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Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects
Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants With Treatment Resistance in Schizophrenia
Functional impact of global rare copy number variation in autism spectrum disorders
A first update on mapping the human genetic architecture of COVID-19
Mapping autism risk loci using genetic linkage and chromosomal rearrangements
Convergence of genes and cellular pathways dysregulated in autism spectrum disorders
Variable DNA methylation in neonates mediates the association between prenatal smoking and birth weight
Genetically elevated high-density lipoprotein cholesterol through the cholesteryl ester transfer protein gene does not associate with risk of Alzheimer's disease
Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism
Refining the role of de novo protein-truncating variants in neurodevelopmental disorders by using population reference samples
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