Nanda M. Verhoeven

5.1k total citations
93 papers, 3.5k citations indexed

About

Nanda M. Verhoeven is a scholar working on Clinical Biochemistry, Molecular Biology and Cell Biology. According to data from OpenAlex, Nanda M. Verhoeven has authored 93 papers receiving a total of 3.5k indexed citations (citations by other indexed papers that have themselves been cited), including 60 papers in Clinical Biochemistry, 47 papers in Molecular Biology and 20 papers in Cell Biology. Recurrent topics in Nanda M. Verhoeven's work include Metabolism and Genetic Disorders (60 papers), Peroxisome Proliferator-Activated Receptors (22 papers) and Amino Acid Enzymes and Metabolism (18 papers). Nanda M. Verhoeven is often cited by papers focused on Metabolism and Genetic Disorders (60 papers), Peroxisome Proliferator-Activated Receptors (22 papers) and Amino Acid Enzymes and Metabolism (18 papers). Nanda M. Verhoeven collaborates with scholars based in Netherlands, United States and France. Nanda M. Verhoeven's co-authors include Cornelis Jakobs, Gajja S. Salomons, Eduard A. Struys, C. Jakobs, Marjo S. van der Knaap, Kim M. Cecil, Ronald J. A. Wanders, Ton J. deGrauw, Erwin E. W. Jansen and Jojanneke H.J. Huck and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Blood and Neurology.

In The Last Decade

Nanda M. Verhoeven

93 papers receiving 3.5k citations

Peers

Countries citing papers authored by Nanda M. Verhoeven

Since Specialization

Citations

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

Fields of papers citing papers by Nanda M. Verhoeven

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Nanda M. Verhoeven. 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 Nanda M. Verhoeven. The network helps show where Nanda M. Verhoeven may publish in the future.

