René Günther Feichtinger (René G Feichtinger, Rene G Feichtinger)

ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 42

Top Venues

Genes

Oxidative medicine and cellular longevity

Journal of medical genetics

Metabolites

Landeskrankenhaus Salzburg - Universitätsklinikum der Paracelsus Medizinischen Privatuniversität

Landeskrankenhaus Salzburg - Universitätsklinikum der Paracelsus Medizinischen Privatuniversität (PHD)

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

Affiliation History

Landeskrankenhaus Salzburg - Universitätsklinikum der Paracelsus Medizinischen Privatuniversität Aug 15 2016

Austria

Senior Researcher, PhD :: Department of Pediatrics

Education History

Landeskrankenhaus Salzburg - Universitätsklinikum der Paracelsus Medizinischen Privatuniversität Oct 08 2006

Austria

PHD :: Department of Pediatrics

Publications

Claire E L Smith, Virginie Laugel-Haushalter, Ummey Hany, Sunayna Best, Rachel L Taylor, James A Poulter, Saskia B Wortmann, René Günther Feichtinger, Johannes A Mayr, Suhaila Al Bahlani, Georgios Nikolopoulos, Alice Rigby, Graeme C Black, Christopher Mark Watson, Sahar Mansour, Chris F Inglehearn, Alan J Mighell, Agnès Bloch-Zupan, null null
Biallelic variants in Plexin B2 ( PLXNB2 ) cause amelogenesis imperfecta, hearing loss and intellectual disability. Journal of medical genetics 61 (7) (2024)
Claire E L Smith, Virginie Laugel-Haushalter, Ummey Hany, Sunayna Best, Rachel L Taylor, James A Poulter, Saskia B Wortmann, René Günther Feichtinger, Johannes A Mayr, Suhaila Al Bahlani, Georgios Nikolopoulos, Alice Rigby, Graeme C Black, Christopher Mark Watson, Sahar Mansour, Chris F Inglehearn, Alan J Mighell, Agnès Bloch-Zupan, null null
Biallelic variants in Plexin B2 ( PLXNB2 ) cause amelogenesis imperfecta, hearing loss and intellectual disability. Journal of medical genetics 61 (7) (2024)
Claire E L Smith, Virginie Laugel-Haushalter, Ummey Hany, Sunayna Best, Rachel L Taylor, James A Poulter, Saskia B Wortmann, René Günther Feichtinger, Johannes A Mayr, Suhaila Al Bahlani, Georgios Nikolopoulos, Alice Rigby, Graeme C Black, Christopher Mark Watson, Sahar Mansour, Chris F Inglehearn, Alan J Mighell, Agnès Bloch-Zupan, null null
Biallelic variants in Plexin B2 ( PLXNB2 ) cause amelogenesis imperfecta, hearing loss and intellectual disability. Journal of medical genetics (2024)
Maximilian Penkl, Johannes Adalbert Mayr, René Günther Feichtinger, Ralf Reilmann, Otfried Debus, Manfred Fobker, Anja Penkl, Janine Reunert, Stephan Rust, Thorsten Marquardt
Anaplerotic Therapy Using Triheptanoin in Two Brothers Suffering from Aconitase 2 Deficiency. Metabolites 14 (4) (2024)
Maximilian Penkl, Johannes Adalbert Mayr, René Günther Feichtinger, Ralf Reilmann, Otfried Debus, Manfred Fobker, Anja Penkl, Janine Reunert, Stephan Rust, Thorsten Marquardt
Anaplerotic Therapy Using Triheptanoin in Two Brothers Suffering from Aconitase 2 Deficiency. Metabolites 14 (4) (2024)
