Matthew Jensen

Single-cell genomics and regulatory networks for 388 human brains

Assortative mating and parental genetic relatedness contribute to the pathogenicity of variably expressive variants

Leveraging a large language model to predict protein phase transition: a physical, multiscale and interpretable approach

Artificial gravity partially protects space-induced neurological deficits in Drosophila melanogaster

Complex genetic interaction patterns determine the phenotypic trajectory of neurodevelopmental disorders

Combinatorial patterns of gene expression changes contribute to variable expressivity of the developmental delay-associated 16p12. 1 deletion

Functional assessment of the “two-hit” model for neurodevelopmental defects in Drosophila and X. laevis

The relevance of deep genomic analyses in families with variably expressive CNVs in the era of personalized medicine