P. A. W. Mooyer

2.0k citations

19 papers · 1.5k indexed · 1 hit paper · h-index 14

Co-authors: Ronald J. A. Wanders Hans R. Waterham Janet Koster Carlo W.T. van Roermund James V. Leonard Stephan Kemp P. G. Barth Sacha Ferdinandusse
Topics: Peroxisome Proliferator-Activated Receptors (14 papers)Metabolism and Genetic Disorders (11 papers)Biochemical and Molecular Research (4 papers)
Cited by: Clinical Biochemistry Biochemistry Molecular Biology
Journals: New England Journal of Medicine Brain Annals of Neurology
Partner nations: Netherlands Spain France

In The Last Decade

P. A. W. Mooyer

19 papers receiving 1.5k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

A Lethal Defect of Mitochondrial and Peroxisomal Fission

2007 583 citations Hans R. Waterham, Janet Koster et al. New England Journal of Medicine profile →

Peers

Countries citing papers authored by P. A. W. Mooyer

Since Specialization

Citations

This map shows the geographic impact of P. A. W. Mooyer'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 P. A. W. Mooyer with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites P. A. W. Mooyer more than expected).

Fields of papers citing papers by P. A. W. Mooyer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by P. A. W. Mooyer. 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 P. A. W. Mooyer. The network helps show where P. A. W. Mooyer may publish in the future.

Co-authorship network of co-authors of P. A. W. Mooyer

This figure shows the co-authorship network connecting the top 25 collaborators of P. A. W. Mooyer. A scholar is included among the top collaborators of P. A. W. Mooyer 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 P. A. W. Mooyer. P. A. W. Mooyer is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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19 of 19 papers shown

