Tracy Fletcher

402 total citations
9 papers, 261 citations indexed

About

Tracy Fletcher is a scholar working on Molecular Biology, Ophthalmology and Epidemiology. According to data from OpenAlex, Tracy Fletcher has authored 9 papers receiving a total of 261 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 3 papers in Ophthalmology and 3 papers in Epidemiology. Recurrent topics in Tracy Fletcher's work include Retinal Development and Disorders (3 papers), Retinal Diseases and Treatments (3 papers) and Genomics and Rare Diseases (2 papers). Tracy Fletcher is often cited by papers focused on Retinal Development and Disorders (3 papers), Retinal Diseases and Treatments (3 papers) and Genomics and Rare Diseases (2 papers). Tracy Fletcher collaborates with scholars based in United Kingdom, Australia and Saudi Arabia. Tracy Fletcher's co-authors include Kim Mulholland, Agustinus Sutanto, Mary Linehan, I Gusti Gede Djelantik, Carib Nelson, David Mercer, Bradford D. Gessner, Vanda Moniaga, Graeme C. Black and Simon Ramsden and has published in prestigious journals such as The Lancet, Scientific Reports and Journal of Medical Genetics.

In The Last Decade

Tracy Fletcher

9 papers receiving 257 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Tracy Fletcher United Kingdom	6	121	102	76	49	45	9	261
Rachael Almond United Kingdom	6	83 0.7×	29 0.3×	30 0.4×	26 0.5×	3 0.1×	9	161
Donald M. Brandon United States	5	48 0.4×	19 0.2×	20 0.3×	7 0.1×	3 0.1×	8	102
Jacob Schrum United States	4	50 0.4×	107 1.0×	5 0.1×	12 0.2×	3 0.1×	4	261
M Knuf Germany	7	264 2.2×	21 0.2×	205 2.7×	2 0.0×		10	320
Susan A. Doyle United States	9	133 1.1×	43 0.4×	6 0.1×	25 0.5×	2 0.0×	10	357
Manuela Bianco Italy	9	150 1.2×	28 0.3×	109 1.4×	6 0.1×		10	236
Isabel Brosius Belgium	8	92 0.8×	79 0.8×	21 0.3×	7 0.1×		18	189
Farbod Alinezhad Iran	7	24 0.2×	32 0.3×	8 0.1×	20 0.4×	8 0.2×	13	167
Michelle M. Thomsen Denmark	8	62 0.5×	49 0.5×	6 0.1×	7 0.1×	4 0.1×	12	244
Maria‐Evangelia Adami Greece	5	40 0.3×	47 0.5×	6 0.1×	28 0.6×		6	311

Countries citing papers authored by Tracy Fletcher

Since Specialization

Citations

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

Fields of papers citing papers by Tracy Fletcher

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tracy Fletcher

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

All Works

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9 of 9 papers shown

1.

Watson, Christopher M., Ian Carr, Martin McKibbin, et al.. (2023). Long-Read Nanopore Sequencing of RPGR ORF15 is Enhanced Following DNase I Treatment of MinION Flow Cells. Molecular Diagnosis & Therapy. 27(4). 525–535. 4 indexed citations

2.

Lenassi, Eva, Ana Carolina de Carvalho, Anja Thormann, et al.. (2023). EyeG2P: an automated variant filtering approach improves efficiency of diagnostic genomic testing for inherited ophthalmic disorders. Journal of Medical Genetics. 60(8). 810–818. 3 indexed citations

3.

Campbell, Patrick, Jamie M. Ellingford, Neil R. A. Parry, et al.. (2019). Clinical and genetic variability in children with partial albinism. Scientific Reports. 9(1). 16576–16576. 30 indexed citations

4.

Lenassi, Eva, Jill Clayton‐Smith, Sofia Douzgou, et al.. (2019). Clinical utility of genetic testing in 201 preschool children with inherited eye disorders. Genetics in Medicine. 22(4). 745–751. 40 indexed citations

5.

Taylor, Rachel L., Eva Lenassi, Jill Smith, et al.. (2019). Diagnostic yield of panel-based genetic testing in syndromic inherited retinal disease. European Journal of Human Genetics. 28(5). 576–586. 20 indexed citations

6.

Kousal, Bohdan, Pavlína Skalická, Tracy Fletcher, et al.. (2014). Severe retinal degeneration in women with a c.2543del mutation in ORF15 of the RPGR gene.. PubMed. 20. 1307–17. 12 indexed citations

7.

Ramsden, Simon, Anna O’Grady, Tracy Fletcher, et al.. (2013). A clinical molecular genetic service for United Kingdom families with choroideraemia. European Journal of Medical Genetics. 56(8). 432–438. 16 indexed citations

8.

Farrell, Michael, David J. Hughes, Mark Drost, et al.. (2013). Multivariate analysis of MLH1 c.1664T>C (p.Leu555Pro) mismatch repair gene variant demonstrates its pathogenicity. Familial Cancer. 12(4). 741–747. 2 indexed citations

9.

Gessner, Bradford D., Agustinus Sutanto, Mary Linehan, et al.. (2005). Incidences of vaccine-preventable Haemophilus influenzae type b pneumonia and meningitis in Indonesian children: hamlet-randomised vaccine-probe trial. The Lancet. 365(9453). 43–52. 134 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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