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PreviewIssue DateTitleAuthor(s)
2020Disentangling the paradox of the PCDH19 clustering epilepsy, a disorder of cellular mosaicsGecz, J.; Thomas, P.Q.
2023Phenotypic consequences of a nanophthalmos-associated TMEM98 variant in human and mouseHassall, M.M.; Javadiyan, S.; Klebe, S.; Awadalla, M.S.; Sharma, S.; Qassim, A.; White, M.; Thomas, P.Q.; Craig, J.E.; Siggs, O.M.
2022Leveraging a natural murine meiotic drive to suppress invasive populationsGierus, L.; Birand, A.; Bunting, M.D.; Godahewa, G.I.; Piltz, S.G.; Oh, K.P.; Piaggio, A.J.; Threadgill, D.W.; Godwin, J.; Edwards, O.; Cassey, P.; Ross, J.V.; Prowse, T.A.A.; Thomas, P.Q.
2021Optimized nickase- and nuclease-based prime editing in human and mouse cellsAdikusuma, F.; Lushington, C.; Arudkumar, J.; Godahewa, G.I.; Chey, Y.C.J.; Gierus, L.; Piltz, S.; Geiger, A.; Jain, Y.; Reti, D.; Wilson, L.O.W.; Bauer, D.C.; Thomas, P.Q.
2021The Nestin neural enhancer is essential for normal levels of endogenous Nestin in neuroprogenitors but is not required for embryo developmentThomson, E.; Dawson, R.; H'ng, C.H.; Adikusuma, F.; Piltz, S.; Thomas, P.Q.; Varshney, G.
2023CRISPR applications for Duchenne muscular dystrophy: From animal models to potential therapiesChey, Y.C.J.; Arudkumar, J.; Aartsma‐Rus, A.; Adikusuma, F.; Thomas, P.Q.
2022Antisense oligonucleotide therapy for KCNT1 encephalopathyBurbano, L.E.; Li, M.; Jancovski, N.; Jafar-Nejad, P.; Richards, K.; Sedo, A.; Soriano, A.; Rollo, B.; Jia, L.; Gazina, E.V.; Piltz, S.; Adikusuma, F.; Thomas, P.Q.; Kopsidas, H.; Rigo, F.; Reid, C.A.; Maljevic, S.; Petrou, S.

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