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

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

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20 of 20 papers shown

#	Work	Indexed citations
1	Novel Synonymous and Deep Intronic Variants Causing Primary and Secondary Pyruvate Dehydrogenase Complex Deficiency 2024 ·Human Mutation ·Helene Bruhn, K Naess, Sofia Ygberg, (unknown), Nicole Lesko, Rolf Wibom, Christoph Freyer, Henrik Stranneheim, Anna Wedell, Anna Wredenberg	1
2	Quantitative proteomics of patient fibroblasts reveal biomarkers and diagnostic signatures of mitochondrial disease 2024 ·JCI Insight ·(unknown), (unknown), (unknown), K Naess, Albert Z. Lim, Robert McFarland, (unknown), (unknown), Rolf Wibom, Martin Engvall, Helene Bruhn, Nicole Lesko, Ákos Végvári, Lukas Käll, (unknown), Charlotte L. Alston, Christoph Freyer, Robert W. Taylor, Anna Wedell, Anna Wredenberg	3
3	Genome sequencing with comprehensive variant calling identifies structural variants and repeat expansions in a large fraction of individuals with ataxia and/or neuromuscular disorders 2023 ·Frontiers in Neurology ·(unknown), Daniel Nilsson, Martin Engvall, Helena Malmgren, Håkan Thonberg, Maria Pettersson, Britt‐Marie Anderlid, Anna Hammarsjö, Hafdís T. Helgadóttir, Snjólaug Arnardottir, K Naess, Inger Nennesmo, Martin Paucar, (unknown), Rayomand Press, Göran Solders, Thomas Sejersen, Anna Lindstrand, Malin Kvarnung	4
4	Unraveling mucolipidosis type III gamma through whole genome sequencing in late-onset retinitis pigmentosa: a case report 2023 ·BMC Ophthalmology ·(unknown), (unknown), K Naess, Eliane Sardh, Anna Lindstrand, Erik Björck	2
5	Phenotypic spectrum and clinical course of single large-scale mitochondrial DNA deletion disease in the paediatric population: a multicentre study 2021 ·Journal of Medical Genetics ·(unknown), John Vissing, Elsebet Østergaard, Laurence A. Bindoff, I.F.M. de Coo, Martin Engvall, Omar Hikmat, Pirjo Isohanni, Gittan Kollberg, Christopher Lindberg, Kari Majamaa, K Naess, Johanna Uusimaa, M. Tulinius, Niklas Darín	11
6	Expanded Screening of One Million Swedish Babies with R4S and CLIR for Post-Analytical Evaluation of Data 2020 ·International Journal of Neonatal Screening ·L. Sørensen, Ulrika von Döbeln, Henrik Åhlman, Annika Ohlsson, Martin Engvall, K Naess, (unknown), (unknown), Anna Wedell, Rolf Zetterström	15
7	The impact of gender, puberty, and pregnancy in patients with POLG disease 2020 ·Annals of Clinical and Translational Neurology ·Omar Hikmat, K Naess, Martin Engvall, Claus Klingenberg, Magnhild Rasmussen, Chantal Tallaksen, Christian Samsonsen, Eylert Brodtkorb, Elsebet Østergaard, I.F.M. de Coo, (unknown), Pirjo Isohanni, Johanna Uusimaa, Niklas Darín, Shamima Rahman, Laurence A. Bindoff	8
8	Simplifying the clinical classification of polymerase gamma (POLG) disease based on age of onset; studies using a cohort of 155 cases 2020 ·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, (unknown), Pirjo Isohanni, Johanna Uusimaa, Niklas Darín, Shamima Rahman, Laurence A. Bindoff	46
9	Segmental and total uniparental isodisomy (UPiD) as a disease mechanism in autosomal recessive lysosomal disorders: evidence from SNP arrays 2019 ·European Journal of Human Genetics ·(unknown), (unknown), (unknown), Marianne Hoogeveen‐Westerveld, Marian A. Kroos, Sirpa Ala‐Mello, Olga Amaral, Clara Sá-Miranda, Irene Mavridou, Helen Michelakakis, K Naess, Frans W. Verheijen, Lies H. Hoefsloot, Trijnie Dijkhuizen, (unknown), (unknown), Ans T. van der Ploeg, W.W.M. Pim Pijnappel, Jasper J. Saris, Dicky Halley	8
