GeNeRARe - German Network of RASopathy Research
What are RASopathies?
RASopathies constitute a heterogeneous group of disorders with a common molecular pathogenesis and overlapping phenotypic patterns. Noonan, cardiofaciocutaneous, Costello, and LEOPARD syndromes belong to this group, as well as neurofibromatosis type 1 and Legius syndrome.
Dysregulation of RAS-dependent signaling due to a germline mutation in one of the pathway components cause a variety of developmental abnormalities such as heart defects, short stature, facial anomalies, cognitive impairment and others. Interestingly, based on the known molecular basis and supported by preliminary animal studies, RASopathies are considered as disorders that might be amenable to treatment with small molecules.
However, translation into clinical trials is still hampered by a limited understanding about the precise mechanisms on cellular and organ levels. There is also a lack of valid genotype-phenotype and long-term follow-up data, making it difficult to define therapeutic targets.
Joint research in the GeNeRaRe network
This consortium aims to fill some of these gaps by a multidisciplinary and multimodal approach. GeNeRare aims to address in particular the pathophysiology and molecular pathogenesis of organ involvement that is critical for long-term outcome, namely development of hypertrophic cardiomyopathy and neurocognitive impairments. But the consortium will also study novel aspects such as epidermal differentiation and cellular senescence. Collection of valid genotype phenotype data as well as the investigation of neurophysiologic parameters in affected humans define further lines of translation of basic research to patient care.
Projects- Mutation spectrum, genotype phenotype correlations and natural history of RASopathies: Prof. Dr. Martin Zenker and Dr. Christina Lißewski, University Hospital Magdeburg – Institute of Human Genetics.
- In vitro models of neuronal dysfunction in RASopathies: Prof. Dr. sc. nat. Anna Fejtova, Universitätsklinikum Erlangen.
- From RASopathiy-associated cardiomyopathy to interaction network profiling and mechanism-based target identification: PD Dr. Reza Ahmadian, Heinrich Heine University Düsseldorf – Institute of Biochemistry and Molecular Biology II.
- Generation of RASopathy patient-derived induced pluripotent stem cells (iPSCs) and in vitro analysis of myocardial genotype-phenotype correlations: Dr. George Kensah, Universitätsmedizin Göttingen.
- Analysis of the pathobiology of dermatological abnormalities in patients with RASopathies: Dr. Georg Rosenberger, Medical Center Hamburg-Eppendorf (UKE) – Institute of Human Genetics.
- Exploration of dysregulated lipid metabolism and mitochondrial activity contribution to the RASopathy pathophenotype : Dr. Ion Cirstea, Ulm University – Institute of Comparative Molecular Endocrinology.
- Dissecting the contribution of GABAergic neurons to neurocognitive defects in RASopathy mouse models: Prof. Dr. Oliver Stork, Otto von Guericke University Magdeburg – Institute for Biology.
- Generation and neurobiological characterisation of human cerebral organoids modelling RASopathies: Prof. Dr. med. Dr. rer. nat. Michael Schmeißer, University Medical Center Mainz
University Hospital Magdeburg
Institute of Human Genetics
Leipziger Str. 44
39120 Magdeburg
Tel.: +49-(0)391-67-15062
Fax: +49-(0)391-67-15066
E-Mail: ihg@med.ovgu.de
Website: www.generare.de
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13. August 2024 (GeNeRARe)
Impaired Intracellular Calcium Buffering Contributes to the Arrhythmogenic Substrate in Atrial Myocytes From Patients With Atrial FibrillationCirculation. 2024 Aug 13. >>Pubmed-Link<<
Funsho E Fakuade, Dominik Hubricht, Vanessa Möller, Izzatullo Sobitov, Aiste Liutkute, Yannic Döring, Fitzwilliam Seibertz, Marcus Gerloff, Julius Ryan D Pronto, Fereshteh Haghighi, Sören Brandenburg, Khaled Alhussini, Nadezda Ignatyeva, Yara Bonhoff, Stefanie Kestel, Aschraf El-Essawi, Ahmad Fawad Jebran, Marius Großmann, Bernhard C Danner, Hassina Baraki, Constanze Schmidt, Samuel Sossalla, Ingo Kutschka, Constanze Bening, Christoph Maack, Wolfgang A Linke, Jordi Heijman, Stephan E Lehnart, George Kensah, Antje Ebert, Fleur E Mason, Niels Voigt
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20. February 2024 (GeNeRARe)
RAS-MAPK Pathway Mutations in Congenital Pulmonary Airway MalformationsAm J Respir Crit Care Med. 2024 Feb 20. >>PubMed-Link<<
Jonas Windrich, Peter Braubach, Florian Länger, Jens Dingemann, Nicolaus Schwerk, Martin Wetzke, Diane M Renz, Martin Zenker, Denny Schanze, Christian P Kratz
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12. October 2023 (GeNeRARe)
Epilepsy in cardiofaciocutaneous syndrome: Clinical burden and response to anti-seizure medicationAm J Med Genet A. 2023 Oct 12. >>PubMed-Link<<
Daniel L Kenney-Jung, Josue E Collazo-Lopez, Dante J Rogers, Ryan Shanley, Abigail L Zatkalik, Ashley E Whitmarsh, Amy E Roberts, Martin Zenker, Elizabeth I Pierpont
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7. September 2023 (GeNeRARe)
Atrial fibrillation-associated electrical remodelling in human induced pluripotent stem cell-derived atrial cardiomyocytes: a novel pathway for antiarrhythmic therapy developmentCardiovasc Res. 2023 Sep 7. >>PubMed-Link<<
