Similar articles for PMID: 23951402

Year	Number of Results
1994	1
1996	1
1997	1
2001	4
2002	4
2003	2
2004	1
2005	1
2006	1
2007	2
2008	3
2009	3
2010	2
2011	1
2012	4
2013	4
2014	3
2015	2
2016	8
2017	9
2018	8
2019	7
2020	9
2021	4
2022	2
2023	1
2024	0

1

An integrative computational analysis provides evidence for FBN1-associated network deregulation in trisomy 21.

Vilardell M, Civit S, Herwig R. Vilardell M, et al. Biol Open. 2013 Jun 20;2(8):771-8. doi: 10.1242/bio.20134408. eCollection 2013 Aug 15. Biol Open. 2013. PMID: 23951402 Free PMC article.

2

Cardiovascular characteristics in Marfan syndrome and their relation to the genotype.

De Backer J. De Backer J. Verh K Acad Geneeskd Belg. 2009;71(6):335-71. Verh K Acad Geneeskd Belg. 2009. PMID: 20232788 Review.

3

Undescribed mutations in FBN1 gene in two family cases of Marfan syndrome.

Cabrera-Bueno F, Fernandez-Rosado F, Alvarez-Cubero MJ, Martinez-Espin E, Entrala-Bernal C. Cabrera-Bueno F, et al. J Cardiol Cases. 2014 Sep 26;10(6):235-237. doi: 10.1016/j.jccase.2014.08.007. eCollection 2014 Dec. J Cardiol Cases. 2014. PMID: 30534251 Free PMC article.

4

Mutation analysis of the FBN1 gene in a cohort of patients with Marfan Syndrome: A 10-year single center experience.

Mannucci L, Luciano S, Salehi LB, Gigante L, Conte C, Longo G, Ferradini V, Piumelli N, Brancati F, Ruvolo G, Novelli G, Sangiuolo F. Mannucci L, et al. Clin Chim Acta. 2020 Feb;501:154-164. doi: 10.1016/j.cca.2019.10.037. Epub 2019 Nov 12. Clin Chim Acta. 2020. PMID: 31730815

5

Genotype and phenotype analysis of 171 patients referred for molecular study of the fibrillin-1 gene FBN1 because of suspected Marfan syndrome.

Loeys B, Nuytinck L, Delvaux I, De Bie S, De Paepe A. Loeys B, et al. Arch Intern Med. 2001 Nov 12;161(20):2447-54. doi: 10.1001/archinte.161.20.2447. Arch Intern Med. 2001. PMID: 11700157

6

Homozygous and compound heterozygous mutations in the FBN1 gene: unexpected findings in molecular diagnosis of Marfan syndrome.

Arnaud P, Hanna N, Aubart M, Leheup B, Dupuis-Girod S, Naudion S, Lacombe D, Milleron O, Odent S, Faivre L, Bal L, Edouard T, Collod-Beroud G, Langeois M, Spentchian M, Gouya L, Jondeau G, Boileau C. Arnaud P, et al. J Med Genet. 2017 Feb;54(2):100-103. doi: 10.1136/jmedgenet-2016-103996. Epub 2016 Aug 31. J Med Genet. 2017. PMID: 27582083 Free article.

7

Mutation screening in the FBN1 gene responsible for Marfan syndrome and related disorder in Chinese families.

Gong B, Yang L, Wang Q, Ye Z, Guo X, Yang C, Hao F, Shi Y, Huang Y, Qu C, Yang Z. Gong B, et al. Mol Genet Genomic Med. 2019 Apr;7(4):e00594. doi: 10.1002/mgg3.594. Epub 2019 Mar 5. Mol Genet Genomic Med. 2019. PMID: 30838813 Free PMC article.

8

Reference Expression Profile of Three FBN1 Transcript Isoforms and Their Association with Clinical Variability in Marfan Syndrome.

Benarroch L, Aubart M, Gross MS, Arnaud P, Hanna N, Jondeau G, Boileau C. Benarroch L, et al. Genes (Basel). 2019 Feb 11;10(2):128. doi: 10.3390/genes10020128. Genes (Basel). 2019. PMID: 30754709 Free PMC article.

9

A novel fibrillin-1 gene missense mutation associated with neonatal Marfan syndrome: a case report and review of the mutation spectrum.

Peng Q, Deng Y, Yang Y, Liu H. Peng Q, et al. BMC Pediatr. 2016 Apr 30;16:60. doi: 10.1186/s12887-016-0598-6. BMC Pediatr. 2016. PMID: 27138491 Free PMC article. Review.

10

Correlation between large FBN1 deletions and severe cardiovascular phenotype in Marfan syndrome: Analysis of two novel cases and analytical review of the literature.

Buki G, Szalai R, Pinter A, Hadzsiev K, Melegh B, Rauch T, Bene J. Buki G, et al. Mol Genet Genomic Med. 2023 Jul;11(7):e2166. doi: 10.1002/mgg3.2166. Epub 2023 Mar 21. Mol Genet Genomic Med. 2023. PMID: 36945115 Free PMC article. Review.

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