Denny Schanze

Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 31

Top Topics

Gene Expression

Internal Carotid Artery

Hypertrophic Cardiomyopathy

Quality Control

Top Venues

Cancer gene therapy

Journal of the American Heart Association

American journal of respiratory and critical care medicine

Nature communications

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

Publications

Jonas Windrich, Peter Braubach, Florian Länger, Jens Dingemann, Nicolaus Schwerk, Martin Wetzke, Diane Miriam Renz, Martin Zenker, Denny Schanze, Christian Peter Kratz
RAS-MAPK Pathway Mutations in Congenital Pulmonary Airway Malformations. American journal of respiratory and critical care medicine 209 (10) (2024)
Vanessa Franziska Schmidt, Friedrich G Kapp, Constantin Goldann, Linda Huthmann, Beatrix Cucuruz, Richard Brill, Veronika Vielsmeier, Caroline T Seebauer, Armin-Johannes Michel, Max Seidensticker, Wibke Uller, Jakob B W Weiß, Alena Sint, Beate Häberle, Julia Küppers, Alexandra Wagner, Johanna Cordes, Annegret Holm, Denny Schanze, Jens Ricke, Melanie A Kimm, Walter A Wohlgemuth, Martin Zenker, Moritz Wildgruber, null null
Extracranial Vascular Anomalies Driven by RAS/MAPK Variants: Spectrum and Genotype-Phenotype Correlations. Journal of the American Heart Association 13 (8) (2024)
Miriam Mengoni, Andreas Dominik Braun, Sahithi Seedarala, Susanne Bonifatius, Evi Kostenis, Denny Schanze, Martin Zenker, Thomas Tüting, Evelyn Gaffal
Transactivation of Met signaling by oncogenic Gnaq drives the evolution of melanoma in Hgf-Cdk4 mice. Cancer gene therapy (2024)
Konrad Lehr, Undine Gabriele Lange, Noam Mathias Hipler, Ramiro Vilchez-Vargas, Albrecht Hoffmeister, Jürgen Feisthammel, Dorina Buchloh, Denny Schanze, Martin Zenker, Ines Gockel, Alexander Link, Boris Jansen-Winkeln
Prediction of anastomotic insufficiency based on the mucosal microbiome prior to colorectal surgery: a proof-of-principle study. Scientific reports 14 (1) (2024)
Miriam Mengoni, Andreas Dominik Braun, Sahithi Seedarala, Susanne Bonifatius, Evi Kostenis, Denny Schanze, Martin Zenker, Thomas Tüting, Evelyn Gaffal
Transactivation of Met signaling by oncogenic Gnaq drives the evolution of melanoma in Hgf-Cdk4 mice. Cancer gene therapy 31 (6) (2024)
Vanessa Franziska Schmidt, Friedrich G Kapp, Constantin Goldann, Linda Huthmann, Beatrix Cucuruz, Richard Brill, Veronika Vielsmeier, Caroline T Seebauer, Armin-Johannes Michel, Max Seidensticker, Wibke Uller, Jakob B W Weiß, Alena Sint, Beate Häberle, Julia Küppers, Alexandra Wagner, Johanna Cordes, Annegret Holm, Denny Schanze, Jens Ricke, Melanie A Kimm, Walter A Wohlgemuth, Martin Zenker, Moritz Wildgruber, null null
Extracranial Vascular Anomalies Driven by RAS/MAPK Variants: Spectrum and Genotype-Phenotype Correlations. Journal of the American Heart Association 13 (8) (2024)
Konrad Lehr, Undine Gabriele Lange, Noam Mathias Hipler, Ramiro Vilchez-Vargas, Albrecht Hoffmeister, Jürgen Feisthammel, Dorina Buchloh, Denny Schanze, Martin Zenker, Ines Gockel, Alexander Link, Boris Jansen-Winkeln
