Gorjana Robevska
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Explore the profile of Gorjana Robevska including associated specialties, affiliations and a list of published articles.
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Articles
43
Citations
540
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Recent Articles
1.
Idris F, van den Bergen J, Robevska G, Ferreira L, Ferreira K, Kizys M, et al.
Mol Cell Endocrinol
. 2025 Jan;
598:112458.
PMID: 39788310
In mammals, male sexual development is initiated by the expression of the Sex-determining-Region-Y (SRY) gene. SRY contains a highly conserved high mobility group (HMG) box essential for DNA binding and...
2.
Kline B, Siddall N, Wijaya F, Stuart C, Orlando L, Bakhshalizadeh S, et al.
Biol Reprod
. 2024 Oct;
112(1):102-118.
PMID: 39400047
Premature ovarian insufficiency (POI) is characterized by the loss or complete absence of ovarian activity in women under the age of 40. Clinical presentation of POI varies with phenotypic severity...
3.
Pachernegg S, Robevska G, Ferreira L, van den Bergen J, Vlahos K, Howden S, et al.
Stem Cell Res
. 2024 Jul;
79:103494.
PMID: 39003885
The transcription factor WT1 plays a critical role in several embryonic developmental processes such as gonadogenesis, nephrogenesis, and cardiac development. We generated a homozygous (MCRIi031-A-3) WT1 knockout induced pluripotent stem...
4.
Pachernegg S, Robevska G, Ferreira L, van den Bergen J, Vlahos K, Howden S, et al.
Stem Cell Res
. 2024 Jun;
79:103484.
PMID: 38924973
The transcription factor SOX9 plays a critical role in several embryonic developmental processes such as gonadogenesis, chrondrogenesis, and cardiac development. We generated heterozygous (MCRIi031-A-1) and homozygous (MCRIi031-A-2) SOX9 knockout induced...
5.
Tucker E, Sharp M, Lokchine A, Bell K, Palmer C, Kline B, et al.
Clin Genet
. 2024 May;
106(3):321-335.
PMID: 38779778
Premature ovarian insufficiency is a common form of female infertility affecting up to 4% of women and characterised by amenorrhea with elevated gonadotropin before the age of 40. Oocytes require...
6.
Bakhshalizadeh S, Bird A, Sreenivasan R, Bell K, Robevska G, van den Bergen J, et al.
Genes (Basel)
. 2024 Mar;
15(3).
PMID: 38540391
Disruption of meiosis and DNA repair genes is associated with female fertility disorders like premature ovarian insufficiency (POI). In this study, we identified a homozygous missense variant in the gene...
7.
Bakhshalizadeh S, Afkhami F, Bell K, Robevska G, van den Bergen J, Cronin S, et al.
Mol Cell Endocrinol
. 2024 Mar;
587:112212.
PMID: 38521400
Research Question: Premature ovarian insufficiency (POI) is characterised by amenorrhea associated with elevated follicle stimulating hormone (FSH) under the age of 40 years and affects 1-3.7% women. Genetic factors explain...
8.
Ferreira L, Cabral-da-Silva M, Pachernegg S, van den Bergen J, Robevska G, Vlahos K, et al.
Stem Cell Res
. 2024 Mar;
76:103374.
PMID: 38458031
The NR2F2 gene encodes the transcription factor COUP-TFII, which is upregulated in embryonic mesoderm. Heterozygous variants in NR2F2 cause a spectrum of congenital anomalies including cardiac and gonadal phenotypes. We...
9.
Ferreira L, Kizys M, Gama G, Pachernegg S, Robevska G, Sinclair A, et al.
Cell Biosci
. 2024 Jan;
14(1):3.
PMID: 38178246
Background: The absence of expression of the Y-chromosome linked testis-determining gene SRY in early supporting gonadal cells (ESGC) leads bipotential gonads into ovarian development. However, genetic variants in NR2F2, encoding...
10.
Ayers K, Eggers S, Rollo B, Smith K, Davidson N, Siddall N, et al.
Nat Commun
. 2023 Jun;
14(1):3566.
PMID: 37322043
No abstract available.