D-Index & Metrics Best Publications

D-Index & Metrics D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines.

Discipline name D-index D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines. Citations Publications World Ranking National Ranking
Medicine D-index 89 Citations 26,695 241 World Ranking 6172 National Ranking 572

Research.com Recognitions

Awards & Achievements

2021 - King Faisal Prize

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Internal medicine
  • Central nervous system

Robin J.M. Franklin mostly deals with Remyelination, Neuroscience, Oligodendrocyte, Multiple sclerosis and Myelin. His Remyelination study combines topics in areas such as Oligodendrocyte differentiation, Cell biology, Immunology and CNS demyelination. He has included themes like White matter, Cellular differentiation, Regeneration and Pathology in his Neuroscience study.

His biological study spans a wide range of topics, including Progenitor cell, Demyelinating disease, Neuroglia and Lesion. His Multiple sclerosis research incorporates themes from Regenerative process, Genetic analysis, Gene and Disease. The various areas that he examines in his Myelin study include Wnt signaling pathway, Neuregulin, Signal transduction and Neuregulin 1.

His most cited work include:

  • Remyelination in the CNS: from biology to therapy (1059 citations)
  • M2 microglia and macrophages drive oligodendrocyte differentiation during CNS remyelination (913 citations)
  • Debris clearance by microglia: an essential link between degeneration and regeneration (706 citations)

What are the main themes of his work throughout his whole career to date?

His primary areas of study are Remyelination, Neuroscience, Oligodendrocyte, Myelin and Multiple sclerosis. His Remyelination study combines topics from a wide range of disciplines, such as Regeneration, Cell biology, Immunology and Transplantation. His research investigates the link between Neuroscience and topics such as Stem cell that cross with problems in Adult stem cell.

Robin J.M. Franklin works mostly in the field of Oligodendrocyte, limiting it down to topics relating to Progenitor cell and, in certain cases, Cell, as a part of the same area of interest. The study incorporates disciplines such as White matter and Microglia in addition to Myelin. His study in Multiple sclerosis is interdisciplinary in nature, drawing from both Precursor cell and Oligodendrocyte progenitor.

He most often published in these fields:

  • Remyelination (56.73%)
  • Neuroscience (48.25%)
  • Oligodendrocyte (35.09%)

What were the highlights of his more recent work (between 2014-2021)?

  • Remyelination (56.73%)
  • Neuroscience (48.25%)
  • Myelin (32.16%)

In recent papers he was focusing on the following fields of study:

His scientific interests lie mostly in Remyelination, Neuroscience, Myelin, Cell biology and Multiple sclerosis. His Remyelination study is concerned with Central nervous system in general. Robin J.M. Franklin has researched Neuroscience in several fields, including Stem cell, Neural stem cell, Disease and Cell type.

His work in Myelin tackles topics such as White matter which are related to areas like Neurodegeneration. His study looks at the relationship between Cell biology and fields such as Lesion, as well as how they intersect with chemical problems. The concepts of his Multiple sclerosis study are interwoven with issues in Regenerative process, Oligodendrocyte progenitor and Microglia.

Between 2014 and 2021, his most popular works were:

  • Single-Cell RNA Sequencing of Microglia throughout the Mouse Lifespan and in the Injured Brain Reveals Complex Cell-State Changes. (424 citations)
  • Regenerating CNS myelin - from mechanisms to experimental medicines. (200 citations)
  • Regulatory T cells promote myelin regeneration in the central nervous system. (166 citations)

In his most recent research, the most cited papers focused on:

  • Gene
  • Internal medicine
  • Neuron

Remyelination, Neuroscience, Myelin, Cell biology and Oligodendrocyte are his primary areas of study. His Remyelination research is multidisciplinary, relying on both Cellular differentiation, Progenitor cell, Stem cell and Multiple sclerosis, Immunology. His study in Neuroscience focuses on Central nervous system and Oligodendrocyte differentiation.

Robin J.M. Franklin interconnects White matter, Innate immune system and Embryonic stem cell in the investigation of issues within Myelin. His work on Cell delivery as part of general Cell biology research is frequently linked to Water exchange, bridging the gap between disciplines. His Oligodendrocyte study integrates concerns from other disciplines, such as Lineage, Neuroglia, Phenotype, Mechanotransduction and Axon.

This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.

Best Publications

Remyelination in the CNS: from biology to therapy

Robin J. M. Franklin;Charles ffrench-Constant.
Nature Reviews Neuroscience (2008)

1668 Citations

M2 microglia and macrophages drive oligodendrocyte differentiation during CNS remyelination

Veronique E. Miron;Amanda Boyd;Jing Wei Zhao;Tracy J. Yuen;Tracy J. Yuen.
Nature Neuroscience (2013)

1424 Citations

Why does remyelination fail in multiple sclerosis

Robin J. M. Franklin.
Nature Reviews Neuroscience (2002)

1053 Citations

Debris clearance by microglia: an essential link between degeneration and regeneration

H P H Neumann;M. R. Kotter;R J M Franklin.
Brain (2008)

930 Citations

Rejuvenation of regeneration in the aging central nervous system

Julia M. Ruckh;Jing-Wei Zhao;Jennifer L. Shadrach;Peter van Wijngaarden.
Cell Stem Cell (2012)

621 Citations

Myelin impairs CNS remyelination by inhibiting oligodendrocyte precursor cell differentiation.

Mark R. Kotter;Wen-Wu Li;Chao Zhao;Robin J. M. Franklin.
The Journal of Neuroscience (2006)

608 Citations

Dysregulation of the Wnt pathway inhibits timely myelination and remyelination in the mammalian CNS

Stephen P.J. Fancy;Sergio E. Baranzini;Chao Zhao;Dong-In Yuk.
Genes & Development (2009)

541 Citations

CNS-resident glial progenitor/stem cells produce Schwann cells as well as oligodendrocytes during repair of CNS demyelination.

Malgorzata Zawadzka;Malgorzata Zawadzka;Leanne E. Rivers;Stephen P.J. Fancy;Stephen P.J. Fancy;Chao Zhao.
Cell Stem Cell (2010)

528 Citations

The Age-Related Decrease in CNS Remyelination Efficiency Is Attributable to an Impairment of Both Oligodendrocyte Progenitor Recruitment and Differentiation

Fraser J. Sim;Chao Zhao;Jacques Penderis;Jacques Penderis;Robin J. M. Franklin.
The Journal of Neuroscience (2002)

501 Citations

Repair of demyelinated lesions by transplantation of purified O-2A progenitor cells

A. K. Groves;S. C. Barnett;R. J. M. Franklin;A. J. Crang.
Nature (1993)

500 Citations

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