Njølstad PR - Search Results

1

Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors.

Warrington NM, Beaumont RN, Horikoshi M, Day FR, Helgeland Ø, Laurin C, Bacelis J, Peng S, Hao K, Feenstra B, Wood AR, Mahajan A, Tyrrell J, Robertson NR, Rayner NW, Qiao Z, Moen GH, Vaudel M, Marsit CJ, Chen J, Nodzenski M, Schnurr TM, Zafarmand MH, Bradfield JP, Grarup N, Kooijman MN, Li-Gao R, Geller F, Ahluwalia TS, Paternoster L, Rueedi R, Huikari V, Hottenga JJ, Lyytikäinen LP, Cavadino A, Metrustry S, Cousminer DL, Wu Y, Thiering E, Wang CA, Have CT, Vilor-Tejedor N, Joshi PK, Painter JN, Ntalla I, Myhre R, Pitkänen N, van Leeuwen EM, Joro R, Lagou V, Richmond RC, Espinosa A, Barton SJ, Inskip HM, Holloway JW, Santa-Marina L, Estivill X, Ang W, Marsh JA, Reichetzeder C, Marullo L, Hocher B, Lunetta KL, Murabito JM, Relton CL, Kogevinas M, Chatzi L, Allard C, Bouchard L, Hivert MF, Zhang G, Muglia LJ, Heikkinen J; EGG Consortium; Morgen CS, van Kampen AHC, van Schaik BDC, Mentch FD, Langenberg C, Luan J, Scott RA, Zhao JH, Hemani G, Ring SM, Bennett AJ, Gaulton KJ, Fernandez-Tajes J, van Zuydam NR, Medina-Gomez C, de Haan HG, Rosendaal FR, Kutalik Z, Marques-Vidal P, Das S, Willemsen G, Mbarek H, Müller-Nurasyid M, Standl M, Appel EVR, Fonvig CE, Trier C, van Beijsterveldt C… See abstract for full author list ➔ Warrington NM, et al. Among authors: njolstad pr. Nat Genet. 2019 May;51(5):804-814. doi: 10.1038/s41588-019-0403-1. Epub 2019 May 1. Nat Genet. 2019. PMID: 31043758 Free PMC article.

2

The genetic abnormality in the beta cell determines the response to an oral glucose load.

Stride A, Vaxillaire M, Tuomi T, Barbetti F, Njølstad PR, Hansen T, Costa A, Conget I, Pedersen O, Søvik O, Lorini R, Groop L, Froguel P, Hattersley AT. Stride A, et al. Among authors: njolstad pr. Diabetologia. 2002 Mar;45(3):427-35. doi: 10.1007/s00125-001-0770-9. Diabetologia. 2002. PMID: 11914749

3

Preserved insulin response to tolbutamide in hepatocyte nuclear factor-1alpha mutation carriers.

Sagen JV, Pearson ER, Johansen A, Spyer G, Søvik O, Pedersen O, Njølstad PR, Hattersley AT, Hansen T. Sagen JV, et al. Among authors: njolstad pr. Diabet Med. 2005 Apr;22(4):406-9. doi: 10.1111/j.1464-5491.2005.01439.x. Diabet Med. 2005. PMID: 15787664

4

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

5

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

6

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

7

The diabetic phenotype in HNF4A mutation carriers is moderated by the expression of HNF4A isoforms from the P1 promoter during fetal development.

Harries LW, Locke JM, Shields B, Hanley NA, Hanley KP, Steele A, Njølstad PR, Ellard S, Hattersley AT. Harries LW, et al. Among authors: njolstad pr. Diabetes. 2008 Jun;57(6):1745-52. doi: 10.2337/db07-1742. Epub 2008 Mar 20. Diabetes. 2008. PMID: 18356407 Free article.

8

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

9

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

10

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

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