Suzanne Drury

2.3k total citations
30 papers, 1.4k citations indexed

About

Suzanne Drury is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Suzanne Drury has authored 30 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 11 papers in Molecular Biology and 8 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Suzanne Drury's work include Prenatal Screening and Diagnostics (8 papers), Estrogen and related hormone effects (7 papers) and Genomics and Rare Diseases (6 papers). Suzanne Drury is often cited by papers focused on Prenatal Screening and Diagnostics (8 papers), Estrogen and related hormone effects (7 papers) and Genomics and Rare Diseases (6 papers). Suzanne Drury collaborates with scholars based in United Kingdom, United States and Italy. Suzanne Drury's co-authors include Mitch Dowsett, Lyn S. Chitty, Sunil Pancholi, Melissa Hill, Nicholas Lench, Alexandra Léary, Lucy Jenkins, C. R. Boustred, Stephen Johnston and Hywel Williams and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Oncology and Brain.

In The Last Decade

Suzanne Drury

29 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Suzanne Drury United Kingdom 22 590 580 366 336 298 30 1.4k
Sophia Apostolidou United Kingdom 18 1.0k 1.7× 533 0.9× 291 0.8× 358 1.1× 320 1.1× 42 1.5k
Ming Gang Lin United States 16 777 1.3× 561 1.0× 410 1.1× 60 0.2× 516 1.7× 17 1.4k
Ina Rhee United States 12 1.8k 3.0× 310 0.5× 520 1.4× 64 0.2× 273 0.9× 14 2.3k
Kathy Chun Canada 22 742 1.3× 319 0.6× 315 0.9× 84 0.3× 63 0.2× 59 1.6k
Eija Mahlamäki Finland 19 781 1.3× 309 0.5× 641 1.8× 59 0.2× 417 1.4× 35 1.7k
Zdeněk Kleibl Czechia 23 745 1.3× 557 1.0× 473 1.3× 50 0.1× 326 1.1× 77 1.4k
E. von Schoultz Sweden 22 429 0.7× 680 1.2× 873 2.4× 46 0.1× 360 1.2× 46 1.6k
F A Firgaira Australia 18 518 0.9× 121 0.2× 471 1.3× 166 0.5× 215 0.7× 32 1.2k
Adam J. Krieg United States 23 1.2k 2.0× 156 0.3× 486 1.3× 76 0.2× 651 2.2× 36 2.0k
Mylan Pho United States 7 690 1.2× 216 0.4× 449 1.2× 49 0.1× 716 2.4× 9 1.4k

