Patricia N. Moretti
Brasilia, DF, Brazil
Last Updated: 09/26/2026
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Found 19 publications
ZDHHC9 X-linked intellectual disability: Clinical and molecular characterization.
Journal: American journal of medical genetics. Part A
Published: March 15, 2022
Cobalamin F deficiency in a girl with severe skin hyperpigmentation and a homozygous LMBRD1 variant.
Cobalamin F deficiency in a girl with severe skin hyperpigmentation and a homozygous LMBRD1 variant.
Journal: Clinical and experimental dermatology
Published: December 01, 2021
Characterization of Associated Nonclassical Phenotypes in Patients with Deletion in the WAGR Region Identified by Chromosomal Microarray: New Insights and Literature Review.
Journal: Molecular syndromology
Published: March 16, 2021
SHORT syndrome in an adult Brazilian patient.
Journal: American journal of medical genetics. Part A
Published: December 16, 2020
Genotype and phenotype correlation in a family with a 2q37 deletion downstream of HDAC4.
Journal: American journal of medical genetics. Part A
Published: September 25, 2019
Defining the Critical Region for Intellectual Disability and Brain Malformations in 6q27 Microdeletions.
Journal: Molecular syndromology
Published: May 07, 2019
Gene expression over the course of schizophrenia: from clinical high-risk for psychosis to chronic stages.
Journal: NPJ schizophrenia
Published: October 19, 2018
DGCR2 influences cortical thickness through a mechanism independent of schizophrenia pathogenesis.
Journal: Psychiatry research
Published: July 23, 2018
Effect of male-specific childhood trauma on telomere length.
Journal: Journal of psychiatric research
Published: June 15, 2018
Polygenic risk score analyses of symptoms and treatment response in an antipsychotic-naive first episode of psychosis cohort.
Journal: Translational psychiatry
Published: September 19, 2017
Accessing Gene Expression in Treatment-Resistant Schizophrenia.
Journal: Molecular neurobiology
Published: August 09, 2017
Last Updated: 09/26/2026