Sam Riedijk

1.3k total citations
37 papers, 889 citations indexed

About

Sam Riedijk is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Molecular Biology. According to data from OpenAlex, Sam Riedijk has authored 37 papers receiving a total of 889 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Pediatrics, Perinatology and Child Health, 17 papers in Genetics and 11 papers in Molecular Biology. Recurrent topics in Sam Riedijk's work include Prenatal Screening and Diagnostics (18 papers), Genomic variations and chromosomal abnormalities (8 papers) and CRISPR and Genetic Engineering (8 papers). Sam Riedijk is often cited by papers focused on Prenatal Screening and Diagnostics (18 papers), Genomic variations and chromosomal abnormalities (8 papers) and CRISPR and Genetic Engineering (8 papers). Sam Riedijk collaborates with scholars based in Netherlands, Denmark and United Kingdom. Sam Riedijk's co-authors include Aad Tibben, John C. van Swieten, Marjolein de Vugt, Frans R.J. Verhey, Martinus F. Niermeijer, Pauline Aalten, H.J. Duivenvoorden, Karin E. M. Diderich, Malgorzata I. Srebniak and Diane Van Opstal and has published in prestigious journals such as PLoS ONE, Trends in biotechnology and EMBO Reports.

In The Last Decade

Sam Riedijk

35 papers receiving 858 citations

Peers

Sam Riedijk
Rhona MacLeod United Kingdom
Magnus Landgren Sweden
Winnie W. Y. Tso Hong Kong
Yuriko Sugawara Japan
Amy Epstein Australia
Wai Lun Alan Fung Canada
Avraham Steinberg Israel
Ayla Humphrey United Kingdom
Rony E. Duncan Australia
Marlene J. Huggins Canada
Rhona MacLeod United Kingdom
Sam Riedijk
Citations per year, relative to Sam Riedijk Sam Riedijk (= 1×) peers Rhona MacLeod

Countries citing papers authored by Sam Riedijk

Since Specialization
Citations

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

Fields of papers citing papers by Sam Riedijk

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Sam Riedijk

This figure shows the co-authorship network connecting the top 25 collaborators of Sam Riedijk. A scholar is included among the top collaborators of Sam Riedijk 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 Sam Riedijk. Sam Riedijk 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.
Arnold, Sophie, et al.. (2025). An exploration of the perspectives of Dutch adults experiencing a genetic condition on human germline gene editing. Journal of Community Genetics. 16(5). 489–501.
2.
Helmrich, Isabel R. A. Retel, Sophie van Baalen, B.C. van Beers, et al.. (2024). The need to set explicit goals for human germline gene editing public dialogues. Journal of Community Genetics. 15(3). 259–265. 4 indexed citations
3.
Helmrich, Isabel R. A. Retel, et al.. (2024). A decade of public engagement regarding human germline gene editing: a systematic scoping review. European Journal of Human Genetics. 33(5). 570–579. 2 indexed citations
4.
Helmrich, Isabel R. A. Retel, et al.. (2023). “What if” should precede “whether” and “how” in the social conversation around human germline gene editing. Journal of Community Genetics. 14(4). 371–375. 5 indexed citations
5.
6.
Polak, Marike, et al.. (2022). Changes in opinions about human germline gene editing as a result of the Dutch DNA-dialogue project. European Journal of Human Genetics. 31(4). 409–416. 12 indexed citations
7.
Buchanan, James, Melissa Hill, Caroline Vass, et al.. (2022). Factors that impact on women's decision‐making around prenatal genomic tests: An international discrete choice survey. Prenatal Diagnosis. 42(7). 934–946. 11 indexed citations
8.
Srebniak, Malgorzata I., Attie T. J. I. Go, Lutgarde Govaerts, et al.. (2021). How to deal with uncertainty in prenatal genomics: A systematic review of guidelines and policies. Clinical Genetics. 100(6). 647–658. 19 indexed citations
9.
Riedijk, Sam, et al.. (2021). In the Era of the Actionable Genome, Everyone is Responsible. Trends in biotechnology. 39(7). 641–643. 2 indexed citations
10.
Baalen, Sophie van, et al.. (2021). The DNA-Dialogue: A Broad Societal Dialogue About Human Germline Genome Editing in the Netherlands. The CRISPR Journal. 4(4). 616–625. 13 indexed citations
11.
Riedijk, Sam, Attie T. J. I. Go, Marike Polak, et al.. (2020). Non-invasive prenatal testing (NIPT): societal pressure or freedom of choice? A vignette study of Dutch citizens’ attitudes. European Journal of Human Genetics. 29(1). 2–10. 10 indexed citations
12.
Riedijk, Sam, et al.. (2019). Germline genome editing: public dialogue is urgent but not self-evident. European Journal of Human Genetics. 28(1). 4–5. 4 indexed citations
13.
Srebniak, Malgorzata I., Karin E. M. Diderich, Lutgarde Govaerts, et al.. (2013). Types of array findings detectable in cytogenetic diagnosis: a proposal for a generic classification. European Journal of Human Genetics. 22(7). 856–858. 27 indexed citations
14.
Riedijk, Sam, Grétel Oudesluijs, & Aad Tibben. (2012). Psychosocial aspects of preconception consultation in primary care: lessons from our experience in clinical genetics. Journal of Community Genetics. 3(3). 213–219. 3 indexed citations
15.
Riedijk, Sam, Hugo J. Duivenvoorden, Sonia M. Rosso, et al.. (2008). Frontotemporal Dementia: Change of Familial Caregiver Burden and Partner Relation in a Dutch Cohort of 63 Patients. Dementia and Geriatric Cognitive Disorders. 26(5). 398–406. 35 indexed citations
16.
Snoo, Femke A. de, Sam Riedijk, Anneke M. van Mil, et al.. (2008). Genetic testing in familial melanoma: uptake and implications. Psycho-Oncology. 17(8). 790–796. 21 indexed citations
17.
Riedijk, Sam, Marjolein de Vugt, H.J. Duivenvoorden, et al.. (2006). Caregiver Burden, Health-Related Quality of Life and Coping in Dementia Caregivers: A Comparison of Frontotemporal Dementia and Alzheimer’s Disease. Dementia and Geriatric Cognitive Disorders. 22(5-6). 405–412. 172 indexed citations
18.
Vugt, Marjolein de, Sam Riedijk, Pauline Aalten, et al.. (2006). Impact of Behavioural Problems on Spousal Caregivers: A Comparison between Alzheimer’s Disease and Frontotemporal Dementia. Dementia and Geriatric Cognitive Disorders. 22(1). 35–41. 186 indexed citations
19.
Oostrom, Iris van, Hanne Meijers‐Heijboer, Hugo J. Duivenvoorden, et al.. (2006). A prospective study of the impact of genetic susceptibility testing for BRCA1/2 or HNPCC on family relationships. Psycho-Oncology. 16(4). 320–328. 47 indexed citations
20.
Riedijk, Sam, Femke A. de Snoo, Sandra van Dijk, et al.. (2005). Hereditary melanoma and predictive genetic testing: why not?. Psycho-Oncology. 14(9). 738–745. 24 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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