Fitzwilliam Seibertz, Tony Rubio, Robin Springer, Fiona Popp, Melanie Ritter, Aiste Liutkute, Lena Bartelt, Lea Stelzer, Fereshteh Haghighi, Jan Pietras, Hendrik Windel, Núria Díaz I Pedrosa, Markus Rapedius, Yannic Döring, Richard Solano, Robin Hindmarsh, Runzhu Shi, Malte Tiburcy, Tobias Brügmann, Ingo Kutschka, Katrin Streckfuss-Bömeke, George Kensah, Lukas Cyganek, Wolfram H Zimmermann, Niels Voigt
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4. July 2023 (GeNeRARe)
The Microenvironment of the Pathogenesis of Cardiac HypertrophyCells. 2023 Jul 4. >>PubMed-Link<<
Farhad Bazgir, Julia Nau, Saeideh Nakhaei-Rad, Ehsan Amin, Matthew J. Wolf, Jeffry J. Saucerman, Kristina Lorenz, Mohammad Reza Ahmadian
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4. July 2023 (GeNeRARe)
ACE2-EGFR-MAPK signaling contributes to SARS-CoV-2 infectionLife Sci. Alliance. 2023 Jul 4. >>PubMed-Link<<
Melanie Engler, Dan Albers, Pascal Von Maltitz, Rüdiger Groß, Jan Münch, Ion Cristian Cirstea
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21. June 2023 (GeNeRARe)
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 tissuesCommun Biol. 2023 Jun 21. >>PubMed-Link<<
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 R Ahmadian
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6. June 2023 (GeNeRARe)
Improvement of synaptic plasticity and cognitive function in RASopathies-a monocentre, randomized, double-blind, parallel-group, placebo-controlled, cross-over clinical trial (SynCoRAS)Trials. 2023 Jun 6. >>PubMed-Link<<
Nikolai H Jung, Silvia Egert-Schwender, Beate Schossow, Victoria Kehl, Ute Wahlländer, Louisa Brich, Viktoria Janke, Christiane Blankenstein, Martin Zenker, Volker Mall
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13. April 2023 (GeNeRARe)
Editorial: Identifying the isoform-specific roles of RAS paralogs in health and diseaseFront Cell Dev Biol. 2023 Apr 13. >>PubMed-Link<<
Saeideh Nakhaei-Rad, Anna Fejtova
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1. February 2023 (GeNeRARe)
Genetic Variants in ARHGEF6 Cause Congenital Anomalies of the Kidneys and Urinary Tract in Humans, Mice, and FrogsJ Am Soc Nephrol. 2023 Feb 1. >>PubMed-Link<<
Verena Klämbt, Florian Buerger, Chunyan Wang, Thomas Naert, Karin Richter, Theresa Nauth, Anna-Carina Weiss, Tobias Sieckmann, Ethan Lai, Dervla M Connaughton, Steve Seltzsam, Nina Mann, Amar J Majmundar, Chen-Han W Wu, Ana C Onuchic-Whitford, Shirlee Shril, Sophia Schneider, Luca Schierbaum, Rufeng Dai, Mir Reza Bekheirnia, Marieke Joosten, Omer Shlomovitz, Asaf Vivante, Ehud Banne, Shrikant Mane, Richard P Lifton, Karin M Kirschner, Andreas Kispert, Georg Rosenberger, Klaus-Dieter Fischer, Soeren S Lienkamp, Mirjam M P Zegers, Friedhelm Hildebrandt
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22. November 2022 (GeNeRARe)
Glucocorticoid receptor and RAS: an unexpected couple in cancerTrends Cell Biol. 2022 Nov 22. >>Web-Link<<
Ion C. Cirstea, Herwig P. Moll, Jan Tuckermann
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18. October 2022 (GeNeRARe)
Increased osteoclastogenesis contributes to bone loss in the Costello syndrome Hras G12V mouse modelFront Cell Dev Biol. 2022 Oct 18. >>PubMed-Link<<
Sayantan Nandi, Saravanakkumar Chennappan, Yannik Andrasch, Miray Fidan, Melanie Engler, Mubashir Ahmad, Jan P Tuckermann, Martin Zenker, Ion Cristian Cirstea
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9. August 2022 (GeNeRARe)
CDC42-IQGAP Interactions Scrutinized: New Insights into the Binding Properties of the GAP-Related DomainInt J Mol Sci. 2022 Aug 9. >>PubMed-Link<<
Niloufar Mosaddeghzadeh, Silke Pudewell, Farhad Bazgir, Neda S Kazemein Jasemi, Oliver H F Krumbach, Lothar Gremer, Dieter Willbold, Radovan Dvorsky, Mohammad R Ahmadian
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2. August 2022 (GeNeRARe)
T cell-specific constitutive active SHP2 enhances T cell memory formation and reduces T cell activationFront Immunol. 2022 Aug 2. >>PubMed-Link<<
Clemens Cammann, Nicole Israel, Sarah Frentzel, Andreas Jeron, Eylin Topfstedt, Thomas Schüler, Luca Simeoni, Martin Zenker, Hans Joerg Fehling, Burkhart Schraven, Dunja Bruder, Ulrike Seifert
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15. July 2022 (GeNeRARe)
Cross-Activation of Hemichannels/Gap Junctions and Immunoglobulin-Like Domains in Innate-Adaptive Immune ResponsesFront Immunol. 2022 Jul 15. >>PubMed-Link<<
Jiang-Hui Meng, Chang-Xu Chen, Mohammad R Ahmadian, Hong Zan, Kai-Jun Luo, Jean X Jiang
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15. July 2022 (GeNeRARe)
Cross-Activation of Hemichannels/Gap Junctions and Immunoglobulin-Like Domains in Innate-Adaptive Immune ResponsesFront Immunol. 2022 Jul 15. >>PubMed-Link<<
Jiang-Hui Meng, Chang-Xu Chen, Mohammad R Ahmadian, Hong Zan, Kai-Jun Luo, Jean X Jiang
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1. July 2022 (GeNeRARe)
Noonan syndrome-associated myocardial malfunctions caused by a RIT1 mutation can be partially rescued by modulating RAS/MAPK signaling in vitroEur J Heart Fail. 2022 Jul.
Kleemann, K., Szallies, H., Haghighi, F., Pietras, J., Busley, A., Dahlmann, J., Rubio, T., Seibertz, F., Moebius, W., Voigt, N., Zenker, M., Cyganek, L., Kutschka, I., Kensah, G.
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1. July 2022 (GeNeRARe)
Electrophysiological anomalies associated with a noonan syndrome mutation in RAF1 contribute to the development of cardiac arrhythmiasEur J Heart Fail. 2022 Jul.
Haghighi, F. F., Boehmker, L., Liutkute, A., Kleemann, K., Busley, A. V., Pietras, J. P., Seibertz, W., Rubio, T., Nourmohammadi, S., Dahlmann, J., Kutschka, I., Zenker, M., Voigt, N., Cyganek, L., Kensah, G.
