Morten Dunø

5.8k total citations
184 papers, 3.8k citations indexed

About

Morten Dunø is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Clinical Biochemistry. According to data from OpenAlex, Morten Dunø has authored 184 papers receiving a total of 3.8k indexed citations (citations by other indexed papers that have themselves been cited), including 130 papers in Molecular Biology, 45 papers in Cellular and Molecular Neuroscience and 34 papers in Clinical Biochemistry. Recurrent topics in Morten Dunø's work include Mitochondrial Function and Pathology (48 papers), Genetic Neurodegenerative Diseases (34 papers) and Metabolism and Genetic Disorders (34 papers). Morten Dunø is often cited by papers focused on Mitochondrial Function and Pathology (48 papers), Genetic Neurodegenerative Diseases (34 papers) and Metabolism and Genetic Disorders (34 papers). Morten Dunø collaborates with scholars based in Denmark, United States and Netherlands. Morten Dunø's co-authors include John Vissing, Marianne Schwartz, Flemming Wibrand, Elsebet Østergaard, Nanna Witting, Thomas Krag, M. Schwartz, Allan M. Lund, Thomas Rosenberg and Tina D. Jeppesen and has published in prestigious journals such as Nucleic Acids Research, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Morten Dunø

177 papers receiving 3.7k citations

Peers

Countries citing papers authored by Morten Dunø

Since Specialization

Citations

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

Fields of papers citing papers by Morten Dunø

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Morten Dunø

This figure shows the co-authorship network connecting the top 25 collaborators of Morten Dunø. A scholar is included among the top collaborators of Morten Dunø 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 Morten Dunø. Morten Dunø 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

