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Publications by Matthew Might
Expanding the Spectrum of BAF-Related Disorders: De Novo Variants in SMARCC2 Cause a Syndrome With Intellectual Disability and Developmental Delay
American Journal of Human Genetics
Genetics
IRF2BPL Is Associated With Neurological Phenotypes
American Journal of Human Genetics
Genetics
De Novo Variants in WDR37 Are Associated With Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia
American Journal of Human Genetics
Genetics
Bi-Allelic Variants in TONSL Cause SPONASTRIME Dysplasia and a Spectrum of Skeletal Dysplasia Phenotypes
American Journal of Human Genetics
Genetics
Pushdown Control-Flow Analysis for Free
ACM SIGPLAN Notices
Computer Science
Abstracting Abstract Machines
ACM SIGPLAN Notices
Computer Science
Flow-Sensitive Type Recovery in Linear-Log Time
ACM SIGPLAN Notices
Computer Science
Environment Analysis via ΔCFA