Claire E L Smith, Virginie Laugel-Haushalter, Ummey Hany, Sunayna Best, Rachel L Taylor, James A Poulter, Saskia B Wortmann, René Günther Feichtinger, Johannes A Mayr, Suhaila Al Bahlani, Georgios Nikolopoulos, Alice Rigby, Graeme C Black, Christopher Mark Watson, Sahar Mansour, Chris F Inglehearn, Alan J Mighell, Agnès Bloch-Zupan, null null
Biallelic variants in Plexin B2 ( PLXNB2 ) cause amelogenesis imperfecta, hearing loss and intellectual disability. Journal of medical genetics 61 (7) (2024)
Claire E L Smith, Virginie Laugel-Haushalter, Ummey Hany, Sunayna Best, Rachel L Taylor, James A Poulter, Saskia B Wortmann, René Günther Feichtinger, Johannes A Mayr, Suhaila Al Bahlani, Georgios Nikolopoulos, Alice Rigby, Graeme C Black, Christopher Mark Watson, Sahar Mansour, Chris F Inglehearn, Alan J Mighell, Agnès Bloch-Zupan, null null
Biallelic variants in Plexin B2 ( PLXNB2 ) cause amelogenesis imperfecta, hearing loss and intellectual disability. Journal of medical genetics (2024)
Maximilian Penkl, Johannes Adalbert Mayr, René Günther Feichtinger, Ralf Reilmann, Otfried Debus, Manfred Fobker, Anja Penkl, Janine Reunert, Stephan Rust, Thorsten Marquardt
Anaplerotic Therapy Using Triheptanoin in Two Brothers Suffering from Aconitase 2 Deficiency. Metabolites 14 (4) (2024)
Katarína Kušíková, Andrea Šoltýsová, Andrej Ficek, René Günther Feichtinger, Johannes Adalbert Mayr, Martina Škopková, Daniela Gasperikova, Miriam Kolníková, Karoline Ornig, Ognian Kalev, Serge Weis, Denisa Weis
Prognostic Value of Genotype-Phenotype Correlations in X-Linked Myotubular Myopathy and the Use of the Face2Gene Application as an Effective Non-Invasive Diagnostic Tool. Genes 14 (12) (2023)
René Günther Feichtinger, Martin Preisel, Karin Brugger, Saskia B Wortmann, Johannes Adalbert Mayr
Case Report-An Inherited Loss-of-Function NRXN3 Variant Potentially Causes a Neurodevelopmental Disorder with Autism Consistent with Previously Described 14q24.3-31.1 Deletions. Genes 14 (6) (2023)
René Günther Feichtinger, Martin Preisel, Karin Brugger, Saskia B Wortmann, Johannes Adalbert Mayr
Case Report-An Inherited Loss-of-Function NRXN3 Variant Potentially Causes a Neurodevelopmental Disorder with Autism Consistent with Previously Described 14q24.3-31.1 Deletions. Genes 14 (6) (2023)
Sara Huber, Theresia Fitzner, René Günther Feichtinger, Sarah Hochmann, Theo F J Kraus, Karl Sotlar, Barbara Kofler, Martin Varga
Galanin System in the Human Bile Duct and Perihilar Cholangiocarcinoma. Cells 12 (13) (2023)
Nathalie Stummer, René Günther Feichtinger, Daniel Weghuber, Barbara Kofler, Anna Maria Schneider
Role of Hydrogen Sulfide in Inflammatory Bowel Disease. Antioxidants (Basel, Switzerland) 12 (8) (2023)
Melanie T Achleitner, Judith J M Jans, Laura Ebner, Johannes Spenger, Vassiliki Konstantopoulou, René Günther Feichtinger, Karin Brugger, Doris Mayr, Ron A Wevers, Christian Thiel, Saskia B Wortmann, Johannes Adalbert Mayr
PPA1 Deficiency Causes a Deranged Galactose Metabolism Recognizable in Neonatal Screening. Metabolites 13 (11) (2023)
