Co-Authors
This is a "connection" page, showing publications co-authored by MICHAEL WANGLER and SCOTT MCLEAN.
Connection Strength
0.311
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Improving access to exome sequencing in a medically underserved population through the Texome Project. Genet Med. 2024 06; 26(6):101102.
Score: 0.209
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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 Sep 21.
Score: 0.062
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Recurrent arginine substitutions in the ACTG2 gene are the primary driver of disease burden and severity in visceral myopathy. Hum Mutat. 2020 03; 41(3):641-654.
Score: 0.039