Similar articles for PMID: 29498494

Year	Number of Results
1992	2
1996	2
1998	1
2003	2
2005	1
2006	2
2007	1
2008	5
2009	10
2010	7
2011	8
2012	5
2013	6
2014	11
2015	9
2016	13
2017	17
2018	18
2019	14
2020	17
2021	16
2022	17
2023	13
2024	8
2025	2
2026	0

1

Potential hot spot for de novo mutations in PTCH1 gene in Gorlin syndrome patients: a case report of twins from Croatia.

Musani V, Ozretić P, Trnski D, Sabol M, Poduje S, Tošić M, Šitum M, Levanat S. Musani V, et al. Croat Med J. 2018 Feb 28;59(1):20-24. doi: 10.3325/cmj.2018.59.20. Croat Med J. 2018. PMID: 29498494 Free PMC article.

2

Multi-layered mutation in hedgehog-related genes in Gorlin syndrome may affect the phenotype.

Onodera S, Saito A, Hasegawa D, Morita N, Watanabe K, Nomura T, Shibahara T, Ohba S, Yamaguchi A, Azuma T. Onodera S, et al. PLoS One. 2017 Sep 15;12(9):e0184702. doi: 10.1371/journal.pone.0184702. eCollection 2017. PLoS One. 2017. PMID: 28915250 Free PMC article.

3

A Novel PTCH1 Frameshift Mutation Leading to Nevoid Basal Cell Carcinoma Syndrome.

Durmaz CD, Evans G, Smith MJ, Ertop P, Akay BN, Tuncalı T. Durmaz CD, et al. Cytogenet Genome Res. 2018;154(2):57-61. doi: 10.1159/000487747. Epub 2018 Mar 16. Cytogenet Genome Res. 2018. PMID: 29544218

4

Germline mutations in SUFU cause Gorlin syndrome-associated childhood medulloblastoma and redefine the risk associated with PTCH1 mutations.

Smith MJ, Beetz C, Williams SG, Bhaskar SS, O'Sullivan J, Anderson B, Daly SB, Urquhart JE, Bholah Z, Oudit D, Cheesman E, Kelsey A, McCabe MG, Newman WG, Evans DG. Smith MJ, et al. J Clin Oncol. 2014 Dec 20;32(36):4155-61. doi: 10.1200/JCO.2014.58.2569. Epub 2014 Nov 17. J Clin Oncol. 2014. PMID: 25403219

5

Spectrum of PTCH1 mutations in French patients with Gorlin syndrome.

Boutet N, Bignon YJ, Drouin-Garraud V, Sarda P, Longy M, Lacombe D, Gorry P. Boutet N, et al. J Invest Dermatol. 2003 Sep;121(3):478-81. doi: 10.1046/j.1523-1747.2003.12423.x. J Invest Dermatol. 2003. PMID: 12925203 Free article.

6

Mutations in SUFU and PTCH1 genes may cause different cutaneous cancer predisposition syndromes: similar, but not the same.

Huq AJ, Walsh M, Rajagopalan B, Finlay M, Trainer AH, Bonnet F, Sevenet N, Winship IM. Huq AJ, et al. Fam Cancer. 2018 Oct;17(4):601-606. doi: 10.1007/s10689-018-0073-7. Fam Cancer. 2018. PMID: 29356994

7

PTCH1 gene mutations in exon 17 and loss of heterozygosity on D9S180 microsatellite in sporadic and inherited human basal cell carcinomas.

Santos DC, Zaphiropoulos PG, Neto CF, Pimentel ER, Sanches JA Jr, Ruiz IR. Santos DC, et al. Int J Dermatol. 2011 Jul;50(7):838-43. doi: 10.1111/j.1365-4632.2010.04866.x. Int J Dermatol. 2011. PMID: 21699520

8

Gorlin Syndrome Associated With a Solitary Circumscribed Retinal Astrocytic Proliferation in a Pediatric Patient.

Lopez-Cañizares A, Al-Khersan H, Carletti P, Shields CL, Berrocal AM. Lopez-Cañizares A, et al. Ophthalmic Surg Lasers Imaging Retina. 2022 Sep;53(9):514-516. doi: 10.3928/23258160-20220811-01. Epub 2022 Sep 1. Ophthalmic Surg Lasers Imaging Retina. 2022. PMID: 36107625

9

Gorlin-like phenotype in a patient with a PTCH2 variant of uncertain significance.

Casano K, Meddaugh H, Zambrano RM, Marble M, Torres JI, Lacassie Y. Casano K, et al. Eur J Med Genet. 2020 Apr;63(4):103842. doi: 10.1016/j.ejmg.2020.103842. Epub 2020 Jan 13. Eur J Med Genet. 2020. PMID: 31945512

10

New mutations and an updated database for the patched-1 (PTCH1) gene.

Reinders MG, van Hout AF, Cosgun B, Paulussen AD, Leter EM, Steijlen PM, Mosterd K, van Geel M, Gille JJ. Reinders MG, et al. Mol Genet Genomic Med. 2018 May;6(3):409-415. doi: 10.1002/mgg3.380. Epub 2018 Mar 25. Mol Genet Genomic Med. 2018. PMID: 29575684 Free PMC article.

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