Timothy J. Cherry, Ph.D.
Affiliations: | 2017- | Center for Developmental Biology and Regenerative Medicine | U Washington/Seattle Children's Research Inst. |
Area:
Retinal DevelopmentWebsite:
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) | S | N | B | C | P |
Parents
Sign in to add mentorChris 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 |
Children
Sign in to add traineeKelsey Luu | research assistant | 2017-2020 | Harvard Medical School |
LuLu Callies | grad student | 2021- | University of Washington |
Brendan McShane | grad student | 2021- | University of Washington |
Cheri Liu | post-doc | UW Medical School | |
Leah VandenBosch | post-doc | 2019- | U of Washington/Seattle Children's Research Inst. |
Santiago P. Fregoso | post-doc | 2021- | U Washington/Seattle Children's Research Inst. (Cell Biology Tree) |
Eric D. Thomas | post-doc | 2019-2022 | Allen Institute |
Liesl Strand | research scientist | 2017-2019 | Stanford (Cell Biology Tree) |
BETA: Related publications
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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 |