PubMed for id: 668

Year	Number of Results
1991	1
1993	1
1999	1
2000	1
2001	5
2002	6
2003	5
2004	7
2005	6
2006	4
2007	7
2008	8
2009	18
2010	24
2011	22
2012	12
2013	20
2014	17
2015	10
2016	9
2017	15
2018	10
2019	8
2020	9
2021	11
2022	6
2023	6
2024	2

1

Deletion of cis-regulatory Element in FOXL2 Promoter in a Chinese Family of Type II Blepharophimosis-ptosis-epicanthus Inversus Syndrome with Polydactyly.

Shen Q, Zhao X, Ji Y, Chai P. Shen Q, et al. J Craniofac Surg. 2024 Jan-Feb 01;35(1):e52-e56. doi: 10.1097/SCS.0000000000009801. Epub 2023 Nov 8. J Craniofac Surg. 2024. PMID: 37938073 Free PMC article.

2

Expanded phenotypic spectrum of FOXL2 Variant c.672_701dup revealed by whole-exome sequencing in a rare blepharophimosis, ptosis, and epicanthus inversus syndrome family.

Lin ZB, Chen ZJ, Yang H, Ding XR, Li J, Pan AP, Sun HS, Yu AY, Chen SH. Lin ZB, et al. BMC Ophthalmol. 2023 Nov 7;23(1):446. doi: 10.1186/s12886-023-03189-5. BMC Ophthalmol. 2023. PMID: 37932670 Free PMC article.

3

FOXL2: a gene central to ovarian function.

Mubeen A, Parra-Herran C. Mubeen A, et al. J Clin Pathol. 2023 Dec;76(12):798-801. doi: 10.1136/jcp-2023-208827. Epub 2023 Oct 5. J Clin Pathol. 2023. PMID: 37798106

4

FOXL2 Mutation Status in Sex Cord-stromal Tumors Cannot be Predicted by Morphology.

Wessman S, Fuentes BB, Severin-Karlsson J, Westbom-Fremer S, Nistér M, Kokaraki G, Petta TB, Haglund F, Carlson JW. Wessman S, et al. Int J Gynecol Pathol. 2024 Jan 1;43(1):78-89. doi: 10.1097/PGP.0000000000000953. Epub 2023 Apr 10. Int J Gynecol Pathol. 2024. PMID: 37255476

5

Incidental FOXL2 mutated adult granulosa cell tumour of the ovary with thecoma-like foci.

Fischer AK, Schömig-Markiefka B, Heydt C, Ratiu D, Mallmann P, Meinel J, Büttner R, Schmidt D, Quaas A. Fischer AK, et al. Virchows Arch. 2023 Jul;483(1):117-124. doi: 10.1007/s00428-022-03452-y. Epub 2022 Nov 18. Virchows Arch. 2023. PMID: 36399188 Free PMC article.

6

The Genetics and Biology of FOXL2.

Tucker EJ. Tucker EJ. Sex Dev. 2022;16(2-3):184-193. doi: 10.1159/000519836. Epub 2021 Nov 2. Sex Dev. 2022. PMID: 34727551 Free article. Review.

7

A Novel Forkhead Box L2 Missense Mutation, c.1068G>C, in a Chinese Family With Blepharophimosis/Ptosis/ Epicanthus Inversus Syndrome.

Wang S, Ge S, Zhuang A. Wang S, et al. J Craniofac Surg. 2022 May 1;33(3):e238-e240. doi: 10.1097/SCS.0000000000008042. Epub 2021 Aug 9. J Craniofac Surg. 2022. PMID: 34374675

8

FOXL2 in adult-type granulosa cell tumour of the ovary: oncogene or tumour suppressor gene?

Pilsworth JA, Todeschini AL, Neilson SJ, Cochrane DR, Lai D, Anttonen M, Heikinheimo M, Huntsman DG, Veitia RA. Pilsworth JA, et al. J Pathol. 2021 Nov;255(3):225-231. doi: 10.1002/path.5771. Epub 2021 Sep 1. J Pathol. 2021. PMID: 34338304

9

The Genetic and Clinical Features of FOXL2-Related Blepharophimosis, Ptosis and Epicanthus Inversus Syndrome.

Méjécase C, Nigam C, Moosajee M, Bladen JC. Méjécase C, et al. Genes (Basel). 2021 Mar 4;12(3):364. doi: 10.3390/genes12030364. Genes (Basel). 2021. PMID: 33806295 Free PMC article. Review.

10

Functional Studies of Novel FOXL2 Variants in Chinese Families With Blepharophimosis-Ptosis-Epicanthus Inversus Syndrome.

Li F, Chen H, Wang Y, Yang J, Zhou Y, Song X, Fan J. Li F, et al. Front Genet. 2021 Mar 16;12:616112. doi: 10.3389/fgene.2021.616112. eCollection 2021. Front Genet. 2021. PMID: 33796131 Free PMC article.

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