Product
Help
Pricing
About
Jobs
Log in
Get started
Author
Add to collection
Janne Molnes
Observed names:
J Molnes,
J. Molnes,
JANNE MOLNES,
Molnes, Janne
Institutions:
Haukeland University Hospital,
University of Bergen
Observed institutions:
University of Copenhagen,
American Diabetes Association,
University of Oslo,
Haukeland University Hospital,
Novo Nordisk Foundation Center for Basic Metabolic Research,
University of Bergen
show all 6
ORCID:
0000-0002-9146-7874
Observed ORCID:
0000-0002-9146-7874
OpenAlex ID:
A5065228244
Activating Mutations in the Gene Encoding the ATP-Sensitive Potassium-Channel Subunit Kir6.2 and Permanent Neonatal Diabetes
2004
·
Anna L. Gloyn
, Ewan R. Pearson
, et al.
·
New England Journal of Medicine
·
1,143
Permanent Neonatal Diabetes due to Mutations in KCNJ11 Encoding Kir6.2
2004
·
Jørn V. Sagen
, Helge Ræder
, et al.
·
Diabetes
·
333
PDF
Second international consensus report on gaps and opportunities for the clinical translation of precision diabetes medicine
2023
·
Deirdre K. Tobias
, Jordi Merino
, et al.
·
Nature Medicine
·
251
PDF
Permanent Neonatal Diabetes Caused by Glucokinase Deficiency
2003
·
Pål R. Njølstad
, Jørn V. Sagen
, et al.
·
Diabetes
·
192
Precision subclassification of type 2 diabetes: a systematic review
2023
·
Shivani Misra
, Robert Wagner
, et al.
·
Communications Medicine
·
139
PDF
Assessing the phenotypic effects in the general population of rare variants in genes for a dominant Mendelian form of diabetes
2013
·
Jason Flannick
, Nicola L Beer
, et al.
·
Nature Genetics
·
137
Targeted next-generation sequencing reveals MODY in up to 6.5% of antibody-negative diabetes cases listed in the Norwegian Childhood Diabetes Registry
2016
·
Bente B. Johansson
, Henrik U. Irgens
, et al.
·
Diabetologia
·
134
PDF
Prevalence of monogenic diabetes in the population-based Norwegian Childhood Diabetes Registry
2013
·
H. U. Irgens
, J. Molnes
, et al.
·
Diabetologia
·
127
PDF
Exome Sequencing and Genetic Testing for MODY
2012
·
Stefan Johansson
, Henrik Irgens
, et al.
·
PLoS ONE
·
112
PDF
Functional Investigations ofHNF1AIdentify Rare Variants as Risk Factors for Type 2 Diabetes in the General Population
2016
·
Laeya Abdoli Najmi
, Ingvild Aukrust
, et al.
·
Diabetes
·
76
PDF
Precision prognostics for cardiovascular disease in Type 2 diabetes: a systematic review and meta-analysis
2024
·
Abrar Ahmad
, Lee-Ling Lim
, et al.
·
Communications Medicine
·
73
PDF
Effective interventions in preventing gestational diabetes mellitus: A systematic review and meta-analysis
2024
·
Wubet Worku Takele
, Kimberly K. Vesco
, et al.
·
Communications Medicine
·
68
PDF
Islet autoantibodies as precision diagnostic tools to characterize heterogeneity in type 1 diabetes: a systematic review
2024
·
Jamie L. Felton
, Maria J. Redondo
, et al.
·
Communications Medicine
·
66
PDF
Kir6.2 mutations causing neonatal diabetes provide new insights into Kir6.2–SUR1 interactions
2005
·
Paolo Tammaro
, Christophe Girard
, et al.
·
The EMBO Journal
·
62
PDF
Diagnostic screening of MODY2/GCKmutations in the Norwegian MODY Registry
2008
·
Jørn V Sagen
, Lise Bjørkhaug
, et al.
·
Pediatric Diabetes
·
57
PDF
The use of precision diagnostics for monogenic diabetes: a systematic review and expert opinion
2023
·
Rinki Murphy
, Kevin Colclough
, et al.
·
Communications Medicine
·
56
PDF
Treatment effect heterogeneity following type 2 diabetes treatment with GLP1-receptor agonists and SGLT2-inhibitors: a systematic review
2023
·
Katherine G. Young
, Eram Haider McInnes
, et al.
·
Communications Medicine
·
49
PDF
Two New Mutations in the CEL Gene Causing Diabetes and Hereditary Pancreatitis: How to Correctly Identify MODY8 Cases
2021
·
Khadija El Jellas
, Petra Dušátková
, et al.
·
The Journal of Clinical Endocrinology & Metabolism
·
49
PDF
Precision gestational diabetes treatment: a systematic review and meta-analyses
2023
·
Jamie L. Benham
, Véronique Gingras
, et al.
·
Communications Medicine
·
48
PDF
Clinical and molecular characterization of neonatal diabetes and monogenic syndromic diabetes in Asian Indian children
2012
·
S Jahnavi
, V Poovazhagi
, et al.
·
Clinical Genetics
·
47
Precision treatment of beta-cell monogenic diabetes: a systematic review
2024
·
Rochelle N. Naylor
, Kashyap A. Patel
, et al.
·
Communications Medicine
·
43
Precision stratification of prognostic risk factors associated with outcomes in gestational diabetes mellitus: a systematic review
2024
·
Zhila Semnani-Azad
, Romy Gaillard
, et al.
·
Communications Medicine
·
43
PDF
Epidermal Growth Factor Receptor Efficiently Activates Mitogen-Activated Protein Kinase in HeLa Cells and Hep2 Cells Conditionally Defective in Clathrin-Dependent Endocytosis
2000
·
Lene Elisabeth Johannessen
, Tove Ringerike
, et al.
·
Experimental Cell Research
·
42
Unsupervised Clustering of Missense Variants in HNF1A Using Multidimensional Functional Data Aids Clinical Interpretation
2020
·
Sara Althari
, Laeya A. Najmi
, et al.
·
The American Journal of Human Genetics
·
40
PDF
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
2008
·
Janne Molnes
, Lise Bjørkhaug
, et al.
·
FEBS Journal
·
38
Show more works
View as search
Works count:
68
Citation count:
3,863
H-index:
30
I10-index:
44
Year
Topic
Type