Author

Eleanor S. Raymond

Institute of Genetics and CancerORCID 0000-0002-2703-7909Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Research Focus:differential expression· 1 Assay:DNA methylation· 1 Approach:experimental assay· 1 Organism:human· 1 Organism:mouse· 1 Assay:proteomics· 1 Approach:statistical model· 1

Frequent Co-Authors

Alex von KriegsheimiD· 1 shared Alison M. MeynertiD· 1 shared Andrew J. FinchiD· 1 shared Andrew P. JacksoniD· 1 shared Archith KamathiD· 1 shared Bernard H. Ramsahoye· 1 shared Chao-Chun Hung· 1 shared David R FitzPatrickiD· 1 shared

Activity by Year

2019-2020 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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1 shared paperGenetics

Alex von KriegsheimORCID

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2 papers

Recent·Most cited

Tex19.1 Regulates Acetylated SMC3 Cohesin and Prevents Aneuploidy in Mouse Oocytes

Judith Reichmann, Karen Dobie, Lisa Lister, Diana Best, James H. Crichton, Marie MacLennan, David Read, Eleanor S. Raymond, Chao-Chun Hung, Shelagh Boyle, Katsuhiko Shirahige, Howard J. Cooke, Wendy A. Bickmore, Mary Herbert, Ian R. Adams

This study shows Tex19.1 maintains acetylated SMC3 and sister chromatid cohesion in mouse oocytes, preventing aneuploidy.

The Journal of Cell Biology · Feb 12, 2020Peer-reviewedGenetics

ITPase Deficiency Causes Martsolf Syndrome With a Lethal Infantile Dilated Cardiomyopathy

Mark T. Handley, Kaalak Reddy, Jimi C. Wills, Elisabeth M. Rosser, Archith Kamath, Mihail R. Halachev, Gavin Falkous, Denise Williams, Phillip M. Cox, Alison M. Meynert, Eleanor S. Raymond, Harris Morrison, S.D.M. Brown, Emma Allan, Irene A. Aligianis, , David R FitzPatrick

This paper identifies ITPA mutations causing a lethal infantile dilated cardiomyopathy with Martsolf syndrome features and describes the molecular consequences of ITPase deficiency.

PLoS Genetics · Mar 11, 2019Peer-reviewedGenetics