Judith Meijer

1.2k citations
33 papers · 650 · h-index 14

Impact in

  • Oncology top 10%
    • Colorectal Cancer Treatments and Studies
    • Pancreatic and Hepatic Oncology Research
  • Clinical Biochemistry top 10%
    • Metabolism and Genetic Disorders

Papers in

  • Molecular Biology 25
    • Biochemical and Molecular Research 23
    • Cancer therapeutics and mechanisms 4
  • Oncology 9
    • Colorectal Cancer Treatments and Studies 7
Co-authors
André B. P. Kuilenburg (30 shared papers)Rutger Meinsma (17 shared papers)Lida Zoetekouw (15 shared papers)Doreen Dobritzsch (12 shared papers)Raoul C. M. Hennekam (10 shared papers)Johan Vande Voorde (1 shared paper)Luke W. Guddat (1 shared paper)Dianne T. Keough (1 shared paper)
Journals
Molecular Genetics and Metabolism (4 papers)Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease (4 papers)Nucleosides Nucleotides & Nucleic Acids (4 papers)Human Genetics (2 papers)British Journal of Cancer (1 paper)
Partner nations
NetherlandsSwedenJapan

In The Last Decade

Judith Meijer

33 papers receiving 648 citations

Peers

Judith Meijer
Comparison fields: 5 of 79
  • Oncology 249
  • Clinical Biochemistry 47
  • Pediatrics, Perinatology and Child Health 101
  • Infectious Diseases 95
  • Molecular Biology 333
Replace Beáta Tóth with:
Beáta Tóth Hungary
Gerard Minuesa Spain
E Ennis United States
Per Olaf Ekstrøm Norway
Marina Lanciotti Italy
Anne Freimoser–Grundschober Switzerland
Tatiana Sedláčková Slovakia
P B Rowe Australia
R. T. MacFarland United States
Hirokazu Hirata Japan
Judith Meijer relative to Beáta Tóth Hungary Beáta Tóth's profile →
Citations per field
00.5×2×4×6.7×
Beáta Tóth · 1×
Citations per year

