Timothy J. Cherry, Ph.D.

Affiliations: 
2017- Center for Developmental Biology and Regenerative Medicine U Washington/Seattle Children's Research Inst. 
Area:
Retinal Development
Website:
http://depts.washington.edu/cdbrm/wordpress/research-labs-center-for-developmental-biology-and-regenerative-medicine/cherry-lab/
Google:
"Timothy Cherry"
Mean distance: 14.92 (cluster 32)
 
SNBCP

Parents

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Chris A. Walsh research assistant 2001-2002 Harvard Medical School
Constance L. Cepko grad student 2002-2009 Harvard
 (An analysis of amacrine cell diversity and development.)
Michael E. Greenberg post-doc 2010-2016 Harvard Medical School
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Publications

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VandenBosch LS, Luu K, Timms AE, et al. (2022) Machine Learning Prediction of Non-Coding Variant Impact in Human Retinal cis-Regulatory Elements. Translational Vision Science & Technology. 11: 16
Bisbach CM, Hass DT, Thomas ED, et al. (2022) Monocarboxylate Transporter 1 (MCT1) Mediates Succinate Export in the Retina. Investigative Ophthalmology & Visual Science. 63: 1
Thomas ED, Timms AE, Giles S, et al. (2022) Cell-specific cis-regulatory elements and mechanisms of non-coding genetic disease in human retina and retinal organoids. Developmental Cell
Lyu P, Hoang T, Santiago CP, et al. (2021) Gene regulatory networks controlling temporal patterning, neurogenesis, and cell-fate specification in mammalian retina. Cell Reports. 37: 109994
Sinha R, Grimes WN, Wallin J, et al. (2021) Transient expression of a GABA receptor subunit during early development is critical for inhibitory synapse maturation and function. Current Biology : Cb
Cherry TJ, Yang MG, Harmin DA, et al. (2020) Mapping the -regulatory architecture of the human retina reveals noncoding genetic variation in disease. Proceedings of the National Academy of Sciences of the United States of America
Majidi SP, Reddy NC, Moore MJ, et al. (2019) Chromatin Environment and Cellular Context Specify Compensatory Activity of Paralogous MEF2 Transcription Factors. Cell Reports. 29: 2001-2015.e5
Van de Sompele S, Smith C, Karali M, et al. (2018) Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease. Genetics in Medicine : Official Journal of the American College of Medical Genetics
Van Schil K, Naessens S, Van de Sompele S, et al. (2018) Correction: Mapping the genomic landscape of inherited retinal disease genes prioritizes genes prone to coding and noncoding copy-number variations. Genetics in Medicine : Official Journal of the American College of Medical Genetics
Jamshidi F, Place EM, Mehrotra S, et al. (2018) Contribution of noncoding pathogenic variants to RPGRIP1-mediated inherited retinal degeneration. Genetics in Medicine : Official Journal of the American College of Medical Genetics
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