Rachel Schot

2.3k total citations
35 papers, 686 citations indexed

About

Rachel Schot is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Rachel Schot has authored 35 papers receiving a total of 686 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Molecular Biology, 19 papers in Genetics and 7 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Rachel Schot's work include Genomic variations and chromosomal abnormalities (8 papers), Genetics and Neurodevelopmental Disorders (8 papers) and Genomics and Rare Diseases (7 papers). Rachel Schot is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Genetics and Neurodevelopmental Disorders (8 papers) and Genomics and Rare Diseases (7 papers). Rachel Schot collaborates with scholars based in Netherlands, United States and Germany. Rachel Schot's co-authors include Frans W. Verheijen, I.F.M. de Coo, Maarten H. Lequin, Grazia M.S. Mancini, Cathryn Poulton, Grazia M.S. Mancini, Marie‐Claire Y. de Wit, Renske Oegema, Peter J. van der Spek and Elly Verbeek and has published in prestigious journals such as Cell, Neurology and The American Journal of Human Genetics.

In The Last Decade

Rachel Schot

32 papers receiving 676 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Rachel Schot Netherlands 16 355 260 107 100 78 35 686
Erik-Jan Kamsteeg Netherlands 15 425 1.2× 320 1.2× 76 0.7× 64 0.6× 65 0.8× 21 874
Anju Shukla India 18 610 1.7× 496 1.9× 106 1.0× 100 1.0× 89 1.1× 112 1.2k
Morad Khayat Israel 16 422 1.2× 162 0.6× 73 0.7× 57 0.6× 37 0.5× 50 664
Davide Tonduti Italy 19 728 2.1× 183 0.7× 51 0.5× 81 0.8× 27 0.3× 64 1.1k
Rowida Almomani Jordan 16 522 1.5× 225 0.9× 57 0.5× 27 0.3× 100 1.3× 26 1.0k
Sahar Mansour United Kingdom 11 575 1.6× 288 1.1× 43 0.4× 33 0.3× 81 1.0× 15 854
Emma Clement United Kingdom 16 968 2.7× 294 1.1× 141 1.3× 53 0.5× 85 1.1× 37 1.3k
Boris Keren France 21 649 1.8× 515 2.0× 65 0.6× 154 1.5× 44 0.6× 70 1.1k
Gretchen Golas United States 16 345 1.0× 320 1.2× 173 1.6× 54 0.5× 24 0.3× 21 869
Paola Prandini Italy 11 799 2.3× 212 0.8× 144 1.3× 43 0.4× 74 0.9× 15 1.0k

