W. Oostheim

719 citations

16 papers · 550 indexed · h-index 13

Impact in

Clinical Biochemistry top 1%
- Metabolism and Genetic Disorders
Biochemistry top 10%
- Amino Acid Enzymes and Metabolism
- Lipid metabolism and biosynthesis

Papers in

Clinical Biochemistry 10
- Metabolism and Genetic Disorders 10
Biochemistry 4
- Amino Acid Enzymes and Metabolism 2
- Lipid metabolism and biosynthesis 2

Co-authors: Ronald J. A. Wanders Lodewijk IJlst Edwin C.J.M. de Vet H. van den Bosch Hans R. Waterham Jos P.N. Ruiter Sacha Ferdinandusse Alisa Gutman
Journals: Human Mutation (2 papers)The American Journal of Human Genetics (2 papers)Journal of Inherited Metabolic Disease (2 papers)Biochemical and Biophysical Research Communications (2 papers)Annals of Human Genetics (1 paper)
Partner nations: Netherlands United States Italy

In The Last Decade

W. Oostheim

16 papers receiving 541 citations

Peers

Countries citing papers authored by W. Oostheim

Since Specialization

Citations

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

Fields of papers citing papers by W. Oostheim

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside W. Oostheim, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with W. Oostheim Line = papers co-authored together W. Oostheim links everyone, so they are left out of the graph.

