Matias Simons

ResearcherID ORCID

Publication Activity (10 Years)

Years Active: 2017-2023
Publications (10 Years): 8

Top Venues

Nature reviews. Nephrology

PLoS genetics

Autophagy

Science (New York, N.Y.)

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

Publications

Julian A T Dow, Matias Simons, Michael F Romero
Publisher Correction: Drosophila melanogaster: a simple genetic model of kidney structure, function and disease. Nature reviews. Nephrology (2023)
Albert Pérez-Martí, Suresh Ramakrishnan, Jiayi Li, Aurélien J F Dugourd, Martijn R Molenaar, Luigi R De La Motte, Kelli Grand, Anis Mansouri, Mélanie Parisot, Soeren S Lienkamp, Julio Saez-Rodriguez, Matias Simons
Reducing lipid bilayer stress by monounsaturated fatty acids protects renal proximal tubules in diabetes. eLife 11 (2022)
Patrick Jouandin, Zvonimir Marelja, Yung-Hsin Shih, Andrey A Parkhitko, Miriam Dambowsky, John M Asara, Ivan Nemazanyy, Christian C Dibble, Matias Simons, Norbert Perrimon
Lysosomal cystine mobilization shapes the response of TORC1 and tissue growth to fasting. Science (New York, N.Y.) 375 (6582) (2022)
Julian A T Dow, Matias Simons, Michael F Romero
Drosophila melanogaster: a simple genetic model of kidney structure, function and disease. Nature reviews. Nephrology 18 (7) (2022)
Magda Cannata Serio, Laurie A Graham, Angel Ashikov, Lars Elmann Larsen, Kimiyo Raymond, Sharita Timal, Gwenn Le Meur, Margret Ryan, Elzbieta Czarnowska, Jos C Jansen, Miao He, Can Ficicioglu, Pavel Pichurin, Linda Hasadsri, Berge Minassian, Alessandra Rugierri, Hannu Kalimo, W Alfredo Ríos-Ocampo, Christian Gilissen, Richard J T Rodenburg, Johan W Jonker, Adriaan G Holleboom, Eva Morava, Joris A Veltman, Piotr Socha, Tom H Stevens, Matias Simons, Dirk J Lefeber
Mutations in the V-ATPase Assembly Factor VMA21 Cause a Congenital Disorder of Glycosylation With Autophagic Liver Disease. Hepatology (Baltimore, Md.) 72 (6) (2021)
Sara Gonçalves, Julie Patat, Maria Clara Guida, Noelle Lachaussée, Christelle Arrondel, Martin Helmstädter, Olivia Boyer, Olivier Gribouval, Marie-Claire Gubler, Geraldine Mollet, Marlène Rio, Marina Charbit, Christine Bole-Feysot, Patrick Nitschke, Tobias B Huber, Patricia G Wheeler, Devon Haynes, Jane Juusola, Thierry Billette de Villemeur, Caroline Nava, Alexandra Afenjar, Boris Keren, Rolf Bodmer, Corinne Antignac, Matias Simons
A homozygous KAT2B variant modulates the clinical phenotype of ADD3 deficiency in humans and flies. PLoS genetics 14 (5) (2018)
Magda Cannata Serio, Maria A Rujano, Matias Simons
Mutations in ATP6AP2 cause autophagic liver disease in humans. Autophagy 14 (6) (2018)
Maria A Rujano, Magda Cannata Serio, Ganna Panasyuk, Romain Péanne, Janine Reunert, Daisy Rymen, Virginie Hauser, Julien H Park, Peter Freisinger, Erika Souche, Maria Clara Guida, Esther M Maier, Yoshinao Wada, Stefanie Jäger, Nevan J Krogan, Oliver Kretz, Susana Nobre, Paula Garcia, Dulce Quelhas, Thomas D Bird, Wendy H Raskind, Michael Schwake, Sandrine Duvet, Francois Foulquier, Gert Matthijs, Thorsten Marquardt, Matias Simons
Mutations in the X-linked ATP6AP2 cause a glycosylation disorder with autophagic defects. The Journal of experimental medicine 214 (12) (2017)

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Publication Activity (10 Years)

Top Topics

Top Venues

Matias Simons