Peter M. van Hasselt

5.6k total citations
114 papers, 2.5k citations indexed

About

Peter M. van Hasselt is a scholar working on Molecular Biology, Physiology and Clinical Biochemistry. According to data from OpenAlex, Peter M. van Hasselt has authored 114 papers receiving a total of 2.5k indexed citations (citations by other indexed papers that have themselves been cited), including 48 papers in Molecular Biology, 43 papers in Physiology and 30 papers in Clinical Biochemistry. Recurrent topics in Peter M. van Hasselt's work include Lysosomal Storage Disorders Research (33 papers), Metabolism and Genetic Disorders (30 papers) and Mitochondrial Function and Pathology (14 papers). Peter M. van Hasselt is often cited by papers focused on Lysosomal Storage Disorders Research (33 papers), Metabolism and Genetic Disorders (30 papers) and Mitochondrial Function and Pathology (14 papers). Peter M. van Hasselt collaborates with scholars based in Netherlands, United States and Germany. Peter M. van Hasselt's co-authors include Nanda M. Verhoeven‐Duif, Judith Jans, Tom J. de Koning, Gepke Visser, Hanneke A. Haijes, Monique G.M. de Sain–van der Velden, Hubertus C.M.T. Prinsen, Sabine A. Fuchs, Jaap Jan Boelens and Maria van der Ham and has published in prestigious journals such as New England Journal of Medicine, Journal of Biological Chemistry and Nature Communications.

In The Last Decade

Peter M. van Hasselt

112 papers receiving 2.5k citations

Peers

Countries citing papers authored by Peter M. van Hasselt

Since Specialization

Citations

This map shows the geographic impact of Peter M. van Hasselt's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Peter M. van Hasselt with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Peter M. van Hasselt more than expected).

Fields of papers citing papers by Peter M. van Hasselt

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Peter M. van Hasselt. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Peter M. van Hasselt. The network helps show where Peter M. van Hasselt may publish in the future.

