Janne Molnes

3.4k citations

35 papers · 1.1k · h-index 17

Impact in

Endocrinology, Diabetes and Metabolism top 2%
- Diabetes Management and Research
- Hyperglycemia and glycemic control in critically ill and hospitalized patients
- Diabetes Treatment and Management
Genetics top 5%
- Diabetes and associated disorders
- Genetics and Neurodevelopmental Disorders

Papers in

Surgery 34
- Pancreatic function and diabetes 33
Genetics 25
- Diabetes and associated disorders 13
- Genetics and Neurodevelopmental Disorders 8
- Genomics and Rare Diseases 6

Co-authors: Pål R. Njølstad (30 shared papers)Anders Molven (14 shared papers)Oddmund Sövik (11 shared papers)Lise Bjørkhaug (15 shared papers)Jørn V. Sagen (8 shared papers)Naim Shehadeh (2 shared papers)Helge Ræder (4 shared papers)Graeme I. Bell (3 shared papers)
Journals: Diabetes (5 papers)Pediatric Diabetes (3 papers)Journal of Biological Chemistry (3 papers)Diabetologia (3 papers)PLoS ONE (3 papers)
Partner nations: Norway United States United Kingdom

In The Last Decade

Janne Molnes

35 papers receiving 1.1k citations

Peers

Countries citing papers authored by Janne Molnes

Since Specialization

Citations

This map shows the geographic impact of Janne Molnes's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Janne Molnes with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Janne Molnes more than expected).

Fields of papers citing papers by Janne Molnes

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Janne Molnes. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Janne Molnes. The network helps show where Janne Molnes may publish in the future.

