Vitenskapelig artikkel

• Kaci, Alba; Solheim, Marie Holm; Silgjerd, Trine et al. (2024). Functional characterization of HNF4A gene variants identify promoter and cell line specific transactivation effects. (ekstern lenke)
• Kuznetsova, Ksenia; Vasicek, Jakub; Skiadopoulou, Dafni et al. (2024). Bioinformatics pipeline for the systematic mining genomic and proteomic variation linked to rare diseases: The example of monogenic diabetes. (ekstern lenke)
• Pavithram, Aishwarya; Zhang, Haichen; Maloney, Kristin A. et al. (2024). In Vitro Functional Analysis Can Aid Precision Diagnostics of HNF1B-MODY. (ekstern lenke)
• Kind, Laura; Molnes, Janne; Tjora, Erling et al. (2024). Molecular mechanism of HNF-1A–mediated HNF4A gene regulation and promoter-driven HNF4A-MODY diabetes. (ekstern lenke)
• Naylor, Rochelle N.; Patel, Kashyap A.; Kettunen, Jarno L. T. et al. (2024). Precision treatment of beta-cell monogenic diabetes: a systematic review. (ekstern lenke)
• Felton, Jamie L.; Redondo, Maria J.; Oram, Richard A. et al. (2024). Islet autoantibodies as precision diagnostic tools to characterize heterogeneity in type 1 diabetes: a systematic review. (ekstern lenke)
• Semnani-Azad, Zhila; Gaillard, Romy; Hughes, Alice E. et al. (2024). Precision stratification of prognostic risk factors associated with outcomes in gestational diabetes mellitus: a systematic review. (ekstern lenke)
• Takele, Wubet Worku; Vesco, Kimberly K.; Josefson, Jami et al. (2024). Effective interventions in preventing gestational diabetes mellitus: A systematic review and meta-analysis. (ekstern lenke)
• Ahmad, Abrar; Lim, Lee-Ling; Morieri, Mario Luca et al. (2024). Precision prognostics for cardiovascular disease in Type 2 diabetes: a systematic review and meta-analysis. (ekstern lenke)
• Tobias, Deirdre K.; Merino, Jordi; Ahmad, Abrar et al. (2023). Second international consensus report on gaps and opportunities for the clinical translation of precision diabetes medicine. (ekstern lenke)
• Svalastoga, Pernille; Kaci, Alba; Molnes, Janne et al. (2023). Characterisation of HNF1A variants in paediatric diabetes in Norway using functional and clinical investigations to unmask phenotype and monogenic diabetes. (ekstern lenke)
• Jellas, Khadija el; Dušátková, Petra; Haldorsen, Ingfrid S. et al. (2022). Two New Mutations in the CEL Gene Causing Diabetes and Hereditary Pancreatitis: How to Correctly Identify MODY8 Cases. (ekstern lenke)
• Kind, Laura; Raasakka, Arne; Molnes, Janne et al. (2022). Structural and biophysical characterization of transcription factor HNF-1A as a tool to study MODY3 diabetes variants. (ekstern lenke)
• Elias-Assad, Ghadir; Saab, Raunak; Molnes, Janne et al. (2021). Maturity onset diabetes of the young type 2 (MODY2): Insight from an extended family. (ekstern lenke)
• Romuld, Ingunn Bratland; Kalleklev, Tine-Lise; Molnes, Janne et al. (2021). Impact of overweight on glucose homeostasis in MODY2 and MODY3. (ekstern lenke)
• Althari, Sara; Najmi, Laeya Abdoli; Bennett, Amanda J. et al. (2020). Unsupervised clustering of missense variants in HNF1A using multidimensional functional data aids clinical interpretation. (ekstern lenke)
• Johansson, Bente Berg; Irgens, Henrik Underthun; Molnes, Janne et al. (2017). Targeted next-generation sequencing reveals MODY in up to 6.5% of antibody-negative diabetes cases listed in the Norwegian Childhood Diabetes Registry. (ekstern lenke)
• Sagen, Jørn V.; Bjørkhaug, Lise; Haukanes, Bjørn Ivar et al. (2017). The HNF1A mutant Ala180Val: Clinical challenges in determining causality of a rare HNF1A variant in familial diabetes. (ekstern lenke)
• Najmi, Laeya Abdoli; Aukrust, Ingvild; Flannick, Jason et al. (2017). Functional investigations of HNF1A identify rare variants as risk factors for type 2 diabetes in the general population. (ekstern lenke)
