Elsebet Østergaard

3.9k total citations
67 papers, 2.2k citations indexed

About

Elsebet Østergaard is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Elsebet Østergaard has authored 67 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 47 papers in Molecular Biology, 19 papers in Clinical Biochemistry and 10 papers in Genetics. Recurrent topics in Elsebet Østergaard's work include Mitochondrial Function and Pathology (30 papers), Metabolism and Genetic Disorders (19 papers) and ATP Synthase and ATPases Research (12 papers). Elsebet Østergaard is often cited by papers focused on Mitochondrial Function and Pathology (30 papers), Metabolism and Genetic Disorders (19 papers) and ATP Synthase and ATPases Research (12 papers). Elsebet Østergaard collaborates with scholars based in Denmark, Netherlands and Sweden. Elsebet Østergaard's co-authors include Flemming Wibrand, Morten Dunø, Jes Olesen, Eric A. Shoubridge, Thomas Rosenberg, Mustafa Batbayli, Ernst Christensen, Michael Bjørn Russell, Richard J. Rodenburg and Lise Lykke Thomsen and has published in prestigious journals such as SHILAP Revista de lepidopterología, Brain and Neurology.

In The Last Decade

Elsebet Østergaard

62 papers receiving 2.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Elsebet Østergaard Denmark 26 1.6k 808 298 241 158 67 2.2k
Esther Leshinsky‐Silver Israel 25 928 0.6× 287 0.4× 522 1.8× 108 0.4× 103 0.7× 76 1.7k
Christine Barnérias France 20 704 0.4× 236 0.3× 283 0.9× 133 0.6× 113 0.7× 73 1.4k
Caterina Garone Italy 21 1.3k 0.8× 641 0.8× 182 0.6× 129 0.5× 78 0.5× 45 1.7k
Eleonora Lamantea Italy 32 3.2k 2.0× 2.0k 2.5× 324 1.1× 59 0.2× 214 1.4× 86 3.7k
Angela Abicht Germany 27 1.2k 0.7× 341 0.4× 269 0.9× 103 0.4× 83 0.5× 124 2.1k
Eeva Nikoskelainen Finland 28 3.7k 2.3× 1.6k 2.0× 242 0.8× 150 0.6× 155 1.0× 70 4.4k
Byung Chan Lim South Korea 23 750 0.5× 179 0.2× 436 1.5× 481 2.0× 130 0.8× 165 1.8k
Jukka S. Moilanen Finland 19 1.2k 0.8× 503 0.6× 386 1.3× 53 0.2× 133 0.8× 61 1.6k
Mohammed Al‐Owain Saudi Arabia 25 1.1k 0.7× 267 0.3× 595 2.0× 51 0.2× 116 0.7× 87 2.0k
Penelope E. Bonnen United States 19 1.8k 1.1× 250 0.3× 389 1.3× 135 0.6× 120 0.8× 37 2.4k

