Vincent R. Harley

13.0k total citations · 2 hit papers
152 papers, 9.1k citations indexed

About

Vincent R. Harley is a scholar working on Genetics, Molecular Biology and Reproductive Medicine. According to data from OpenAlex, Vincent R. Harley has authored 152 papers receiving a total of 9.1k indexed citations (citations by other indexed papers that have themselves been cited), including 127 papers in Genetics, 120 papers in Molecular Biology and 48 papers in Reproductive Medicine. Recurrent topics in Vincent R. Harley's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (118 papers), Sexual Differentiation and Disorders (72 papers) and Sperm and Testicular Function (47 papers). Vincent R. Harley is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (118 papers), Sexual Differentiation and Disorders (72 papers) and Sperm and Testicular Function (47 papers). Vincent R. Harley collaborates with scholars based in Australia, United States and United Kingdom. Vincent R. Harley's co-authors include Peter N. Goodfellow, Robin Lovell‐Badge, Benoît De Crombrugghe, Véronique Lefebvre, Wendong Huang, Pascal Bernard, Peter Koopman, Anthony Argentaro, Stefan Bagheri‐Fam and Helena Sim and has published in prestigious journals such as Science, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

In The Last Decade

Vincent R. Harley

149 papers receiving 8.9k citations

Hit Papers

2 papers align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

SOX9 Is a Potent Activator of the Chondrocyte-Specific Enhancer of the Proα1(II) Collagen Gene

1997 934 citations Véronique Lefebvre, Wendong Huang et al. Molecular and Cellular Biology profile →
Sox9 expression during gonadal development implies a conserved role for the gene in testis differentiation in mammals and birds

1996 663 citations Vincent R. Harley, Peter N. Goodfellow et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Vincent R. Harley Australia	54	6.1k	5.3k	1.9k	946	747	152	9.1k
Seppo Vainio Finland	56	9.0k 1.5×	2.9k 0.6×	622 0.3×	787 0.8×	608 0.8×	229	12.1k
Philippe Berta France	38	6.5k 1.1×	5.8k 1.1×	1.7k 0.9×	143 0.2×	429 0.6×	83	9.4k
Orsetta Zuffardi Italy	56	6.8k 1.1×	7.3k 1.4×	1.2k 0.6×	211 0.2×	429 0.6×	324	12.2k
Paul A. Overbeek United States	64	9.6k 1.6×	3.2k 0.6×	454 0.2×	208 0.2×	907 1.2×	166	13.0k
Yumiko Saga Japan	60	9.6k 1.6×	3.1k 0.6×	1.2k 0.7×	212 0.2×	710 1.0×	181	13.1k
Patrick Tam Australia	74	14.1k 2.3×	5.0k 1.0×	452 0.2×	1.0k 1.1×	1.2k 1.6×	275	18.1k
Marc Fellous France	54	5.3k 0.9×	5.3k 1.0×	2.0k 1.1×	140 0.1×	357 0.5×	174	9.0k
Andrea Münsterberg United Kingdom	35	5.3k 0.9×	2.7k 0.5×	823 0.4×	196 0.2×	1.0k 1.4×	85	6.6k
Bernhard Zabel Germany	50	7.2k 1.2×	4.7k 0.9×	284 0.2×	1.5k 1.6×	1.1k 1.4×	166	11.0k
Robert Sullivan Canada	52	5.1k 0.8×	1.2k 0.2×	3.7k 2.0×	417 0.4×	1.4k 1.9×	128	9.5k

Countries citing papers authored by Vincent R. Harley

Since Specialization

Citations

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

Fields of papers citing papers by Vincent R. Harley

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Vincent R. Harley. 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 Vincent R. Harley. The network helps show where Vincent R. Harley may publish in the future.

Co-authorship network of co-authors of Vincent R. Harley

This figure shows the co-authorship network connecting the top 25 collaborators of Vincent R. Harley. A scholar is included among the top collaborators of Vincent R. Harley 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 Vincent R. Harley. Vincent R. Harley 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

Bird, Anthony D., Stefan Bagheri‐Fam, Brittany Croft, et al.. (2023). Somatic FGFR2 is Required for Germ Cell Maintenance in the Mouse Ovary. Endocrinology. 164(5). 3 indexed citations

Croft, Brittany, Anthony D. Bird, Makoto Ono, et al.. (2022). FGF9 variant in 46, XY DSD patient suggests a role for dimerization in sex determination. Clinical Genetics. 103(3). 277–287. 9 indexed citations

Harley, Vincent R., et al.. (2021). ATR-X syndrome: genetics, clinical spectrum, and management. Human Genetics. 140(12). 1625–1634. 14 indexed citations

