Kristian Tveten
8PUBLICATIONS
65CO-AUTHORS
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Publications (8)
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|Aug 27, 2025
ANKRD26 Gene Mutation and Thrombocytopenia-Is the Risk of Malignancy Dependent on the Mutation Variant?Eirik B Tjønnfjord, Kristian Tveten, Signe Spetalen
|Apr 22, 2025
Healthcare needs, care use and health status outcomes in adults with Bardet-Biedl syndrome: a cross-sectional study in Norway.Cecilie Fremstad Rustad, Ragnheidur Bragadottir, Hilde Nordgarden
|May 22, 2024
Comparison of the ABC and ACMG systems for variant classification.Gunnar Houge, Eirik Bratland, Ingvild Aukrust
|Feb 17, 2023
Alternative polyadenylation alters protein dosage by switching between intronic and 3'UTR sites.Nicola de Prisco, Caitlin Ford, Nathan D Elrod
|May 13, 2021
RBL2 bi-allelic truncating variants cause severe motor and cognitive impairment without evidence for abnormalities in DNA methylation or telomeric function.Nadra Samra, Shir Toubiana, Hilde Yttervik
|Dec 08, 2020
Benefits of clinical criteria and high-throughput sequencing for diagnosing children with syndromic craniosynostosis.Elin Tønne, Bernt Johan Due-Tønnessen, Inger-Lise Mero
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Frequent Collaborators
2 joint publications
A Micheil Innes
2 joint publications
Cecilie Fremstad Rustad
1 joint publications
Sandra Jansen
1 joint publications
Ilse M van der Werf
1 joint publications
Anke van Dijck
1 joint publications
Charu Kaiwar
1 joint publications
Tuula Rinne
1 joint publications
Corrado Romano
1 joint publications
David A Sweetser
1 joint publications
R Frank Kooy