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29. June 2022 (GeNeRARe)
Bassoon controls synaptic vesicle release via regulation of presynaptic phosphorylation and cAMPEMBO Rep. 2022 Jun 29. >>PubMed-Link<<
Carolina Montenegro-Venegas, Debarpan Guhathakurta, Eneko Pina-Fernandez, Maria Andres-Alonso, Florian Plattner, Eckart D Gundelfinger, Anna Fejtova
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29. June 2022 (GeNeRARe)
A novel HRAS c.466C>T p.(Phe156Leu) variant in two patients with attenuated features of Costello syndromeEur J Hum Genet. 2022 Jun 29. >>PubMed-Link<<
Suzanna Lindsey-Temple, Matt Edwards, Verena Rickassel, Theresa Nauth, Georg Rosenberger
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24. May 2022 (GeNeRARe)
Real-Time Optical Mapping of Contracting Cardiac Tissues With GPU-Accelerated Numerical Motion TrackingFront Cardiovasc Med. 2022 May 24. >>PubMed-Link<<
Jan Lebert, Namita Ravi, George Kensah, Jan Christoph
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18. May 2022 (GeNeRARe)
Cutis marmorata telangiectatica congenita being caused by postzygotic GNA11 mutationsEur J Med Genet. 2022 May; Epub 2022 Mar 26. >>PubMed-Link<<
Claudia Schuart, Andrea Bassi, Friedrich Kapp, Ilse Wieland, Angelica Pagliazzi, Heike Losch, Carlo Mazzatenta, Giacomo M Bacci, Teresa Oranges, Denny Schanze, Klaus Mohnik9, Arti Nanda, Judith Fischer, Martin Zenker, Rudolf Happle
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26. March 2022 (GeNeRARe)
Expanding the molecular spectrum of pathogenic SHOC2 variants underlying Mazzanti syndromeHum Mol Genet. 2022 Mar 26. >>PubMed-Link<<
Marialetizia Motta, Maja Solman, Adeline A Bonnard, Alma Kuechler, Francesca Pantaleoni, Manuela Priolo, Balasubramanian Chandramouli, Simona Coppola, Simone Pizzi, Erika Zara, Marco Ferilli, Hülya Kayserili, Roberta Onesimo, Chiara Leoni, Julia Brinkmann, Yoann Vial, Susanne B Kamphausen, Cécile Thomas-Teinturier, Anne Guimier, Viviana Cordeddu, Laura Mazzanti, Giuseppe Zampino, Giovanni Chillemi, Martin Zenker, Hélène Cavé, Jeroen Hertog, Marco Tartaglia
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22. March 2022 (GeNeRARe)
The glucocorticoid receptor associates with RAS complexes to inhibit cell proliferation and tumor growthSci Signal. 2022 Mar 22. >>PubMed-Link<<
Bozhena Caratti, Miray Fidan, Giorgio Caratti, Kristina Breitenecker, Melanie Engler, Naser Kazemitash, Rebecca Traut, Rainer Wittig, Emilio Casanova, Mohammad Reza Ahmadian, Jan P Tuckermann, Herwig P Moll, Ion Cristian Cirstea
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16. February 2022 (GeNeRARe)
The Pseudo-Natural Product Rhonin Targets RHOGDIAngew Chem Int Ed Engl. 2022 Feb 16. >>PubMed-Link<<
Mohammad Akbarzadeh, Jana Flegel, Sumersing Patil, Erchang Shang, Rishikesh Narayan, Marcel Buchholzer, Neda S Kazemein Jasemi, Michael Grigalunas, Adrian Krzyzanowski, Daniel Abegg, Anton Shuster, Marco Potowski, Hacer Karatas, George Karageorgis, Niloufar Mosaddeghzadeh, Mia-Lisa Zischinsky, Christian Merten, Christopher Golz, Lucas Brieger, Carsten Strohmann, Andrey P Antonchick, Petra Janning, Alexander Adibekian, Roger S Goody, Mohammad Reza Ahmadian, Slava Ziegler, Herbert Waldmann
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22. November 2021 (GeNeRARe)
Selectivity Determinants of RHO GTPase Binding to IQGAPsInt. J. Mol. Sci. 2021 Nov 22. >>PubMed-Link<<
Niloufar Mosaddeghzadeh, Kazem Nouri, Oliver H F Krumbach, Ehsan Amin, Radovan Dvorsky, Mohammad R Ahmadian
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19. November 2021 (GeNeRARe)
Electrostatic Forces Mediate the Specificity of RHO GTPase-GDI InteractionsInt J Mol Sci. 2021 Nov 19. >>PubMed-Link<<
Niloufar Mosaddeghzadeh, Neda S Kazemein Jasemi, Jisca Majolée, Si-Cai Zhang, Peter L Hordijk, Radovan Dvorsky, Mohammad Reza Ahmadian
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4. November 2021 (GeNeRARe)
SPRED2 loss-of-function causes a recessive Noonan syndrome-like phenotypeAm J Hum Genet. 2021 Nov 4. >>PubMed-Link<<
Marialetizia Motta, Giulia Fasano, Sina Gredy, Julia Brinkmann, Adeline Alice Bonnard, Pelin Ozlem Simsek-Kiper, Elif Yilmaz Gulec, Leila Essaddam, Gulen Eda Utine, Ingrid Guarnetti Prandi, Martina Venditti, Francesca Pantaleoni, Francesca Clementina Radio, Andrea Ciolfi, Stefania Petrini, Federica Consoli, Cédric Vignal, Denis Hepbasli, Melanie Ullrich, Elke de Boer, Lisenka E L M Vissers, Sami Gritli, Cesare Rossi, Alessandro De Luca, Saayda Ben Becher, Bruce D Gelb, Bruno Dallapiccola, Antonella Lauri, Giovanni Chillemi, Kai Schuh, Hélène Cavé, Martin Zenker, Marco Tartaglia
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30. October 2021 (GeNeRARe)
Translating the Role of mTOR- and RAS-Associated Signalopathies in Autism Spectrum Disorder: Models, Mechanisms and TreatmentGenes (Basel). 2021 Oct 30. >>PubMed-Link<<
Verica Vasic, Mattson S O Jones, Denise Haslinger, Lisa S Knaus, Michael J Schmeisser, Gaia Novarino, Andreas G Chiocchett
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28. October 2021 (GeNeRARe)
Inhibition of the RacGEF VAV3 by the small molecule IODVA1 impedes RAC signaling and overcomes resistance to tyrosine kinase inhibition in acute lymphoblastic leukemiaLeukemia. 2021 Oct 28. >>PubMed-Link<<
Shailaja Hegde, Anjelika Gasilina, Mark Wunderlich, Yuan Lin, Marcel Buchholzer, Oliver H F Krumbach, Mohammad Akbarzadeh, Mohammad Reza Ahmadian, William Seibel, Yi Zheng, John P Perentesis, Benjamin E Mizukawa, Lisa Privette Vinnedge, José A Cancelas, Nicolas N Nassar
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27. October 2021 (GeNeRARe)
RHO GTPase-Related Long Noncoding RNAs in Human CancersCancers (Basel). 2021 Oct 27. >>PubMed-Link<<
Mahsa Saliani, Amin Mirzaiebadizi, Niloufar Mosaddeghzadeh, Mohammad Reza Ahmadian
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4. October 2021 (GeNeRARe)
Galloway-Mowat syndrome: New insights from bioinformatics and expression during Xenopus embryogenesisGene Expr Patterns. 2021 Oct 4. >>PubMed-Link<<
Ernestine Treimer, Kathrin Niedermayer, Sven Schumann, Martin Zenker, Michael J Schmeisser, Susanne J Kühl
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3. September 2021 (GeNeRARe)
Criss-crossing autism spectrum disorder and adult neurogenesisJ Neurochem. 2021 Sep 3. >>PubMed-Link<<
Frank Bicker, Leonardo Nardi, Jannik Maier, Verica Vasic, Michael J Schmeisser
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1. September 2021 (GeNeRARe)
Rigosertib elicits potent anti-tumor responses in colorectal cancer by inhibiting Ras signaling pathwayCell Signal. 2021 Sep. >>PubMed-Link<<
Rahmani, F., Hashemzehi, M., Avan, A., Barneh, F., Asgharzadeh, F., Marjaneh, R. M., Soleimani, A., Parizadeh, M., Ferns, G. A., Mobarhan, M. G., Ryzhikov, M., Afshari, A. R., Ahmadian, M. R., Giovannetti, E., Jafari, M., Khazaei, M., Hassanian, S. M.
