K Naess

2.2k total citations
41 papers, 974 citations indexed

About

K Naess is a scholar working on Molecular Biology, Clinical Biochemistry and Physiology. According to data from OpenAlex, K Naess has authored 41 papers receiving a total of 974 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 21 papers in Clinical Biochemistry and 8 papers in Physiology. Recurrent topics in K Naess's work include Mitochondrial Function and Pathology (22 papers), Metabolism and Genetic Disorders (21 papers) and ATP Synthase and ATPases Research (10 papers). K Naess is often cited by papers focused on Mitochondrial Function and Pathology (22 papers), Metabolism and Genetic Disorders (21 papers) and ATP Synthase and ATPases Research (10 papers). K Naess collaborates with scholars based in Sweden, Finland and Netherlands. K Naess's co-authors include Rolf Wibom, Ulrika von Döbeln, Niklas Darín, Michela Barbaro, Laurence A. Bindoff, Pirjo Isohanni, Helene Bruhn, Johanna Uusimaa, I.F.M. de Coo and Elsebet Østergaard and has published in prestigious journals such as New England Journal of Medicine, SHILAP Revista de lepidopterología and Annals of Neurology.

In The Last Decade

K Naess

41 papers receiving 958 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
K Naess Sweden 15 740 466 117 112 89 41 974
Valentina Emmanuele United States 16 895 1.2× 361 0.8× 72 0.6× 99 0.9× 105 1.2× 39 1.1k
Lynne A. Wolfe United States 15 742 1.0× 297 0.6× 120 1.0× 264 2.4× 42 0.5× 49 1.1k
Daria Diodato Italy 18 868 1.2× 535 1.1× 88 0.8× 89 0.8× 78 0.9× 44 1.2k
Nataliya Povalko Japan 14 830 1.1× 510 1.1× 166 1.4× 43 0.4× 76 0.9× 20 1.0k
Shoji Yano United States 17 386 0.5× 269 0.6× 166 1.4× 162 1.4× 49 0.6× 57 858
I. E. M. Luyt‐Houwen Netherlands 14 866 1.2× 564 1.2× 120 1.0× 78 0.7× 59 0.7× 26 1.1k
Emma Footitt United Kingdom 17 387 0.5× 412 0.9× 92 0.8× 78 0.7× 126 1.4× 29 735
María Teresa García‐Silva Spain 12 392 0.5× 234 0.5× 83 0.7× 71 0.6× 80 0.9× 24 595
Iris Marquardt Germany 11 347 0.5× 401 0.9× 120 1.0× 101 0.9× 44 0.5× 15 796
Langping He United Kingdom 25 1.8k 2.5× 959 2.1× 98 0.8× 152 1.4× 45 0.5× 52 2.0k

Countries citing papers authored by K Naess

Since Specialization
Citations

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

Fields of papers citing papers by K Naess

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of K Naess

This figure shows the co-authorship network connecting the top 25 collaborators of K Naess. A scholar is included among the top collaborators of K Naess 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 K Naess. K Naess 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.
Bruhn, Helene, K Naess, Sofia Ygberg, et al.. (2024). Novel Synonymous and Deep Intronic Variants Causing Primary and Secondary Pyruvate Dehydrogenase Complex Deficiency. Human Mutation. 2024. 1–16. 1 indexed citations
2.
Naess, K, Albert Z. Lim, Robert McFarland, et al.. (2024). Quantitative proteomics of patient fibroblasts reveal biomarkers and diagnostic signatures of mitochondrial disease. JCI Insight. 9(20). 3 indexed citations
3.
Nilsson, Daniel, Martin Engvall, Helena Malmgren, et al.. (2023). Genome sequencing with comprehensive variant calling identifies structural variants and repeat expansions in a large fraction of individuals with ataxia and/or neuromuscular disorders. Frontiers in Neurology. 14. 1170005–1170005. 4 indexed citations
4.
Naess, K, et al.. (2023). Unraveling mucolipidosis type III gamma through whole genome sequencing in late-onset retinitis pigmentosa: a case report. BMC Ophthalmology. 23(1). 394–394. 2 indexed citations
5.
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
6.
Sørensen, L., Ulrika von Döbeln, Henrik Åhlman, et al.. (2020). Expanded Screening of One Million Swedish Babies with R4S and CLIR for Post-Analytical Evaluation of Data. International Journal of Neonatal Screening. 6(2). 42–42. 15 indexed citations
7.
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
8.
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
9.
Hoogeveen‐Westerveld, Marianne, Marian A. Kroos, Sirpa Ala‐Mello, et al.. (2019). Segmental and total uniparental isodisomy (UPiD) as a disease mechanism in autosomal recessive lysosomal disorders: evidence from SNP arrays. European Journal of Human Genetics. 27(6). 919–927. 8 indexed citations
10.
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
11.
Falkenberg, Kim D., Nancy Braverman, Ann B. Moser, et al.. (2017). Allelic Expression Imbalance Promoting a Mutant PEX6 Allele Causes Zellweger Spectrum Disorder. The American Journal of Human Genetics. 101(6). 965–976. 34 indexed citations
12.
Stranneheim, Henrik, Martin Engvall, K Naess, et al.. (2014). Rapid pulsed whole genome sequencing for comprehensive acute diagnostics of inborn errors of metabolism. BMC Genomics. 15(1). 1090–1090. 44 indexed citations
13.
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
14.
Shahim, Pashtun, Niklas Darín, Ulf Andréasson, et al.. (2013). Cerebrospinal Fluid Brain Injury Biomarkers in Children: A Multicenter Study. Pediatric Neurology. 49(1). 31–39.e2. 36 indexed citations
15.
Tuppen, Helen, K Naess, Nancy G. Kennaway, et al.. (2012). Mutations in the mitochondrial tRNASer(AGY) gene are associated with deafness, retinal degeneration, myopathy and epilepsy. European Journal of Human Genetics. 20(8). 897–904. 11 indexed citations
16.
Naess, K, Michela Barbaro, Helene Bruhn, et al.. (2011). Complete Deletion of a POLG1 Allele in a Patient with Alpers Syndrome. JIMD Reports. 4. 67–73. 4 indexed citations
17.
Fahnehjelm, Kristina Teär, Monica Olsson, K Naess, et al.. (2010). Visual function, ocular motility and ocular characteristics in patients with mitochondrial complex I deficiency. Acta Ophthalmologica. 90(1). 32–43. 8 indexed citations
18.
Hoefs, Saskia J.G., Cindy E. Dieteren, Richard J. Rodenburg, et al.. (2009). Baculovirus complementation restores a novelNDUFAF2mutation causing complex I deficiency. Human Mutation. 30(7). E728–E736. 41 indexed citations
19.
Naess, K, Christoph Freyer, Helene Bruhn, et al.. (2008). MtDNA mutations are a common cause of severe disease phenotypes in children with Leigh syndrome. Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1787(5). 484–490. 47 indexed citations
20.
Malm, Gunilla, Britt Gustafsson, Gunilla Berglund, et al.. (2008). Outcome in six children with mucopolysaccharidosis type IH, hurler syndrome, after haematopoietic stem cell transplantation (HSCT). Acta Paediatrica. 97(8). 1108–1112. 34 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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