❭ Research by medical division ❭ Paediatric & Adolescent Medicine ❭ Dept. of Rare Disorders & Disabilities [Nærland] ❭ Group members ❭ Centre for Rare Disorders ❭

Cecilie Rustad

  • Consultant, geneticist, PhD student
 
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Home Paediatric & Adolescent Medicine Dept. of Rare Disorders & Disabilities [Nærland]

  • Group members
    • Norwegian Centre for Cystic Fibrosis
    • National Competence Centre for Rare Epilepsy-Related Diagnoses
    • Nevsom
    • Centre for Rare Disorders
    • Alphabetical listing
  • Publications
  • Research projects
  • Norwegian Resource Centre for Cystic Fibrosis
  • National Competence Centre for Rare Epilepsy-Related Diagnoses
  • Nevsom
  • Centre for Rare Disorders

Recent publications

Hope S, Lin A, Rodevand L, Hübenette SJ, Quintana DS, Sønderby IE, Cheng W, Frei O, Bahrami S, Hindley GFL, Kaale A, Shadrin AA, O'Connell KS, Parker N, Djurovic S, Nærland T, Andreassen OA (2025)
Shared genetic architecture between autism spectrum disorder, loneliness, and social isolation reveals novel genetic loci
Psychiatr Genet (in press)
DOI 10.1097/YPG.0000000000000406, PubMed 41263488

Weedon-Fekjær MS, Pihlstrøm HK, Weedon-Fekjær H, Berentsen B, Hatlebakk JG, Bjerkely B, Solberg OK, Heimdal KR, Ørstavik K, Jenssen TG, Sigurdardottir S (2025)
Gastrointestinal symptoms in adults with Fabry disease and their associations with physical and mental health
BMC Gastroenterol, 25 (1), 819
DOI 10.1186/s12876-025-04439-0, PubMed 41257599

Bakke KA, Brunborg C, Midtlyng E, Helverschou SB, Skrivarhaug T (2025)
Comorbidity of Type 1 Diabetes and ADHD: A Longitudinal Cohort Study in Males and Females From the Norwegian Childhood Diabetes Registry
Pediatr Diabetes, 2025, 9574797
DOI 10.1155/pedi/9574797, PubMed 41255955

More publications

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