Countries citing papers authored by Judith Meijer

Since Specialization
Citations

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

Fields of papers citing papers by Judith Meijer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 33 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Role of Human Hypoxanthine Guanine Phosphoribosyltransferase in Activation of the Antiviral Agent T-705 (Favipiravir)
Molecular Pharmacology ·Lieve Naesens, Luke W. Guddat, Dianne T. Keough, André B. P. Kuilenburg, Judith Meijer, Johan Vande Voorde, Jan Balzarini
201398
2
Intragenic deletions and a deep intronic mutation affecting pre-mRNA splicing in the dihydropyrimidine dehydrogenase gene as novel mechanisms causing 5-fluorouracil toxicity
Human Genetics ·André B. P. Kuilenburg, Judith Meijer, Adri N. Mul, Rutger Meinsma, Veronika Schmid, Doreen Dobritzsch, Raoul C. M. Hennekam, Marcel M. A. M. Mannens, Marion Kiechle, Marie-Christine Étienne-Grimaldi, Heinz‐Josef Klümpen, Jan Gerard Maring, Veerle A. Derleyn, Ed Maartense, G. Milano, Raymon Vijzelaar, Eva Groß
201093
3
Rapid detection of chromosomal aneuploidies in uncultured amniocytes by multiplex ligation-dependent probe amplification (MLPA)
Prenatal Diagnosis ·Ron Hochstenbach, Judith Meijer, J. van de Brug, I. Vossebeld-Hoff, Renée S. Jansen, Rob B. van der Luijt, Richard J. Sinke, Godelieve C.M.L. Page‐Christiaens, Johannes Kristian Ploos van Amstel, Jennie M. Pater
200552
4
Phenotypic and clinical implications of variants in the dihydropyrimidine dehydrogenase gene
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·André B. P. Kuilenburg, Judith Meijer, Michael W.T. Tanck, Doreen Dobritzsch, Lida Zoetekouw, Lois-Lee Dekkers, Jeroen Roelofsen, Rutger Meinsma, Machteld Wymenga, Wim Kulik, Barbara Büchel, Raoul C. M. Hennekam, Carlo R. Largiadèr
201642
5
Analysis of severely affected patients with dihydropyrimidine dehydrogenase deficiency reveals large intragenic rearrangements of DPYD and a de novo interstitial deletion del(1)(p13.3p21.3)
Human Genetics ·André B. P. Kuilenburg, Judith Meijer, Adri N. Mul, Raoul C. M. Hennekam, J.M.N. Hoovers, Christine de Die‐Smulders, Christian Weber, Andrea Mori, Jörgen Bierau, Brian Fowler, Klaus Macke, Jörn Oliver Sass, Rutger Meinsma, Julia B. Hennermann, Peter Miny, Lida Zoetekouw, Raymon Vijzelaar, Joost Nicolai, Bauke Ylstra, M. Estela Rubio‐Gozalbo
200939
6
Severe fluoropyrimidine toxicity due to novel and rare DPYD missense mutations, deletion and genomic amplification affecting DPD activity and mRNA splicing
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·André B. P. Kuilenburg, Judith Meijer, Dirk Maurer, Doreen Dobritzsch, Rutger Meinsma, Maartje Los, Lia Knegt, Lida Zoetekouw, Rob L. H. Jansen, Vincent O. Dezentjé, Lieke H. van Huis‐Tanja, Roel J.W. van Kampen, Jens Michael Hertz, Raoul C. M. Hennekam
201636
7
Clinical, biochemical and genetic findings in two siblings with a dihydropyrimidinase deficiency
Molecular Genetics and Metabolism ·André B. P. Kuilenburg, Judith Meijer, Doreen Dobritzsch, Rutger Meinsma, Marinus Durán, Bernhard Lohkamp, Lida Zoetekouw, N. G. G. M. Abeling, Harm van Tinteren, Annet M. Bosch
200726
8
Evaluation of an oral uracil loading test to identify DPD‐deficient patients using a limited sampling strategy
British Journal of Clinical Pharmacology ·Maurice C. van Staveren, André B. P. Kuilenburg, Henk‐Jan Guchelaar, Judith Meijer, Cornelis J.A. Punt, Robert S. de Jong, Hans Gelderblom, Jan Gerard Maring
201523
9
ß-Ureidopropionase deficiency: Phenotype, genotype and protein structural consequences in 16 patients
Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·André B. P. Kuilenburg, Doreen Dobritzsch, Judith Meijer, Michael Krumpel, Laila Selim, Mohamed S. Rashed, Birgit Assmann, Rutger Meinsma, Bernhard Lohkamp, Tetsuya Ito, N. G. G. M. Abeling, Kayoko Saito, Kaoru Eto, Martin Smitka, Martin Engvall, Chunhua Zhang, Xu Wang, Lida Zoetekouw, Raoul C. M. Hennekam
201223
10
Capecitabine‐based treatment of a patient with a novel DPYD genotype and complete dihydropyrimidine dehydrogenase deficiency
International Journal of Cancer ·Linda M. Henricks, Ester Siemerink, Hilde Rosing, Judith Meijer, Susan Goorden, Abeltje M. Polstra, Lida Zoetekouw, Annemieke Cats, Jan H.M. Schellens, André B. P. Kuilenburg
201723
11
Clinical, biochemical and molecular analysis of 13 Japanese patients with β‐ureidopropionase deficiency demonstrates high prevalence of the c.977G > A (p.R326Q) mutation
Journal of Inherited Metabolic Disease ·Yoko Nakajima, Judith Meijer, Doreen Dobritzsch, Tetsuya Ito, Rutger Meinsma, N. G. G. M. Abeling, Jeroen Roelofsen, Lida Zoetekouw, Yoriko Watanabe, Kyoko Tashiro, Tomoko Lee, Yasuhiro Takeshima, Hiroshi Mitsubuchi, Akira Yoneyama, Kazuhide Ohta, Kaoru Eto, Kayoko Saito, Tomiko Kuhara, André B. P. Kuilenburg
201420
12
β-Ureidopropionase deficiency presenting with congenital anomalies of the urogenital and colorectal systems
Molecular Genetics and Metabolism ·Joy Yaplito‐Lee, James Pitt, Judith Meijer, Lida Zoetekouw, Rutger Meinsma, André B. P. Kuilenburg
200719
13
Patients homozygous for DPYD c.1129-5923C>G/haplotype B3 have partial DPD deficiency and require a dose reduction when treated with fluoropyrimidines
Cancer Chemotherapy and Pharmacology ·Didier Meulendijks, Linda M. Henricks, André B. P. Kuilenburg, Bart Jacobs, Abidin Aliev, Lisette Rozeman, Judith Meijer, Jos H. Beijnen, Hiltje de Graaf, Annemieke Cats, Jan H.M. Schellens
201618
14
Dihydropyrimidinase deficiency in four East Asian patients due to novel and rare DPYS mutations affecting protein structural integrity and catalytic activity
Molecular Genetics and Metabolism ·Yoko Nakajima, Judith Meijer, Doreen Dobritzsch, Tetsuya Ito, Chunhua Zhang, Xu Wang, Yoriko Watanabe, Kyoko Tashiro, Rutger Meinsma, Jeroen Roelofsen, Lida Zoetekouw, André B. P. Kuilenburg
201714
15
Novel Genetic Mutations in the First Swedish Patient with Purine Nucleoside Phosphorylase Deficiency and Clinical Outcome After Hematopoietic Stem Cell Transplantation with HLA-Matched Unrelated Donor
JIMD Reports ·Nicholas Brodszki, Maria Svensson, André B. P. Kuilenburg, Judith Meijer, Lida Zoetekouw, Lennart Truedsson, Jacek Toporski
201512
16
Dihydropyrimidine Dehydrogenase Deficiency: Metabolic Disease or Biochemical Phenotype?
JIMD Reports ·Martin Fleger, J. Willomitzer, Rutger Meinsma, Mariëlle Alders, Judith Meijer, Raoul C. M. Hennekam, Martina Huemer, André B. P. Kuilenburg
201712
17
Children with atopic dermatitis show increased activity of β‐glucocerebrosidase and stratum corneum levels of glucosylcholesterol that are strongly related to the local cytokine milieu
British Journal of Dermatology ·Sanja Kežić, Maeve A. McAleer, Ivone Jakaša, Susan Goorden, Karen Ghauharali‐van der Vlugt, F.S. Beers-Stet, Judith Meijer, Jeroen Roelofsen, Monique M. Nieman, André B. P. Kuilenburg, Alan D. Irvine
202212
18
Dihydropyrimidine Dehydrogenase Deficiency in Two Malaysian Siblings with Abnormal MRI Findings
Molecular Syndromology ·Bee Chin Chen, Rowani Mohd Rawi, Rutger Meinsma, Judith Meijer, Raoul C. M. Hennekam, André B. P. Kuilenburg
201410
19
Somatic copy number changes in DPYD are associated with lower risk of recurrence in triple-negative breast cancers
British Journal of Cancer ·(unknown), Christina Meul, Sandra Raab, Corinna Propping, Stefanie Avril, Michaela Aubele, Apostolos Gkazepis, Tibor Schuster, Nicolaï Grebenchtchikov, Manfred Schmitt, Marion Kiechle, Judith Meijer, Raymon Vijzelaar, A Meindl, André B. P. Kuilenburg
201310
20
Altered Pre-mRNA Splicing Caused by a Novel Intronic Mutation c.1443+5G>A in the Dihydropyrimidinase (DPYS) Gene
International Journal of Molecular Sciences ·Yoko Nakajima, Judith Meijer, Chunhua Zhang, Xu Wang, Tomomi Kondo, Tetsuya Ito, Doreen Dobritzsch, André B. P. Kuilenburg
20169