Prediction of anastomotic insufficiency based on the mucosal microbiome prior to colorectal surgery: a proof-of-principle study. Scientific reports 14 (1) (2024)
Vanessa Franziska Schmidt, Friedrich G Kapp, Constantin Goldann, Linda Huthmann, Beatrix Cucuruz, Richard Brill, Veronika Vielsmeier, Caroline T Seebauer, Armin-Johannes Michel, Max Seidensticker, Wibke Uller, Jakob B W Weiß, Alena Sint, Beate Häberle, Julia Küppers, Alexandra Wagner, Johanna Cordes, Annegret Holm, Denny Schanze, Jens Ricke, Melanie A Kimm, Walter A Wohlgemuth, Martin Zenker, Moritz Wildgruber, null null
Extracranial Vascular Anomalies Driven by RAS/MAPK Variants: Spectrum and Genotype-Phenotype Correlations. Journal of the American Heart Association 13 (8) (2024)
Jonas Windrich, Peter Braubach, Florian Länger, Jens Dingemann, Nicolaus Schwerk, Martin Wetzke, Diane Miriam Renz, Martin Zenker, Denny Schanze, Christian Peter Kratz
RAS-MAPK Pathway Mutations in Congenital Pulmonary Airway Malformations. American journal of respiratory and critical care medicine 209 (10) (2024)
Miriam Mengoni, Andreas Dominik Braun, Sahithi Seedarala, Susanne Bonifatius, Evi Kostenis, Denny Schanze, Martin Zenker, Thomas Tüting, Evelyn Gaffal
Transactivation of Met signaling by oncogenic Gnaq drives the evolution of melanoma in Hgf-Cdk4 mice. Cancer gene therapy 31 (6) (2024)
Jonas Windrich, Peter Braubach, Florian Länger, Jens Dingemann, Nicolaus Schwerk, Martin Wetzke, Diane Miriam Renz, Martin Zenker, Denny Schanze, Christian Peter Kratz
RAS-MAPK Pathway Mutations in Congenital Pulmonary Airway Malformations. American journal of respiratory and critical care medicine 209 (10) (2024)
Jonas Windrich, Peter Braubach, Florian Länger, Jens Dingemann, Nicolaus Schwerk, Martin Wetzke, Diane Miriam Renz, Martin Zenker, Denny Schanze, Christian Peter Kratz
RAS-MAPK Pathway Mutations in Congenital Pulmonary Airway Malformations. American journal of respiratory and critical care medicine 209 (10) (2024)
Dorothee Maria Gescher, Denny Schanze, Peter Vavra, Philip Wolff, Geraldine Zimmer-Bensch, Martin Zenker, Thomas Frodl, Christian Schmahl
Differential methylation of OPRK1 in borderline personality disorder is associated with childhood trauma. Molecular psychiatry (2024)
Vanessa Franziska Schmidt, Friedrich G Kapp, Constantin Goldann, Linda Huthmann, Beatrix Cucuruz, Richard Brill, Veronika Vielsmeier, Caroline T Seebauer, Armin-Johannes Michel, Max Seidensticker, Wibke Uller, Jakob B W Weiß, Alena Sint, Beate Häberle, Julia Küppers, Alexandra Wagner, Johanna Cordes, Annegret Holm, Denny Schanze, Jens Ricke, Melanie A Kimm, Walter A Wohlgemuth, Martin Zenker, Moritz Wildgruber, null null
Extracranial Vascular Anomalies Driven by RAS/MAPK Variants: Spectrum and Genotype-Phenotype Correlations. Journal of the American Heart Association 13 (8) (2024)
Konrad Lehr, Undine Gabriele Lange, Noam Mathias Hipler, Ramiro Vilchez-Vargas, Albrecht Hoffmeister, Jürgen Feisthammel, Dorina Buchloh, Denny Schanze, Martin Zenker, Ines Gockel, Alexander Link, Boris Jansen-Winkeln
