Greice A. Molfetta

Otorhynolaryngology And Head And Neck Surgery
Ribeirao Preto, SP, Brazil

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 14 publications

Familial keratoconus across three generations: Co-segregation of a COL11A1 c.3185G>A (p.Arg1062His) variant.

Familial keratoconus across three generations: Co-segregation of a COL11A1 c.3185G>A (p.Arg1062His) variant.

Journal: The ocular surface

Published: May 16, 2026

Novel germline GATA1s-generating variant associates with somatic STAG2 variants in hypoplastic myelodysplastic neoplasm.

Novel germline GATA1s-generating variant associates with somatic STAG2 variants in hypoplastic myelodysplastic neoplasm.

Journal: British journal of haematology

Published: March 16, 2026

Non-Syndromic Intellectual Disability and Its Pathways: A Long Noncoding RNA Perspective.

Non-Syndromic Intellectual Disability and Its Pathways: A Long Noncoding RNA Perspective.

Journal: Non-coding RNA

Published: November 12, 2020

Molecular basis of various forms of maple syrup urine disease in Chilean patients.

Molecular basis of various forms of maple syrup urine disease in Chilean patients.

Journal: Molecular genetics & genomic medicine

Published: July 10, 2020

Lynch syndrome identification in a Brazilian cohort of endometrial cancer screened by a universal approach.

Lynch syndrome identification in a Brazilian cohort of endometrial cancer screened by a universal approach.

Journal: Gynecologic oncology

Published: June 03, 2020

Germline variants in DNA repair genes associated with hereditary breast and ovarian cancer syndrome: analysis of a 21 gene panel in the Brazilian population.

Germline variants in DNA repair genes associated with hereditary breast and ovarian cancer syndrome: analysis of a 21 gene panel in the Brazilian population.

Journal: BMC medical genomics

Published: October 14, 2019

Molecular basis of familial adenomatous polyposis in the southeast of Brazil: identification of six novel mutations.

Molecular basis of familial adenomatous polyposis in the southeast of Brazil: identification of six novel mutations.

Journal: The International journal of biological markers

Published: March 12, 2019

Whole transcriptome analysis reveals correlation of long noncoding RNA ZEB1-AS1 with invasive profile in melanoma.

Whole transcriptome analysis reveals correlation of long noncoding RNA ZEB1-AS1 with invasive profile in melanoma.

Journal: Scientific reports

Published: August 21, 2018

A non-functional galanin receptor-2 in a multiple sclerosis patient.

A non-functional galanin receptor-2 in a multiple sclerosis patient.

Journal: The pharmacogenomics journal

Published: November 26, 2017

Mutational screening in the LDLR gene among patients presenting familial hypercholesterolemia in the Southeast of Brazil.

Mutational screening in the LDLR gene among patients presenting familial hypercholesterolemia in the Southeast of Brazil.

Journal: Genetics and molecular research : GMR

Published: September 06, 2017

Mitochondrial transcription factor A (TFAM) shapes metabolic and invasion gene signatures in melanoma.

Mitochondrial transcription factor A (TFAM) shapes metabolic and invasion gene signatures in melanoma.

Journal: Scientific reports

Published: July 13, 2017

Clinical profile and molecular characterization of Galactosemia in Brazil: identification of seven novel mutations.

Clinical profile and molecular characterization of Galactosemia in Brazil: identification of seven novel mutations.

Journal: BMC medical genetics

Published: June 20, 2015

Showing 1-12 of 14

Last Updated: 09/26/2026