Lesley McGregor

1.3k total citations
10 papers, 380 citations indexed

About

Lesley McGregor is a scholar working on Genetics, Molecular Biology and Cell Biology. According to data from OpenAlex, Lesley McGregor has authored 10 papers receiving a total of 380 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 5 papers in Molecular Biology and 2 papers in Cell Biology. Recurrent topics in Lesley McGregor's work include Connective tissue disorders research (3 papers), Cancer-related gene regulation (2 papers) and Congenital heart defects research (2 papers). Lesley McGregor is often cited by papers focused on Connective tissue disorders research (3 papers), Cancer-related gene regulation (2 papers) and Congenital heart defects research (2 papers). Lesley McGregor collaborates with scholars based in Australia, United Kingdom and United States. Lesley McGregor's co-authors include Benjamin A. Alman, Gavin Chapman, Yumiko Saga, Kenro Kusumi, Victoria C. O׳Reilly, Elaine H. Zackai, John P. Dormans, Sally L. Dunwoodie, Duncan B. Sparrow and Ryoichiro Kageyama and has published in prestigious journals such as Cell, Nature Genetics and American Journal of Medical Genetics Part B Neuropsychiatric Genetics.

In The Last Decade

Lesley McGregor

10 papers receiving 373 citations

Peers

Lesley McGregor
Marybeth Hummel United States
Elizabeth Wohler United States
Morad Ansari United Kingdom
Debora Plehn-Dujowich Israel
Esther Geán Spain
Frank Oeffner Germany
Miriam Entesarian Sweden
Julie Plaisancié France
E K Pivnick United States
Marta Owczarek‐Lipska Switzerland
Marybeth Hummel United States
Lesley McGregor
Citations per year, relative to Lesley McGregor Lesley McGregor (= 1×) peers Marybeth Hummel

Countries citing papers authored by Lesley McGregor

Since Specialization
Citations

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

Fields of papers citing papers by Lesley McGregor

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lesley McGregor

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

All Works

10 of 10 papers shown
1.
Tofts, Louise, Penny Ireland, Craig F. Munns, et al.. (2024). Consensus Guidelines for the Use of Vosoritide in Children with Achondroplasia in Australia. Children. 11(7). 789–789. 5 indexed citations
2.
Tofts, Louise, Jennifer A. Armstrong, Katherine Langdon, et al.. (2023). Australian guidelines for the management of children with achondroplasia. Journal of Paediatrics and Child Health. 59(2). 229–241. 7 indexed citations
3.
Souzeau, Emmanuelle, Owen M. Siggs, Francesca Pasutto, et al.. (2020). Gene‐specific facial dysmorphism in Axenfeld‐Rieger syndrome caused by FOXC1 and PITX2 variants. American Journal of Medical Genetics Part A. 185(2). 434–439. 8 indexed citations
4.
Corbett, Mark, et al.. (2013). De novo intragenic deletion of the autism susceptibility candidate 2 (AUTS2) gene in a patient with developmental delay: A case report and literature review. American Journal of Medical Genetics Part A. 161(6). 1508–1512. 27 indexed citations
5.
Nicholl, Jillian, Susan J. Brown, Michael Harbord, et al.. (2012). Epilepsy with cognitive deficit and autism spectrum disorders: Prospective diagnosis by array CGH. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 162(1). 24–35. 17 indexed citations
6.
Sparrow, Duncan B., Gavin Chapman, Victoria C. O׳Reilly, et al.. (2012). A Mechanism for Gene-Environment Interaction in the Etiology of Congenital Scoliosis. Cell. 149(2). 295–306. 155 indexed citations
7.
Williams, Vaughan, et al.. (2011). Investigation of inflicted injury in a young girl reveals mild haemophilia A and Turner’s syndrome. International Journal of Laboratory Hematology. 34(1). 98–101. 4 indexed citations
8.
Boyce, Aaron, John A. McGrath, Tanasit Techanukul, et al.. (2011). Ectodermal dysplasia‐skin fragility syndrome due to a new homozygous internal deletion mutation in the PKP1 gene. Australasian Journal of Dermatology. 53(1). 61–65. 22 indexed citations
9.
Jadeja, Shalini, Ian Smyth, Jolanta E. Pitera, et al.. (2005). Identification of a new gene mutated in Fraser syndrome and mouse myelencephalic blebs. Nature Genetics. 37(5). 520–525. 124 indexed citations
10.
McGregor, Lesley, Sean P. Flaherty, & W. G. Breed. (1989). Structure of the zona pellucida and cumulus oophorus in three species of native Australian rodents. Gamete Research. 23(3). 279–287. 11 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Marybeth Hummel Breakdown of academic impact, for papers by Elizabeth Wohler Breakdown of academic impact, for papers by Morad Ansari Breakdown of academic impact, for papers by Debora Plehn-Dujowich Breakdown of academic impact, for papers by Esther Geán Breakdown of academic impact, for papers by Frank Oeffner Breakdown of academic impact, for papers by Miriam Entesarian Breakdown of academic impact, for papers by Julie Plaisancié Breakdown of academic impact, for papers by E K Pivnick Breakdown of academic impact, for papers by Marta Owczarek‐Lipska
Rankless by CCL
2026