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Human Genetics|January 5, 2007
Evidence for epistasis between SLC6A4 and ITGB3 in autism etiology and in the determination of platelet serotonin levelsAna M Coutinho, Inês Sousa, Madalena Martins, et al.NPJ Genomic Medicine|November 29, 2025
UBR5 loss-of-function variants in autism spectrum disorder and intellectual disability: case series and review of the literatureMiriam S Reuter, Nelson Bautista Salazar, Jennifer L Howe, et al.BMC Immunology|January 29, 2009
Low frequency of CD4+CD25+ Treg in SLE patients: a heritable trait associated with CTLA4 and TGFbeta gene variantsMarta Barreto, Ricardo C Ferreira, Lara Lourenço, et al.Plos One|April 6, 2012
Compensatory T-cell regulation in unaffected relatives of SLE patients, and opposite IL-2/CD25-mediated effects suggested by coreferentiality modelingConstantin Fesel, Marta Barreto, Ricardo C Ferreira, et al.Frontiers in Genetics|April 19, 2013
Dysfunction of the Heteromeric KV7.3/KV7.5 Potassium Channel is Associated with Autism Spectrum DisordersMette Gilling, Hanne B Rasmussen, Kirstine Calloe, et al.Journal of Clinical Epidemiology|February 22, 2025
A scoping review of the assessment reports of genetic or genomic tests reveals inconsistent consideration of key dimensions of clinical utilityAngelo Maria Pezzullo, Angelica Valz Gris, Nicolò Scarsi, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|April 12, 2007
MECP2 coding sequence and 3'UTR variation in 172 unrelated autistic patientsAna M Coutinho, Guiomar Oliveira, Cécile Katz, et al.Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism|March 29, 2012
TTC7B emerges as a novel risk factor for ischemic stroke through the convergence of several genome-wide approachesTiago Krug, João Paulo Gabriel, Ricardo Taipa, et al.Cerebrovascular Diseases (Basel, Switzerland)|April 2, 2010
Association of a genetic variant in the ALOX5AP with higher risk of ischemic stroke: a case-control, meta-analysis and functional studySophie Domingues-Montanari, Israel Fernández-Cadenas, Alberto del Rio-Espinola, et al.Molecular Autism|April 12, 2014
Recurrent duplications of the annexin A1 gene (ANXA1) in autism spectrum disordersCatarina T Correia, Inês C Conceição, Bárbara Oliveira, et al.Pageof 5