Santos C - Search Results

1

Identification of SPRY4 as a Novel Candidate Susceptibility Gene for Familial Nonmedullary Thyroid Cancer.

Marques IJ, Gomes I, Pojo M, Pires C, Moura MM, Cabrera R, Santos C, van IJcken WFJ, Teixeira MR, Ramalho JS, Leite V, Cavaco BM. Marques IJ, et al. Among authors: santos c. Thyroid. 2021 Sep;31(9):1366-1375. doi: 10.1089/thy.2020.0290. Epub 2021 Jun 3. Thyroid. 2021. PMID: 33906393

2

The c.156_157insAlu BRCA2 rearrangement accounts for more than one-fourth of deleterious BRCA mutations in northern/central Portugal.

Peixoto A, Santos C, Rocha P, Pinheiro M, Príncipe S, Pereira D, Rodrigues H, Castro F, Abreu J, Gusmão L, Amorim A, Teixeira MR. Peixoto A, et al. Among authors: santos c. Breast Cancer Res Treat. 2009 Mar;114(1):31-8. doi: 10.1007/s10549-008-9978-4. Epub 2008 Mar 25. Breast Cancer Res Treat. 2009. PMID: 18363094

3

Haplotype and quantitative transcript analyses of Portuguese breast/ovarian cancer families with the BRCA1 R71G founder mutation of Galician origin.

Santos C, Peixoto A, Rocha P, Vega A, Soares MJ, Cerveira N, Bizarro S, Pinheiro M, Pereira D, Rodrigues H, Castro F, Henrique R, Teixeira MR. Santos C, et al. Fam Cancer. 2009;8(3):203-8. doi: 10.1007/s10689-008-9229-1. Epub 2009 Jan 3. Fam Cancer. 2009. PMID: 19123044

4

Feasibility of differential diagnosis of kidney tumors by comparative genomic hybridization of fine needle aspiration biopsies.

Vieira J, Henrique R, Ribeiro FR, Barros-Silva JD, Peixoto A, Santos C, Pinheiro M, Costa VL, Soares MJ, Oliveira J, Jerónimo C, Teixeira MR. Vieira J, et al. Among authors: santos c. Genes Chromosomes Cancer. 2010 Oct;49(10):935-47. doi: 10.1002/gcc.20805. Genes Chromosomes Cancer. 2010. PMID: 20629095

5

FOXE1 polymorphisms are associated with familial and sporadic nonmedullary thyroid cancer susceptibility.

Tomaz RA, Sousa I, Silva JG, Santos C, Teixeira MR, Leite V, Cavaco BM. Tomaz RA, et al. Among authors: santos c. Clin Endocrinol (Oxf). 2012 Dec;77(6):926-33. doi: 10.1111/j.1365-2265.2012.04505.x. Clin Endocrinol (Oxf). 2012. PMID: 22882326

6

Genomic characterization of two large Alu-mediated rearrangements of the BRCA1 gene.

Peixoto A, Pinheiro M, Massena L, Santos C, Pinto P, Rocha P, Pinto C, Teixeira MR. Peixoto A, et al. Among authors: santos c. J Hum Genet. 2013 Feb;58(2):78-83. doi: 10.1038/jhg.2012.137. Epub 2012 Dec 6. J Hum Genet. 2013. PMID: 23223007

7

Pathogenicity evaluation of BRCA1 and BRCA2 unclassified variants identified in Portuguese breast/ovarian cancer families.

Santos C, Peixoto A, Rocha P, Pinto P, Bizarro S, Pinheiro M, Pinto C, Henrique R, Teixeira MR. Santos C, et al. J Mol Diagn. 2014 May;16(3):324-34. doi: 10.1016/j.jmoldx.2014.01.005. Epub 2014 Mar 5. J Mol Diagn. 2014. PMID: 24607278 Free article.

8

Identification of Two Novel HOXB13 Germline Mutations in Portuguese Prostate Cancer Patients.

Maia S, Cardoso M, Pinto P, Pinheiro M, Santos C, Peixoto A, Bento MJ, Oliveira J, Henrique R, Jerónimo C, Teixeira MR. Maia S, et al. Among authors: santos c. PLoS One. 2015 Jul 15;10(7):e0132728. doi: 10.1371/journal.pone.0132728. eCollection 2015. PLoS One. 2015. PMID: 26176944 Free PMC article.

9

The role of germline mutations in the BRCA1/2 and mismatch repair genes in men ascertained for early-onset and/or familial prostate cancer.

Maia S, Cardoso M, Paulo P, Pinheiro M, Pinto P, Santos C, Pinto C, Peixoto A, Henrique R, Teixeira MR. Maia S, et al. Among authors: santos c. Fam Cancer. 2016 Jan;15(1):111-21. doi: 10.1007/s10689-015-9832-x. Fam Cancer. 2016. PMID: 26289772

10

Co-occurrence of nonsense mutations in MSH6 and MSH2 in Lynch syndrome families evidencing that not all truncating mutations are equal.

Pinto C, Pinheiro M, Peixoto A, Santos C, Veiga I, Rocha P, Pinto P, Lopes P, Baptista M, Henrique R, Teixeira MR. Pinto C, et al. Among authors: santos c. J Hum Genet. 2016 Feb;61(2):151-6. doi: 10.1038/jhg.2015.124. Epub 2015 Oct 8. J Hum Genet. 2016. PMID: 26446363

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