Sandra Donkervoort

9.1k total citations
115 papers, 2.8k citations indexed

About

Sandra Donkervoort is a scholar working on Molecular Biology, Surgery and Genetics. According to data from OpenAlex, Sandra Donkervoort has authored 115 papers receiving a total of 2.8k indexed citations (citations by other indexed papers that have themselves been cited), including 48 papers in Molecular Biology, 34 papers in Surgery and 22 papers in Genetics. Recurrent topics in Sandra Donkervoort's work include Muscle Physiology and Disorders (31 papers), Neurogenetic and Muscular Disorders Research (20 papers) and Gallbladder and Bile Duct Disorders (19 papers). Sandra Donkervoort is often cited by papers focused on Muscle Physiology and Disorders (31 papers), Neurogenetic and Muscular Disorders Research (20 papers) and Gallbladder and Bile Duct Disorders (19 papers). Sandra Donkervoort collaborates with scholars based in United States, Netherlands and United Kingdom. Sandra Donkervoort's co-authors include Carsten G. Bönnemann, A. Reghan Foley, Diana Bharucha‐Goebel, Alexander T. Chesler, Lea M. Dijksman, Djamila Boerma, Marcin Szczot, Marja A. Boermeester, Payam Mohassel and Bert van Ramshorst and has published in prestigious journals such as Science, New England Journal of Medicine and The Lancet.

In The Last Decade

Sandra Donkervoort

109 papers receiving 2.8k citations

Peers

Sandra Donkervoort
Shenandoah Robinson United States
Sandra Donkervoort
Citations per year, relative to Sandra Donkervoort Sandra Donkervoort (= 1×) peers Shenandoah Robinson

Countries citing papers authored by Sandra Donkervoort

Since Specialization
Citations

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

Fields of papers citing papers by Sandra Donkervoort

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sandra Donkervoort

This figure shows the co-authorship network connecting the top 25 collaborators of Sandra Donkervoort. A scholar is included among the top collaborators of Sandra Donkervoort 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 Sandra Donkervoort. Sandra Donkervoort 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.
Donkervoort, Sandra, Ying Hu, Sarah Neuhaus, et al.. (2024). Clinical, immunohistochemical, and genetic characterization of splice-altering biallelic DES variants: Therapeutic implications. Human Genetics and Genomics Advances. 5(2). 100274–100274. 1 indexed citations
2.
Hayes, Leslie H., Sarah Neuhaus, Sandra Donkervoort, et al.. (2024). Taking on the Titin: Muscle imaging as a diagnostic marker of biallelic TTN- related myopathy. Journal of Neuromuscular Diseases. 11(6). 1211–1220. 1 indexed citations
3.
Mohassel, Payam, Maike F. Dohrn, Museer A. Lone, et al.. (2023). P169 Childhood onset amyotrophic lateral sclerosis associated with SPTLC2 gain-of-function pathogenic variants: clinical, genetic, and biochemical insights. Neuromuscular Disorders. 33. S107–S107.
4.
Moreno, Cristiane Araújo Martins, Gisele Chagas de Medeiros, Fernanda Chiarion Sassi, et al.. (2023). Clinical Manifestation of Nebulin-Associated Nemaline Myopathy. Neurology Genetics. 9(1). e200056–e200056. 4 indexed citations
5.
Alili, Mohamed El, Laura A M Duineveld, Thijs Wieldraaijer, et al.. (2023). Cost-effectiveness of general practitioner- versus surgeon-led colon cancer survivorship care: an economic evaluation alongside a randomised controlled trial. Journal of Cancer Survivorship. 18(4). 1393–1402. 1 indexed citations
6.
Donkervoort, Sandra, Pelin Özlem Şimşek‐Kiper, Rahşan Göçmen, et al.. (2022). A Life-Threatening Complication in a Patient with Ehlers-Danlos Syndrome Musculocontractural Type. SHILAP Revista de lepidopterología. 9(3). 297–301. 1 indexed citations
7.
Mroczek, Magdalena, Cheryl Longman, Maria Elena Farrugia, et al.. (2022). FXR1-related congenital myopathy: expansion of the clinical and genetic spectrum. Journal of Medical Genetics. 59(11). 1069–1074. 3 indexed citations
8.
Duineveld, Laura A M, Thijs Wieldraaijer, Sandra Donkervoort, et al.. (2021). Recruitment challenges to the I CARE study: a randomised trial on general practitioner-led colon cancer survivorship care. BMJ Open. 11(8). e048985–e048985. 5 indexed citations
9.
Sirisena, Nirmala D., Osório Lopes Abath Neto, A. Reghan Foley, et al.. (2021). A novel variant in the COL6A1 gene causing Ullrich congenital muscular dystrophy in a consanguineous family: a case report. BMC Neurology. 21(1). 105–105. 1 indexed citations
10.
Mohammadi, Pejman, Stephane E. Castel, Beryl B. Cummings, et al.. (2019). Genetic regulatory variation in populations informs transcriptome analysis in rare disease. Science. 366(6463). 351–356. 64 indexed citations
11.
Cocanougher, Ben, Minal Jain, M. Waite, et al.. (2019). Adult MTM1 -related myopathy carriers. Neurology. 93(16). e1535–e1542. 16 indexed citations
12.
Nagi, Saad S., Andrew Marshall, Ewa Jarocka, et al.. (2019). An ultrafast system for signaling mechanical pain in human skin. Science Advances. 5(7). eaaw1297–eaaw1297. 84 indexed citations
13.
Lornage, Xavière, Norma B. Romero, Sandra Donkervoort, et al.. (2019). ACTN2 mutations cause “Multiple structured Core Disease” (MsCD). Acta Neuropathologica. 137(3). 501–519. 35 indexed citations
14.
Szczot, Marcin, Jaquette Liljencrantz, Nima Ghitani, et al.. (2018). PIEZO2 mediates injury-induced tactile pain in mice and humans. Science Translational Medicine. 10(462). 212 indexed citations
15.
Wieldraaijer, Thijs, Laura A M Duineveld, Kristel M. van Asselt, et al.. (2016). Follow-up of colon cancer patients; causes of distress and need for supportive care. European Journal of Surgical Oncology. 43(1). 118–125. 21 indexed citations
16.
Vuillerot, Carole, Katherine G. Meilleur, Minal Jain, et al.. (2014). English cross-cultural translation and validation of the NM-Score: A system for motor function classification in patients with neuromuscular diseases. Annals of Physical and Rehabilitation Medicine. 57. e105–e105. 1 indexed citations
17.
Donkervoort, Sandra, et al.. (2014). Enterocolic lymphocytic phlebitis: an oncologic surgical resection without a preoperative pathologic diagnosis. Journal of Surgical Case Reports. 2014(5). rju037–rju037. 4 indexed citations
18.
Vuillerot, Carole, Katherine G. Meilleur, Minal Jain, et al.. (2014). English Cross-Cultural Translation and Validation of the Neuromuscular Score: A System for Motor Function Classification in Patients With Neuromuscular Diseases. Archives of Physical Medicine and Rehabilitation. 95(11). 2064–2070.e1. 7 indexed citations
19.
Donkervoort, Sandra, et al.. (2013). Surgeon’s Volume Is Not Associated with Complication Outcome After Laparoscopic Cholecystectomy. Digestive Diseases and Sciences. 59(1). 39–45. 20 indexed citations
20.
Dijksman, Lea M., et al.. (2010). Safety and outcome of general surgical open and laparoscopic procedures during pregnancy. Surgical Endoscopy. 25(5). 1574–1578. 30 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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