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
Biology and Biochemistry D-index 65 Citations 28,050 206 World Ranking 5763 National Ranking 2738

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Enzyme
  • Cancer

His scientific interests lie mostly in Neuroscience, Genetics, Histone, Small molecule and Cell biology. His Neuroscience study integrates concerns from other disciplines, such as Alzheimer's disease, Neurodegeneration and Pharmacology. His work on FMR1, Epigenetics, Exome and Allele as part of his general Genetics study is frequently connected to Multifactorial Inheritance, thereby bridging the divide between different branches of science.

In the subject of general Histone, his work in Histone deacetylase 2 is often linked to Epigenetics of cocaine addiction, thereby combining diverse domains of study. His Small molecule research includes themes of Immunology, Drug repositioning, Zebrafish, Computational biology and Drug discovery. Stephen J. Haggarty combines subjects such as Drug action, Disease, Function and Molecular targets with his study of Computational biology.

His most cited work include:

  • The Connectivity Map: Using Gene-Expression Signatures to Connect Small Molecules, Genes, and Disease (3268 citations)
  • The Connectivity Map: Using Gene-Expression Signatures to Connect Small Molecules, Genes, and Disease (3268 citations)
  • Small Molecule Inhibitor of Mitotic Spindle Bipolarity Identified in a Phenotype-Based Screen (1436 citations)

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

Stephen J. Haggarty spends much of his time researching Cell biology, Neuroscience, Histone deacetylase, Epigenetics and Small molecule. The study incorporates disciplines such as Molecular biology and Neurodegeneration in addition to Cell biology. His work deals with themes such as Induced pluripotent stem cell and Drug discovery, which intersect with Neuroscience.

His Histone deacetylase research focuses on subjects like Pharmacology, which are linked to Kinase and In vitro. Stephen J. Haggarty has included themes like Histone and Memory consolidation in his Epigenetics study. His research links Computational biology with Small molecule.

He most often published in these fields:

  • Cell biology (29.85%)
  • Neuroscience (29.48%)
  • Histone deacetylase (13.43%)

What were the highlights of his more recent work (between 2018-2021)?

  • Cell biology (29.85%)
  • Neuroscience (29.48%)
  • Neurodegeneration (6.34%)

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

Cell biology, Neuroscience, Neurodegeneration, Induced pluripotent stem cell and Frontotemporal dementia are his primary areas of study. His study in Cell biology is interdisciplinary in nature, drawing from both Histone deacetylase, microRNA, Peptide and Tauopathy. His studies deal with areas such as Psychiatric Disease, Circular RNA, Gene expression and Cereblon as well as Neuroscience.

As a part of the same scientific family, he mostly works in the field of Neurodegeneration, focusing on Activator and, on occasion, Gliosis. Stephen J. Haggarty studied Frontotemporal dementia and Tau protein that intersect with Cell, Drug discovery, Disease mechanisms, Disease etiology and DNA ligase. His Psychological repression study is concerned with the field of Gene as a whole.

Between 2018 and 2021, his most popular works were:

  • Targeted degradation of aberrant tau in frontotemporal dementia patient-derived neuronal cell models (74 citations)
  • Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia (41 citations)
  • A farnesyltransferase inhibitor activates lysosomes and reduces tau pathology in mice with tauopathy (31 citations)

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

  • Gene
  • Enzyme
  • Cancer

His main research concerns Cell biology, Drug discovery, Neural stem cell, Neurodegeneration and Tauopathy. His Cell biology research incorporates themes from Autophagy and Downregulation and upregulation, Gene. His Drug discovery research is multidisciplinary, incorporating elements of Ex vivo, Computational biology and Drug.

His work carried out in the field of Computational biology brings together such families of science as Precision medicine, Stem cell, Disease, Translational science and Cell type. His research integrates issues of Cancer research, Neurite, Corticobasal degeneration, Induced pluripotent stem cell and Neurogenesis in his study of Neural stem cell. His work in Tauopathy covers topics such as Tau protein which are related to areas like Frontotemporal dementia, Cell and Neuroscience.

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

The Connectivity Map: Using Gene-Expression Signatures to Connect Small Molecules, Genes, and Disease

Justin Lamb;Emily D. Crawford;David Peck;Joshua W. Modell.
Science (2006)

4549 Citations

Small Molecule Inhibitor of Mitotic Spindle Bipolarity Identified in a Phenotype-Based Screen

Thomas U. Mayer;Tarun M. Kapoor;Stephen J. Haggarty;Stephen J. Haggarty;Randall W. King.
Science (1999)

2146 Citations

A Next Generation Connectivity Map: L1000 Platform and the First 1,000,000 Profiles.

Aravind Subramanian;Rajiv Narayan;Steven M. Corsello;Steven M. Corsello;David D. Peck.
Cell (2017)

1662 Citations

HDAC2 negatively regulates memory formation and synaptic plasticity

Ji Song Guan;Stephen J. Haggarty;Emanuela Giacometti;Jan Hermen Dannenberg;Jan Hermen Dannenberg.
Nature (2009)

1586 Citations

A polygenic burden of rare disruptive mutations in schizophrenia

Shaun M Purcell;Jennifer L Moran;Menachem Fromer;Douglas Ruderfer.
Nature (2014)

1428 Citations

Domain-selective small-molecule inhibitor of histone deacetylase 6 (HDAC6)-mediated tubulin deacetylation

Stephen J. Haggarty;Kathryn M. Koeller;Jason C. Wong;Christina M. Grozinger.
Proceedings of the National Academy of Sciences of the United States of America (2003)

1191 Citations

Disrupted in Schizophrenia 1 Regulates Neuronal Progenitor Proliferation via Modulation of GSK3β/β-Catenin Signaling

Yingwei Mao;Xuecai Ge;Xuecai Ge;Xuecai Ge;Christopher L. Frank;Christopher L. Frank;Jon M. Madison.
Cell (2009)

855 Citations

Chemical phylogenetics of histone deacetylases

James E Bradner;Nathan West;Nathan West;Melissa L Grachan;Edward F Greenberg;Edward F Greenberg.
Nature Chemical Biology (2010)

766 Citations

An epigenetic blockade of cognitive functions in the neurodegenerating brain

Johannes Gräff;Damien Rei;Damien Rei;Ji-Song Guan;Ji-Song Guan;Wen-Yuan Wang;Wen-Yuan Wang.
Nature (2012)

764 Citations

Inhibitors of class 1 histone deacetylases reverse contextual memory deficits in a mouse model of Alzheimer's disease.

Mark Kilgore;Courtney A Miller;Daniel M Fass;Daniel M Fass;Krista M Hennig;Krista M Hennig.
Neuropsychopharmacology (2010)

699 Citations

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