| Discordant congenital Zika syndrome twins show differential in vitro viral susceptibility of neural progenitor cells LC Caires-Júnior, E Goulart, US Melo, BHS Araujo, L Alvizi, ... Nature communications 9 (1), 475, 2018 | 123 | 2018 |
| Overexpression of KLC2 due to a homozygous deletion in the non-coding region causes SPOAN syndrome US Melo, LI Macedo-Souza, T Figueiredo, AR Muotri, JG Gleeson, ... Human molecular genetics 24 (24), 6877-6885, 2015 | 57 | 2015 |
| A homozygous loss-of-function mutation in inositol monophosphatase 1 (IMPA1) causes severe intellectual disability T Figueiredo, US Melo, ALS Pessoa, PR Nobrega, JP Kitajima, H Rusch, ... Molecular psychiatry 21 (8), 1125-1129, 2016 | 30 | 2016 |
| Homozygous missense mutation in MED25 segregates with syndromic intellectual disability in a large consanguineous family T Figueiredo, US Melo, ALS Pessoa, PR Nobrega, JP Kitajima, I Correa, ... Journal of Medical Genetics 52 (2), 123-127, 2015 | 29 | 2015 |
| Reconsidering the association between the major histocompatibility complex and bipolar disorder TC Figueiredo, JRM de Oliveira Journal of molecular neuroscience 47, 26-30, 2012 | 27 | 2012 |
| Molecular analysis of brazilian patients with combined pituitary hormone deficiency and orthotopic posterior pituitary lobe reveals eight different PROP1 alterations … JLO Madeira, MY Nishi, M Nakaguma, AF Benedetti, IP Biscotto, ... Clinical endocrinology 87 (6), 725-732, 2017 | 16 | 2017 |
| Different gene expression profiles in iPSC-derived motor neurons from ALS8 patients with variable clinical courses suggest mitigating pathways for neurodegeneration D Oliveira, DA Morales-Vicente, MS Amaral, L Luz, AL Sertié, FS Leite, ... Human molecular genetics 29 (9), 1465-1475, 2020 | 14 | 2020 |
| Inositol monophosphatase 1 (IMPA1) mutation in intellectual disability patients impairs neurogenesis but not gliogenesis T Figueiredo, APD Mendes, DP Moreira, E Goulart, D Oliveira, ... Molecular Psychiatry 26 (7), 3558-3571, 2021 | 9 | 2021 |
| Reliability of information on people with disabilities gathered by community health workers in highly consanguineous communities of Northeastern Brazil FRL Lopes, KS Monteiro, T Figueiredo, TC Wanderley, TA Pequeno, ... BMC Health Services Research 17, 1-9, 2017 | 9 | 2017 |
| Loss-of-function mutation in inositol monophosphatase 1 (IMPA1) results in abnormal synchrony in resting-state EEG CP Walker, ALS Pessoa, T Figueiredo, M Rafferty, US Melo, PR Nóbrega, ... Orphanet Journal of Rare Diseases 14, 1-10, 2019 | 5 | 2019 |
| Discordant congenital Zika syndrome twins show differen‑tial in vitro viral susceptibility of neural progenitor cells. Nat Commun 9 (1): 475 LC Caires-Junior, E Goulart, US Melo, BHS Araujo, L Alvizi, ... | 5 | 2018 |
| Publisher Correction: Discordant congenital Zika syndrome twins show differential in vitro viral susceptibility of neural progenitor cells LC Caires-Júnior, E Goulart, US Melo, BHS Araujo, L Alvizi, ... Nature Communications 9 (1), 1114, 2018 | 4 | 2018 |
| Discordant congenital Zika syndrome twins show differential in vitro viral susceptibility of neural progenitor cells LC CAIRES JR, E GOULART, US MELO, BSH ARAUJO, L ALVIZI, ... Nature Communications, 2018 | 2 | 2018 |
| Neuropsychological Characterization of Autosomal Recessive Intellectual Developmental Disorder 59 Associated with IMPA1 (MRT59) ALS Pessoa, AA Quesada, PR Nóbrega, APO Viana, KT de Oliveira, ... Brain Sciences 13 (7), 1048, 2023 | 1 | 2023 |
| Novel ERLIN2 variant expands the phenotype of Spastic Paraplegia 18 GC de Souza, MC Malta, MRS Santos, MÍB Fontes, JL de Sousa Anjos, ... Neurological Sciences 45 (6), 2705-2710, 2024 | | 2024 |
| DEFICIÊNCIA INTELECTUAL EM MACEIÓ-AL: UM RETRATO EPIDEMIOLÓGICO EM INSTITUIÇÕES DE REABILITAÇÃO INTELECTUAL MRS Santos, MC Malta, RWP Malta, JLD Lima, JBBC Santos, ... Gep News 7 (2), 208-214, 2023 | | 2023 |
| PREVALÊNCIA DOS NASCIDOS VIVOS COM ANOMALIAS CONGÊNITAS E SUA RELAÇÃO COM A MORTALIDADE FETAL E INFANTIL EM ALAGOAS MC Malta, T Figueiredo Gep News 5 (1), 55-57, 2021 | | 2021 |
| Using ESTs database to predict and validate single polymorphisms at the HLA system TC Figueiredo, JRM de Oliveira International Journal of Immunogenetics 39 (3), 253-257, 2012 | | 2012 |
