Njølstad PR - Search Results

1

Genome-wide analyses of neonatal jaundice reveal a marked departure from adult bilirubin metabolism.

Solé-Navais P, Juodakis J, Ytterberg K, Wu X, Bradfield JP, Vaudel M, LaBella AL, Helgeland Ø, Flatley C, Geller F, Finel M, Zhao M, Lazarus P, Hakonarson H, Magnus P, Andreassen OA, Njølstad PR, Grant SFA, Feenstra B, Muglia LJ, Johansson S, Zhang G, Jacobsson B. Solé-Navais P, et al. Among authors: njolstad pr. Nat Commun. 2024 Aug 30;15(1):7550. doi: 10.1038/s41467-024-51947-w. Nat Commun. 2024. PMID: 39214992 Free PMC article.

2

Mutations in the CEL VNTR cause a syndrome of diabetes and pancreatic exocrine dysfunction.

Raeder H, Johansson S, Holm PI, Haldorsen IS, Mas E, Sbarra V, Nermoen I, Eide SA, Grevle L, Bjørkhaug L, Sagen JV, Aksnes L, Søvik O, Lombardo D, Molven A, Njølstad PR. Raeder H, et al. Among authors: njolstad pr. Nat Genet. 2006 Jan;38(1):54-62. doi: 10.1038/ng1708. Epub 2005 Dec 20. Nat Genet. 2006. PMID: 16369531

3

A hepatocyte nuclear factor-4 alpha gene (HNF4A) P2 promoter haplotype linked with late-onset diabetes: studies of HNF4A variants in the Norwegian MODY registry.

Raeder H, Bjørkhaug L, Johansson S, Mangseth K, Sagen JV, Hunting A, Følling I, Johansen O, Bjørgaas M, Paus PN, Søvik O, Molven A, Njølstad PR. Raeder H, et al. Among authors: njolstad pr. Diabetes. 2006 Jun;55(6):1899-903. doi: 10.2337/db05-1677. Diabetes. 2006. PMID: 16731861

4

Studies in 3,523 Norwegians and meta-analysis in 11,571 subjects indicate that variants in the hepatocyte nuclear factor 4 alpha (HNF4A) P2 region are associated with type 2 diabetes in Scandinavians.

Johansson S, Raeder H, Eide SA, Midthjell K, Hveem K, Søvik O, Molven A, Njølstad PR. Johansson S, et al. Among authors: njolstad pr. Diabetes. 2007 Dec;56(12):3112-7. doi: 10.2337/db07-0513. Epub 2007 Sep 7. Diabetes. 2007. PMID: 17827402

5

Pancreatic exocrine dysfunction in maturity-onset diabetes of the young type 3.

Vesterhus M, Raeder H, Johansson S, Molven A, Njølstad PR. Vesterhus M, et al. Among authors: njolstad pr. Diabetes Care. 2008 Feb;31(2):306-10. doi: 10.2337/dc07-1002. Epub 2007 Nov 5. Diabetes Care. 2008. PMID: 17989309

6

Genetic analysis of recently identified type 2 diabetes loci in 1,638 unselected patients with type 2 diabetes and 1,858 control participants from a Norwegian population-based cohort (the HUNT study).

Hertel JK, Johansson S, Raeder H, Midthjell K, Lyssenko V, Groop L, Molven A, Njølstad PR. Hertel JK, et al. Among authors: njolstad pr. Diabetologia. 2008 Jun;51(6):971-7. doi: 10.1007/s00125-008-0982-3. Epub 2008 Apr 24. Diabetologia. 2008. PMID: 18437351

7

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

Eide SA, Raeder H, Johansson S, Midthjell K, Søvik O, Njølstad PR, Molven A. Eide SA, et al. Among authors: njolstad pr. Diabet Med. 2008 Jul;25(7):775-81. doi: 10.1111/j.1464-5491.2008.02459.x. Diabet Med. 2008. PMID: 18513305

8

A coding polymorphism in NALP1 confers risk for autoimmune Addison's disease and type 1 diabetes.

Magitta NF, Bøe Wolff AS, Johansson S, Skinningsrud B, Lie BA, Myhr KM, Undlien DE, Joner G, Njølstad PR, Kvien TK, Førre Ø, Knappskog PM, Husebye ES. Magitta NF, et al. Among authors: njolstad pr. Genes Immun. 2009 Mar;10(2):120-4. doi: 10.1038/gene.2008.85. Epub 2008 Oct 23. Genes Immun. 2009. PMID: 18946481

9

Mutations in the VNTR of the carboxyl-ester lipase gene (CEL) are a rare cause of monogenic diabetes.

Torsvik J, Johansson S, Johansen A, Ek J, Minton J, Raeder H, Ellard S, Hattersley A, Pedersen O, Hansen T, Molven A, Njølstad PR. Torsvik J, et al. Among authors: njolstad pr. Hum Genet. 2010 Jan;127(1):55-64. doi: 10.1007/s00439-009-0740-8. Epub 2009 Sep 17. Hum Genet. 2010. PMID: 19760265

10

[Progress in diabetes genetics].

Njølstad PR, Hertel JK, Søvik O, Raeder H, Johansson S, Molven A. Njølstad PR, et al. Tidsskr Nor Laegeforen. 2010 Jun 3;130(11):1145-9. doi: 10.4045/tidsskr.09.1035. Tidsskr Nor Laegeforen. 2010. PMID: 20531501 Free article. Review. Norwegian.

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