Ingvild Aukrust

2.0k total citations
41 papers, 709 citations indexed

About

Ingvild Aukrust is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Ingvild Aukrust has authored 41 papers receiving a total of 709 indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Molecular Biology, 19 papers in Genetics and 17 papers in Surgery. Recurrent topics in Ingvild Aukrust's work include Pancreatic function and diabetes (17 papers), Genetics and Neurodevelopmental Disorders (10 papers) and Genomics and Rare Diseases (6 papers). Ingvild Aukrust is often cited by papers focused on Pancreatic function and diabetes (17 papers), Genetics and Neurodevelopmental Disorders (10 papers) and Genomics and Rare Diseases (6 papers). Ingvild Aukrust collaborates with scholars based in Norway, United States and France. Ingvild Aukrust's co-authors include Torgeir Flatmark, Pål R. Njølstad, Lise Bjørkhaug, Anni Vedeler, Hanne Hollås, Janne Molnes, Stefan Johansson, Anders Molven, Gunnar Houge and Oddmund Sövik and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Molecular Biology and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Ingvild Aukrust

40 papers receiving 702 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Ingvild Aukrust Norway	16	464	275	260	129	77	41	709
Paola Benaglio United States	14	530 1.1×	324 1.2×	132 0.5×	88 0.7×	23 0.3×	21	795
Tarjinder Singh United States	8	256 0.6×	269 1.0×	322 1.2×	130 1.0×	100 1.3×	16	629
Qing V. Li United States	8	847 1.8×	218 0.8×	282 1.1×	61 0.5×	27 0.4×	9	1000
Eric D. Bankaitis United States	9	293 0.6×	236 0.9×	402 1.5×	136 1.1×	50 0.6×	11	698
Leonard Anderson United States	12	296 0.6×	153 0.6×	42 0.2×	56 0.4×	40 0.5×	18	581
Laura Erker United States	12	533 1.1×	108 0.4×	281 1.1×	11 0.1×	51 0.7×	16	918
Cristina Méndez‐Vidal Spain	16	595 1.3×	122 0.4×	32 0.1×	30 0.2×	52 0.7×	28	725
Casey L. Moulson United States	12	770 1.7×	52 0.2×	53 0.2×	43 0.3×	201 2.6×	13	1.0k
Anja A. T. Geisterfer-Lowrance United States	8	1.3k 2.8×	176 0.6×	85 0.3×	22 0.2×	107 1.4×	9	2.2k
Pratima Karnik United States	14	385 0.8×	249 0.9×	68 0.3×	46 0.4×	96 1.2×	20	752

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-authorship network of co-authors of Ingvild Aukrust

This figure shows the co-authorship network connecting the top 25 collaborators of Ingvild Aukrust. A scholar is included among the top collaborators of Ingvild Aukrust based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Ingvild Aukrust. Ingvild Aukrust is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Aukrust, Ingvild, Laurie L. Molday, Siren Berland, et al.. (2024). Functional Characterization of ABCA4 Missense Variants Aids Variant Interpretation and Phenotype Prediction in Patients With ABCA4-Retinal Dystrophies. Investigative Ophthalmology & Visual Science. 65(10). 2–2.

Molnes, Janne, André Madsen, Christine Bellanné‐Chantelot, et al.. (2024). Functional characterization of HNF4A gene variants identify promoter and cell line specific transactivation effects. Human Molecular Genetics. 33(10). 894–904. 1 indexed citations

Høberg‐Vetti, Hildegunn, Sarah Ariansen, Wenche Sjursen, et al.. (2023). Functional Analyses of Rare Germline Missense BRCA1 Variants Located within and outside Protein Domains with Known Functions. Genes. 14(2). 262–262. 1 indexed citations

Svalastoga, Pernille, Janne Molnes, Bente B. Johansson, et al.. (2023). Characterisation of HNF1A variants in paediatric diabetes in Norway using functional and clinical investigations to unmask phenotype and monogenic diabetes. Diabetologia. 66(12). 2226–2237. 1 indexed citations

Larasati, Yonika Arum, Gonzalo P. Solis, Alexey Koval, et al.. (2023). Clinical Cases and the Molecular Profiling of a Novel Childhood Encephalopathy-Causing GNAO1 Mutation P170R. Cells. 12(20). 2469–2469. 7 indexed citations

