J. Almeida

发表

Functional impact of global rare copy number variation in autism spectrum disorders

Gary D Bader, Joseph T. Glessner, Stephen J. Guter, 2010, Nature.

A genome-wide scan for common alleles affecting risk for autism

Margaret A. Pericak-Vance, Kathryn Roeder, Thomas Bourgeron, 2010, Human molecular genetics.

Individual common variants exert weak effects on the risk for autism spectrum disorders

Margaret A. Pericak-Vance, Kathryn Roeder, Thomas Bourgeron, 2012, Human molecular genetics.

Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders

Stephen J. Guter, Emily L. Crawford, D. Pinto, 2014, American journal of human genetics.

Intellectual Profiles in the Autism Spectrum and Other Neurodevelopmental Disorders

J. Almeida, F. Duque, G. Oliveira, 2016, Journal of Autism and Developmental Disorders.

Dysfunction of the Heteromeric KV7.3/KV7.5 Potassium Channel is Associated with Autism Spectrum Disorders

J. Almeida, G. Oliveira, A. Sequeira, 2012, Front. Genet..

Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia

Christopher S. Poultney, Stephan J Sanders, Stephen J. Guter, 2017, Molecular Autism.

Definition of a putative pathological region in PARK2 associated with autism spectrum disorder through in silico analysis of its functional structure

J. Almeida, F. Duque, G. Oliveira, 2017, Psychiatric genetics.

The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism

Thomas Bourgeron, Ellen M. Wijsman, Gillian Baird, 2014, Nature Communications.

Recurrent duplications of the annexin A1 gene (ANXA1) in autism spectrum disorders

D. Pinto, S. Scherer, D. Geschwind, 2014, Molecular Autism.

Dysfunction of the heteromeric K V 7 . 3 / K V 7 . 5 potassium channel is associated with autism spectrum disorders

J. Almeida, G. Oliveira, A. Sequeira, 2013 .

A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder

Joseph T. Glessner, Stephen J. Guter, D. Pinto, 2011, Human Genetics.

Copy number variations in chromosome 16p13.11-The neurodevelopmental clinical spectrum

J. Almeida, G. Oliveira, A. Vicente, 2017 .

Neurodevelopmental regression and Rett syn- drome - a variant form

J. Almeida, G. Oliveira, S. Loureiro, 2010 .

Pharmacogenetics of risperidone therapy in autism: association analysis of eight candidate genes with drug efficacy and adverse drug reactions

J. Almeida, G. Oliveira, A. Sequeira, 2010, The Pharmacogenomics Journal.

Adaptive Profiles in Autism and Other Neurodevelopmental Disorders

J. Almeida, F. Duque, G. Oliveira, 2015, Journal of autism and developmental disorders.

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

Jin Yan, Catarina Correia, Astrid M Vicente, 2007, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Adaptive Profiles in Autism and Other Neurodevelopmental Disorders

J. Almeida, F. Duque, G. Oliveira, 2014, Journal of Autism and Developmental Disorders.

Association of the α4 integrin subunit gene (ITGA4) with autism

M. Gill, L. Gallagher, J. Conroy, 2009, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

A Direct Comparison of Local-Global Integration in Autism and other Developmental Disorders: Implications for the Central Coherence Hypothesis

Miguel Castelo-Branco, Inês Bernardino, Susana Mouga, 2012, PloS one.

Brief Report: High Frequency of Biochemical Markers for Mitochondrial Dysfunction in Autism: No Association with the Mitochondrial Aspartate/Glutamate Carrier SLC25A12 Gene

Catarina Correia, Astrid M Vicente, C. Correia, 2006, Journal of autism and developmental disorders.

Increased BDNF levels and NTRK2 gene association suggest a disruption of BDNF/TrkB signaling in autism

M. Gill, L. Gallagher, J. Conroy, 2010, Genes, brain, and behavior.

Intellectual Profiles in the Autism Spectrum and Other Neurodevelopmental Disorders

J. Almeida, F. Duque, G. Oliveira, 2016, Journal of Autism and Developmental Disorders.

Autism Spectrum Disorder: FRAXE Mutation, a Rare Etiology

J. Almeida, G. Oliveira, S. Mouga, 2015, Journal of autism and developmental disorders.

Autism Spectrum Disorder: FRAXE Mutation, a Rare Etiology

J. Almeida, G. Oliveira, S. Mouga, 2014, Journal of Autism and Developmental Disorders.

Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia

Christopher S. Poultney, Stephan J Sanders, Stephen J. Guter, 2017, Molecular Autism.

A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder

Stephen J. Guter, D. Pinto, S. Scherer, 2011, Human Genetics.

Increased BDNF levels and association with the NTRK2 gene suggest a disruption of BDNF/TRKB signaling in autism

L. Gallagher, J. Almeida, G. Oliveira, 2010, International Journal of Developmental Neuroscience.