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Biology and Biochemistry

D-Index
67
Citations
35535
World Ranking
8029
National Ranking
3638

Overview

Danilo A. Tagle is affiliated with the National Institutes of Health in the United States. Their research spans the fields of biochemistry, genetics, molecular biology, and engineering, with a focus on subfields such as biomedical engineering, molecular biology, and cancer research.

The scientist's work covers a range of topics, including:

  • 3D Printing in Biomedical Research
  • Pluripotent Stem Cells Research
  • Biomedical and Engineering Education
  • Extracellular vesicles in disease
  • Neuroscience and Neural Engineering
  • MicroRNA in disease regulation
  • Cancer-related molecular mechanisms research

Danilo A. Tagle has published extensively, with notable recent papers including:

  • Organs-on-chips: into the next decade, 2020, Nature Reviews Drug Discovery
  • Emerging technologies and their impact on regulatory science, 2021, Experimental Biology and Medicine
  • Extracellular RNAs as potential biomarkers for cancer, 2020, Journal of Cancer Metastasis and Treatment
  • Microphysiological Systems: Stakeholder Challenges to Adoption in Drug Development, 2021, Cells Tissues Organs
  • Organs-on-a-Chip, 2020, Advances in Experimental Medicine and Biology

The venues where Danilo A. Tagle frequently publishes include:

  • Experimental Biology and Medicine
  • ALTEX
  • NAM journal.
  • Nature Reviews Drug Discovery
  • Journal of Cancer Metastasis and Treatment

Frequent coauthors who have collaborated with Danilo A. Tagle are:

  • Lucie A. Low
  • Christine Happel
  • Janny van den Eijnden-van Raaij
  • Passley Hargrove-Grimes
  • Christine L. Mummery

Best Publications

  • A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes

    Marcy E. MacDonald;Christine M. Ambrose;Mabel P. Duyao;Richard H. Myers

  • A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. The Huntington's Disease Collaborative Research Group.

    M Shah;N Datson;L Srinidhi;VP Stanton

  • A SINGLE ATAXIA TELANGIECTASIA GENE WITH A PRODUCT SIMILAR TO PI-3 KINASE

    Kinneret Savitsky;Anat Bar-Shira;Shlomit Gilad;Galit Rotman

  • Atm-deficient mice: a paradigm of ataxia telangiectasia.

    Carrolee Barlow;Shinji Hirotsune;Richard Paylor;Marek Liyanage

  • Niemann-Pick C1 disease gene: homology to mediators of cholesterol homeostasis.

    Eugene D. Carstea;Jill A. Morris;Katherine G. Coleman;Stacie K. Loftus

  • Murine model of Niemann-Pick C disease: mutation in a cholesterol homeostasis gene.

    Stacie K. Loftus;Jill A. Morris;Eugene D. Carstea;Jessie Z. Gu

  • The complete sequence of the coding region of the ATM gene reveals similarity to cell cycle regulators in different species

    Kinneret Savitsky;Sharon Sfez;Danilo A. Tagle;Yael Ziv

  • Organs-on-chips: into the next decade

    Lucie A. Low;Christine Mummery;Christine Mummery;Brian R. Berridge;Christopher P. Austin

  • Widespread expression of the human and rat Huntington's disease gene in brain and nonneural tissues.

    Theresa V. Strong;Danilo A. Tagle;John M. Valdes;Lawrence W. Elmer

  • Behavioural abnormalities and selective neuronal loss in HD transgenic mice expressing mutated full-length HD cDNA

    P. Hemachandra Reddy;Maya Williams;Vinod Charles;Lisa Garrett

  • Embryonic epsilon and gamma globin genes of a prosimian primate (Galago crassicaudatus). Nucleotide and amino acid sequences, developmental regulation and phylogenetic footprints

    Danilo A. Tagle;Ben F. Koop;Morris Goodman;Jerry L. Slightom;Jerry L. Slightom

  • TEL1, an S. cerevisiae homolog of the human gene mutated in ataxia telangiectasia, is functionally related to the yeast checkpoint gene MEC1

    Dwight M Morrow;Danilo A Tagle;Yosef Shiloh;Francis S Collins

  • Abnormal mitochondrial dynamics, mitochondrial loss and mutant huntingtin oligomers in Huntington's disease: implications for selective neuronal damage

    Ulziibat Shirendeb;Arubala P. Reddy;Maria Manczak;Marcus J. Calkins

  • Mutant huntingtin expression in clonal striatal cells: dissociation of inclusion formation and neuronal survival by caspase inhibition.

    Manho Kim;H. S. Lee;Genevieve LaForet;Charmian McIntyre

  • Atm deficiency results in severe meiotic disruption as early as leptonema of prophase I

    Carrolee Barlow;Marek Liyanage;Peter B. Moens;Madalina Tarsounas

  • Phenylketonuria Scientific Review Conference: state of the science and future research needs.

    Kathryn M. Camp;Melissa A. Parisi;Phyllis B. Acosta;Gerard T. Berry

  • Changes in cortical and striatal neurons predict behavioral and electrophysiological abnormalities in a transgenic murine model of Huntington's disease

    G A Laforet;E Sapp;K Chase;C McIntyre

  • Biology-inspired microphysiological system approaches to solve the prediction dilemma of substance testing.

    Uwe Marx;Tommy B Andersson;Anthony Bahinski;Mario Beilmann

  • Atm selectively regulates distinct p53-dependent cell-cycle checkpoint and apoptotic pathways

    Carrolee Barlow;Kevin D. Brown;Chu Xia Deng;Danilo A. Tagle

  • Structure, expression, and function of kynurenine aminotransferases in human and rodent brains

    Qian Han;Tao Cai;Danilo A. Tagle;Jianyong Li

Frequent Co-Authors

Francis S. Collins
Francis S. Collins National Institutes of Health
Jerry L. Slightom
Jerry L. Slightom AureoGen Biosciences (United States)
Yosef Shiloh
Yosef Shiloh Tel Aviv University
Morris Goodman
Morris Goodman Wayne State University
P. Hemachandra Reddy
P. Hemachandra Reddy Texas Tech University Health Sciences Center
Anthony Wynshaw-Boris
Anthony Wynshaw-Boris Case Western Reserve University
Ben F. Koop
Ben F. Koop University of Victoria
Marcy E. MacDonald
Marcy E. MacDonald Harvard University
William J. Pavan
William J. Pavan National Institutes of Health
Peter G. Pentchev
Peter G. Pentchev National Institutes of Health

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