Prediction of anastomotic insufficiency based on the mucosal microbiome prior to colorectal surgery: a proof-of-principle study. Scientific reports 14 (1) (2024)
Vanessa Franziska Schmidt, Friedrich G Kapp, Constantin Goldann, Linda Huthmann, Beatrix Cucuruz, Richard Brill, Veronika Vielsmeier, Caroline T Seebauer, Armin-Johannes Michel, Max Seidensticker, Wibke Uller, Jakob B W Weiß, Alena Sint, Beate Häberle, Julia Küppers, Alexandra Wagner, Johanna Cordes, Annegret Holm, Denny Schanze, Jens Ricke, Melanie A Kimm, Walter A Wohlgemuth, Martin Zenker, Moritz Wildgruber, null null
Extracranial Vascular Anomalies Driven by RAS/MAPK Variants: Spectrum and Genotype-Phenotype Correlations. Journal of the American Heart Association 13 (8) (2024)
Jonas Windrich, Peter Braubach, Florian Länger, Jens Dingemann, Nicolaus Schwerk, Martin Wetzke, Diane Miriam Renz, Martin Zenker, Denny Schanze, Christian Peter Kratz
RAS-MAPK Pathway Mutations in Congenital Pulmonary Airway Malformations. American journal of respiratory and critical care medicine 209 (10) (2024)
Miriam Mengoni, Andreas Dominik Braun, Sahithi Seedarala, Susanne Bonifatius, Evi Kostenis, Denny Schanze, Martin Zenker, Thomas Tüting, Evelyn Gaffal
Transactivation of Met signaling by oncogenic Gnaq drives the evolution of melanoma in Hgf-Cdk4 mice. Cancer gene therapy 31 (6) (2024)
Miriam Mengoni, Andreas Dominik Braun, Sahithi Seedarala, Susanne Bonifatius, Evi Kostenis, Denny Schanze, Martin Zenker, Thomas Tüting, Evelyn Gaffal
Transactivation of Met signaling by oncogenic Gnaq drives the evolution of melanoma in Hgf-Cdk4 mice. Cancer gene therapy (2024)
Miriam Mengoni, Andreas Dominik Braun, Sahithi Seedarala, Susanne Bonifatius, Evi Kostenis, Denny Schanze, Martin Zenker, Thomas Tüting, Evelyn Gaffal
Transactivation of Met signaling by oncogenic Gnaq drives the evolution of melanoma in Hgf-Cdk4 mice. Cancer gene therapy 31 (6) (2024)
Vanessa Franziska Schmidt, Friedrich G Kapp, Constantin Goldann, Linda Huthmann, Beatrix Cucuruz, Richard Brill, Veronika Vielsmeier, Caroline T Seebauer, Armin-Johannes Michel, Max Seidensticker, Wibke Uller, Jakob B W Weiß, Alena Sint, Beate Häberle, Julia Küppers, Alexandra Wagner, Johanna Cordes, Annegret Holm, Denny Schanze, Jens Ricke, Melanie A Kimm, Walter A Wohlgemuth, Martin Zenker, Moritz Wildgruber, null null
Extracranial Vascular Anomalies Driven by RAS/MAPK Variants: Spectrum and Genotype-Phenotype Correlations. Journal of the American Heart Association (2024)
Katrin Vogel, Aditya Arra, Holger Lingel, Dirk Bretschneider, Florian Prätsch, Denny Schanze, Martin Zenker, Silke Balk, Dunja Bruder, Robert Geffers, Thomas Hachenberg, Christoph Arens, Monika C Brunner-Weinzierl
Bifidobacteria shape antimicrobial T-helper cell responses during infancy and adulthood. Nature communications 14 (1) (2023)
Saeideh Nakhaei-Rad, Fereshteh Haghighi, Farhad Bazgir, Julia Dahlmann, Alexandra Viktoria Busley, Marcel Buchholzer, Karolin Kleemann, Anne Schänzer, Andrea Borchardt, Andreas Hahn, Sebastian Kötter, Denny Schanze, Ruchika Anand, Florian Funk, Annette Vera Kronenbitter, Jürgen Scheller, Roland P Piekorz, Andreas S Reichert, Marianne Volleth, Matthew J Wolf, Ion Cristian Cirstea, Bruce D Gelb, Marco Tartaglia, Joachim P Schmitt, Martina Krüger, Ingo Kutschka, Lukas Cyganek, Martin Zenker, George Kensah, Mohammad Reza Ahmadian