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7. July 2021 (GeNeRARe)
The intramolecular allostery of GRB2 governing its interaction with SOS1 is modulated by phosphotyrosine ligandsBiochem J. 2021 Jul 7. >>PubMed-Link<<
Jasemi, N. S. K., Herrmann, C., Estirado, E. M., Gremer, L., Willbold, D., Brunsveld, L., Dvorsky, R., Ahmadian, M. R.
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1. July 2021 (GeNeRARe)
The RHO Family GTPases: Mechanisms of Regulation and SignalingCells. 2021 Jul. >>PubMed-Link<<
Mosaddeghzadeh Niloufar; Ahmadian, Mohammad Reza
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16. June 2021 (GeNeRARe)
Spotlight on Accessory Proteins: RTK-RAS-MAPK Modulators as New Therapeutic TargetsBiomolecules. 2021 Jun. >>PubMed-Link<<
Silke Pudewell and Mohammad Reza Ahmadian
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14. May 2021 (GeNeRARe)
Early life adversity targets the transcriptional signature of hippocampal NG2+ glia and affects voltage gated sodium (Na v) channels propertiesNeurobiol Stress. 2021 May 14. >>PubMed-Link<<
Giulia Treccani, Hatice Yigit, Thomas Lingner, Vanessa Schleuβner, Franziska Mey, Michael A van der Kooij, Malin Wennström, David P Herzog, Matthias Linke, Markus Fricke, Michael J Schmeisser, Gregers Wegener, Thomas Mittmann, Jacqueline Trotter, Marianne B Müller
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28. April 2021 (GeNeRARe)
A comprehensive analysis of RAS-effector interactions reveals interaction hotspots and new binding partnersJ Biol Chem. Jan-Jun 2021. >>PubMed-Link<<
Soheila Rezaei Adariani, Neda S Kazemein Jasemi, Farhad Bazgir, Christoph Wittich, Ehsan Amin, Claus A M Seidel, Radovan Dvorsky, Mohammad R Ahmadian
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17. April 2021 (GeNeRARe)
Aβ1-16 controls synaptic vesicle pools at excitatory synapses via cholinergic modulation of synapsin phosphorylationCell Mol Life Sci. 2021 Apr 17. >>PubMed-Link<<
Daniela Anni, Eva-Maria Weiss, Debarpan Guhathakurta, Yagiz Enes Akdas, Julia Klueva, Stefanie Zeitler, Maria Andres-Alonso, Tobias Huth, Anna Fejtova
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8. April 2021 (GeNeRARe)
Accessory proteins of the RAS-MAPK pathway: moving from the side line to the front lineCommunications Biology. 2021 Jun 8. >>PubMed-Link<<
Pudewell, Silke; Wittich, Christoph; Jasemi, Neda S. Kazemein; Bazgir, Farhad; Ahmadian, Mohammad R.
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1. March 2021 (GeNeRARe)
Senescence in RASopathies, a possible novel contributor to a complex pathophenoypeMech Ageing Dev. 2021 Mar. >>PubMed-Link<<
Melanie Engler, Miray Fidan, Sayantan Nandi, Ion Cristian Cirstea
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1. January 2021 (GeNeRARe)
Genetic influences of autism candidate genes on circuit wiring and olfactory decodingCell Tissue Res. 2021 Jan. >>PubMed-Link<<
Renée Hartig, David Wolf, Michael J Schmeisser, Wolfgang Kelsch
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18. December 2020 (GeNeRARe)
Abnormalities of synaptic mitochondria in autism spectrum disorder and related neurodevelopmental disordersJ Mol Med. 2020 Dec 18. [Epub ahead of print] >>PubMed-Link<<
Liliana Rojas-Charry, Leonardo Nardi, Axel Methner, Michael J. Schmeisser -
7. December 2020 (GeNeRARe)
Aplasia cutis congenita in a CDC42-related developmental phenotypeAm J Med Genet A. 2020 Dec 7. [Epub ahead of print] >>PubMed-Link<<
Franziska Schnabel, Susanne B Kamphausen, Rudolf Funke, Silke Kaulfuß, Bernd Wollnik, Martin Zenker
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20. October 2020 (GeNeRARe)
The clinical significance ofA2ML1variants in Noonan syndrome has to be reconsideredEur J Hum Genet. 2020 Oct 20. [Epub ahead of print] >>PubMed-Link<<
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, Marco Tartaglia, Hélène Cavé, Martin Zenker
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1. September 2020 (GeNeRARe)
Anti-tumor mechanisms of rigosertib in colorectal cancerAnn Oncol. 2020 Sep 01. [Epub ahead of print]
S.M. Hassanian Mehr, F. Rahmani, M. Hashemzehi, A. Avan, F. Barneh, F. Asgharzadeh, R. Moradi-Marjaneh, A. Soleimani, M. Parizadeh, G.A. Ferns, M. Ghayour Mobarhan, M. Ryzhikov, A.R. Afshari, M.R. Ahmadian, E. Giovannetti, M. Jafari, A.R. Rezaei, M. Khazaei
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12. August 2020 (GeNeRARe)
Variants of SOS2 are a rare cause of Noonan syndrome with particular predisposition for lymphatic complicationsEur J Hum Genet. 2020 Aug 12. [Epub ahead of print] >>PubMed-Link<<
