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Henrique C. R. Galvão
Henrique C. R. Galvão
Gerente médico na Dasa Genômica / Médico Geneticista
Email confirmado em dasa.com.br - Página inicial
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Ano
Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations
TR Rebbeck, TM Friebel, E Friedman, U Hamann, D Huo, A Kwong, ...
Human mutation 39 (5), 593-620, 2018
2932018
Large scale multifactorial likelihood quantitative analysis of BRCA1 and BRCA2 variants: An ENIGMA resource to support clinical variant classification
MT Parsons, E Tudini, H Li, E Hahnen, B Wappenschmidt, L Feliubadaló, ...
Human mutation 40 (9), 1557-1578, 2019
1212019
Prevalence of BRCA1/BRCA2 mutations in a Brazilian population sample at-risk for hereditary breast cancer and characterization of its genetic ancestry
GC Fernandes, RAD Michelli, HCR Galvão, AE Paula, R Pereira, ...
Oncotarget 7 (49), 80465, 2016
882016
The germline mutational landscape of BRCA1 and BRCA2 in Brazil
EI Palmero, DM Carraro, B Alemar, MAM Moreira, A Ribeiro-dos-Santos, ...
Scientific reports 8 (1), 9188, 2018
782018
Whole‐exome sequencing of non‐BRCA1/BRCA2 mutation carrier cases at high‐risk for hereditary breast/ovarian cancer
PS Felicio, RS Grasel, N Campacci, AE de Paula, HCR Galvão, ...
Human mutation 42 (3), 290-299, 2021
462021
XAF1 as a modifier of p53 function and cancer susceptibility
EM Pinto, BC Figueiredo, W Chen, HCR Galvao, MN Formiga, ...
Science advances 6 (26), eaba3231, 2020
442020
A survey of the clinicopathological and molecular characteristics of patients with suspected Lynch syndrome in Latin America
BM Rossi, EI Palmero, F López-Kostner, C Sarroca, CA Vaccaro, ...
Bmc Cancer 17, 1-26, 2017
412017
Genotype and phenotype landscape of MEN2 in 554 medullary thyroid cancer patients: the BrasMEN study
RMB Maciel, CP Camacho, LVM Assumpção, NE Bufalo, AL Carvalho, ...
Endocrine connections 8 (3), 289-298, 2019
402019
Molecular analysis of TSC1 and TSC2 genes and phenotypic correlations in Brazilian families with tuberous sclerosis
C Rosset, F Vairo, IC Bandeira, RL Correia, FV De Goes, RTB Da Silva, ...
PLoS One 12 (10), e0185713, 2017
322017
From colorectal cancer pattern to the characterization of individuals at risk: Picture for genetic research in Latin America
CA Vaccaro, F López‐Kostner, DV Adriana, EI Palmero, BM Rossi, ...
International journal of cancer 145 (2), 318-326, 2019
262019
Oncogenetics service and the Brazilian public health system: the experience of a reference Cancer Hospital
EI Palmero, HCR Galvão, GC Fernandes, AE Paula, JC Oliveira, ...
Genetics and Molecular Biology 39 (2), 168-177, 2016
232016
A snapshot of current genetic testing practice in Lynch syndrome: The results of a representative survey of 33 Latin American existing centres/registries
A Della Valle, BM Rossi, EI Palmero, M Antelo, CA Vaccaro, ...
European Journal of Cancer 119, 112-121, 2019
202019
Ocular features in 16 Brazilian patients with Williams-Beuren syndrome
MM Viana, M Frasson, H Galvao, LL Leão, M Stofanko, ...
Ophthalmic Genetics 36 (3), 234-238, 2015
182015
New insights on familial colorectal cancer type X syndrome
FAO Garcia, ES de Andrade, H de Campos Reis Galvão, ...
Scientific Reports 12 (1), 2846, 2022
172022
Germline MLH1, MSH2 and MSH6 variants in Brazilian patients with colorectal cancer and clinical features suggestive of Lynch Syndrome
NB Schneider, T Pastor, AE Paula, MI Achatz, ÂR Santos, FSL Vianna, ...
Cancer medicine 7 (5), 2078-2088, 2018
172018
p53 signaling pathway polymorphisms, cancer risk and tumor phenotype in TP53 R337H mutation carriers
GS Macedo, IA Vieira, FSL Vianna, B Alemar, J Giacomazzi, ...
Familial Cancer 17, 269-274, 2018
172018
TP53 variants of uncertain significance: increasing challenges in variant interpretation and genetic counseling
CM Bittar, IA Vieira, CS Sabato, TF Andreis, B Alemar, O Artigalás, ...
Familial cancer 18, 451-456, 2019
132019
The Brazilian TP53 mutation (R337H) and sarcomas
SM Volc, CRN Ramos, HCR Galvão, PS Felicio, AS Coelho, ...
PLoS One 15 (1), e0227260, 2020
102020
Clinicopathological and molecular characterization of Brazilian families at risk for Lynch syndrome
AE de Paula, HCR Galvão, M Bonatelli, C Sabato, GC Fernandes, ...
Cancer Genetics 254, 82-91, 2021
92021
Using Co-segregation and loss of heterozygosity analysis to define the pathogenicity of unclassified variants in hereditary breast cancer patients
RS Grasel, PS Felicio, AE De Paula, N Campacci, FANDO Garcia, ...
Frontiers in Oncology 10, 571330, 2020
92020
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