Lena E. Hjermind

3.2k total citations
47 papers, 904 citations indexed

About

Lena E. Hjermind is a scholar working on Cellular and Molecular Neuroscience, Neurology and Molecular Biology. According to data from OpenAlex, Lena E. Hjermind has authored 47 papers receiving a total of 904 indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Cellular and Molecular Neuroscience, 24 papers in Neurology and 23 papers in Molecular Biology. Recurrent topics in Lena E. Hjermind's work include Genetic Neurodegenerative Diseases (26 papers), Neurological disorders and treatments (19 papers) and Mitochondrial Function and Pathology (12 papers). Lena E. Hjermind is often cited by papers focused on Genetic Neurodegenerative Diseases (26 papers), Neurological disorders and treatments (19 papers) and Mitochondrial Function and Pathology (12 papers). Lena E. Hjermind collaborates with scholars based in Denmark, Germany and Netherlands. Lena E. Hjermind's co-authors include Jørgen E. Nielsen, Tua Vinther‐Jensen, Troels T. Nielsen, Esben Budtz–Jørgensen, Anne Nørremølle, Poul Hyttel, Sven Asger Sørensen, Gunhild Waldemar, Kristine Freude and Cecilie Ammitzbøll and has published in prestigious journals such as PLoS ONE, Annals of Neurology and Journal of neurosurgery.

In The Last Decade

Lena E. Hjermind

47 papers receiving 876 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Lena E. Hjermind Denmark	18	405	403	388	119	100	47	904
Shabnam Ghazi‐Noori United Kingdom	7	782 1.9×	594 1.5×	339 0.9×	125 1.1×	83 0.8×	7	1.2k
Sara Duarte‐Silva Portugal	18	502 1.2×	489 1.2×	200 0.5×	108 0.9×	65 0.7×	38	811
Paweł Tacik Germany	20	278 0.7×	222 0.6×	492 1.3×	378 3.2×	245 2.5×	46	960
Kathrin N. Karle Germany	18	893 2.2×	467 1.2×	203 0.5×	121 1.0×	258 2.6×	24	1.4k
Nayana Lahiri United Kingdom	15	610 1.5×	575 1.4×	206 0.5×	57 0.5×	113 1.1×	27	1.0k
Dennis R. Mosier United States	15	474 1.2×	460 1.1×	448 1.2×	244 2.1×	99 1.0×	21	1.1k
Aurélie Méneret France	14	159 0.4×	195 0.5×	240 0.6×	84 0.7×	81 0.8×	46	704
Ikuru Yazawa Japan	15	434 1.1×	469 1.2×	438 1.1×	167 1.4×	237 2.4×	34	907
Oswaldo Lorenzo‐Betancor Spain	19	357 0.9×	348 0.9×	806 2.1×	139 1.2×	189 1.9×	36	1.1k
Ana Djarmati Germany	19	499 1.2×	605 1.5×	845 2.2×	162 1.4×	233 2.3×	29	1.3k

Countries citing papers authored by Lena E. Hjermind

Since Specialization

Citations

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

Fields of papers citing papers by Lena E. Hjermind

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Lena E. Hjermind. 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 Lena E. Hjermind. The network helps show where Lena E. Hjermind may publish in the future.

Co-authorship network of co-authors of Lena E. Hjermind

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

All Works

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20 of 20 papers shown

Hjermind, Lena E., et al.. (2022). On the association between apathy and deficits of social cognition and executive functions in Huntington’s disease. Journal of the International Neuropsychological Society. 29(4). 369–376. 7 indexed citations

Ortigoza‐Escobar, Juan Darío, Jean‐Marc Burgunder, Caterina Mariotti, et al.. (2022). Corrigendum: Combining Literature Review With a Ground Truth Approach for Diagnosing Huntington's Disease Phenocopy. Frontiers in Neurology. 13. 891800–891800. 1 indexed citations

Vinther‐Jensen, Tua, Esben Budtz–Jørgensen, Lena E. Hjermind, et al.. (2021). Hybrid 2-[18F] FDG PET/MRI in premanifest Huntington’s disease gene-expansion carriers: The significance of partial volume correction. PLoS ONE. 16(6). e0252683–e0252683. 8 indexed citations

Vinther‐Jensen, Tua, Ida Unmack Larsen, Troels T. Nielsen, et al.. (2021). Endophenotypical drift in Huntington’s disease: a 5-year follow-up study. Orphanet Journal of Rare Diseases. 16(1). 340–340. 4 indexed citations

Toft, Anders, Steffen Birk, Martin Ballegaard, et al.. (2019). Peripheral neuropathy in hereditary spastic paraplegia caused by REEP1 variants. Journal of Neurology. 266(3). 735–744. 10 indexed citations

