Detalhe da pesquisa
1.
SH2B1 variants as potential causes of non-syndromic monogenic obesity in a Brazilian cohort.
Eat Weight Disord
; 27(8): 3665-3674, 2022 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-36436143
2.
Study of LEP, MRAP2 and POMC genes as potential causes of severe obesity in Brazilian patients.
Eat Weight Disord
; 26(5): 1399-1408, 2021 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-32578125
3.
Association of the MC4R rs17782313 polymorphism with plasma ghrelin, leptin, IL6 and TNFα concentrations, food intake and eating behaviors in morbidly obese women.
Eat Weight Disord
; 26(4): 1079-1087, 2021 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-32918257
4.
Application of WHO International Biological Reference Standards to evaluate commercial serological tests for chronic Chagas disease.
Mem Inst Oswaldo Cruz
; 115: e200214, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32725060
5.
Genetic variants in the fat mass and obesity-associated (FTO) gene confer risk for extreme obesity and modulate adiposity in a Brazilian population.
Genet Mol Biol
; 43(1): e20180264, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32154826
6.
Human glutathione S-transferase polymorphisms associated with prostate cancer in the Brazilian population.
Int Braz J Urol
; 40(4): 463-73, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-25251951
7.
Human N-acetyltransferase 2 (NAT2) gene variability in Brazilian populations from different geographical areas.
Front Pharmacol
; 14: 1278720, 2023.
Artigo
em Inglês
| MEDLINE | ID: mdl-38035025
8.
Polymorphisms upstream of the melanocortin-1 receptor coding region are associated with human pigmentation variation in a Brazilian population.
Am J Hum Biol
; 24(6): 853-5, 2012.
Artigo
em Inglês
| MEDLINE | ID: mdl-22961816
9.
HLA-A*01 allele: a risk factor for dengue haemorrhagic fever in Brazil's population.
Mem Inst Oswaldo Cruz
; 107(2): 224-30, 2012 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-22415262
10.
Identification of Variants Responsible for Monogenic Forms of Diabetes in Brazil.
Front Endocrinol (Lausanne)
; 13: 827325, 2022.
Artigo
em Inglês
| MEDLINE | ID: mdl-35592779
11.
Genetic polymorphisms of NAT2, CYP2E1 and GST enzymes and the occurrence of antituberculosis drug-induced hepatitis in Brazilian TB patients.
Mem Inst Oswaldo Cruz
; 106(6): 716-24, 2011 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-22012226
12.
Next-Generation Sequencing for Molecular Diagnosis of Cystic Fibrosis in a Brazilian Cohort.
Dis Markers
; 2021: 9812074, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33613790
13.
A Rare Potential Pathogenic Variant in the BDNF Gene is Found in a Brazilian Patient with Severe Childhood-Onset Obesity.
Diabetes Metab Syndr Obes
; 14: 11-22, 2021.
Artigo
em Inglês
| MEDLINE | ID: mdl-33442278
14.
Identification of the First PAX4-MODY Family Reported in Brazil.
Diabetes Metab Syndr Obes
; 13: 2623-2631, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32801813
15.
Genetic Variants in the Activation of the Brown-Like Adipocyte Pathway and the Risk for Severe Obesity.
Obes Facts
; 13(2): 130-143, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32325455
16.
Identification of a Rare and Potential Pathogenic MC4R Variant in a Brazilian Patient With Adulthood-Onset Severe Obesity.
Front Genet
; 11: 608840, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-33362866
17.
The association of the fat mass and obesity-associated gene (FTO) rs9939609 polymorphism and the severe obesity in a Brazilian population.
Diabetes Metab Syndr Obes
; 12: 667-684, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31213864
18.
Identification of a novel large deletion and other copy number variations in the CFTR gene in patients with Cystic Fibrosis from a multiethnic population.
Mol Genet Genomic Med
; 7(7): e00645, 2019 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-31199594
19.
The first case of NEUROD1-MODY reported in Latin America.
Mol Genet Genomic Med
; 7(12): e989, 2019 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-31578821
20.
Identification of the MC4R start lost mutation in a morbidly obese Brazilian patient.
Diabetes Metab Syndr Obes
; 12: 257-266, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-30863132