List of works - Mónica Santos

A whole genome screen for association with multiple sclerosis in Portuguese patients

scientific article published in October 2003

Aberrant neuronal activity-induced signaling and gene expression in a mouse model of RASopathy.

scientific article

An explanation for another familial case of Rett syndrome: maternal germline mosaicism

scientific article published on 18 April 2007

Analysis of highly conserved regions of the 3'UTR of MECP2 gene in patients with clinical diagnosis of Rett syndrome and other disorders associated with mental retardation.

scientific article published on January 2008

Chromatin remodeling and neuronal function: exciting links

scientific article (publication date: June 2006)

Correction: Aberrant neuronal activity-induced signaling and gene expression in a mouse model of RASopathy.

scientific article published on 16 June 2017

Detection of heterozygous deletions and duplications in the MECP2 gene in Rett syndrome by Robust Dosage PCR (RD-PCR).

scientific article

Evidence for abnormal early development in a mouse model of Rett syndrome.

scientific article published on 17 July 2006

Fragile X-Associated Tremor/Ataxia Syndrome (FXTAS) Motor Dysfunction Modeled in Mice

scientific article published on 2 June 2016

From neural to genetic substrates of panic disorder: Insights from human and mouse studies

scientific article published on 24 March 2015

Genome-wide miR-155 and miR-802 target gene identification in the hippocampus of Ts65Dn Down syndrome mouse model by miRNA sponges

scientific article

Genotypes at the APOE and SCA2 loci do not predict the course of multiple sclerosis in patients of Portuguese origin

scientific article published in April 2004

Hippocampal hyperexcitability underlies enhanced fear memories in TgNTRK3, a panic disorder mouse model.

scientific article

Infralimbic Neurotrophin-3 Infusion Rescues Fear Extinction Impairment in a Mouse Model of Pathological Fear

scientific article

Lack of MeCP2 leads to region-specific increase of doublecortin in the olfactory system

scientific article published on 28 March 2019

MECP2 coding sequence and 3'UTR variation in 172 unrelated autistic patients

scientific article published in June 2007

Male-specific features are reduced in Mecp2-null mice: analyses of vasopressinergic innervation, pheromone production and social behaviour

scientific article published on 04 August 2020

Monoamine deficits in the brain of methyl-CpG binding protein 2 null mice suggest the involvement of the cerebral cortex in early stages of Rett syndrome

scientific article published on 13 July 2010

Mutations in the MECP2 gene are not a major cause of Rett syndrome-like or related neurodevelopmental phenotype in male patients

scientific article published on January 2009

Selective rescue of heightened anxiety but not gait ataxia in a premutation 90CGG mouse model of Fragile X-associated tremor/ataxia syndrome.

scientific article

T-1237C polymorphism of TLR9 gene is not associated with multiple sclerosis in the Portuguese population.

scientific article published on 21 January 2008

The C677T polymorphism in MTHFR is not associated with migraine in Portugal.

scientific article published on January 2008

List of works by Mónica Santos

A whole genome screen for association with multiple sclerosis in Portuguese patients

Aberrant neuronal activity-induced signaling and gene expression in a mouse model of RASopathy.

An explanation for another familial case of Rett syndrome: maternal germline mosaicism

Analysis of highly conserved regions of the 3'UTR of MECP2 gene in patients with clinical diagnosis of Rett syndrome and other disorders associated with mental retardation.

Chromatin remodeling and neuronal function: exciting links

Correction: Aberrant neuronal activity-induced signaling and gene expression in a mouse model of RASopathy.

Detection of heterozygous deletions and duplications in the MECP2 gene in Rett syndrome by Robust Dosage PCR (RD-PCR).

Evidence for abnormal early development in a mouse model of Rett syndrome.

Fragile X-Associated Tremor/Ataxia Syndrome (FXTAS) Motor Dysfunction Modeled in Mice

From neural to genetic substrates of panic disorder: Insights from human and mouse studies

Genome-wide miR-155 and miR-802 target gene identification in the hippocampus of Ts65Dn Down syndrome mouse model by miRNA sponges

Genotypes at the APOE and SCA2 loci do not predict the course of multiple sclerosis in patients of Portuguese origin

Hippocampal hyperexcitability underlies enhanced fear memories in TgNTRK3, a panic disorder mouse model.

Infralimbic Neurotrophin-3 Infusion Rescues Fear Extinction Impairment in a Mouse Model of Pathological Fear

Lack of MeCP2 leads to region-specific increase of doublecortin in the olfactory system

MECP2 coding sequence and 3'UTR variation in 172 unrelated autistic patients

Male-specific features are reduced in Mecp2-null mice: analyses of vasopressinergic innervation, pheromone production and social behaviour

Monoamine deficits in the brain of methyl-CpG binding protein 2 null mice suggest the involvement of the cerebral cortex in early stages of Rett syndrome

Mutations in the MECP2 gene are not a major cause of Rett syndrome-like or related neurodevelopmental phenotype in male patients

Selective rescue of heightened anxiety but not gait ataxia in a premutation 90CGG mouse model of Fragile X-associated tremor/ataxia syndrome.

T-1237C polymorphism of TLR9 gene is not associated with multiple sclerosis in the Portuguese population.

The C677T polymorphism in MTHFR is not associated with migraine in Portugal.