Christina Lissewski, Valérie Chune, Francesca Pantaleoni, Alessandro De Luca, Yline Capri, Julia Brinkmann, Francesca Lepri, Paola Daniele, Erika Leenders, Laura Mazzanti, Emanuela Scarano, Francesca Clementina Radio, Kerstin Kutsche, Alma Kuechler, Marion Gérard, Kara Ranguin, Marine Legendre, Yoann Vial, Ineke van der Burgt, Tuula Rinne, Elena Andreucci, Gioia Mastromoro, Maria Cristina Digilio, Hélène Cave, Marco Tartaglia, Martin Zenker
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21. July 2020 (GeNeRARe)
Activating MRAS mutations cause Noonan syndrome associated with hypertrophic cardiomyopathyHum Mol Genet. 2020 Jul 21. [Epub ahead of print] >>PubMed-Link<<
Marialetizia Motta, Lena Sagi-Dain, Oliver H F Krumbach, Andreas Hahn, Amir Peleg, Alina German, Christina Lissewski, Simona Coppola, Francesca Pantaleoni, Luisa Kocherscheid, Franziska Altmüller, Denny Schanze, Thushiha Logeswaran, Soheyla Chahrokh-Zadeh, Anna Munzig, Saeideh Nakhaei-Rad, Hélène Cavé, Mohammad R Ahmadian, Marco Tartaglia, Martin Zenker
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24. June 2020 (GeNeRARe)
Expanding the genotypic and phenotypic spectrum of severe serine biosynthesis disordersHum Mutat. 2020 Jun 24. [Epub ahead of print] >>PubMed-Link<<
Fatima Abdelfattah, Ariana Kariminejad, Anne-Karin Kahlert, Patrick J Morrison, Evren Gumus, Katherine D Mathews, Benjamin W Darbro, David J Amor, Maie Walsh, Yves Sznajer, Luisa Weiß, Sabine Weidensee, David Chitayat, Patrick Shannon, Eva Bermejo-Sánchez, Isolina Riaño-Galán, Ian Hayes, Gemma Poke, Caroline Rooryck, Perrine Pennamen, Suonavy Khung-Savatovsky, Annick Toutain, Marie-Laure Vuillaume, Siavash Ghaderi-Sohi, Mohamad H Kariminejad, Sönke Weinert, Heinrich Sticht, Martin Zenker, Denny Schanze
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11. June 2020 (GeNeRARe)
Novel FMRP interaction networks linked to cellular stressFEBS J. 2020 Jun 11. [Epub ahead of print] >>PubMed-Link<<
Mohamed S Taha, Fereshteh Haghighi, Anja Stefanski, Saeideh Nakhaei-Rad, Neda S Kazemein Jasemi, Mohamed Aghyad Al Kabbani, Boris Görg, Masahiro Fujii, Phillip A Lang, Dieter Häussinger, Roland P Piekorz, Kai Stühler, Mohammad R Ahmadian
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4. June 2020 (GeNeRARe)
The novel duplication HRAS c.186_206dup p.(Glu62_Arg68dup): clinical and functional aspectsEur J Hum Genet. 2020 Jun 4. [Epub ahead of print] >>PubMed-Link<<
Karen W Gripp, Laura Baker, Katherine M Robbins, Deborah L Stabley, Gary A Bellus, Verena Kolbe, Theresa Nauth, Georg Rosenberger
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1. June 2020 (GeNeRARe)
Pathogenic PTPN11 variants involving the poly-glutamine Gln255 -Gln256 -Gln257 stretch highlight the relevance of helix B in SHP2’s functional regulationHum Mutat. 2020 Jun;41(6):1171-1182. Epub 2020 Mar 11 >>PubMedLink<<Martinelli S, Pannone L, Lissewski C, Brinkmann J, Flex E, Schanze D, Calligari P, Anselmi M, Pantaleoni F, Canale VC, Radio FC, Ioannides A, Rahner N, Schanze I, Josifova D, Bocchinfuso G, Ryten M, Stella L, Tartaglia M, Zenker M
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2. December 2019 (GeNeRARe)
A novel disorder involving dyshematopoiesis, inflammation, and HLH due to aberrant CDC42 functionJ Exp Med. 2019 Dec 2. [Epub ahead of print] >>PubMed-Link<<
Michael T Lam , Simona Coppola, Oliver H F Krumbach, Giusi Prencipe, Antonella Insalaco, Cristina Cifaldi, Immacolata Brigida, Erika Zara, Serena Scala, Silvia Di Cesare, Simone Martinelli, Martina Di Rocco, Antonia Pascarella, Marcello Niceta, Francesca Pantaleoni, Andrea Ciolfi, Petra Netter, Alexandre F Carisey, Michael Diehl, Mohammad Akbarzadeh, Francesca Conti, Pietro Merli, Anna Pastore, Stefano Levi Mortera, Serena Camerini, Luciapia Farina, Marcel Buchholzer, Luca Pannone, Tram N Cao, Zeynep H Coban-Akdemir, Shalini N Jhangiani, Donna M Muzny, Richard A Gibbs, Luca Basso-Ricci, Maria Chiriaco, Radovan Dvorsky, Lorenza Putignani, Rita Carsetti, Petra Janning, Asbjorg Stray-Pedersen, Hans Christian Erichsen, AnnaCarin Horne, Yenan T Bryceson, Lamberto Torralba-Raga, Kim Ramme, Vittorio Rosti, Claudia Bracaglia, Virginia Messia, Paolo Palma, Andrea Finocchi , Franco Locatelli, Ivan K Chinn, James R Lupski, Emily M Mace, Caterina Cancrini, Alessandro Aiuti, Mohammad R Ahmadian, Jordan S Orange, Fabrizio De Benedetti, Marco Tartaglia
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1. December 2019 (GeNeRARe)
Variants in nuclear factor I genes influence growth and developmentAm J Med Genet C Semin Med Genet. 2019 Dec. [Epub ahead of print] >>PubMed-Link<<
Martin Zenker, Jens Bunt, Ina Schanze, Denny Schanze, Michael Piper, Manuela Priolo, Erica H Gerkes, Richard M Gronostajski, Linda J Richards, Julie Vogt, Marja W Wessels, Raoul C Hennekam
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1. November 2019 (GeNeRARe)
NFIB Haploinsufficiency Is Associated with Intellectual Disability and MacrocephalyAm J Hum Genet. 2018 Nov 1. [Epub ahead of print] >>PubMed-Link<<
