Stephanie Allen

1.8k total citations
43 papers, 1.1k citations indexed

About

Stephanie Allen is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Molecular Biology. According to data from OpenAlex, Stephanie Allen has authored 43 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Pediatrics, Perinatology and Child Health, 18 papers in Genetics and 12 papers in Molecular Biology. Recurrent topics in Stephanie Allen's work include Prenatal Screening and Diagnostics (33 papers), Fetal and Pediatric Neurological Disorders (18 papers) and Genomic variations and chromosomal abnormalities (12 papers). Stephanie Allen is often cited by papers focused on Prenatal Screening and Diagnostics (33 papers), Fetal and Pediatric Neurological Disorders (18 papers) and Genomic variations and chromosomal abnormalities (12 papers). Stephanie Allen collaborates with scholars based in United Kingdom, United States and Greece. Stephanie Allen's co-authors include Mark D. Kilby, Jo Leonardi‐Bee, John Britton, R. Katie Morris, Karla Hemming, Trevor Cole, Samuel Clokie, Denise Williams, Lucy Jenkins and Susan Hamilton and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Clinical Chemistry.

In The Last Decade

Stephanie Allen

41 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Stephanie Allen United Kingdom 16 653 325 316 183 111 43 1.1k
Min Pan China 15 470 0.7× 236 0.7× 281 0.9× 224 1.2× 21 0.2× 79 924
Shuenn‐Dyh Chang Taiwan 19 672 1.0× 205 0.6× 185 0.6× 87 0.5× 19 0.2× 103 1.3k
M J Mahoney United States 21 655 1.0× 329 1.0× 435 1.4× 146 0.8× 43 0.4× 37 1.2k
C Nessmann France 22 701 1.1× 273 0.8× 225 0.7× 89 0.5× 36 0.3× 45 1.4k
Tonia C. Carter United States 20 177 0.3× 214 0.7× 185 0.6× 39 0.2× 40 0.4× 33 762
David M. Iovannisci United States 21 176 0.3× 399 1.2× 240 0.8× 63 0.3× 53 0.5× 33 1.2k
Jo‐Ann Brock Canada 14 681 1.0× 155 0.5× 200 0.6× 113 0.6× 21 0.2× 39 1.0k
Robert M. Greenstein United States 19 281 0.4× 231 0.7× 270 0.9× 46 0.3× 65 0.6× 39 904
Inusha Panigrahi India 17 153 0.2× 267 0.8× 254 0.8× 47 0.3× 93 0.8× 145 1.0k
Frans J. Los Netherlands 22 1.1k 1.6× 226 0.7× 519 1.6× 110 0.6× 38 0.3× 70 1.4k

