Ed J. Ryder

University of Cambridge, Cambridge, England, United Kingdom 
Genetics, Bioinformatics
"Ed Ryder"
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Reissig LF, Herdina AN, Rose J, et al. (2019) The mouse line - lessons from the deciphering the mechanisms of developmental disorders (DMDD) program. Biology Open
Collins JE, White RJ, Staudt N, et al. (2019) Common and distinct transcriptional signatures of mammalian embryonic lethality. Nature Communications. 10: 2792
Ballesteros Reviriego C, Clare S, Arends MJ, et al. (2019) FBXO7 sensitivity of phenotypic traits elucidated by a hypomorphic allele. Plos One. 14: e0212481
O'Connell AE, Gerashchenko MV, O'Donohue MF, et al. (2019) Mammalian Hbs1L deficiency causes congenital anomalies and developmental delay associated with Pelota depletion and 80S monosome accumulation. Plos Genetics. 15: e1007917
Iyer V, Boroviak K, Thomas M, et al. (2018) No unexpected CRISPR-Cas9 off-target activity revealed by trio sequencing of gene-edited mice. Plos Genetics. 14: e1007503
Perez-Garcia V, Fineberg E, Wilson R, et al. (2018) Placentation defects are highly prevalent in embryonic lethal mouse mutants. Nature
Weyden LV, Arends MJ, Campbell AD, et al. (2017) Genome-wide in vivo screen identifies novel host regulators of metastatic colonization. Nature
Dickinson ME, Flenniken AM, Ji X, et al. (2016) High-throughput discovery of novel developmental phenotypes. Nature
Kaloff C, Anastassiadis K, Ayadi A, et al. (2016) Genome wide conditional mouse knockout resources Drug Discovery Today: Disease Models. 20: 3-12
de Angelis MH, Nicholson G, Selloum M, et al. (2015) Analysis of mammalian gene function through broad-based phenotypic screens across a consortium of mouse clinics. Nature Genetics
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