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Branca Maria Cavaco

Observed names: B Cavaco, B M Cavaco, B. CAVACO, B. Cavaco, B. M Cavaco, B. M. CAVACO, B. M. Cavaco, B.M. Cavaco, Branca Cavaco, Branca M Cavaco, Branca M. Cavaco, Cavaco, Branca, Cavaco, Branca M.
Observed institutions: University of Lisbon, Instituto Português de Oncologia de Coimbra Francisco Gentil, Utrecht University, Churchill Hospital, Hammersmith Hospital, Nuffield Orthopaedic Centre, University of Oxford, Instituto Português de Oncologia Francisco Gentil, Oxford Centre for Diabetes, Endocrinology and Metabolism, Instituto Português de Oncologia de Coimbra Francisco Gentil, Instituto de Medicina Molecular João Lobo Antunes, Imperial College London, Universidade Nova de Lisboa
ORCID: 0000-0001-8946-8635
Observed ORCID: 0000-0001-8946-8635
OpenAlex ID: A5065364190
HRPT2, encoding parafibromin, is mutated in hyperparathyroidism–jaw tumor syndrome
2002 · J.D. Carpten, C.M. Robbins, et al. · Nature Genetics · 754
TERT Promoter Mutations Are a Major Indicator of Poor Outcome in Differentiated Thyroid Carcinomas
2014 · Miguel Melo, Adriana Gaspar da Rocha, et al. · The Journal of Clinical Endocrinology & Metabolism · 555
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High Prevalence of RAS Mutations in RET -Negative Sporadic Medullary Thyroid Carcinomas
2011 · Margarida M. Moura, Branca M. Cavaco, et al. · The Journal of Clinical Endocrinology & Metabolism · 244
Correlation of RET somatic mutations with clinicopathological features in sporadic medullary thyroid carcinomas
2009 · M M Moura, B M Cavaco, et al. · British Journal of Cancer · 177
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Uterine tumours are a phenotypic manifestation of the hyperparathyroidism‐jaw tumour syndrome
2004 · K. J. BRADLEY, M. R. HOBBS, et al. · Journal of Internal Medicine · 161
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A Study of MECT1-MAML2 in Mucoepidermoid Carcinoma and Warthin's Tumor of Salivary Glands
2004 · Carmo Martins, Branca Cavaco, et al. · Journal of Molecular Diagnostics · 138
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Genomic profiling reveals mutational landscape in parathyroid carcinomas
2017 · Chetanya Pandya, Andrew V. Uzilov, et al. · JCI Insight · 127
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Parafibromin mutations in hereditary hyperparathyroidism syndromes and parathyroid tumours
2006 · K. J. Bradley, B. M. Cavaco, et al. · Clinical Endocrinology · 114
Screening for a BRCA2 Rearrangement in High-Risk Breast/Ovarian Cancer Families: Evidence for a Founder Effect and Analysis of the Associated Phenotypes
2007 · Patrícia M. Machado, Rita D. Brandão, et al. · Journal of Clinical Oncology · 113
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RAS proto-oncogene in medullary thyroid carcinoma
2015 · Margarida M Moura, Branca M Cavaco, et al. · Endocrine Related Cancer · 111
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Some forms of big big prolactin behave as a complex of monomeric prolactin with an immunoglobulin G in patients with macroprolactinemia or prolactinoma
1995 · B Cavaco, V Leite, et al. · The Journal of Clinical Endocrinology & Metabolism · 109
Whole-Exome Sequencing Studies of Parathyroid Carcinomas Reveal Novel PRUNE2 Mutations, Distinctive Mutational Spectra Related to APOBEC-Catalyzed DNA Mutagenesis and Mutational Enrichment in Kinases Associated With Cell Migration and Invasion
2014 · Willie Yu, John R McPherson, et al. · The Journal of Clinical Endocrinology & Metabolism · 106
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Cell Cycle Deregulation and TP53 and RAS Mutations Are Major Events in Poorly Differentiated and Undifferentiated Thyroid Carcinomas
2014 · Jaime Miguel Pita, Inês Filipa Figueiredo, et al. · The Journal of Clinical Endocrinology & Metabolism · 98
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Gene expression profiling associated with the progression to poorly differentiated thyroid carcinomas
2009 · J M Pita, A Banito, et al. · British Journal of Cancer · 90
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Mapping a New Familial Thyroid Epithelial Neoplasia Susceptibility Locus to Chromosome 8p23.1-p22 by High-Density Single-Nucleotide Polymorphism Genome-Wide Linkage Analysis
2008 · Branca M. Cavaco, Pedro F. Batista, et al. · The Journal of Clinical Endocrinology & Metabolism · 79
Multiple endocrine neoplasia type 1 (MEN1) germline mutations in familial isolated primary hyperparathyroidism
2003 · A. A. J. Pannett, A. M. Kennedy, et al. · Clinical Endocrinology · 79
Expression of vascular endothelial growth factor (VEGF) and its receptors in thyroid carcinomas of follicular origin: a potential autocrine loop
2005 · Joaquim Miguel Vieira, Susana C Rosa Santos, et al. · European Journal of Endocrinology · 78
Identification of a novel germline FOXE1 variant in patients with familial non-medullary thyroid carcinoma (FNMTC)
2014 · Joana S. Pereira, Joana Gomes da Silva, et al. · Endocrine · 76
The hyperparathyroidism-jaw tumour syndrome in a Portuguese kindred
2001 · B.M. Cavaco · QJM · 75
Hyperprolactinemia due to big big prolactin is differently detected by commercially available immunoassays
1999 · B. Cavaco, S. Prazeres, et al. · Journal of Endocrinological Investigation · 75
Hyperparathyroidism-Jaw Tumor Syndrome in Roma Families from Portugal Is Due to a Founder Mutation of the HRPT2 Gene
2004 · Branca M. Cavaco, Laura Guerra, et al. · The Journal of Clinical Endocrinology & Metabolism · 68
FOXE1 polymorphisms are associated with familial and sporadic nonmedullary thyroid cancer susceptibility
2012 · Rute A. Tomaz, Inês Sousa, et al. · Clinical Endocrinology · 62
Expression and function of the chemokine receptor CCR7 in thyroid carcinomas
2006 · Margarida Sancho, Joaquim Miguel Vieira, et al. · Journal of Endocrinology · 62
Familial non-medullary thyroid carcinoma (FNMTC): analysis of fPTC/PRN, NMTC1, MNG1 and TCO susceptibility loci and identification of somatic BRAF and RAS mutations
2008 · B. M Cavaco, P. F Batista, et al. · Endocrine Related Cancer · 59
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Mutational analysis of Portuguese families with multiple endocrine neoplasia type 1 reveals large germline deletions
2002 · B. M. Cavaco, R. Domingues, et al. · Clinical Endocrinology · 58
Works count: 134
Citation count: 4,444
H-index: 31
I10-index: 53
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