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Publications by H. A. Stessman

Recurrent De Novo Mutations Implicate Novel Genes Underlying Simplex Autism Risk

Nature Communications

Molecular Biology

English

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Recurrent De Novo Mitochondrial DNA Mutations in Respiratory Chain Deficiency

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Inherited and De Novo Genetic Risk for Autism Impacts Shared Networks

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Genes and Mutations Underlying Domestication Transitions in Grasses

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De Novo Mutations in FOXP1 in Cases With Intellectual Disability, Autism, and Language Impairment

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Altered Spinogenesis in iPSC-derived Cortical Neurons From Patients With Autism Carrying De Novo SHANK3 Mutations

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Genes With De Novo Mutations Are Shared by Four Neuropsychiatric Disorders Discovered From NPdenovo Database

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De Novo Mutations From Sporadic Schizophrenia Cases Highlight Important Signaling Genes in an Independent Sample

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Exonic Mosaic Mutations Contribute Risk for Autism Spectrum Disorder

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Protein-Coding Variants Implicate Novel Genes Related to Lipid Homeostasis Contributing to Body-Fat Distribution

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