Lavínia Schüler-Faccini

51PUBLICATIONS
165CO-AUTHORS
African languagesNeurogeneticsInfant and child healthPublic health nutritionGene mapping
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Publications (51)

|Sep 24, 2026
A novel TYR variant implicated in oculocutaneous albinism type 1 (OCA1): a study in an indigenous population in Southern Brazil.

|Apr 08, 2026
Genetic disorders and congenital anomalies in Nigeria: a scoping review.

Ayoade Desmond Babalola, Nitza Ferreira Muniz, Lavinia Schuler-Faccini

|Mar 25, 2026
Impact of congenital anomalies on infant mortality in the 14th Health Region of Paraná, from 2010 to 2019.

Nitza Ferreira Muniz, Ayoade Desmond Babalola, Maria Antonia Ramos Costa

|Sep 13, 2025
Scientific and Public Health Challenges in Folic Acid Supplementation: Insights from Brazil and Global Implications.

Marília Körbes Rockenbach, Ricardo Rohweder, Lavinia Schuler-Faccini

|May 14, 2025
Spatial analysis of risk areas of congenital anomalies in Brazil, 2012-2021.

Suzana de Souza, Clarissa Gutierrez Carvalho, Lavinia Schuler-Faccini

|May 14, 2025
Orofacial clefts in newborns in Brazil: a time series study, 2010-2021.

Karoline Machado Vieira, Verônica Canarim Menezes, Augusto César Cardoso-Dos-Santos

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Frequent Collaborators

8 joint publications

Fernanda Sales Luiz Vianna

8 joint publications

Maria Teresa Vieira Sanseverino

8 joint publications

Augusto César Cardoso-Dos-Santos

5 joint publications

Lucas Rosa Fraga