Annet M. Bosch

6.9k total citations · 2 hit papers
118 papers, 4.2k citations indexed

About

Annet M. Bosch is a scholar working on Clinical Biochemistry, Physiology and Molecular Biology. According to data from OpenAlex, Annet M. Bosch has authored 118 papers receiving a total of 4.2k indexed citations (citations by other indexed papers that have themselves been cited), including 98 papers in Clinical Biochemistry, 46 papers in Physiology and 39 papers in Molecular Biology. Recurrent topics in Annet M. Bosch's work include Metabolism and Genetic Disorders (98 papers), Diet and metabolism studies (41 papers) and Mitochondrial Function and Pathology (33 papers). Annet M. Bosch is often cited by papers focused on Metabolism and Genetic Disorders (98 papers), Diet and metabolism studies (41 papers) and Mitochondrial Function and Pathology (33 papers). Annet M. Bosch collaborates with scholars based in Netherlands, United States and Switzerland. Annet M. Bosch's co-authors include Francjan J. van Spronsen, Alberto Burlina, Frits A. Wijburg, Nenad Blau, Stephan C. J. Huijbregts, M. Estela Rubio‐Gozalbo, Carla E. M. Hollak, Vincenzo Leuzzi, Maria Giżewska and François Feillet and has published in prestigious journals such as PEDIATRICS, Clinical Infectious Diseases and Journal of Neurology Neurosurgery & Psychiatry.

In The Last Decade

Annet M. Bosch

112 papers receiving 4.1k citations

Hit Papers

The complete European gui... 2017 2026 2020 2023 2017 2021 100 200 300 400 500

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Annet M. Bosch Netherlands 34 3.3k 1.9k 1.6k 865 844 118 4.2k
Peter Burgard Germany 36 3.3k 1.0× 2.2k 1.1× 1.1k 0.7× 838 1.0× 776 0.9× 112 4.0k
Barbara Plecko Austria 37 1.9k 0.6× 2.3k 1.2× 984 0.6× 747 0.9× 597 0.7× 138 4.6k
Johan L.K. Van Hove United States 32 2.0k 0.6× 2.2k 1.2× 732 0.5× 500 0.6× 466 0.6× 93 3.8k
Avihu Boneh Australia 33 2.7k 0.8× 3.8k 2.0× 992 0.6× 512 0.6× 497 0.6× 111 5.3k
Friedrich K. Trefz Germany 38 3.5k 1.1× 2.7k 1.4× 1.5k 1.0× 691 0.8× 885 1.0× 105 4.4k
Vassili Valayannopoulos France 39 1.4k 0.4× 1.5k 0.8× 2.0k 1.3× 595 0.7× 900 1.1× 125 4.7k
Cary O. Harding United States 33 2.0k 0.6× 1.9k 1.0× 1.1k 0.7× 291 0.3× 416 0.5× 120 3.4k
Toshihiro Ohura Japan 27 1.8k 0.5× 1.5k 0.8× 654 0.4× 574 0.7× 691 0.8× 90 3.0k
Diego Martinelli Italy 30 1.4k 0.4× 1.5k 0.8× 421 0.3× 386 0.4× 433 0.5× 105 3.0k
Olaf A. Bodamer United States 34 1.0k 0.3× 1.4k 0.7× 1.9k 1.2× 470 0.5× 913 1.1× 156 4.2k

