Geoff Shaw

6.8k total citations
193 papers, 4.9k citations indexed

About

Geoff Shaw is a scholar working on Genetics, Molecular Biology and Reproductive Medicine. According to data from OpenAlex, Geoff Shaw has authored 193 papers receiving a total of 4.9k indexed citations (citations by other indexed papers that have themselves been cited), including 87 papers in Genetics, 81 papers in Molecular Biology and 40 papers in Reproductive Medicine. Recurrent topics in Geoff Shaw's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (44 papers), Sexual Differentiation and Disorders (39 papers) and Sperm and Testicular Function (35 papers). Geoff Shaw is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (44 papers), Sexual Differentiation and Disorders (39 papers) and Sperm and Testicular Function (35 papers). Geoff Shaw collaborates with scholars based in Australia, United States and Japan. Geoff Shaw's co-authors include Marilyn B. Renfree, Andrew J. Pask, R. V. Short, Jean D. Wilson, Michael W. Leihy, Shunsuke Suzuki, Jennifer A. Marshall Graves, Stephen Frankenberg, Hongshi Yu and Douglas Coveney and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and The Lancet.

In The Last Decade

Geoff Shaw

189 papers receiving 4.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Geoff Shaw Australia 35 2.4k 2.3k 826 665 659 193 4.9k
Luiz R. França Brazil 46 1.6k 0.7× 3.0k 1.3× 3.8k 4.7× 292 0.4× 1.8k 2.7× 99 7.0k
Thomas B. Hildebrandt Germany 38 844 0.4× 1.2k 0.5× 923 1.1× 181 0.3× 1.1k 1.6× 198 4.2k
Horacio Merchant‐Larios Mexico 33 1.3k 0.6× 1.4k 0.6× 1.1k 1.4× 163 0.2× 791 1.2× 138 3.3k
William B. Neaves United States 34 1.2k 0.5× 929 0.4× 1.9k 2.4× 156 0.2× 753 1.1× 80 4.3k
Jack Hearn United Kingdom 34 1.4k 0.6× 668 0.3× 557 0.7× 193 0.3× 718 1.1× 116 3.8k
Anthony Michael Carter Denmark 35 774 0.3× 483 0.2× 260 0.3× 1.7k 2.6× 551 0.8× 171 4.4k
Leslie A. Lyons United States 40 2.6k 1.1× 3.3k 1.4× 170 0.2× 171 0.3× 720 1.1× 198 6.2k
Peter Šutovský United States 53 4.2k 1.8× 2.3k 1.0× 4.7k 5.7× 604 0.9× 4.7k 7.2× 235 9.0k
Allen C. Enders United States 46 1.7k 0.7× 873 0.4× 1.3k 1.5× 1.1k 1.7× 1.6k 2.4× 108 6.5k
Minoo Rassoulzadegan France 37 3.8k 1.6× 1.8k 0.7× 683 0.8× 588 0.9× 791 1.2× 113 5.8k

