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Author Details

Dimitre R Simeonov
University of California San Francisco
2008
26
19
PMIDPaper TitleJournal TitlePublished Year
37503101Non-coding sequence variation reveals fragility within interleukin 2 feedback circuitry and shapes autoimmune disease risk.bioRxiv2023
37547023The lncRNA Malat1 Inhibits miR-15/16 to Enhance Cytotoxic T Cell Activation and Memory Cell Formation.bioRxiv2023
32499641CRISPR screen in regulatory T cells reveals modulators of Foxp3.Nature2020
32989329Functional CRISPR dissection of gene networks controlling human regulatory T cell identity.Nat Immunol2020
30698999CRISPR-Based Tools in Immunity.Annu Rev Immunol2019
31433990miR-15/16 Restrain Memory T Cell Differentiation, Cell Cycle, and Survival.Cell Rep2019
30643267Thymic regulatory T cells arise via two distinct developmental programs.Nat Immunol2019
28742462A novel iris transillumination grading scale allowing flexible assessment with quantitative image analysis and visual matching.Ophthalmic Genet2018
29899441Author Correction: Discovery of stimulation-responsive immune enhancers with CRISPR activation.Nature2018
29980618Revisiting IL-2: Biology and therapeutic prospects.Sci Immunol2018
28603714Defining Disease, Diagnosis, and Translational Medicine within a Homeostatic Perturbation Paradigm: The National Institutes of Health Undiagnosed Diseases Program Experience.Front Med (Lausanne)2017
28945252Enhancer connectome in primary human cells identifies target genes of disease-associated DNA elements.Nat Genet2017
28880873"T-bet"-ing on autoimmunity variants.PLoS Genet2017
28854172Discovery of stimulation-responsive immune enhancers with CRISPR activation.Nature2017
26216948Generation of knock-in primary human T cells using Cas9 ribonucleoproteins.Proc Natl Acad Sci U S A2015
24839611<i>GRIN2A</i> mutation and early-onset epileptic encephalopathy: personalized therapy with memantine.Ann Clin Transl Neurol2014
25251875ERCC6 dysfunction presenting as progressive neurological decline with brain hypomyelination.Am J Med Genet A2014
23103514A divalent interaction between HPS1 and HPS4 is required for the formation of the biogenesis of lysosome-related organelle complex-3 (BLOC-3).Biochim Biophys Acta2013
23504663DNA variations in oculocutaneous albinism: an updated mutation list and current outstanding issues in molecular diagnostics.Hum Mutat2013
22146942Exome sequencing and SNP analysis detect novel compound heterozygosity in fatty acid hydroxylase-associated neurodegeneration.Eur J Hum Genet2012
22675082Exome sequencing as a diagnostic tool in a case of undiagnosed juvenile-onset GM1-gangliosidosis.Neurology2012
22290570VAR-MD: a tool to analyze whole exome-genome variants in small human pedigrees with mendelian inheritance.Hum Mutat2012
21968110Nitisinone improves eye and skin pigmentation defects in a mouse model of oculocutaneous albinism.J Clin Invest2011
20371321The mechanical properties of Drosophila jump muscle expressing wild-type and embryonic Myosin isoforms.Biophys J2010
19838064Distinct Kinesin-14 mitotic mechanisms in spindle bipolarity.Cell Cycle2009
18418055Protein complexes at the microtubule organizing center regulate bipolar spindle assembly.Cell Cycle2008
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Collaborators

Alexander Marson
Gladstone-UCSF Institute of Genomic Immunology
Co-authored papers 13
William A Gahl
National Human Genome Research Institute, National Institutes of Health
Co-authored papers 10
David R Adams
National Human Genome Research Institute, National Institutes of Health
Co-authored papers 8
Cornelius F Boerkoel
University of British Columbia
Co-authored papers 6
Thomas C Markello
National Institutes of Health
Co-authored papers 5
Cynthia J Tifft
National Human Genome Research Institute
Co-authored papers 5
Jonathan M Woo
University of California san francisco
Co-authored papers 5
Kathrin Schumann
Institute for Medical Microbiology, Technical University of Munich (TUM)
Co-authored papers 4
Gretchen Golas
National Human Genome Research Institute, National Institutes of Health
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Murat Sincan
Boston University School of Public Health
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Theodore L Roth
Stanford University
Co-authored papers 4
Chun Jimmie Ye
University of California san francisco
Co-authored papers 4
Jacob E Corn
Co-authored papers 3
Ansuman T Satpathy
Stanford University
Co-authored papers 3
James C Mullikin
National Human Genome Research Institute, National Institutes of Health
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William J Greenleaf
Stanford University
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Brian P Brooks
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Maxwell R Mumbach
Broad Institute of MIT and Harvard
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Howard Y Chang
Center for Personal Dynamic Regulomes, Stanford University
Co-authored papers 3
Camilo Toro
National Human Genome Research Institute, National Institutes of Health
Co-authored papers 3
Youjin V Lee
University of Chicago
Co-authored papers 3
Nancy F Hansen
National Human Genome Research Institute, National Institutes of Health
Co-authored papers 2
Miao He
Children's Hospital of Philadelphia
Co-authored papers 2
Mark J Daly
Massachusetts General Hospital
Co-authored papers 2
Roxanne Fischer
National Human Genome Research Institute, National Institutes of Health
Co-authored papers 2
Victoria Tobin
California Institute of Technology
Co-authored papers 2
Zaheer Valivullah
Center for Mendelian Genomics, Broad Institute of MIT and Harvard
Co-authored papers 2
Lynne A Wolfe
National Institutes of Health Undiagnosed Diseases Program
Co-authored papers 2
Hailiang Huang
Massachusetts General Hospital
Co-authored papers 2
Eric Shifrut
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Release 1.2