Gorjana Robevska

1.5k total citations
33 papers, 556 citations indexed

About

Gorjana Robevska is a scholar working on Molecular Biology, Genetics and Reproductive Medicine. According to data from OpenAlex, Gorjana Robevska has authored 33 papers receiving a total of 556 indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 20 papers in Genetics and 6 papers in Reproductive Medicine. Recurrent topics in Gorjana Robevska's work include Sexual Differentiation and Disorders (19 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (18 papers) and Reproductive Biology and Fertility (4 papers). Gorjana Robevska is often cited by papers focused on Sexual Differentiation and Disorders (19 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (18 papers) and Reproductive Biology and Fertility (4 papers). Gorjana Robevska collaborates with scholars based in Australia, France and Indonesia. Gorjana Robevska's co-authors include Andrew Sinclair, Katie Ayers, Jocelyn van den Bergen, Elena J. Tucker, Sonia Grover, Ingrid Knarston, Sultana MH Faradz, Peter Koopman, Rajini Sreenivasan and Brittany Croft and has published in prestigious journals such as Journal of Biological Chemistry, Nature Communications and SHILAP Revista de lepidopterología.

In The Last Decade

Gorjana Robevska

31 papers receiving 552 citations

Peers

Gorjana Robevska
Gorjana Robevska
Citations per year, relative to Gorjana Robevska Gorjana Robevska (= 1×) peers Shinji Komori

Countries citing papers authored by Gorjana Robevska

Since Specialization
Citations

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

Fields of papers citing papers by Gorjana Robevska

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gorjana Robevska

This figure shows the co-authorship network connecting the top 25 collaborators of Gorjana Robevska. A scholar is included among the top collaborators of Gorjana Robevska 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 Gorjana Robevska. Gorjana Robevska 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.
Bergen, Jocelyn van den, Gorjana Robevska, Marina M. L. Kizys, et al.. (2025). Functional analysis of SRY variants in individuals with 46,XY differences of sex development. Molecular and Cellular Endocrinology. 598. 112458–112458.
2.
Kizys, Marina M. L., et al.. (2024). COUP-TFII regulates early bipotential gonad signaling and commitment to ovarian progenitors. Cell & Bioscience. 14(1). 3–3. 3 indexed citations
3.
Tucker, Elena J., Michael F. Sharp, Katrina M. Bell, et al.. (2024). Biallelic FANCA variants detected in sisters with isolated premature ovarian insufficiency. Clinical Genetics. 106(3). 321–335. 2 indexed citations
4.
Cabral-da-Silva, Mauricio Castro, Jocelyn A. van den Bergen, Gorjana Robevska, et al.. (2024). Generation of heterozygous (MCRIi030-A-1) and homozygous (MCRIi030-A-2) NR2F2/COUP-TFII knockout human iPSC lines. Stem Cell Research. 76. 103374–103374. 1 indexed citations
5.
Bakhshalizadeh, Shabnam, Katrina M. Bell, Gorjana Robevska, et al.. (2024). Diverse genetic causes of amenorrhea in an ethnically homogeneous cohort and an evolving approach to diagnosis. Molecular and Cellular Endocrinology. 587. 112212–112212. 2 indexed citations
6.
Robevska, Gorjana, Jocelyn van den Bergen, Jennifer Couper, et al.. (2023). Genetic Variants in SRD5A2 in a Spectrum of DSD Patients from Australian Clinics Highlight Importance of Genetic Testing alongside Typical First-Line Investigations. Sexual Development. 17(1). 8–15. 3 indexed citations
7.
Sreenivasan, Rajini, Katrina M. Bell, Jocelyn van den Bergen, et al.. (2022). Whole exome sequencing reveals copy number variants in individuals with disorders of sex development. Molecular and Cellular Endocrinology. 546. 111570–111570. 7 indexed citations
8.
Juniarto, Achmad Zulfa, et al.. (2021). Analysis of the androgen receptor (AR) gene in a cohort of Indonesian undermasculinized 46, XY DSD patients. SHILAP Revista de lepidopterología. 22(1). 5 indexed citations
9.
Tucker, Elena J., Katrina M. Bell, Gorjana Robevska, et al.. (2021). Meiotic genes in premature ovarian insufficiency: variants in HROB and REC8 as likely genetic causes. European Journal of Human Genetics. 30(2). 219–228. 23 indexed citations
10.
Bagheri‐Fam, Stefan, Huijun Chen, Sean B. Wilson, et al.. (2020). The gene encoding the ketogenic enzyme HMGCS2 displays a unique expression during gonad development in mice. PLoS ONE. 15(1). e0227411–e0227411. 13 indexed citations
11.
Knarston, Ingrid, Gorjana Robevska, Irene M. Ghobrial, et al.. (2020). An In Vitro Differentiation Protocol for Human Embryonic Bipotential Gonad and Testis Cell Development. Stem Cell Reports. 15(6). 1377–1391. 27 indexed citations
12.
Jaillard, Sylvie, Rajini Sreenivasan, Gorjana Robevska, et al.. (2019). Analysis of NR5A1 in 142 patients with premature ovarian insufficiency, diminished ovarian reserve, or unexplained infertility. Maturitas. 131. 78–86. 26 indexed citations
13.
Thorpe, Frazer, Christopher B. Gorman, Gorjana Robevska, et al.. (2019). A citizen science model for implementing statewide educational DNA barcoding. PLoS ONE. 14(1). e0208604–e0208604. 8 indexed citations
14.
Ayers, Katie, Rakesh Kumar, Gorjana Robevska, et al.. (2019). Familial bilateral cryptorchidism is caused by recessive variants in RXFP2. Journal of Medical Genetics. 56(11). 727–733. 23 indexed citations
15.
Robevska, Gorjana, Aurore Bouty, Achmad Zulfa Juniarto, et al.. (2019). Genetic Analysis Reveals Complete Androgen Insensitivity Syndrome in Female Children Surgically Treated for Inguinal Hernia. Journal of Investigative Surgery. 34(2). 227–233. 7 indexed citations
16.
Robevska, Gorjana, Jocelyn van den Bergen, Emanuele Pelosi, et al.. (2018). Identification of Candidate Genes for Mayer-Rokitansky-Küster-Hauser Syndrome Using Genomic Approaches. Sexual Development. 13(1). 26–34. 29 indexed citations
17.
Croft, Brittany, Thomas Ohnesorg, Jacqueline Hewitt, et al.. (2018). Human sex reversal is caused by duplication or deletion of core enhancers upstream of SOX9. Nature Communications. 9(1). 5319–5319. 117 indexed citations
18.
Tucker, Elena J., et al.. (2018). Identification of variants in pleiotropic genes causing “isolated” premature ovarian insufficiency: implications for medical practice. European Journal of Human Genetics. 26(9). 1319–1328. 29 indexed citations
19.
Ayers, Katie, Dave Tang, Jocelyn A. van den Bergen, et al.. (2018). A novel, homozygous mutation in desert hedgehog (DHH) in a 46, XY patient with dysgenetic testes presenting with primary amenorrhoea: a case report. International Journal of Pediatric Endocrinology. 2018(1). 2–2. 13 indexed citations
20.
Zeng, Weiguang, Gorjana Robevska, Chinn Yi Wong, et al.. (2011). A Modular Approach to Assembly of Totally Synthetic Self-adjuvanting Lipopeptide-based Vaccines Allows Conformational Epitope Building. Journal of Biological Chemistry. 286(15). 12944–12951. 24 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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