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Ron A. Wevers

helmholtz-center munich - german research center for environmental health

89H-index
713Paper Count
2.9WCitation Count
Published Papers 256
Publication Date
Untargeted Metabolomics for Diagnosis, Monitoring, and Understanding the Pathophysiology of Inherited Metabolic Disorders
err2025-12-02
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errMartens, Jonathan; Engelke, Udo F. H.; Wevers, Ron A.; Lefeber, Dirk J.; Kulkarni, Purva
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Newborn Screening by DNA-First: Systematic Evaluation of the Eligibility of Inherited Metabolic Disorders Based on Treatability
err2025-08-21
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PREAI
errAbigail Veldman; Birgit Sikkema-Raddatz; Terry G. J. Derks; Clara D. M. van Karnebeek; M. B. Gea Kiewiet; Margaretha F. Mulder; Marcel R. Nelen; M. Estela Rubio-Gozalbo; Richard J. Sinke; Monique G. de Sain-van der Velden; Gepke Visser; Maaike C. de Vries; Dineke Westra; Monique Williams; Ron A. Wevers; M. Rebecca Heiner-Fokkema; Francjan J. van Spronsen
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New treatment for pyridoxine-dependent epilepsy due to ALDH7A1 deficiency: first proof-of-principle of upstream enzyme inhibition in the mouse
err2025-01-01
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errvan Karnebeek, Clara D. M.; Gailus-Durner, Valerie; Engelke, Udo F.; Seisenberger, Claudia; Marschall, Susan; Dragano, Nathalia R., V; da Silva-Buttkus, Patricia; Leuchtenberger, Stefanie; Fuchs, Helmut; Hrabe de Angelis, Martin; Wevers, Ron A.; Coughlin, Curtis R.; Lefeber, Dirk J.
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Newborn Screening by DNA-First: Systematic Evaluation of the Eligibility of Inherited Metabolic Disorders Based on Treatability
err2024-12-28
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errVeldman, Abigail; Sikkema-Raddatz, Birgit; Derks, Terry G. J.; van Karnebeek, Clara D. M.; Kiewiet, M. B. Gea; Mulder, Margaretha F.; Nelen, Marcel R.; Rubio-Gozalbo, M. Estela; Sinke, Richard J.; de van der Velden, Monique G.; Visser, Gepke; de Vries, Maaike C.; Westra, Dineke; Williams, Monique; Wevers, Ron A.; Heiner-Fokkema, M. Rebecca; van Spronsen, Francjan J.
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A rare homozygous INS variant causes adult-onset diabetes
err2024-12-20
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errTans, Roel; Glendorf, Tine; van Herwaarden, Antonius E.; Venselaar, Hanka; van Rijswijck, Danique M. H.; Wevers, Ron A.; Gloerich, Jolein; van Gool, Alain; Tack, Cees J.
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Impact of Phenylketonuria on the Serum Metabolome and Plasma Lipidome: A Study in Early-Treated Patients
err2024-08-30
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errvan der Weerd, Jorine C.; van Wegberg, Annemiek M. J.; Boer, Theo S.; Engelke, Udo F. H.; Coene, Karlien L. M.; Wevers, Ron A.; Bakker, Stephan J. L.; de Blaauw, Pim; Groen, Joost; van Spronsen, Francjan J.; Heiner-Fokkema, M. Rebecca
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Genome and RNA sequencing were essential to reveal cryptic intronic variants associated to defective ATP6AP1 mRNA processing
err2024-07-01
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PREAI
errMorales-Romero, Blai; Munoz-Pujol, Gerard; Artuch, Rafael; Garcia-Cazorla, Angels; O'Callaghan, Mar; Sykut-Cegielska, Jolanta; Campistol, Jaume; Moreno-Lozano, Pedro Juan; Oud, Machteld M.; Wevers, Ron A.; Lefeber, Dirk J.; Esteve-Codina, Anna; Yepez, Vicente A.; Gagneur, Julien; Wortmann, Saskia B.; Prokisch, Holger; Ribes, Antonia; Garcia-Villoria, Judit; Tort, Frederic
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Consensus guidelines for the diagnosis and management of succinic semialdehyde dehydrogenase deficiency
err2024-05-01
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PREAI
errLatzer, Itay Tokatly; Bertoldi, Mariarita; Blau, Nenad; DiBacco, Melissa L.; Elsea, Sarah H.; Garcia-Cazorla, Angels; Gibson, K. Michael; Gropman, Andrea L.; Hanson, Ellen; Hoffman, Carolyn; Jeltsch, Kathrin; Julia-Palacios, Natalia; Knerr, Ina; Lee, Henry H. C.; Malaspina, Patrizia; McConnell, Alice; Opladen, Thomas; Oppeboen, Mari; Rotenberg, Alexander; Walterfang, Mark; Wang-Tso, Lee; Wevers, Ron A.; Roullet, Jean-Baptiste; Pearl, Phillip L.
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Clinical, Neuroimaging, and Metabolic Footprint of the Neurodevelopmental Disorder Caused by Monoallelic HK1 Variants
err2024-04-01
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errWortmann, Saskia B.; Feichtinger, Rene G.; Abela, Lucia; van Gemert, Loes A.; Aubart, Melodie; Dufeu-Berat, Claire-Marine; Boddaert, Nathalie; de Coo, Rene; Stuehn, Lara; Hebbink, Jasmijn; Heinritz, Wolfram; Hildebrandt, Julia; Himmelreich, Nastassja; Korenke, Christoph; Lehman, Anna; Leyland, Thomas; Makowski, Christine; Martinez Marin, Rafael Jenaro; Marzin, Pauline; Muehlhausen, Chris; Rio, Marlene; Rotig, Agnes; Roux, Charles-Joris; Schiff, Manuel; Haack, Tobias B.; Syrbe, Steffen; Zylicz, Stas A.; Thiel, Christian; Veiga da Cunha, Maria; van Schaftingen, Emile; Wagner, Matias; Mayr, Johannes A.; Wevers, Ron A.; Boltshauser, Eugen; Willemsen, Michel A.
