Vidur Garg

Employment

• Sloan-Kettering Institute Research Scholar
  2021 - Present
• Weill Cornell Graduate School of Medical Sciences Graduate Student
  2013 - 2021
• Sloan-Kettering Institute Research Technician
  2012 - 2013
• Weill Cornell Medical College Undergraduate Research Associate
  2010 - 2012

Education

• Weill Cornell Graduate School of Medical Sciences Doctor of Philosophy
  2013 - Present
• Henry Ford Community College Associate in Science (Biology)
  2008 - 2009
• Hunter College Bachelor of Arts, Biochemistry
  2007 - 2012

Projects & Funding

Projects & funding information is unavailable.

Publications (13)

• 3D Enhancer–promoter networks provide predictive features for gene expression and coregulation in early embryonic lineages
  Nature Structural & Molecular Biology 2024 DOI: 10.1038/s41594-023-01130-4
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• Systematic mapping and modeling of 3D enhancer-promoter interactions in early mouse embryonic lineages reveal regulatory principles that determine the levels and cell-type specificity of gene expression
  2023 DOI: 10.1101/2023.07.19.549714
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• Single-cell analysis of bidirectional reprogramming between early embryonic states reveals mechanisms of differential lineage plasticities
  2023 DOI: 10.1101/2023.03.28.534648
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• 3D genome topologies distinguish pluripotent epiblast and primitive endoderm cells in the mouse blastocyst
  2022 DOI: 10.1101/2022.10.19.512781
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• Single-Cell Transcriptomics Reveals Early Emergence of Liver Parenchymal and Non-parenchymal Cell Lineages
  Cell 2020 DOI: 10.1016/j.cell.2020.09.012
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• The emergent landscape of the mouse gut endoderm at single-cell resolution.
  Nature 2019 DOI: 10.1038/s41586-019-1127-1
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• Ex Utero Culture and Imaging of Mouse Embryos.
  Methods in molecular biology (Clifton, N.J.) 2019 DOI: 10.1007/978-1-4939-9009-2_11
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• A Sprouty4 reporter to monitor FGF/ERK signaling activity in ESCs and mice.
  Developmental biology 2018 DOI: 10.1016/j.ydbio.2018.06.017
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• Lineage Establishment and Progression within the Inner Cell Mass of the Mouse Blastocyst Requires FGFR1 and FGFR2.
  Developmental cell 2017 DOI: 10.1016/j.devcel.2017.05.003
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• Widespread Mitotic Bookmarking by Histone Marks and Transcription Factors in Pluripotent Stem Cells.
  Cell reports 2017 DOI: 10.1016/j.celrep.2017.04.067
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