Co-authors

The 25 scholars most cited alongside Janne Molnes, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Janne Molnes Line = papers co-authored together Janne Molnes links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 35 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Permanent Neonatal Diabetes due to Mutations in KCNJ11 Encoding Kir6.2 Diabetes ·Jørn V. Sagen, Helge Ræder, Eba Hathout, Naim Shehadeh, Kolbeinn Gudmundsson, H Baevre, Dianne Abuelo, Chanika Phornphutkul, Janne Molnes, Graeme I. Bell, Anna L. Gloyn, Andrew T. Hattersley, Anders Molven, Oddmund Sövik, Pål R. Njølstad	2004	259
2	Permanent Neonatal Diabetes Caused by Glucokinase Deficiency Diabetes ·Pål R. Njølstad, Jørn V. Sagen, Lise Bjørkhaug, Stella Odili, Naim Shehadeh, Doua Bakry, S. Ümit Sarící, Faruk Alpay, Janne Molnes, Anders Molven, Oddmund Sövik, Franz M. Matschinsky	2003	135
3	Prevalence of monogenic diabetes in the population-based Norwegian Childhood Diabetes Registry Diabetologia ·Henrik Irgens, Janne Molnes, Bente B. Johansson, Monika Ringdal, Torild Skrivarhaug, Dag E. Undlien, O Søvik, Geir Joner, Anders Molven, Pål R. Njølstad	2013	92
4	Targeted next-generation sequencing reveals MODY in up to 6.5% of antibody-negative diabetes cases listed in the Norwegian Childhood Diabetes Registry Diabetologia ·Bente B. Johansson, Henrik Irgens, Janne Molnes, Paweł Sztromwasser, Ingvild Aukrust, Pétur Benedikt Júlíusson, Oddmund Sövik, Shawn Levy, Torild Skrivarhaug, Geir Joner, Anders Molven, Stefan Johansson, Pål R. Njølstad	2016	92
5	Exome Sequencing and Genetic Testing for MODY PLoS ONE ·Stefan Johansson, Henrik Irgens, Kishan Chudasama, Janne Molnes, Jan Aerts, Francisco S. Roque, Inge Jonassen, Shawn Levy, Kari Lima, Per M. Knappskog, Graeme I. Bell, Anders Molven, Pål R. Njølstad	2012	88
6	Kir6.2 mutations causing neonatal diabetes provide new insights into Kir6.2–SUR1 interactions The EMBO Journal ·Paolo Tammaro, Christophe A. Girard, Janne Molnes, Pål R. Njølstad, Frances M. Ashcroft	2005	52
7	Functional Investigations ofHNF1AIdentify Rare Variants as Risk Factors for Type 2 Diabetes in the General Population Diabetes ·Laeya A. Najmi, Ingvild Aukrust, Jason Flannick, Janne Molnes, Noël P. Burtt, Anders Molven, Leif Groop, David Altshuler, Stefan Johansson, Lise Bjørkhaug, Pål R. Njølstad	2016	51
8	Diagnostic screening of MODY2/GCKmutations in the Norwegian MODY Registry Pediatric Diabetes ·Jørn V. Sagen, Lise Bjørkhaug, Janne Molnes, Helge Ræder, Louise Grevle, Oddmund Sövik, Anders Molven, Pål R. Njølstad	2008	43
9	Clinical and molecular characterization of neonatal diabetes and monogenic syndromic diabetes in Asian Indian children Clinical Genetics ·S Jahnavi, Poovazhagi Varadarajan, Viswanathan Mohan, Dhanasekaran Bodhini, P. Raghupathy, Anandakumar Amutha, Priya Kumar, P Adhikari, M Shriraam, Tanvir Kaur, AK Das, Janne Molnes, PR Njølstad, Ranjit Unnikrishnan, Venkatesan Radha	2012	37
10	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 FEBS Journal ·Janne Molnes, Lise Bjørkhaug, Oddmund Sövik, Pål R. Njølstad, Torgeir Flatmark	2008	36
11	Epidermal Growth Factor Receptor Efficiently Activates Mitogen-Activated Protein Kinase in HeLa Cells and Hep2 Cells Conditionally Defective in Clathrin-Dependent Endocytosis Experimental Cell Research ·Lene E. Johannessen, Tove Ringerike, Janne Molnes, Inger Helene Madshus	2000	35
12	Allosteric Activation of Human Glucokinase by Free Polyubiquitin Chains and Its Ubiquitin-dependent Cotranslational Proteasomal Degradation Journal of Biological Chemistry ·Lise Bjørkhaug, Janne Molnes, Oddmund Sövik, Paål Rasmus Njølstad, Torgeir Flatmark	2007	31
13	SUMOylation of Pancreatic Glucokinase Regulates Its Cellular Stability and Activity* Journal of Biological Chemistry ·Ingvild Aukrust, Lise Bjørkhaug, M Negahdar, Janne Molnes, Bente B. Johansson, Yvonne Müller, Wilhelm Haas, Steven P. Gygi, Oddmund Sövik, Torgeir Flatmark, Rohit Kulkarni, Pål R. Njølstad	2013	28
14	Unsupervised Clustering of Missense Variants in HNF1A Using Multidimensional Functional Data Aids Clinical Interpretation The American Journal of Human Genetics ·Sara Althari, Laeya A. Najmi, Amanda J. Bennett, Ingvild Aukrust, Jana K. Rundle, Kevin Colclough, Janne Molnes, Alba Kaci, Sameena Nawaz, Timme van der Lugt, Neelam Hassanali, Anubha Mahajan, Anders Molven, Sian Ellard, Mark I. McCarthy, Lise Bjørkhaug, Pål R. Njølstad, Anna L. Gloyn	2020	22
15	Two New Mutations in the CEL Gene Causing Diabetes and Hereditary Pancreatitis: How to Correctly Identify MODY8 Cases The Journal of Clinical Endocrinology & Metabolism ·Khadija El Jellas, Petra Dušátková, Ingfrid S. Haldorsen, Janne Molnes, Erling Tjora, Bente B. Johansson, Karianne Fjeld, Stefan Johansson, Štěpánka Průhová, Leif Groop, Matthias Löhr, Pål R. Njølstad, Anders Molven	2021	21
16	An Egyptian family with H syndrome due to a novel mutation inSLC29A3illustrating overlapping features with pigmented hypertrichotic dermatosis with insulin-dependent diabetes and Faisalabad histiocytosis Pediatric Diabetes ·Nancy Samir Elbarbary, Erling Tjora, Janne Molnes, Benedicte A. Lie, Mohammad Asadul Habib, Mona A. Salem, Pål R. Njølstad	2012	20
17	Binding of ATP at the active site of human pancreatic glucokinase – nucleotide‐induced conformational changes with possible implications for its kinetic cooperativity FEBS Journal ·Janne Molnes, Knut Teigen, Ingvild Aukrust, Lise Bjørkhaug, Oddmund Sövik, Torgeir Flatmark, Pål R. Njølstad	2011	19
18	GCK-MODY diabetes associated with protein misfolding, cellular self-association and degradation Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·M Negahdar, Ingvild Aukrust, Bente B. Johansson, Janne Molnes, Anders Molven, Franz M. Matschinsky, Oddmund Sövik, Rohit Kulkarni, Torgeir Flatmark, Pål R. Njølstad, Lise Bjørkhaug	2012	14
19	HNF1B mutation in a Turkish child with renal and exocrine pancreas insufficiency, diabetes and liver disease Pediatric Diabetes ·E. Nazlı Gönç, Burcu Bulum Öztürk, Ingfrid S. Haldorsen, Janne Molnes, Heike Immervoll, Helge Ræder, Anders Molven, Oddmund Sövik, Pål R. Njølstad	2011	12
20	GCK-MODY diabetes as a protein misfolding disease: The mutation R275C promotes protein misfolding, self-association and cellular degradation Molecular and Cellular Endocrinology ·M Negahdar, Ingvild Aukrust, Janne Molnes, Marie H. Solheim, Bente B. Johansson, Jørn V. Sagen, Knut Dahl‐Jørgensen, Rohit Kulkarni, Oddmund Sövik, Torgeir Flatmark, Pål R. Njølstad, Lise Bjørkhaug	2013	11

About Janne Molnes

Janne Molnes is a scholar working on Surgery, Genetics, Molecular Biology, Endocrinology, Diabetes and Metabolism and Cell Biology, having authored 35 papers that have together received 1.1k indexed citations. Recurring topics across this work include Pancreatic function and diabetes (33 papers), Diabetes and associated disorders (13 papers), Metabolism, Diabetes, and Cancer (12 papers), Genetics and Neurodevelopmental Disorders (8 papers), Diabetes Treatment and Management (7 papers), Genomics and Rare Diseases (6 papers), Diabetes Management and Research (5 papers) and Endoplasmic Reticulum Stress and Disease (4 papers). The work is most often cited by research in Endocrinology, Diabetes and Metabolism (533 citations), Genetics (659 citations), Surgery (950 citations), Molecular Biology (483 citations) and Pathology and Forensic Medicine (84 citations). Janne Molnes has collaborated with scholars based in Norway, United States and United Kingdom. Frequent co-authors include Pål R. Njølstad, Anders Molven, Oddmund Sövik, Lise Bjørkhaug, Jørn V. Sagen, Naim Shehadeh, Helge Ræder, Graeme I. Bell, Henrik Irgens and Bente B. Johansson. Their work appears in journals such as Diabetes, Pediatric Diabetes, Journal of Biological Chemistry, Diabetologia and PLoS ONE.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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