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Discovery of novel diagnostic biomarkers for Sjogren-Larsson syndrome by untargeted lipidomics
err2024-03-01
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errVaz, Frederic M.; Staps, Pippa; Klinken, Jan Bert van; van Lenthe, Henk; Vervaart, Martin; Wanders, Ronald J. A.; Pras-Raves, Mia L.; van Weeghel, Michel; Salomons, Gajja S.; Ferdinandusse, Sacha; Wevers, Ron A.; Willemsen, Michel A. A. P.
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A spectroscopic test suggests that fragment ion structure annotations in MS/MS libraries are frequently incorrect
err2024-02-14
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errvan Tetering, Lara; Spies, Sylvia; Wildeman, Quirine D. K.; Houthuijs, Kas J.; van Outersterp, Rianne E.; Martens, Jonathan; Wevers, Ron A.; Wishart, David S.; Berden, Giel; Oomens, Jos
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A framework for evaluating long-term impact of newborn screening ( oct , 2023 , 10.1038/s41431-023-01469-8)
err2023-11-29
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errKalkman, Shona; Wevers, Ron A.; Wijburg, Frits A.; Leeflang, Mariska M. G.
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PPA1 Deficiency Causes a Deranged Galactose Metabolism Recognizable in Neonatal Screening
err2023-11-10
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errAchleitner, Melanie T.; Jans, Judith J. M.; Ebner, Laura; Spenger, Johannes; Konstantopoulou, Vassiliki; Feichtinger, Rene G.; Brugger, Karin; Mayr, Doris; Wevers, Ron A.; Thiel, Christian; Wortmann, Saskia B.; Mayr, Johannes A.
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A Delphi Survey Study to Formulate Statements on the Treatability of Inherited Metabolic Disorders to Decide on Eligibility for Newborn Screening
err2023-10-11
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errVeldman, Abigail; Kiewiet, M. B. Gea; Westra, Dineke; Bosch, Annet M.; Brands, Marion M. G.; de Coo, Rene I. F. M.; Derks, Terry G. J.; Fuchs, Sabine A.; van den Hout, Johanna. M. P.; Huidekoper, Hidde H.; Kluijtmans, Leo A. J.; Koop, Klaas; Lubout, Charlotte M. A.; Mulder, Margaretha F.; Panis, Bianca; Rubio-Gozalbo, M. Estela; de van der Velden, Monique G.; Schaefers, Jaqueline; Schreuder, Andrea B.; Visser, Gepke; Wevers, Ron A.; Wijburg, Frits A.; Heiner-Fokkema, M. Rebecca; van Spronsen, Francjan J.
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A framework for evaluating long-term impact of newborn screening
err2023-10-03
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errKalkman, Shona; Wevers, Ron A.; Wijburg, Frits A.; Leeflang, Mariska M. G.
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Exome sequencing links the SUMO protease SENP7 with fatal arthrogryposis multiplex congenita, early respiratory failure and neutropenia
err2023-07-17
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errSamra, Nadra; Jansen, Nicolette S.; Morani, Ilham; Kakun, Reli Rachel; Zaid, Rinat; Paperna, Tamar; Garcia-Dominguez, Mario; Viner, Yuri; Frankenthal, Hilel; Shinwell, Eric S.; Portnov, Igor; Bakry, Doua; Shalata, Adel; Shapira Rootman, Mika; Kidron, Dvora; Claessens, Laura A.; Wevers, Ron A.; Mandel, Hanna; Vertegaal, Alfred C. O.; Weiss, Karin
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Distinguishing Oligosaccharide Isomers Using Far-Infrared Ion Spectroscopy: Identification of Biomarkers for Inborn Errors of Metabolism
err2023-06-21
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errvan Outersterp, Rianne E.; Kooijman, Pieter C.; Merx, Jona; Engelke, Udo F. H.; Omidikia, Nematollah; Tonneijck, Mei-Lan H.; Houthuijs, Kas J.; Berden, Giel; Peters, Tessa M. A.; Lefeber, Dirk J.; Willemsen, Michel A. A. P.; Mecinovic, Jasmin; Jansen, Jeroen J.; Coene, Karlien L. M.; Wevers, Ron A.; Boltje, Thomas J.; Oomens, Jos; Martens, Jonathan
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An In Silico Infrared Spectral Library of Molecular Ions for Metabolite Identification
err2023-06-01
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errHouthuijs, Kas J.; Berden, Giel; Engelke, Udo F. H.; Gautam, Vasuk; Wishart, David S.; Wevers, Ron A.; Martens, Jonathan; Oomens, Jos
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Newborn screening for Cerebrotendinous Xanthomatosis: A retrospective biomarker study using both flow-injection and UPLC-MS/MS analysis in newborns
err2023-01-01
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errVaz, Frederic M.; Jamal, Youssra; Barto, Rob; Gelb, Michael H.; DeBarber, Andrea E.; Wevers, Ron A.; Nelen, Marcel R.; Verrips, Aad; Bootsma, Albert H.; Bouva, Marelle J.; Kleise, Nick; van der Zee, Walter; He, Tao; Salomons, Gajja S.; Huidekoper, Hidde H.
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