Co-authorship network of co-authors of Nanda M. Verhoeven

This figure shows the co-authorship network connecting the top 25 collaborators of Nanda M. Verhoeven. A scholar is included among the top collaborators of Nanda M. Verhoeven 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 Nanda M. Verhoeven. Nanda M. Verhoeven 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	Overexpression of GAMT restores GAMT activity in primary GAMT-deficient fibroblasts 2006 ·Molecular Genetics and Metabolism ·Lígia S. Almeida, Efraim H. Rosenberg, (unknown), Nanda M. Verhoeven, Laura Vilarinho, C. Jakobs, Gajja S. Salomons	6
2	Global developmental delay in guanidionacetate methyltransferase deficiency: differences in formal testing and clinical observation 2006 ·European Journal of Pediatrics ·K. T. Verbruggen, (unknown), R. J. Soorani‐Lunsing, Paul E. Sijens, Nanda M. Verhoeven, Gajja S. Salomons, S.M. Goorhuis-Brouwer, Francjan J. van Spronsen	11
3	A novel, quantitative assay for homocarnosine in cerebrospinal fluid using stable-isotope dilution liquid chromatography–tandem mass spectrometry 2005 ·Journal of Chromatography B ·Erwin E. W. Jansen, K. Michael Gibson, Yosuke Shigematsu, Cornelis Jakobs, Nanda M. Verhoeven	23
4	Quantification of sugar phosphate intermediates of the pentose phosphate pathway by LC–MS/MS: application to two new inherited defects of metabolism 2005 ·Journal of Chromatography B ·Mirjam M. C. Wamelink, Eduard A. Struys, Jojanneke H.J. Huck, Birthe Roos, Marjo S. van der Knaap, Cornelis Jakobs, Nanda M. Verhoeven	55
5	Mutations in the d-2-Hydroxyglutarate Dehydrogenase Gene Cause d-2-Hydroxyglutaric Aciduria 2005 ·The American Journal of Human Genetics ·Eduard A. Struys, Gajja S. Salomons, Younès Achouri, Emile Van Schaftingen, Salvatore Grosso, William J. Craigen, Nanda M. Verhoeven, Cornelis Jakobs	126
6	Ribose-5-Phosphate Isomerase Deficiency: New Inborn Error in the Pentose Phosphate Pathway Associated with a Slowly Progressive Leukoencephalopathy 2004 ·The American Journal of Human Genetics ·Jojanneke H.J. Huck, Nanda M. Verhoeven, Eduard A. Struys, Gajja S. Salomons, Cornelis Jakobs, Marjo S. van der Knaap	99
7	Evaluation of pentitol metabolism in mammalian tissues provides new insight into disorders of human sugar metabolism 2004 ·Molecular Genetics and Metabolism ·Jojanneke H.J. Huck, Birthe Roos, Cornelis Jakobs, Marjo S. van der Knaap, Nanda M. Verhoeven	27
8	l-2-Hydroxyglutaric Aciduria in Staffordshire Bull Terriers 2003 ·Journal of Veterinary Internal Medicine ·(unknown), Simon R. Platt, Cornelis Jakobs, Nanda M. Verhoeven, Ruth Dennis, Laurent Garosi, G. Diane Shelton	4
9	L-2-Hydroxyglutaric Aciduria in Staffordshire Bull Terriers 2003 ·Journal of Veterinary Internal Medicine ·(unknown), Simon R. Platt, Cornelis Jakobs, Nanda M. Verhoeven, Ruth Dennis, Laurent Garosi, G. Diane Shelton	28
10	Carnitine-acylcarnitine translocase deficiency: phenotype, residual enzyme activity and outcome 2001 ·European Journal of Pediatrics ·Enrico Lopriore, Reinoud J. B. J. Gemke, Nanda M. Verhoeven, Cornelis Jakobs, Ronald J. A. Wanders, (unknown), Bwee Tien Poll‐The	30
11	In vivo and in vitro NMR spectroscopy reveal a putative novel inborn error involving polyol metabolism 2001 ·NMR in Biomedicine ·Sytske H. Moolenaar, Marjo S. van der Knaap, Udo F. H. Engelke, Petra J. W. Pouwels, (unknown), Nanda M. Verhoeven, Cornelis Jakobs, Ron A. Wevers	27
12	Transaldolase Deficiency: Liver Cirrhosis Associated with a New Inborn Error in the Pentose Phosphate Pathway 2001 ·The American Journal of Human Genetics ·Nanda M. Verhoeven, Jojanneke H.J. Huck, Birthe Roos, Eduard A. Struys, Gajja S. Salomons, A. C. Douwes, Marjo S. van der Knaap, Cornelis Jakobs	90
13	Irreversible brain creatine deficiency with elevated serum and urine creatine: A creatine transporter defect? 2001 ·Annals of Neurology ·Kim M. Cecil, G. S. Salomons, William S. Ball, Brenda Wong, Gail Chuck, Nanda M. Verhoeven, (unknown), Ton J. deGrauw	137
14	X-Linked Creatine-Transporter Gene (SLC6A8) Defect: A New Creatine-Deficiency Syndrome 2001 ·The American Journal of Human Genetics ·Gajja S. Salomons, Silvy J.M. van Dooren, Nanda M. Verhoeven, Kim M. Cecil, William S. Ball, Ton J. deGrauw, Cornelis Jakobs	289
15	Mental retardation and behavioral problems as presenting signs of a creatine synthesis defect 2000 ·Annals of Neurology ·Marjo S. van der Knaap, Nanda M. Verhoeven, P. D. Maaswinkel‐Mooij, Petra J. W. Pouwels, (unknown), E Peeters, Sylvia Stöckler‐Ipsiroglu, (unknown)	18
16	Leukoencephalopathy associated with a disturbance in the metabolism of polyols 1999 ·Annals of Neurology ·Marjo S. van der Knaap, Ron A. Wevers, Eduard A. Struys, Nanda M. Verhoeven, Petra J. W. Pouwels, Udo F. H. Engelke, (unknown), J. Valk, (unknown)	50
17	Clinical approach to inherited peroxisomal disorders: A series of 27 patients 1998 ·Annals of Neurology ·Matthias R. Baumgartner, Bwee Tien Poll‐The, Nanda M. Verhoeven, C. Jakobs, Marc Espeel, Frank Roels, Daniel Rabier, Thierry Levade, Marie-Odile Rolland, Maria Carmen Martínez, R. J. A. Wanders, Jean Marie Saudubray	41
18	An accurate stable isotope dilution gas chromatographic–mass spectrometric approach to the diagnosis of guanidinoacetate methyltransferase deficiency 1998 ·Journal of Pharmaceutical and Biomedical Analysis ·Eduard A. Struys, Erwin E. W. Jansen, H.J. ten Brink, Nanda M. Verhoeven, Marjo S. van der Knaap, C. Jakobs	69
19	Iron Release From Human Monocytes After Erythrophagocytosis In Vitro: An Investigation in Normal Subjects and Hereditary Hemochromatosis Patients 1998 ·Blood ·(unknown), Minke A. Noordermeer, Nanda M. Verhoeven, (unknown), Joannes J.M. Marx	111
20	Resolution of the Phytanic Acid α-Oxidation Pathway: Identification of Pristanal as Product of the Decarboxylation of 2-Hydroxyphytanoyl-CoA 1997 ·Biochemical and Biophysical Research Communications ·Nanda M. Verhoeven, D. S. M. Schor, H.J. ten Brink, Ronald J. A. Wanders, C. Jakobs	45

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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