Tom Sante

905 total citations
16 papers, 473 citations indexed

About

Tom Sante is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Tom Sante has authored 16 papers receiving a total of 473 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 8 papers in Molecular Biology and 4 papers in Plant Science. Recurrent topics in Tom Sante's work include Genomic variations and chromosomal abnormalities (9 papers), Chromosomal and Genetic Variations (4 papers) and Genomics and Rare Diseases (3 papers). Tom Sante is often cited by papers focused on Genomic variations and chromosomal abnormalities (9 papers), Chromosomal and Genetic Variations (4 papers) and Genomics and Rare Diseases (3 papers). Tom Sante collaborates with scholars based in Belgium, Netherlands and United States. Tom Sante's co-authors include Björn Menten, Annelies Dheedene, Elfride De Baere, Sarah Vergult, Katleen De Preter, Bram De Wilde, Hannah Verdin, Dieter Deforce, Nadine Van Roy and Björn Heindryckx and has published in prestigious journals such as PLoS ONE, Scientific Reports and Clinical Cancer Research.

In The Last Decade

Tom Sante

16 papers receiving 456 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Tom Sante Belgium 12 246 209 121 91 43 16 473
Shlomit Rienstein Israel 14 277 1.1× 161 0.8× 94 0.8× 107 1.2× 60 1.4× 28 559
Ruth Charlton United Kingdom 12 240 1.0× 168 0.8× 118 1.0× 23 0.3× 88 2.0× 25 477
Nadine Jalkh Lebanon 13 541 2.2× 238 1.1× 90 0.7× 25 0.3× 48 1.1× 38 751
Janneke Schuurs-Hoeijmakers Netherlands 14 463 1.9× 398 1.9× 37 0.3× 63 0.7× 76 1.8× 29 773
Olga Jarinova Canada 10 439 1.8× 300 1.4× 151 1.2× 47 0.5× 16 0.4× 19 695
Teresa Neuhann Germany 14 215 0.9× 189 0.9× 35 0.3× 62 0.7× 17 0.4× 38 425
Avni Santani United States 16 405 1.6× 439 2.1× 110 0.9× 43 0.5× 26 0.6× 39 781
Lisa H. Gibson United States 12 335 1.4× 266 1.3× 50 0.4× 98 1.1× 53 1.2× 17 559
Vera Uliana Italy 13 163 0.7× 189 0.9× 23 0.2× 37 0.4× 46 1.1× 30 377
Maja Klug Germany 9 660 2.7× 139 0.7× 86 0.7× 48 0.5× 66 1.5× 10 857

Countries citing papers authored by Tom Sante

Since Specialization
Citations

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

Fields of papers citing papers by Tom Sante

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tom Sante

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

All Works

16 of 16 papers shown
1.
Hellemans, Jan, et al.. (2022). Evaluation of efficiency and sensitivity of 1D and 2D sample pooling strategies for SARS-CoV-2 RT-qPCR screening purposes. Scientific Reports. 12(1). 6603–6603. 3 indexed citations
2.
Linden, Malaïka Van Der, Annelies Dheedene, Tom Sante, et al.. (2019). Detection of Copy Number Alterations by Shallow Whole-Genome Sequencing of Formalin-Fixed, Paraffin-Embedded Tumor Tissue. Archives of Pathology & Laboratory Medicine. 144(8). 974–981. 7 indexed citations
3.
Hemelsoet, Dimitri, Arnaud Vanlander, Joél Smet, et al.. (2018). Leigh syndrome followed by parkinsonism in an adult with homozygous c.626C>T mutation in MTFMT. Neurology Genetics. 4(6). e298–e298. 5 indexed citations
4.
Roy, Nadine Van, Malaïka Van Der Linden, Björn Menten, et al.. (2017). Shallow Whole Genome Sequencing on Circulating Cell-Free DNA Allows Reliable Noninvasive Copy-Number Profiling in Neuroblastoma Patients. Clinical Cancer Research. 23(20). 6305–6314. 81 indexed citations
5.
Cauwenbergh, Caroline Van, Kristof Van Schil, Robrecht Cannoodt, et al.. (2016). arrEYE: a customized platform for high-resolution copy number analysis of coding and noncoding regions of known and candidate retinal dystrophy genes and retinal noncoding RNAs. Genetics in Medicine. 19(4). 457–466. 28 indexed citations
6.
Dheedene, Annelies, Tom Sante, Bernard Grisart, et al.. (2016). Implementation of non‐invasive prenatal testing by semiconductor sequencing in a genetic laboratory. Prenatal Diagnosis. 36(8). 699–707. 12 indexed citations
7.
Coninck, Dieter De, Christodoulos Christodoulou, Tom Sante, et al.. (2015). Whole genome amplification with SurePlex results in better copy number alteration detection using sequencing data compared to the MALBAC method. Scientific Reports. 5(1). 11711–11711. 41 indexed citations
8.
Dheedene, Annelies, Dieter De Coninck, Tom Sante, et al.. (2015). Shallow whole genome sequencing is well suited for the detection of chromosomal aberrations in human blastocysts. Fertility and Sterility. 104(5). 1276–1285.e1. 38 indexed citations
9.
Vanlander, Arnaud, Björn Menten, Joél Smet, et al.. (2014). Two Siblings with Homozygous Pathogenic Splice-Site Variant in Mitochondrial Asparaginyl-tRNA Synthetase (NARS2). Human Mutation. 36(2). 222–231. 43 indexed citations
10.
Coppieters, Frauke, Kristof Van Schil, Miriam Bauwens, et al.. (2014). Identity-by-descent–guided mutation analysis and exome sequencing in consanguineous families reveals unusual clinical and molecular findings in retinal dystrophy. Genetics in Medicine. 16(9). 671–680. 47 indexed citations
11.
Sante, Tom, Sarah Vergult, Pieter‐Jan Volders, et al.. (2014). ViVar: A Comprehensive Platform for the Analysis and Visualization of Structural Genomic Variation. PLoS ONE. 9(12). e113800–e113800. 35 indexed citations
12.
Vergult, Sarah, Ellen van Binsbergen, Tom Sante, et al.. (2013). Mate pair sequencing for the detection of chromosomal aberrations in patients with intellectual disability and congenital malformations. European Journal of Human Genetics. 22(5). 652–659. 25 indexed citations
13.
Verdin, Hannah, Barbara D′haene, Diane Beysen, et al.. (2013). Microhomology-Mediated Mechanisms Underlie Non-Recurrent Disease-Causing Microdeletions of the FOXL2 Gene or Its Regulatory Domain. PLoS Genetics. 9(3). e1003358–e1003358. 56 indexed citations
14.
Vergult, Sarah, A. Jeannette M. Hoogeboom, Emilia K. Bijlsma, et al.. (2012). Complex genetics of radial ray deficiencies: screening of a cohort of 54 patients. Genetics in Medicine. 15(3). 195–202. 22 indexed citations
15.
Vergult, Sarah, Ellen van Binsbergen, Tom Sante, et al.. (2012). Matepair sequencing for the detection of chromosomal aberrations in patients with intellectual disability and congenital malformations. Ghent University Academic Bibliography (Ghent University). 3 indexed citations
16.
Dycke, Annelies Van, Robrecht Raedt, Ine Dauwe, et al.. (2010). Continuous local intrahippocampal delivery of adenosine reduces seizure frequency in rats with spontaneous seizures. Epilepsia. 51(9). 1721–1728. 27 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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