Andreas Walter Kuss (Andreas W Kuss)

Publication Activity (10 Years)

Years Active: 2018-2023
Publications (10 Years): 14

Top Topics

Machine Learning

Cardiovascular Disease

Top Venues

Journal of clinical medicine

International journal of molecular sciences

European journal of human genetics : EJHG

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

Publications

Simone Venz, Viola von Bohlen Und Halbach, Christian Hentschker, Heike Junker, Andreas Walter Kuss, Thomas Sura, Elke Krüger, Linus Völker, Oliver von Bohlen Und Halbach, Lars Riff Jensen, Elke Hammer
Global Protein Profiling in Processed Immunohistochemistry Tissue Sections. International journal of molecular sciences 24 (14) (2023)
Heiko Dunkel, Henning Wehrmann, Lars Riff Jensen, Andreas Walter Kuss, Stefan Simm
MncR: Late Integration Machine Learning Model for Classification of ncRNA Classes Using Sequence and Structural Encoding. International journal of molecular sciences 24 (10) (2023)
Wolfgang Poller, Bettina Heidecker, Enrico Ammirati, Andreas Walter Kuss, Ana Tzvetkova, Wolfram C Poller, Carsten Skurk, Arash Haghikia
Innate Immunity in Cardiovascular Diseases-Identification of Novel Molecular Players and Targets. Journal of clinical medicine 12 (1) (2023)
Wolfgang Poller, Bettina Heidecker, Enrico Ammirati, Andreas Walter Kuss, Ana Tzvetkova, Wolfram C Poller, Carsten Skurk, Arash Haghikia
Innate Immunity in Cardiovascular Diseases-Identification of Novel Molecular Players and Targets. Journal of clinical medicine 12 (1) (2023)
Wolfgang Poller, Bettina Heidecker, Enrico Ammirati, Andreas Walter Kuss, Ana Tzvetkova, Wolfram C Poller, Carsten Skurk, Arash Haghikia
Innate Immunity in Cardiovascular Diseases-Identification of Novel Molecular Players and Targets. Journal of clinical medicine 12 (1) (2023)
Martina Gast, Vanasa Nageswaran, Andreas Walter Kuss, Ana Tzvetkova, Xiaomin Wang, Liliana H Mochmann, Pegah Ramezani Rad, Stefan Weiss, Stefan Simm, Tanja Zeller, Henry Voelzke, Wolfgang U Hoffmann, Linus Völker, Stefan B Felix, Marcus Dörr, Antje Beling, Carsten Skurk, David-Manuel Leistner, Bernhard H Rauch, Tetsuro Hirose, Bettina Heidecker, Karin Klingel, Shinichi Nakagawa, Wolfram C Poller, Filip K Swirski, Arash Haghikia, Wolfgang Poller
tRNA-like Transcripts from the NEAT1-MALAT1 Genomic Region Critically Influence Human Innate Immunity and Macrophage Functions. Cells 11 (24) (2022)
Martina Gast, Vanasa Nageswaran, Andreas Walter Kuss, Ana Tzvetkova, Xiaomin Wang, Liliana H Mochmann, Pegah Ramezani Rad, Stefan Weiss, Stefan Simm, Tanja Zeller, Henry Voelzke, Wolfgang U Hoffmann, Linus Völker, Stefan B Felix, Marcus Dörr, Antje Beling, Carsten Skurk, David-Manuel Leistner, Bernhard H Rauch, Tetsuro Hirose, Bettina Heidecker, Karin Klingel, Shinichi Nakagawa, Wolfram C Poller, Filip K Swirski, Arash Haghikia, Wolfgang Poller
tRNA-like Transcripts from the NEAT1-MALAT1 Genomic Region Critically Influence Human Innate Immunity and Macrophage Functions. Cells 11 (24) (2022)
Viola von Bohlen Und Halbach, Simone Venz, Simon Nwakor, Christian Hentschker, Elke Hammer, Heike Junker, Andreas Walter Kuss, Oliver von Bohlen Und Halbach, Lars R Jensen
