Elsebet Østergaard

3.9k citations

67 papers · 2.2k indexed · h-index 26

Impact in

Clinical Biochemistry top 0.2%
- Metabolism and Genetic Disorders
Molecular Biology top 5%
- Mitochondrial Function and Pathology
- ATP Synthase and ATPases Research
- RNA modifications and cancer
- RNA and protein synthesis mechanisms
- Retinal Development and Disorders

Papers in ⓘ

Clinical Biochemistry 19
- Metabolism and Genetic Disorders 19
Molecular Biology 47
- Mitochondrial Function and Pathology 30
- ATP Synthase and ATPases Research 12
- RNA and protein synthesis mechanisms 7
- RNA modifications and cancer 6
- RNA regulation and disease 5

Co-authors: Flemming Wibrand (20 shared papers)Morten Dunø (16 shared papers)Jes Olesen (3 shared papers)Eric A. Shoubridge (4 shared papers)Thomas Rosenberg (5 shared papers)Mustafa Batbayli (5 shared papers)Ernst Christensen (4 shared papers)Michael Bjørn Russell (1 shared paper)
Journals: Journal of Medical Genetics (6 papers)Human Molecular Genetics (5 papers)The American Journal of Human Genetics (5 papers)Journal of Inherited Metabolic Disease (5 papers)Neurology (3 papers)
Partner nations: Denmark Netherlands Sweden

