Yvonne Boyd

4.1k total citations
84 papers, 3.1k citations indexed

About

Yvonne Boyd is a scholar working on Molecular Biology, Genetics and Immunology. According to data from OpenAlex, Yvonne Boyd has authored 84 papers receiving a total of 3.1k indexed citations (citations by other indexed papers that have themselves been cited), including 58 papers in Molecular Biology, 33 papers in Genetics and 10 papers in Immunology. Recurrent topics in Yvonne Boyd's work include Animal Genetics and Reproduction (15 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (12 papers) and Muscle Physiology and Disorders (10 papers). Yvonne Boyd is often cited by papers focused on Animal Genetics and Reproduction (15 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (12 papers) and Muscle Physiology and Disorders (10 papers). Yvonne Boyd collaborates with scholars based in United Kingdom, United States and France. Yvonne Boyd's co-authors include Ian Craig, Neil J. Fraser, Anthony P. Monaco, Veronica J. Buckle, Kay E. Davies, Simon C. Riley, Jean‐Louis Mandel, H.F. Willard, Robert L. Nussbaum and Nat Bumstead and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and The Lancet.

In The Last Decade

Yvonne Boyd

84 papers receiving 3.0k citations

Peers

Yvonne Boyd

GENET

IMMUN

HEMAT

GENET

Dean Nižetić United Kingdom

C. Conover Talbot United States

Nicholas M. Gough Australia

James W. Nagle United States

Rudolf Jaenisch United States

Christine A. Kozak United States

Linda D. Siracusa United States

Clare Huxley United Kingdom

Manabu Nakayama Japan

Dong Sung An United States

Dean Nižetić United Kingdom

Yvonne Boyd

1.8k ×1.0

977 ×0.9

GENET

334 ×0.7

IMMUN

421 ×1.6

HEMAT

168 ×0.8

GENET

Citations per year, relative to Yvonne Boyd Yvonne Boyd (= 1×) peers Dean Nižetić

Countries citing papers authored by Yvonne Boyd

Since Specialization

Citations

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

Fields of papers citing papers by Yvonne Boyd

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yvonne Boyd

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

All Works

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20 of 20 papers shown

Taggart, Tamara, Allison Mathews, Yvonne Boyd, et al.. (2024). PrEP your step: Implementing an online crowdsourcing contest to engage young people in HIV prevention in Washington DC, USA. PLoS ONE. 19(11). e0313882–e0313882. 1 indexed citations

Jamieson, Robyn V., Rahat Perveen, P. H. Glenister, et al.. (2003). A dominant mutation within the DNA-binding domain of the bZIP transcription factor Maf causes murine cataract and results in selective alteration in DNA binding. Human Molecular Genetics. 12(6). 585–594. 45 indexed citations

Boyd, Yvonne, et al.. (2002). Orthologs of seven genes (AKT1, CDC42BPB, DIO3, EIF5, JAG2, KLC, NDUFB1) from human Chromosome 14q32 map to distal chicken Chromosome 5. Mammalian Genome. 13(2). 120–122. 3 indexed citations

Salomonsen, J., et al.. (2001). Structure and Chromosomal Localization of Chicken CD5. Scandinavian Journal of Immunology. 54(1-2). 141–145. 7 indexed citations

Fenner, Martin, Julia Parrish, Yvonne Boyd, et al.. (1998). MSG1(Melanocyte-Specific Gene 1): Mapping to Chromosome Xq13.1, Genomic Organization, and Promoter Analysis. Genomics. 51(3). 401–407. 23 indexed citations

Boyd, Yvonne, et al.. (1998). Mouse chromosome X. Mammalian Genome. 8(S1). S361–S377. 5 indexed citations

Blair, Helen J., et al.. (1996). The Mouse X-Linked Developmental Mutant, Tattered, Lies betweenDXMit55andXkhand Is Associated with Hyperkeratinization. Genomics. 37(2). 238–241. 9 indexed citations

Masson, W.K., Sylvester Holt, Victoria Reed, & Yvonne Boyd. (1996). The use of compound heterozygotes and Hprt selection to analyze X-linked mottled alleles associated with prenatal lethality. Mammalian Genome. 7(7). 486–489. 1 indexed citations

Calabi, Franco, et al.. (1995). Identification and chromosomal mapping of a third mouse runt-like locus. Genomics. 26(3). 607–610. 15 indexed citations

10.

Matthews, Paul M., M. V. Squier, L. V. B. Nicholson, et al.. (1995). Muscle X-inactivation patterns and dystrophin expression in Duchenne muscular dystrophy carriers. Neuromuscular Disorders. 5(3). 209–220. 45 indexed citations

11.

Glenister, P. H., Jamel Chelly, Zeynep Tümer, et al.. (1994). Analysis of Mnk, the Murine Homologue of the Locus for Menkes Disease, in Normal and Mottled (Mo) Mice. Genomics. 22(1). 27–35. 19 indexed citations

12.

Baldini, Antonio, Thomas M. Gress, Ketan Patel, et al.. (1993). Mapping on Human and Mouse Chromosomes of the Gene for the β-Galactoside-Binding Protein, an Autocrine-Negative Growth Factor. Genomics. 15(1). 216–218. 17 indexed citations

13.

Reed, Victoria, Steven H. Laval, G. Maslen, & Yvonne Boyd. (1993). Partial sequence data from three evolutionarily conserved loci from the proximal short arm of the human X chromosome; assignment of DXF34S1 to Xp11.21-cen. Cytogenetic and Genome Research. 62(2-3). 153–155. 1 indexed citations

14.

Robinson, David, Yvonne Boyd, D.J. Cockburn, et al.. (1990). The parental origin of de novo X-autosome translocations in females with Duchenne muscular dystrophy revealed by M27ß methylation analysis. Genetics Research. 56(2-3). 135–140. 20 indexed citations

15.

Oerlemans, Frank, H.J.M. Smeets, Jan Schepens, et al.. (1989). Definition of subchromosomal intervals around the myotonic dystrophy gene region at 19q. Genomics. 4(3). 384–396. 67 indexed citations

16.

Goundis, Dimitrios, Scott M. Holt, Yvonne Boyd, & K.B.M. Reid. (1989). Localization of the properdin structural locus to Xp11.23–Xp21.1. Genomics. 5(1). 56–60. 32 indexed citations

17.

Fraser, Neil J., Yvonne Boyd, & Ian Craig. (1989). Isolation and characterization of a human variable copy number tandem repeat at Xcen-p11.22. Genomics. 5(1). 144–148. 84 indexed citations

18.

Buckle, Veronica J., Yvonne Boyd, Niall J. Fraser, et al.. (1987). Localisation of Y chromosome sequences in normal and 'XX' males.. Journal of Medical Genetics. 24(4). 197–203. 27 indexed citations

19.

Burn, John, S Povey, Yvonne Boyd, et al.. (1986). Duchenne muscular dystrophy in one of monozygotic twin girls.. Journal of Medical Genetics. 23(6). 494–500. 73 indexed citations

20.

Povey, Sue, Yvonne Boyd, M.E. Duncan, S.J. Jeremiah, & B. Carritt. (1978). Factors affecting the expression of genes on chromosome 9. Cytogenetic and Genome Research. 22(1-6). 461–464. 2 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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