Caio Robledo D'Angioli Costa Quaio

12PUBLICATIONS
56CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Developmental genetics (incl. sex determination)Epigenetics (incl. genome methylation and epigenomics)Epidemiological modelling
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Publications (12)

|May 13, 2025
A decade of whole-exome sequencing in Brazilian Neurology: from past insights to future perspectives.

Caio Robledo D'Angioli Costa Quaio, Thiago Yoshinaga Tonholo Silva, Orlando G Barsottini

|Aug 14, 2024
Principles of clinical genetics for rheumatologists: clinical indications and interpretation of broad-based genetic testing.

Renan Rodrigues Neves Ribeiro do Nascimento, Caio Robledo D'Angioli Costa Quaio, Christine Hsiaoyun Chung

|Mar 07, 2024
EVALUATION OF AGREEMENT BETWEEN C/T-13910 POLYMORPHISM GENOTYPING RESULTS AND LACTOSE TOLERANCE TEST RESULTS: A RETROSPECTIVE POPULATION-BASED STUDY IN BRAZIL.

Marcia Wehba Esteves Cavichio, Caio Robledo D'Angioli Costa Quaio, Wagner Antonio da Rosa Baratela

|Nov 16, 2023
The hospital Israelita Albert Einstein standards for constitutional sequence variants classification: version 2023.

Caio Robledo D'Angioli Costa Quaio, José Ricardo Magliocco Ceroni, Michele Araújo Pereira

|Sep 14, 2022
Exome sequencing of 500 Brazilian patients with rare diseases: what we have learned.

Caio Robledo D'Angioli Costa Quaio, Caroline Monaco Moreira, Christine Hsiaoyun Chung

|Aug 18, 2022
Expansion and mechanistic insights into de novo DEAF1 variants in DEAF1-associated neurodevelopmental disorders.

Stacey R McGee, Shivakumar Rajamanickam, Sandeep Adhikari

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Frequent Collaborators

2 joint publications

Christine Hsiaoyun Chung

2 joint publications

Sandro Felix Perazzio

2 joint publications

Thiago Yoshinaga Tonholo Silva

1 joint publications

Letícia Rocha