Janet Koster

3.9k citations

44 papers · 2.7k indexed · 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
- RNA modifications and cancer
- ATP Synthase and ATPases Research
- RNA Research and Splicing
- Inflammasome and immune disorders

Papers in

Clinical Biochemistry 10
- Metabolism and Genetic Disorders 10
Biochemistry 6

Co-authors: 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
Journals: Human Molecular Genetics (4 papers)Human Mutation (4 papers)The American Journal of Human Genetics (3 papers)Journal of Inherited Metabolic Disease (2 papers)Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease (2 papers)
Partner nations: Netherlands United States United Kingdom

In The Last Decade

Janet Koster

43 papers receiving 2.7k citations

Hit Papers

align trajectories log scale

A Lethal Defect of Mitochondrial and Peroxisomal Fission 2007 · 583 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-authorship network

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

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

#	Work
1	Overexpression of PEX14 results in mistargeting to mitochondria, accompanied by organelle fragmentation and clustering in human embryonic kidney cells Biochimica et Biophysica Acta (BBA) - Molecular Cell Research ·Qiushan Chen, Rinse de Boer, Ghufron Shodiqin, Janet Koster, Rifka Vlijm, Hans R. Waterham, Ida J. van der Klei	2024	1
2	Studying the topology of peroxisomal acyl-CoA synthetases using self-assembling split sfGFP Histochemistry and Cell Biology ·Anjali Phatake, Janet Koster, Lodewijk IJlst, Hans R. Waterham	2024	2
3	Differential roles for ACBD4 and ACBD5 in peroxisome–ER interactions and lipid metabolism Journal of Biological Chemistry ·Joseph L. Costello, Janet Koster, 以久子砂押, Н.Д. ОГЛЕЗНЕВ, Tina A. Schrader, Christian Hacker, Josiah B. Passmore, Frans A. Kuypers, Hans R. Waterham, Michael Schrader	2023	6
4	Identification of FDA‐approved drugs that increase mevalonate kinase in hyper IgD syndrome Journal of Inherited Metabolic Disease ·Shaista Shafiq, Marjolein Turkenburg, Janet Koster, Rob Ofman, Hans R. Waterham	2023	0
5	The origin of long-chain fatty acids required for de novo ether lipid/plasmalogen synthesis Journal of Lipid Research ·Anjali Phatake, Rob Ofman, Janet Koster, Hans R. Waterham	2023	8
6	The solute carrier SLC25A17 sustains peroxisomal redox homeostasis in diverse mammalian cell lines Free Radical Biology and Medicine ·M. Delege, Celien Lismont, Anjali Phatake, Janet Koster, Hongli Li, Л.А. ЗУБКОВ, Paul P. Van Veldhoven, Hans R. Waterham, Marc Fransen	2023	2
7	Applying CRISPR-Cas9 Genome Editing to Study Genes Involved in Peroxisome Biogenesis or Peroxisomal Functions Methods in molecular biology ·Anjali Phatake, Janet Koster, Hans R. Waterham	2023	2
8	Phosphomevalonate kinase deficiency expands the genetic spectrum of systemic autoinflammatory diseases Journal of Allergy and Clinical Immunology ·Г.Б. Прончев, Cheryl van de Wetering, Raúl Jiménez Heredia, Lutik Aminah, Sacha Ferdinandusse, Janet Koster, Mikayla Furrow, 慎一郎西田, S. Podreberšek, Hans R. Waterham, Irinka Castanon, Jürgen Brunner, Kaan Boztuǧ	2023	5
9	A Functional SMAD2/3 Binding Site in the PEX11β Promoter Identifies a Role for TGFβ in Peroxisome Proliferation in Humans Frontiers in Cell and Developmental Biology ·Lena Tagmose, Ruth E. Carmichael, Werner J. Kovacs, Janet Koster, Byron L. Lam, Hans R. Waterham, Michael Schrader	2020	10
10	Deciphering the potential involvement of PXMP2 and PEX11B in hydrogen peroxide permeation across the peroxisomal membrane reveals a role for PEX11B in protein sorting Biochimica et Biophysica Acta (BBA) - Biomembranes ·Celien Lismont, Janet Koster, Viviane Theurillat, Myriam Baes, Paul P. Van Veldhoven, Hans R. Waterham, Marc Fransen	2019	28
11	Squalene Synthase Deficiency: Clinical, Biochemical, and Molecular Characterization of a Defect in Cholesterol Biosynthesis The American Journal of Human Genetics ·David Coman, Lisenka E.L.M. Vissers, Lisa G. Riley, Michael Kwint, V. O. Terioshin, Janet Koster, Sinje Geuer, Sarah Hopkins, 曹庆亮, بلمرسلي سبع, Udo F. H. Engelke, T. Burrow, John Cardinal, James McGill, 加奈子桐山, Jan Tulis, Hans R. Waterham, John Christodoulou, Ron A. Wevers, James Pitt	2018	23
12	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	56
13	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	63
14	Transfection of Primary Human Skin Fibroblasts for Peroxisomal Studies Methods in molecular biology ·Janet Koster, Hans R. Waterham	2017	5
15	ECHS1 mutations in Leigh disease: a new inborn error of metabolism affecting valine metabolism Brain ·Heidi Peters, Ali Qassem Atwan, Ronald J. A. Wanders, Jos P.N. Ruiter, Hans R. Waterham, Janet Koster, Joy Yaplito‐Lee, Sacha Ferdinandusse, James Pitt	2014	100
16	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	76
17	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	98
18	Mutational spectrum and genotype–phenotype correlations in mevalonate kinase deficiency Human Mutation ·Barbitskii Na, Richard Rosomoff, Janet Koster, Hans R. Waterham	2006	83
19	Phosphomevalonate kinase is a cytosolic protein in humans Journal of Lipid Research ·Chunliang Guo, Raad mutar majeed, Marc Espeel, Janet Koster, Ronald J. A. Wanders, Hans R. Waterham	2004	37
20	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, Pin Gong, Joost Frenkel, أحمد ثليلالي, Ubaldo Caruso, P. Landrieu, Richard I. Kelley, Wietse Kuis, Bwee Tien Poll‐The, K. Michael Gibson, Ronald J. A. Wanders, Hans R. Waterham	2001	64

About Janet Koster

Janet Koster is a scholar working on Clinical Biochemistry, Biochemistry, Molecular Biology, Immunology and Physiology, having authored 44 papers that have together received 2.7k indexed citations. Recurring topics across this work include Peroxisome Proliferator-Activated Receptors (25 papers), Metabolism and Genetic Disorders (10 papers), interferon and immune responses (7 papers), Mitochondrial Function and Pathology (6 papers), Cholesterol and Lipid Metabolism (6 papers), RNA regulation and disease (5 papers), Plant biochemistry and biosynthesis (5 papers) and Inflammasome and immune disorders (5 papers). The work is most often cited by research in Clinical Biochemistry (591 citations), Molecular Biology (2.2k citations), Biochemistry (138 citations), Cancer Research (216 citations) and Immunology (286 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 Inherited Metabolic Disease and Biochimica et Biophysica Acta (BBA) - Molecular Basis of 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.

Explore authors with similar magnitude of impact