About Judith Meijer

Judith Meijer is a scholar working on Molecular Biology, Oncology, Clinical Biochemistry, Genetics and Pediatrics, Perinatology and Child Health, having authored 33 papers that have together received 650 indexed citations. Recurring topics across this work include Biochemical and Molecular Research (23 papers), Metabolism and Genetic Disorders (7 papers), Colorectal Cancer Treatments and Studies (7 papers), Cancer therapeutics and mechanisms (4 papers), Neonatal Health and Biochemistry (4 papers), HIV/AIDS drug development and treatment (4 papers), Genetic factors in colorectal cancer (3 papers) and Adenosine and Purinergic Signaling (3 papers). The work is most often cited by research in Oncology (249 citations), Clinical Biochemistry (47 citations), Pediatrics, Perinatology and Child Health (101 citations), Infectious Diseases (95 citations) and Molecular Biology (333 citations). Judith Meijer has collaborated with scholars based in Netherlands, Sweden and Japan. Frequent co-authors include André B. P. Kuilenburg, Rutger Meinsma, Lida Zoetekouw, Doreen Dobritzsch, Raoul C. M. Hennekam, Johan Vande Voorde, Luke W. Guddat, Dianne T. Keough, Lieve Naesens and Jan Balzarini. Their work appears in journals such as Molecular Genetics and Metabolism, Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease, Nucleosides Nucleotides & Nucleic Acids, Human Genetics and British Journal of Cancer.

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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