Molecular and cellular evidence for the impact of a hypertrophic cardiomyopathy-associated RAF1 variant on the structure and function of contractile machinery in bioartificial cardiac tissues. Communications biology 6 (1) (2023)
Ramiro Vilchez-Vargas, Franz Salm, Eva B Znalesniak, Katharina Haupenthal, Denny Schanze, Martin Zenker, Alexander Link, Werner Hoffmann
Profiling of the Bacterial Microbiota along the Murine Alimentary Tract. International journal of molecular sciences 23 (3) (2022)
Julia Brinkmann, Christina Lissewski, Valentina Pinna, Yoann Vial, Francesca Pantaleoni, Francesca Lepri, Paola Daniele, Birute Burnyte, Goran Cuturilo, Christine Fauth, Alper Gezdirici, Dieter Kotzot, Elif Yılmaz Güleç, Violeta Iotova, Denny Schanze, Francis Ramond, Markéta Havlovicová, Gulen Eda Utine, Pelin Ozlem Simsek-Kiper, Milena Stoyanova, Alain Verloes, Alessandro De Luca, Tartaglia Marco, Hélène Cave, Martin Zenker
The clinical significance of A2ML1 variants in Noonan syndrome has to be reconsidered. European journal of human genetics : EJHG 29 (3) (2020)
Paige B Martin, Yu Kigoshi-Tansho, Roger B Sher, Gianina Ravenscroft, Jennifer E Stauffer, Rajesh Kumar, Ryo Yonashiro, Tina Müller, Christopher Griffith, William Allen, Davut Pehlivan, Tamar Harel, Martin Zenker, Denise Howting, Denny Schanze, Eissa A Faqeih, Naif A M Almontashiri, Reza Maroofian, Henry Houlden, Neda Mazaheri, Hamid Galehdari, F Nienke Boonstra, Jennifer E Posey, Monique M Ryan, James R Lupski, Nigel G Laing, Claudio A P Joazeiro, Gregory A Cox
NEMF mutations that impair ribosome-associated quality control are associated with neuromuscular disease. Nature communications 11 (1) (2020)
Paige B Martin, Yu Kigoshi-Tansho, Roger B Sher, Gianina Ravenscroft, Jennifer E Stauffer, Rajesh Kumar, Ryo Yonashiro, Tina Müller, Christopher Griffith, William Allen, Davut Pehlivan, Tamar Harel, Martin Zenker, Denise Howting, Denny Schanze, Eissa A Faqeih, Naif A M Almontashiri, Reza Maroofian, Henry Houlden, Neda Mazaheri, Hamid Galehdari, F Nienke Boonstra, Jennifer E Posey, Monique M Ryan, James R Lupski, Nigel G Laing, Claudio A P Joazeiro, Gregory A Cox
Author Correction: NEMF mutations that impair ribosome-associated quality control are associated with neuromuscular disease. Nature communications 11 (1) (2020)
Ante Karoglan, Denny Schanze, Claudia Bär, Petra Muschke, Martin Zenker, Ina Schanze
A 2q24.2 microdeletion containing TANK as novel candidate gene for intellectual disability. American journal of medical genetics. Part A 179 (5) (2019)
