Tatiana Ferreira de Almeida

Exomic variants of an elderly cohort of Brazilians in the ABraOM database

D. Y. Sunaga, Nam Pho, E. Amaro, 2017, Human mutation.

The role of the doctor in precision medicine

Tatiana Ferreira de Almeida, 2019, Einstein.

Genomic study of nonsyndromic hearing loss in unaffected individuals: Frequency of pathogenic and likely pathogenic variants in a Brazilian cohort of 2,097 genomes

M. Cervato, R. Guedes, Tatiana Ferreira de Almeida, 2022, Frontiers in Genetics.

A clinical follow-up of 35 Brazilian patients with Prader-Willi Syndrome

C. Kim, Tatiana Ferreira de Almeida, D. Bertola, 2012, Clinics.

Tegumentary manifestations of Noonan and Noonan-related syndromes

A. Pereira, C. Kim, Tatiana Ferreira de Almeida, 2013, Clinics.

Meta‐Analyses Support Previous and Novel Autism Candidate Genes: Outcomes of an Unexplored Brazilian Cohort

S. Scherer, A. Chan, M. Passos-Bueno, 2019, Autism research : official journal of the International Society for Autism Research.

The hospital Israelita Albert Einstein standards for constitutional sequence variants classification: version 2023

M. Cervato, Tatiana Ferreira de Almeida, J. Ceroni, 2023, Human Genomics.