Co-Authors
This is a "connection" page, showing publications co-authored by MICHAEL WANGLER and Jung-Wan Mok.
Connection Strength
0.672
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A rare recurring gain-of-function variant in BMPR2 causes neurodevelopmental phenotypes in humans and flies. Am J Hum Genet. 2026 Oct 01; 113(10):2178-2194.
Score: 0.250
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C-terminal frameshift variants in GPKOW are associated with a multisystemic X-linked disorder. Genet Med. 2025 07; 27(7):101429.
Score: 0.226
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De novo variants in MRTFB have gain-of-function activity in Drosophila and are associated with a novel neurodevelopmental phenotype with dysmorphic features. Genet Med. 2023 06; 25(6):100833.
Score: 0.196