Becky Treacy

994 total citations
5 papers, 195 citations indexed

About

Becky Treacy is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Becky Treacy has authored 5 papers receiving a total of 195 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Genetics, 1 paper in Molecular Biology and 1 paper in Pediatrics, Perinatology and Child Health. Recurrent topics in Becky Treacy's work include Connective tissue disorders research (4 papers), Moyamoya disease diagnosis and treatment (1 paper) and Congenital limb and hand anomalies (1 paper). Becky Treacy is often cited by papers focused on Connective tissue disorders research (4 papers), Moyamoya disease diagnosis and treatment (1 paper) and Congenital limb and hand anomalies (1 paper). Becky Treacy collaborates with scholars based in United Kingdom. Becky Treacy's co-authors include Arabella Poulson, John C. Whittaker, Allan J. Richards, Martin P. Snead, Annie McNinch, Sarah Waller, Howard Martin, Sarah Meredith, Alan Ang and John D. Scott and has published in prestigious journals such as Human Mutation and European Journal of Human Genetics.

In The Last Decade

Becky Treacy

5 papers receiving 191 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Becky Treacy United Kingdom	5	139	60	48	34	31	5	195
Jaume Crespí Spain	8	99 0.7×	99 1.6×	56 1.2×	6 0.2×	110 3.5×	15	255
Luís Alexandre Rassi Gabriel United States	6	64 0.5×	74 1.2×	18 0.4×	3 0.1×	58 1.9×	9	173
Joel T. Gibson Australia	8	64 0.5×	94 1.6×	121 2.5×	5 0.1×	12 0.4×	9	238
Mirella Bruttini Italy	6	24 0.2×	73 1.2×	28 0.6×	7 0.2×	77 2.5×	7	157
Richard Lao United States	4	68 0.5×	51 0.8×	9 0.2×	4 0.1×	13 0.4×	7	117
Huferesh K. Darbary United States	5	54 0.4×	159 2.6×	16 0.3×	16 0.5×	10 0.3×	6	223
Kim Jenny United States	4	160 1.2×	188 3.1×	2 0.0×	45 1.3×	10 0.3×	6	265
Pavlína Skalická Czechia	10	40 0.3×	92 1.5×	9 0.2×	3 0.1×	93 3.0×	34	250
Shu Yau United Kingdom	8	90 0.6×	130 2.2×	77 1.6×	38 1.1×	1 0.0×	10	258
G. A. Williams United Kingdom	6	38 0.3×	70 1.2×	10 0.2×	3 0.1×	120 3.9×	9	190

Countries citing papers authored by Becky Treacy

Since Specialization

Citations

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

Fields of papers citing papers by Becky Treacy

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Becky Treacy

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

All Works

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5 of 5 papers shown

1.

Richards, Allan J., Annie McNinch, John C. Whittaker, et al.. (2011). Splicing analysis of unclassified variants in COL2A1 and COL11A1 identifies deep intronic pathogenic mutations. European Journal of Human Genetics. 20(5). 552–558. 29 indexed citations

2.

Richards, Allan J., Annie McNinch, Howard Martin, et al.. (2010). Stickler syndrome and the vitreous phenotype: mutations in COL2A1 and COL11A1. Human Mutation. 31(6). E1461–E1471. 99 indexed citations

3.

Mountford, Roger, et al.. (2008). Practice guidelines for the Testing for maternal cell contamination (MCC) in prenatal samples for molecular studies.. 13 indexed citations

4.

Richards, Allan J., John C. Whittaker, Becky Treacy, et al.. (2006). High efficiency of mutation detection in type 1 stickler syndrome using a two-stage approach: vitreoretinal assessment coupled with exon sequencing for screening COL2A1. Human Mutation. 27(7). 696–704. 48 indexed citations

5.

Richards, Allan J., John C. Whittaker, Becky Treacy, et al.. (2006). High efficiency of mutation detection in type 1 Stickler syndrome using a two-stage approach: vitreoretinal assessment coupled with exon sequencing for screening COL2A1. Human Mutation. 27(11). 1156–1156. 6 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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