Katarína Kušíková, Andrea Šoltýsová, Andrej Ficek, René Günther Feichtinger, Johannes Adalbert Mayr, Martina Škopková, Daniela Gasperikova, Miriam Kolníková, Karoline Ornig, Ognian Kalev, Serge Weis, Denisa Weis
Prognostic Value of Genotype-Phenotype Correlations in X-Linked Myotubular Myopathy and the Use of the Face2Gene Application as an Effective Non-Invasive Diagnostic Tool. Genes 14 (12) (2023)
René Günther Feichtinger, Martin Preisel, Karin Brugger, Saskia B Wortmann, Johannes Adalbert Mayr
Case Report-An Inherited Loss-of-Function NRXN3 Variant Potentially Causes a Neurodevelopmental Disorder with Autism Consistent with Previously Described 14q24.3-31.1 Deletions. Genes 14 (6) (2023)
Frédéric Ebstein, Sébastien Küry, Victoria Most, Cory Scott Rosenfelt, Marie-Pier Scott-Boyer, Geeske M van Woerden, Thomas Besnard, Jonas Johannes Papendorf, Maja Studencka-Turski, Tianyun Wang, Tzung-Chien Hsieh, Richard Golnik, Dustin Baldridge, Cara Forster, Charlotte de Konink, Selina M W Teurlings, Virginie Vignard, Richard H van Jaarsveld, Lesley Ades, Benjamin Cogné, Cyril Mignot, Wallid Deb, Marjolijn C J Jongmans, F Sessions Cole, Marie-José H van den Boogaard, Jennifer A Wambach, Daniel J Wegner, Sandra Yang, Vickie Hannig, Jennifer Ann Brault, Neda Zadeh, Bruce Bennetts, Boris Keren, Anne-Claire Gélineau, Zöe Powis, Meghan C Towne, Kristine Bachman, Andrea Seeley, Anita E Beck, Jennifer Morrison, Rachel Westman, Kelly Averill, Theresa Brunet, Judith Haasters, Melissa T Carter, Matthew Osmond, Patricia G Wheeler, Francesca Forzano, Shehla Mohammed, Yannis Trakadis, Andrea Accogli, Rachel Harrison, Yiran Guo, Hakon H Hakonarson, Sophie Rondeau, Geneviève Baujat, Giulia Barcia, René Günther Feichtinger, Johannes Adalbert Mayr, Martin Preisel, Frederic Laumonnier, Tilmann Kallinich, Alexej Knaus, Bertrand Isidor, Peter M Krawitz, Linus Völker, Elke Hammer, Arnaud Droit, Evan E Eichler, Ype Elgersma, Peter W Hildebrand, Francois V Bolduc, Elke Krüger, Stephane Bezieau
PSMC3 proteasome subunit variants are associated with neurodevelopmental delay and type I interferon production. Science translational medicine 15 (698) (2023)
Katarína Kušíková, Andrea Šoltýsová, Andrej Ficek, René Günther Feichtinger, Johannes Adalbert Mayr, Martina Škopková, Daniela Gasperikova, Miriam Kolníková, Karoline Ornig, Ognian Kalev, Serge Weis, Denisa Weis
Prognostic Value of Genotype-Phenotype Correlations in X-Linked Myotubular Myopathy and the Use of the Face2Gene Application as an Effective Non-Invasive Diagnostic Tool. Genes 14 (12) (2023)
René Günther Feichtinger, Martin Preisel, Karin Brugger, Saskia B Wortmann, Johannes Adalbert Mayr
Case Report-An Inherited Loss-of-Function NRXN3 Variant Potentially Causes a Neurodevelopmental Disorder with Autism Consistent with Previously Described 14q24.3-31.1 Deletions. Genes 14 (6) (2023)
Luca Catalano, Sepideh Aminzadeh-Gohari, Daniela D Weber, Rodolphe Poupardin, Victoria E Stefan, William J Smiles, Julia Tevini, René Günther Feichtinger, Sophia Derdak, Martin Bilban, Stefan Bareswill, Markus M Heimesaat, Barbara Kofler
