Get started
Author

Clarissa Gondim Picanço-Albuquerque

Observed names: C. G. Picanço-Albuquerque, C.G. Picanço-Albuquerque, Clarissa G. Picanço-Albuquerque, Clarissa Gondim Picanço, Clarissa Picanço
ORCID: 0000-0002-9711-6362
Observed ORCID: 0000-0002-9711-6362
OpenAlex ID: A5003943291
In prostate cancer needle biopsies, detections of PTEN loss by fluorescence in situ hybridization (FISH) and by immunohistochemistry (IHC) are concordant and show consistent association with upgrading
2016 · C. G. Picanço-Albuquerque, C. L. Morais, et al. · Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin · 39
Risk Stratification of Prostate Cancer Through Quantitative Assessment of PTEN Loss (qPTEN)
2020 · Tamara Jamaspishvili, Palak G Patel, et al. · JNCI Journal of the National Cancer Institute · 25
High throughput assessment of biomarkers in tissue microarrays using artificial intelligence: PTEN loss as a proof-of-principle in multi-center prostate cancer cohorts
2020 · Stephanie A. Harmon, Palak G. Patel, et al. · Modern Pathology · 22
The breast cancer immunophenotype of TP53-p.R337H carriers is different from that observed among other pathogenic TP53 mutation carriers
2015 · Mariana Fitarelli-Kiehl, Juliana Giacomazzi, et al. · Familial Cancer · 11
Familial chromosomal translocation X; 22 associated with infertility and recurrent X mosaicism
2016 · Juliana Dourado Grzesiuk, Ciro Silveira Pereira, et al. · Molecular Cytogenetics · 9
PDF
Contribution of SLC26A4 to the molecular diagnosis of nonsyndromic prelingual sensorineural hearing loss in a Brazilian cohort
2018 · Simone da Costa e Silva Carvalho, Carlos Henrique Paiva Grangeiro, et al. · BMC Research Notes · 8
PDF
Hypothenar hammer syndrome: case report and literature review
2013 · Márcia Maria Muniz de Queiroz, Lícia Pachêco Pereira, et al. · Revista Brasileira de Ortopedia (English Edition) · 7
Síndrome do martelo hipotenar: relato de caso e revisão da literatura
2013 · Márcia Maria Muniz de Queiroz, Lícia Pachêco Pereira, et al. · Revista Brasileira de Ortopedia · 6
PTEN loss in Gleason grade 7 prostate tumors exhibits intratumoral heterogeneity and is associated with unfavorable pathological features
2019 · C. G. Picanço-Albuquerque, T. Vidotto, et al. · Applied cancer research/Applied Cancer Research · 5
PDF
Are pathogenic BRCA1 mutations associated with parotid mucoepidermoid carcinoma? A case report
2020 · Paulo Goberlânio de Barros Silva, Rosane Oliveira de Sant'ana, et al. · Oral Surgery Oral Medicine Oral Pathology and Oral Radiology · 3
Evaluation of pathogenic variants detected in high homology regions of the PMS2 gene. How effective is long-range PCR?
2024 · Daniele Paixão, Thalitta Hetamaro Ayala Lima, et al. · Frontiers in Oncology · 2
Effects of the coronavirus disease 2019 pandemic on anxiety and spirituality in patients with cancer undergoing chemotherapy: A cross-sectional study.
2023 · Francisca Fernanda Barbosa Oliveira, Rosane Oliveira Sant'Ana, et al. · Journal of Clinical Oncology · 1
P075: Evaluation of PMS2 gene variant c.2182_2184delinsG by NGS in a Brazilian sample: How long-range PCR can solve homology?
2023 · Daniele Paixão, Thalitta Hetamaro Ayala Lima, et al. · Genetics in Medicine Open · 1
Prevalence of pathogenic non-BRCA1/2 gene variants in patients with suspected hereditary breast and ovarian cancer at a referral hospital in northeastern Brazil.
2020 · Rosane Oliveira Sant'Ana, Clarissa Gondim Picanço-Albuquerque, et al. · Journal of Clinical Oncology · 1
A new PMS2 gene variant of unknown significance: How pathogenic is it?
2020 · Clarissa Gondim Picanço-Albuquerque, Maria Júlia Barbosa Bezerra, et al. · Journal of Clinical Oncology · 1
Erratum to: Familial chromosomal translocation X; 22 associated with infertility and recurrent X mosaicism
2016 · Juliana Dourado Grzesiuk, Ciro Silveira Pereira, et al. · Molecular Cytogenetics · 1
PDF
Frequent Detection of KRAS ‐G12C and PIK3CA ‐Q546K Mutations in MAP Tumors Highlights their Role in MUTYH Variants of Uncertain Significance Reclassification
2026 · Ana Beatriz Deleame Medeiros, Vanessa Nascimento Kozak, et al. · Human Mutation
Prevalence and clinical correlations of Lynch syndrome (LS) in northeast Brazil.
2023 · Rosane Oliveira Sant'Ana, Isabelle Joyce de Lima Silva-Fernandes, et al. · Journal of Clinical Oncology
Optimization of protein extraction for proteomic analysis of formalin-fixed and paraffin-embedding (FFPE) biopsy specimens from males with breast cancer.
2023 · Maria Júlia Barbosa Bezerra, Jackeline Almeida Silva, et al. · Journal of Clinical Oncology
PDF
Evaluation of the psychological state of patients suspected of Lynch syndrome after the germline genetic testing result.
2023 · Francisca Fernanda Barbosa Oliveira, Rosane Oliveira Sant'Ana, et al. · Journal of Clinical Oncology
MUTYH-related polyposis syndrome associated with a variant of uncertain significance mutation: A new pathogenic mutation?
2022 · Clarissa Gondim Picanço-Albuquerque, Rosane Oliveira Sant'Ana, et al. · Journal of Clinical Oncology
Effects of anxiety and depression on the quality of life of male cancer patients undergoing genetic investigation for hereditary cancer predisposition syndromes.
2022 · Francisca Fernanda Barbosa Oliveira, Paulo Goberlânio de Barros Silva, et al. · Journal of Clinical Oncology
Monoallelic MUTYH mutations and hereditary breast cancer - results of an epidemiologic study in Brazil
2021 · R.O. Sant’Ana, I.J.L. Silva, et al. · The Breast
PDF
Abstract PS9-37: Hereditary breast and ovarian cancer syndrome (HBOC) diagnosis impacts more the life quality of women than men: A case-control report
2021 · Francisca Fernanda Barbosa Oliveira, Paulo Goberlanio de Barros Silva, et al. · Cancer Research
Abstract PS14-27: Oncogenetic caracterization and imunohistochemistry patterns of male cancer breast diagnosticated in Haroldo JuaÇaba hospital, Northeast of Brazil
2021 · Maria Claudia dos Santos Luciano, Maria Júlia Barbosa Bezerra, et al. · Cancer Research
Works count: 32
Citation count: 142
H-index: 7
I10-index: 4
Year
Topic
Type