Countries citing papers authored by Elsebet Østergaard

Since Specialization
Citations

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

Fields of papers citing papers by Elsebet Østergaard

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elsebet Østergaard

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

All Works

20 of 20 papers shown
1.
Bak, Mads, Kristín Rós Kjartansdóttir, Thomas van Overeem Hansen, et al.. (2024). Novel Alu insertion in the ZEB2 gene causing Mowat‐Wilson syndrome. American Journal of Medical Genetics Part A. 194(8). e63581–e63581. 1 indexed citations
2.
Østergaard, Elsebet, et al.. (2024). mTORC1 hampers Hedgehog signaling inTsc2deficient cells. Life Science Alliance. 7(11). e202302419–e202302419.
3.
Dunø, Morten, Ulf Birkedal, John Vissing, et al.. (2023). Homozygous splice variant (c.1741-6G>A) of the COL6A1 gene in three patients with Ullrich congenital muscular dystrophy. Neuromuscular Disorders. 33(7). 539–545.
4.
Lund, Allan M., et al.. (2021). Excellent response to asfotase alfa treatment in an adolescent patient with hypophosphatasia. JIMD Reports. 59(1). 10–15. 3 indexed citations
5.
Vogel, Ida, et al.. (2021). A novel homozygous variant in C1QBP causes severe IUGR, edema, and cardiomyopathy in two fetuses. JIMD Reports. 59(1). 20–25. 4 indexed citations
6.
Vissing, John, Elsebet Østergaard, Laurence A. Bindoff, et al.. (2021). Phenotypic spectrum and clinical course of single large-scale mitochondrial DNA deletion disease in the paediatric population: a multicentre study. Journal of Medical Genetics. 60(1). 65–73. 11 indexed citations
7.
Thompson, Kyle, Emanuele Bellacchio, Courtney E. French, et al.. (2021). Elucidating the molecular mechanisms associated with TARS2-related mitochondrial disease. Human Molecular Genetics. 31(4). 523–534. 13 indexed citations
8.
Hikmat, Omar, K Naess, Martin Engvall, et al.. (2020). The impact of gender, puberty, and pregnancy in patients with POLG disease. Annals of Clinical and Translational Neurology. 7(10). 2019–2025. 8 indexed citations
9.
Hikmat, Omar, K Naess, Martin Engvall, et al.. (2020). Simplifying the clinical classification of polymerase gamma (POLG) disease based on age of onset; studies using a cohort of 155 cases. Journal of Inherited Metabolic Disease. 43(4). 726–736. 46 indexed citations
10.
Wibrand, Flemming, et al.. (2019). Genotype and phenotype classification of 29 patients affected by Krabbe disease. JIMD Reports. 46(1). 35–45. 10 indexed citations
11.
Grønborg, Sabine, Lotte Risom, Jakob Ek, et al.. (2018). A Faroese founder variant in TBCD causes early onset, progressive encephalopathy with a homogenous clinical course. European Journal of Human Genetics. 26(10). 1512–1520. 12 indexed citations
12.
13.
Saunders, Carol, Laurie D. Smith, Flemming Wibrand, et al.. (2015). CLPB Variants Associated with Autosomal-Recessive Mitochondrial Disorder with Cataract, Neutropenia, Epilepsy, and Methylglutaconic Aciduria. The American Journal of Human Genetics. 96(2). 258–265. 44 indexed citations
14.
Valencia, Eulalia, José A. Caparrós‐Martín, Ma Salomé Sirerol-Piquer, et al.. (2014). Report of a newly indentified patient with mutations in BMP1 and underlying pathogenetic aspects. American Journal of Medical Genetics Part A. 164(5). 1143–1150. 24 indexed citations
15.
Dobolyi, Árpád, Elsebet Østergaard, Attila G. Bagó, et al.. (2013). Exclusive neuronal expression of SUCLA2 in the human brain. Brain Structure and Function. 220(1). 135–151. 16 indexed citations
16.
Grønskov, Karen, Christopher M. Dooley, Elsebet Østergaard, et al.. (2013). Mutations in C10orf11, a Melanocyte-Differentiation Gene, Cause Autosomal-Recessive Albinism. The American Journal of Human Genetics. 92(3). 415–421. 86 indexed citations
17.
Østergaard, Elsebet, et al.. (2011). A novel MERTK deletion is a common founder mutation in the Faroe Islands and is responsible for a high proportion of retinitis pigmentosa cases.. PubMed. 17. 1485–92. 50 indexed citations
18.
Miller, Chaya, Liya Wang, Elsebet Østergaard, Phyllis Dan, & Ann Saada. (2011). The interplay between SUCLA2, SUCLG2, and mitochondrial DNA depletion. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1812(5). 625–629. 40 indexed citations
19.
Janssen, Rolf J. R. J., Felix Distelmaier, Roel Smeets, et al.. (2009). Contiguous gene deletion of ELOVL7, ERCC8 and NDUFAF2 in a patient with a fatal multisystem disorder. Human Molecular Genetics. 18(18). 3365–3374. 28 indexed citations
20.
Østergaard, Elsebet, et al.. (2003). Sporadic Hemiplegic Migraine is an Aetiologically Heterogeneous Disorder. Cephalalgia. 23(9). 921–928. 32 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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