H-Index & Metrics Best Publications

H-Index & Metrics

Discipline name H-index Citations Publications World Ranking National Ranking
Neuroscience D-index 66 Citations 17,857 138 World Ranking 1044 National Ranking 111
Biology and Biochemistry D-index 75 Citations 26,936 171 World Ranking 2251 National Ranking 164

Research.com Recognitions

Awards & Achievements

2018 - Member of Academia Europaea

2011 - Fellow of the Royal Society of Edinburgh

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • DNA
  • Genetics

Seth G. N. Grant mostly deals with Neuroscience, Cell biology, Synaptic plasticity, Long-term potentiation and Synapse. His Neuroscience study combines topics in areas such as Neurotransmission, Function and Guanylate kinase. Seth G. N. Grant has researched Cell biology in several fields, including NMDA receptor, Receptor and Peptide.

His work carried out in the field of Synaptic plasticity brings together such families of science as Glutamatergic and Untranslated region. His Long-term potentiation study incorporates themes from Tyrosine kinase, FYN and Protein kinase A. His biological study spans a wide range of topics, including Proteomics and Postsynaptic potential.

His most cited work include:

  • An anatomically comprehensive atlas of the adult human brain transcriptome (1443 citations)
  • De novo mutations in schizophrenia implicate synaptic networks (1120 citations)
  • Proteomic analysis of NMDA receptor-adhesion protein signaling complexes. (1071 citations)

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

The scientist’s investigation covers issues in Neuroscience, Cell biology, Synapse, Postsynaptic density and Postsynaptic potential. Seth G. N. Grant combines subjects such as Synaptic plasticity, Long-term potentiation, Neurotransmission and AMPA receptor with his study of Neuroscience. His Cell biology research is multidisciplinary, incorporating perspectives in NMDA receptor, Receptor and Biochemistry.

The study incorporates disciplines such as Proteome, Human brain and Nervous system in addition to Synapse. While the research belongs to areas of Proteome, Seth G. N. Grant spends his time largely on the problem of Computational biology, intersecting his research to questions surrounding Genetics and Bioinformatics. His research in Postsynaptic density intersects with topics in Dendritic spine, Scaffold protein, Signal transducing adaptor protein and Guanylate kinase.

He most often published in these fields:

  • Neuroscience (48.36%)
  • Cell biology (29.61%)
  • Synapse (23.03%)

What were the highlights of his more recent work (between 2017-2021)?

  • Neuroscience (48.36%)
  • Synapse (23.03%)
  • Excitatory postsynaptic potential (14.47%)

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

Seth G. N. Grant mainly focuses on Neuroscience, Synapse, Excitatory postsynaptic potential, Proteome and Postsynaptic potential. The concepts of his Neuroscience study are interwoven with issues in Long-term potentiation and Coronal plane. His Synapse study also includes

  • Forebrain which intersects with area such as NMDA receptor,
  • Cell biology that connect with fields like Synaptic plasticity.

His studies deal with areas such as Neocortex, Biophysics, Electrophysiology and Neurotransmitter receptor as well as Excitatory postsynaptic potential. His Proteome research is multidisciplinary, incorporating elements of Resource, Proteomics, Gene and Computational biology. His studies examine the connections between Postsynaptic potential and genetics, as well as such issues in Vertebrate, with regards to Hindbrain.

Between 2017 and 2021, his most popular works were:

  • Architecture of the Mouse Brain Synaptome (66 citations)
  • In vivo STED microscopy visualizes PSD95 sub-structures and morphological changes over several hours in the mouse visual cortex. (59 citations)
  • Proteomic analysis of postsynaptic proteins in regions of the human neocortex (46 citations)

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

  • Gene
  • DNA
  • Genetics

His primary areas of study are Excitatory postsynaptic potential, Neuroscience, Synapse, Postsynaptic density and Proteome. His studies in Excitatory postsynaptic potential integrate themes in fields like Live cell imaging, Postsynaptic potential, Spine, Glutamate receptor and Biophysics. The various areas that Seth G. N. Grant examines in his Neuroscience study include Genetic disorder and Longevity.

His studies deal with areas such as Early adulthood, Long-term potentiation, Forebrain and Intellectual ability as well as Synapse. His Forebrain research incorporates elements of Synaptic plasticity, Ca2+/calmodulin-dependent protein kinase and Cell biology, Phosphorylation, Synaptogenesis. His Proteome study combines topics in areas such as Autism, Transcription, Gene, Human brain and Proteostasis.

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

An anatomically comprehensive atlas of the adult human brain transcriptome

Michael J. Hawrylycz;Ed S. Lein;Angela L. Guillozet-Bongaarts;Elaine H. Shen.
Nature (2012)

1707 Citations

Differential plasmid rescue from transgenic mouse DNAs into Escherichia coli methylation-restriction mutants.

Seth G. N. Grant;Joel Jessee;Fredric R. Bloom;Douglas Hanahan.
Proceedings of the National Academy of Sciences of the United States of America (1990)

1419 Citations

Proteomic analysis of NMDA receptor-adhesion protein signaling complexes.

Holger Husi;Malcolm A. Ward;Jyoti S. Choudhary;Walter P. Blackstock.
Nature Neuroscience (2000)

1371 Citations

Impaired long-term potentiation, spatial learning, and hippocampal development in fyn mutant mice.

Seth G. N. Grant;Thomas J. O'dell;Kevin A. Karl;Paul L. Stein.
Science (1992)

1340 Citations

Enhanced long-term potentiation and impaired learning in mice with mutant postsynaptic density-95 protein

Martine Migaud;Paul Charlesworth;Maureen Dempster;Lorna C. Webster.
Nature (1998)

1288 Citations

De novo mutations in schizophrenia implicate synaptic networks

Menachem Fromer;Andrew Pocklington;David Kavanagh;Hywel John Williams.
Nature (2014)

1272 Citations

A polygenic burden of rare disruptive mutations in schizophrenia

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

1201 Citations

Arc/Arg3.1 Is Essential for the Consolidation of Synaptic Plasticity and Memories

Niels Plath;Ora Ohana;Ora Ohana;Björn Dammermann;Mick L. Errington.
Neuron (2006)

820 Citations

De Novo CNV Analysis Implicates Specific Abnormalities of Postsynaptic Signalling Complexes in the Pathogenesis of Schizophrenia

George Kirov;Andrew Pocklington;Peter Alan Holmans;Dobril Ivanov.
Molecular Psychiatry (2012)

758 Citations

The HUPO PSI's Molecular Interaction format—a community standard for the representation of protein interaction data

Henning Hermjakob;Luisa Montecchi-Palazzi;Gary Bader;Jérôme Wojcik.
Nature Biotechnology (2004)

713 Citations

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