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
Chemistry D-index 57 Citations 9,104 223 World Ranking 5864 National Ranking 149
Biology and Biochemistry D-index 60 Citations 9,864 200 World Ranking 5450 National Ranking 107

Overview

What is he best known for?

The fields of study he is best known for:

  • Enzyme
  • Gene
  • DNA

The scientist’s investigation covers issues in Biochemistry, Stereochemistry, Receptor, Adenosine receptor and Binding site. Stefano Moro works mostly in the field of Stereochemistry, limiting it down to concerns involving Structure–activity relationship and, occasionally, Radioligand Assay. His study in Amino acid extends to Receptor with its themes.

His study in Adenosine receptor is interdisciplinary in nature, drawing from both G protein-coupled receptor, Adenosine, Ligand, Chemical synthesis and Carboxamide. His Binding site research includes themes of Protein structure and Biophysics. As a part of the same scientific study, Stefano Moro usually deals with the Docking, concentrating on Drug discovery and frequently concerns with Computational biology.

His most cited work include:

  • FAM/USP9x, a Deubiquitinating Enzyme Essential for TGFβ Signaling, Controls Smad4 Monoubiquitination (389 citations)
  • Medicinal Chemistry and the Molecular Operating Environment (MOE): Application of QSAR and Molecular Docking to Drug Discovery (335 citations)
  • The mitochondrial calcium uniporter is a multimer that can include a dominant-negative pore-forming subunit. (306 citations)

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

Stereochemistry, Receptor, Molecular model, Adenosine receptor and Biochemistry are his primary areas of study. His research integrates issues of Structure–activity relationship, Chemical synthesis and DNA in his study of Stereochemistry. Many of his studies involve connections with topics such as Pharmacophore and Receptor.

His study explores the link between Molecular model and topics such as Docking that cross with problems in Ligand. His Adenosine receptor research is multidisciplinary, relying on both Adenosine, Potency, Xanthine, Selectivity and Pharmacology. His work carried out in the field of G protein-coupled receptor brings together such families of science as Biophysics, Computational biology and Binding site.

He most often published in these fields:

  • Stereochemistry (34.57%)
  • Receptor (22.86%)
  • Molecular model (22.00%)

What were the highlights of his more recent work (between 2015-2021)?

  • Molecular dynamics (6.86%)
  • Computational biology (12.57%)
  • Stereochemistry (34.57%)

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

Stefano Moro focuses on Molecular dynamics, Computational biology, Stereochemistry, Adenosine receptor and Molecular model. His Molecular dynamics research is multidisciplinary, incorporating elements of Protein ligand, Molecule, Chemical physics and Ligand. His Computational biology study incorporates themes from Molecular recognition, In silico and Drug discovery.

His studies in Stereochemistry integrate themes in fields like Alkyl and Amide. His Adenosine receptor study is related to the wider topic of Receptor. Stefano Moro combines subjects such as Moiety, Docking and Antagonist with his study of Molecular model.

Between 2015 and 2021, his most popular works were:

  • Bridging Molecular Docking to Molecular Dynamics in Exploring Ligand-Protein Recognition Process: An Overview. (108 citations)
  • Deciphering the Complexity of Ligand–Protein Recognition Pathways Using Supervised Molecular Dynamics (SuMD) Simulations (49 citations)
  • Ciprofloxacin and levofloxacin attenuate microglia inflammatory response via TLR4/NF-kB pathway. (47 citations)

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

  • Enzyme
  • Gene
  • DNA

Stefano Moro mainly focuses on Molecular dynamics, Molecular model, Ligand, Stereochemistry and Computational biology. He focuses mostly in the field of Molecular model, narrowing it down to topics relating to Drug discovery and, in certain cases, Biochemical engineering and Virology. His studies deal with areas such as Apoptosis, Structure–activity relationship and Adenosine receptor as well as Stereochemistry.

His Adenosine receptor research integrates issues from Wild type and Potency. His study looks at the relationship between Binding site and topics such as Biophysics, which overlap with Receptor. Receptor is a subfield of Biochemistry that he explores.

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

FAM/USP9x, a Deubiquitinating Enzyme Essential for TGFβ Signaling, Controls Smad4 Monoubiquitination

Sirio Dupont;Anant Mamidi;Michelangelo Cordenonsi;Marco Montagner.
Cell (2009)

534 Citations

Medicinal Chemistry and the Molecular Operating Environment (MOE): Application of QSAR and Molecular Docking to Drug Discovery

Santiago Vilar;Giorgio Cozza;Stefano Moro.
Current Topics in Medicinal Chemistry (2008)

464 Citations

The mitochondrial calcium uniporter is a multimer that can include a dominant-negative pore-forming subunit.

Anna Raffaello;Diego De Stefani;Davide Sabbadin;Enrico Teardo.
The EMBO Journal (2013)

380 Citations

Synthesis, CoMFA analysis, and receptor docking of 3,5-diacyl-2, 4-dialkylpyridine derivatives as selective A3 adenosine receptor antagonists.

An-Hu Li;Stefano Moro;Nancy Forsyth;Neli Melman.
Journal of Medicinal Chemistry (1999)

252 Citations

DNA Binding Site Selection of Dimeric and Tetrameric Stat5 Proteins Reveals a Large Repertoire of Divergent Tetrameric Stat5a Binding Sites

Elisabetta Soldaini;Susan John;Stefano Moro;Julie Bollenbacher.
Molecular and Cellular Biology (2000)

237 Citations

Toward the rational design of protein kinase casein kinase-2 inhibitors.

Stefania Sarno;Stefano Moro;Flavio Meggio;Giuseppe Zagotto.
Pharmacology & Therapeutics (2002)

206 Citations

USP15 is a deubiquitylating enzyme for receptor-activated SMADs

Masafumi Inui;Andrea Manfrin;Anant Mamidi;Graziano Martello.
Nature Cell Biology (2011)

203 Citations

Human P2Y1 Receptor: Molecular Modeling and Site-Directed Mutagenesis as Tools To Identify Agonist and Antagonist Recognition Sites

Stefano Moro;Danping Guo;Emidio Camaioni;José L. Boyer.
Journal of Medicinal Chemistry (1998)

198 Citations

Progress in the pursuit of therapeutic adenosine receptor antagonists.

Stefano Moro;Zhan-Guo Gao;Kenneth A. Jacobson;Giampiero Spalluto.
Medicinal Research Reviews (2006)

190 Citations

Bridging Molecular Docking to Molecular Dynamics in Exploring Ligand-Protein Recognition Process: An Overview.

Veronica Salmaso;Stefano Moro.
Frontiers in Pharmacology (2018)

173 Citations

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