C. Rocha

The CIITA genetic polymorphism rs4774*C in combination with the HLA-DRB1*15:01 allele as a putative susceptibility factor to multiple sclerosis in Brazilian females.

E. Gasparetto, S. Alves-Leon, F. Malfetano, 2015, Arquivos de neuro-psiquiatria.

Prader-Willi-like phenotypes: a systematic review of their chromosomal abnormalities.

C. Rocha, C. Paiva, 2014, Genetics and molecular research : GMR.

Haplotype analysis of the CAG and CCG repeats in 21 Brazilian families with Huntington’s disease

P. Cabello, E. Medina-Acosta, R. Alvarenga, 2012, Journal of Human Genetics.

Monosomy 1 p 36 syndrome : reviewing the correlation between deletion sizes and phenotypes

S. Santos, C. Rocha, C. Paiva, 2016 .

SOD1 in amyotrophic lateral sclerosis development – in silico analysis and molecular dynamics of A4F and A4V variants

Lorena Giannini Alves Moreira, G. Pereira, A. N. R. Da Silva, 2019, Journal of cellular biochemistry.

Mini-Review: Monosomy 1p36 syndrome: reviewing the correlation between deletion sizes and phenotypes.

S. Santos, C. Rocha, C. Paiva, 2016, Genetics and Molecular Research.

Haplotype analysis of the CAG and CCG repeats in 21 Brazilian families with Huntington's disease This article has been corrected since Advance Online Publication, and an erratum is also printed in this issue.

S. Santos, E. Paradela, C. Rocha, 2012 .