Co-authorship network of co-authors of Peter M. van Hasselt

This figure shows the co-authorship network connecting the top 25 collaborators of Peter M. van Hasselt. A scholar is included among the top collaborators of Peter M. van Hasselt based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Peter M. van Hasselt. Peter M. van Hasselt is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Novel Insights Into Gyrate Atrophy of the Choroid and Retina (GACR): A Cohort Study 2025 ·Journal of Inherited Metabolic Disease ·(unknown), (unknown), Camiel J. F. Boon, Martijn C.G.J. Brouwers, Roselie M.H. Diederen, (unknown), Peter M. van Hasselt, Bregje Jaeger, (unknown), Alexander J. Rennings, Francjan J. van Spronsen, (unknown), Margreet A. E. M. Wagenmakers, Julie De Zaeytijd, Bart P. Leroy, Andreas Schulze, Clara D. van Karnebeek, Marion M. Brands	1
2	Correction of pathogenic mitochondrial DNA in patient-derived disease models using mitochondrial base editors 2025 ·PLoS Biology ·Indi P. Joore, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Wilbert P. Vermeij, Richard J. Rodenburg, Raymond M. Schiffelers, Edward E. S. Nieuwenhuis, Peter M. van Hasselt, Sabine A. Fuchs, Martijn Koppens	2
3	Longitudinal volumetric analysis of gray matter atrophy in metachromatic leukodystrophy 2024 ·Journal of Inherited Metabolic Disease ·(unknown), (unknown), (unknown), Shanice Beerepoot, Caroline A. Lindemans, Peter M. van Hasselt, Marjo S. van der Knaap, (unknown), Petra J. W. Pouwels	2
4	Timing of cerebral damage in molybdenum cofactor deficiency: A meta-analysis of case reports 2024 ·Genetics in Medicine Open ·(unknown), Floris C. Hofstede, Hanneke A. Haijes, Klaske D. Lichtenbelt, L. R. Pistorius, Monique G.M. de Sain–van der Velden, Peter G. J. Nikkels, Maarten H. Lequin, Linda S. de Vries, Saskia N. van der Crabben, Peter M. van Hasselt	2
5	Neurodegenerative disease after hematopoietic stem cell transplantation in metachromatic leukodystrophy 2023 ·Annals of Clinical and Translational Neurology ·(unknown), Shanice Beerepoot, (unknown), Marjolein Breur, (unknown), Petra J. W. Pouwels, Jaap Jan Boelens, Caroline A. Lindemans, Peter M. van Hasselt, Ulrich Matzner, Adeline Vanderver, Marianna Bugiani, Marjo S. van der Knaap, Nicole I. Wolf	6
6	A second case of glutaminase hyperactivity: Expanding the phenotype with epilepsy 2023 ·JIMD Reports ·(unknown), Petra J. W. Pouwels, Nicole I. Wolf, Holger Rehmann, Mirjam M. C. Wamelink, Quinten Waisfisz, Judith Jans, Hubertus C.M.T. Prinsen, Jiddeke M. van de Kamp, Peter M. van Hasselt	3
7	Development of a compounded propofol nanoemulsion using multiple non-invasive process analytical technologies 2023 ·International Journal of Pharmaceutics ·(unknown), (unknown), (unknown), (unknown), (unknown), Peter M. van Hasselt, (unknown), Cornelus F. van Nostrum, Michiel Hermes, R. Besseling, (unknown)	3
8	Aberrant cyclin C nuclear release induces mitochondrial fragmentation and dysfunction in MED13L syndrome fibroblasts 2022 ·iScience ·Kai‐Ti Chang, Jan Ježek, (unknown), (unknown), (unknown), (unknown), Ping Jiang, Hyung‐Ok Lee, Warren D. Kruger, Peter M. van Hasselt, Randy Strich	6
9	Long-term effect of hematopoietic cell transplantation on systemic inflammation in patients with mucopolysaccharidoses 2021 ·Blood Advances ·(unknown), Caroline A. Lindemans, Jaap Jan Boelens, Eveline M. Delemarre, Julia Drylewicz, Nanda M. Verhoeven‐Duif, Peter M. van Hasselt, Stefan Nierkens	3
10	The potential and limitations of intrahepatic cholangiocyte organoids to study inborn errors of metabolism 2021 ·Journal of Inherited Metabolic Disease ·(unknown), Imre F. Schene, Arif Ibrahim Ardisasmita, Nalan Liv, Tineke Veenendaal, Judith Klumperman, Hubert P. J. van der Doef, Henkjan J. Verkade, Monique M.A. Verstegen, Luc J. W. van der Laan, Judith Jans, Nanda M. Verhoeven‐Duif, Peter M. van Hasselt, Edward E. S. Nieuwenhuis, Bart Spee, Sabine A. Fuchs	8
11	Hurdles in treating Hurler disease: potential routes to achieve a “real” cure 2020 ·Blood Advances ·(unknown), Jaap van Doorn, (unknown), Stefan Nierkens, Caroline A. Lindemans, Nanda M. Verhoeven‐Duif, Jaap Jan Boelens, Peter M. van Hasselt	10
12	Variants in NGLY1 lead to intellectual disability, myoclonus epilepsy, sensorimotor axonal polyneuropathy and mitochondrial dysfunction 2020 ·Clinical Genetics ·(unknown), Saskia B. Wortmann, Charlotte A. Haaxma, Peter M. van Hasselt, Nicole I. Wolf, Yvonne Hendriks, Benno Küsters, (unknown), (unknown), Werner J.H. Koopman, Liesbeth T. Wintjes, (unknown), Maaike de Vries, Dirk J. Lefeber, Jan Smeıtınk, Richard J. Rodenburg	23
13	Influence of PEGylation of Vitamin-K-Loaded Mixed Micelles on the Uptake by and Transport through Caco-2 Cells 2018 ·Molecular Pharmaceutics ·(unknown), Max Adrian, Nataliia Beztsinna, (unknown), Roel F. Maas-Bakker, Peter M. van Hasselt, Mies J. van Steenbergen, (unknown), Lukas C. Kapitein, Wim E. Hennink, Cornelus F. van Nostrum	7
14	Identification of a Loss-of-Function Mutation in the Context of Glutaminase Deficiency and Neonatal Epileptic Encephalopathy 2018 ·JAMA Neurology ·(unknown), (unknown), Oliver Maier, Holger Rehmann, Maarten H. Lequin, Jan-Ulrich Schlump, Bernhard Schmitt, (unknown), Hubertus C.M.T. Prinsen, (unknown), Ralph Fingerhut, Johannes R. Lemke, Fried Zwartkruis, Roderick H.J. Houwen, Judith Jans, Nanda M. Verhoeven‐Duif, Peter M. van Hasselt, Rami Abou Jamra	34
15	Mutated PET117 causes complex IV deficiency and is associated with neurodevelopmental regression and medulla oblongata lesions 2017 ·Human Genetics ·G. Herma Renkema, Gepke Visser, Fabian Baertling, Liesbeth T. Wintjes, Victorien M. Wolters, Joris van Montfrans, G.A.P. de Kort, Peter G. J. Nikkels, Peter M. van Hasselt, Saskia N. van der Crabben, Richard J. Rodenburg	27
16	Incomplete biomarker response in mucopolysaccharidosis type I after successful hematopoietic cell transplantation 2017 ·Molecular Genetics and Metabolism ·(unknown), Peter M. van Hasselt, Jaap Jan Boelens, Frits A. Wijburg, Eveline J. Langereis	4
17	Effectiveness of whole-exome sequencing and costs of the traditional diagnostic trajectory in children with intellectual disability 2016 ·Genetics in Medicine ·Glen R. Monroe, G. W. J. Frederix, Sanne M. C. Savelberg, Tamar I. de Vries, Karen Duran, Jasper J. van der Smagt, Pauline Terhal, Peter M. van Hasselt, Hester Y. Kroes, Nanda M. Verhoeven‐Duif, Isaäc J. Nijman, Ellen C. Carbo, Koen L.I. van Gassen, Nine Knoers, Anke M. Hövels, Mieke M. van Haelst, Gepke Visser, Gijs van Haaften	125
18	A New Approach for Fast Metabolic Diagnostics in CMAMMA 2016 ·JIMD Reports ·Monique G.M. de Sain–van der Velden, Maria van der Ham, Judith Jans, Gepke Visser, Hubertus C.M.T. Prinsen, Nanda M. Verhoeven‐Duif, Koen L.I. van Gassen, Peter M. van Hasselt	5
19	Hereditaire fructose-intolerantie 2014 ·Nederlandsch tijdschrift voor geneeskunde/Nederlands tijdschrift voor geneeskunde/NTvG-databank ·(unknown), Hans R. Waterham, (unknown), Peter M. van Hasselt, Gepke Visser	1
20	Prevalence and Development of Orthopaedic Symptoms in the Dutch Hurler Patient Population after Haematopoietic Stem Cell Transplantation 2012 ·JIMD Reports ·(unknown), Moyo C. Kruyt, (unknown), Ralph J. B. Sakkers, Peter M. van Hasselt, René M. Castelein	20

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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