Helle Høyer

558 total citations
17 papers, 329 citations indexed

About

Helle Høyer is a scholar working on Cellular and Molecular Neuroscience, Molecular Biology and Neurology. According to data from OpenAlex, Helle Høyer has authored 17 papers receiving a total of 329 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Cellular and Molecular Neuroscience, 5 papers in Molecular Biology and 5 papers in Neurology. Recurrent topics in Helle Høyer's work include Hereditary Neurological Disorders (13 papers), Genetic Neurodegenerative Diseases (6 papers) and Neurological diseases and metabolism (5 papers). Helle Høyer is often cited by papers focused on Hereditary Neurological Disorders (13 papers), Genetic Neurodegenerative Diseases (6 papers) and Neurological diseases and metabolism (5 papers). Helle Høyer collaborates with scholars based in Norway, United States and Denmark. Helle Høyer's co-authors include Geir J. Braathen, Michael Bjørn Russell, Camilla Furu Skjelbred, Øyvind L. Busk, Linda M. Strand, Øystein L. Holla, Sine Godiksen, Gry B. N. Nordang, Egil Johnson and Mona Sæbø and has published in prestigious journals such as PLoS ONE, Brain and BioMed Research International.

In The Last Decade

Helle Høyer

16 papers receiving 324 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Helle Høyer Norway	8	243	105	97	96	50	17	329
Simona Capponi Italy	12	222 0.9×	74 0.7×	211 2.2×	92 1.0×	76 1.5×	16	405
Fiorella Speziani United States	9	252 1.0×	146 1.4×	259 2.7×	79 0.8×	101 2.0×	9	529
Xiaohong Zi China	11	155 0.6×	86 0.8×	192 2.0×	59 0.6×	15 0.3×	25	355
Maria Schabhüttl Austria	9	202 0.8×	101 1.0×	162 1.7×	51 0.5×	132 2.6×	9	382
Menelaos Pipis United Kingdom	7	214 0.9×	79 0.8×	90 0.9×	74 0.8×	41 0.8×	10	289
Rita-Eva Varga Germany	5	149 0.6×	75 0.7×	74 0.8×	44 0.5×	100 2.0×	6	277
Tomoya Nishimura Japan	8	111 0.5×	50 0.5×	109 1.1×	62 0.6×	33 0.7×	17	246
Claudia Stendel Germany	9	279 1.1×	75 0.7×	223 2.3×	84 0.9×	102 2.0×	17	443
Stefania Magri Italy	13	271 1.1×	66 0.6×	296 3.1×	115 1.2×	54 1.1×	33	477
Christelle Tesson France	10	211 0.9×	124 1.2×	196 2.0×	208 2.2×	88 1.8×	17	496

Countries citing papers authored by Helle Høyer

Since Specialization

Citations

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

Fields of papers citing papers by Helle Høyer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Helle Høyer

This figure shows the co-authorship network connecting the top 25 collaborators of Helle Høyer. A scholar is included among the top collaborators of Helle Høyer 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 Helle Høyer. Helle Høyer 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:

17 of 17 papers shown

Busk, Øyvind L., Øystein L. Holla, Kristian Tveten, et al.. (2023). Genetic overlap between ALS and other neurodegenerative or neuromuscular disorders. Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration. 25(1-2). 177–187. 7 indexed citations

Høyer, Helle, et al.. (2022). A woman in her fifties with progressive walking difficulties. Tidsskrift for Den norske legeforening. 142(11).

Løseth, Sissel, Helle Høyer, Eric Delpire, et al.. (2022). Late-onset sensory-motor axonal neuropathy, a novelSLC12A6-related phenotype. Brain. 146(3). 912–922. 3 indexed citations

Høyer, Helle, Øyvind L. Busk, Oddveig Røsby, et al.. (2022). Clinical characteristics and proteome modifications in two Charcot-Marie-Tooth families with the AARS1 Arg326Trp mutation. BMC Neurology. 22(1). 299–299. 3 indexed citations

Høyer, Helle, et al.. (2021). HINT1 neuropathy in Norway: clinical, genetic and functional profiling. Orphanet Journal of Rare Diseases. 16(1). 116–116. 8 indexed citations

Fabrizi, Gian Maria, Helle Høyer, Federica Taioli, et al.. (2020). Inherited motor-sensory neuropathy with upper limb predominance associated with the tropomyosin-receptor kinase fused gene. Neuromuscular Disorders. 30(3). 227–231. 2 indexed citations

Arntzen, Kjell Arne, Helle Høyer, Kristin Ørstavik, et al.. (2018). Charcot–Marie–Tooth disease type 4C in Norway: Clinical characteristics, mutation spectrum and minimum prevalence. Neuromuscular Disorders. 28(8). 639–645. 5 indexed citations

Høyer, Helle, Øyvind L. Busk, Øystein L. Holla, et al.. (2015). Arvelige perifere nevropatier diagnostisert ved dypsekvensering. Tidsskrift for Den norske legeforening. 135(20). 1838–1843. 6 indexed citations

Holla, Øystein L., Øyvind L. Busk, Kristian Tveten, et al.. (2015). Diagnostisk eksomsekvensering – norske erfaringer. Tidsskrift for Den norske legeforening. 135(20). 1833–1837. 3 indexed citations

10.

Høyer, Helle, et al.. (2015). Copy Number Variations in a Population-Based Study of Charcot-Marie-Tooth Disease. BioMed Research International. 2015. 1–7. 18 indexed citations

11.

Braathen, Geir J., Helle Høyer, Øyvind L. Busk, et al.. (2015). Variants in the genesDCTN2,DNAH10,LRIG3,andMYO1Aare associated with intermediate Charcot–Marie–Tooth disease in a Norwegian family. Acta Neurologica Scandinavica. 134(1). 67–75. 11 indexed citations

12.

Vogel, Lotte K., Mona Sæbø, Helle Høyer, et al.. (2014). Intestinal PTGS2 mRNA Levels, PTGS2 Gene Polymorphisms, and Colorectal Carcinogenesis. PLoS ONE. 9(8). e105254–e105254. 34 indexed citations

13.

Høyer, Helle, Geir J. Braathen, Øyvind L. Busk, et al.. (2014). Genetic Diagnosis of Charcot-Marie-Tooth Disease in a Population by Next-Generation Sequencing. BioMed Research International. 2014. 1–13. 47 indexed citations

14.

Høyer, Helle, et al.. (2011). Charcot-Marie-Tooth caused by a copy number variation in myelin protein zero. European Journal of Medical Genetics. 54(6). e580–e583. 22 indexed citations

15.

Braathen, Geir J., et al.. (2010). MFN2point mutations occur in 3.4% of Charcot-Marie-Tooth families. An investigation of 232 Norwegian CMT families. BMC Medical Genetics. 11(1). 48–48. 42 indexed citations

16.

Braathen, Geir J., et al.. (2010). Genetic epidemiology of Charcot–Marie–Tooth in the general population. European Journal of Neurology. 18(1). 39–48. 117 indexed citations

17.

Høyer, Helle. (1986). [Mongolism and orthodontics: early treatment is often successful].. PubMed. 76(18). 1993–7. 1 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