Ina Schanze, Jens Bunt, Jonathan W C Lim, Denny Schanze, Ryan J Dean, Marielle Alders, Patricia Blanchet, Tania Attié-Bitach, Siren Berland, Steven Boogert, Sangamitra Boppudi, Caitlin J Bridges, Megan T Cho, William B Dobyns, Dian Donnai, Jessica Douglas, Dawn L Earl, Timothy J Edwards, Laurence Faivre, Brieana Fregeau, David Genevieve, Marion Gérard, Vincent Gatinois, Muriel Holder-Espinasse, Samuel F Huth, Kosuke Izumi, Bronwyn Kerr, Elodie Lacaze, Phillis Lakeman, Sonal Mahida, Ghayda M Mirzaa, Sian M Morgan, Catherine Nowak, Hilde Peeters, Florence Petit, Daniela T Pilz, Jacques Puechberty, Eyal Reinstein, Jean-Baptiste Rivière, Avni B Santani, Anouck Schneider, Elliott H Sherr, Constance Smith-Hicks, Ilse Wieland, Elaine Zackai, Xiaonan Zhao, Richard M Gronostajski, Martin Zenker, Linda J Richards
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1. August 2019 (GeNeRARe)
From basic researches to new achievements in therapeutic strategies of KRAS-driven cancersCancer Biol Med. 2019 Aug. [Epub ahead of print] >>PubMed-Link<<
Mahsa Saliani, Razieh Jalal, Mohammad Reza Ahmadian
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1. August 2019 (GeNeRARe)
Next-generation sequencing of 32 genes associated with hereditary aortopathies and related disorders of connective tissue in a cohort of 199 patientsGenet Med. 2019 Aug. [Epub ahead of print] >>PubMed-Link<<
Sina Renner, Helke Schüler, Malik Alawi, Verena Kolbe, Meike Rybczynski, Rixa Woitschach, Sara Sheikhzadeh, Veronika C Stark, Jakob Olfe, Elke Roser, Friederike Sophia Seggewies, Adrian Mahlmann, Maja Hempel, Melanie J Hartmann, Mathias Hillebrand, Dagmar Wieczorek, Alexander Erich Volk, Katja Kloth, Margarete Koch-Hogrebe, Rami Abou Jamra, Diana Mitter, Janine Altmüller, Alexandra Wey-Fabrizius, Christine Petersen, Isabella Rau, Guntram Borck, Christian Kubisch, Thomas S Mir, Yskert von Kodolitsch, Kerstin Kutsche, Georg Rosenberger
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10. July 2019 (GeNeRARe)
Cdk5 Deletion Enhances the Anti-inflammatory Potential of GC-Mediated GR Activation During InflammationFront Immunol. 2019 Jul 10. [Epub ahead of print] >>PubMed-Link<<
Pauline Pfänder, Miray Fidan, Ute Burret, Lena Lipinski, Sabine Vettorazzi
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6. June 2019 (GeNeRARe)
Activating Mutations of RRAS2 Are a Rare Cause of Noonan SyndromeAm J Hum Genet. 2019 Jun 6. [Epub ahead of print] >>PubMed-Link<<
Yline Capri, Elisabetta Flex, Oliver H F Krumbach, Giovanna Carpentieri, Serena Cecchetti, Christina Lißewski, Soheila Rezaei Adariani, Denny Schanze, Julia Brinkmann, Juliette Piard, Francesca Pantaleoni, Francesca R Lepri, Elaine Suk-Ying Goh, Karen Chong, Elliot Stieglitz, Julia Meyer, Alma Kuechler, Nuria C Bramswig, Stephanie Sacharow, Marion Strullu, Yoann Vial, Cédric Vignal, George Kensah, Goran Cuturilo, Neda S Kazemein Jasemi, Radovan Dvorsky, Kristin G Monaghan, Lisa M Vincent, Hélène Cavé, Alain Verloes, Mohammad R Ahmadian, Marco Tartaglia, Martin Zenker
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21. May 2019 (GeNeRARe)
Activating MRAS mutations cause Noonan syndrome associated with hypertrophic cardiomyopathyHuman Molecular Genetics, Published 21 May 2019
Marialetizia Motta,Lena Sagi-Dain, Oliver H.F. Krumbach, Andreas , Amir Peleg, Alina
German, Christina Lissewski, Simona Coppola, Francesca Pantaleoni, Luisa Kocherscheid,
Franziska Altmüller, Denny Schanze, Thushiha Logeswaran, Soheyla Chahrokh-Zadeh, Anna
Munzig, Saeideh Nakhaei-Rad, Hélène Cavé, Mohammad R. Ahmadian, Marco Tartaglia,
Martin Zenker -
13. May 2019 (GeNeRARe)
Activating Mutations of RRAS2 Are a Rare Cause of Noonan SyndromeAm J Hum Genet. 2019 May 13. pii: S0002-9297(19)30161-2. doi: 10.1016/j.ajhg.2019.04.013. [Epub ahead of print]
Capri Y, Flex E, Krumbach OHF, Carpentieri G, Cecchetti S, Lißewski C, Rezaei Adariani S, Schanze D, Brinkmann J, Piard J, Pantaleoni F, Lepri FR, Goh ES, Chong K, Stieglitz E, Meyer J, Kuechler A, Bramswig NC, Sacharow S, Strullu M, Vial Y, Vignal C, Kensah G, Cuturilo G, Kazemein Jasemi NS, Dvorsky R, Monaghan KG, Vincent LM, Cavé H, Verloes A, Ahmadian MR, Tartaglia M, Zenker M.
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7. May 2019 (GeNeRARe)
Hypertrophic Cardiomyopathy in Noonan Syndrome Treated by MEK-InhibitionJ Am Coll Cardiol. 2019 May 7;73(17):2237-2239. doi: 10.1016/j.jacc.2019.01.066.
Andelfinger G, Marquis C, Raboisson MJ, Théoret Y, Waldmüller S, Wiegand G, Gelb BD, Zenker M, Delrue MA, Hofbeck M
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7. May 2019 (GeNeRARe)
Deregulation of Hepatic Mek1/2⁻Erk1/2 Signaling Module in Iron Overload ConditionsPharmaceuticals (Basel). 2019 May 7;12(2). pii: E70. doi: 10.3390/ph12020070.
