Anna Wredenberg

7.1k total citations · 1 hit paper
49 papers, 4.7k citations indexed

About

Anna Wredenberg is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, Anna Wredenberg has authored 49 papers receiving a total of 4.7k indexed citations (citations by other indexed papers that have themselves been cited), including 47 papers in Molecular Biology, 18 papers in Clinical Biochemistry and 7 papers in Genetics. Recurrent topics in Anna Wredenberg's work include Mitochondrial Function and Pathology (32 papers), Metabolism and Genetic Disorders (18 papers) and RNA modifications and cancer (10 papers). Anna Wredenberg is often cited by papers focused on Mitochondrial Function and Pathology (32 papers), Metabolism and Genetic Disorders (18 papers) and RNA modifications and cancer (10 papers). Anna Wredenberg collaborates with scholars based in Sweden, Germany and United Kingdom. Anna Wredenberg's co-authors include Nils‐Göran Larsson, Rolf Wibom, Aleksandra Trifunović, Anja T. Rovio, Johannes N. Spelbrink, Howard T. Jacobs, Anders Oldfors, Maria Falkenberg, Jan Törnell and Mohammad Bohlooly‐Y and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Anna Wredenberg

49 papers receiving 4.7k citations

Hit Papers

align trajectories sort by overperformance

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.

Premature ageing in mice expressing defective mitochondrial DNA polymerase

2004 2.0k citations Aleksandra Trifunović, Anna Wredenberg et al. Nature profile →

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author						Papers	Cites
Anna Wredenberg	4.0k	1.2k	926	560	383	49	4.7k
Gregory C. Kujoth	2.7k 0.7×	678 0.6×	933 1.0×	481 0.9×	380 1.0×	36	3.7k
Rolf Wibom	5.5k 1.4×	1.6k 1.3×	1.5k 1.6×	547 1.0×	516 1.3×	80	6.8k
Johannes N. Spelbrink	6.6k 1.6×	2.6k 2.2×	968 1.0×	543 1.0×	459 1.2×	69	7.5k
Carl E.G. Bruder	2.2k 0.6×	534 0.5×	548 0.6×	373 0.7×	389 1.0×	33	3.2k
Carlo Viscomi	4.4k 1.1×	1.6k 1.3×	810 0.9×	139 0.2×	345 0.9×	94	5.8k
Anja T. Rovio	2.2k 0.6×	693 0.6×	656 0.7×	449 0.8×	235 0.6×	12	2.8k
Marc Vermulst	2.0k 0.5×	527 0.4×	513 0.6×	278 0.5×	243 0.6×	29	2.5k
Henna Tyynismaa	3.0k 0.7×	1.1k 0.9×	405 0.4×	115 0.2×	184 0.5×	82	3.8k
Rudolf J. Wiesner	2.9k 0.7×	506 0.4×	947 1.0×	117 0.2×	279 0.7×	107	4.3k
Erik E. Griffin	2.4k 0.6×	606 0.5×	357 0.4×	255 0.5×	363 0.9×	17	2.8k

Countries citing papers authored by Anna Wredenberg

Since Specialization

Citations

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

Fields of papers citing papers by Anna Wredenberg

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anna Wredenberg

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

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

Filograna, Roberta, Giovanni Rigoni, Michela Barbaro, et al.. (2024). PARKIN is not required to sustain OXPHOS function in adult mammalian tissues. npj Parkinson s Disease. 10(1). 93–93. 10 indexed citations

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

Kvarnung, Malin, Wolfgang Sperker, Helene Bruhn, et al.. (2023). Ataxia Syndrome With Hearing Loss and Nephronophthisis Associated With a Novel Homozygous Variant in XPNPEP3. Neurology Genetics. 9(6). e200100–e200100. 1 indexed citations

Milenkovic, Dusanka, Xie Xie, Min Jiang, et al.. (2022). Mammalian RNase H1 directs RNA primer formation for mtDNA replication initiation and is also necessary for mtDNA replication completion. Nucleic Acids Research. 50(15). 8749–8766. 14 indexed citations

Engvall, Martin, Aki Kawasaki, Valério Carelli, et al.. (2021). Case Report: A Novel Mutation in the Mitochondrial MT-ND5 Gene Is Associated With Leber Hereditary Optic Neuropathy (LHON). Frontiers in Neurology. 12. 652590–652590. 7 indexed citations