Deficiency in FTSJ1 Affects Neuronal Plasticity in the Hippocampal Formation of Mice. Biology 11 (7) (2022)
Martina Gast, Vanasa Nageswaran, Andreas Walter Kuss, Ana Tzvetkova, Xiaomin Wang, Liliana H Mochmann, Pegah Ramezani Rad, Stefan Weiss, Stefan Simm, Tanja Zeller, Henry Voelzke, Wolfgang U Hoffmann, Linus Völker, Stefan B Felix, Marcus Dörr, Antje Beling, Carsten Skurk, David-Manuel Leistner, Bernhard H Rauch, Tetsuro Hirose, Bettina Heidecker, Karin Klingel, Shinichi Nakagawa, Wolfram C Poller, Filip K Swirski, Arash Haghikia, Wolfgang Poller
tRNA-like Transcripts from the NEAT1-MALAT1 Genomic Region Critically Influence Human Innate Immunity and Macrophage Functions. Cells 11 (24) (2022)
Martina Gast, Vanasa Nageswaran, Andreas Walter Kuss, Ana Tzvetkova, Xiaomin Wang, Liliana H Mochmann, Pegah Ramezani Rad, Stefan Weiss, Stefan Simm, Tanja Zeller, Henry Voelzke, Wolfgang U Hoffmann, Linus Völker, Stefan B Felix, Marcus Dörr, Antje Beling, Carsten Skurk, David-Manuel Leistner, Bernhard H Rauch, Tetsuro Hirose, Bettina Heidecker, Karin Klingel, Shinichi Nakagawa, Wolfram C Poller, Filip K Swirski, Arash Haghikia, Wolfgang Poller
tRNA-like Transcripts from the NEAT1-MALAT1 Genomic Region Critically Influence Human Innate Immunity and Macrophage Functions. Cells 11 (24) (2022)
Martina Gast, Vanasa Nageswaran, Andreas Walter Kuss, Ana Tzvetkova, Xiaomin Wang, Liliana H Mochmann, Pegah Ramezani Rad, Stefan Weiss, Stefan Simm, Tanja Zeller, Henry Voelzke, Wolfgang U Hoffmann, Linus Völker, Stefan B Felix, Marcus Dörr, Antje Beling, Carsten Skurk, David-Manuel Leistner, Bernhard H Rauch, Tetsuro Hirose, Bettina Heidecker, Karin Klingel, Shinichi Nakagawa, Wolfram C Poller, Filip K Swirski, Arash Haghikia, Wolfgang Poller
tRNA-like Transcripts from the NEAT1-MALAT1 Genomic Region Critically Influence Human Innate Immunity and Macrophage Functions. Cells 11 (24) (2022)
Neetika Nath, Lisa Hagenau, Stefan Weiss, Ana Tzvetkova, Lars Riff Jensen, Lars Kaderali, Matthias Port, Harry Scherthan, Andreas Walter Kuss
Genome-Wide DNA Alterations in X-Irradiated Human Gingiva Fibroblasts. International journal of molecular sciences 21 (16) (2020)
Masoud Garshasbi, Mahdi Mahmoudi, Ehsan Razmara, Mahdi Vojdanian, Saeed Aslani, Elham Farhadi, Lars Riff Jensen, Seyed Masoud Arzaghi, Shiva Poursani, Amirreza Bitaraf, Milad Eidi, Elika Esmaeilzadeh Gharehdaghi, Andreas Walter Kuss, Ahmadreza Jamshidi
Identification of RELN variant p.(Ser2486Gly) in an Iranian family with ankylosing spondylitis; the first association of RELN and AS. European journal of human genetics : EJHG 28 (6) (2020)
Laura van Diepen, Falk F R Büttner, Dirk Hoffmann, Christina T Thiesler, Oliver von Bohlen Und Halbach, Viola von Bohlen Und Halbach, Lars Riff Jensen, Doris Steinemann, Simon Edvardson, Orly Elpeleg, Axel Schambach, Rita Gerardy-Schahn, Andreas Walter Kuss
A patient-specific induced pluripotent stem cell model for West syndrome caused by ST3GAL3 deficiency. European journal of human genetics : EJHG 26 (12) (2018)