René Feichtinger

Phone0043 662 4482 4753
Emailr.feichtingersalkat

Research activity per year

Fingerprint

Dive into the research topics where René Feichtinger is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

8 Similar Profiles

91 Original Article
16 Abstract (Journal)
10 Review article
9 Case report
More

Anaplerotic Therapy Using Triheptanoin in Two Brothers Suffering from Aconitase 2 Deficiency
Penkl, M., Mayr, J. A. (Co-author), Feichtinger, R. G. (Co-author), Reilmann, R., Debus, O., Fobker, M., Penkl, A., Reunert, J., Rust, S. & Marquardt, T., 20 Apr 2024, In: METABOLITES. 14, 4, 12 p., 238.
Research output: Contribution to journal › Original Article › peer-review

Open Access
Biallelic Cys141Tyr variant of SEL1L is associated with neurodevelopmental disorders, agammaglobulinemia, and premature death
Weis, D., Lin, L. L., Wang, H. H., Li, Z. J., Kusikova, K., Ciznar, P., Wolf, H. M., Leiss-Piller, A., Wang, Z., Wei, X., Weis, S., Skalicka, K., Hrckova, G., Danisovic, L., Soltysova, A., Yang, T. T., Feichtinger, R. G. (Last author), Mayr, J. A. (Last author) & Qi, L., 16 Jan 2024, In: JOURNAL OF CLINICAL INVESTIGATION. 134, 2, 15 p., e170882.
Research output: Contribution to journal › Original Article › peer-review

Open Access
5 Citations (Web of Science)
Biallelic variants in Plexin B2 (PLXNB2) cause amelogenesis imperfecta, hearing loss and intellectual disability
Smith, C., Laugel-Haushalter, V., Hany, U., Best, S., Taylor, R., Poulter, J., Wortmann, S. (Co-author), Feichtinger, R. (Co-author), Mayr, J. (Co-author), Al Bahlani, S., Nikolopoulos, G., Rigby, A., Black, G., Watson, C., Mansour, S., Inglehearn, C., Mighell, A., Bloch-Zupan, A., UK Inherited Retinal Dystrophy Consortium (UKIRDC) & Genomes England Research Consortium (GERC), Jul 2024, In: JOURNAL OF MEDICAL GENETICS . 61, 7, p. 689-698 10 p.
Research output: Contribution to journal › Original Article › peer-review

Open Access
Clinical, Neuroimaging, and Metabolic Footprint of the Neurodevelopmental Disorder Caused by Monoallelic HK1 Variants
Wortmann, S. B. (First author), Feichtinger, R. G. (Co-author), Abela, L., van Gemert, L. A., Aubart, M., Dufeu-Berat, C.-M., Boddaert, N., de Coo, R., Stühn, L., Hebbink, J., Heinritz, W., Hildebrandt, J., Himmelreich, N., Korenke, C., Lehman, A., Leyland, T., Makowski, C., Martinez Marin, R. J., Marzin, P. & Mühlhausen, C. & 15 others, Rio, M., Rotig, A., Roux, C.-J., Schiff, M., Haack, T. B., Syrbe, S., Zylicz, S. A., Thiel, C., Veiga da Cunha, M., van Schaftingen, E., Wagner, M., Mayr, J. A. (Co-author), Wevers, R. A., Boltshauser, E. & Willemsen, M. A., Apr 2024, In: NEUROLOGY-GENETICS. 10, 2, p. e200146 13 p., e200146.
Research output: Contribution to journal › Original Article › peer-review

Open Access
Loss-of-Function Variants in <i>CUL3</i> Cause a Syndromic Neurodevelopmental Disorder
Blackburn, P. R., Ebstein, F., Hsieh, T.-C., Motta, M., Radio, F. C., Herkert, J. C., Rinne, T., Thiffault, I., Rapp, M., Alders, M., Maas, S., Gerard, B., Smol, T., Vincent-Delorme, C., Cogne, B., Isidor, B., Vincent, M., Bachmann-Gagescu, R., Rauch, A. & Joset, P. & 59 others, Ferrero, G. B., Ciolfi, A., Husson, T., Guerrot, A.-M., Bacino, C., Macmurdo, C., Thompson, S. S., Rosenfeld, J. A., Faivre, L., Mau-Them, F. T., Deb, W., Vignard, V., Agrawal, P. B., Madden, J. A., Goldenberg, A., Lecoquierre, F., Zech, M., Prokisch, H., Necpal, J., Jech, R., Winkelmann, J., Koprusakova, M. T., Konstantopoulou, V., Younce, J. R., Shinawi, M., Mighton, C., Fung, C., Morel, C. F., Lerner-Ellis, J., Ditroia, S., Barth, M., Bonneau, D., Krapels, I., Stegmann, A. P. A., van Der Schoot, V., Brunet, T., Bussmann, C., Mignot, C., Zampino, G., Wortmann, S. B. (Co-author), Mayr, J. A. (Co-author), Feichtinger, R. G. (Co-author), Courtin, T., Ravelli, C., Keren, B., Ziegler, A., Hasadsri, L., Pichurin, P. N., Klee, E. W., Grand, K., Sanchez-Lara, P. A., Krueger, E., Bezieau, S., Klinkhammer, H., Krawitz, P. M., Eichler, E. E., Tartaglia, M., Kuery, S. & Wang, T., 20 Sept 2024, In: ANNALS OF NEUROLOGY . 14 p.
Research output: Contribution to journal › Original Article › peer-review

1 Active
7 Finished

GENOMIT: A multi-omics approach for diagnostics and monitoring of mitochondrial disorders
Mayr, J. A. (PI), Achleitner, M. (Further contributor), Feichtinger, R. (Further contributor) & Wortmann, S. (Further contributor)
1/07/23 → 1/07/26
Project: Research
Mitochondial dysfunction in preeclampsia (PE)
Feichtinger, R. (CoPI) & Jaksch-Bogensperger, H. (Further contributor)
1/10/22 → 1/10/24
Project: Research
Investigation of disorders in the pathway of ADP ribosylation in pediatric patients
Mayr, J. A. (PI), Koch, J. (Further contributor) & Feichtinger, R. (Further contributor)
1/09/19 → 1/11/20
Project: Research
Feasibility of flow cytometric analysis of the mitochondrial energy metabolism in fibroblasts and peripheral blood
Feichtinger, R. (PI) & Koller, A. (CoPI)
1/06/17 → 1/06/18
Project: Research
TRANSMIT (TRANSlating the role of Mitochondria in Tumorigenesis)
Kofler, B. (PI), Feichtinger, R. (Further contributor) & Aminzadeh-Gohari, S. (Further contributor)
1/01/17 → 1/01/21
Project: Research

Award of Excellence 2009 from the Bundesministerium für Wissenschaft und Forschung (Dr. Johannes Hahn) for one of the best dissertations 2009
Feichtinger, R. (Recipient), 2009
Prize
Best Abstract Award 2010 (48. Jahrestagung der ÖGKJ)
Feichtinger, R. (Recipient), 2010
Prize
Best Poster Award 2009 (47. Jahrestagung der ÖGKJ)
Feichtinger, R. (Recipient), 2009
Prize
Golden scientific award of the Paracelsus Medical University 2014
Feichtinger, R. (Recipient), 2014
Prize
Golden scientific award of the Paracelsus Medical University 2019
Feichtinger, R. (Recipient), 2019
Prize

René Feichtinger

Fingerprint

Research output

Projects

Prizes