Get started
Author

Mariana Moysés‐Oliveira

Observed names: M. Moyses-Oliveira, M. Moysés-Oliveira, M. Moysés‐Oliveira, M.M. Oliveira, M.M.-O. Moysés-Oliveira, Mariana M. Oliveira, Mariana Moyses Oliveira, Mariana Moyses-Oliveira, Mariana Moyses-oliveira, Mariana Moysés Oliveira, Mariana Moysés-Oliveira, Moyses-Oliveira, Mariana, Moysés-Oliveira, M., Moysés-Oliveira, Mariana, Moysés-Oliveira,Mariana
Institutions: Broad Institute, Massachusetts General Hospital, Associação Fundo de Incentivo à Pesquisa, Instituto do Sono, Stanley Center for Psychiatric Research, Massachusetts Institute of Technology, Universidade Federal de São Paulo
Observed institutions: Broad Institute, Harvard University, Yale University, Massachusetts General Hospital, Associação Fundo de Incentivo à Pesquisa, Instituto do Sono, Stanley Center for Psychiatric Research, Massachusetts Institute of Technology, Universidade Federal de São Paulo, University of Lausanne
ORCID: 0000-0002-3233-932X
Observed ORCID: 0000-0002-3233-932X
OpenAlex ID: A5000893407
Genetic mechanisms leading to primary amenorrhea in balanced X-autosome translocations
2015 · Mariana Moysés-Oliveira, Roberta dos Santos Guilherme, et al. · Fertility and Sterility · 64
19q13.33→qter trisomy in a girl with intellectual impairment and seizures
2014 · Gianna Carvalheira, Mariana Moysés Oliveira, et al. · Meta Gene · 53
PDF
New gene discoveries highlight functional convergence in autism and related neurodevelopmental disorders
2020 · Mariana Moyses-Oliveira, Rachita Yadav, et al. · Current Opinion in Genetics & Development · 46
Position effect modifying gene expression in a patient with ring chromosome 14
2015 · Roberta Santos Guilherme, Mariana Moysés-Oliveira, et al. · Journal of Applied Genetics · 45
Genetics of premature ovarian insufficiency and the association with X-autosome translocations
2020 · Adriana Di-Battista, Mariana Moysés-Oliveira, et al. · Reproduction · 43
Unusual X‐chromosome inactivation pattern in patients with Xp11.23‐p11.22 duplication: Report and review
2016 · Adriana Di‐Battista, Vera Ayres Meloni, et al. · American Journal of Medical Genetics Part A · 40
X‐linked intellectual disability related genes disrupted by balanced X‐autosome translocations
2015 · Mariana Moysés‐Oliveira, Roberta Santos Guilherme, et al. · American Journal of Medical Genetics Part B Neuropsychiatric Genetics · 39
Transcriptional and functional consequences of alterations to MEF2C and its topological organization in neuronal models
2022 · Kiana Mohajeri, Rachita Yadav, et al. · The American Journal of Human Genetics · 34
The Natural History of a Man With Ovotesticular 46,XX DSD Caused by a Novel 3-Mb 15q26.2 Deletion Containing NR2F2 Gene
2019 · Gianna Carvalheira, Andrea M Malinverni, et al. · Journal of the Endocrine Society · 31
Inactivation of AMMECR1 is associated with growth, bone, and heart alterations
2017 · Mariana Moysés-Oliveira, Giuliana Giannuzzi, et al. · Human Mutation · 28
PDF
Convergent coexpression of autism-associated genes suggests some novel risk genes may not be detectable in large-scale genetic studies
2023 · Calwing Liao, Mariana Moyses-Oliveira, et al. · Cell Genomics · 24
The impact of 22q11.2 copy-number variants on human traits in the general population
2023 · Malú Zamariolli, Chiara Auwerx, et al. · The American Journal of Human Genetics · 20
Incorporation of 5-ethynyl-2′-deoxyuridine (EdU) as a novel strategy for identification of the skewed X inactivation pattern in balanced and unbalanced X-rearrangements
2015 · Luiza Sisdelli, Angela Cristina Vidi, et al. · Human Genetics · 20
Sclerocornea in a patient with van den Ende–Gupta syndrome homozygous for a SCARF2 microdeletion
2014 · Michele P. Migliavacca, Nara L. M. Sobreira, et al. · American Journal of Medical Genetics Part A · 19
PDF
Breakpoint mapping at nucleotide resolution in X-autosome balanced translocations associated with clinical phenotypes
2019 · Mariana Moysés-Oliveira, Adriana Di-Battista, et al. · European Journal of Human Genetics · 18
PDF
Copy number variation (CNV) identification, interpretation, and database from Brazilian patients
2020 · Victória Cabral Silveira Monteiro de Godoy, Fernanda Teixeira Bellucco, et al. · Genetics and Molecular Biology · 16
PDF
Rare single‐nucleotide variants in oculo‐auriculo‐vertebral spectrum (OAVS)
2019 · Malú Zamariolli, Mileny Colovati, et al. · Molecular Genetics & Genomic Medicine · 14
PDF
Genetic basis of sleep phenotypes and rare neurodevelopmental syndromes reveal shared molecular pathways
2023 · Mariana Moysés‐Oliveira, Mayara Paschalidis, et al. · Journal of Neuroscience Research · 11
Novel MYT1 variants expose the complexity of oculo‐auriculo‐vertebral spectrum genetic mechanisms
2021 · Malú Zamariolli, Bruna Burssed, et al. · American Journal of Medical Genetics Part A · 11
Premature ovarian insufficiency is associated with global alterations in the regulatory landscape and gene expression in balanced X-autosome translocations
2023 · Adriana Di-Battista, Bianca Pereira Favilla, et al. · Epigenetics & Chromatin · 10
PDF
Search for appropriate reference genes for quantitative reverse transcription PCR studies in somite, prosencephalon and heart of early mouse embryo
2019 · Mariana Moysés-Oliveira, Victória Cabral, et al. · Gene · 10
Shared genetic mechanisms underlying association between sleep disturbances and depressive symptoms
2024 · Mariana Moyses-Oliveira, Malu Zamariolli, et al. · Sleep Medicine · 8
Parallelized engineering of mutational models using piggyBac transposon delivery of CRISPR libraries
2023 · Xander Nuttle, Nicholas D. Burt, et al. · Cell Reports Methods · 7
22q11.2 Deletion Syndrome due to a Translocation t(6;22) in a Patient Conceived via in vitro Fertilization
2015 · Anelisa Gollo Dantas, Adriana Bortolai, et al. · Molecular Syndromology · 7
Unlocking the role of Galectin-3: Implications for sleep disorders and health
2024 · Monica Levy Andersen, Mariana Moyses-Oliveira, et al. · Sleep Medicine · 6
Works count: 109
Citation count: 714
H-index: 16
I10-index: 21
Year
Topic
Type