Countries citing papers authored by Annet M. Bosch

Since Specialization
Citations

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

Fields of papers citing papers by Annet M. Bosch

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Annet M. Bosch

This figure shows the co-authorship network connecting the top 25 collaborators of Annet M. Bosch. A scholar is included among the top collaborators of Annet M. Bosch 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 Annet M. Bosch. Annet M. Bosch is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Dussen, Laura van, Marion M. Brands, Bregje Jaeger, et al.. (2025). Effectiveness of Pyridoxal‐5′‐Phosphate in PNPO Deficiency: A Systematic Review. Journal of Inherited Metabolic Disease. 48(5). e70074–e70074.
2.
Ahmad, Mehtab, Annet M. Bosch, Vincent de Groot, et al.. (2025). Bone Biopsy not Superior to Ulcer Bed Biopsy–guided Antibacterial Therapy on Remission of Diabetic Foot Osteomyelitis: A Randomized Controlled Trial. Clinical Infectious Diseases. 82(3). 436–442.
3.
Geurtsen, Gert J., Carla E. M. Hollak, Mirian C. H. Janssen, et al.. (2024). Social cognition, emotion regulation and social competence in classical galactosemia patients without intellectual disability. Acta Neuropsychiatrica. 36(6). 378–389. 1 indexed citations
4.
Geurtsen, Gert J., et al.. (2024). Neuropsychological stability in classical galactosemia: A pilot study in 10 adult patients. JIMD Reports. 65(2). 110–115. 2 indexed citations
5.
Jaeger, Bregje, Mirjam Langeveld, Robert Brunkhorst, et al.. (2024). Riboflavin transporter deficiency in young adults unmasked by dietary changes. JIMD Reports. 65(4). 233–238. 1 indexed citations
6.
Häberle, Johannes, et al.. (2024). Mapping challenges in the accessibility of treatment products for urea cycle disorders: A survey of European healthcare professionals. Journal of Inherited Metabolic Disease. 48(1). e12815–e12815.
7.
Bosch, Annet M., David Cassiman, Mirian C. H. Janssen, et al.. (2024). Impact of theta transcranial alternating current stimulation on language production in adult classic galactosemia patients. Journal of Inherited Metabolic Disease. 47(4). 703–715. 2 indexed citations
8.
Jaeger, Bregje, et al.. (2024). Riboflavin transporter deficiency, the search for the undiagnosed: a retrospective data mining study. Orphanet Journal of Rare Diseases. 19(1). 410–410.
9.
Boelen, Anita, Annet M. Bosch, Nitash Zwaveling‐Soonawala, et al.. (2024). The Value of Reducing Inconclusive and False-Positive Newborn Screening Results for Congenital Hypothyroidism, Congenital Adrenal Hyperplasia and Maple Syrup Urine Disease in The Netherlands. International Journal of Neonatal Screening. 10(4). 70–70. 2 indexed citations
10.
Bosch, Annet M., et al.. (2021). Inflammatory arthritis complicating galactosialidosis: a case report. BMC Rheumatology. 5(1). 41–41. 2 indexed citations
11.
Bleeker, Jeannette C., Sacha Ferdinandusse, Maaike de Vries, et al.. (2019). Proposal for an individualized dietary strategy in patients with very long‐chain acyl‐CoA dehydrogenase deficiency. Journal of Inherited Metabolic Disease. 42(1). 159–168. 18 indexed citations
12.
Bosch, Annet M., Margot F. Mulder, M. Estela Rubio‐Gozalbo, et al.. (2019). A nationwide retrospective observational study of population newborn screening for medium‐chain acyl‐CoA dehydrogenase (MCAD) deficiency in the Netherlands. Journal of Inherited Metabolic Disease. 42(5). 890–897. 22 indexed citations
13.
Arrieta, Francisco, François Feillet, Maria Giżewska, et al.. (2019). Bone mineral density is within normal range in most adult phenylketonuria patients. Journal of Inherited Metabolic Disease. 43(2). 251–258. 14 indexed citations
14.
Landolt, Markus A., Annet M. Bosch, Sarah C. Grünert, et al.. (2019). Reducing complexity: explaining inborn errors of metabolism and their treatment to children and adolescents. Orphanet Journal of Rare Diseases. 14(1). 248–248. 9 indexed citations
15.
Jahja, Rianne, Francjan J. van Spronsen, Leo de Sonneville, et al.. (2017). Long-Term Follow-Up of Cognition and Mental Health in Adult Phenylketonuria: A PKU-COBESO Study. Behavior Genetics. 47(5). 486–497. 47 indexed citations
16.
Jahja, Rianne, Stephan C. J. Huijbregts, Leo de Sonneville, et al.. (2017). Cognitive profile and mental health in adult phenylketonuria: A PKU-COBESO study.. Neuropsychology. 31(4). 437–447. 55 indexed citations
17.
MacDonald, Anita, M. van Rijn, François Feillet, et al.. (2012). Adherence Issues in Inherited Metabolic Disorders Treated by Low Natural Protein Diets. Annals of Nutrition and Metabolism. 61(4). 289–295. 74 indexed citations
18.
Smit, Gerrit, Maaike de Vries, Johannis B.C. de Klerk, et al.. (2012). Risk stratification by residual enzyme activity after newborn screening for medium-chain acyl-CoA dehyrogenase deficiency: data from a cohort study. Orphanet Journal of Rare Diseases. 7(1). 30–30. 24 indexed citations
19.
Gentile, Jennifer, Amber E. ten Hoedt, & Annet M. Bosch. (2009). Psychosocial aspects of PKU: Hidden disabilities – A review☆. Molecular Genetics and Metabolism. 99. S64–S67. 70 indexed citations
20.
Bosch, Annet M., H. R. Waterham, M. Durán, & H. D. Bakker. (2003). Een premature tweeling met icterus, stollingsstoornissen en een E. coli-sepsis. Data Archiving and Networked Services (DANS). 28. 341–343.

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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