Ingvild Aukrust

2.0k citations

41 papers · 709 indexed · h-index 16

Impact in

Genetics top 10%
- Diabetes and associated disorders
- Genetics and Neurodevelopmental Disorders
Endocrinology, Diabetes and Metabolism top 10%
- Diabetes Management and Research

Papers in ⓘ

Genetics 19
- Genetics and Neurodevelopmental Disorders 10
- Genomics and Rare Diseases 6
Immunology and Allergy 4
- Cell Adhesion Molecules Research 4

Co-authors: Torgeir Flatmark (9 shared papers)Pål R. Njølstad (17 shared papers)Lise Bjørkhaug (16 shared papers)Hanne Hollås (5 shared papers)Anni Vedeler (5 shared papers)Janne Molnes (12 shared papers)Stefan Johansson (8 shared papers)Anders Molven (7 shared papers)
Journals: Diabetologia (3 papers)Acta Ophthalmologica (2 papers)Diabetes (2 papers)Journal of Biological Chemistry (2 papers)Molecular and Cellular Endocrinology (2 papers)
Partner nations: Norway United States United Kingdom

In The Last Decade

Ingvild Aukrust

40 papers receiving 702 citations

Peers

Countries citing papers authored by Ingvild Aukrust

Since Specialization

Citations

This map shows the geographic impact of Ingvild Aukrust'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 Ingvild Aukrust with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ingvild Aukrust more than expected).

Fields of papers citing papers by Ingvild Aukrust

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Ingvild Aukrust. 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 Ingvild Aukrust. The network helps show where Ingvild Aukrust may publish in the future.

