Sandra Janssens

4.6k total citations
66 papers, 1.5k citations indexed

About

Sandra Janssens is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Sandra Janssens has authored 66 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Genetics, 16 papers in Molecular Biology and 16 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Sandra Janssens's work include Prenatal Screening and Diagnostics (15 papers), Neurofibromatosis and Schwannoma Cases (12 papers) and Cystic Fibrosis Research Advances (9 papers). Sandra Janssens is often cited by papers focused on Prenatal Screening and Diagnostics (15 papers), Neurofibromatosis and Schwannoma Cases (12 papers) and Cystic Fibrosis Research Advances (9 papers). Sandra Janssens collaborates with scholars based in Belgium, United States and United Kingdom. Sandra Janssens's co-authors include Pascal Borry, Geert Mortier, Davit Chokoshvili, Anne De Paepe, Björn Menten, Eric Legius, Sofie De Schepper, Hilde Brems, Ludwine Messiaen and Jo Vandesompele and has published in prestigious journals such as Nature Communications, Journal of Fluid Mechanics and Scientific Reports.

In The Last Decade

Sandra Janssens

61 papers receiving 1.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Sandra Janssens Belgium 20 483 430 325 293 202 66 1.5k
Salmo Raskin Brazil 28 1.5k 3.0× 578 1.3× 332 1.0× 134 0.5× 670 3.3× 147 2.8k
Hubert Journel France 23 563 1.2× 559 1.3× 229 0.7× 191 0.7× 36 0.2× 57 1.4k
Livia Garavelli Italy 23 715 1.5× 670 1.6× 161 0.5× 116 0.4× 102 0.5× 110 1.6k
Rena E. Falk United States 19 408 0.8× 447 1.0× 75 0.2× 174 0.6× 71 0.4× 39 1.0k
Chitra Prasad Canada 23 687 1.4× 409 1.0× 335 1.0× 223 0.8× 100 0.5× 72 1.7k
Donatella Milani Italy 24 1.3k 2.6× 994 2.3× 84 0.3× 180 0.6× 91 0.5× 118 2.1k
David R. Witt United States 17 694 1.4× 444 1.0× 619 1.9× 186 0.6× 106 0.5× 23 1.9k
Wendy L. Golden United States 25 642 1.3× 393 0.9× 118 0.4× 136 0.5× 94 0.5× 63 1.7k
Zvi Borochowitz Israel 24 1.0k 2.2× 875 2.0× 123 0.4× 134 0.5× 27 0.1× 67 2.2k
Arpad von Moers Germany 22 1.1k 2.3× 533 1.2× 159 0.5× 222 0.8× 64 0.3× 58 2.3k

