Lista de obras - Carla Lintas - Dominio Público Uruguay

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

artículo científico publicado en 2013

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).

artículo científico publicado en 2007

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

artículo científico publicado en 2020

Association of autism with polyomavirus infection in postmortem brains

artículo científico publicado en 2010

Autism genetics: Methodological issues and experimental design

artículo científico

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

artículo científico publicado en 2009

Decreased serum arylesterase activity in autism spectrum disorders

artículo científico publicado en 2010

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

artículo científico publicado en 2016

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

artículo científico publicado en 2006

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

artículo científico publicado en 2020

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

artículo científico publicado en 2020

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

artículo científico publicado en 2010

Genomic and epigenetic evidence for oxytocin receptor deficiency in autism

artículo científico publicado en 2009

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

artículo científico publicado en 2008

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

artículo científico publicado en 2009

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

artículo científico publicado en 2011

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

artículo científico publicado en 2006

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

artículo científico publicado en 2003

Neocortical RELN promoter methylation increases significantly after puberty

artículo científico publicado en 2010

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

artículo científico publicado en 2019

Reelin Gene Polymorphisms in Autistic Disorder

article

Unraveling molecular pathways shared by Kabuki and Kabuki-like syndromes

artículo científico

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

artículo científico publicado en 2016

Lista de obras de 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