Countries citing papers authored by Stephanie Allen

Since Specialization
Citations

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

Fields of papers citing papers by Stephanie Allen

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stephanie Allen

This figure shows the co-authorship network connecting the top 25 collaborators of Stephanie Allen. A scholar is included among the top collaborators of Stephanie Allen 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 Stephanie Allen. Stephanie Allen 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.
Rolnik, Daniel L., Stephanie Allen, Alexandros Sotiriadis, et al.. (2025). Performance of international phenotypic criteria for prenatal exome sequencing: systematic review and comparative diagnostic accuracy study using historical individual participant data. Ultrasound in Obstetrics and Gynecology. 66(3). 282–289.
2.
Allen, Stephanie, Dae Yong Park, Evangelia Vemmou, et al.. (2024). Clinical Interpretation of Serum Troponin in the Era of High-Sensitivity Testing. Diagnostics. 14(5). 503–503. 9 indexed citations
3.
Allen, Stephanie, et al.. (2024). Chapter 2: Non-invasive prenatal diagnosis. Best Practice & Research Clinical Obstetrics & Gynaecology. 97. 102544–102544.
4.
Walton, Holly, Michelle Peter, Rhiannon Mellis, et al.. (2024). Evaluating the Implementation of the Rapid Prenatal Exome Sequencing Service in England. Public Health Genomics. 28(1). 34–52. 3 indexed citations
5.
Allen, Stephanie, Natalie Chandler, Esther Kinning, et al.. (2023). Diagnosis of inborn errors of metabolism through prenatal exome sequencing with targeted analysis for fetal structural anomalies. Prenatal Diagnosis. 44(4). 432–442. 3 indexed citations
6.
7.
Agarwal, Umber, Žarko Alfirević, Stephanie Allen, et al.. (2022). Prenatal exome sequencing and impact on perinatal outcome: cohort study. Ultrasound in Obstetrics and Gynecology. 61(3). 339–345. 6 indexed citations
8.
Mone, Fionnuala, Susan Hamilton, Anna N. Seale, et al.. (2021). The Diagnostic Yield of Prenatal Genetic Technologies in Congenital Heart Disease: A Prospective Cohort Study. Fetal Diagnosis and Therapy. 48(2). 112–119. 11 indexed citations
9.
Fratter, Carl, Raymond Dalgleish, Stephanie Allen, et al.. (2020). EMQN best practice guidelines for genetic testing in dystrophinopathies. European Journal of Human Genetics. 28(9). 1141–1159. 39 indexed citations
10.
Togneri, Fiona S., et al.. (2020). Cytogenomic results following high-chance non-invasive prenatal testing: a UK national audit. Genetics Research. 102. e7–e7. 3 indexed citations
11.
Mone, Fionnuala, Clare O’Connor, Susan Hamilton, et al.. (2020). Evolution of a prenatal genetic clinic—A 10‐year cohort study. Prenatal Diagnosis. 40(5). 618–625. 11 indexed citations
12.
Hamilton, Susan, Fionnuala Mone, Ka Wang Cheung, et al.. (2019). Prenatal chromosomal microarray testing of fetuses with ultrasound structural anomalies: A prospective cohort study of over 1000 consecutive cases. Prenatal Diagnosis. 39(12). 1064–1069. 20 indexed citations
13.
Hamilton, Susan, et al.. (2019). Potential genetic causes of miscarriage in euploid pregnancies: a systematic review. Human Reproduction Update. 25(4). 452–472. 87 indexed citations
14.
Webb, Emma, Samuel Clokie, Zahurin Mohamed, et al.. (2019). Next generation sequencing (NGS) to improve the diagnosis and management of patients with disorders of sex development (DSD). Endocrine Connections. 8(2). 100–110. 60 indexed citations
15.
Togneri, Fiona S., Mark D. Kilby, Elizabeth Young, et al.. (2019). Implementation of cell-free DNA-based non-invasive prenatal testing in a National Health Service Regional Genetics Laboratory. Genetics Research. 101. e11–e11. 6 indexed citations
16.
Mackie, Fiona L., Stephanie Allen, R. Katie Morris, & Mark D. Kilby. (2017). Cell‐free fetal DNA ‐based noninvasive prenatal testing of aneuploidy. The Obstetrician & Gynaecologist. 19(3). 211–218. 5 indexed citations
17.
Parks, Michael, Siobhán Cleary, Samuel Clokie, et al.. (2017). Non-invasive prenatal diagnosis of spinal muscular atrophy by relative haplotype dosage. European Journal of Human Genetics. 25(4). 416–422. 74 indexed citations
18.
Hemming, Karla, et al.. (2016). The accuracy of cell‐free fetal DNA ‐based non‐invasive prenatal testing in singleton pregnancies: a systematic review and bivariate meta‐analysis. BJOG An International Journal of Obstetrics & Gynaecology. 124(1). 32–46. 182 indexed citations
19.
Allen, Stephanie. (2014). Establishing the scope of pilates through systematic evaluation: evidence and current practice. OpenGrey (Institut de l'Information Scientifique et Technique). 2 indexed citations
20.
Allen, Stephanie, John Britton, & Jo Leonardi‐Bee. (2009). Association between antioxidant vitamins and asthma outcome measures: systematic review and meta-analysis. Thorax. 64(7). 610–619. 151 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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