Nadia Schoenmakers

5.6k total citations
47 papers, 1.2k citations indexed

About

Nadia Schoenmakers is a scholar working on Endocrinology, Diabetes and Metabolism, Molecular Biology and Genetics. According to data from OpenAlex, Nadia Schoenmakers has authored 47 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Endocrinology, Diabetes and Metabolism, 20 papers in Molecular Biology and 11 papers in Genetics. Recurrent topics in Nadia Schoenmakers's work include Thyroid Disorders and Treatments (34 papers), Growth Hormone and Insulin-like Growth Factors (15 papers) and Congenital heart defects research (9 papers). Nadia Schoenmakers is often cited by papers focused on Thyroid Disorders and Treatments (34 papers), Growth Hormone and Insulin-like Growth Factors (15 papers) and Congenital heart defects research (9 papers). Nadia Schoenmakers collaborates with scholars based in United Kingdom, Netherlands and Italy. Nadia Schoenmakers's co-authors include Krishna Chatterjee, A S Paul van Trotsenburg, Mehul Dattani, Catherine Peters, Carla Moran, Erik Schoenmakers, Luca Persani, Greta Lyons, Mark Gurnell and Maura Agostini and has published in prestigious journals such as Journal of Clinical Investigation, The Journal of Clinical Endocrinology & Metabolism and PLoS Computational Biology.

In The Last Decade

Nadia Schoenmakers

44 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Nadia Schoenmakers United Kingdom 21 929 442 246 174 127 47 1.2k
Caterina Di Cosmo Italy 20 934 1.0× 328 0.7× 230 0.9× 141 0.8× 77 0.6× 38 1.2k
Giuseppina De Marco Italy 19 542 0.6× 334 0.8× 126 0.5× 68 0.4× 60 0.5× 47 859
C. Mammoli Italy 23 1.0k 1.1× 248 0.6× 200 0.8× 83 0.5× 129 1.0× 37 1.4k
Yardena Tenenbaum‐Rakover Israel 20 537 0.6× 609 1.4× 395 1.6× 119 0.7× 66 0.5× 52 1.3k
Donald F. Sellitti United States 18 319 0.3× 357 0.8× 94 0.4× 69 0.4× 147 1.2× 47 899
Junta Takamatsu Japan 20 785 0.8× 256 0.6× 152 0.6× 46 0.3× 97 0.8× 57 989
Rita van Bree Belgium 22 295 0.3× 316 0.7× 148 0.6× 530 3.0× 154 1.2× 47 1.4k
Eriko Takimoto Japan 7 526 0.6× 445 1.0× 92 0.4× 187 1.1× 77 0.6× 9 1.2k
Mandy Donaldson United Kingdom 15 457 0.5× 429 1.0× 118 0.5× 31 0.2× 74 0.6× 27 1.3k
Damiano Gullo Italy 16 543 0.6× 185 0.4× 105 0.4× 62 0.4× 79 0.6× 40 815