Countries citing papers authored by Sandra Janssens

Since Specialization
Citations

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

Fields of papers citing papers by Sandra Janssens

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sandra Janssens

This figure shows the co-authorship network connecting the top 25 collaborators of Sandra Janssens. A scholar is included among the top collaborators of Sandra Janssens 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 Janssens. Sandra Janssens 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.
Fındıklı, Necati, et al.. (2025). The Effects of Endometriosis on Oocyte and Embryo Quality. Journal of Clinical Medicine. 14(7). 2339–2339. 1 indexed citations
2.
Baetens, Machteld, Leander Meuris, Nico Callewaert, et al.. (2024). Advancing diagnosis and early risk assessment of preeclampsia through noninvasive cell-free DNA methylation profiling. Clinical Epigenetics. 16(1). 182–182. 2 indexed citations
3.
Baetens, Machteld, Kelly Tilleman, Frauke Vanden Meerschaut, et al.. (2024). Aligning genotyping and copy number data in single trophectoderm biopsies for aneuploidy prediction: uncovering incomplete concordance. Human Reproduction Open. 2024(4). hoae056–hoae056. 2 indexed citations
4.
Wilderman, Andrea, Machteld Baetens, Ellen Roets, et al.. (2024). A distant global control region is essential for normal expression of anterior HOXA genes during mouse and human craniofacial development. Nature Communications. 15(1). 3 indexed citations
5.
Verdin, Hannah, et al.. (2024). Accepting or declining preconception expanded carrier screening: An exploratory study with 407 couples. Journal of Genetic Counseling. 34(1). e1899–e1899. 1 indexed citations
6.
Tilleman, Kelly, et al.. (2024). Managing risks for genetic conditions in donor sperm treatment: current practices in Belgian fertility clinics. Reproductive BioMedicine Online. 49(5). 104352–104352. 2 indexed citations
7.
8.
Acke, Frederic, Wim Wuyts, Kristof Van Schil, et al.. (2022). Negative Molecular Diagnostics in Non-Syndromic Hearing Loss: What Next?. Genes. 14(1). 105–105. 3 indexed citations
9.
Janssens, Sandra, et al.. (2017). FLM volume 830 Cover and Front matter. Journal of Fluid Mechanics. 830. f1–f4. 1 indexed citations
10.
Acke, Frederic, et al.. (2014). Etiological approach in patients with unidentified hearing loss. International Journal of Pediatric Otorhinolaryngology. 79(2). 216–222. 17 indexed citations
11.
Houtte, Evelyne Van, Jan Casselman, Sandra Janssens, et al.. (2014). Middle and inner ear malformations in two siblings exposed to valproic acid during pregnancy: A case report. International Journal of Pediatric Otorhinolaryngology. 78(11). 2007–2010. 8 indexed citations
12.
Møller, Lisbeth Birk, Małgorzata Lenartowicz, M. T. Zabot, et al.. (2012). Clinical expression of Menkes disease in females with normal karyotype. Orphanet Journal of Rare Diseases. 7(1). 6–6. 36 indexed citations
13.
Janssens, Sandra, Anne De Paepe, & Pascal Borry. (2012). Attitudes of health care professionals toward carrier screening for cystic fibrosis. A review of the literature. Journal of Community Genetics. 5(1). 13–29. 17 indexed citations
14.
Cosyns, Marjan, et al.. (2010). Speech disorders in neurofibromatosis type 1: a sample survey. International Journal of Language & Communication Disorders. 45(5). 600–607. 10 indexed citations
15.
Cosyns, Marjan, et al.. (2010). Speech fluency in neurofibromatosis type 1. Journal of Fluency Disorders. 35(1). 59–69. 5 indexed citations
16.
Leenheer, Els De, et al.. (2010). Etiological diagnosis in the hearing impaired newborn: Proposal of a flow chart. International Journal of Pediatric Otorhinolaryngology. 75(1). 27–32. 24 indexed citations
17.
Menten, Björn, Katrien Swerts, Barbara Delle Chiaie, et al.. (2009). Array comparative genomic hybridization and flow cytometry analysis of spontaneous abortions and mors in utero samples. BMC Medical Genetics. 10(1). 89–89. 60 indexed citations
18.
Mhatre, Anand N., Sandra Janssens, Michael Nardi, Yan Li, & Anil K. Lalwani. (2009). Clinical and molecular genetic analysis of a family with macrothrombocytopenia and early onset sensorineural hearing loss. European Journal of Medical Genetics. 52(4). 185–190. 2 indexed citations
19.
Maertens, Ophélia, Sofie De Schepper, Jo Vandesompele, et al.. (2007). Molecular Dissection of Isolated Disease Features in Mosaic Neurofibromatosis Type 1. The American Journal of Human Genetics. 81(2). 243–251. 97 indexed citations
20.
Coster, Rudy N. Van, Sandra Janssens, Jean‐Paul Misson, Alain Verloès, & J. G. Leroy. (1998). Prenatal diagnosis of pyruvate carboxylase deficiency by direct measurement of catalytic activity on chorionic villi samples. Prenatal Diagnosis. 18(10). 1041–1044. 10 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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