Dagmar Tapon

2.1k total citations
11 papers, 311 citations indexed

About

Dagmar Tapon is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Infectious Diseases. According to data from OpenAlex, Dagmar Tapon has authored 11 papers receiving a total of 311 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Pediatrics, Perinatology and Child Health, 6 papers in Genetics and 2 papers in Infectious Diseases. Recurrent topics in Dagmar Tapon's work include Prenatal Screening and Diagnostics (8 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genomics and Rare Diseases (3 papers). Dagmar Tapon is often cited by papers focused on Prenatal Screening and Diagnostics (8 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genomics and Rare Diseases (3 papers). Dagmar Tapon collaborates with scholars based in United Kingdom, United States and Italy. Dagmar Tapon's co-authors include Ronald A. Perez, David N. Louis, Mia MacCollin, David J. Kwiatkowski, Katherine B. Sims, Vijaya Ramesh, Marian L. Logrip, Yo Niida, Anat Stemmer‐Rachamimov and Lyn S. Chitty and has published in prestigious journals such as The American Journal of Human Genetics, Ultrasound in Obstetrics and Gynecology and Genetics in Medicine.

In The Last Decade

Dagmar Tapon

10 papers receiving 305 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Dagmar Tapon United Kingdom 5 134 123 115 93 43 11 311
Shu‐Chin Chien Taiwan 10 73 0.5× 55 0.4× 67 0.6× 84 0.9× 36 0.8× 32 309
Petra Kapaun Germany 7 49 0.4× 157 1.3× 34 0.3× 73 0.8× 34 0.8× 7 331
Leslie Steele Canada 14 274 2.0× 57 0.5× 175 1.5× 232 2.5× 30 0.7× 23 525
M. Elizabeth McCready Canada 10 120 0.9× 38 0.3× 39 0.3× 80 0.9× 17 0.4× 25 254
Parag Tamhankar India 10 67 0.5× 57 0.5× 34 0.3× 95 1.0× 9 0.2× 32 272
G. Wendell Richmond United States 9 37 0.3× 65 0.5× 31 0.3× 88 0.9× 54 1.3× 18 325
Michael T. Gabbett Australia 11 168 1.3× 14 0.1× 59 0.5× 116 1.2× 19 0.4× 25 313
Christina Hung United States 11 84 0.6× 101 0.8× 15 0.1× 223 2.4× 37 0.9× 21 370
B. Petrák Czechia 8 66 0.5× 35 0.3× 26 0.2× 44 0.5× 16 0.4× 19 212
Layla Shahmirzadi United States 8 268 2.0× 31 0.3× 101 0.9× 135 1.5× 6 0.1× 8 412

Countries citing papers authored by Dagmar Tapon

Since Specialization
Citations

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

Fields of papers citing papers by Dagmar Tapon

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dagmar Tapon

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

All Works

11 of 11 papers shown
1.
Peter, Michelle, Melissa Hill, Jane Fisher, et al.. (2024). Equity and timeliness as factors in the effectiveness of an ethical prenatal sequencing service: reflections from parents and professionals. European Journal of Human Genetics. 33(3). 360–367. 1 indexed citations
2.
Mellis, Rhiannon, Dagmar Tapon, Nora Shannon, et al.. (2022). Implementing a rapid fetal exome sequencing service: What do parents and health professionals think?. Prenatal Diagnosis. 42(6). 783–795. 8 indexed citations
3.
Peter, Michelle, et al.. (2021). What's out there for parents? A systematic review of online information about prenatal microarray and exome sequencing. Prenatal Diagnosis. 42(1). 97–108. 2 indexed citations
4.
Chandler, Natalie, Sunayna Best, Jane Hayward, et al.. (2019). Rapid Prenatal Diagnosis Using Targeted Exome Sequencing: A Cohort Study to Assess Feasibility and Potential Impact on Prenatal Counseling and Pregnancy Management. Obstetrical & Gynecological Survey. 74(4). 202–204. 2 indexed citations
5.
Chandler, Natalie, Sunayna Best, Jane Hayward, et al.. (2018). Rapid prenatal diagnosis using targeted exome sequencing: a cohort study to assess feasibility and potential impact on prenatal counseling and pregnancy management. Genetics in Medicine. 20(11). 1430–1437. 104 indexed citations
6.
Dall’Asta, A., Dagmar Tapon, Kathy Mann, et al.. (2016). Gestation related karyotype, QF-PCR and CGH-array failure rates in diagnostic amniocentesis. Prenatal Diagnosis. 36(8). 708–713. 4 indexed citations
7.
Tapon, Dagmar, et al.. (2015). OC20.06: Late amniocentesis: is our counselling up to date?. Ultrasound in Obstetrics and Gynecology. 46(S1). 44–45. 1 indexed citations
8.
Morgan, Tim, Geneviève Baujat, Valérie Cormier‐Daire, et al.. (2012). Osteopathia striata congenita with cranial sclerosis and intellectual disability due to contiguous gene deletions involving the WTX locus. Clinical Genetics. 83(3). 251–256. 20 indexed citations
9.
Tapon, Dagmar. (2009). Prenatal Testing for Down Syndrome: Comparison of Screening Practices in the UK and USA. Journal of Genetic Counseling. 19(2). 112–130. 18 indexed citations
10.
Niida, Yo, Anat Stemmer‐Rachamimov, Marian L. Logrip, et al.. (2001). Survey of Somatic Mutations in Tuberous Sclerosis Complex (TSC) Hamartomas Suggests Different Genetic Mechanisms for Pathogenesis of TSC Lesions. The American Journal of Human Genetics. 69(3). 493–503. 148 indexed citations
11.
Tapon, Dagmar. (1999). Case Report: Object Relations Family Therapy as a Model for Genetic Counseling. Journal of Genetic Counseling. 8(4). 235–246. 3 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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