Anna Wredenberg

Publication Activity (10 Years)

Years Active: 2019-2024
Publications (10 Years): 13

Top Topics

Hypertrophic Cardiomyopathy

Pluripotent Stem Cells

Mitochondrial Dna

Top Venues

Stem cells translational medicine

Human molecular genetics

Molecular genetics & genomic medicine

Science advances

This page only lists publications with an associated author ORCID identifier.

Publications

Ana Vučković, Christoph Freyer, Anna Wredenberg, Hauke S Hillen
The molecular machinery for maturation of primary mtDNA transcripts. Human molecular genetics 33 (R1) (2024)
Julia Rogal, Laura Nicoleti Zamproni, Polyxeni Nikolakopoulou, Sofia Ygberg, Anna Wedell, Anna Wredenberg, Anna Herland
Human In Vitro Models of Neuroenergetics and Neurometabolic Disturbances: Current Advances and Clinical Perspectives. Stem cells translational medicine 13 (6) (2024)
Julia Rogal, Laura Nicoleti Zamproni, Polyxeni Nikolakopoulou, Sofia Ygberg, Anna Wedell, Anna Wredenberg, Anna Herland
Human In Vitro Models of Neuroenergetics and Neurometabolic Disturbances: Current Advances and Clinical Perspectives. Stem cells translational medicine 13 (6) (2024)
Julia Rogal, Laura Nicoleti Zamproni, Polyxeni Nikolakopoulou, Sofia Ygberg, Anna Wedell, Anna Wredenberg, Anna Herland
Human In Vitro Models of Neuroenergetics and Neurometabolic Disturbances: Current Advances and Clinical Perspectives. Stem cells translational medicine (2024)
Julia Rogal, Laura Nicoleti Zamproni, Polyxeni Nikolakopoulou, Sofia Ygberg, Anna Wedell, Anna Wredenberg, Anna Herland
Human In Vitro Models of Neuroenergetics and Neurometabolic Disturbances: Current Advances and Clinical Perspectives. Stem cells translational medicine 13 (6) (2024)
Ana Vučković, Christoph Freyer, Anna Wredenberg, Hauke S Hillen
The molecular machinery for maturation of primary mtDNA transcripts. Human molecular genetics 33 (R1) (2024)
Ana Vučković, Christoph Freyer, Anna Wredenberg, Hauke S Hillen
The molecular machinery for maturation of primary mtDNA transcripts. Human molecular genetics 33 (R1) (2024)
Ilan Ben-Shabat, Malin Kvarnung, Wolfgang Sperker, Helene Bruhn, Anna Wredenberg, Rolf Wibom, Inger Nennesmo, Martin Engvall, Martin Paucar
Ataxia Syndrome With Hearing Loss and Nephronophthisis Associated With a Novel Homozygous Variant in XPNPEP3 . Neurology. Genetics 9 (6) (2023)
Paula Clemente, Javier Calvo-Garrido, Sarah F Pearce, Florian A Schober, Megumi Shigematsu, Stefan J Siira, Isabelle Laine, Henrik Spåhr, Christian Steinmetzger, Katja Petzold, Yohei Kirino, Rolf Wibom, Oliver Rackham, Aleksandra Filipovska, Joanna Rorbach, Christoph Freyer, Anna Wredenberg
ANGEL2 phosphatase activity is required for non-canonical mitochondrial RNA processing. Nature communications 13 (1) (2022)
Florian A Schober, David Moore, Ilian Atanassov, Marco F Moedas, Paula Clemente, Ákos Végvári, Najla El Fissi, Roberta Filograna, Anna-Lena Bucher, Yvonne Hinze, Matthew The, Erik Hedman, Ekaterina Chernogubova, Arjana Begzati, Rolf Wibom, Mohit Jain, Roland Nilsson, Lukas Käll, Anna Wedell, Christoph Freyer, Anna Wredenberg
The one-carbon pool controls mitochondrial energy metabolism via complex I and iron-sulfur clusters. Science advances 7 (8) (2021)
Sandrina P Correia, Marco F Moedas, Karin Naess, Helene Bruhn, Camilla Maffezzini, Javier Calvo-Garrido, Nicole Lesko, Rolf Wibom, Florian A Schober, Anders Jemt, Henrik Stranneheim, Christoph Freyer, Anna Wedell, Anna Wredenberg
Severe congenital lactic acidosis and hypertrophic cardiomyopathy caused by an intronic variant in NDUFB7. Human mutation 42 (4) (2021)
Aleksandra Pajak, Isabelle Laine, Paula Clemente, Najla El-Fissi, Florian A Schober, Camilla Maffezzini, Javier Calvo-Garrido, Rolf Wibom, Roberta Filograna, Ashish Dhir, Anna Wedell, Christoph Freyer, Anna Wredenberg
Defects of mitochondrial RNA turnover lead to the accumulation of double-stranded RNA in vivo. PLoS genetics 15 (7) (2019)
Camilla Maffezzini, Isabelle Laine, Cristina Dallabona, Paula Clemente, Javier Calvo-Garrido, Rolf Wibom, Karin Naess, Michela Barbaro, Anna Falk, Claudia Donnini, Christoph Freyer, Anna Wredenberg, Anna Wedell
Mutations in the mitochondrial tryptophanyl-tRNA synthetase cause growth retardation and progressive leukoencephalopathy. Molecular genetics & genomic medicine 7 (6) (2019)