Co-Authors
This is a "connection" page, showing publications co-authored by MICHAEL WANGLER and LISA EMRICK.
Connection Strength
0.165
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Cross-species functional analysis of a de novo DCLK1 variant associated with a neurodevelopmental disorder. Res Sq. 2026 Jul 23.
Score: 0.062
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Disruptive mutations in TANC2 define a neurodevelopmental syndrome associated with psychiatric disorders. Nat Commun. 2019 10 15; 10(1):4679.
Score: 0.039
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Clinically severe CACNA1A alleles affect synaptic function and neurodegeneration differentially. PLoS Genet. 2017 Jul; 13(7):e1006905.
Score: 0.033
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Diagnosis of adenylosuccinate lyase deficiency by metabolomic profiling in plasma reveals a phenotypic spectrum. Mol Genet Metab Rep. 2016 Sep; 8:61-6.
Score: 0.031