10	Elevated cerebrospinal fluid protein in POLG‐related epilepsy: Diagnostic and prognostic implications 2018 ·Epilepsia ·Omar Hikmat, K Naess, Martin Engvall, Claus Klingenberg, Magnhild Rasmussen, Chantal Tallaksen, Eylert Brodtkorb, Torunn Fiskerstrand, Pirjo Isohanni, Johanna Uusimaa, Niklas Darín, Shamima Rahman, Laurence A. Bindoff	6
11	Allelic Expression Imbalance Promoting a Mutant PEX6 Allele Causes Zellweger Spectrum Disorder 2017 ·The American Journal of Human Genetics ·Kim D. Falkenberg, Nancy Braverman, Ann B. Moser, Steven J. Steinberg, Femke C. C. Klouwer, Agatha Schlüter, Montserrat Ruíz, Aurora Pujol, Martin Engvall, K Naess, (unknown), (unknown), M. Estela Rubio‐Gozalbo, Sacha Ferdinandusse, Ronald J. A. Wanders, Hans R. Waterham	34
12	Rapid pulsed whole genome sequencing for comprehensive acute diagnostics of inborn errors of metabolism 2014 ·BMC Genomics ·Henrik Stranneheim, Martin Engvall, K Naess, Nicole Lesko, Pontus Larsson, (unknown), (unknown), Anna Wredenberg, Christoph Freyer, Michela Barbaro, Helene Bruhn, (unknown), Måns Magnusson, Rolf Wibom, Rolf Zetterström, Valtteri Wirta, Ulrika von Döbeln, Anna Wedell	44
13	A multicenter study on Leigh syndrome: disease course and predictors of survival 2014 ·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, (unknown), Tuula Lönnqvist, Helena Pihko, Katariina Mankinen, Laurence A. Bindoff, M. Tulinius, Niklas Darín	161
14	Cerebrospinal Fluid Brain Injury Biomarkers in Children: A Multicenter Study 2013 ·Pediatric Neurology ·Pashtun Shahim, Niklas Darín, Ulf Andréasson, Kaj Blennow, (unknown), Johan Lundgren, Jan‐Eric Månsson, K Naess, Carl‐Johan Törnhage, Henrik Zetterberg, Niklas Mattsson	36
15	Mutations in the mitochondrial tRNASer(AGY) gene are associated with deafness, retinal degeneration, myopathy and epilepsy 2012 ·European Journal of Human Genetics ·Helen Tuppen, K Naess, Nancy G. Kennaway, Mazhor Aldosary, Nicole Lesko, John W. Yarham, Helene Bruhn, Rolf Wibom, Inger Nennesmo, Richard G. Weleber, Emma L. Blakely, Robert W. Taylor, Robert McFarland	11
16	Complete Deletion of a POLG1 Allele in a Patient with Alpers Syndrome 2011 ·JIMD Reports ·K Naess, Michela Barbaro, Helene Bruhn, Rolf Wibom, Inger Nennesmo, Ulrika von Döbeln, Nils‐Göran Larsson, Antal Németh, Nicole Lesko	4
17	Visual function, ocular motility and ocular characteristics in patients with mitochondrial complex I deficiency 2010 ·Acta Ophthalmologica ·Kristina Teär Fahnehjelm, Monica Olsson, K Naess, Maria Kristoffersen Wiberg, Jan Ygge, Lene Martin, Ulrika von Döbeln	8
18	Baculovirus complementation restores a novelNDUFAF2mutation causing complex I deficiency 2009 ·Human Mutation ·Saskia J.G. Hoefs, Cindy E. Dieteren, Richard J. Rodenburg, K Naess, Helene Bruhn, Rolf Wibom, Esther Wagena, Peter H.G.M. Willems, Jan Smeıtınk, Leo Nijtmans, Lambert P. van den Heuvel	41
19	MtDNA mutations are a common cause of severe disease phenotypes in children with Leigh syndrome 2008 ·Biochimica et Biophysica Acta (BBA) - Bioenergetics ·K Naess, Christoph Freyer, Helene Bruhn, Rolf Wibom, Gunilla Malm, Inger Nennesmo, Ulrika von Döbeln, Nils‐Göran Larsson	47
20	Outcome in six children with mucopolysaccharidosis type IH, hurler syndrome, after haematopoietic stem cell transplantation (HSCT) 2008 ·Acta Paediatrica ·Gunilla Malm, Britt Gustafsson, Gunilla Berglund, (unknown), K Naess, Birgit Borgström, Ulrika von Döbeln, Olle Ringdén	34

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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