Triple Therapy with Metformin, Ketogenic Diet, and Metronomic Cyclophosphamide Reduced Tumor Growth in MYCN-Amplified Neuroblastoma Xenografts. Metabolites 13 (8) (2023)
Sara Carvalhal, Ingrid Bader, Martin A Rooimans, Anneke B Oostra, Jesper A Balk, René Günther Feichtinger, Christine Beichler, Michael R Speicher, Johanna M van Hagen, Quinten Waisfisz, Mieke van Haelst, Martijn Bruijn, Alexandra Tavares, Johannes Adalbert Mayr, Rob M F Wolthuis, Raquel de Vasconcellos Carvalhaes de Oliveira, Job de Lange
Biallelic BUB1 mutations cause microcephaly, developmental delay, and variable effects on cohesion and chromosome segregation. Science advances 8 (3) (2022)
Nathalie Stummer, Daniel Weghuber, René Günther Feichtinger, Sara Huber, Johannes Adalbert Mayr, Barbara Kofler, Daniel Neureiter, Eckhard Klieser, Sarah Hochmann, Wanda Lauth, Anna Maria Schneider
Hydrogen Sulfide Metabolizing Enzymes in the Intestinal Mucosa in Pediatric and Adult Inflammatory Bowel Disease. Antioxidants (Basel, Switzerland) 11 (11) (2022)
Anna Maria Schneider, Mihriban Özsoy, Franz A Zimmermann, Susanne Maria Brunner, René Günther Feichtinger, Johannes Adalbert Mayr, Barbara Kofler, Daniel Neureiter, Eckhard Klieser, Elmar Aigner, Sebastian Schütz, Nathalie Stummer, Wolfgang Sperl, Daniel Weghuber
Expression of Oxidative Phosphorylation Complexes and Mitochondrial Mass in Pediatric and Adult Inflammatory Bowel Disease. Oxidative medicine and cellular longevity 2022 (2022)
René Günther Feichtinger, Martin Preisel, Katja Steinbrücker, Karin Brugger, Alexandra Radda, Saskia B Wortmann, Johannes Adalbert Mayr
A TSHZ3 Frame-Shift Variant Causes Neurodevelopmental and Renal Disorder Consistent with Previously Described Proximal Chromosome 19q13.11 Deletion Syndrome. Genes 13 (12) (2022)
René Günther Feichtinger, Martin Preisel, Katja Steinbrücker, Karin Brugger, Alexandra Radda, Saskia B Wortmann, Johannes Adalbert Mayr
A TSHZ3 Frame-Shift Variant Causes Neurodevelopmental and Renal Disorder Consistent with Previously Described Proximal Chromosome 19q13.11 Deletion Syndrome. Genes 13 (12) (2022)
René Günther Feichtinger, Martin Preisel, Katja Steinbrücker, Karin Brugger, Alexandra Radda, Saskia B Wortmann, Johannes Adalbert Mayr
A TSHZ3 Frame-Shift Variant Causes Neurodevelopmental and Renal Disorder Consistent with Previously Described Proximal Chromosome 19q13.11 Deletion Syndrome. Genes 13 (12) (2022)
Michael Zech, Matthias Elstner, Katja Steinbrücker, Céline Bris, Naig Gueguen, René Günther Feichtinger, Melanie T Achleitner, Neslihan Duzkale, Maximilien Périvier, Johannes Koch, Harald Engelhardt, Peter Freisinger, Matias Wagner, Theresa Brunet, Riccardo Berutti, Dmitrii Smirnov, Tharsini Navaratnarajah, Richard J T Rodenburg, Lynn S Pais, Christina Austin-Tse, Melanie O'Leary, Sylvia Boesch, Robert Jech, Somayeh Bakhtiari, Sheng Chih Jin, Friederike Wilbert, Michael C Kruer, Saskia B Wortmann, Matthias Eckenweiler, Johannes A Mayr, Felix Distelmaier, Robert Steinfeld, Juliane Winkelmann, Holger Prokisch