#	Work	Indexed citations
1	Variants in CAPN3 Causing Autosomal Dominant Limb–Girdle Muscular Dystrophy Combined With Calpain‐3 Deficiency 2025 ·Human Mutation ·Thomas Krag, (unknown), Lauren Brady, (unknown), France Leturcq, Edoardo Malfatti, Morten Dunø, Mark A. Tarnopolsky, John Vissing	1
2	Muscle fat replacement and contractility in patients with skeletal muscle sodium channel disorders 2023 ·Scientific Reports ·(unknown), (unknown), (unknown), (unknown), (unknown), Morten Dunø, John Vissing	9
3	DNA methylation signature classification of rare disorders using publicly available methylation data 2023 ·Clinical Genetics ·(unknown), (unknown), Tina Duelund Hjortshøj, Morten Dunø, Lotte Risom, Mads Bak, Jakob Ek, Rikke S. Møller, Andrea Ciolfi, Marco Tartaglia, Zeynep Tümer	1
4	Homozygous splice variant (c.1741-6G>A) of the COL6A1 gene in three patients with Ullrich congenital muscular dystrophy 2023 ·Neuromuscular Disorders ·(unknown), Morten Dunø, Ulf Birkedal, John Vissing, Alfred Peter Born, Thomas Krag, Thomas van Overeem Hansen, Elsebet Østergaard	0
5	Cell-Free Fetal DNA for Genetic Evaluation in Copenhagen Pregnancy Loss Study (COPL): A Prospective Cohort Study 2023 ·Obstetrical & Gynecological Survey ·Tanja Schlaikjær Hartwig, Louise Ambye, Jennifer R. Gruhn, (unknown), (unknown), Letizia Amato, Andrew C. Chan, Boyang Ji, (unknown), (unknown), (unknown), (unknown), (unknown), Morten Dunø, Iben Bache, Markus J. Herrgård, Finn Stener Jørgensen, Eva R. Hoffmann, Henriette Svarre Nielsen	0
6	Epidemiology and diagnostic trends of congenital adrenal hyperplasia in Denmark: a retrospective, population-based study 2023 ·The Lancet Regional Health - Europe ·Agnethe Berglund, Marie Juul Ørnstrup, (unknown), Morten Dunø, Marie Bækvad‐Hansen, Anders Juul, Luise Borch, Niklas Rye Jørgensen, Åse Krogh Rasmussen, Marianne Andersen, Katharina M. Main, (unknown), Claus Højbjerg Gravholt	10
7	Myopathy can be a key phenotype of membrin (GOSR2) deficiency 2021 ·Human Mutation ·(unknown), (unknown), Morten Dunø, Thomas Krag, John Vissing	2
8	upd(20)mat is a rare cause of the Silver‐Russell‐syndrome‐like phenotype: Two unrelated cases and screening of large cohorts 2020 ·Clinical Genetics ·Tina Duelund Hjortshøj, A.R. Sørensen, (unknown), Bo Mølholm Hansen, Morten Dunø, Marie Balslev‐Harder, Karen Grønskov, Johanna M. van Hagen, Abeltje M. Polstra, Thomas Eggermann, Martijn J.J. Finken, Zeynep Tümer	9
9	Successful treatment with dupilumab of an adult with Netherton syndrome 2020 ·Clinical and Experimental Dermatology ·(unknown), (unknown), Morten Dunø, Ulrikke Lei, Claus Zachariae, Jacob P. Thyssen	30
10	A single c.1715G>C calpain 3 gene variant causes dominant calpainopathy with loss of calpain 3 expression and activity 2020 ·Human Mutation ·John Vissing, Julia R. Dahlqvist, Carinne Roudaut, Jérôme Poupiot, Isabelle Richard, Morten Dunø, Thomas Krag	10
11	Genotype and phenotype classification of 29 patients affected by Krabbe disease 2019 ·JIMD Reports ·(unknown), Flemming Wibrand, Allan M. Lund, Jakob Ek, Morten Dunø, Elsebet Østergaard	10
12	Hydroxylated long-chain acylcarnitines are biomarkers of mitochondrial myopathy 2019 ·The Journal of Clinical Endocrinology & Metabolism ·Christoffer Rasmus Vissing, Morten Dunø, Flemming Wibrand, Mette Christensen, John Vissing	24
13	Adaptations in Mitochondrial Enzymatic Activity Occurs Independent of Genomic Dosage in Response to Aerobic Exercise Training and Deconditioning in Human Skeletal Muscle 2019 ·Cells ·Andreas M. Fritzen, (unknown), Kasper Højgaard Thybo, Christoffer Rasmus Vissing, Thomas Krag, (unknown), Lotte Risom, Flemming Wibrand, Louise D. Høeg, Bente Kiens, Morten Dunø, John Vissing, Tina D. Jeppesen	27
14	BAG3 myopathy is not always associated with cardiomyopathy 2018 ·Neuromuscular Disorders ·Annarita Ghosh Andersen, (unknown), Henrik Daa Schrøder, Thomas Krag, Volker Straub, Morten Dunø, John Vissing	9
15	[Clinical molecular genetics diagnostics of Rett syndrome in Denmark]. 2015 ·PubMed ·Bitten Schönewolf‐Greulich, Morten Dunø, Kirstine Ravn, Karen Brøndum‐Nielsen, Anne‐Marie Bisgaard	1
16	Carnitine levels in 26,462 individuals from the nationwide screening program for primary carnitine deficiency in the Faroe Islands 2013 ·Journal of Inherited Metabolic Disease ·Jan Rasmussen, Olav Wendelboe Nielsen, Nils Janzen, Morten Dunø, Lars Køber, Ulrike Steuerwald, Allan M. Lund	64
17	Pharmacokinetic variability of clarithromycin and differences in CYP3A4 activity in patients with cystic fibrosis 2013 ·Journal of Cystic Fibrosis ·(unknown), Xiaohui Chen Nielsen, Kim Dalhoff, Jan‐Willem C. Alffenaar, Morten Dunø, Anders Buchard, Donald R. A. Uges, Allan G. Jensen, Gesche Jürgens, T. Pressler, Helle Krogh Johansen, Niels Høiby	10
18	A novel MERTK deletion is a common founder mutation in the Faroe Islands and is responsible for a high proportion of retinitis pigmentosa cases. 2011 ·PubMed ·Elsebet Østergaard, Morten Dunø, Mustafa Batbayli, (unknown), Thomas Rosenberg	50
19	Improved Molecular Diagnosis of Dystrophin Gene Mutations Using the Multiplex Ligation-Dependent Probe Amplification Method 2004 ·Genetic Testing ·Marianne Schwartz, Morten Dunø	75
20	Decrement of compound muscle action potential is related to mutation type in myotonia congenita 2003 ·Muscle & Nerve ·Eskild Colding‐Jørgensen, Morten Dunø, Marianne Schwartz, John Vissing	31

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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