Don Leigh

1.5k total citations
43 papers, 933 citations indexed

About

Don Leigh is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Molecular Biology. According to data from OpenAlex, Don Leigh has authored 43 papers receiving a total of 933 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Pediatrics, Perinatology and Child Health, 17 papers in Genetics and 14 papers in Molecular Biology. Recurrent topics in Don Leigh's work include Prenatal Screening and Diagnostics (17 papers), Genomic variations and chromosomal abnormalities (9 papers) and Reproductive Biology and Fertility (5 papers). Don Leigh is often cited by papers focused on Prenatal Screening and Diagnostics (17 papers), Genomic variations and chromosomal abnormalities (9 papers) and Reproductive Biology and Fertility (5 papers). Don Leigh collaborates with scholars based in Australia, United States and China. Don Leigh's co-authors include Steven J. McArthur, Robert P.S. Jansen, James Marshall, R.K. Scopes, Peter L. Rogers, Louise Carey, James Catt, Alison Gee, David S. Cram and Stuart Purvis‐Smith and has published in prestigious journals such as Nucleic Acids Research, Genome Research and American Journal of Obstetrics and Gynecology.

In The Last Decade

Don Leigh

41 papers receiving 841 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Don Leigh Australia 15 548 387 329 200 126 43 933
Manuel Viotti United States 16 609 1.1× 323 0.8× 720 2.2× 358 1.8× 128 1.0× 41 1.3k
Michael V. Zaragoza United States 21 602 1.1× 431 1.1× 580 1.8× 467 2.3× 77 0.6× 31 1.4k
Dehua Cheng China 12 307 0.6× 300 0.8× 242 0.7× 162 0.8× 47 0.4× 44 618
Atsushi Fukuda Japan 15 235 0.4× 474 1.2× 1.3k 3.9× 185 0.9× 80 0.6× 38 1.5k
Mina Popovic Belgium 14 341 0.6× 147 0.4× 438 1.3× 312 1.6× 44 0.3× 51 787
G. L. Terzoli Italy 10 517 0.9× 397 1.0× 237 0.7× 84 0.4× 146 1.2× 14 843
Judy Chernos Canada 15 286 0.5× 521 1.3× 375 1.1× 180 0.9× 97 0.8× 38 859
Guang‐lun Zhuang China 16 300 0.5× 99 0.3× 331 1.0× 466 2.3× 65 0.5× 56 796
Sophie Brouillet France 20 272 0.5× 135 0.3× 345 1.0× 329 1.6× 53 0.4× 64 1.1k
Maribel Grande Spain 16 476 0.9× 173 0.4× 270 0.8× 106 0.5× 131 1.0× 33 826

Countries citing papers authored by Don Leigh

Since Specialization
Citations

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

Fields of papers citing papers by Don Leigh

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Don Leigh

This figure shows the co-authorship network connecting the top 25 collaborators of Don Leigh. A scholar is included among the top collaborators of Don Leigh 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 Don Leigh. Don Leigh 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.
Vera, Daniel L., Patrick Griffin, Don Leigh, et al.. (2025). Multiomic clocks to predict phenotypic age in mice. The Journals of Gerontology Series A. 80(11).
2.
Liang, H., Duo Chen, Yanjie Xia, et al.. (2023). The uncertainty of copy number variants: pregnancy decisions and clinical follow-up. American Journal of Obstetrics and Gynecology. 229(2). 170.e1–170.e8. 14 indexed citations
3.
Cheng, Yanfei, Qian Yu, Minyue Ma, et al.. (2021). Variant haplophasing by long-read sequencing: a new approach to preimplantation genetic testing workups. Fertility and Sterility. 116(3). 774–783. 22 indexed citations
4.
Liu, Sai, Hui Wang, Don Leigh, et al.. (2020). Third-generation sequencing: any future opportunities for PGT?. Journal of Assisted Reproduction and Genetics. 38(2). 357–364. 23 indexed citations
5.
6.
Rechitsky, Svetlana, Anver Kuliev, Ilan Tur-Kaspa, et al.. (2019). Single-Molecule Sequencing. Journal of Molecular Diagnostics. 22(2). 220–227. 3 indexed citations
7.
Wang, Li, Jiandong Shen, David S. Cram, et al.. (2017). Preferential selection and transfer of euploid noncarrier embryos in preimplantation genetic diagnosis cycles for reciprocal translocations. Fertility and Sterility. 108(4). 620–627.e4. 21 indexed citations
8.
9.
McArthur, Steven J., et al.. (2005). Pregnancies and live births after trophectoderm biopsy and preimplantation genetic testing of human blastocysts. Fertility and Sterility. 84(6). 1628–1636. 181 indexed citations
10.
Catt, James, et al.. (2004). Moving to blastocyst biopsy for preimplantation genetic diagnosis and single embryo transfer at sydney IVF. Fertility and Sterility. 82(2). 295–298. 79 indexed citations
11.
Faradz, Sultana MH, Don Leigh, Mark A. Jenkins, et al.. (2000). Genetic diversity at the FMR1 locus in the Indonesian population. Annals of Human Genetics. 64(4). 329–339. 19 indexed citations
12.
13.
Ziegler, John B., et al.. (1998). Mosaicism in X-linked severe combined immunodeficiency. The Journal of Pediatrics. 133(4). 575–576. 1 indexed citations
14.
Palasanthiran, Pamela, et al.. (1994). Early detection of human immunodeficiency virus type 1 infection in Australian infants at risk of perinatal infection and factors affecting transmission. The Pediatric Infectious Disease Journal. 13(12). 1083–1090. 6 indexed citations
15.
Cairns, Murray J., et al.. (1993). Detection of polymorphisms using thermal cycling with a single oligonucleotide on a DNA sequencing gel. Human Mutation. 2(2). 118–122. 1 indexed citations
16.
Neilan, Brett A., et al.. (1993). Rapid preparation of limited biological samples for small-volume PCR.. Genome Research. 2(3). 261–262. 8 indexed citations
17.
Murray, Vincent, et al.. (1992). Direct PCR Sequencing of Dystrophin Polymorphic CACA Alleles after Purification to Remove Shadow Bands. DNA and Cell Biology. 11(8). 637–640. 3 indexed citations
18.
Smith, Garry J., et al.. (1991). EGF-Receptor and Extracellular Matrix Changes in Mouse Pulmonary Carcinogenesis. Experimental Lung Research. 17(2). 327–340. 5 indexed citations
19.
20.
Leigh, Don, et al.. (1988). Nucleotide sequence of a developmentally regulated Dictyostelium discoideum endogenous plasmid gene and 5' flanking region. Nucleic Acids Research. 16(22). 10914–10914. 3 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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