– Variants in the fetal genome near FLT1 are associated with risk of preeclampsia
– Genetic loci associated with coronary artery disease harbor evidence of selection and antagonistic pleiotropy.
– Truncating mutations in RBM12 are associated with psychosis
– Germline hypomorphic CARD11 mutations in severe atopic disease
– Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorder
– A novel UBE2A mutation causes X-linked intellectual disability type Nascimento
– Large-scale analyses of common and rare variants identify 12 new loci associated with atrial fibrillation
– Genome-wide association meta-analysis of 78,308 individuals identifies new loci and genes influencing human intelligence
– Rare Copy Number Variants in NRXN1 and CNTN6 Increase Risk for Tourette Syndrome
Nuevas variantes, mutaciones y asociaciones
Filed under Medicina personalizada, Neurología, Patógenos, Polimorfismos by on . 
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