Zoe Docherty

2.2k total citations
36 papers, 1.1k citations indexed

About

Zoe Docherty is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Zoe Docherty has authored 36 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Genetics, 14 papers in Molecular Biology and 13 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Zoe Docherty's work include Genomic variations and chromosomal abnormalities (19 papers), Prenatal Screening and Diagnostics (13 papers) and Chromosomal and Genetic Variations (12 papers). Zoe Docherty is often cited by papers focused on Genomic variations and chromosomal abnormalities (19 papers), Prenatal Screening and Diagnostics (13 papers) and Chromosomal and Genetic Variations (12 papers). Zoe Docherty collaborates with scholars based in United Kingdom, Canada and Egypt. Zoe Docherty's co-authors include Caroline Mackie Ogilvie, Kathy Mann, Celia Donaghue, Paul N. Scriven, Shu C. Yau, Stephen Abbs, Chris Bennett, David Grant, S. Robb and J. Ross Hawkins and has published in prestigious journals such as The Lancet, British Journal of Cancer and International Journal of Cancer.

In The Last Decade

Zoe Docherty

36 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
Zoe Docherty United Kingdom 18 787 540 378 192 78 36 1.1k
Ikuko Teshima Canada 23 797 1.0× 292 0.5× 731 1.9× 171 0.9× 25 0.3× 61 1.5k
Philippos C. Patsalis Cyprus 27 1.2k 1.5× 705 1.3× 1.0k 2.8× 266 1.4× 114 1.5× 100 2.0k
Amber N. Pursley United States 20 1.1k 1.4× 690 1.3× 498 1.3× 250 1.3× 59 0.8× 28 1.4k
Justine Coppinger United States 16 1.2k 1.6× 857 1.6× 480 1.3× 182 0.9× 45 0.6× 24 1.5k
Harriet von Koskull Finland 19 689 0.9× 272 0.5× 465 1.2× 85 0.4× 37 0.5× 52 1.1k
Franz Binkert Switzerland 24 1.3k 1.7× 932 1.7× 585 1.5× 403 2.1× 84 1.1× 50 1.7k
Beth S. Torchia United States 23 1.2k 1.5× 686 1.3× 693 1.8× 171 0.9× 43 0.6× 34 1.6k
Griet Van Buggenhout Belgium 20 1.2k 1.5× 444 0.8× 1.0k 2.7× 200 1.0× 27 0.3× 63 1.9k
Tsang‐Ming Ko Taiwan 18 463 0.6× 409 0.8× 483 1.3× 75 0.4× 101 1.3× 83 1.3k
P.A. Jacobs United Kingdom 19 1.1k 1.4× 336 0.6× 723 1.9× 360 1.9× 33 0.4× 28 1.8k

