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Asbjørg Stray-Pedersen

Norway

Research Interests

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Professors in Norway Professors in Immunology Immunology professors in Norway

Articles (20)

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Collaborators (16)

Hilde Nilsen

Professor

University of Oslo

NORWAY

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Malgorzata Borowiak

Professor, Program Leader

Adam Mickiewicz University in Poznań

POLAND

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Gareth Sullivan

PI and Senior Forsker

Oslo University Hospital

NORWAY

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Laurent Ferron

University College London

UNITED KINGDOM

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Kirsi Jahnukainen

University of Helsinki

FINLAND

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Jolan E. Walter

UNITED STATES

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Simon Eastham

University of Bristol

UNITED KINGDOM

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Bernard Malissen

Researcher / CNRS Investigator (Directeur de Recherche de Classe Exceptionnelle)

CNRS

FRANCE

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Evandro F Fang

Group Leader

University of Oslo

NORWAY

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Joan Boyes

Associate Professor

University of Leeds

UNITED KINGDOM

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Panagiotis Baliakas

Uppsala University

SWEDEN

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Johannes Raedler

GERMANY

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Venetia Bigley

Clinical Senior Lecturer/Hon Consultant

Newcastle University

UNITED KINGDOM

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Mana Momenilandi

Imagine Institute for Genetic Diseases

FRANCE

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Katta Girisha

Professor

Sultan Qaboos University

OMAN

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Outi Kilpivaara

University of Helsinki

FINLAND

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Asbjørg Stray-Pedersen

Research Interests

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Articles (20)

Transcriptional Profiling Shows Dampening of Interferon Gene Signatures by NAD<sup>+</sup> Augmentation in Ataxia-Telangiectasia

The c.64 + 2 T > A Founder Variant Hits Home: Report on 14 Patients Expands the Phenotypic Landscape of Inherited ARPC1B Deficiency — a Comparative Analysis

A pathological missense mutation in the deubiquitinase USP5 leads to insensitivity to pain

How to manage patients with germline DDX41 variants

<i>NUDCD3</i> deficiency disrupts V(D)J recombination to cause SCID and Omenn syndrome.

Newborn Genetic Screening—Still a Role for Sanger Sequencing in the Era of NGS

Long‐Term Nicotinamide Riboside Use Improves Coordination and Eye Movements in Ataxia Telangiectasia

Aagenaes syndrome/lymphedema cholestasis syndrome 1 is caused by a founder variant in the 5’-untranslated region of UNC45A

Adult presentation of ornithine transcarbamylase deficiency: a possible cause of hyperammonemia after high-dose chemotherapy and stem cell transplantation

Persontilpasset medisin ved utviklingsforstyrrelser

Human CARMIL2 deficiency underlies a broader immunological and clinical phenotype than CD28 deficiency.

A Nationwide Study of GATA2 Deficiency in Norway—the Majority of Patients Have Undergone Allo-HSCT

En mann i 6o-årene med kondritt og benmargssvikt

Human NK cell deficiency as a result of biallelic mutations in MCM10.

Next-generation sequencing of newborn screening genes: the accuracy of short-read mapping.

Disease-associated CTNNBL1 mutation impairs somatic hypermutation by decreasing nuclear AID.

Disease-associated CTNNBL1 mutation impairs somatic hypermutation by decreasing nuclear AID

Second-Tier Next Generation Sequencing Integrated in Nationwide Newborn Screening Provides Rapid Molecular Diagnostics of Severe Combined Immunodeficiency.

Performance of Expanded Newborn Screening in Norway Supported by Post-Analytical Bioinformatics Tools and Rapid Second-Tier DNA Analyses.

Delayed Radiation Myelopathy in a Child With Hodgkin Lymphoma and ARTEMIS Mutation.

Collaborators (16)

Hilde Nilsen

Malgorzata Borowiak

Gareth Sullivan

Laurent Ferron

Kirsi Jahnukainen

Jolan E. Walter

Simon Eastham

Bernard Malissen

Evandro F Fang

Joan Boyes

Panagiotis Baliakas

Johannes Raedler

Venetia Bigley

Mana Momenilandi

Katta Girisha

Outi Kilpivaara

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