Authors: Lovlie, R Daly, AK Matre, GE Molven, A Steen, VM

Citation: R. Lovlie et al., Polymorphisms in CYP2D6 duplication-negative individuals with the ultrarapid metabolizer phenotype: a role for the CYP2D635 allele in ultrarapid metabolism?, PHARMACOGEN, 11(1), 2001, pp. 45-55

Authors: Njolstad, PR Sovik, O Cuesta-Munoz, A Bjorkhaug, L Massa, O Barbetti, F Undlien, DE Shiota, C Magnuson, MA Molven, A Matschinsky, FM Bell, GI

Citation: Pr. Njolstad et al., Neonatal diabetes mellitus due to complete glucokinase deficiency., N ENG J MED, 344(21), 2001, pp. 1588-1592

Authors: Sjoholt, G Gulbrandsen, AK Lovlie, R Berle, JO Molven, A Steen, VM

Citation: G. Sjoholt et al., A human myo-inositol monophosphatase gene (IMPA2) localized in a putative susceptibility region for bipolar disorder on chromosome 18p11.2: genomic structure and polymorphism screening in manic-depressive patients, MOL PSYCHI, 5(2), 2000, pp. 172-180

Authors: Bjorkhaug, L Sovik, O Bell, GI Njolstad, PR Molven, A

Citation: L. Bjorkhaug et al., A simple test for the high-frequency P291fsinsC mutation in the HNF1 alpha/MODY3 gene, DIABETOLOG, 43(6), 2000, pp. 818-819

Authors: Bjorkhaug, L Ye, HG Horikawa, Y Sovik, O Molven, A Njolstad, PR

Citation: L. Bjorkhaug et al., MODY associated with two novel hepatocyte nuclear factor-1 alpha loss-of-function mutations (P112L and Q466X), BIOC BIOP R, 279(3), 2000, pp. 792-798

Authors: Lovlie, R Gulbrandsen, AK Molven, A Steen, VM

Citation: R. Lovlie et al., Genomic structure and sequence analysis of a human inositol polyphosphate 1-phosphatase gene (INPP1), PHARMACOGEN, 9(4), 1999, pp. 517-528