Hans Christian Erichsen Landsverk
- PhD; MD
- +47 23 07 39 03
Publications 2024
NUDCD3 deficiency disrupts V(D)J recombination to cause SCID and Omenn syndrome
Sci Immunol, 9 (95), eade5705
DOI 10.1126/sciimmunol.ade5705, PubMed 38787962
Publications 2021
Primary antibody deficiency: The impact on the quality of life and mental health of affected children and their parents
Acta Paediatr, 110 (5), 1645-1652
DOI 10.1111/apa.15752, PubMed 33420742
Publications 2020
Second-Tier Next Generation Sequencing Integrated in Nationwide Newborn Screening Provides Rapid Molecular Diagnostics of Severe Combined Immunodeficiency
Front Immunol, 11, 1417
DOI 10.3389/fimmu.2020.01417, PubMed 32754152
Publications 2019
Allogeneic hematopoietic stem cell transplant outcomes for patients with dominant negative IKZF1/IKAROS mutations
J Allergy Clin Immunol, 144 (1), 339-342
DOI 10.1016/j.jaci.2019.03.025, PubMed 30965037
A novel disorder involving dyshematopoiesis, inflammation, and HLH due to aberrant CDC42 function
J Exp Med, 216 (12), 2778-2799
DOI 10.1084/jem.20190147, PubMed 31601675
A combined immunodeficiency with severe infections, inflammation, and allergy caused by ARPC1B deficiency
J Allergy Clin Immunol, 143 (6), 2296-2299
DOI 10.1016/j.jaci.2019.02.003, PubMed 30771411
Publications 2017
Thymus transplantation for complete DiGeorge syndrome: European experience
J Allergy Clin Immunol, 140 (6), 1660-1670.e16
DOI 10.1016/j.jaci.2017.03.020, PubMed 28400115
Publications 2016
A potential founder variant in CARMIL2/RLTPR in three Norwegian families with warts, molluscum contagiosum, and T-cell dysfunction
Mol Genet Genomic Med, 4 (6), 604-616
DOI 10.1002/mgg3.237, PubMed 27896283
Primary immunodeficiency diseases: Genomic approaches delineate heterogeneous Mendelian disorders
J Allergy Clin Immunol, 139 (1), 232-245
DOI 10.1016/j.jaci.2016.05.042, PubMed 27577878
Publications 2015
Targeted high-throughput sequencing for genetic diagnostics of hemophagocytic lymphohistiocytosis
Genome Med, 7, 130
DOI 10.1186/s13073-015-0244-1, PubMed 26684649
Publications 2014
PGM3 mutations cause a congenital disorder of glycosylation with severe immunodeficiency and skeletal dysplasia
Am J Hum Genet, 95 (1), 96-107
DOI 10.1016/j.ajhg.2014.05.007, PubMed 24931394
Publications 2008
Genetic variation in sodium-dependent vitamin C transporters SLC23A1 and SLC23A2 and risk of advanced colorectal adenoma
Nutr Cancer, 60 (5), 652-9
DOI 10.1080/01635580802033110, PubMed 18791929
Publications 2007
Genomic and functional analysis of the sodium-dependent vitamin C transporter SLC23A1-SVCT1
Genes Nutr, 2 (1), 143-5
DOI 10.1007/s12263-007-0040-7, PubMed 18850166
Single nucleotide polymorphisms in genes encoding vitaminC transport proteins and inflammatory cytokines: risk of colon adenoma and preterm birth
In Series of dissertations submitted to the Faculty of Medicine, University of Oslo, Unipub, Oslo, no. 477, 1 b. (flere pag.)
BIBSYS 070353905, ISBN 978-82-8072-683-4
Publications 2005
Risk of spontaneous preterm birth is associated with common proinflammatory cytokine polymorphisms
Epidemiology, 16 (4), 469-77
DOI 10.1097/01.ede.0000164539.09250.31, PubMed 15951664
Risk of small-for-gestational age is associated with common anti-inflammatory cytokine polymorphisms
Epidemiology, 16 (4), 478-86
DOI 10.1097/01.ede.0000164535.36412.6b, PubMed 15951665
Genetic variation in the sodium-dependent vitamin C transporters, SLC23A1, and SLC23A2 and risk for preterm delivery
Am J Epidemiol, 163 (3), 245-54
DOI 10.1093/aje/kwj035, PubMed 16357110
Publications 2004
Comparison of the genomic structure and variation in the two human sodium-dependent vitamin C transporters, SLC23A1 and SLC23A2
Hum Genet, 115 (4), 285-94
DOI 10.1007/s00439-004-1167-x, PubMed 15316768
Publications 2003
Association between chronic disseminated candidiasis in adult acute leukemia and common IL4 promoter haplotypes
J Infect Dis, 187 (7), 1153-6
DOI 10.1086/368345, PubMed 12660931