Raasakka, Arne, Janne Molnes, Ingvild Aukrust, et al.. (2022). Structural and biophysical characterization of transcription factor HNF-1A as a tool to study MODY3 diabetes variants. Journal of Biological Chemistry. 298(4). 101803–101803. 4 indexed citations

Ariansen, Sarah, Marijke Van Ghelue, Wenche Sjursen, et al.. (2022). BRCA1 Norway: comparison of classification for BRCA1 germline variants detected in families with suspected hereditary breast and ovarian cancer between different laboratories. Familial Cancer. 21(4). 389–398. 3 indexed citations

Preuß, Michael, Roelof A. J. Smit, Nathalie Chami, et al.. (2022). The contribution of functional HNF1A variants and polygenic susceptibility to risk of type 2 diabetes in ancestrally diverse populations. Diabetologia. 66(1). 116–126. 5 indexed citations

Denker, Elsa, William Norton, Laurence A. Bindoff, et al.. (2021). Chip Protein U-Box Domain Truncation Affects Purkinje Neuron Morphology and Leads to Behavioral Changes in Zebrafish. Frontiers in Molecular Neuroscience. 14. 723912–723912. 1 indexed citations

10.

Malíková, Jana, Petra Dušátková, Ingvild Aukrust, et al.. (2020). Functional Analyses of HNF1A-MODY Variants Refine the Interpretation of Identified Sequence Variants. The Journal of Clinical Endocrinology & Metabolism. 105(4). e1377–e1386. 15 indexed citations

11.

Najmi, Laeya A., Amanda J. Bennett, Ingvild Aukrust, et al.. (2020). Unsupervised Clustering of Missense Variants in HNF1A Using Multidimensional Functional Data Aids Clinical Interpretation. The American Journal of Human Genetics. 107(4). 670–682. 22 indexed citations

12.

Støve, Svein I., et al.. (2018). 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. 19(1). 47–47. 24 indexed citations

13.

Berland, Siren, Trine L. Toft‐Bertelsen, Ingvild Aukrust, et al.. (2018). A de novo Ser111Thr variant in aquaporin-4 in a patient with intellectual disability, transient signs of brain ischemia, transient cardiac hypertrophy, and progressive gait disturbance. Molecular Case Studies. 4(1). a002303–a002303. 3 indexed citations

14.

Keindl, Magdalena, et al.. (2018). The E3 SUMO ligase PIASγ is a novel interaction partner regulating the activity of diabetes associated hepatocyte nuclear factor-1α. Scientific Reports. 8(1). 12780–12780. 10 indexed citations

15.

Storbeck, Markus, Beate Horsberg Eriksen, Andreas Unger, et al.. (2017). Phenotypic extremes of BICD2-opathies: from lethal, congenital muscular atrophy with arthrogryposis to asymptomatic with subclinical features. European Journal of Human Genetics. 25(9). 1040–1048. 34 indexed citations

16.

Aukrust, Ingvild, Lise Bjørkhaug, Janne Molnes, et al.. (2013). SUMOylation of Pancreatic Glucokinase Regulates Its Cellular Stability and Activity*. Journal of Biological Chemistry. 288(8). 5951–5962. 28 indexed citations

17.

Aukrust, Ingvild, Bente B. Johansson, Janne Molnes, et al.. (2012). GCK-MODY diabetes associated with protein misfolding, cellular self-association and degradation. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1822(11). 1705–1715. 14 indexed citations

18.

Molnes, Janne, Knut Teigen, Ingvild Aukrust, 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. FEBS Journal. 278(13). 2372–2386. 19 indexed citations

19.

Aukrust, Ingvild, Lasse Evensen, Hanne Hollås, et al.. (2006). 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. 363(2). 469–481. 16 indexed citations

20.

Hollås, Hanne, Ingvild Aukrust, Stine Grimmer, et al.. (2006). Annexin A2 recognises a specific region in the 3′-UTR of its cognate messenger RNA. Biochimica et Biophysica Acta (BBA) - Molecular Cell Research. 1763(11). 1325–1334. 48 indexed citations

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.

Explore authors with similar magnitude of impact