Tangudu NK, Buth N, Strnad P, Cirstea IC, Spasić MV
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7. May 2019 (GeNeRARe)
Hypertrophic Cardiomyopathy in Noonan Syndrome Treated by MEK-InhibitionJ Am Coll Cardiol. 2019 May 7. [Epub ahead of print] >>PubMed-Link<<
Gregor Andelfinger, Christopher Marquis, Marie-Josée Raboisson, Yves Théoret, Stephan Waldmüller, Gesa Wiegand, Bruce D Gelb, Martin Zenker, Marie-Ange Delrue, Michael Hofbeck
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7. May 2019 (GeNeRARe)
Deregulation of Hepatic Mek1/2⁻Erk1/2 Signaling Module in Iron Overload ConditionsPharmaceuticals (Basel). 2019 May 7. [Epub ahead of print] >>PubMed-Link<<
Naveen Kumar Tangudu, Nils Buth, Pavel Strnad, Ion C Cirstea, Maja Vujić Spasić
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1. May 2019 (GeNeRARe)
Detection of a multilineage mosaic NRAS mutation c.181C>A (p.Gln61Lys) in an individual with a complex congenital nevus syndromePigment Cell Melanoma Res. 2019 May;32(3):470-473. doi: 10.1111/pcmr.12761. Epub 2018 Dec 21
Ulrich M, Tinschert S, Siebert E, Franke I, Tüting T, Ulrich J, Schanze D, Wieland I, Zenker M
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15. March 2019 (GeNeRARe)
Dominant Noonan syndrome-causing LZTR1 mutations specifically affect the Kelch domain substrate-recognition surface and enhance RAS-MAPK signalingHum Mol Genet. 2019 Mar 15. [Epub ahead of print] >>PubMed-Link<<
Marialetizia Motta, Miray Fidan, Emanuele Bellacchio, Francesca Pantaleoni, Konstantin Schneider-Heieck, Simona Coppola, Guntram Borck, Leonardo Salviati, Martin Zenker, Ion C Cirstea, Marco Tartaglia
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24. January 2019 (GeNeRARe)
Next-generation sequencing of 32 genes associated with hereditary aortopathies and related disorders of connective tissue in a cohort of 199 patientsGenet Med. 2019 Jan 24. doi: 10.1038/s41436-019-0435-z. [Epub ahead of print]
Renner S, Schüler H, Alawi M, Kolbe V, Rybczynski M, Woitschach R, Sheikhzadeh S, Stark VC, Olfe J, Roser E, Seggewies FS, Mahlmann A, Hempel M, Hartmann MJ, Hillebrand M, Wieczorek D, Volk AE, Kloth K, Koch-Hogrebe M, Abou Jamra R, Mitter D, Altmüller J, Wey-Fabrizius A, Petersen C, Rau I, Borck G, Kubisch C, Mir TS, von Kodolitsch Y, Kutsche K, Rosenberger G.
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5. December 2018 (GeNeRARe)
bFGF-mediated pluripotency maintenance in human induced pluripotent stem cells is associated with NRAS-MAPK signalingCell Commun Signal. 2018 Dec 5;16(1):96. doi: 10.1186/s12964-018-0307-1.
Haghighi F, Dahlmann J, Nakhaei-Rad S, Lang A, Kutschka I, Zenker M, Kensah G, Piekorz RP, Ahmadian MR.
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5. December 2018 (GeNeRARe)
bFGF-mediated pluripotency maintenance in human induced pluripotent stem cells is associated with NRAS-MAPK signalingCell Commun Signal. 2018 Dec 5. [Epub ahead of print] >>PubMed-Link<<
Fereshteh Haghighi, Julia Dahlmann, Saeideh Nakhaei-Rad, Alexander Lang, Ingo Kutschka, Martin Zenke, George Kensah, Roland P Piekorz, Mohammad Reza Ahmadian
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30. November 2018 (GeNeRARe)
Dominant Noonan syndrome-causing LZTR1 mutations specifically affect the kelch domain substrate-recognition surface and enhance RAS-MAPK signalingHum Mol Genet. 2018 Nov 27. doi: 10.1093/hmg/ddy412.
Motta M, Fidan M, Bellacchio E, Pantaleoni F, Schneider-Heieck K, Coppola S3, Borck G, Salviati L, Zenker M, Cirstea IC2, Tartaglia M.
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5. November 2018 (GeNeRARe)
Assessing the gene–disease association of 19 genes with the RASopathies using the ClinGen gene curation frameworkHum Mutat. 2018 Nov. >>PubMed-Link<<
Grant AR, Cushman BJ, Cavé H, Dillon MW, Gelb BD, Gripp KW, Lee JA, Mason-Suares H, Rauen KA, Tartaglia M, Vincent LM, Zenker M.
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1. November 2018 (GeNeRARe)
ClinGen’s RASopathy Expert Panel consensus methods for variant interpretationGenet Med. 2018 Nov. [Epub ahead of print] >>PubMed-Link<<
Bruce D Gelb, Hélène Cavé, Mitchell W Dillon, Karen W Gripp, Jennifer A Lee, Heather Mason-Suares, Katherine A Rauen, Bradley Williams, Martin Zenker, Lisa M Vincent, ClinGen RASopathy Working Group
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1. October 2018 (GeNeRARe)
Autosomal recessive Noonan syndrome associated with biallelic LZTR1 variantsGenet Med. 2018 Oct. [Epub ahead of print] >>PubMed-Link<<
Jennifer J Johnston, Jasper J van der Smagt, Jill A Rosenfeld, Alistair T Pagnamenta, Abdulrahman Alswaid, Eva H Baker, Edward Blair, Guntram Borck, Julia Brinkmann, William Craigen, Vu Chi Dung, Lisa Emrick, David B Everman, Koen L van Gassen, Suleyman Gulsuner, Margaret H Harr, Mahim Jain, Alma Kuechler, Kathleen A Leppig, Donna M McDonald-McGinn, Ngoc Thi Bich Can, Amir Peleg, Elizabeth R Roeder, R Curtis Rogers, Lena Sagi-Dain, Julie C Sapp, Alejandro A Schäffer, Denny Schanze, Helen Stewart, Jenny C Taylor, Nienke E Verbeek, Magdalena A Walkiewicz, Elaine H Zackai, Christiane Zweier, Members of the Undiagnosed Diseases Network; Martin Zenker, Brendan Lee, Leslie G Biesecker
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7. September 2018 (GeNeRARe)
RIT1 controls actin dynamics via complex formation with RAC1/CDC42 and PAK1PLoS Genet. 2018 May 7;14(5):e1007370. doi: 10.1371/journal.pgen.1007370. eCollection 2018 May.
zum Büschenfelde UM, Brandenstein LI, von Elsner L, Flato K, Holling T, Zenker M, Rosenberger G, Kutsche K.
