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 62 Citations 14,454 331 World Ranking 5647 National Ranking 141
Biology and Biochemistry D-index 67 Citations 16,888 286 World Ranking 5201 National Ranking 119

Overview

What is he best known for?

The fields of study he is best known for:

  • Enzyme
  • Organic chemistry
  • Gene

Roberto Pellicciari mostly deals with Biochemistry, Internal medicine, Kynurenic acid, Endocrinology and Pharmacology. His Biochemistry study frequently draws parallels with other fields, such as Cell biology. In his study, which falls under the umbrella issue of Internal medicine, Bile acid, Small heterodimer partner, Retinoid X receptor and Adipogenesis is strongly linked to Farnesoid X receptor.

His Bile acid study frequently links to other fields, such as Stereochemistry. The concepts of his Kynurenic acid study are interwoven with issues in Quinolinic acid, Kynurenine pathway, Kynurenine and Indoleamine 2,3-dioxygenase. His Pharmacology study combines topics from a wide range of disciplines, such as Glutamate receptor, Metabotropic glutamate receptor 1 and Metabotropic glutamate receptor.

His most cited work include:

  • TGR5-Mediated Bile Acid Sensing Controls Glucose Homeostasis (1079 citations)
  • Targeting bile-acid signalling for metabolic diseases (796 citations)
  • Manipulation of Brain Kynurenines: Glial Targets, Neuronal Effects, and Clinical Opportunities (450 citations)

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

His main research concerns Stereochemistry, Biochemistry, Organic chemistry, Bile acid and Metabotropic glutamate receptor. Roberto Pellicciari has included themes like Agonist, Glycine, NMDA receptor and Chemical synthesis in his Stereochemistry study. In general Bile acid, his work in G protein-coupled bile acid receptor is often linked to Side chain linking many areas of study.

His Metabotropic glutamate receptor research is multidisciplinary, incorporating elements of Antagonist and Metabotropic receptor. His research investigates the connection with Kynurenic acid and areas like Quinolinic acid which intersect with concerns in Kynurenine. His Farnesoid X receptor study combines topics in areas such as Internal medicine and Chenodeoxycholic acid.

He most often published in these fields:

  • Stereochemistry (30.71%)
  • Biochemistry (21.57%)
  • Organic chemistry (13.20%)

What were the highlights of his more recent work (between 2010-2021)?

  • Biochemistry (21.57%)
  • Bile acid (13.20%)
  • Receptor (10.91%)

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

Roberto Pellicciari focuses on Biochemistry, Bile acid, Receptor, Stereochemistry and Farnesoid X receptor. His Biochemistry study frequently draws connections between adjacent fields such as In vivo. Roberto Pellicciari focuses mostly in the field of Bile acid, narrowing it down to topics relating to Cholestasis and, in certain cases, Metabolism.

Many of his studies on Stereochemistry involve topics that are commonly interrelated, such as Structure–activity relationship. His Farnesoid X receptor research is multidisciplinary, incorporating perspectives in Chenodeoxycholic acid, Ligand, Transactivation, Biological activity and Allosteric regulation. His work deals with themes such as Combinatorial chemistry and Signal transduction, Cell biology, which intersect with G protein-coupled bile acid receptor.

Between 2010 and 2021, his most popular works were:

  • Family-wide chemical profiling and structural analysis of PARP and tankyrase inhibitors (339 citations)
  • TGR5 activation inhibits atherosclerosis by reducing macrophage inflammation and lipid loading. (300 citations)
  • De novo NAD + synthesis enhances mitochondrial function and improves health (121 citations)

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

  • Enzyme
  • Organic chemistry
  • Gene

His primary scientific interests are in Biochemistry, G protein-coupled bile acid receptor, Farnesoid X receptor, Stereochemistry and Receptor. His study on G protein-coupled bile acid receptor also encompasses disciplines like

  • Inflammation, which have a strong connection to PI3K/AKT/mTOR pathway, CCAAT-Enhancer-Binding Protein-beta, Adipose tissue and mTORC1,
  • Signal transduction that connect with fields like Internal medicine, Proinflammatory cytokine and Macrophage,
  • Immunology that intertwine with fields like Endocrinology. His Farnesoid X receptor research incorporates elements of Virtual screening and Plasma protein binding.

His Stereochemistry research is multidisciplinary, relying on both Agonist, Potency and Transactivation. His studies deal with areas such as Homology modeling and Site-directed mutagenesis as well as Receptor. Chenodeoxycholic acid is the focus of his Bile acid research.

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

TGR5-Mediated Bile Acid Sensing Controls Glucose Homeostasis

Charles W. Thomas;Antimo Gioiello;Lilia G Noriega;Lilia G Noriega;Axelle Strehle.
Cell Metabolism (2009)

1594 Citations

Targeting bile-acid signalling for metabolic diseases

Charles Thomas;Roberto Pellicciari;Mark Pruzanski;Johan Auwerx.
Nature Reviews Drug Discovery (2008)

1211 Citations

Manipulation of Brain Kynurenines: Glial Targets, Neuronal Effects, and Clinical Opportunities

Robert Schwarcz;Roberto Pellicciari.
Journal of Pharmacology and Experimental Therapeutics (2002)

737 Citations

Family-wide chemical profiling and structural analysis of PARP and tankyrase inhibitors

Elisabet Wahlberg;Tobias Karlberg;Ekaterina Kouznetsova;Ekaterina Kouznetsova;Natalia Markova;Natalia Markova.
Nature Biotechnology (2012)

481 Citations

The nuclear receptor SHP mediates inhibition of hepatic stellate cells by FXR and protects against liver fibrosis

Stefano Fiorucci;Elisabetta Antonelli;Giovanni Rizzo;Barbara Renga.
Gastroenterology (2004)

460 Citations

TGR5 activation inhibits atherosclerosis by reducing macrophage inflammation and lipid loading.

Thijs Pols;Mitsunori Nomura;Taoufiq Harach;Giuseppe Lo Sasso.
Cell Metabolism (2011)

379 Citations

Structural Basis for Bile Acid Binding and Activation of the Nuclear Receptor FXR

Li Zhi Mi;Srikripa Devarakonda;Joel M. Harp;Qing Han.
Molecular Cell (2003)

303 Citations

Novel Potent and Selective Bile Acid Derivatives as TGR5 Agonists: Biological Screening, Structure−Activity Relationships, and Molecular Modeling Studies

Hiroyuki Sato;Antonio Macchiarulo;Charles Thomas;Antimo Gioiello.
Journal of Medicinal Chemistry (2008)

291 Citations

Bile Acid Derivatives as Ligands of the Farnesoid X Receptor. Synthesis, Evaluation, and Structure−Activity Relationship of a Series of Body and Side Chain Modified Analogues of Chenodeoxycholic Acid

Roberto Pellicciari;Gabriele Costantino;Emidio Camaioni;Bahman M. Sadeghpour.
Journal of Medicinal Chemistry (2004)

267 Citations

Protective effects of 6-ethyl chenodeoxycholic acid, a farnesoid x receptor ligand, in estrogen-induced cholestasis

Stefano Fiorucci;Carlo Clerici;Elisabetta Antonelli;Stefano Orlandi.
Journal of Pharmacology and Experimental Therapeutics (2005)

259 Citations

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