Karina Griesi-Oliveira
Karina Griesi-Oliveira
Scientific Researcher at Albert Einstein Hospital, São Paulo, Brasil
Verified email at
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Cited by
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
Transtornos do espectro autista: um guia atualizado para aconselhamento genético
K Griesi-Oliveira, AL Sertié
Einstein (São Paulo) 15, 233-238, 2017
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
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
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
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
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
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
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
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
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
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
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
Improvement of in vitro osteogenic potential through differentiation of induced pluripotent stem cells from human exfoliated dental tissue towards mesenchymal-like stem cells
FAA Ishiy, RD Fanganiello, K Griesi-Oliveira, AM Suzuki, GS Kobayashi, ...
Stem Cells International 2015, 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
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
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
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
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
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
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