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A Novel CDC42 Variant with Impaired Thymopoiesis, IL-7R Signaling, PAK1 Binding, and TCR Repertoire Diversity

Journal of clinical immunology, 2023-11, Vol.43 (8), p.1927-1940

2023

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Altered Antibody Response to Epstein-Barr Virus in Patients With Rheumatoid Arthritis and Healthy Subjects Predisposed to the Disease. A Twin Study

Frontiers in immunology, 2021-03, Vol.12, p.650713

2021

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Clinical characteristics and real-life diagnostic approaches in all Danish children with hereditary angioedema

Orphanet journal of rare diseases, 2017-03, Vol.12 (1), p.55-55, Article 55

2017

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White blood cell mitochondrial DNA copy number is decreased in rheumatoid arthritis and linked with risk factors. A twin study

Journal of autoimmunity, 2019-01, Vol.96, p.142-146

2019

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Impact of RHD genotyping on transfusion practice in Denmark and the United States and identification of novel RHD alleles

Transfusion (Philadelphia, Pa.), 2021-01, Vol.61 (1), p.256-265

2021

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Results of noninvasive prenatal RHD testing in Gestation Week 25 are not affected by maternal body mass index

Transfusion (Philadelphia, Pa.), 2018-10, Vol.58 (10), p.2421-2425

2018

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Pyrin Inflammasome Activation Abrogates Interleukin‐1 Receptor Antagonist, Suggesting a New Mechanism Underlying Familial Mediterranean Fever Pathogenesis

Arthritis & rheumatology (Hoboken, N.J.), 2021-11, Vol.73 (11), p.2116-2126

2021

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STK4 Deficiency Impairs Innate Immunity and Interferon Production Through Negative Regulation of TBK1-IRF3 Signaling

Journal of clinical immunology, 2021, Vol.41 (1), p.109-124

2021

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The development of an indel panel for microchimerism detection

Experimental and molecular pathology, 2022-08, Vol.127, p.104804-104804, Article 104804

2022

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Gene therapy of X-linked severe combined immunodeficiency by use of a pseudotyped gammaretroviral vector

The Lancet (British edition), 2004-12, Vol.364 (9452), p.2181-2187

2004

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A case of high-titer anti-D hemolytic disease of the newborn in which late onset and mild course is associated with the D variant, RHD-CE(9)-D

Transfusion (Philadelphia, Pa.), 2014-10, Vol.54 (10), p.2463-2467

2014

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A novel ABO allele with a 21‐bp duplication identified in two unrelated European individuals with weak A expression

Transfusion medicine (Oxford, England), 2020-12, Vol.30 (6), p.508-512

2020

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Immunodeficiency Associated with a Nonsense Mutation of IKBKB

Journal of clinical immunology, 2014-11, Vol.34 (8), p.916-921

2014

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CD18 is redundant for the response to multiple vaccines: A case study

Pediatric allergy and immunology, 2019-02, Vol.30 (1), p.136-139

2019

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Infantile hemophagocytic lymphohistiocytosis in a case of chediak-higashi syndrome caused by a mutation in the LYST/CHS1 gene presenting with delayed umbilical cord detachment and diarrhea

Journal of pediatric hematology/oncology, 2015-03, Vol.37 (2), p.e73-e79

2015

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Noninvasive fetal RHD genotyping to guide targeted anti‐D prophylaxis–an external quality assessment workshop

Vox sanguinis, 2019-05, Vol.114 (4), p.386-393

2019

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Identification of a novel STAT3 mutation in a patient with hyper-IgE syndrome

Scandinavian journal of infectious diseases, 2013-03, Vol.45 (3), p.235-238

2013

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Interleukin 10 Induces the Maturation of Putative Tolerogenic Monocyte-derived Dendritic Cells as Revealed by GeneArray Analysis

American journal of immunology, 2005-04, Vol.1 (4), p.135-142

2005

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CD18 is redundant for the response to multiple vaccines: A case study

Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology, 2019, Vol.30 (1), p.136-139

2019

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Identification of a novel STAT3 mutation in a patient with hyper-IgE syndrome

Scandinavian Journal of Infectious Diseases, 2013, Vol.45 (3), p.235-238

2013

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Long COVID in a prospective cohort of home-isolated patients

Nature medicine, 2021-09, Vol.27 (9), p.1607-1613

2021

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Ovarian carcinoma histotype determination is highly reproducible, and is improved through the use of immunohistochemistry

Histopathology, 2014-06, Vol.64 (7), p.1004-1013

2014

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Major types of dietary fat and risk of coronary heart disease: a pooled analysis of 11 cohort studies

The American journal of clinical nutrition, 2009-05, Vol.89 (5), p.1425-1432

2009

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Palindromic sequence artifacts generated during next generation sequencing library preparation from historic and ancient DNA

PloS one, 2014-03, Vol.9 (3), p.e89676-e89676

2014

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Selective serotonin reuptake inhibitors versus placebo in patients with major depressive disorder. A systematic review with meta-analysis and Trial Sequential Analysis

BMC psychiatry, 2017-02, Vol.17 (1), p.58, Article 58

2017

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A Novel CDC42 Variant with Impaired Thymopoiesis, IL-7R Signaling, PAK1 Binding, and TCR Repertoire Diversity

Altered Antibody Response to Epstein-Barr Virus in Patients With Rheumatoid Arthritis and Healthy Subjects Predisposed to the Disease. A Twin Study

Clinical characteristics and real-life diagnostic approaches in all Danish children with hereditary angioedema

White blood cell mitochondrial DNA copy number is decreased in rheumatoid arthritis and linked with risk factors. A twin study

Impact of RHD genotyping on transfusion practice in Denmark and the United States and identification of novel RHD alleles

Results of noninvasive prenatal RHD testing in Gestation Week 25 are not affected by maternal body mass index

Pyrin Inflammasome Activation Abrogates Interleukin‐1 Receptor Antagonist, Suggesting a New Mechanism Underlying Familial Mediterranean Fever Pathogenesis

STK4 Deficiency Impairs Innate Immunity and Interferon Production Through Negative Regulation of TBK1-IRF3 Signaling

The development of an indel panel for microchimerism detection

Gene therapy of X-linked severe combined immunodeficiency by use of a pseudotyped gammaretroviral vector

A case of high-titer anti-D hemolytic disease of the newborn in which late onset and mild course is associated with the D variant, RHD-CE(9)-D

A novel ABO allele with a 21‐bp duplication identified in two unrelated European individuals with weak A expression

Immunodeficiency Associated with a Nonsense Mutation of IKBKB

CD18 is redundant for the response to multiple vaccines: A case study

Infantile hemophagocytic lymphohistiocytosis in a case of chediak-higashi syndrome caused by a mutation in the LYST/CHS1 gene presenting with delayed umbilical cord detachment and diarrhea

Noninvasive fetal RHD genotyping to guide targeted anti‐D prophylaxis–an external quality assessment workshop

Identification of a novel STAT3 mutation in a patient with hyper-IgE syndrome

Interleukin 10 Induces the Maturation of Putative Tolerogenic Monocyte-derived Dendritic Cells as Revealed by GeneArray Analysis

CD18 is redundant for the response to multiple vaccines: A case study

Identification of a novel STAT3 mutation in a patient with hyper-IgE syndrome

Long COVID in a prospective cohort of home-isolated patients

Ovarian carcinoma histotype determination is highly reproducible, and is improved through the use of immunohistochemistry

Major types of dietary fat and risk of coronary heart disease: a pooled analysis of 11 cohort studies

Palindromic sequence artifacts generated during next generation sequencing library preparation from historic and ancient DNA

Selective serotonin reuptake inhibitors versus placebo in patients with major depressive disorder. A systematic review with meta-analysis and Trial Sequential Analysis

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