Bruun, Marie, Esben Budtz–Jørgensen, Lena E. Hjermind, et al.. (2018). Quantitative Measurements of Motor Function in Alzheimer’s Disease, Frontotemporal Dementia, and Dementia with Lewy Bodies: A Proof-of-Concept Study. Dementia and Geriatric Cognitive Disorders. 46(3-4). 168–179. 11 indexed citations

Schmid, Benjamin, Troels T. Nielsen, Gunhild Waldemar, et al.. (2016). Generation of a gene-corrected isogenic control cell line from an Alzheimer's disease patient iPSC line carrying a A79V mutation in PSEN1. Stem Cell Research. 17(2). 285–288. 42 indexed citations

Schmid, Benjamin, Troels T. Nielsen, Lena E. Hjermind, et al.. (2016). Generation of a gene-corrected isogenic control hiPSC line derived from a familial Alzheimer's disease patient carrying a L150P mutation in presenilin 1. Stem Cell Research. 17(3). 466–469. 30 indexed citations

Li, Tong, Troels T. Nielsen, Gunhild Waldemar, et al.. (2016). Generation of induced pluripotent stem cells (iPSCs) from an Alzheimer's disease patient carrying an A79V mutation in PSEN1. Stem Cell Research. 16(2). 229–232. 30 indexed citations

10.

Li, Tong, Troels T. Nielsen, Gunhild Waldemar, et al.. (2016). Generation of induced pluripotent stem cells (iPSCs) from an Alzheimer's disease patient carrying a M146I mutation in PSEN1. Stem Cell Research. 16(2). 334–337. 12 indexed citations

11.

Bertelsen, Birgitte, Lusine Nazaryan‐Petersen, Wei Sun, et al.. (2015). A germline chromothripsis event stably segregating in 11 individuals through three generations. Genetics in Medicine. 18(5). 494–500. 54 indexed citations

12.

Rasmussen, Mikkel A., Lena E. Hjermind, Lis Hasholt, et al.. (2015). Induced pluripotent stem cells (iPSCs) derived from a patient with frontotemporal dementia caused by a R406W mutation in microtubule-associated protein tau (MAPT). Stem Cell Research. 16(1). 75–78. 8 indexed citations

13.

Tubsuwan, Alisa, Mikkel A. Rasmussen, Benjamin Schmid, et al.. (2015). Generation of induced pluripotent stem cells (iPSCs) from an Alzheimer's disease patient carrying a L150P mutation in PSEN-1. Stem Cell Research. 16(1). 110–112. 19 indexed citations

14.

Rasmussen, Mikkel A., Lena E. Hjermind, Lis Hasholt, et al.. (2015). Induced pluripotent stem cells (iPSCs) derived from a pre-symptomatic carrier of a R406W mutation in microtubule-associated protein tau (MAPT) causing frontotemporal dementia. Stem Cell Research. 16(1). 105–109. 7 indexed citations

15.

Bech, Sára, Lena E. Hjermind, Lisette Salvesen, et al.. (2011). Amyloid-related biomarkers and axonal damage proteins in parkinsonian syndromes. Parkinsonism & Related Disorders. 18(1). 69–72. 37 indexed citations

16.

Simonsen, Anja Hviid, Sára Bech, Inga Laursen, et al.. (2010). Proteomic investigations of the ventriculo-lumbar gradient in human CSF. Journal of Neuroscience Methods. 191(2). 244–248. 19 indexed citations

17.

Nilsson, Karin, Jørgen E. Nielsen, Suzanne Granhøj Lindquist, et al.. (2009). Reduced CSF CART in dementia with Lewy bodies. Neuroscience Letters. 453(2). 104–106. 22 indexed citations

18.

Asmus, Friedrich, Farid Salih, Lena E. Hjermind, et al.. (2005). Myoclonus‐dystonia due to genomic deletions in the epsilon‐sarcoglycan gene. Annals of Neurology. 58(5). 792–797. 49 indexed citations

19.

Lindquist, Suzanne Granhøj, Anne Nørremølle, Lena E. Hjermind, Lis Hasholt, & Jørgen E. Nielsen. (2005). Meiotic CAG repeat instability in spinocerebellar ataxia type 6: Maternally transmitted elongation in a presumed sporadic case. Journal of the Neurological Sciences. 241(1-2). 95–98. 6 indexed citations

20.

Hjermind, Lena E., Lis Johannsen, Nenad Blau, et al.. (2005). Dopa‐responsive dystonia and early‐onset Parkinson's disease in a patient with GTP cyclohydrolase I deficiency?. Movement Disorders. 21(5). 679–682. 23 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.

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