Countries citing papers authored by Geoff Shaw

Since Specialization
Citations

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

Fields of papers citing papers by Geoff Shaw

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Geoff Shaw

This figure shows the co-authorship network connecting the top 25 collaborators of Geoff Shaw. A scholar is included among the top collaborators of Geoff Shaw 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 Geoff Shaw. Geoff Shaw 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.
Shaw, Geoff, et al.. (2025). Ontogeny of RSPO1 , FOXL2 , and RUNX1 during ovarian differentiation in the marsupial tammar wallaby. Developmental Dynamics. 255(3). 340–361.
2.
Newman, Trent, Donna M. Bond, Quentin Gouil, et al.. (2024). PRKACB is a novel imprinted gene in marsupials. Epigenetics & Chromatin. 17(1). 29–29. 3 indexed citations
3.
Peiris, Madusha, Yu Chen, Geoff Shaw, & Marilyn B. Renfree. (2024). Early ovarian differentiation in the tammar wallaby and the effects of exposure to bisphenol A. Reproduction. 169(1). 1 indexed citations
4.
Suzuki, Shunsuke, Trent Newman, Jane C. Fenelon, et al.. (2023). Marsupials have monoallelic MEST expression with a conserved antisense lncRNA but MEST is not imprinted. Heredity. 132(1). 5–17. 1 indexed citations
5.
Solé, M, Roberto de la Fuente, Marilyn B. Renfree, et al.. (2023). Divergent patterns of meiotic double strand breaks and synapsis initiation dynamics suggest an evolutionary shift in the meiosis program between American and Australian marsupials. Frontiers in Cell and Developmental Biology. 11. 1147610–1147610. 4 indexed citations
6.
Chew, Keng Yih, Geoff Shaw, Hongshi Yu, Andrew J. Pask, & Marilyn B. Renfree. (2013). Heterochrony in the regulation of the developing marsupial limb. Developmental Dynamics. 243(2). 324–338. 22 indexed citations
7.
Suzuki, Shunsuke, Geoff Shaw, & Marilyn B. Renfree. (2013). Postnatal epigenetic reprogramming in the germline of a marsupial, the tammar wallaby. Epigenetics & Chromatin. 6(1). 14–14. 12 indexed citations
8.
Stringer, Jessica M., Shunsuke Suzuki, Andrew J. Pask, Geoff Shaw, & Marilyn B. Renfree. (2012). Selected imprinting of INS in the marsupial. Epigenetics & Chromatin. 5(1). 14–14. 27 indexed citations
9.
Frankenberg, Stephen, et al.. (2011). Identification of two distinct genes at the vertebrate TRPC2 locus and their characterisation in a marsupial and a monotreme. BMC Molecular Biology. 12(1). 39–39. 4 indexed citations
10.
Edwards, Carol A., Andrew J. Mungall, Lucy Matthews, et al.. (2008). The evolution of an imprinted domain in mammals. Genetics Research. 90(3). 3 indexed citations
11.
Suzuki, Shunsuke, Ryuichi Ono, Takanori Narita, et al.. (2007). Retrotransposon Silencing by DNA Methylation Can Drive Mammalian Genomic Imprinting. PLoS Genetics. 3(4). e55–e55. 166 indexed citations
12.
Ager, Eleanor I, Shunsuke Suzuki, Andrew J. Pask, et al.. (2007). Insulin is imprinted in the placenta of the marsupial, Macropus eugenii. Developmental Biology. 309(2). 317–328. 35 indexed citations
13.
Armati, Patricia J., Michael Archer, William B. Sherwin, et al.. (2006). Marsupials. Cambridge University Press eBooks. 13 indexed citations
14.
Pask, Andrew J., Deanne J. Whitworth, Chai‐An Mao, et al.. (2004). Marsupial Anti-Müllerian Hormone Gene Structure, Regulatory Elements, and Expression1. Biology of Reproduction. 70(1). 160–167. 26 indexed citations
15.
Wilson, Jean D., Michael W. Leihy, Geoff Shaw, & Marilyn B. Renfree. (2003). Unsolved problems in male physiology: studies in a marsupial. Molecular and Cellular Endocrinology. 211(1-2). 33–36. 22 indexed citations
16.
Renfree, Marilyn B., Jean D. Wilson, & Geoff Shaw. (2002). The Hormonal Control of Sexual Development. Novartis Foundation symposium. 244. 136–156. 34 indexed citations
17.
Renfree, Marilyn B., et al.. (2001). Differential Regulation of Contractility and Nitric Oxide Sensitivity in Gravid and Nongravid Myometrium during Late Pregnancy in a Marsupial1. Endocrinology. 142(6). 2244–2251. 10 indexed citations
18.
Renfree, Marilyn B. & Geoff Shaw. (2001). Germ cells, gonads and sex reversal in marsupials. The International Journal of Developmental Biology. 45(3). 557–567. 21 indexed citations
19.
Sebastian, Lucille, et al.. (1998). Mesotocin receptors during pregnancy, parturition and lactation in the tammar wallaby. Animal Reproduction Science. 51(1). 57–74. 13 indexed citations
20.
Shaw, Geoff. (1996). The uterine environment in early pregnancy in the tammar wallaby. Reproduction Fertility and Development. 8(4). 811–818. 22 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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