Countries citing papers authored by Zoe Docherty

Since Specialization
Citations

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

Fields of papers citing papers by Zoe Docherty

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Zoe Docherty

This figure shows the co-authorship network connecting the top 25 collaborators of Zoe Docherty. A scholar is included among the top collaborators of Zoe Docherty 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 Zoe Docherty. Zoe Docherty 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.
2.
Hills, Alison, Celia Donaghue, Jonathan J. Waters, et al.. (2010). QF‐PCR as a stand‐alone test for prenatal samples: the first 2 years' experience in the London region. Prenatal Diagnosis. 30(6). 509–517. 57 indexed citations
3.
Donaghue, Celia, et al.. (2009). Combined QF‐PCR and MLPA molecular analysis of miscarriage products: an efficient and robust alternative to karyotype analysis. Prenatal Diagnosis. 30(2). 133–137. 32 indexed citations
4.
Barwell, Julian, Laurent Pangon, Shirley Hodgson, et al.. (2007). Biallelic mutation of MSH2 in primary human cells is associated with sensitivity to irradiation and altered RAD51 foci kinetics. Journal of Medical Genetics. 44(8). 516–520. 15 indexed citations
5.
Barwell, Julian, Laurent Pangon, Zoe Docherty, et al.. (2007). Is telomere length in peripheral blood lymphocytes correlated with cancer susceptibility or radiosensitivity?. British Journal of Cancer. 97(12). 1696–1700. 37 indexed citations
6.
Willatt, Lionel, John Barber, Ingrid Simonic, et al.. (2006). Novel deletion variants of 9q13–q21.12 and classical euchromatic variants of 9q12/qh involve deletion, duplication and triplication of large tracts of segmentally duplicated pericentromeric euchromatin. European Journal of Human Genetics. 15(1). 45–52. 12 indexed citations
7.
Docherty, Zoe, Caroline Langman, Ian Kesterton, et al.. (2006). Is chromosome radiosensitivity and apoptotic response to irradiation correlated with cancer susceptibility?. International Journal of Radiation Biology. 83(1). 1–12. 19 indexed citations
8.
Donaghue, Celia, Kathy Mann, Zoe Docherty, & Caroline Mackie Ogilvie. (2005). Detection of mosaicism for primary trisomies in prenatal samples by QF-PCR and karyotype analysis. Prenatal Diagnosis. 25(1). 65–72. 76 indexed citations
9.
Mann, Kathy, et al.. (2005). Maternal cell contamination of prenatal samples assessed by QF-PCR genotyping. Prenatal Diagnosis. 25(1). 79–83. 45 indexed citations
10.
Ogilvie, Caroline Mackie, et al.. (2005). Rapid Prenatal Diagnosis of Aneuploidy Using Quantitative Fluorescence-PCR (QF-PCR). Journal of Histochemistry & Cytochemistry. 53(3). 285–288. 52 indexed citations
11.
Mann, Kathy, et al.. (2004). Strategies for the rapid prenatal diagnosis of chromosome aneuploidy. European Journal of Human Genetics. 12(11). 907–915. 112 indexed citations
12.
Davies, Angela, et al.. (2003). Characterization of terminal chromosome anomalies using multisubtelomere FISH. American Journal of Medical Genetics Part A. 120A(4). 483–489. 28 indexed citations
13.
Mann, Kathy, Stephen Abbs, Shu C. Yau, et al.. (2001). Development and implementation of a new rapid aneuploidy diagnostic service within the UK National Health Service and implications for the future of prenatal diagnosis. The Lancet. 358(9287). 1057–1061. 160 indexed citations
14.
Hanson, Helen, Christopher G. Mathew, Zoe Docherty, & Caroline Mackie Ogilvie. (2001). Telomere shortening in Fanconi anaemia demonstrated by a direct FISH approach. Cytogenetic and Genome Research. 93(3-4). 203–206. 37 indexed citations
15.
Baird, Gillian, et al.. (2000). Support for linkage of autism and specific language impairment to 7q3 from two chromosome rearrangements involving band 7q31. American Journal of Medical Genetics. 96(2). 228–234. 57 indexed citations
16.
Behjati, Farkhondeh, et al.. (1997). Chromosome deletion 17pl 1.2 (Smith‐Magenis syndrome) in seven new patients, four of whom had been referred for fragile‐X investigation. Clinical Genetics. 51(1). 71–74. 10 indexed citations
17.
Barnicoat, Angela, E. Boyd, Zoe Docherty, et al.. (1996). Down syndrome with partial duplication and del (21) syndrome: study protocol and call for collaboration. Study I: clinical assessment. Clinical Genetics. 49(1). 20–27. 11 indexed citations
18.
Barnicoat, Angela, Zoe Docherty, & Martin Bobrow. (1993). WHERE HAVE ALL THE FRAGILE X BOYS GONE?. Developmental Medicine & Child Neurology. 35(6). 532–539. 9 indexed citations
19.
Docherty, Zoe, et al.. (1988). X-linked lymphoproliferative disease: a karyotype analysis. Cytogenetic and Genome Research. 47(1-2). 92–94. 7 indexed citations
20.
Docherty, Zoe, et al.. (1984). A rare heterochromatic variant of chromosome 4.. Journal of Medical Genetics. 21(6). 470–472. 4 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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