Publications 2021

Berg AK, Diseth TH, Abrahamsen TG, Halvorsen K, Reinfjell T, Erichsen HC (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

Publications 2020

Strand J, Gul KA, Erichsen HC, Lundman E, Berge MC, Tromborg AK, Sorgjerd LK, Ytre-Arne M, Hogner S, Halsne R, Gaup HJ, Osnes LT, Kro GAB, Sorte HS, Morkrid L, Rowe AD, Tangeraas T, Jorgensen JV, Alme C, Bjorndalen TEH, Ronnestad AE, Lang AM, Rootwelt T, Buechner J, Overland T et al. (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

Publications 2019

Kellner ES, Krupski C, Kuehn HS, Rosenzweig SD, Yoshida N, Kojima S, Boutboul D, Latour S, Barlogis V, Galambrun C, Stray-Pedersen A, Erichsen HC, Marsh RA (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

Lam MT, Coppola S, Krumbach OHF, Prencipe G, Insalaco A, Cifaldi C, Brigida I, Zara E, Scala S, Di Cesare S, Martinelli S, Di Rocco M, Pascarella A, Niceta M, Pantaleoni F, Ciolfi A, Netter P, Carisey AF, Diehl M, Akbarzadeh M, Conti F, Merli P, Pastore A, Mortera SL, Camerini S et al. (2019)
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

Volpi S, Cicalese MP, Tuijnenburg P, Tool ATJ, Cuadrado E, Abu-Halaweh M, Ahanchian H, Alzyoud R, Akdemir ZC, Barzaghi F, Blank A, Boisson B, Bottino C, Brigida I, Caorsi R, Casanova JL, Chiesa S, Chinn IK, Duckers G, Enders A, Erichsen HC, Forbes LR, Gambin T, Gattorno M, Karimiani EG et al. (2019)
A combined immunodeficiency with severe infections, inflammation, and allergy caused by ARPC1B deficiency
J. Allergy Clin. Immunol., 143 (6), 2296-+
DOI 10.1016/j.jaci.2019.02.003

Publications 2017

Davies EG, Cheung M, Gilmour K, Maimaris J, Curry J, Furmanski A, Sebire N, Halliday N, Mengrelis K, Adams S, Bernatoniene J, Bremner R, Browning M, Devlin B, Erichsen HC, Gaspar HB, Hutchison L, Ip W, Ifversen M, Leahy TR, McCarthy E, Moshous D, Neuling K, Pac M, Papadopol A et al. (2017)
Thymus transplantation for complete DiGeorge syndrome: European experience
J. Allergy Clin. Immunol., 140 (6), 1660-+
DOI 10.1016/j.jaci.2017.03.020

Stray-Pedersen A, Sorte HS, Samarakoon P, Gambin T, Chinn IK, Akdemir ZHC, Erichsen HC, Forbes LR, Gu S, Yuan B, Jhangiani SN, Muzny DM, Rodningen OK, Sheng Y, Nicholas SK, Noroski LM, Seeborg FO, Davis CM, Canter DL, Mace EM, Vece TJ, Allen CE, Abhyankar HA, Boone PM, Beck CR et al. (2017)
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

Publications 2016

Sorte HS, Osnes LT, Fevang B, Aukrust P, Erichsen HC, Backe PH, Abrahamsen TG, Kittang OB, Overland T, Jhangiani SN, Muzny DM, Vigeland MD, Samarakoon P, Gambin T, Akdemir ZHC, Gibbs RA, Rodningen OK, Lyle R, Lupski JR, Stray-Pedersen A (2016)
A potential founder variant in CARMIL2/RLTPR in three Norwegian families with warts, molluscum contagiosum, and T-cell dysfunction
Mol. Genet. Genom. Med., 4 (6), 604-616
DOI 10.1002/mgg3.237

Publications 2015

Tesi B, Lagerstedt-Robinson K, Chiang SCC, Ben Bdira E, Abboud M, Belen B, Devecioglu O, Fadoo Z, Yeoh AEJ, Erichsen HC, Mottonen M, Akar HH, Hastbacka J, Kaya Z, Nunes S, Patiroglu T, Sabel M, Saribeyoglu ET, Tvedt TH, Unal E, Unal S, Unuvar A, Meeths M, Henter JI, Nordenskjold M et al. (2015)
Targeted high-throughput sequencing for genetic diagnostics of hemophagocytic lymphohistiocytosis
Genome Med., 7, 130
DOI 10.1186/s13073-015-0244-1

Publications 2014

Stray-Pedersen A, Backe PH, Sorte HS, Morkrid L, Chokshi NY, Erichsen HC, Gambin T, Elgstoen KBP, Bjoras M, Wlodarski MW, Kruger M, Jhangiani SN, Muzny DM, Patel A, Raymond KM, Sasa GS, Krance RA, Martinez CA, Abraham SM, Speckmann C, Ehl S, Hall P, Forbes LR, Merckoll E, Westvik J et al. (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

Publications 2007

Erichsen HC (2007)
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