Countries citing papers authored by Nadia Schoenmakers

Since Specialization
Citations

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

Fields of papers citing papers by Nadia Schoenmakers

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nadia Schoenmakers

This figure shows the co-authorship network connecting the top 25 collaborators of Nadia Schoenmakers. A scholar is included among the top collaborators of Nadia Schoenmakers 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 Nadia Schoenmakers. Nadia Schoenmakers 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.
Yao, Yihan, Nadia A. Erkamp, Tomas Šneideris, et al.. (2025). Extracellular phase separation mediates storage and release of thyroglobulin in the thyroid follicular lumen. Communications Biology. 8(1). 466–466. 1 indexed citations
2.
Stoupa, Athanasia, Aurore Carré, Michel Polak, Gabor Szinnai, & Nadia Schoenmakers. (2025). Genetics of primary congenital hypothyroidism: three decades of discoveries and persisting etiological challenges. European Thyroid Journal. 14(2). 4 indexed citations
3.
Schoenmakers, Nadia, et al.. (2024). Congenital Central Hypothyroidism Caused by Novel Variants in <i>IGSF1</i> Gene: Case Series of 3 Patients. Hormone Research in Paediatrics. 98(1). 1–7. 1 indexed citations
4.
Ruiz, M., Melissa Cabecinha, Rachel L Knowles, et al.. (2022). Establishing risk factors and outcomes for congenital hypothyroidism with gland in situ using population-based data linkage methods: study protocol. BMJ Paediatrics Open. 6(1). e001341–e001341. 1 indexed citations
5.
Nicholas, Adeline K., Erik Schoenmakers, Jennifer A. Dickens, et al.. (2021). Brief Report: A Novel Sodium/Iodide Symporter Mutation, S356F, Causing Congenital Hypothyroidism. Thyroid. 32(2). 215–218. 3 indexed citations
6.
Schoenmakers, Nadia, et al.. (2021). A Novel Mutation in the Thyroglobulin Gene Resulting in Neonatal Goiter and Congenital Hypothyroidism in an Eritrean Infant. Journal of Clinical Research in Pediatric Endocrinology. 14(2). 221–226. 5 indexed citations
7.
Kahaly, George J., Joanne Jones, Paul W. Sanders, et al.. (2019). Meeting Abstracts from the 67th Annual British Thyroid Association Meeting. Thyroid Research. 12(S1).
8.
Peters, Catherine, Adeline K. Nicholas, Erik Schoenmakers, et al.. (2019). DUOX2 / DUOXA2 Mutations Frequently Cause Congenital Hypothyroidism that Evades Detection on Newborn Screening in the United Kingdom. Thyroid. 29(6). 790–801. 33 indexed citations
9.
Prasad, Rathi, Adeline K. Nicholas, Nadia Schoenmakers, & John Barton. (2019). Haploinsufficiency of <b><i>NKX2-1</i></b> in Brain-Lung-Thyroid Syndrome with Additional Multiple Pituitary Dysfunction. Hormone Research in Paediatrics. 92(5). 340–344. 10 indexed citations
10.
Aycan, Zehra, Hakan Cangül, Marina Muzza, et al.. (2017). Digenic DUOX1 and DUOX2 Mutations in Cases With Congenital Hypothyroidism. The Journal of Clinical Endocrinology & Metabolism. 102(9). 3085–3090. 46 indexed citations
11.
Boudellioua, Imane, Rozaimi Razali, Maxat Kulmanov, et al.. (2017). Semantic prioritization of novel causative genomic variants. PLoS Computational Biology. 13(4). e1005500–e1005500. 25 indexed citations
12.
Joustra, Sjoerd D., Charlotte A. Heinen, Nadia Schoenmakers, et al.. (2016). IGSF1 Deficiency: Lessons From an Extensive Case Series and Recommendations for Clinical Management. The Journal of Clinical Endocrinology & Metabolism. 101(4). 1627–1636. 58 indexed citations
13.
Koulouri, Olympia, Adeline K. Nicholas, Erik Schoenmakers, et al.. (2016). A Novel Thyrotropin-Releasing Hormone Receptor Missense Mutation (P81R) in Central Congenital Hypothyroidism. The Journal of Clinical Endocrinology & Metabolism. 101(3). 847–851. 17 indexed citations
14.
Schoenmakers, Nadia & Krishna Chatterjee. (2015). TSHR mutations and subclinical congenital hypothyroidism. Nature Reviews Endocrinology. 11(5). 258–259. 11 indexed citations
15.
Schoenmakers, Nadia, Kyriaki S. Alatzoglou, Krishna Chatterjee, & Mehul Dattani. (2015). Recent advances in central congenital hypothyroidism. Journal of Endocrinology. 227(3). R51–R71. 69 indexed citations
16.
Schoenmakers, Nadia, Hakan Cangül, Adeline K. Nicholas, et al.. (2013). A comprehensive next generation sequencing-based strategy for genetic diagnosis in congenital hypothyroidism. 33. 8 indexed citations
17.
Watson, Laura, Philippa Raymond‐Barker, Carla Moran, et al.. (2013). An approach to quantifying abnormalities in energy expenditure and lean mass in metabolic disease. European Journal of Clinical Nutrition. 68(2). 234–240. 15 indexed citations
18.
Schoenmakers, Nadia, Carla Moran, Robin P. Peeters, et al.. (2013). Resistance to thyroid hormone mediated by defective thyroid hormone receptor alpha. Biochimica et Biophysica Acta (BBA) - General Subjects. 1830(7). 4004–4008. 39 indexed citations
19.
Schoenmakers, Nadia. (2012). Genetic disorders of thyroid physiology and development. 30. 1 indexed citations
20.
Savage, David B., Sylvie Dufour, Nadia Schoenmakers, et al.. (2010). Resistance to thyroid hormone is associated with raised energy expenditure, muscle mitochondrial uncoupling, and hyperphagia. Journal of Clinical Investigation. 120(4). 1345–1354. 90 indexed citations

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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