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The Journal of Molecular Diagnostics : JMD|March 11, 2014
Pathogenicity evaluation of BRCA1 and BRCA2 unclassified variants identified in Portuguese breast/ovarian cancer familiesCatarina Santos, Ana Peixoto, Patrícia Rocha, et al.
International Journal of Cancer|December 30, 2003
Highly sensitive detection of the MGB1 transcript (mammaglobin) in the peripheral blood of breast cancer patientsNuno Cerveira, Lurdes Torres, Patrícia Rocha, et al.
European Journal of Endocrinology|November 26, 2013
Familial vs sporadic papillary thyroid carcinoma: a matched-case comparative study showing similar clinical/prognostic behaviourAntónio E Pinto, Giovani L Silva, Rui Henrique, et al.
Oncoscience|June 23, 2015
Uncovering potential downstream targets of oncogenic GRPR overexpression in prostate carcinomas harboring ETS rearrangementsJoana Santos, Diana Mesquita, João D Barros-Silva, et al.
Virchows Archiv : an International Journal of Pathology|March 3, 2007
Expression changes of the MAD mitotic checkpoint gene family in renal cell carcinomas characterized by numerical chromosome changesMafalda Pinto, Maria J Soares, Nuno Cerveira, et al.
BMC Cancer|July 25, 2007
Quantitative promoter methylation analysis of multiple cancer-related genes in renal cell tumorsVera L Costa, Rui Henrique, Franclim R Ribeiro, et al.
Plos One|August 23, 2013
Assessment of fusion gene status in sarcomas using a custom made fusion gene microarrayMarthe Løvf, Gard O S Thomassen, Fredrik Mertens, et al.
Breast Cancer Research and Treatment|August 25, 2016
Implementation of next-generation sequencing for molecular diagnosis of hereditary breast and ovarian cancer highlights its genetic heterogeneityPedro Pinto, Paula Paulo, Catarina Santos, et al.
DNA and Cell Biology|April 7, 2005
Frequent 14-3-3 sigma promoter methylation in benign and malignant prostate lesionsRui Henrique, Carmen Jerónimo, Mohammad O Hoque, et al.
Virchows Archiv : an International Journal of Pathology|December 5, 2016
Ovarian metastasis from uveal melanoma with MLH1/PMS2 protein loss in a patient with germline MLH1 mutated Lynch syndrome: consequence or coincidence?João Lobo, Carla Pinto, Micaela Freitas, et al.
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