Cláudia Fernandes Lorea (Cláudia F Lorea)

Publication Activity (10 Years)

Years Active: 2020-2021
Publications (10 Years): 2

Top Topics

Autism Spectrum Disorder

Pulmonary Hypertension

Aortic Valve Replacement

Top Venues

Proceedings of the National Academy of Sciences of the United States of America

Journal of pediatric genetics

Hospital Escola da Universidade Federal de Pelotas

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Hospital Escola da Universidade Federal de Pelotas Jul 01 2016

Brazil

Médica Geneticista :: Unidade de Atenção à saúde da criança e do adolescente

Publications

Carson J Bryant, Cláudia Fernandes Lorea, Hiram Larangeira de Almeida, Letícia Weinert, Leonardo Vedolin, Filippo Pinto E Vairo, Susan J Baserga
Biallelic splicing variants in the nucleolar 60S assembly factor RBM28 cause the ribosomopathy ANE syndrome. Proceedings of the National Academy of Sciences of the United States of America 118 (19) (2021)
Bruna Lixinski Diniz, Andressa Schneiders Santos, Andressa Barreto Glaeser, Bruna Baierle Guaraná, Cláudia Fernandes Lorea, Juliana Alves Josahkian, Janaína Huber, Rafael Fabiano Machado Rosa, Paulo Ricardo Gazzola Zen
Congenital Heart Defects and Dysmorphic Facial Features in Patients Suspicious of 22q11.2 Deletion Syndrome in Southern Brazil. Journal of pediatric genetics 9 (4) (2020)