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7. May 2018 (GeNeRARe)
RIT1 controls actin dynamics via complex formation with RAC1/CDC42 and PAK1PLoS Genet. 2018 May 7. [Epub ahead of print] >>PubMed-Link<<
Uta Meyer Zum Büschenfelde, Laura Isabel Brandenstein, Leonie von Elsner, Kristina Flato, Tess Holling, Martin Zenker, Georg Rosenberger, Kerstin Kutsche
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11. March 2018 (GeNeRARe)
ClinGen’s RASopathy Expert Panel consensus methods for variant interpretationClinGen’s RASopathy Expert Panel consensus methods for variant interpretation. Genet Med. 2018 Mar 1
Gelb BD, Cavé H, Dillon MW, Gripp KW, Lee JA, Mason-Suares H, Rauen KA, Williams B, Zenker M, Vincent LM.
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22. February 2018 (GeNeRARe)
Autosomal recessive Noonan syndrome associated with biallelic LZTR1 variantsGenet Med. 2018 Feb 22. doi: 10.1038/gim.2017.249.
Johnston JJ, van der Smagt JJ, Rosenfeld JA, Pagnamenta AT, Alswaid A, Baker EH, Blair E, Borck G, Brinkmann J, Craigen W, Dung VC, Emrick L, Everman DB, van Gassen KL, Gulsuner S, Harr MH, Jain M, Kuechler A, Leppig KA, McDonald-McGinn DM, Can NTB, Peleg A, Roeder ER, Rogers RC, Sagi-Dain L, Sapp JC, Schäffer AA, Schanze D, Stewart H, Taylor JC, Verbeek NE, Walkiewicz MA,Zackai EH, Zweier C; Members of the Undiagnosed Diseases Network, Zenker M, Lee B, Biesecker LG
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10. February 2018 (GeNeRARe)
The novel RAF1 mutation p.(Gly361Ala) located outside the kinase domain of the CR3 region in two patients with Noonan syndrome, including one with a rare brain tumorAm J Med Genet A. 2018 Feb;176(2):470-476. doi: 10.1002/ajmg.a.38569.
Harms FL, Alawi M, Amor DJ, Tan TY, Cuturilo G, Lissewski C, Brinkmann J, Schanze D, Kutsche K, Zenker M.
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1. February 2018 (GeNeRARe)
The novel RAF1 mutation p.(Gly361Ala) located outside the kinase domain of the CR3 region in two patients with Noonan syndrome, including one with a rare brain tumorAm J Med Genet A. 2018 Feb. [Epub ahead of print] >>PubMed-Link<<
Frederike L Harms, Malik Alawi, David J Amor, Tiong Y Tan, Goran Cuturilo, Christina Lissewski, Julia Brinkmann, Denny Schanze, Kerstin Kutsche, Martin Zenker
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1. September 2017 (GeNeRARe)
Attenuated phenotype of Costello syndrome and early death in a patient with an HRAS mutation (c.179G>T; p.Gly60Val) affecting signalling dynamicsClin Genet. 2017 Sep. [Epub ahead of print] >>PubMed-Link<<
K W Gripp, V Kolbe, L I Brandenstein, G Rosenberger
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25. June 2017 (GeNeRARe)
Genotype and phenotype spectrum of NRAS germline variants.Eur J Hum Genet. 2017 Jun;25(7):823-831.
Altmüller F, Lissewski C, Bertola D, Flex E, Stark Z, Spranger S, Baynam G, Buscarilli de Moraes M, Dyack S, Gillis J, Yntema HG, Pantaleoni F, van Loon RL, MacKay S, Mina K, Schanze I, Tan TY, Walsh M, White SM, Niewisch MR, García-Miñaúr S, Plaza D, Ahmadian MR, Cavé H, Tartaglia M, Zenker M. -
16. June 2017 (GeNeRARe)
Correction: Aberrant neuronal activity-induced signaling and gene expression in a mouse model of RASopathyPLoS Genet. 2017 Jun 16;13(6):e1006843. doi:10.1371/journal.pgen.1006843. eCollection 2017 Jun.
Altmüller F, Pothula S, Annamneedi A, Nakhaei-Rad S, Montenegro-Venegas C, Pina-Fernández E, Marini C, Santos M, Schanze D, Montag D, Ahmadian MR, Stork O, Zenker M, Fejtova A.
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1. June 2017 (GeNeRARe)
Genotype and phenotype spectrum of NRAS germline variantsEur J Hum Genet. 2017 Jun. [Epub ahead of print] >>PubMed-Link<<
Franziska Altmüller, Christina Lissewski, Debora Bertola, Elisabetta Flex, Zornitza Stark, Stephanie Spranger, Gareth Baynam, Michelle Buscarilli, Sarah Dyack, Jane Gillis, Helger G Yntema, Francesca Pantaleoni, Rosa LE van Loon, Sara MacKay, Kym Mina, Ina Schanze, Tiong Yang Tan, Maie Walsh, Susan M White, Marena R Niewisch, Sixto García-Miñaúr, Diego Plaza, Mohammad Reza Ahmadian, Hélène Cavé, Marco Tartaglia, Martin Zenker
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27. March 2017 (GeNeRARe)
Aberrant neuronal activity-induced signaling and gene expression in a mouse model of RASopathyPLoS Genet. 2017 Mar 27. [Epub ahead of print] >>PubMed-Link<<
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
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31. January 2017 (GeNeRARe)
Attenuated phenotype of Costello syndrome and early death in a patient with an HRAS Mutation (c.179G>T; p.Gly60Val) affecting signalling dynamicsClin Genet. 2017 Jan 31. doi: 10.1111/cge.12980. [Epub ahead of print] Gripp KW, Kolbe V, Brandenstein LI, Rosenberger G
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9. December 2016 (GeNeRARe)
The RAS-Effector Interface: Isoform-Specific Differences in the Effector Binding RegionsPLoS One. 2016 Dec 9;11(12):e0167145. doi: 10.1371/journal.pone.0167145.
Nakhaeizadeh H, Amin E, Nakhaei-Rad S, Dvorsky R, Ahmadian MR.
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9. December 2016 (GeNeRARe)
The RAS-Effector Interface: Isoform-Specific Differences in the Effector Binding RegionsPLoS One. 2016 Dec 9. >>PubMed-Link<<
Hossein Nakhaeizadeh, Ehsan Amin, Saeideh Nakhaei-Rad, Radovan Dvorsky, Mohammad Reza Ahmadian