Janet Koster

3.9k citations

44 papers · 2.9k · 1 hit paper · h-index 24

Impact in

Clinical Biochemistry top 0.5%
- Metabolism and Genetic Disorders
Molecular Biology top 5%
- Peroxisome Proliferator-Activated Receptors
- Mitochondrial Function and Pathology
- ATP Synthase and ATPases Research
- RNA modifications and cancer
- Inflammasome and immune disorders
- RNA Research and Splicing

Papers in

Molecular Biology 42
- Peroxisome Proliferator-Activated Receptors 25
- Mitochondrial Function and Pathology 6
- Plant biochemistry and biosynthesis 5
- Inflammasome and immune disorders 5
Clinical Biochemistry 8
- Metabolism and Genetic Disorders 8

Co-authors: Hans R. Waterham (41 shared papers)Ronald J. A. Wanders (23 shared papers)Carlo W.T. van Roermund (4 shared papers)P. A. W. Mooyer (4 shared papers)James V. Leonard (1 shared paper)Richard I. Kelley (4 shared papers)Sacha Ferdinandusse (12 shared papers)Merel S. Ebberink (6 shared papers)
Journals: Human Molecular Genetics (4 papers)Human Mutation (4 papers)The American Journal of Human Genetics (3 papers)Journal of Lipid Research (2 papers)Journal of Inherited Metabolic Disease (2 papers)
Partner nations: Netherlands United States United Kingdom

In The Last Decade

Janet Koster

44 papers receiving 2.9k citations

Janet Koster's Hit Papers

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A Lethal Defect of Mitochondrial and Peroxisomal Fission 2007 · 618 citations

