Andrea Citterio

Exploring the relationship between OXTR DNA methylation and temperament in children with neurodevelopmental disabilities.

Journal: Frontiers in psychology

Published: December 09, 2025

Expanding the clinical spectrum of RNU4ATAC-opathies: More frequent and diverse than assumed.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: October 01, 2025

Expanding the clinical spectrum of RNU4ATAC-opathies: more frequent and diverse than assumed.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: October 01, 2025

Exploring PIEZO1 DNA methylation in infants with neurodevelopmental disorders.

Journal: Frontiers in psychology

Published: March 14, 2025

Case report: A novel FARS2 deletion and a missense variant in a child with complicated, rapidly progressive spastic paraplegia.

Journal: Frontiers in genetics

Published: December 23, 2022

Whole-genome sequencing of hMPXV1 in five Italian cases confirms the occurrence of the predominant epidemic lineage.

Journal: Journal of medical virology

Published: December 06, 2022

Is Brain-Derived Neurotropic Factor Methylation Involved in the Association Between Prenatal Stress and Maternal Postnatal Anxiety During the COVID-19 Pandemic?

Journal: Frontiers in psychiatry

Published: May 22, 2022

A case of a childhood onset developmental encephalopathy with a novel de novo truncating variant in the Membrane Protein Palmitoylated 5 (MPP5) gene.

Journal: Seizure

Published: May 20, 2022

Case Reports: Novel Missense Variants in the Filamin C Actin Binding Domain Cause Variable Phenotypes.

Journal: Frontiers in neurology

Published: April 27, 2022

Hidden pandemic: COVID-19-related stress, SLC6A4 methylation, and infants' temperament at 3 months.

Journal: Scientific reports

Published: May 03, 2021

Novel SPTBN2 gene mutation and first intragenic deletion in early onset spinocerebellar ataxia type 5.

Journal: Annals of clinical and translational neurology

Published: February 11, 2021

U-Fiber Leukoencephalopathy Due to a Novel Mutation in the TACO1 Gene.

Journal: Neurology. Genetics

Published: September 29, 2020

Exploring the relationship between OXTR DNA methylation and temperament in children with neurodevelopmental disabilities.

Exploring the relationship between OXTR DNA methylation and temperament in children with neurodevelopmental disabilities.

Expanding the clinical spectrum of RNU4ATAC-opathies: More frequent and diverse than assumed.

Expanding the clinical spectrum of RNU4ATAC-opathies: More frequent and diverse than assumed.

Expanding the clinical spectrum of RNU4ATAC-opathies: more frequent and diverse than assumed.

Expanding the clinical spectrum of RNU4ATAC-opathies: more frequent and diverse than assumed.

Exploring PIEZO1 DNA methylation in infants with neurodevelopmental disorders.

Exploring PIEZO1 DNA methylation in infants with neurodevelopmental disorders.

Case report: A novel FARS2 deletion and a missense variant in a child with complicated, rapidly progressive spastic paraplegia.

Case report: A novel FARS2 deletion and a missense variant in a child with complicated, rapidly progressive spastic paraplegia.

Whole-genome sequencing of hMPXV1 in five Italian cases confirms the occurrence of the predominant epidemic lineage.

Whole-genome sequencing of hMPXV1 in five Italian cases confirms the occurrence of the predominant epidemic lineage.

Is Brain-Derived Neurotropic Factor Methylation Involved in the Association Between Prenatal Stress and Maternal Postnatal Anxiety During the COVID-19 Pandemic?

Is Brain-Derived Neurotropic Factor Methylation Involved in the Association Between Prenatal Stress and Maternal Postnatal Anxiety During the COVID-19 Pandemic?

A case of a childhood onset developmental encephalopathy with a novel de novo truncating variant in the Membrane Protein Palmitoylated 5 (MPP5) gene.

A case of a childhood onset developmental encephalopathy with a novel de novo truncating variant in the Membrane Protein Palmitoylated 5 (MPP5) gene.

Case Reports: Novel Missense Variants in the Filamin C Actin Binding Domain Cause Variable Phenotypes.

Case Reports: Novel Missense Variants in the Filamin C Actin Binding Domain Cause Variable Phenotypes.

﻿Hidden pandemic: COVID-19-related stress, SLC6A4 methylation, and infants' temperament at 3 months.

﻿Hidden pandemic: COVID-19-related stress, SLC6A4 methylation, and infants' temperament at 3 months.

Novel SPTBN2 gene mutation and first intragenic deletion in early onset spinocerebellar ataxia type 5.

Novel SPTBN2 gene mutation and first intragenic deletion in early onset spinocerebellar ataxia type 5.

U-Fiber Leukoencephalopathy Due to a Novel Mutation in the TACO1 Gene.

U-Fiber Leukoencephalopathy Due to a Novel Mutation in the TACO1 Gene.

Hidden pandemic: COVID-19-related stress, SLC6A4 methylation, and infants' temperament at 3 months.

Hidden pandemic: COVID-19-related stress, SLC6A4 methylation, and infants' temperament at 3 months.