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Matthew Might
Matthew Might
Hugh Kaul Precision Medicine Institute, University of Alabama at Birmingham
Adresse e-mail validée de uab.edu - Page d'accueil
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Année
Metformin use is associated with reduced mortality in a diverse population with COVID-19 and diabetes
AB Crouse, T Grimes, P Li, M Might, F Ovalle, A Shalev
Frontiers in endocrinology 11, 600439, 2021
2022021
Abstracting abstract machines
D Van Horn, M Might
Proceedings of the 15th ACM SIGPLAN international conference on Functional …, 2010
1892010
MARRVEL: integration of human and model organism genetic resources to facilitate functional annotation of the human genome
J Wang, R Al-Ouran, Y Hu, SY Kim, YW Wan, MF Wangler, S Yamamoto, ...
The American Journal of Human Genetics 100 (6), 843-853, 2017
1762017
The undiagnosed diseases network: accelerating discovery about health and disease
RB Ramoni, JJ Mulvihill, DR Adams, P Allard, EA Ashley, JA Bernstein, ...
The American Journal of Human Genetics 100 (2), 185-192, 2017
1592017
Improving flow analyses via ΓCFA: Abstract garbage collection and counting
M Might, O Shivers
Proceedings of the eleventh ACM SIGPLAN international conference on …, 2006
1302006
A syndromic neurodevelopmental disorder caused by de novo variants in EBF3
HT Chao, M Davids, E Burke, JG Pappas, JA Rosenfeld, AJ McCarty, ...
The American Journal of Human Genetics 100 (1), 128-137, 2017
1142017
Resolving and exploiting the k-CFA paradox: illuminating functional vs. object-oriented program analysis
M Might, Y Smaragdakis, D Van Horn
Proceedings of the 31st ACM SIGPLAN Conference on Programming Language …, 2010
1142010
The shifting model in clinical diagnostics: how next-generation sequencing and families are altering the way rare diseases are discovered, studied, and treated
M Might, M Wilsey
Genetics in Medicine 16 (10), 736-737, 2014
912014
IRF2BPL is associated with neurological phenotypes
PC Marcogliese, V Shashi, RC Spillmann, N Stong, JA Rosenfeld, ...
The American Journal of Human Genetics 103 (2), 245-260, 2018
902018
Parsing with derivatives: a functional pearl
M Might, D Darais, D Spiewak
Acm sigplan notices 46 (9), 189-195, 2011
812011
EigenCFA: Accelerating flow analysis with GPUs
T Prabhu, S Ramalingam, M Might, M Hall
ACM SIGPLAN Notices 46 (1), 511-522, 2011
792011
Induced pluripotent stem cells for neural drug discovery
A Farkhondeh, R Li, K Gorshkov, KG Chen, M Might, S Rodems, DC Lo, ...
Drug discovery today 24 (4), 992-999, 2019
772019
A comprehensive iterative approach is highly effective in diagnosing individuals who are exome negative
V Shashi, K Schoch, R Spillmann, H Cope, QKG Tan, N Walley, L Pena, ...
Genetics in Medicine 21 (1), 161-172, 2019
762019
Environment analysis of higher-order languages
M Might
Georgia Institute of Technology, 2007
732007
Biallelic mutations in ATP5F1D, which encodes a subunit of ATP synthase, cause a metabolic disorder
M Oláhová, WH Yoon, K Thompson, S Jangam, L Fernandez, ...
The American Journal of Human Genetics 102 (3), 494-504, 2018
722018
Sound and precise malware analysis for Android via pushdown reachability and entry-point saturation
S Liang, AW Keep, M Might, S Lyde, T Gilray, P Aldous, D Van Horn
Proceedings of the Third ACM workshop on Security and privacy in smartphones …, 2013
712013
Expanding the spectrum of BAF-related disorders: de novo variants in SMARCC2 cause a syndrome with intellectual disability and developmental delay
K Machol, J Rousseau, S Ehresmann, T Garcia, TTM Nguyen, ...
The American Journal of Human Genetics 104 (1), 164-178, 2019
702019
De novo truncating variants in ASXL2 are associated with a unique and recognizable clinical phenotype
V Shashi, LDM Pena, K Kim, B Burton, M Hempel, K Schoch, ...
The American Journal of Human Genetics 99 (4), 991-999, 2016
682016
Introspective pushdown analysis of higher-order programs
C Earl, I Sergey, M Might, D Van Horn
Proceedings of the 17th ACM SIGPLAN international conference on Functional …, 2012
682012
Transcriptome and functional analysis in a Drosophila model of NGLY1 deficiency provides insight into therapeutic approaches
KG Owings, JB Lowry, Y Bi, M Might, CY Chow
Human molecular genetics 27 (6), 1055-1066, 2018
652018
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