List of works - Carla Lintas

Age-dependent decrease and alternative splicing of methionine synthase mRNA in human cerebral cortex and an accelerated decrease in autism

scientific article

An 8-year-old boy with autoimmune hepatitis and Candida onychosis as the first symptoms of autoimmune polyglandular syndrome (APS1): identification of a new homozygous mutation in the autoimmune regulator gene (AIRE).

scientific article published on 21 September 2007

Appropriateness of array-CGH in the ADHD clinics: a comparative study

scientific article published on 06 March 2020

Association of autism with polyomavirus infection in postmortem brains

scientific article published in March 2010

Autism genetics: Methodological issues and experimental design

scientific article published on 02 September 2015

Autistic phenotypes and genetic testing: state-of-the-art for the clinical geneticist

scientific article

Decreased serum arylesterase activity in autism spectrum disorders

scientific article published on 21 May 2010

Differential methylation at the RELN gene promoter in temporal cortex from autistic and typically developing post-puberal subjects

scientific article published on 29 April 2016

Do mutations of RAG genes have a role in human autoimmunity? The Notarangelo's hypothesis revisited

scientific article

FARP-1 deletion is associated with lack of response to autism treatment by early start denver model in a multiplex family

scientific article published on 25 June 2020

Genetic and epigenetic MTHFR gene variants in the mothers of attention-deficit/hyperactivity disorder affected children as possible risk factors for neurodevelopmental disorders

scientific article published on 02 June 2020

Genome-wide expression studies in autism spectrum disorder, Rett syndrome, and Down syndrome

scientific article published on 02 December 2010

Genomic and epigenetic evidence for oxytocin receptor deficiency in autism

scientific article

Immune transcriptome alterations in the temporal cortex of subjects with autism.

scientific article published on 10 March 2008

Involvement of the PRKCB1 gene in autistic disorder: significant genetic association and reduced neocortical gene expression

scientific article

Lack of infection with XMRV or other MLV-related viruses in blood, post-mortem brains and paternal gametes of autistic individuals

scientific article

Linking genetics to epigenetics: The role of folate and folate-related pathways in neurodevelopmental disorders

article

Methylation profile in tumor and sputum samples of lung cancer patients detected by spiral computed tomography: a nested case-control study

scientific article

Mutations that affect the ability of the vnd/NK-2 homeoprotein to regulate gene expression: transgenic alterations and tertiary structure

scholarly article

Neocortical RELN promoter methylation increases significantly after puberty

scientific article

Phenotypic spectrum of NRXN1 mono- and bi-allelic deficiency: A systematic review

scientific article published on 14 March 2019

Reelin Gene Polymorphisms in Autistic Disorder

article

Unraveling molecular pathways shared by Kabuki and Kabuki-like syndromes

scientific article published on 31 January 2017

Xp22.33p22.12 Duplication in a Patient with Intellectual Disability and Dysmorphic Facial Features

scientific article

List of works by Carla Lintas

Age-dependent decrease and alternative splicing of methionine synthase mRNA in human cerebral cortex and an accelerated decrease in autism

An 8-year-old boy with autoimmune hepatitis and Candida onychosis as the first symptoms of autoimmune polyglandular syndrome (APS1): identification of a new homozygous mutation in the autoimmune regulator gene (AIRE).

Appropriateness of array-CGH in the ADHD clinics: a comparative study

Association of autism with polyomavirus infection in postmortem brains

Autism genetics: Methodological issues and experimental design

Autistic phenotypes and genetic testing: state-of-the-art for the clinical geneticist

Decreased serum arylesterase activity in autism spectrum disorders

Differential methylation at the RELN gene promoter in temporal cortex from autistic and typically developing post-puberal subjects

Do mutations of RAG genes have a role in human autoimmunity? The Notarangelo's hypothesis revisited

FARP-1 deletion is associated with lack of response to autism treatment by early start denver model in a multiplex family

Genetic and epigenetic MTHFR gene variants in the mothers of attention-deficit/hyperactivity disorder affected children as possible risk factors for neurodevelopmental disorders

Genome-wide expression studies in autism spectrum disorder, Rett syndrome, and Down syndrome

Genomic and epigenetic evidence for oxytocin receptor deficiency in autism

Immune transcriptome alterations in the temporal cortex of subjects with autism.

Involvement of the PRKCB1 gene in autistic disorder: significant genetic association and reduced neocortical gene expression

Lack of infection with XMRV or other MLV-related viruses in blood, post-mortem brains and paternal gametes of autistic individuals

Linking genetics to epigenetics: The role of folate and folate-related pathways in neurodevelopmental disorders

Methylation profile in tumor and sputum samples of lung cancer patients detected by spiral computed tomography: a nested case-control study

Mutations that affect the ability of the vnd/NK-2 homeoprotein to regulate gene expression: transgenic alterations and tertiary structure

Neocortical RELN promoter methylation increases significantly after puberty

Phenotypic spectrum of NRXN1 mono- and bi-allelic deficiency: A systematic review

Reelin Gene Polymorphisms in Autistic Disorder

Unraveling molecular pathways shared by Kabuki and Kabuki-like syndromes

Xp22.33p22.12 Duplication in a Patient with Intellectual Disability and Dysmorphic Facial Features