Countries citing papers authored by Rachel Schot

Since Specialization
Citations

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

Fields of papers citing papers by Rachel Schot

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rachel Schot

This figure shows the co-authorship network connecting the top 25 collaborators of Rachel Schot. A scholar is included among the top collaborators of Rachel Schot 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 Rachel Schot. Rachel Schot 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.
Perenthaler, Elena, Soheil Yousefi, Kristina Lanko, et al.. (2025). BRAIN-MAGNET: A functional genomics atlas for interpretation of non-coding variants. Cell. 189(2). 676–695.e24.
2.
Schot, Rachel, et al.. (2024). Re‐analysis of whole genome sequencing ends a diagnostic odyssey: Case report of an RNU4‐2 related neurodevelopmental disorder. Clinical Genetics. 106(4). 512–517. 11 indexed citations
3.
Schot, Rachel, et al.. (2024). BRCC3 ‐Associated Syndromic Moyamoya Angiopathy Diagnosed Through Clinical RNA Sequencing. Clinical Genetics. 107(3). 341–347.
4.
Smits, Daphne J., Rachel Schot, Brahim Tabarki, et al.. (2022). CLEC16A interacts with retromer and TRIM27, and its loss impairs endosomal trafficking and neurodevelopment. Human Genetics. 142(3). 379–397. 8 indexed citations
5.
Mancini, Grazia M.S., Daphne J. Smits, Rachel Schot, et al.. (2021). Multidisciplinary interaction and MCD gene discovery. The perspective of the clinical geneticist. European Journal of Paediatric Neurology. 35. 27–34. 1 indexed citations
6.
Schot, Rachel, A. Jeannette M. Hoogeboom, Carsten R. Lincke, et al.. (2018). Mutated zinc finger protein of the cerebellum 1 leads to microcephaly, cortical malformation, callosal agenesis, cerebellar dysplasia, tethered cord and scoliosis. European Journal of Medical Genetics. 61(12). 783–789. 7 indexed citations
7.
Stroobants, Stijn, Frans W. Verheijen, Ilse Goris, et al.. (2017). Progressive leukoencephalopathy impairs neurobehavioral development in sialin-deficient mice. Experimental Neurology. 291. 106–119. 11 indexed citations
8.
Verbeek, Elly, Marije Meuwissen, Frans W. Verheijen, et al.. (2012). COL4A2 mutation associated with familial porencephaly and small-vessel disease. European Journal of Human Genetics. 20(8). 844–851. 73 indexed citations
9.
Poulton, Cathryn, Renske Oegema, Daphne Heijsman, et al.. (2012). Progressive cerebellar atrophy and polyneuropathy: expanding the spectrum of PNKP mutations. Neurogenetics. 14(1). 43–51. 55 indexed citations
10.
Oegema, Renske, Maarten H. Lequin, Rachel Schot, et al.. (2012). Asymmetric polymicrogyria and periventricular nodular heterotopia due to mutation in ARX. American Journal of Medical Genetics Part A. 158A(6). 1472–1476. 6 indexed citations
11.
Wit, Marie‐Claire Y. de, I.F.M. de Coo, Rachel Schot, et al.. (2010). Periventricular nodular heterotopia and distal limb deficiency: A recurrent association. American Journal of Medical Genetics Part A. 152A(4). 954–959. 5 indexed citations
12.
Oegema, Renske, Annelies de Klein, Annemieke J.M.H. Verkerk, et al.. (2010). Distinctive Phenotypic Abnormalities Associated with Submicroscopic 21q22 Deletion Including DYRK1A. Molecular Syndromology. 1(3). 113–120. 39 indexed citations
13.
Verkerk, Annemieke J.M.H., Rachel Schot, Hannie Douben, et al.. (2010). Unbalanced der(5)t(5;20) translocation associated with megalencephaly, perisylvian polymicrogyria, polydactyly and hydrocephalus. American Journal of Medical Genetics Part A. 152A(6). 1488–1497. 5 indexed citations
14.
Oegema, Renske, Rachel Schot, Marie‐Claire Y. de Wit, et al.. (2010). KBG syndrome associated with periventricular nodular heterotopia. Clinical Dysmorphology. 19(3). 164–165. 8 indexed citations
15.
Lequin, Maarten H., I.F.M. de Coo, Esther Brusse, et al.. (2008). Cortical Brain Malformations. Archives of Neurology. 65(3). 358–66. 24 indexed citations
16.
Garavelli, Livia, Anna De Simoni, Marcella Zollino, et al.. (2007). Megalencephaly and Perisylvian Polymicrogyria with Postaxial Polydactyly and Hydrocephalus (MPPH): Report of a New Case. Neuropediatrics. 38(4). 200–203. 17 indexed citations
17.
Dewit, Olivier, I.F.M. de Coo, Elly Verbeek, et al.. (2005). Brain abnormalities in a case of malonyl-CoA decarboxylase deficiency. Molecular Genetics and Metabolism. 87(2). 102–106. 28 indexed citations
18.
Biancheri, Roberta, Andrea Rossi, Rachel Schot, et al.. (2005). Homozygosity for the p.K136E mutation in the SLC17A5 gene as cause of an Italian severe Salla disease. Neurogenetics. 6(4). 195–199. 13 indexed citations
19.
Birkenhäger-Frenkel, D.H., H.A.P. Pols, Rachel Schot, et al.. (1995). Effects of 24r,25-dihydroxyvitamin D3 in combination with 1α-hydroxyvitamin D3 in predialysis renal insufficiency: Biochemistry and histomorphometry of cancellous bone. Journal of Bone and Mineral Research. 10(2). 197–204. 25 indexed citations
20.
Asselt, Els van, Rachel Schot, & R. van Mastrigt. (1993). Cell length measurements in longitudinal smooth muscle strips of the pig urinary bladder. Urological Research. 21(4). 253–256. 2 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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