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Author Details

Timothy J Cherry
University of Washington
2003
23
16
PMIDPaper TitleJournal TitlePublished Year
37502987Lipid nanoparticle-mediated delivery of mRNA into the mouse and human retina and other ocular tissues.bioRxiv2023
34929105Distinct features of brain perivascular fibroblasts and mural cells revealed by <i>in vivo</i> two-photon imaging.J Cereb Blood Flow Metab2022
35435921Machine Learning Prediction of Non-Coding Variant Impact in Human Retinal cis-Regulatory Elements.Transl Vis Sci Technol2022
35363247Monocarboxylate Transporter 1 (MCT1) Mediates Succinate Export in the Retina.Invest Ophthalmol Vis Sci2022
35303433Cell-specific cis-regulatory elements and mechanisms of non-coding genetic disease in human retina and retinal organoids.Dev Cell2022
34216551Targeted long-read sequencing identifies missing disease-causing variation.Am J Hum Genet2021
34788628Gene regulatory networks controlling temporal patterning, neurogenesis, and cell-fate specification in mammalian retina.Cell Rep2021
34433078Transient expression of a GABA receptor subunit during early development is critical for inhibitory synapse maturation and function.Curr Biol2021
32265282Mapping the <i>cis</i>-regulatory architecture of the human retina reveals noncoding genetic variation in disease.Proc Natl Acad Sci U S A2020
30670881ABCA4-associated disease as a model for missing heritability in autosomal recessive disorders: novel noncoding splice, cis-regulatory, structural, and recurrent hypomorphic variants.Genet Med2019
31722213Chromatin Environment and Cellular Context Specify Compensatory Activity of Paralogous MEF2 Transcription Factors.Cell Rep2019
30072743Contribution of noncoding pathogenic variants to RPGRIP1-mediated inherited retinal degeneration.Genet Med2019
30377383Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease.Genet Med2019
30297699Correction: Mapping the genomic landscape of inherited retinal disease genes prioritizes genes prone to coding and noncoding copy-number variations.Genet Med2019
30607024Correction: Biallelic sequence and structural variants in RAX2 are a novel cause for autosomal recessive inherited retinal disease.Genet Med2019
28749477Mapping the genomic landscape of inherited retinal disease genes prioritizes genes prone to coding and noncoding copy-number variations.Genet Med2018
25801704MEF2D drives photoreceptor development through a genome-wide competition for tissue-specific enhancers.Neuron2015
21593321NeuroD factors regulate cell fate and neurite stratification in the developing retina.J Neurosci2011
19470466Development and diversification of retinal amacrine interneurons at single cell resolution.Proc Natl Acad Sci U S A2009
15894532Early asymmetry of gene transcription in embryonic human left and right cerebral cortex.Science2005
15165674Etiological heterogeneity of familial periventricular heterotopia and hydrocephalus.Brain Dev2004
12682315Autosomal recessive form of periventricular heterotopia.Neurology2003
12687690Characterization of Foxp2 and Foxp1 mRNA and protein in the developing and mature brain.J Comp Neurol2003
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Collaborators

Christopher A Walsh
Broad Institute of MIT and Harvard
Co-authored papers 4
Andrew E Timms
Center for Integrative Brain Research, Seattle Children's Research Institute
Co-authored papers 4
Martin McKibbin
Leeds Teaching Hospitals NHS Trust
Co-authored papers 2
Seth Blackshaw
Johns Hopkins University School of Medicine.
Co-authored papers 2
Jiang Qian
Co-authored papers 2
Robert Sean Hill
Co-authored papers 2
Rando Allikmets
Columbia University Medical Center
Co-authored papers 2
Constance L Cepko
Howard Hughes Medical Institute, Harvard Medical School
Co-authored papers 2
Martin Friedlander
the Scripps Research Institute
Co-authored papers 1
Jeffrey M Trimarchi
Inc., Lehigh University
Co-authored papers 1
Andrew S Allen
Duke University School of Medicine
Co-authored papers 1
Shriya Challam
Co-authored papers 1
Mary-Claire King
University of Washington
Co-authored papers 1
Gavin Arno
Institute of Ophthalmology, University College London
Co-authored papers 1
Alexias Safi
Center for Genomic and Computational Biology, Duke University Medical Center
Co-authored papers 1
Deborah A Nickerson
University of Washington
Co-authored papers 1
Monkol Lek
Co-authored papers 1
Daniel H Geschwind
University of California los angeles
Co-authored papers 1
Rui Chen
Co-authored papers 1
Stuart H Orkin
Boston Children's Hospital and Dana-Farber Cancer Institute, Harvard Medical School
Co-authored papers 1
Emily S Bonkowski
University of Washington School of Public Health.
Co-authored papers 1
Michael J Bamshad
University of Washington
Co-authored papers 1
Andrew R Webster
Institute of Ophthalmology, University College London
Co-authored papers 1
Kelsey Luu
Co-authored papers 1
Dawn Earl
Co-authored papers 1
Melanie Bahlo
Co-authored papers 1
Tom Walsh
University of Washington
Co-authored papers 1
Aaron Lee
Harvard University, Moorfields Eye Hospital NHS Foundation Trust, St. John's Mercy Hospital, University of British Columbia, University of Washington, Washington University in Saint Louis
Co-authored papers 1
Timothy E Reddy
Co-authored papers 1
Dan Doherty
University of Washington
Co-authored papers 1
Release 1.2