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A Phenotypic Paradigm for Cerebral Palsy Genetics

2026-01-18

Abstract excerpt

Disease-causing genetic variants can be found in a subset of individuals with cerebral palsy (CP), with variants deemed causal of CP having been published for at least 515 genes. We develop a statistical approach that treats CP as a phenotypic feature for which some genetic disorders confer an increased risk. Based on comprehensive literature curation we show that the null hypothesis of no CP association can be re...

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Literature Corpus work
8bc74f94-f2b8-582f-a5e2-f0f1b84dcbf1
DOI
10.64898/2026.01.13.25341946
Open publication

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A Phenotypic Paradigm for Cerebral Palsy GeneticsDOI 10.64898/2026.01.13.25341946
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