Eirene Markenscoff-Papadimitriou

Affiliations: 
2014 Neuroscience University of California, San Francisco, San Francisco, CA 
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"Eirene Markenscoff-Papadimitriou"
Mean distance: 15.39 (cluster 11)
 
SNBCP

Parents

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David Julius grad student 2014 UCSF
 (The regulatory architecture of olfactory receptor gene enhancers.)
Matthew W. State post-doc UCSF
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Publications

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Liu Z, Ypsilanti AR, Markenscoff-Papadimitriou E, et al. (2024) enhancers have distinct functions in controlling expression during cortical development. Proceedings of the National Academy of Sciences of the United States of America. 121: e2402368121
Chen Y, Dawes R, Kim HC, et al. (2024) De novo variants in the RNU4-2 snRNA cause a frequent neurodevelopmental syndrome. Nature
Chen Y, Dawes R, Kim HC, et al. (2024) variants in the non-coding spliceosomal snRNA gene are a frequent cause of syndromic neurodevelopmental disorders. Medrxiv : the Preprint Server For Health Sciences
Markenscoff-Papadimitriou E, Binyameen F, Whalen S, et al. (2021) Autism risk gene POGZ promotes chromatin accessibility and expression of clustered synaptic genes. Cell Reports. 37: 110089
Markenscoff-Papadimitriou E, Whalen S, Przytycki P, et al. (2020) A Chromatin Accessibility Atlas of the Developing Human Telencephalon. Cell
Markenscoff-Papadimitriou E. (2019) 42.1 Chromatin Regulation In A Mouse Model Of Asd Journal of the American Academy of Child and Adolescent Psychiatry. 58
An JY, Lin K, Zhu L, et al. (2018) Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder. Science (New York, N.Y.). 362
Werling DM, Brand H, An JY, et al. (2018) An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder. Nature Genetics
Markenscoff-Papadimitriou E. (2018) 5.3 Epigenetic Mechanisms of Gene Repression in ASD Journal of the American Academy of Child and Adolescent Psychiatry. 57
Akbarian S, Liu C, Knowles JA, et al. (2015) The PsychENCODE project. Nature Neuroscience. 18: 1707-1712
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