Niklas Darín

8.1k total citations · 1 hit paper
105 papers, 4.8k citations indexed

About

Niklas Darín is a scholar working on Molecular Biology, Clinical Biochemistry and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Niklas Darín has authored 105 papers receiving a total of 4.8k indexed citations (citations by other indexed papers that have themselves been cited), including 71 papers in Molecular Biology, 37 papers in Clinical Biochemistry and 16 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Niklas Darín's work include Mitochondrial Function and Pathology (43 papers), Metabolism and Genetic Disorders (37 papers) and ATP Synthase and ATPases Research (21 papers). Niklas Darín is often cited by papers focused on Mitochondrial Function and Pathology (43 papers), Metabolism and Genetic Disorders (37 papers) and ATP Synthase and ATPases Research (21 papers). Niklas Darín collaborates with scholars based in Sweden, Netherlands and Finland. Niklas Darín's co-authors include M. Tulinius, Anders Oldfors, Elisabeth Holme, Ali‐Reza Moslemi, T Hallböök, Sverker Jern, Per Mårin, Teiko Amemiya, Björn Andersson and Kalliopi Sofou and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and Nature Medicine.

In The Last Decade

Niklas Darín

103 papers receiving 4.7k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Systemic Administration of PRO051 in Duchenne's Muscular Dystrophy

2011 518 citations M. Tulinius, Niklas Darín et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Niklas Darín Sweden	36	3.2k	1.3k	616	550	509	105	4.8k
G. Scarlato Italy	51	3.7k 1.1×	980 0.8×	706 1.1×	1.1k 2.1×	449 0.9×	264	8.1k
Masanori Nakagawa Japan	48	3.0k 0.9×	438 0.3×	576 0.9×	1.3k 2.4×	415 0.8×	324	8.3k
D. Pongratz Germany	39	2.3k 0.7×	576 0.5×	308 0.5×	898 1.6×	499 1.0×	185	5.0k
F.J.M. Gabreëls Netherlands	43	2.6k 0.8×	1.0k 0.8×	269 0.4×	606 1.1×	177 0.3×	202	6.1k
Masayuki Sasaki Japan	34	3.3k 1.0×	368 0.3×	438 0.7×	822 1.5×	282 0.6×	303	6.4k
Makiko Ōsawa Japan	36	2.4k 0.7×	351 0.3×	359 0.6×	581 1.1×	386 0.8×	196	4.9k
Mark Johnson United Kingdom	30	2.7k 0.9×	351 0.3×	200 0.3×	453 0.8×	527 1.0×	55	5.0k
Oebele F. Brouwer Netherlands	44	1.8k 0.6×	273 0.2×	498 0.8×	386 0.7×	491 1.0×	154	5.2k
Roberta Battini Italy	29	1.2k 0.4×	555 0.4×	237 0.4×	354 0.6×	98 0.2×	178	2.9k
Serenella Servidei Italy	51	6.8k 2.1×	3.3k 2.6×	745 1.2×	791 1.4×	980 1.9×	224	9.4k

Countries citing papers authored by Niklas Darín

Since Specialization

Citations

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

Fields of papers citing papers by Niklas Darín

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Niklas Darín

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

Karlsson, Michael, Fredrik Sjövall, Eleonor Åsander Frostner, et al.. (2024). Correlation of mitochondrial respiration in platelets, peripheral blood mononuclear cells and muscle fibers. Heliyon. 10(5). e26745–e26745. 6 indexed citations

Geoerger, Birgit, Manuel Schiff, Virginie Penard‐Lacronique, et al.. (2023). Enasidenib treatment in two individuals with D-2-hydroxyglutaric aciduria carrying a germline IDH2 mutation. Nature Medicine. 29(6). 1358–1363. 5 indexed citations

Darín, Niklas, Triinu Siibak, Bradley Peter, et al.. (2021). Functional analysis of a novel POLγA mutation associated with a severe perinatal mitochondrial encephalomyopathy. Neuromuscular Disorders. 31(4). 348–358. 1 indexed citations

