Vera Lúcia Gil-da-Silva-Lopes

22PUBLICATIONS
50CO-AUTHORS
Molecular evolutionGenetic immunologyEpigenetics (incl. genome methylation and epigenomics)Social epidemiologyDevelopmental genetics (incl. sex determination)
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Publications (22)

|Oct 16, 2026
A Novel Homozygous Nonsense Variant in DCHS1 in a Brazilian Patient With Van Maldergem Syndrome Type 1: Clinical Report and Literature Review.

|Jul 29, 2026
Whole-genome sequencing in Brazilian patients with neurofibromatosis type 1, including novel variants, incidental findings, and dual diagnoses.

|May 21, 2026
A comprehensive approach to users from a Brazilian clinical genetics service: an observational study.

|Jul 06, 2024
Comprehensive insights into health services accessibility and quality of life of families with individuals with 22q11.2 deletion syndrome in Brazil.

Isabela Mayá Wayhs Silva, Vera Lúcia Gil-da-Silva-Lopes

|Apr 27, 2024
22q11.2 Deletion Syndrome: Influence of Parental Origin on Clinical Heterogeneity.

Melissa Bittencourt de Wallau, Ana Carolina Xavier, Carolina Araújo Moreno

|Apr 27, 2024
Syndromic Retinitis Pigmentosa: A 15-Patient Study.

Ianne Pessoa Holanda, Priscila Hae Hyun Rim, Rare Genomes Project Consortium

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Frequent Collaborators

9 joint publications

Társis Paiva Vieira

5 joint publications

Carlos Eduardo Steiner

3 joint publications

Milena Atique-Tacla

2 joint publications

Ilária Cristina Sgardioli