Shazia Ashraf, Hiroki Kudo, Jia Rao, Atsuo Kikuchi, Eugen Widmeier, Jennifer A Lawson, Weizhen Tan, Tobias Hermle, Jillian K Warejko, Shirlee Shril, Merlin Airik, Tilman Jobst-Schwan, Svjetlana Lovric, Daniela A Braun, Heon Yung Gee, David Schapiro, Amar J Majmundar, Carolin E Sadowski, Werner L Pabst, Ankana Daga, Amelie T van der Ven, Johanna M Schmidt, Boon Chuan Low, Anjali Bansal Gupta, Brajendra K Tripathi, Jenny Wong, Kirk Campbell, Kay Metcalfe, Denny Schanze, Tetsuya Niihori, Hiroshi Kaito, Kandai Nozu, Hiroyasu Tsukaguchi, Ryojiro Tanaka, Kiyoshi Hamahira, Yasuko Kobayashi, Takumi Takizawa, Ryo Funayama, Keiko Nakayama, Yoko Aoki, Naonori Kumagai, Kazumoto Iijima, Henry Fehrenbach, Jameela A Kari, Sherif El Desoky, Sawsan Jalalah, Radovan Bogdanovic, Nataša Stajić, Hildegard Zappel, Assel Rakhmetova, Sharon-Rose Wassmer, Therese Jungraithmayr, Juergen Strehlau, Aravind Selvin Kumar, Arvind Bagga, Neveen A Soliman, Shrikant M Mane, Lewis Kaufman, Douglas R Lowy, Mohamad A Jairajpuri, Richard P Lifton, York Pei, Martin Zenker, Shigeo Kure, Friedhelm Hildebrandt
Mutations in six nephrosis genes delineate a pathogenic pathway amenable to treatment. Nature communications 9 (1) (2018)
Franziska Altmüller, Santosh Pothula, Anil Annamneedi, Saeideh Nakhaei-Rad, Carolina Montenegro-Venegas, Eneko Pina-Fernández, Claudia Marini, Monica Santos, Denny Schanze, Dirk Montag, Mohammad R Ahmadian, Oliver Stork, Martin Zenker, Anna Fejtova
Aberrant neuronal activity-induced signaling and gene expression in a mouse model of RASopathy. PLoS genetics 13 (3) (2017)
Daniela A Braun, Jia Rao, Geraldine Mollet, David Schapiro, Marie-Claire Daugeron, Weizhen Tan, Olivier Gribouval, Olivia Boyer, Patrick Revy, Tilman Jobst-Schwan, Johanna Magdalena Schmidt, Jennifer A Lawson, Denny Schanze, Shazia Ashraf, Jeremy F P Ullmann, Charlotte A Hoogstraten, Nathalie Boddaert, Bruno Collinet, Gaëlle Martin, Dominique Liger, Svjetlana Lovric, Monica Furlano, I Chiara Guerrera, Oraly Sanchez-Ferras, Jennifer F Hu, Anne-Claire Boschat, Sylvia Sanquer, Björn Menten, Sarah Vergult, Nina De Rocker, Merlin Airik, Tobias Hermle, Shirlee Shril, Eugen Widmeier, Heon Yung Gee, Won-Il Choi, Carolin E Sadowski, Werner L Pabst, Jillian K Warejko, Ankana Daga, Tamara Basta, Verena Matejas, Karin Scharmann, Sandra D Kienast, Babak Behnam, Brendan Beeson, Amber Begtrup, Malcolm Bruce, Gaik-Siew Ch'ng, Shuan-Pei Lin, Jui-Hsing Chang, Chao-Huei Chen, Megan T Cho, Patrick M Gaffney, Patrick E Gipson, Chyong-Hsin Hsu, Jameela A Kari, Yu-Yuan Ke, Cathy Kiraly-Borri, Wai-Ming Lai, Emmanuelle Lemyre, Rebecca Okashah Littlejohn, Amira Masri, Mastaneh Moghtaderi, Kazuyuki Nakamura, Fatih Ozaltin, Marleen Praet, Chitra Prasad, Agnieszka Prytuła, Elizabeth R Roeder, Patrick Rump, Rhonda E Schnur, Takashi Shiihara, Manish D Sinha, Neveen A Soliman, Kenza Soulami, David A Sweetser, Wen-Hui Tsai, Jeng-Daw Tsai, Rezan Topaloglu, Udo Vester, David H Viskochil, Nithiwat Vatanavicharn, Jessica L Waxler, Klaas J Wierenga, Matthias T F Wolf, Sik-Nin Wong, Sebastian A Leidel, Gessica Truglio, Peter C Dedon, Annapurna Poduri, Shrikant Mane, Richard P Lifton, Maxime Bouchard, Peter Kannu, David Chitayat, Daniella Magen, Bert Callewaert, Herman van Tilbeurgh, Martin Zenker, Corinne Antignac, Friedhelm Hildebrandt
Mutations in KEOPS-complex genes cause nephrotic syndrome with primary microcephaly. Nature genetics 49 (10) (2017)