Countries citing papers authored by Suzanne Drury

Since Specialization
Citations

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

Fields of papers citing papers by Suzanne Drury

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Suzanne Drury

This figure shows the co-authorship network connecting the top 25 collaborators of Suzanne Drury. A scholar is included among the top collaborators of Suzanne Drury 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 Suzanne Drury. Suzanne Drury 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., Frank Casey, Anna N. Seale, et al.. (2024). The incremental yield of prenatal exome sequencing over chromosome microarray for congenital heart abnormalities: A systematic review and meta‐analysis. Prenatal Diagnosis. 44(6-7). 821–831. 4 indexed citations
2.
Haworth, A., Eva Serra, Janna Kenny, et al.. (2020). A report on the impact of rapid prenatal exome sequencing on the clinical management of 52 ongoing pregnancies: a retrospective review. BJOG An International Journal of Obstetrics & Gynaecology. 128(6). 1012–1019. 29 indexed citations
3.
Mestek, Lamia, Emma Clement, Wendy D. Jones, et al.. (2018). Rapid Paediatric Sequencing (RaPS): comprehensive real-life workflow for rapid diagnosis of critically ill children. Journal of Medical Genetics. 55(11). 721–728. 89 indexed citations
4.
Reid, Emma, Apostolos Papandreou, Suzanne Drury, et al.. (2016). Advantages and pitfalls of an extended gene panel for investigating complex neurometabolic phenotypes. Brain. 139(11). 2844–2854. 27 indexed citations
5.
Drury, Suzanne, Melissa Hill, & Lyn S. Chitty. (2016). Cell-Free Fetal DNA Testing for Prenatal Diagnosis. Advances in clinical chemistry. 76. 1–35. 41 indexed citations
6.
Drury, Suzanne, Sarah Mason, Fiona McKay, et al.. (2016). Implementing Non-Invasive Prenatal Diagnosis (NIPD) in a National Health Service Laboratory; From Dominant to Recessive Disorders. Advances in experimental medicine and biology. 924. 71–75. 32 indexed citations
7.
Hill, Melissa, Philip Twiss, Talitha I. Verhoef, et al.. (2015). Non‐invasive prenatal diagnosis for cystic fibrosis: detection of paternal mutations, exploration of patient preferences and cost analysis. Prenatal Diagnosis. 35(10). 950–958. 61 indexed citations
8.
Drury, Suzanne, Hywel Williams, Natalie Trump, et al.. (2015). Exome sequencing for prenatal diagnosis of fetuses with sonographic abnormalities. Prenatal Diagnosis. 35(10). 1010–1017. 129 indexed citations
9.
Drury, Suzanne, C. R. Boustred, Mehmet Tekman, et al.. (2014). A novel homozygous ERCC5 truncating mutation in a family with prenatal arthrogryposis—Further evidence of genotype–phenotype correlation. American Journal of Medical Genetics Part A. 164(7). 1777–1783. 21 indexed citations
10.
Kelberman, Daniel, Renata S. Auriemma, Suzanne Drury, et al.. (2013). A novel heterozygous SOX2 mutation causing congenital bilateral anophthalmia, hypogonadotropic hypogonadism and growth hormone deficiency. Gene. 534(2). 282–285. 20 indexed citations
11.
Hills, Margaret, Suzanne Drury, Janine Salter, et al.. (2012). ER and HER2 expression are positively correlated in HER2 non-overexpressing breast cancer. Breast Cancer Research. 14(2). R46–R46. 49 indexed citations
12.
Dunbier, Anita K., H Anderson, Zara Ghazoui, et al.. (2011). ESR1 Is Co-Expressed with Closely Adjacent Uncharacterised Genes Spanning a Breast Cancer Susceptibility Locus at 6q25.1. PLoS Genetics. 7(4). e1001382–e1001382. 43 indexed citations
13.
Drury, Suzanne, Simone Detre, Alexandra Léary, et al.. (2011). Changes in breast cancer biomarkers in the IGF1R/PI3K pathway in recurrent breast cancer after tamoxifen treatment. Endocrine Related Cancer. 18(5). 565–577. 67 indexed citations
14.
15.
Drury, Suzanne, Janine Salter, Frederick L. Baehner, Steven Shak, & Mitch Dowsett. (2010). Feasibility of using tissue microarray cores of paraffin-embedded breast cancer tissue for measurement of gene expression: a proof-of-concept study. Journal of Clinical Pathology. 63(6). 513–517. 21 indexed citations
16.
Plaza-Menacho, Iván, Andrea Morandi, David Robertson, et al.. (2010). Targeting the receptor tyrosine kinase RET sensitizes breast cancer cells to tamoxifen treatment and reveals a role for RET in endocrine resistance. Oncogene. 29(33). 4648–4657. 111 indexed citations
17.
Drury, Suzanne, H Anderson, & Mitch Dowsett. (2009). Selection of REFERENCE Genes for Normalization of qRT-PCR Data Derived From FFPE Breast Tumors. Diagnostic Molecular Pathology. 18(2). 103–107. 26 indexed citations
18.
Pancholi, Sunil, Caroline Hilmi, Susana Banerjee, et al.. (2008). ERBB2 influences the subcellular localization of the estrogen receptor in tamoxifen-resistant MCF-7 cells leading to the activation of AKT and RPS6KA2. Endocrine Related Cancer. 15(4). 985–1002. 70 indexed citations
19.
Arriola, Edurne, Caterina Marchiò, David S.P. Tan, et al.. (2008). Genomic analysis of the HER2/TOP2A amplicon in breast cancer and breast cancer cell lines. Laboratory Investigation. 88(5). 491–503. 115 indexed citations
20.
Mackay, Alan, Ander Urruticoechea, J. Michael Dixon, et al.. (2007). Molecular response to aromatase inhibitor treatment in primary breast cancer. Breast Cancer Research. 9(3). R37–R37. 97 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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