Variants in Mitochondrial ATP Synthase Cause Variable Neurologic Phenotypes. Annals of neurology 91 (2) (2022)
René Günther Feichtinger, Martin Preisel, Katja Steinbrücker, Karin Brugger, Alexandra Radda, Saskia B Wortmann, Johannes Adalbert Mayr
A TSHZ3 Frame-Shift Variant Causes Neurodevelopmental and Renal Disorder Consistent with Previously Described Proximal Chromosome 19q13.11 Deletion Syndrome. Genes 13 (12) (2022)
René Günther Feichtinger, Andreas Hüllen, Andreas Koller, Dieter Kotzot, Valerian Grote, Erdmann Rapp, Peter Hofbauer, Karin Brugger, Christian Thiel, Johannes Adalbert Mayr, Saskia B Wortmann
A spoonful of L-fucose-an efficient therapy for GFUS-CDG, a new glycosylation disorder. EMBO molecular medicine 13 (9) (2021)
Daniela D Weber, Maheshwor Thapa, Sepideh Aminzadeh-Gohari, Anna-Sophia Redtenbacher, Luca Catalano, René Günther Feichtinger, Peter Koelblinger, Guido Dallmann, Michael Emberger, Barbara Kofler, Roland Lang
Targeted Metabolomics Identifies Plasma Biomarkers in Mice with Metabolically Heterogeneous Melanoma Xenografts. Cancers 13 (3) (2021)
Anne Schänzer, Melanie T Achleitner, Dietrich Trümbach, Laurence Hubert, Arnold Munnich, Barbara Ahlemeyer, Maha M AlAbdulrahim, Philipp A Greif, Sebastian Vosberg, Blake Hummer, René Günther Feichtinger, Johannes A Mayr, Saskia B Wortmann, Heidi Aichner, Sabine Rudnik-Schöneborn, Anna Ruiz, Elisabeth Gabau, Jacobo Pérez Sánchez, Sian Ellard, Tessa Homfray, Karen L Stals, Wolfgang Wurst, Bernd A Neubauer, Till Acker, Stefan K Bohlander, Cédric Asensio, Claude Besmond, Fowzan Sami Alkuraya, Moenaldeen D AlSayed, Andreas Hahn, Axel Weber
Mutations in HID1 Cause Syndromic Infantile Encephalopathy and Hypopituitarism. Annals of neurology 90 (1) (2021)
Silvia Vidali, Raffaele Gerlini, Kyle Thompson, Jill E Urquhart, Jana Meisterknecht, Juan Antonio Aguilar-Pimentel, Oana V Amarie, Lore Becker, Catherine Breen, Julia Calzada-Wack, Nirav F Chhabra, Yi-Li Cho, Patricia da Silva-Buttkus, René Günther Feichtinger, Kristine Gampe, Lillian Garrett, Kai P Hoefig, Sabine Maria Hölter, Elisabeth Jameson, Tanja Klein-Rodewald, Stefanie Leuchtenberger, Susan Marschall, Philipp Mayer-Kuckuk, Gregor Miller, Manuela A Oestereicher, Kristina Pfannes, Birgit Rathkolb, Jan Rozman, Charlotte Sanders, Nadine Spielmann, Claudia Stoeger, Marten Szibor, Irina Treise, John H Walter, Wolfgang Wurst, Johannes Adalbert Mayr, Helmut Fuchs, Ulrich Gärtner, Ilka Wittig, Robert W Taylor, William G Newman, Holger Prokisch, Valérie Gailus-Durner, Martin Hrabě de Angelis
Characterising a homozygous two-exon deletion in UQCRH: comparing human and mouse phenotypes. EMBO molecular medicine 13 (12) (2021)
Wolfgang Sperl, Saskia B Wortmann, René Günther Feichtinger, Johannes Adalbert Mayr
The switch in the diagnosis of mitochondrial diseases from the classical 'function first' to the NGS-based 'genetics first' diagnostic era. Journal of mother and child 24 (2) (2020)