• Negahdar, Maria; Aukrust, Ingvild; Molnes, Janne et al. (2014). GCK-MODY diabetes as a protein misfolding disease: The mutation R275C promotes protein misfolding, self-association and cellular degradation. (ekstern lenke)
• Flannick, Jason; Beer, Nicola L.; Bick, Alexander G. et al. (2013). Assessing the phenotypic effects in the general population of rare variants in genes for a dominant Mendelian form of diabetes. (ekstern lenke)
• Eifes, Serge; Chudasama, Kishan Kumar; Molnes, Janne et al. (2013). A novel GATA6 mutation in a child with congenital heart malformation and neonatal diabetes. (ekstern lenke)
• Søvik, Oddmund; Irgens, Henrik Underthun; Molnes, Janne et al. (2013). Monogenetic diabetes mellitus in Norway :. (ekstern lenke)
• Aukrust, Ingvild; Bjørkhaug, Lise; Negahdar, Maria et al. (2013). SUMOylation of pancreatic glucokinase regulates its cellular stability and activity. (ekstern lenke)
• Irgens, Henrik Underthun; Molnes, Janne; Johansson, Bente Berg et al. (2013). Prevalence of monogenic diabetes in the population-based Norwegian Childhood Diabetes Registry. (ekstern lenke)
• Jahnavi, S; Poovazhagi, V; Mohan, V et al. (2013). Clinical and molecular characterization of neonatal diabetes and monogenic syndromic diabetes in Asian Indian children. (ekstern lenke)
• Elbarbary, Nancy S.; Tjora, Erling; Molnes, Janne et al. (2013). An Egyptian family with H syndrome due to a novel mutation in SLC29A3 illustrating overlapping features with pigmented hypertrichotic dermatosis with insulin-dependent diabetes and Faisalabad histiocytosis. (ekstern lenke)
• Gonc, E. Nazli; Ozturk, Burcu Bulum; Haldorsen, Ingfrid S. et al. (2012). HNF1B mutation in a Turkish child with renal and exocrine pancreas insufficiency, diabetes and liver disease. (ekstern lenke)
• Johansson, Stefan; Irgens, Henrik Underthun; Chudasama, Kishankumar et al. (2012). Exome sequencing and genetic testing for MODY. (ekstern lenke)
• Negahdar, Maria; Aukrust, Ingvild; Johansson, Bente Berg et al. (2012). GCK-MODY diabetes associated with protein misfolding, cellular self-association and degradation. (ekstern lenke)
• Molnes, Janne; Teigen, Knut; Aukrust, Ingvild et al. (2011). Binding of ATP at the active site of human pancreatic glucokinase - nucleotide-induced conformational changes with possible implications for its kinetic cooperativity. (ekstern lenke)
• Sagen, Jørn V.; Bjørkhaug, Lise; Molnes, Janne et al. (2008). Diagnostic screening of MODY2/GCK mutations in the Norwegian MODY Registry. (ekstern lenke)
• Molnes, Janne; Bjørkhaug, Lise; Søvik, Oddmund et al. (2008). Catalytic activation of human glucokinase by substrate binding - residue contacts involved in the binding of D-glucose to the super-open form and conformational transitions. (ekstern lenke)
• Bjørkhaug, Lise; Molnes, Janne; Søvik, Oddmund et al. (2007). Allosteric activation of human glucokinase by free polyubiquitin chains and its ubiquitin-dependent cotranslational proteasomal degradation. (ekstern lenke)
• Tammaro, Paolo; Girard, Christophe; Molnes, Janne et al. (2005). Kir6.2 mutations causing neonatal diabetes provide new insights into Kir6.2-SUR1 interactions. (ekstern lenke)
• Gloyn, AL; Pearson, ER; Antcliff, JF et al. (2004). Activating mutations in the gene encoding the ATP-sensitive potassium-channel subunit Kir6.2 and permanent neonatal diabetes. (ekstern lenke)
• Sagen, Jørn V.; Ræder, Helge; Hathout, Eba et al. (2004). Permanent neonatal diabetes due to mutations in KCNJ11 encoding Kir6.2 - Patient characteristics and initial response to sulfonylurea therapy. (ekstern lenke)
• Njølstad, Pål Rasmus; Sagen, Jørn; Bjørkhaug, Lise et al. (2003). Permanent neonatal diabetes mellitus due to glucokinase deficiency- an inborn error of the glucose-insulin signalling pathway. (ekstern lenke)
• Njølstad, Pål Rasmus; Sagen, Jørn V.; Bjørkhaug, Lise et al. (2003). Permanent neonatal diabetes caused by glucokinase deficiency; inborn error of the glucose-insulin signaling pathway. (ekstern lenke)

