| Transtornos do espectro autista: um guia atualizado para aconselhamento genético K Griesi-Oliveira, AL Sertié Einstein (São Paulo) 15, 233-238, 2017 | 223* | 2017 |
| Modeling non-syndromic autism and the impact of TRPC6 disruption in human neurons K Griesi-Oliveira, A Acab, AR Gupta, DY Sunaga, T Chailangkarn, X Nicol, ... Molecular psychiatry 20 (11), 1350-1365, 2015 | 222 | 2015 |
| 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 | 131 | 2018 |
| Transcriptome of iPSC-derived neuronal cells reveals a module of co-expressed genes consistently associated with autism spectrum disorder K Griesi-Oliveira, MS Fogo, BGG Pinto, AY Alves, AM Suzuki, AG Morales, ... Molecular psychiatry 26 (5), 1589-1605, 2021 | 74 | 2021 |
| Maintenance and differentiation of neural stem cells KB Massirer, C Carromeu, K Griesi‐Oliveira, AR Muotri Wiley Interdisciplinary Reviews: Systems Biology and Medicine 3 (1), 107-114, 2011 | 64 | 2011 |
| Dysfunctional mTORC1 signaling: a convergent mechanism between syndromic and nonsyndromic forms of autism spectrum disorder? J Magdalon, SM Sánchez-Sánchez, K Griesi-Oliveira, AL Sertié International Journal of Molecular Sciences 18 (3), 659, 2017 | 62 | 2017 |
| 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 | 59 | 2015 |
| Rare RELN variants affect Reelin–DAB1 signal transduction in autism spectrum disorder SM Sánchez‐Sánchez, J Magdalon, K Griesi‐Oliveira, GL Yamamoto, ... Human mutation 39 (10), 1372-1383, 2018 | 45 | 2018 |
| Auriculo-condylar syndrome: mapping of a first locus and evidence for genetic heterogeneity C Masotti, KG Oliveira, F Poerner, A Splendore, J Souza, RS Freitas, ... European journal of human genetics 16 (2), 145-152, 2008 | 45 | 2008 |
| EIF4A3 deficient human iPSCs and mouse models demonstrate neural crest defects that underlie Richieri-Costa-Pereira syndrome EE Miller, GS Kobayashi, CM Musso, M Allen, FAA Ishiy, LC de Caires Jr, ... Human molecular genetics 26 (12), 2177-2191, 2017 | 41 | 2017 |
| Collybistin binds and inhibits mTORC1 signaling: a potential novel mechanism contributing to intellectual disability and autism COF Machado, K Griesi-Oliveira, C Rosenberg, F Kok, S Martins, ... European Journal of Human Genetics 24 (1), 59-65, 2016 | 39 | 2016 |
| HTR1B and HTR2C in autism spectrum disorders in Brazilian families GM Orabona, K Griesi-Oliveira, E Vadasz, VLS Bulcão, V Takahashi, ... Brain Research 1250, 14-19, 2009 | 38 | 2009 |
| Actin cytoskeleton dynamics in stem cells from autistic individuals K Griesi-Oliveira, AM Suzuki, AY Alves, ACCN Mafra, GL Yamamoto, ... Scientific reports 8 (1), 11138, 2018 | 37 | 2018 |
| Improvement of In Vitro Osteogenic Potential through Differentiation of Induced Pluripotent Stem Cells from Human Exfoliated Dental Tissue towards Mesenchymal … FAA Ishiy, RD Fanganiello, K Griesi-Oliveira, AM Suzuki, GS Kobayashi, ... Stem Cells International 2015 (1), 249098, 2015 | 37 | 2015 |
| Investigation of 15q11-q13, 16p11. 2 and 22q13 CNVs in autism spectrum disorder Brazilian individuals with and without epilepsy DP Moreira, K Griesi-Oliveira, AL Bossolani-Martins, NCV Lourenço, ... PLoS One 9 (9), e107705, 2014 | 32 | 2014 |
| Altered mTORC1 signaling in multipotent stem cells from nearly 25% of patients with nonsyndromic autism spectrum disorders AM Suzuki, K Griesi-Oliveira, C de Oliveira Freitas Machado, E Vadasz, ... Molecular psychiatry 20 (5), 551-552, 2015 | 25 | 2015 |
| Stem cells as a good tool to investigate dysregulated biological systems in autism spectrum disorders K Griesi‐Oliveira, DY Sunaga, L Alvizi, E Vadasz, MR Passos‐Bueno Autism Research 6 (5), 354-361, 2013 | 18 | 2013 |
| Complement C4 is reduced in iPSC-derived astrocytes of autism spectrum disorder subjects F Mansur, AL Teles e Silva, AKS Gomes, J Magdalon, JS de Souza, ... International Journal of Molecular Sciences 22 (14), 7579, 2021 | 17 | 2021 |
| Detection of small copy number variations (CNVs) in autism spectrum disorder (ASD) by custom array comparative genomic hybridization (aCGH) ES Moreira, IMW Silva, N Lourenco, DP Moreira, CM Ribeiro, ALB Martins, ... Research in Autism Spectrum Disorders 23, 145-151, 2016 | 14 | 2016 |
| A complex chromosomal rearrangement involving chromosomes 2, 5, and X in autism spectrum disorder K Griesi‐Oliveira, DP Moreira, N Davis‐Wright, S Sanders, C Mason, ... American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 159 …, 2012 | 11 | 2012 |
Alysson MuotriUniversity of California, San DiegoVerified email at ucsd.edu