Rosenberger, Florian A., Ilian Atanassov, David Moore, et al.. (2021). Stable Isotope Labeling of Amino Acids in Flies (SILAF) Reveals Differential Phosphorylation of Mitochondrial Proteins Upon Loss of OXPHOS Subunits. Molecular & Cellular Proteomics. 20. 100065–100065. 8 indexed citations

Alsina, David, Oleksandr Lytovchenko, Ilian Atanassov, et al.. (2020). FBXL 4 deficiency increases mitochondrial removal by autophagy. EMBO Molecular Medicine. 12(7). e11659–e11659. 43 indexed citations

Maffezzini, Camilla, Javier Calvo‐Garrido, Anna Wredenberg, & Christoph Freyer. (2020). Metabolic regulation of neurodifferentiation in the adult brain. Cellular and Molecular Life Sciences. 77(13). 2483–2496. 59 indexed citations

10.

Naess, K, Helene Bruhn, Henrik Stranneheim, et al.. (2020). Clinical Presentation, Genetic Etiology, and Coenzyme Q10 Levels in 55 Children with Combined Enzyme Deficiencies of the Mitochondrial Respiratory Chain. The Journal of Pediatrics. 228. 240–251.e2. 8 indexed citations

11.

Schober, F., Ilian Atanassov, Christoph Freyer, & Anna Wredenberg. (2020). Quantitative Proteomics in Drosophila with Holidic Stable-Isotope Labeling of Amino Acids in Fruit Flies (SILAF). Methods in molecular biology. 2192. 75–87. 4 indexed citations

12.

Calvo‐Garrido, Javier, Camilla Maffezzini, F. Schober, et al.. (2019). SQSTM1/p62-Directed Metabolic Reprogramming Is Essential for Normal Neurodifferentiation. Stem Cell Reports. 12(4). 696–711. 36 indexed citations

13.

Tegelberg, Saara, Jukka Kallijärvi, Janne Purhonen, et al.. (2017). Respiratory chain complex III deficiency due to mutated BCS1L: a novel phenotype with encephalomyopathy, partially phenocopied in a Bcs1l mutant mouse model. Orphanet Journal of Rare Diseases. 12(1). 73–73. 18 indexed citations

14.

Herebıan, Diran, Annette Seibt, Sander H. J. Smits, et al.. (2017). Detection of 6-demethoxyubiquinone in CoQ10 deficiency disorders: Insights into enzyme interactions and identification of potential therapeutics. Molecular Genetics and Metabolism. 121(3). 216–223. 25 indexed citations

15.

Wredenberg, Anna, Marie Lagouge, Ana Bratić, et al.. (2013). MTERF3 Regulates Mitochondrial Ribosome Biogenesis in Invertebrates and Mammals. PLoS Genetics. 9(1). e1003178–e1003178. 82 indexed citations

16.

Edgar, Daniel, Irina G. Shabalina, Yolanda Cámara, et al.. (2009). Random Point Mutations with Major Effects on Protein-Coding Genes Are the Driving Force behind Premature Aging in mtDNA Mutator Mice. Cell Metabolism. 10(2). 131–138. 167 indexed citations

17.

Aydin, Jan, Daniel Andersson, Sandra L. Hänninen, et al.. (2008). Increased mitochondrial Ca 2+ and decreased sarcoplasmic reticulum Ca 2+ in mitochondrial myopathy. Human Molecular Genetics. 18(2). 278–288. 64 indexed citations

18.

Stewart, James B., Christoph Freyer, Joanna L. Elson, et al.. (2008). Strong Purifying Selection in Transmission of Mammalian Mitochondrial DNA. PLoS Biology. 6(1). e10–e10. 388 indexed citations

19.

Wredenberg, Anna, Christoph Freyer, Marie Sandström, et al.. (2006). Respiratory chain dysfunction in skeletal muscle does not cause insulin resistance. Biochemical and Biophysical Research Communications. 350(1). 202–207. 118 indexed citations

20.

Trifunović, Aleksandra, Anna Wredenberg, Maria Falkenberg, et al.. (2004). Premature ageing in mice expressing defective mitochondrial DNA polymerase. Nature. 429(6990). 417–423. 2050 indexed citations breakdown →

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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