All Works

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16 of 16 papers shown

#	Work
1	A mutation creating an upstream translation initiation codon in SLC22A5 5′UTR is a frequent cause of primary carnitine deficiency Human Mutation ·Sacha Ferdinandusse, Heleen te Brinke, Jos P.N. Ruiter, Janet Haasjes, W. Oostheim, Henk van Lenthe, Lodewijk IJlst, Merel S. Ebberink, Ronald J. A. Wanders, Frédéric M. Vaz, Hans R. Waterham	2019	18
2	Identification of a Missense Mutation in a Patient with Lethal Carnitine Acyl-Carnitine Carrier Deficiency Kluwer Academic Publishers eBooks ·Lodewijk IJlst, Jos P.N. Ruiter, W. Oostheim, Klary E. Niezen‐Koning, Ferdinando Palmieri, R. J. A. Wanders	2006	4
3	Mutational Spectrum of d-Bifunctional Protein Deficiency and Structure-Based Genotype-Phenotype Analysis The American Journal of Human Genetics ·Sacha Ferdinandusse, Rabita Karanjit, Jolein Gloerich, M. Kristian Koski, W. Oostheim, Hans R. Waterham, J. Kalervo Hiltunen, Ronald J. A. Wanders, Tuomo Glumoff	2005	66
4	Identification of novel mutations in classical galactosemia Human Mutation ·Annet M. Bosch, Lodewijk IJlst, W. Oostheim, Joyce Mulders, H. D. Bakker, Frits A. Wijburg, Ronald J. A. Wanders, Hans R. Waterham	2005	28
5	Identification of three patients with a very mild form of Smith‐Lemli‐Opitz syndrome American Journal of Medical Genetics Part A ·Cathrine Garp, Hans R. Waterham, G. J. Romeijn, W. Oostheim, Martina M.J. de Barse, L. Dorland, Marinus Durán, Frits A. Beemer, Ronald J. A. Wanders, Bwee Tien Poll‐The	2003	23
6	Reinvestigation of Peroxisomal 3-Ketoacyl-CoA Thiolase Deficiency: Identification of the True Defect at the Level of d-Bifunctional Protein The American Journal of Human Genetics ·Sacha Ferdinandusse, E.G. van Grunsven, W. Oostheim, Frank Hentschel, Eveline M. Hogenhout, Lodewijk IJlst, Carlo W.T. van Roermund, Hans R. Waterham, Sidney Goldfischer, Ronald J. A. Wanders	2002	36
7	Functional Analysis of Mutant Human Carnitine Acylcarnitine Translocases in Yeast Biochemical and Biophysical Research Communications ·Lodewijk IJlst, Carlo W.T. van Roermund, Vito Iacobazzi, W. Oostheim, Jos P.N. Ruiter, Joel Williams, Ferdinando Palmieri, Ronald J. A. Wanders	2001	36
8	Novel mutations in the 7‐dehydrocholesterol reductase gene of 13 patients with Smith–Lemli–Opitz syndrome Annals of Human Genetics ·Petr Jira, Ronald J. A. Wanders, Jan A. M. Smeitink, Jeroen de Jong, Ron A. Wevers, W. Oostheim, J.H.A.M. Tuerlings, R Hennekam, R. C. A. Sengers, H. R. Waterham	2001	26
9	Novel mutations in the 7-dehydrocholesterol reductase gene of 13 patients with Smith--Lemli--Opitz syndrome. PubMed ·Petr Jira, Ronald J. A. Wanders, Jan A. M. Smeitink, Jeroen de Jong, Ron A. Wevers, W. Oostheim, J.H.A.M. Tuerlings, Raoul C. M. Hennekam, R. C. A. Sengers, Hans R. Waterham	2001	26
10	Molecular Cloning and Expression of Human L-Pipecolate Oxidase Biochemical and Biophysical Research Communications ·Lodewijk IJlst, Wenjin Xu, W. Oostheim, Ronald J. A. Wanders	2000	21
11	Heterozygosity for the Common LCHAD Mutation (1528G>C) Is Not a Major Cause of HELLP Syndrome and the Prevalence of the Mutation in the Dutch Population Is Low Pediatric Research ·M. E. J. den Boer, Lodewijk IJlst, Frits A. Wijburg, W. Oostheim, 晴久日吉, Maria G. van Pampus, H. S. A. Heymans, Ronald J. A. Wanders	2000	44
12	Ether lipid biosynthesis: alkyl-dihydroxyacetonephosphate synthase protein deficiency leads to reduced dihydroxyacetonephosphate acyltransferase activities Journal of Lipid Research ·Edwin C.J.M. de Vet, Lodewijk IJlst, W. Oostheim, Pan Xin-hong, H. W. Moser, H. van den Bosch, Ronald J. A. Wanders	1999	43
13	Molecular basis of Sjögren‐Larsson syndrome: Frequency of the 1297–1298 del GA and 943C→T mutation in 29 patients Journal of Inherited Metabolic Disease ·Lodewijk IJlst, W. Oostheim, 順治中田, Michèl A.A.P. Willemsen, Ronald J. A. Wanders	1999	7
14	Molecular basis of hepatic carnitine palmitoyltransferase I deficiency. Journal of Clinical Investigation ·Lodewijk IJlst, Hanna Mandel, W. Oostheim, Jos P.N. Ruiter, Alisa Gutman, R. J. A. Wanders	1998	75
15	Alkyl-Dihydroxyacetonephosphate Synthase Journal of Biological Chemistry ·Edwin C.J.M. de Vet, Lodewijk IJlst, W. Oostheim, Ronald J. A. Wanders, H. van den Bosch	1998	87
16	Molecular basis of long‐chain 3‐hydroxyacyl‐CoA dehydrogenase deficiency: Identification of two new mutations Journal of Inherited Metabolic Disease ·Lodewijk IJlst, W. Oostheim, LU Ying-li, Ronald J. A. Wanders	1997	10

About W. Oostheim

W. Oostheim is a scholar working on Clinical Biochemistry, Biochemistry, Molecular Biology, Nephrology and Physiology, having authored 16 papers that have together received 550 indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (10 papers), Peroxisome Proliferator-Activated Receptors (6 papers), Mitochondrial Function and Pathology (5 papers), Cholesterol and Lipid Metabolism (3 papers), Amino Acid Enzymes and Metabolism (2 papers), Lipid metabolism and biosynthesis (2 papers), RNA and protein synthesis mechanisms (2 papers) and Diet and metabolism studies (2 papers). The work is most often cited by research in Clinical Biochemistry (266 citations), Biochemistry (70 citations), Molecular Biology (398 citations), Pediatrics, Perinatology and Child Health (64 citations) and Cancer Research (45 citations). W. Oostheim has collaborated with scholars based in Netherlands, United States and Italy. Frequent co-authors include Ronald J. A. Wanders, Lodewijk IJlst, Edwin C.J.M. de Vet, H. van den Bosch, Hans R. Waterham, Jos P.N. Ruiter, Sacha Ferdinandusse, Alisa Gutman, Hanna Mandel and R. J. A. Wanders. Their work appears in journals such as Human Mutation, The American Journal of Human Genetics, Journal of Inherited Metabolic Disease, Biochemical and Biophysical Research Communications and Annals of Human Genetics.

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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