Teresa Davies

1.3k total citations · 1 hit paper
9 papers, 719 citations indexed

About

Teresa Davies is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, Teresa Davies has authored 9 papers receiving a total of 719 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 3 papers in Pediatrics, Perinatology and Child Health and 3 papers in Genetics. Recurrent topics in Teresa Davies's work include Prenatal Screening and Diagnostics (3 papers), Chronic Lymphocytic Leukemia Research (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). Teresa Davies is often cited by papers focused on Prenatal Screening and Diagnostics (3 papers), Chronic Lymphocytic Leukemia Research (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). Teresa Davies collaborates with scholars based in United Kingdom, Netherlands and Canada. Teresa Davies's co-authors include Gerard C. Grosveld, Ton van Agthoven, Anne Hagemeijer, John Stephenson, Ad Geurts van Kessel, Nora Heisterkamp, Marion E. Stone, Annelies de Klein, Claus R. Bartram and John Groffen and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and British Journal of Haematology.

In The Last Decade

Teresa Davies

9 papers receiving 668 citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Translocation of c-abl oncogene correlates with the presence of a Philadelphia chromosome in chronic myelocytic leukaemia

1983 551 citations Claus R. Bartram, Annelies de Klein et al. Nature profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Teresa Davies United Kingdom	7	482	340	210	160	149	9	719
Costanza Bosi Italy	13	385 0.8×	210 0.6×	281 1.3×	76 0.5×	98 0.7×	25	630
SL George United States	9	457 0.9×	169 0.5×	169 0.8×	264 1.6×	62 0.4×	14	597
Nicolas Duployez France	17	621 1.3×	303 0.9×	375 1.8×	190 1.2×	135 0.9×	67	950
Mauro Nanni Italy	16	456 0.9×	294 0.9×	402 1.9×	112 0.7×	97 0.7×	43	804
Marie‐Josée Le Bris France	18	551 1.1×	235 0.7×	420 2.0×	245 1.5×	63 0.4×	55	986
G Meloni Italy	11	461 1.0×	268 0.8×	81 0.4×	99 0.6×	118 0.8×	24	547
Odile Maarek France	13	645 1.3×	411 1.2×	352 1.7×	120 0.8×	231 1.6×	24	1.0k
Sonja Schindela Germany	13	620 1.3×	314 0.9×	368 1.8×	158 1.0×	34 0.2×	25	830
Yue‐Yun Lai China	14	542 1.1×	256 0.8×	196 0.9×	159 1.0×	101 0.7×	79	693
Lucia Casarino Italy	13	323 0.7×	163 0.5×	162 0.8×	50 0.3×	67 0.4×	26	608

Countries citing papers authored by Teresa Davies

Since Specialization

Citations

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

Fields of papers citing papers by Teresa Davies

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Teresa Davies

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

All Works

Sort: Min cites: Since: Top N: Style:

9 of 9 papers shown

1.

Attilakos, George, Deborah G. Maddocks, Teresa Davies, et al.. (2011). Quantification of free fetal DNA in multiple pregnancies and relationship with chorionicity. Prenatal Diagnosis. 31(10). 967–972. 16 indexed citations

2.

Ellard, Sian, et al.. (2009). Evaluation of 13q14 Status in Patients with Chronic Lymphocytic Leukemia Using Single Nucleotide Polymorphism-Based Techniques. Journal of Molecular Diagnostics. 11(4). 298–305. 4 indexed citations

3.

Parker, Helen, Qian An, Kerry E. Barber, et al.. (2008). The complex genomic profile of ETV6‐RUNX1 positive acute lymphoblastic leukemia highlights a recurrent deletion of TBL1XR1. Genes Chromosomes and Cancer. 47(12). 1118–1125. 43 indexed citations

4.

Paulsson, Kajsa, Qian An, Anthony V. Moorman, et al.. (2008). Methylation of tumour suppressor gene promoters in the presence and absence of transcriptional silencing in high hyperdiploid acute lymphoblastic leukaemia. British Journal of Haematology. 144(6). 838–847. 23 indexed citations

5.

An, Qian, Sarah Wright, Zoë J. Konn, et al.. (2008). Variable breakpoints target PAX5 in patients with dicentric chromosomes: A model for the basis of unbalanced translocations in cancer. Proceedings of the National Academy of Sciences. 105(44). 17050–17054. 55 indexed citations

6.

Charles, Adrian, et al.. (2001). The role of comparative genomic hybridisation in prenatal diagnosis. BJOG An International Journal of Obstetrics & Gynaecology. 108(6). 642–648. 2 indexed citations

7.

Carroll, Stephen G., Teresa Davies, Phillipa M. Kyle, Sherif A. Abdel‐Fattah, & Peter Soothill. (1999). Fetal karyotyping by chorionic villus sampling after the first trimester. BJOG An International Journal of Obstetrics & Gynaecology. 106(10). 1035–1040. 8 indexed citations

8.

Howell, R T & Teresa Davies. (1994). Diagnosis of Bloom's syndrome by sister chromatid exchange evaluation in chorionic villus cultures. Prenatal Diagnosis. 14(11). 1071–1073. 17 indexed citations

9.

Bartram, Claus R., Annelies de Klein, Anne Hagemeijer, et al.. (1983). Translocation of c-abl oncogene correlates with the presence of a Philadelphia chromosome in chronic myelocytic leukaemia. Nature. 306(5940). 277–280. 551 indexed citations breakdown →

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.

Explore authors with similar magnitude of impact