Anna M Schneider, Mihriban Özsoy, Franz A Zimmermann, René Günther Feichtinger, Johannes Adalbert Mayr, Barbara Kofler, Wolfgang Sperl, Daniel Weghuber, Katharina Mörwald
Age-Related Deterioration of Mitochondrial Function in the Intestine. Oxidative medicine and cellular longevity 2020 (2020)
Sepideh Aminzadeh-Gohari, Daniela D Weber, Luca Catalano, René Günther Feichtinger, Barbara Kofler, Roland Lang
Targeting Mitochondria in Melanoma. Biomolecules 10 (10) (2020)
Silvia Vidali, Sepideh Aminzadeh-Gohari, Renaud Vatrinet, Luisa Iommarini, Anna Maria Porcelli, Barbara Kofler, René Günther Feichtinger
Lithium and Not Acetoacetate Influences the Growth of Cells Treated with Lithium Acetoacetate. International journal of molecular sciences 20 (12) (2019)
David Licha, Silvia Vidali, Sepideh Aminzadeh-Gohari, Oliver Alka, Leander Breitkreuz, Oliver Kohlbacher, Roland J Reischl, René Günther Feichtinger, Barbara Kofler, Christian G Huber
Untargeted Metabolomics Reveals Molecular Effects of Ketogenic Diet on Healthy and Tumor Xenograft Mouse Models. International journal of molecular sciences 20 (16) (2019)
René Günther Feichtinger, Roland Lang
Targeting L-Lactate Metabolism to Overcome Resistance to Immune Therapy of Melanoma and Other Tumor Entities. Journal of oncology 2019 (2019)
Enrico Bugiardini, Simon Pope, René Günther Feichtinger, Olivia V Poole, Alan M Pittman, Cathy E Woodward, Simon Heales, Rosaline Quinlivan, Henry Houlden, Johannes A Mayr, Michael G Hanna, Robert D S Pitceathly
Utility of Whole Blood Thiamine Pyrophosphate Evaluation in TPK1-Related Diseases. Journal of clinical medicine 8 (7) (2019)
René Günther Feichtinger, Georg Schäfer, Christof Seifarth, Johannes Adalbert Mayr, Barbara Kofler, Helmut Klocker
Reduced Levels of ATP Synthase Subunit ATP5F1A Correlate with Earlier-Onset Prostate Cancer. Oxidative medicine and cellular longevity 2018 (2018)
René Günther Feichtinger, Daniel Neureiter, Tom Skaria, Silja Wessler, Timothy L Cover, Johannes Adalbert Mayr, Franz A Zimmermann, Gernot Posselt, Wolfgang Sperl, Barbara Kofler
Oxidative Phosphorylation System in Gastric Carcinomas and Gastritis. Oxidative medicine and cellular longevity 2017 (2017)
René Günther Feichtinger, Michaela Brunner-Krainz, Bader Alhaddad, Saskia B Wortmann, Reka Kovacs-Nagy, Tatjana Stojakovic, Wolfgang Erwa, Bernhard Resch, Werner Windischhofer, Sarah Verheyen, Sabine Uhrig, Christian Windpassinger, Felix Locker, Christine Makowski, Tim M Strom, Thomas Meitinger, Holger Prokisch, Wolfgang Sperl, Tobias B Haack, Johannes Adalbert Mayr
Combined Respiratory Chain Deficiency and UQCC2 Mutations in Neonatal Encephalomyopathy: Defective Supercomplex Assembly in Complex III Deficiencies. Oxidative medicine and cellular longevity 2017 (2017)

René Günther Feichtinger.css-eqlu8i{font-size:small;padding-left:4px;} (René G Feichtinger, Rene G Feichtinger)

Publication Activity (10 Years)

Top Topics

Top Venues

René Günther Feichtinger (René G Feichtinger, Rene G Feichtinger)