P. R. Njølstad

Clinical reappraisal of SHORT syndrome with PIK3R1 mutations: toward recommendation for molecular testing and management

C. Fagour, P. Njølstad, J. Bernstein, 2016, Clinical genetics.

ISPAD Clinical Practice Consensus Guidelines 2018: The diagnosis and management of monogenic diabetes in children and adolescents

A. Hattersley, S. Ellard, M. Polak, 2018, Pediatric diabetes.

A Trans-ancestral Meta-Analysis of Genome-Wide Association Studies Reveals Loci Associated with Childhood Obesity.

Christopher D. Brown, A. Uitterlinden, M. McCarthy, 2019, Human molecular genetics.

Causes of death in childhood‐onset Type 1 diabetes: long‐term follow‐up

P. Njølstad, T. Skrivarhaug, L. Sandvik, 2017, Diabetic medicine : a journal of the British Diabetic Association.

Genome-wide analyses of vocabulary size in infancy and toddlerhood: associations with ADHD, literacy and cognition-related traits

Pashupati P. Mishra, N. Timpson, T. Ahluwalia, 2023, Biological Psychiatry.

Research Online Research Online Continuing stability of center differences in pediatric diabetes care: do Continuing stability of center differences in pediatric diabetes care: do advances in diabetes treatment improve outcome? advances in diabetes treatment improve outcome?

D. Daneman, E. Kaprio, T. Urakami, 2020 .

CIITA gene variants are associated with rheumatoid arthritis in Scandinavian populations

B. Lie, P. Njølstad, L. Alfredsson, 2012, Genes and Immunity.

Genome-Wide Analyses of Vocabulary Size in Infancy and Toddlerhood: Associations With Attention-Deficit/Hyperactivity Disorder, Literacy, and Cognition-Related Traits

Chin Yang Shapland, Pashupati P. Mishra, N. Timpson, 2023, Biological Psychiatry.

Prevalence of HNF1A (MODY3) mutations in a Norwegian population (the HUNT2 Study)

A. Molven, P. Njølstad, O. Søvik, 2008, Diabetic medicine : a journal of the British Diabetic Association.

Hyperexcitability to sulphonylurea in MODY3

P. Njølstad, O. Søvik, G. Bell, 1998, Diabetologia.