Mariana Moysés‐Oliveira

Author

Also Known As

M. Moyses-Oliveira, M. Moysés 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

103

Publications

711

Citations

H-Index

Concepts

All Affiliations

Universidade Federal de São Paulo University of Lausanne Jena University Hospital Friedrich Schiller University Jena Broad Institute

About

Mariana Moysés‐Oliveira is an author at Universidade Federal de São Paulo specializing in medicine, genetics, and molecular genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	7	7	258
2	Natural Sciences	2	2	65
3	Engineering	1	1	19
4	Public Health	1	1	19
5	Social Sciences	1	1	27

Mariana Moysés‐Oliveira

Publications

483

Citations

H-Index

Page 1

	Year	Citations
Genetic mechanisms leading to primary amenorrhea in balanced X-autosome translocations Mariana Moysés‐Oliveira, Roberta dos Santos Guilherme, Anelisa Gollo Dantas, Fertility and Sterility Primary AmenorrheaChromosome DynamicsCell DivisionGenetic DisorderGenetics	2015	65
19q13.33→qter trisomy in a girl with intellectual impairment and seizures Gianna Carvalheira, Mariana Moysés‐Oliveira, S.S. Takeno, Meta Gene CytogeneticsGeneticsMolecular BiologyMolecular GeneticsGenomics	2014	49
Position effect modifying gene expression in a patient with ring chromosome 14 Roberta Santos Guilherme, Mariana Moysés‐Oliveira, Anelisa Gollo Dantas, Journal of Applied Genetics ChromatinChromosome DynamicsChromatin StructurePosition EffectNatural Sciences	2015	46
Plasmid-mediated extended-spectrum beta-lactamase-producing strains of Enterobacteriaceae isolated from diabetes foot infections in a Brazilian diabetic center Renato Motta, Mariana Moysés‐Oliveira, P S F Magalhães, The Brazilian Journal of Infectious Diseases	2003	42
X‐linked intellectual disability related genes disrupted by balanced X‐autosome translocations Mariana Moysés‐Oliveira, Roberta Santos Guilherme, Vera Ayres Meloni, American Journal of Medical Genetics Part B Neuropsychiatric Genetics	2015	38
Inactivation of <i>AMMECR1</i> is associated with growth, bone, and heart alterations Mariana Moysés‐Oliveira, Giuliana Giannuzzi, Richard J. Fish, Human Mutation Cardiac MuscleHeart AlterationsX-linked Ammecr1SclerostinGenetics	2017	33
The Natural History of a Man With Ovotesticular 46,XX DSD Caused by a Novel 3-Mb 15q26.2 Deletion Containing NR2F2 Gene Gianna Carvalheira, Andréa Cristina de Moraes Malinverni, Mariana Moysés‐Oliveira, Journal of the Endocrine Society	2019	31
Transcriptional and functional consequences of alterations to MEF2C and its topological organization in neuronal models Kiana Mohajeri, Rachita Yadav, Eva D’haene, The American Journal of Human Genetics Molecular PhysiologySignal TransductionMolecular NeuroscienceTopological OrganizationNeuroanatomy	2022	27
Convergent coexpression of autism-associated genes suggests some novel risk genes may not be detectable in large-scale genetic studies Calwing Liao, Mariana Moysés‐Oliveira, Celine E.F. De Esch, Cell Genomics	2023	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 Luiza Sisdelli, Angela Cristina Vidi, Mariana Moysés‐Oliveira, Human Genetics EngineeringNovel StrategyUnbalanced X-rearrangementsMolecular BiologyOrganic Chemistry	2015	19

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