Cited In for PMID: 32867104

Year	Number of Results
2020	1
2021	3
2022	5
2023	7
2024	13
2025	13
2026	2

1

Stickler Syndrome: A Review of Clinical Manifestations and the Genetics Evaluation.

Boothe M, Morris R, Robin N. Boothe M, et al. J Pers Med. 2020 Aug 27;10(3):105. doi: 10.3390/jpm10030105. J Pers Med. 2020. PMID: 32867104 Free PMC article. Review.

2

Paediatric Retinal Detachment in a Patient With Coexistent Stickler and Noonan Syndromes: The Importance of a Multidisciplinary Approach.

Bakr Y, Helmy Y, Qin C, Kalogeropoulos D, Latasiewicz M. Bakr Y, et al. Cureus. 2026 Jan 8;18(1):e101111. doi: 10.7759/cureus.101111. eCollection 2026 Jan. Cureus. 2026. PMID: 41658696 Free PMC article.

3

Rare heterozygous missense variants in VSX2 are associated with retinal detachment.

Brock DC, Dhindsa JS, Chen Y, Ravanmehr V, Mitchell J, Hu F, Li X, Nandigam L, Wang Q, Wu K, Butts JC, Dhindsa HS, Frankfort BJ, Tran NM, Petrovski S, Dhindsa RS. Brock DC, et al. PLoS Genet. 2026 Feb 3;22(2):e1012027. doi: 10.1371/journal.pgen.1012027. eCollection 2026 Feb. PLoS Genet. 2026. PMID: 41632798 Free PMC article.

4

Immediate sequential bilateral retinal detachment repair in a patient with suspected COL2A1 and APC mutations.

Arias-González N, Kiryakoza L, Fernandez MP, Negron CI, Lopez-Cañizares A, Malek DA, Berrocal AM. Arias-González N, et al. J Vitreoretin Dis. 2025 Dec 16:24741264251404645. doi: 10.1177/24741264251404645. Online ahead of print. J Vitreoretin Dis. 2025. PMID: 41415015

5

Inherited Retinal Diseases with High Myopia: A Review.

Liu C, Sheri N, Benson MD. Liu C, et al. Genes (Basel). 2025 Oct 11;16(10):1183. doi: 10.3390/genes16101183. Genes (Basel). 2025. PMID: 41153400 Free PMC article. Review.

6

Novel pathogenic splicing mutation in COL11A1 in a patient with Stickler syndrome verified by minigene splicing assay.

Zhang J, Huang Y, Deng Y, Yang X, Shi H, Yang Y, Lv T, Yan Y, He M, Liu F. Zhang J, et al. Front Genet. 2025 Aug 22;16:1642604. doi: 10.3389/fgene.2025.1642604. eCollection 2025. Front Genet. 2025. PMID: 40919431 Free PMC article.

7

Genetics and Clinical Findings Associated with Early-Onset Myopia and Retinal Detachment in Saudi Arabia.

AlEissa MM, Alhawsawi AA, Milibari D, Schatz P, AlBalawi HB, Alali NM, Abu-Amero KK, Hameed S, Magliyah MS. AlEissa MM, et al. Genes (Basel). 2025 Jul 21;16(7):848. doi: 10.3390/genes16070848. Genes (Basel). 2025. PMID: 40725504 Free PMC article. Review.

8

Mutation of beta-tubulin 4B gene (TUBB4B) causes autosomal dominant retinitis pigmentosa with sensorineural hearing loss in a multigenerational family.

Gregory-Evans CY, Joe AW, Gregory-Evans K. Gregory-Evans CY, et al. Mol Vis. 2025 May 16;31:175-188. eCollection 2025. Mol Vis. 2025. PMID: 40606475 Free PMC article.

9

First-trimester Diagnosis of Micrognathia as a Presentation of Stickler Syndrome.

Chen GL, Li DZ. Chen GL, et al. J Med Ultrasound. 2024 Sep 5;33(2):179-180. doi: 10.4103/jmu.jmu_58_24. eCollection 2025 Apr-Jun. J Med Ultrasound. 2024. PMID: 40521313 Free PMC article. No abstract available.

10

Syndromic forms of inherited retinal dystrophies: a comprehensive molecular diagnosis of consanguineous Pakistani families using capture panel sequencing.

Asghar A, Wazir S, Fatima S, Bilal H, Shoaib M, Rehman SU, Altaf S, Li Y, Afshan K, Chen R, Firasat S. Asghar A, et al. Mol Vis. 2025 Mar 26;31:69-83. eCollection 2025. Mol Vis. 2025. PMID: 40384762 Free PMC article.

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Cited In for PMID: 32867104

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