Øyvind L. Busk

844 total citations
12 papers, 244 citations indexed

About

Øyvind L. Busk is a scholar working on Cellular and Molecular Neuroscience, Genetics and Neurology. According to data from OpenAlex, Øyvind L. Busk has authored 12 papers receiving a total of 244 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Cellular and Molecular Neuroscience, 3 papers in Genetics and 2 papers in Neurology. Recurrent topics in Øyvind L. Busk's work include Hereditary Neurological Disorders (4 papers), Genetic Neurodegenerative Diseases (4 papers) and Neurological diseases and metabolism (2 papers). Øyvind L. Busk is often cited by papers focused on Hereditary Neurological Disorders (4 papers), Genetic Neurodegenerative Diseases (4 papers) and Neurological diseases and metabolism (2 papers). Øyvind L. Busk collaborates with scholars based in Norway and United States. Øyvind L. Busk's co-authors include Øystein L. Holla, Helle Høyer, Kristian Tveten, Geir Mathiesen, Geir J. Braathen, Wolfgang Egge‐Jacobsen, Tahira Riaz, Vincent G. H. Eijsink, Morten Skaugen and Camilla Furu Skjelbred and has published in prestigious journals such as BMC Genomics, BioMed Research International and Toxicon.

In The Last Decade

Øyvind L. Busk

12 papers receiving 242 citations

Peers

Countries citing papers authored by Øyvind L. Busk

Since Specialization

Citations

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

Fields of papers citing papers by Øyvind L. Busk

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Øyvind L. Busk. 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 Øyvind L. Busk. The network helps show where Øyvind L. Busk may publish in the future.

Co-authorship network of co-authors of Øyvind L. Busk

This figure shows the co-authorship network connecting the top 25 collaborators of Øyvind L. Busk. A scholar is included among the top collaborators of Øyvind L. Busk 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 Øyvind L. Busk. Øyvind L. Busk is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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12 of 12 papers shown

#	Work	Indexed citations
1	Genetic overlap between ALS and other neurodegenerative or neuromuscular disorders 2023 ·Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration ·(unknown), Øyvind L. Busk, Øystein L. Holla, Kristian Tveten, Trygve Holmøy, Ole‐Bjørn Tysnes, Helle Høyer	7
2	Clinical characteristics and proteome modifications in two Charcot-Marie-Tooth families with the AARS1 Arg326Trp mutation 2022 ·BMC Neurology ·Helle Høyer, Øyvind L. Busk, (unknown), Oddveig Røsby, (unknown), Michael Bjørn Russell, Tuula A. Nyman, Geir J. Braathen, Hilde Nilsen	3
3	Genetic and Phenotypic Characterization of Community Hospital Patients With QT Prolongation 2018 ·Journal of the American Heart Association ·Charlotte Gibbs, (unknown), Kristian Tveten, Øyvind L. Busk, (unknown), Kristina H. Haugaa, Øystein L. Holla	5
4	Next-generation sequencing of the monogenic obesity genes LEP , LEPR , MC4R , PCSK1 and POMC in a Norwegian cohort of patients with morbid obesity and normal weight controls 2017 ·Molecular Genetics and Metabolism ·Gry B. N. Nordang, Øyvind L. Busk, Kristian Tveten, Hans Ivar Hanevik, Anne Kristin Møller Fell, Jøran Hjelmesæth, Øystein L. Holla, Jens Kristoffer Hertel	49
5	Arvelige perifere nevropatier diagnostisert ved dypsekvensering 2015 ·Tidsskrift for Den norske legeforening ·Helle Høyer, Øyvind L. Busk, Øystein L. Holla, Linda M. Strand, Michael Bjørn Russell, Camilla Furu Skjelbred, Geir J. Braathen	6
6	Diagnostisk eksomsekvensering – norske erfaringer 2015 ·Tidsskrift for Den norske legeforening ·Øystein L. Holla, Øyvind L. Busk, Kristian Tveten, (unknown), Linda M. Strand, Helle Høyer, (unknown), Camilla Furu Skjelbred, Geir J. Braathen	3
7	Variants in the genesDCTN2,DNAH10,LRIG3,andMYO1Aare associated with intermediate Charcot–Marie–Tooth disease in a Norwegian family 2015 ·Acta Neurologica Scandinavica ·Geir J. Braathen, Helle Høyer, Øyvind L. Busk, Kristian Tveten, Camilla Furu Skjelbred, Michael Bjørn Russell	11
8	Familial visceral myopathy diagnosed by exome sequencing of a patient with chronic intestinal pseudo-obstruction 2014 ·Endoscopy ·Øystein L. Holla, Günter Bock, Øyvind L. Busk, (unknown)	24
9	Genetic Diagnosis of Charcot-Marie-Tooth Disease in a Population by Next-Generation Sequencing 2014 ·BioMed Research International ·Helle Høyer, Geir J. Braathen, Øyvind L. Busk, Øystein L. Holla, (unknown), (unknown), Linda M. Strand, Camilla Furu Skjelbred, Michael Bjørn Russell	47
10	Cytosol protein regulation in H295R steroidogenesis model induced by the zearalenone metabolites, α- and β-zearalenol 2011 ·Toxicon ·Øyvind L. Busk, Caroline Frizzell, Steven Verhaegen, Silvio Uhlig, Lisa Connolly, Erik Ropstad, Morten Sørlie	14
11	Identification of surface proteins in Enterococcus faecalis V583 2011 ·BMC Genomics ·(unknown), Tahira Riaz, Wolfgang Egge‐Jacobsen, Morten Skaugen, Øyvind L. Busk, Vincent G. H. Eijsink, Geir Mathiesen	61
12	Relative quantification of the proteomic changes associated with the mycotoxin zearalenone in the H295R steroidogenesis model 2011 ·Toxicon ·Øyvind L. Busk, Doreen Ndossi, Steven Verhaegen, Lisa Connolly, Gunnar Sundstøl Eriksen, Erik Ropstad, Morten Sørlie	14

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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