Detalhe da pesquisa
1.
Bilateral Peters' anomaly, aniridia and Wilms tumour (WAGR syndrome) in monozygotic twins.
Acta Paediatr;
113(6): 1420-1425, 2024 Jun.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38363039
2.
IFITM3 rs12252 polymorphism association with COVID-19 severity and mortality in a Brazilian sample: an update and a meta-analysis.
An Acad Bras Cienc;
96(2): e20231160, 2024.
Artigo
em Inglês
| MEDLINE
| ID: mdl-38808879
3.
Chronic rhinosinusitis with nasal polyps does not harbor KRAS, BRAF, and EGFR mutations.
J Oral Pathol Med;
52(5): 426-430, 2023 May.
Artigo
em Inglês
| MEDLINE
| ID: mdl-36116035
4.
Association of 3p21.31 Locus (CXCR6 and LZTFL1) with COVID-19 Outcomes in Brazilian Hospitalyzed Subjects.
Curr Microbiol;
80(10): 319, 2023 Aug 14.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37578643
5.
Adenoid ameloblastoma harbors beta-catenin mutations.
Mod Pathol;
35(11): 1562-1569, 2022 11.
Artigo
em Inglês
| MEDLINE
| ID: mdl-35840721
6.
Whole-exome sequencing reveals novel vacuolar ATPase genes' variants and variants in genes involved in lysosomal biology and autophagosomal formation in oral granular cell tumors.
J Oral Pathol Med;
50(4): 410-417, 2021 Apr.
Artigo
em Inglês
| MEDLINE
| ID: mdl-33289181
7.
Definition of Late Onset Alzheimer's Disease and Anticipation Effect of Genome-Wide Significant Risk Variants: Pilot Study of the APOE e4 Allele.
Neuropsychobiology;
77(1): 8-12, 2019.
Artigo
em Inglês
| MEDLINE
| ID: mdl-30110694
8.
Ocular alterations, molecular findings, and three novel pathological mutations in a series of NF2 patients.
Graefes Arch Clin Exp Ophthalmol;
257(7): 1453-1458, 2019 Jul.
Artigo
em Inglês
| MEDLINE
| ID: mdl-31089872
9.
Spectrum of germline mutations in smokers and non-smokers in Brazilian non-small-cell lung cancer (NSCLC) patients.
Carcinogenesis;
38(11): 1112-1118, 2017 10 26.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28968711
10.
The In Vitro and In Vivo Antiangiogenic Effects of Flavokawain B.
Phytother Res;
31(10): 1607-1613, 2017 Oct.
Artigo
em Inglês
| MEDLINE
| ID: mdl-28816367
11.
Malignant phenotype and two SDHD mutations in a family with paraganglioma syndrome type 1.
Genet Res (Camb);
97: e3, 2015 Mar 30.
Artigo
em Inglês
| MEDLINE
| ID: mdl-25819804
12.
Spectrum of somatic EGFR, KRAS, BRAF, PTEN mutations and TTF-1 expression in Brazilian lung cancer patients.
Genet Res (Camb);
96: e002, 2014.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24594201
13.
Association of angiotensin type 2 receptor gene polymorphisms with ureteropelvic junction obstruction in Brazilian patients.
Nephrology (Carlton);
19(11): 714-20, 2014 Nov.
Artigo
em Inglês
| MEDLINE
| ID: mdl-24995698
14.
Sociodemographic characteristics, clinical factors, and genetic polymorphisms associated with Alzheimer's disease.
Int J Geriatr Psychiatry;
28(6): 640-6, 2013 Jun.
Artigo
em Inglês
| MEDLINE
| ID: mdl-22899317
15.
Association analysis of CFH and ARMS2 gene polymorphisms in a Brazilian cohort with age-related macular degeneration.
Ophthalmic Res;
50(2): 117-22, 2013.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23867343
16.
Evaluation of clinical and genetic factors in obstructive sleep apnoea.
Acta Otorhinolaryngol Ital;
43(6): 409-416, 2023 Dec.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37814975
17.
Whole-exome identifies germline variants in families with obstructive sleep apnea syndrome.
Front Genet;
14: 1137817, 2023.
Artigo
em Inglês
| MEDLINE
| ID: mdl-37229194
18.
The contribution of FTO and UCP-1 SNPs to extreme obesity, diabetes and cardiovascular risk in Brazilian individuals.
BMC Med Genet;
13: 101, 2012 Nov 07.
Artigo
em Inglês
| MEDLINE
| ID: mdl-23134754
19.
Genetic association of the PERIOD3 (PER3) Clock gene with extreme obesity.
Obes Res Clin Pract;
15(4): 334-338, 2021.
Artigo
em Inglês
| MEDLINE
| ID: mdl-34215556
20.
Germline Mutations in Familial Papillary Thyroid Cancer.
Endocr Pathol;
31(1): 14-20, 2020 Mar.
Artigo
em Inglês
| MEDLINE
| ID: mdl-32034658