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

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

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

Veenstra‐Knol, Hermine E., Fleur Vansenne, Erica H. Gerkes, et al.. (2020). De novo variants in CAMTA1 cause a syndrome variably associated with spasticity, ataxia, and intellectual disability. European Journal of Human Genetics. 28(6). 763–769. 8 indexed citations

Szakács, Attila, John Eric Chaplin, Pontus Tideman, et al.. (2019). A population-based and case-controlled study of children and adolescents with narcolepsy: Health-related quality of life, adaptive behavior and parental stress. European Journal of Paediatric Neurology. 23(2). 288–295. 14 indexed citations

Hikmat, Omar, K Naess, Martin Engvall, et al.. (2018). Elevated cerebrospinal fluid protein in POLG‐related epilepsy: Diagnostic and prognostic implications. Epilepsia. 59(8). 1595–1602. 6 indexed citations

10.

Szakács, Attila, T Hallböök, Pontus Tideman, Niklas Darín, & Elisabet Wentz. (2015). Psychiatric Comorbidity and Cognitive Profile in Children with Narcolepsy with or without Association to the H1N1 Influenza Vaccination. SLEEP. 38(4). 615–621. 56 indexed citations

11.

Sofou, Kalliopi, I.F.M. de Coo, Pirjo Isohanni, et al.. (2014). A multicenter study on Leigh syndrome: disease course and predictors of survival. Orphanet Journal of Rare Diseases. 9(1). 52–52. 161 indexed citations

12.

Sofou, Kalliopi, et al.. (2013). MRI of the brain in childhood-onset mitochondrial disorders with central nervous system involvement. Mitochondrion. 13(4). 364–371. 36 indexed citations

13.

Darín, Niklas, Eva Lagberg Arkblad, Anna‐Karin Kroksmark, et al.. (2007). G.P.2.11 Spinal muscular atrophy. The mutational spectra in children from Western Sweden. Neuromuscular Disorders. 17(9-10). 779–779.

14.

Darín, Niklas, et al.. (2007). M.P.1.12 Progressive encephalopathy and complex I deficiency associated with novel mutations in MTND1. Neuromuscular Disorders. 17(9-10). 771–771. 4 indexed citations

15.

Darín, Niklas, Oluf Andersen, Lars‐Martin Wiklund, Daniel Holmgren, & Elisabeth Holme. (2007). 3-Methylcrotonyl-CoA Carboxylase Deficiency and Severe Multiple Sclerosis. Pediatric Neurology. 36(2). 132–134. 9 indexed citations

16.

Tajsharghi, Homa, Niklas Darín, M. Tulinius, & Anders Oldfors. (2005). Early onset myopathy with a novel mutation in the Selenoprotein N gene (SEPN1). Neuromuscular Disorders. 15(4). 299–302. 31 indexed citations

17.

Géromel, Vanna, Niklas Darín, Dominique Chrétien, et al.. (2002). Coenzyme Q10 and idebenone in the therapy of respiratory chain diseases: rationale and comparative benefits. Molecular Genetics and Metabolism. 77(1-2). 21–30. 135 indexed citations

18.

Martinsson, Tommy, Niklas Darín, Mårten Kyllerman, et al.. (1999). Dominant Hereditary Inclusion-Body Myopathy Gene (IBM3) Maps to Chromosome Region 17p13.1. The American Journal of Human Genetics. 64(5). 1420–1426. 33 indexed citations

19.

Darín, Niklas, Mårten Kyllerman, J. Wahlström, Tommy Martinsson, & Anders Oldfors. (1998). Autosomal dominant myopathy with congenital joint contractures, ophthalmoplegia, and rimmed vacuoles. Annals of Neurology. 44(2). 242–248. 62 indexed citations

20.

Darín, Niklas & Per Hanner. (1997). Changes in prevalence, aetiology, age at detection, and associated disabilities in preschool children with hearing impairment born in Göteborg. Developmental Medicine & Child Neurology. 39(12). 797–802. 27 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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