Peter van Hasselt

Associate Professor - medical

Strategic program(s):

Biography

2020-present Member of the board of the WKZ Research Fund

2020-2022 Manager Research of the Division 'Child' at the UMC Utrecht

2019-present Associate Professor (Universitair hoofddocent UHD)

2017-present Head of Department Metabolic diseases

2017-present 'Opleider' at department of Metabolic Diseases

2017-2020 Head of Cluster C (portfolios Science, Finance, Operational Excellence, Capacity management) at WKZ

2017-2022 Member of Leadership team Division 'Child', UMC Utrecht

2016-2020 Member of the scientific committee of the WKZ Research Fund

2015-present Head of Section Metabolic Diseases NVK

2012-2017 'Plaatsvervangend Opleider' Metabolic Diseases (WKZ)

2009-present Staff member at department of Metabolic Diseases

2007-present Pediatrician for Metabolic Diseases, Wilhelmina Children’s Hospital, Utrecht.

2007-2009 Temporary Staff Metabolic Diseases & PhD (WKZ)

2004-2007 Subspecialty training (fellowship) for Metabolic Diseases, Wilhelmina Children’s Hospital. Head: Dr. T.J. de Koning

1998-1999 Physician-researcher (Herseninstituut, Amsterdam)

1997-1998 Pediatrician non-trainee (WKZ, Neonatology)

1995 Student-researcher (UMCG Pharmacology)

Strategic program(s):

Contact

phassel2@umcutrecht.nl

Pure profile

Recent publications

All publications

UPLC-Orbitrap-HRMS application for analysis of plasma sterols Maria van der Ham, Johan Gerrits, Berthil Prinsen, Peter van Hasselt, Sabine Fuchs, Judith Jans, Anke Willems, Monique de Sain-van der Velden
Analytica Chimica Acta, 2024, vol. 1296

Neddylation orchestrates the complex transcriptional and posttranscriptional program that drives Schwann cell myelination Paula Ayuso-García, Alejandro Sánchez-Rueda, Sergio Velasco-Avilés, Miguel Tamayo-Caro, Aroa Ferrer-Pinós, Cecilia Huarte-Sebastian, Vanesa Alvarez, Cristina Riobello, Selene Jiménez-Vega, Izaskun Buendia, Jorge Cañas-Martin, Héctor Fernández-Susavila, Adrián Aparicio-Rey, Eva M. Esquinas-Román, Carlos Rodríguez Ponte, Romane Guhl, Nicolas Laville, Encarni Pérez-Andrés, José L. Lavín, Monika González-Lopez, Nuria Macías Cámara, Ana M. Aransay, Juan José Lozano, James D. Sutherland, Rosa Barrio, María Luz Martinez-Chantar, Mikel Azkargorta, Félix Elortza, Mario Soriano-Navarro, Carlos Matute, María Victoria Sánchez-Gómez, Laura Bayón-Cordero, Alberto Pérez-Samartín, Susana B. Bravo, Thimo Kurz, Tomas Lama-Díaz, Miguel G. Blanco, Saif Haddad, Christopher J. Record, Peter M. van Hasselt, Mary M. Reilly, Marta Varela-Rey, Ashwin Woodhoo
Science advances, 2024, vol. 10

Newborn screening in metachromatic leukodystrophy – European consensus-based recommendations on clinical management Lucia Laugwitz, Daphne H. Schoenmakers, Laura A. Adang, Stefanie Beck-Woedl, Caroline Bergner, Geneviève Bernard, Annette Bley, Audrey Boyer, Valeria Calbi, Hanka Dekker, Florian Eichler, Erik Eklund, Francesca Fumagalli, Francesco Gavazzi, Sabine W. Grønborg, Peter van Hasselt, Mirjam Langeveld, Caroline Lindemans, Fanny Mochel, Andreas Oberg, Dipak Ram, Elise Saunier-Vivar, Ludger Schöls, Michael Scholz, Caroline Sevin, Ayelet Zerem, Nicole I. Wolf, Samuel Groeschel
European Journal of Paediatric Neurology, 2024, vol. 49, p.141-154

Mono-allelic KCNB2 variants lead to a neurodevelopmental syndrome caused by altered channel inactivation Shreyas Bhat, Justine Rousseau, Coralie Michaud, Charles Marques Lourenço, Joan M. Stoler, Raymond J. Louie, Lola K. Clarkson, Angie Lichty, Daniel C. Koboldt, Shalini C. Reshmi, Sanjay M. Sisodiya, Eva M.M. Hoytema van Konijnenburg, Klaas Koop, Peter M. van Hasselt, Florence Démurger, Christèle Dubourg, Bonnie R. Sullivan, Susan S. Hughes, Isabelle Thiffault, Elisabeth Simard Tremblay, Andrea Accogli, Myriam Srour, Rikard Blunck, Philippe M. Campeau
American Journal of Human Genetics, 2024, vol. 111, p.761-777

Longitudinal volumetric analysis of gray matter atrophy in metachromatic leukodystrophy Murtadha L. Al-Saady, Hristina Galabova, Daphne H. Schoenmakers, Shanice Beerepoot, Caroline Lindemans, Peter M. van Hasselt, Marjo S. van der Knaap, Nicole I. Wolf, Petra J.W. Pouwels
Journal of Inherited Metabolic Disease, 2024, vol. 47, p.792-804

Severity-adjusted evaluation of liver transplantation on health outcomes in urea cycle disorders Roland Posset, Sven F. Garbade, Florian Gleich, Svenja Scharre, Jürgen G. Okun, Andrea L. Gropman, Sandesh C.S. Nagamani, Ann Catrin Druck, Friederike Epp, Georg F. Hoffmann, Stefan Kölker, Matthias Zielonka, Nicholas Ah Mew, Jennifer Seminara, Lindsay C. Burrage, Gerard T. Berry, Margo Breilyn, Andreas Schulze, Cary O. Harding, Susan A. Berry, Derek Wong, Shawn E. McCandless, Matthias R. Baumgartner, Laura Konczal, Can Ficicioglu, George A. Diaz, Curtis R. Coughlin, Gregory M. Enns, Renata C. Gallagher, Christina Lam, Tamar Stricker, Greta Wilkening, Carlo Dionisi-Vici, Dries Dobbelaere, Javier Blasco-Alonso, Alberto B. Burlina, Peter Freisinger, Peter M. van Hasselt, Anastasia Skouma, Allan M. Lund, Roshni Vara, Adrijan Sarajlija, Andrew A. Morris, Anupam Chakrapani, Ivo Barić, Persephone Augoustides-Savvopoulou, Yin Hsiu Chien, Elisenda Cortès-Saladelafont, Francois Eyskens, Gwendolyn Gramer, ,
Genetics in Medicine, 2024, vol. 26

Fellowships & Awards

2022: UMD Catalyst Grant - Morpholomics: the Imagestream as a read out to visualize aberrant cellular pathways in patients with genetic Variants of Unknown Significance

2022: Prijs beste abstract 2022

2022: Rotary 2022: Oog voor de toekomst

2022: For Wishdom 2022: Oog voor de toekomst

2022: Stichting de Merel 2022: Vroege voorspellers voor het ziektebeloop van MLD

2021: NWA-ORC: NANOSPRESSO-NL: op maat gemaakte gepersonaliseerde geneesmiddelen versus grootschalige industriële productie van geneesmiddelen

2015: Prijs voor het beste artikel 2015

External positions

bestuurslid - UMD is een samenwerking tussen de zes universitaire metabole centra en de patientenvereniging - UMD

advies - toekomstige medicatie metabole ziekten - ZIN (Zorg Instituut Nederland, previously VWS)