Monica B. Melo

Campinas, RS, Brazil

Last Updated: 09/26/2026

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Found 8 publications

GWAS for primary angle-closure glaucoma identifies loci related to ocular biometry and morphology.

GWAS for primary angle-closure glaucoma identifies loci related to ocular biometry and morphology.

Journal: Nature communications

Published: November 02, 2024

Angiogenesis-Related Genes in Endothelial Progenitor Cells May Be Involved in Sickle Cell Stroke.

Angiogenesis-Related Genes in Endothelial Progenitor Cells May Be Involved in Sickle Cell Stroke.

Journal: Journal of the American Heart Association

Published: February 04, 2020

Evaluation of oxidative stress-related genetic variants for predicting stroke in patients with sickle cell anemia.

Evaluation of oxidative stress-related genetic variants for predicting stroke in patients with sickle cell anemia.

Journal: Journal of the neurological sciences

Published: December 07, 2019

Association of Genetic Variants With Primary Open-Angle Glaucoma Among Individuals With African Ancestry.

Association of Genetic Variants With Primary Open-Angle Glaucoma Among Individuals With African Ancestry.

Journal: JAMA

Published: November 06, 2019

Association of the CFH Y402H Polymorphism with the 1-Year Response of Exudative AMD to Intravitreal Anti-VEGF Treatment in the Brazilian Population.

Association of the CFH Y402H Polymorphism with the 1-Year Response of Exudative AMD to Intravitreal Anti-VEGF Treatment in the Brazilian Population.

Journal: Ophthalmic research

Published: November 21, 2016

Pharmacogenetic Effect of Complement Factor H Gene Polymorphism in Response to the Initial Intravitreal Injection of Bevacizumab for Wet Age-Related Macular Degeneration.

Pharmacogenetic Effect of Complement Factor H Gene Polymorphism in Response to the Initial Intravitreal Injection of Bevacizumab for Wet Age-Related Macular Degeneration.

Journal: Ophthalmic research

Published: May 31, 2015

Polymorphism in the HMOX1 gene is associated with high levels of fetal hemoglobin in Brazilian patients with sickle cell anemia.

Polymorphism in the HMOX1 gene is associated with high levels of fetal hemoglobin in Brazilian patients with sickle cell anemia.

Journal: Hemoglobin

Published: June 04, 2013

Haptoglobin polymorphism and diabetic retinopathy in Brazilian patients.

Haptoglobin polymorphism and diabetic retinopathy in Brazilian patients.

Journal: Diabetes research and clinical practice

Published: December 15, 2006

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Last Updated: 09/26/2026