T. Miguel

Evidence for epistasis between SLC6A4 and ITGB3 in autism etiology and in the determination of platelet serotonin levels

Astrid M. Vicente, Catarina Correia, Celeste Bento, 2007, Human Genetics.

Variants of the serotonin transporter gene (SLC6A4) significantly contribute to hyperserotonemia in autism

G. Oliveira, A. Vicente, C. Bento, 2004, Molecular Psychiatry.

Neurodevelopmental regression and Rett syn- drome - a variant form

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

Mitochondrial dysfunction in autism spectrum disorders: a population-based study.

G. Oliveira, A. Vicente, L. Diogo, 2005, Developmental medicine and child neurology.

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.

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.

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.

Partial Tetrasomy of Chromosome 3q and Mosaicism in a Child with Autism

G. Oliveira, A. Vicente, J. Saraiva, 2003, Journal of autism and developmental disorders.

Autoantibody repertoires to brain tissue in autism nuclear families

G. Oliveira, A. Vicente, C. Correia, 2004, Journal of Neuroimmunology.

Epidemiology of autism spectrum disorder in Portugal: prevalence, clinical characterization, and medical conditions

Esmeralda Gonçalves, Ana Margarida Coutinho, Astrid Moura Vicente, 2007, Developmental medicine and child neurology.

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.

Mitochondrial dysfunction in autism spectrum disorders: a population‐based study

G. Oliveira, A. Vicente, L. Diogo, 2005, Developmental medicine and child neurology.