Poster

• Kaci, Alba; Aukrust, Ingvild; Bjørkhaug, Lise et al. (2019). Functional characterization of HNF1A variants identified in Norwegian MODY diabetes registry can implement precision medicine in diabetes clinics. (ekstern lenke)
• Bjørkhaug, Lise; Aukrust, Ingvild; Kaci, Alba et al. (2018). Functional characterization of HNF1A variants identified in Norwegian diabetes registries can be important for precision medicine in diabetes clinics. (ekstern lenke)
• Njølstad, Pål Rasmus; Dahl-Jørgensen, Knut; Sarici, U et al. (2002). Mild diabetes or permanent neonatal diabetes: Localization of glukoinase mutations linked to severity of phenotype. (ekstern lenke)
• Njølstad, Pål Rasmus; Dahl-Jørgensen, Knut; Sarici, U et al. (2002). Mild diabetes or permanent neonatal diabetes: Localization of glucoinase mutations linked to severity of phenotype. (ekstern lenke)

Vitenskapelig foredrag

• Kaci, Alba; Aukrust, Ingvild; Njølstad, Pål Rasmus et al. (2019). Functional characterization of diabetes gene variants is important for precision medicine . (ekstern lenke)
• Haaheim, Lars Reinhardt; Cox, RJ; Molnes, Janne et al. (1997). Plasmacute - A diagnostic tool for influenza?. (ekstern lenke)

Doktorgradsavhandling

• Molnes, Janne (2012). Human pancreatic glucokinase; Structural and physico-chemical studies related to catalytic activation, kinetic cooperativity and GCK-diabetes. (ekstern lenke)

Sammendrag/abstract

• Tammaro, P; Girard, C; Molnes, Janne et al. (2005). Two novel Kir6.2 mutations affecting the ATP sensitivity of the K-ATP channel are the cause of Permanent Neonatal Diabetes. (ekstern lenke)

Hovedfagsoppgave

• Molnes, Janne (1998). Antigenic drift in the HA1 domain of influenza A(H3N2) strains isolated in Norway in 1992-6 and relationship to vaccine and reference viruses. (ekstern lenke)
• Molnes, Janne (1997). Antigenic drift in the HA<SUB>1</SUB> domain of influenza A(H3N2) strains isolated in Norway in 1992-6 and relationship to vaccine and reference viruses. (ekstern lenke)

Se en full oversikt over publikasjoner i Cristin

https://bora.uib.no/bora-xmlui/bitstream/handle/1956/6235/45423%20Molnes%20main_thesis.pdf?sequence=1&isAllowed=y