#	Work	Indexed citations
1	Biochemical Studies in Fibroblasts to Interpret Variants of Unknown Significance in the ABCD1 Gene 2021 ·Genes ·(unknown),P. A. W. Mooyer,Inge M. E. Dijkstra,Conny Dekker,(unknown),(unknown),Maura Ruzhnikov,Keith Van Haren,Nelson L.S. Tang,Klaas Koop,Michèl A.A.P. Willemsen,Joannie Hui,Frédéric M. Vaz,Merel S. Ebberink,Marc Engelen,Stephan Kemp,Sacha Ferdinandusse	8
2	ACBD5 deficiency causes a defect in peroxisomal very long-chain fatty acid metabolism 2016 ·Journal of Medical Genetics ·Sacha Ferdinandusse,Kim D. Falkenberg,Janet Koster,P. A. W. Mooyer,Richard O. Jones,Carlo W.T. van Roermund,Amy Pizzino,Michael Schrader,Ronald J. A. Wanders,Adeline Vanderver,Hans R. Waterham	87
3	Specific combination of compound heterozygous mutations in 17β-hydroxysteroid dehydrogenase type 4 (HSD17B4) defines a new subtype of D-bifunctional protein deficiency 2012 ·Orphanet Journal of Rare Diseases ·Hugh J. McMillan,(unknown),Jeremy Schwartzentruber,Chloe Gottlieb,Sarah Lawrence,Alex MacKenzie,Chandree L. Beaulieu,P. A. W. Mooyer,Ronald J. A. Wanders,Jacek Majewski,Dennis E. Bulman,Michael T. Geraghty,Sacha Ferdinandusse,Kym M. Boycott	48
4	Plasmalogens participate in very-long-chain fatty acid-induced pathology 2008 ·Brain ·Pedro Brites,P. A. W. Mooyer,(unknown),Hans R. Waterham,R. J. A. Wanders	82
5	A key role for the peroxisomalABCD2transporter in fatty acid homeostasis 2008 ·American Journal of Physiology-Endocrinology and Metabolism ·Stéphane Fourcade,Montserrat Ruíz,Carme Camps,Agatha Schlüter,Sander M. Houten,P. A. W. Mooyer,Teresa Pàmpols,G. Dacremont,Ronald J. A. Wanders,M. Girós,Aurora Pujol	86
6	Genotype-phenotype correlation in PEX5-deficient peroxisome biogenesis defective cell lines 2008 ·Human Mutation ·Merel S. Ebberink,P. A. W. Mooyer,Janet Koster,Conny Dekker,François Eyskens,Carlo Dionisi‐Vici,Peter T. Clayton,P. G. Barth,Ronald J. A. Wanders,Hans R. Waterham	16
7	A Lethal Defect of Mitochondrial and Peroxisomal Fissionbreakdown → 2007 ·New England Journal of Medicine ·Hans R. Waterham,Janet Koster,Carlo W.T. van Roermund,P. A. W. Mooyer,Ronald J. A. Wanders,James V. Leonard	583
8	Inactivation of the peroxisomal ABCD2 transporter in the mouse leads to late-onset ataxia involving mitochondria, Golgi and endoplasmic reticulum damage 2005 ·Human Molecular Genetics ·Isidró Ferrer,Josef P. Kapfhammer,C. Hindelang,Stephan Kemp,N. Troffer-Charlier,Vania Broccoli,(unknown),P. A. W. Mooyer,(unknown),P. Vreken,Ronald J. A. Wanders,Jean‐Louis Mandel,Aurora Pujol	86
9	Clinical and biochemical spectrum of D‐bifunctional protein deficiency 2005 ·Annals of Neurology ·Sacha Ferdinandusse,Simone Denis,P. A. W. Mooyer,Conny Dekker,Marinus Durán,R. J. Soorani‐Lunsing,Eugen Boltshauser,Alfons Macaya,Jutta Gärtner,Charles B.L.M. Majoie,P. G. Barth,Ronald J. A. Wanders,Bwee Tien Poll‐The	138
10	Identification of fatty acid oxidation disorder patients with lowered acyl‐CoA thioesterase activity in human skin fibroblasts 2005 ·European Journal of Clinical Investigation ·Mary C. Hunt,(unknown),P. A. W. Mooyer,(unknown),Rob Ofman,Lodewijk IJlst,Ronald J. A. Wanders	8
11	Elongation of very long-chain fatty acids is enhanced in X-linked adrenoleukodystrophy 2004 ·Molecular Genetics and Metabolism ·Stephan Kemp,Fredoen Valianpour,Simone Denis,Rob Ofman,(unknown),P. A. W. Mooyer,P. G. Barth,Ronald J. A. Wanders	72
12	Method for Measurement of Peroxisomal Very-Long-Chain Fatty Acid β-Oxidation in Human Skin Fibroblasts Using Stable-Isotope-Labeled Tetracosanoic Acid 2004 ·Clinical Chemistry ·Stephan Kemp,Fredoen Valianpour,P. A. W. Mooyer,Willem Kulik,Ronald J. A. Wanders	32
13	Autosomal Recessive HEM/Greenberg Skeletal Dysplasia Is Caused by 3β-Hydroxysterol Δ14-Reductase Deficiency Due to Mutations in the Lamin B Receptor Gene 2003 ·The American Journal of Human Genetics ·Hans R. Waterham,Janet Koster,P. A. W. Mooyer,Gerard van Noort,Richard I. Kelley,William R. Wilcox,Jennifer Wanders,(unknown),Cor Oosterwijk	159
14	Clinical, enzymatic, and molecular genetic characterization of a biochemical variant type of argininosuccinic aciduria: prenatal and postnatal diagnosis in five unrelated families 2002 ·Journal of Inherited Metabolic Disease ·Wim J. Kleijer,Victor H. Garritsen,Michael Linnebank,P. A. W. Mooyer,J. G. M. Huijmans,Aki Mustonen,K. O. J. Simola,Mine Arslan‐Kirchner,Roberta Battini,P. Briones,E Cardó,Hanna Mandel,Eva Tschiedel,Ronald J. A. Wanders,Hans‐Georg Koch	31
15	Atypical Refsum disease with pipecolic acidemia and abnormal catalase distribution 2000 ·Annals of Neurology ·Matthias R. Baumgartner,Gerbert A. Jansen,Nanda M. Verhoeven,P. A. W. Mooyer,C. Jakobs,Frank Roels,Marc Espeel,(unknown),H. Bellet,R. J. A. Wanders,J. M. Saudubray	2
16	Atypical Refsum disease with pipecolic acidemia and abnormal catalase distribution 2000 ·Annals of Neurology ·Matthias R. Baumgartner,Gerbert A. Jansen,Nanda M. Verhoeven,P. A. W. Mooyer,C. Jakobs,Frank Roels,Marc Espeel,A Fourmaintraux,H. Bellet,R. J. A. Wanders,Jean Marie Saudubray	12
17	ALDP expression in fibroblasts of patients with X‐linked adrenoleukodystrophy 1995 ·Journal of Inherited Metabolic Disease ·Stephan Kemp,P. A. W. Mooyer,P. A. Bolhuis,Björn M. van Geel,Jean‐Louis Mandel,P. G. Barth,Patrick Aubourg,Ronald J. A. Wanders	29
18	The IMP dehydrogenase inhibitor mycophenolic acid antagonizes the CTP synthetase inhibitor 3-deazauridine in MOLT-3 human leukemia cells: A central role for phosphoribosyl pyrophosphate 1995 ·Biochemical Pharmacology ·A Berg,P. A. W. Mooyer,Henk van Lenthe,(unknown),Ronney A. De Abreu,(unknown),Albert H. Gennip	3
19	d‐2‐Hydroxyglutaric acidaemia: identification of a new enzyme,d‐2‐hydroxyglutarate dehydrogenase, localized in mitochondria 1995 ·Journal of Inherited Metabolic Disease ·R. J. A. Wanders,P. A. W. Mooyer	21

About P. A. W. Mooyer

P. A. W. Mooyer is a scholar working on Clinical Biochemistry, Biochemistry and Molecular Biology, having authored 19 papers that have together received 1.5k indexed citations. Recurring topics across this work include Peroxisome Proliferator-Activated Receptors (14 papers), Metabolism and Genetic Disorders (11 papers) and Biochemical and Molecular Research (4 papers). The work is most often cited by research in Clinical Biochemistry (526 citations), Biochemistry (156 citations) and Molecular Biology (1.4k citations). P. A. W. Mooyer has collaborated with scholars based in Netherlands, Spain and France. Frequent co-authors include Ronald J. A. Wanders, Hans R. Waterham, Janet Koster, Carlo W.T. van Roermund, James V. Leonard, Stephan Kemp, P. G. Barth, Sacha Ferdinandusse, Simone Denis and Jennifer Wanders. Their work appears in journals such as New England Journal of Medicine, Brain and Annals of Neurology.

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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