Thuresson, Ann‐Charlotte, et al.. (2020). A novel heterozygous variant in FGF9 associated with previously unreported features of multiple synostosis syndrome 3. Clinical Genetics. 99(2). 325–329. 7 indexed citations

Hare, Lauren, et al.. (2018). Genetic Link Between Gender Dysphoria and Sex Hormone Signaling. The Journal of Clinical Endocrinology & Metabolism. 104(2). 390–396. 44 indexed citations

Barseghyan, Hayk, Ascia Eskin, Matthew S. Bramble, et al.. (2018). Identification of novel candidate genes for 46,XY disorders of sex development (DSD) using a C57BL/6J-Y POS mouse model. Biology of Sex Differences. 9(1). 8–8. 21 indexed citations

Lavery, Rowena, Nicolás Bellora, Gayle K. Philip, et al.. (2017). In mammalian foetal testes, SOX9 regulates expression of its target genes by binding to genomic regions with conserved signatures. Nucleic Acids Research. 45(12). 7191–7211. 78 indexed citations

Eggers, Stefanie, Katherine R. Smith, Melanie Bahlo, et al.. (2014). Whole exome sequencing combined with linkage analysis identifies a novel 3 bp deletion in NR5A1. European Journal of Human Genetics. 23(4). 486–493. 25 indexed citations

Hersmus, Remko, Yvonne G. van der Zwan, Hans Stoop, et al.. (2012). A 46,XY Female DSD Patient with Bilateral Gonadoblastoma, a Novel SRY Missense Mutation Combined with a WT1 KTS Splice-Site Mutation. PLoS ONE. 7(7). e40858–e40858. 27 indexed citations

10.

Argentaro, Anthony, Andrew J. Pask, Liza O’Donnell, et al.. (2011). Localization of the Chromatin Remodelling Protein, ATRX in the Adult Testis. Journal of Reproduction and Development. 57(3). 317–321. 8 indexed citations

11.

Bagheri‐Fam, Stefan, Anthony Argentaro, Terje Svingen, et al.. (2011). Defective survival of proliferating Sertoli cells and androgen receptor function in a mouse model of the ATR-X syndrome (vol 20, pg 2213, 2011). Human Molecular Genetics. 20(17). 1 indexed citations

12.

Bagheri‐Fam, Stefan, Anthony Argentaro, Terje Svingen, et al.. (2011). Defective survival of proliferating Sertoli cells and androgen receptor function in a mouse model of the ATR-X syndrome. Human Molecular Genetics. 20(11). 2213–2224. 52 indexed citations

13.

White, Stefan J., Jacqueline Hewitt, Erin Turbitt, et al.. (2011). A multi-exon deletion within WWOX is associated with a 46,XY disorder of sex development. European Journal of Human Genetics. 20(3). 348–351. 40 indexed citations

14.

Hersmus, Remko, Hans Stoop, Pascal Bernard, et al.. (2009). A novel SRY missense mutation affecting nuclear import in a 46,XY female patient with bilateral gonadoblastoma. European Journal of Human Genetics. 17(12). 1642–1649. 28 indexed citations

15.

Vilain, Éric, John C. Achermann, Erica A. Eugster, et al.. (2007). We used to call them hermaphrodites. Genetics in Medicine. 9(2). 65–66. 23 indexed citations

16.

Moreno-Méndoza, Norma, Leda Torres, Jesús Chimal‐Monroy, Vincent R. Harley, & Horacio Merchant‐Larios. (2004). Disturbed Expression of Sox9 in Pre-Sertoli Cells Underlies Sex-Reversal in Mice B6.Ytir1. Biology of Reproduction. 70(1). 114–122. 13 indexed citations

17.

Kelly, Sabine, et al.. (2003). Recombinant Expression, Purification and Characterisation of the Hmg Domain of Human Sry. Protein and Peptide Letters. 10(3). 281–286. 8 indexed citations

18.

Kelly, Sharon M., et al.. (2003). Turning on the male – SRY, SOX9 and sex determination in mammals. Cytogenetic and Genome Research. 101(3-4). 185–198. 54 indexed citations

19.

Lefebvre, Véronique, Wendong Huang, Vincent R. Harley, Peter N. Goodfellow, & Benoît De Crombrugghe. (1997). SOX9 Is a Potent Activator of the Chondrocyte-Specific Enhancer of the Proα1(II) Collagen Gene. Molecular and Cellular Biology. 17(4). 2336–2346. 934 indexed citations breakdown →

20.

Mitchell, Claire H. & Vincent R. Harley. (1997). Phage display - A powerful genetic probe of biomolecular interactions. 7(4). 218–222. 1 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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