In The Last Decade

Elsebet Østergaard

62 papers receiving 2.2k citations

Peers

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-authors

The 25 scholars most cited alongside Elsebet Østergaard, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Elsebet Østergaard Line = papers co-authored together Elsebet Østergaard links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 67 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	A multicenter study on Leigh syndrome: disease course and predictors of survival Orphanet Journal of Rare Diseases ·Kalliopi Sofou, I.F.M. de Coo, Pirjo Isohanni, Elsebet Østergaard, K Naess, Linda De Meırleır, Charalampos Tzoulis, Johanna Uusimaa, Isabell B De Angst, Tuula Lönnqvist, Helena Pihko, Katariina Mankinen, Laurence A. Bindoff, M. Tulinius, Niklas Darín	2014	161
2	Mitochondrial encephalomyopathy with elevated methylmalonic acid is caused by SUCLA2 mutations Brain ·Elsebet Østergaard, Flemming Juul Hansen, N. Sörensen, Morten Dunø, John Vissing, P L Larsen, O. Faeroe, Sigurður Þorgrímsson, Flemming Wibrand, E. Christensen, M. Schwartz	2007	140
3	Deficiency of the α Subunit of Succinate–Coenzyme A Ligase Causes Fatal Infantile Lactic Acidosis with Mitochondrial DNA Depletion The American Journal of Human Genetics ·Elsebet Østergaard, Ernst Christensen, Elisabeth Kristensen, Bodil Mogensen, Morten Dunø, Eric A. Shoubridge, Flemming Wibrand	2007	135
4	Mutations in C12orf65 in Patients with Encephalomyopathy and a Mitochondrial Translation Defect The American Journal of Human Genetics ·Hana Antonická, Elsebet Østergaard, Florin Sasarman, Woranontee Weraarpachai, Flemming Wibrand, Anne Marie B. Pedersen, Richard J. Rodenburg, Marjo S. van der Knaap, Jan Smeıtınk, Zofia M. Chrzanowska‐Lightowlers, Eric A. Shoubridge	2010	115
5	POLG mutations in Alpers syndrome Neurology ·Khue Vu Nguyen, Elsebet Østergaard, Søren Ravn, Thomas Balslev, Else Rubæk Danielsen, A. Vardag, P. J. McKiernan, Glenda Gray, Robert K. Naviaux	2005	103
6	Evidence for a separate type of migraine with aura Neurology ·Lise Lykke Thomsen, Elsebet Østergaard, Jes Olesen, Michael Bjørn Russell	2003	100
7	Natural disease course and genotype‐phenotype correlations in Complex I deficiency caused by nuclear gene defects: what we learned from 130 cases Journal of Inherited Metabolic Disease ·Saskia Koene, Richard J. Rodenburg, Marjo S. van der Knaap, Michèl A.A.P. Willemsen, Wolfgang Sperl, Vincent Laugel, Elsebet Østergaard, Mark A. Tarnopolsky, Miguel A. Martı́n, Victoria Nesbitt, Janice M. Fletcher, Simon Edvardson, Vincent Procaccio, Abdelhamid Slama, Lambert P. W. J. den van Heuvel, J.A.M. Smeitink	2012	100
8	An Epidemiological Survey of Hemiplegic Migraine Cephalalgia ·Lars Lykke Thomsen, M K Eriksen, S Faerch Romer, Ingelise Andersen, Elsebet Østergaard, Niels Keiding, Jes Olesen, MB Russell	2002	97
9	Mutations in C10orf11, a Melanocyte-Differentiation Gene, Cause Autosomal-Recessive Albinism The American Journal of Human Genetics ·Karen Grønskov, Christopher M. Dooley, Elsebet Østergaard, Robert N. Kelsh, Lars Hestbjerg Hansen, Mitchell P. Levesque, Kaj Vilhelmsen, Kjeld Møllgård, Derek L. Stemple, Thomas Rosenberg	2013	86
10	Recessive mutations in PTHR1 cause contrasting skeletal dysplasias in Eiken and Blomstrand syndromes Human Molecular Genetics ·Sabine Duchatelet, Elsebet Østergaard, Dina Cortes, Arnaud Lemainque, Cécile Julier	2004	83
11	Autosomal-Recessive Posterior Microphthalmos Is Caused by Mutations in PRSS56, a Gene Encoding a Trypsin-Like Serine Protease The American Journal of Human Genetics ·Andreas Gal, Isabella Rau, (unknown), Hans‐Jürgen Kreienkamp, Susanne Fehr, K. Baklouti, Ibtissem Chouchane, Yun Li, Monika Rehbein, Josefine Fuchs, Hans C. Fledelius, Kaj Vilhelmsen, Daniel F. Schorderet, Francis L. Munier, Elsebet Østergaard, Debra A. Thompson, Thomas Rosenberg	2011	60
12	Phenotype-genotype correlations in Leigh syndrome: new insights from a multicentre study of 96 patients Journal of Medical Genetics ·Kalliopi Sofou, I.F.M. de Coo, Elsebet Østergaard, Pirjo Isohanni, K Naess, Linda De Meırleır, Charalampos Tzoulis, Johanna Uusimaa, Tuula Lönnqvist, Laurence A. Bindoff, M. Tulinius, Niklas Darín	2017	55
13	Disorders caused by deficiency of succinate‐CoA ligase Journal of Inherited Metabolic Disease ·Elsebet Østergaard	2008	52
14	The effects of wound infiltration with bupivacaine versus saline on postoperative pain and opioid requirements after herniorrhaphy Acta Anaesthesiologica Scandinavica ·G. W. DlERKING, Elsebet Østergaard, H. T. ØSTERGÅRD, J. B. Dahl	1994	51
15	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 ·Elsebet Østergaard, Morten Dunø, Mustafa Batbayli, Kaj Vilhelmsen, Thomas Rosenberg	2011	50
16	Respiratory chain complex I deficiency due to NDUFA12 mutations as a new cause of Leigh syndrome Journal of Medical Genetics ·Elsebet Østergaard, Richard J. Rodenburg, Michiel van den Brand, L. L. Thomsen, Morten Dunø, Mustafa Batbayli, Flemming Wibrand, Leo Nijtmans	2011	49
17	Mutations in PCDH21 cause autosomal recessive cone-rod dystrophy Journal of Medical Genetics ·Elsebet Østergaard, Mustafa Batbayli, Morten Dunø, Kaj Vilhelmsen, Thomas Rosenberg	2010	48
18	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 ·Omar Hikmat, K Naess, Martin Engvall, Claus Klingenberg, Magnhild Rasmussen, Chantal Tallaksen, Eylert Brodtkorb, Elsebet Østergaard, I.F.M. de Coo, Leticia Pías‐Peleteiro, Pirjo Isohanni, Johanna Uusimaa, Niklas Darín, Shamima Rahman, Laurence A. Bindoff	2020	46
19	Mutations in COA3 cause isolated complex IV deficiency associated with neuropathy, exercise intolerance, obesity, and short stature Journal of Medical Genetics ·Elsebet Østergaard, Woranontee Weraarpachai, Kirstine Ravn, Alfred Peter Born, Lars Jønson, Morten Dunø, Flemming Wibrand, Eric A. Shoubridge, John Vissing	2015	45
20	CLPB Variants Associated with Autosomal-Recessive Mitochondrial Disorder with Cataract, Neutropenia, Epilepsy, and Methylglutaconic Aciduria The American Journal of Human Genetics ·Carol Saunders, Laurie D. Smith, Flemming Wibrand, Kirstine Ravn, Peter Bross, Isabelle Thiffault, Mette Christensen, Andrea M. Atherton, Emily Farrow, Neil Miller, Stephen F. Kingsmore, Elsebet Østergaard	2015	44

About Elsebet Østergaard

Elsebet Østergaard is a scholar working on Clinical Biochemistry, Molecular Biology, Family Practice, Sensory Systems and Genetics, having authored 67 papers that have together received 2.2k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (30 papers), Metabolism and Genetic Disorders (19 papers), ATP Synthase and ATPases Research (12 papers), RNA and protein synthesis mechanisms (7 papers), RNA modifications and cancer (6 papers), RNA regulation and disease (5 papers), Migraine and Headache Studies (4 papers) and Genomics and Rare Diseases (4 papers). The work is most often cited by research in Clinical Biochemistry (808 citations), Molecular Biology (1.6k citations), Psychiatry and Mental health (241 citations), Neurology (121 citations) and Sensory Systems (62 citations). Elsebet Østergaard has collaborated with scholars based in Denmark, Netherlands and Sweden. Frequent co-authors include Flemming Wibrand, Morten Dunø, Jes Olesen, Eric A. Shoubridge, Thomas Rosenberg, Mustafa Batbayli, Ernst Christensen, Michael Bjørn Russell, Lise Lykke Thomsen and Richard J. Rodenburg. Their work appears in journals such as Journal of Medical Genetics, Human Molecular Genetics, The American Journal of Human Genetics, Journal of Inherited Metabolic Disease and Neurology.

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