Co-authors

The 25 scholars most cited alongside Ingvild Aukrust, 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 Ingvild Aukrust Line = papers co-authored together Ingvild Aukrust 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 41 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	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
2	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
3	Annexin A2 recognises a specific region in the 3′-UTR of its cognate messenger RNA Biochimica et Biophysica Acta (BBA) - Molecular Cell Research ·Hanne Hollås, Ingvild Aukrust, Stine Grimmer, Elin Strand, Torgeir Flatmark, Anni Vedeler	2006	48
4	STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity Orphanet Journal of Rare Diseases ·Ketil Heimdal, Mònica Sánchez-Guixé, Ingvild Aukrust, Jens Bollerslev, Ove Bruland, Greg Eigner Jablonski, Anne Kjersti Erichsen, (unknown), Jeanette Koht, Sigrid Erdal, Torunn Fiskerstrand, Bjørn Ivar Haukanes, Helge Boman, Lise Bjørkhaug, Chantal Tallaksen, Per M. Knappskog, Stefan Johansson	2014	43
5	The intronic ABCA4 c.5461‐10T>C variant, frequently seen in patients with Stargardt disease, causes splice defects and reduced ABCA4 protein level Acta Ophthalmologica ·Ingvild Aukrust, Ragnhild Wivestad Jansson, Cecilie Bredrup, Hilde E. Rusaas, Siren Berland, Agnete Jørgensen, Marte G. Haug, Eyvind Rødahl, Gunnar Houge, Per M. Knappskog	2016	40
6	The mRNA-binding Site of Annexin A2 Resides in Helices C–D of its Domain IV Journal of Molecular Biology ·Ingvild Aukrust, Hanne Hollås, Elin Strand, Lasse Evensen, Gilles Travé, Torgeir Flatmark, Anni Vedeler	2007	37
7	Phenotypic extremes of BICD2-opathies: from lethal, congenital muscular atrophy with arthrogryposis to asymptomatic with subclinical features European Journal of Human Genetics ·Markus Storbeck, Beate Horsberg Eriksen, Andreas Unger, Irmgard Hölker, Ingvild Aukrust, Lilian A. Martinez-Carrera, Wolfgang A. Linke, A. Ferbert, Raoul Heller, Matthias Vorgerd, Gunnar Houge, Brunhilde Wirth	2017	34
8	High Incidence of HeterozygousABCC8andHNF1AMutations in Czech Patients With Congenital Hyperinsulinism The Journal of Clinical Endocrinology & Metabolism ·Klára Roženková, Jana Malíková, Azizun Nessa, Lenka Dušátková, Lise Bjørkhaug, Barbora Obermannová, Petra Dušátková, Jitka Kytnarová, Ingvild Aukrust, Laeya A. Najmi, Blanka Rypáčková, Zdenĕk Šumnı́k, Jan Lebl, Pål R. Njølstad, Khalid Hussain, Štěpánka Průhová	2015	33
9	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
10	Ubiquitinated annexin A2 is enriched in the cytoskeleton fraction FEBS Letters ·Silje U. Lauvrak, Hanne Hollås, Anne P. Døskeland, Ingvild Aukrust, Torgeir Flatmark, Anni Vedeler	2004	28
11	NAA10 dysfunction with normal NatA-complex activity in a girl with non-syndromic ID and a de novo NAA10 p.(V111G) variant – a case report BMC Medical Genetics ·Nina McTiernan, Svein I. Støve, Ingvild Aukrust, Marita Torrisen Mårli, Line M. Myklebust, Gunnar Houge, Thomas Arnesen	2018	24
12	Post‐translational modifications of Annexin A2 are linked to its association with perinuclear nonpolysomal mRNP complexes FEBS Open Bio ·Ingvild Aukrust, Linn Andersen Rosenberg, Mia Madeleine Ankerud, Vibeke Bertelsen, Hanne Hollås, Jaakko Saraste, Ann Kari Grindheim, Anni Vedeler	2016	24
13	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
14	In vitro characterization of six STUB1 variants in spinocerebellar ataxia 16 reveals altered structural properties for the encoded CHIP proteins Bioscience Reports ·Yasaman Pakdaman, Mònica Sánchez-Guixé, Rune Kleppe, Sigrid Erdal, Helene J. Bustad, Lise Bjørkhaug, Kristoffer Haugarvoll, Charalampos Tzoulis, Ketil Heimdal, Per M. Knappskog, Stefan Johansson, Ingvild Aukrust	2017	20
15	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
16	Engineering, Biophysical Characterisation and Binding Properties of a Soluble Mutant form of Annexin A2 Domain IV that Adopts a Partially Folded Conformation Journal of Molecular Biology ·Ingvild Aukrust, Lasse Evensen, Hanne Hollås, Frode S. Berven, Roger Atkinson, Gilles Travé, Torgeir Flatmark, Anni Vedeler	2006	16
17	Functional Analyses of HNF1A-MODY Variants Refine the Interpretation of Identified Sequence Variants The Journal of Clinical Endocrinology & Metabolism ·Jana Malíková, Alba Kaci, Petra Dušátková, Ingvild Aukrust, Janniche Torsvik, Klára Veselá, Pavla Dvorakova Kankova, Pål R. Njølstad, Štěpánka Průhová, Lise Bjørkhaug	2020	15
18	DominantARL3-related retinitis pigmentosa Ophthalmic Genetics ·Josephine Prener Holtan, Knut Teigen, Ingvild Aukrust, Ragnheiður Bragadóttir, Gunnar Houge	2019	15
19	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
20	Genetic Dominant Variants in STUB1, Segregating in Families with SCA48, Display In Vitro Functional Impairments Indistinctive from Recessive Variants Associated with SCAR16 International Journal of Molecular Sciences ·Yasaman Pakdaman, Siren Berland, Helene J. Bustad, Sigrid Erdal, Bryony A. Thompson, Paul A. James, Kjersti Nesheim Power, Ståle Ellingsen, Martin Krooni, Line Iden Berge, Adrienne Sexton, Laurence A. Bindoff, Per M. Knappskog, Stefan Johansson, Ingvild Aukrust	2021	13

About Ingvild Aukrust

Ingvild Aukrust is a scholar working on Genetics, Immunology and Allergy, Endocrinology, Diabetes and Metabolism, Molecular Biology and Surgery, having authored 41 papers that have together received 709 indexed citations. Recurring topics across this work include Pancreatic function and diabetes (17 papers), Genetics and Neurodevelopmental Disorders (10 papers), Genomics and Rare Diseases (6 papers), Metabolism, Diabetes, and Cancer (5 papers), S100 Proteins and Annexins (5 papers), Endoplasmic Reticulum Stress and Disease (4 papers), Cell Adhesion Molecules Research (4 papers) and RNA Research and Splicing (4 papers). The work is most often cited by research in Genetics (275 citations), Endocrinology, Diabetes and Metabolism (129 citations), Molecular Biology (464 citations), Surgery (260 citations) and Cell Biology (77 citations). Ingvild Aukrust has collaborated with scholars based in Norway, United States and United Kingdom. Frequent co-authors include Torgeir Flatmark, Pål R. Njølstad, Lise Bjørkhaug, Hanne Hollås, Anni Vedeler, Janne Molnes, Stefan Johansson, Anders Molven, Gunnar Houge and Oddmund Sövik. Their work appears in journals such as Diabetologia, Acta Ophthalmologica, Diabetes, Journal of Biological Chemistry and Molecular and Cellular Endocrinology.

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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