples

Idiopathic hypereosinophilic syndrome: A rare diagnosis in children

Host Genetics, Innate Immune Responses, and Cellular Death Pathways in Poliomyelitis Patients

Ectodermal dysplasia with immunodeficiency caused by a branch-point mutation in IKBKG/NEMO

Interview with Mette Christiansen (September 2021)

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

Cooperation of the Cockayne Syndrome Group B Protein and Poly(ADP-Ribose) Polymerase 1 in the Response to Oxidative Stress

Islands of linkage in an ocean of pervasive recombination reveals two-speed evolution of human cytomegalovirus genomes

Cockayne syndrome group B protein is engaged in processing of DNA adducts of lipid peroxidation product trans-4-hydroxy-2-nonenal

Functional crosstalk between hOgg1 and the helicase domain of Cockayne syndrome group B protein

Refined Method for Droplet Microfluidics-Enabled Detection of Plasmodium falciparum Encoded Topoisomerase I in Blood from Malaria Patients

Increased transmissibility of SARS-CoV-2 lineage B.1.1.7 by age and viral load

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

Detecting mismatched donor HLA types from allograft biopsies – An easily applicable tool for improved individualized risk assessment

Functional IRF3 deficiency in a patient with herpes simplex encephalitis

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