Peers

Countries citing papers authored by Janet Koster

Since Specialization

Citations

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

Fields of papers citing papers by Janet Koster

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Janet Koster, 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 Janet Koster Line = papers co-authored together Janet Koster links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 44 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	A Lethal Defect of Mitochondrial and Peroxisomal Fission 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 Hit paper breakdown →	2007	618
2	Mutations in the 3β-Hydroxysterol Δ24-Reductase Gene Cause Desmosterolosis, an Autosomal Recessive Disorder of Cholesterol Biosynthesis The American Journal of Human Genetics ·Hans R. Waterham, Janet Koster, G. J. Romeijn, Raoul C. M. Hennekam, P. Vreken, Hans C. Andersson, David Fitzpatrick, Richard I. Kelley, Ronald J. A. Wanders	2001	303
3	Autosomal Recessive HEM/Greenberg Skeletal Dysplasia Is Caused by 3β-Hydroxysterol Δ14-Reductase Deficiency Due to Mutations in the Lamin B Receptor Gene 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, C.M. Raoul Hennekam, Cor Oosterwijk	2003	176
4	Sodium taurocholate cotransporting polypeptide (SLC10A1) deficiency: Conjugated hypercholanemia without a clear clinical phenotype Hepatology ·Frédéric M. Vaz, Coen C. Paulusma, Hidde H. Huidekoper, Minke H. de Ru, Cynthia Ciwei Lim, Janet Koster, Kam S. Ho‐Mok, Albert H. Bootsma, Albert K. Groen, Frank G. Schaap, Ronald P.J. Oude Elferink, Hans R. Waterham, Ronald J. A. Wanders	2014	161
5	Clinical, biochemical, and mutational spectrum of peroxisomal acyl–coenzyme A oxidase deficiency Human Mutation ·Sacha Ferdinandusse, Simone Denis, Eveline M. Hogenhout, Janet Koster, Carlo W.T. van Roermund, Lodewijk IJlst, Ann B. Moser, Ronald J. A. Wanders, Hans R. Waterham	2007	124
6	Genetic classification and mutational spectrum of more than 600 patients with a Zellweger syndrome spectrum disorder Human Mutation ·Merel S. Ebberink, Petra A.W. Mooijer, Jeannette Gootjes, Janet Koster, Ronald J. A. Wanders, Hans R. Waterham	2010	120
7	HMG-CoA reductase inhibition induces IL-1β release through Rac1/PI3K/PKB-dependent caspase-1 activation Blood ·Loes M. Kuijk, Jeffrey M. Beekman, Janet Koster, Hans R. Waterham, Joost Frenkel, Paul J. Coffer	2008	119
8	A novel bile acid biosynthesis defect due to a deficiency of peroxisomal ABCD3 Human Molecular Genetics ·Sacha Ferdinandusse, Gerardo Jiménez‐Sánchez, Janet Koster, Simone Denis, C W van Roermund, Irma Silva‐Zolezzi, Ann B. Moser, Wouter F. Visser, Mine Güllüoğlu, Özlem Durmaz, Mübeccel Demirkol, Hans R. Waterham, Gülden Gökçay, Ronald J. A. Wanders, David Valle	2014	109
9	A novel defect of peroxisome division due to a homozygous non-sense mutation in the PEX11β gene Journal of Medical Genetics ·Merel S. Ebberink, Janet Koster, Gepke Visser, Francjan van Spronsen, Irene Stolte‐Dijkstra, Gerrit Smit, Johanna M. Fock, Stephan Kemp, Ronald J. A. Wanders, Hans R. Waterham	2012	105
10	ECHS1 mutations in Leigh disease: a new inborn error of metabolism affecting valine metabolism Brain ·Heidi Peters, Nicole E. Buck, Ronald J. A. Wanders, Jos P.N. Ruiter, Hans R. Waterham, Janet Koster, Joy Yaplito‐Lee, Sacha Ferdinandusse, James Pitt	2014	105
11	ACBD5 deficiency causes a defect in peroxisomal very long-chain fatty acid metabolism 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	2016	96
12	Mutational spectrum and genotype–phenotype correlations in mevalonate kinase deficiency Human Mutation ·Saskia H. L. Mandey, Marit S. Schneiders, Janet Koster, Hans R. Waterham	2006	92
13	Substrate specificity of human carnitine acetyltransferase: Implications for fatty acid and branched-chain amino acid metabolism Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Sara Violante, Lodewijk IJlst, Jos P.N. Ruiter, Janet Koster, Henk van Lenthe, Marinus Durán, Isabel Tavares de Almeida, Ronald J. A. Wanders, Sander M. Houten, Fátima V. Ventura	2013	80
14	Peroxisomes contribute to the acylcarnitine production when the carnitine shuttle is deficient Biochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids ·Sara Violante, Lodewijk IJlst, Heleen te Brinke, Janet Koster, Isabel Tavares de Almeida, Ronald J. A. Wanders, Fátima V. Ventura, Sander M. Houten	2013	78
15	Organization of the mevalonate kinase (MVK) gene and identification of novel mutations causing mevalonic aciduria and hyperimmunoglobulinaemia D and periodic fever syndrome European Journal of Human Genetics ·Sander M. Houten, Janet Koster, Gerrit-Jan Romeijn, Joost Frenkel, Maja Di Rocco, Ubaldo Caruso, P. Landrieu, Richard I. Kelley, Wietse Kuis, Bwee Tien Poll‐The, K. Michael Gibson, Ronald J. A. Wanders, Hans R. Waterham	2001	70
16	A novel case of ACOX2 deficiency leads to recognition of a third human peroxisomal acyl-CoA oxidase Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Sacha Ferdinandusse, Simone Denis, Carlo W.T. van Roermund, Mary Anne Preece, Janet Koster, Merel S. Ebberink, Hans R. Waterham, Ronald J. A. Wanders	2017	68
17	A novel type of rhizomelic chondrodysplasia punctata, RCDP5, is caused by loss of the PEX5 long isoform Human Molecular Genetics ·Tuva Barøy, Janet Koster, Petter Strømme, Merel S. Ebberink, Doriana Misceo, Sacha Ferdinandusse, Asbjørn Holmgren, Timothy Hughes, Else Merckoll, Jostein Westvik, Berit Woldseth, John H. Walter, (unknown), Bjørn Tvedt, Kristine Stadskleiv, Ronald J. A. Wanders, Hans R. Waterham, Eirik Frengen	2015	63
18	A homozygous missense mutation in ERAL1, encoding a mitochondrial rRNA chaperone, causes Perrault syndrome Human Molecular Genetics ·Iliana A. Chatzispyrou, Mariëlle Alders, Sergio Guerrero‐Castillo, Rubén Zapata‐Pérez, Martin A. Haagmans, Laurent Mouchiroud, Janet Koster, Rob Ofman, Frank Baas, Hans R. Waterham, Johannes N. Spelbrink, Johan Auwerx, Marcel M. A. M. Mannens, Riekelt H. Houtkooper, Astrid S. Plomp	2017	59
19	Identification and Characterization of Three Novel Missense Mutations in Mevalonate Kinase cDNA Causing Mevalonic Aciduria, a Disorder of Isoprene Biosynthesis Human Molecular Genetics ·Sander M. Houten, G. J. Romeijn, Janet Koster, R. G. F. Gray, Philip Darbyshire, G. P. A. Smit, J. B. C. de Klerk, M. Durán, K. Michael Gibson, Ronald J. A. Wanders, Hans R. Waterham	1999	53
20	Desmosterolosis—phenotypic and molecular characterization of a third case and review of the literature American Journal of Medical Genetics Part A ·Christian P. Schaaf, Janet Koster, Panagiotis Katsonis, Lisa E. Kratz, Oleg A. Shchelochkov, Fernando Scaglia, Richard I. Kelley, Olivier Lichtarge, Hans R. Waterham, Marwan Shinawi	2011	51

About Janet Koster

Janet Koster is a scholar working on Molecular Biology, Clinical Biochemistry, Surgery, Biochemistry and Immunology, having authored 44 papers that have together received 2.9k indexed citations. Recurring topics across this work include Peroxisome Proliferator-Activated Receptors (25 papers), Metabolism and Genetic Disorders (8 papers), Cholesterol and Lipid Metabolism (6 papers), Mitochondrial Function and Pathology (6 papers), interferon and immune responses (5 papers), Plant biochemistry and biosynthesis (5 papers), Inflammasome and immune disorders (5 papers) and Lipid metabolism and biosynthesis (4 papers). The work is most often cited by research in Clinical Biochemistry (612 citations), Molecular Biology (2.2k citations), Biochemistry (133 citations), Cancer Research (210 citations) and Physiology (337 citations). Janet Koster has collaborated with scholars based in Netherlands, United States and United Kingdom. Frequent co-authors include Hans R. Waterham, Ronald J. A. Wanders, Carlo W.T. van Roermund, P. A. W. Mooyer, James V. Leonard, Richard I. Kelley, Sacha Ferdinandusse, Merel S. Ebberink, G. J. Romeijn and Raoul C. M. Hennekam. Their work appears in journals such as Human Molecular Genetics, Human Mutation, The American Journal of Human Genetics, Journal of Lipid Research and Journal of Inherited Metabolic Disease.

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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Janet Koster's Hit Papers

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About Janet Koster

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