World's Best Scientists 2026 revealed!

D-Index & Metrics

Chemistry

D-Index
60
Citations
13289
World Ranking
9668
National Ranking
287

Marco Mor publication distribution in Chemistry in 2026

The chart shows the distribution of publications by all Research.com ranked scientists in the field of Chemistry in 2026. The highlighted bar marks where Marco Mor sits on this spectrum.

61–80 publications: 66 scientists 81–100 publications: 302 scientists 101–120 publications: 623 scientists 121–140 publications: 918 scientists 141–160 publications: 1,218 scientists 161–180 publications: 1,350 scientists 181–200 publications: 1,344 scientists 201–220 publications: 1,281 scientists 221–240 publications: 1,216 scientists 241–260 publications: 1,100 scientists 261–280 publications: 979 scientists 281–300 publications: 939 scientists 301–320 publications: 764 scientists 321–340 publications: 643 scientists 341–360 publications: 628 scientists 361–380 publications: 522 scientists 381–400 publications: 459 scientists 401–420 publications: 397 scientists 421–440 publications: 327 scientists 441–460 publications: 270 scientists 461–480 publications: 265 scientists 481–500 publications: 252 scientists 501–520 publications: 201 scientists 521–540 publications: 185 scientists 541–560 publications: 148 scientists 561–580 publications: 148 scientists 581–600 publications: 132 scientists 601–620 publications: 114 scientists 621–640 publications: 104 scientists 641–660 publications: 91 scientists 661–680 publications: 92 scientists 681–700 publications: 73 scientists 701–720 publications: 57 scientists 721–740 publications: 54 scientists 741–760 publications: 67 scientists 761–780 publications: 45 scientists 781–800 publications: 46 scientists 801–820 publications: 39 scientists 821–840 publications: 32 scientists 841–860 publications: 36 scientists 861–880 publications: 29 scientists 881–900 publications: 26 scientists 901–920 publications: 24 scientists 921–940 publications: 14 scientists 941–960 publications: 23 scientists 961–980 publications: 28 scientists 981–1,000 publications: 15 scientists 1,001–1,020 publications: 29 scientists 1,021–1,040 publications: 12 scientists 1,041–1,060 publications: 19 scientists 1,061–1,080 publications: 12 scientists 1,081–1,100 publications: 6 scientists 1,101–1,120 publications: 8 scientists 1,121–1,140 publications: 12 scientists 1,141–1,160 publications: 5 scientists 1,161–1,180 publications: 6 scientists 1,181–1,200 publications: 14 scientists 1,201–1,220 publications: 7 scientists 1,221–1,240 publications: 2 scientists 1,241–1,260 publications: 6 scientists 1,261–1,280 publications: 4 scientists 1,281–1,294 publications: 6 scientists 1,295+ publications: 100 scientists
61 publications 1,295+

This scientist: 247 publications — 49th percentile

49% of scientists in this discipline score the same or lower.

The last bar groups every scientist with 1,295 publications or more.

Marco Mor D-index placement in Chemistry in 2026

The chart shows the D-index (discipline H-index) distribution of Chemistry scientists ranked by Research.com in 2026. The highlighted bar marks where Marco Mor sits on this spectrum.

40–41 D-Index: 289 scientists 42–43 D-Index: 612 scientists 44–45 D-Index: 808 scientists 46–47 D-Index: 776 scientists 48–49 D-Index: 835 scientists 50–51 D-Index: 861 scientists 52–53 D-Index: 872 scientists 54–55 D-Index: 933 scientists 56–57 D-Index: 1,051 scientists 58–59 D-Index: 930 scientists 60–61 D-Index: 882 scientists 62–63 D-Index: 834 scientists 64–65 D-Index: 731 scientists 66–67 D-Index: 775 scientists 68–69 D-Index: 683 scientists 70–71 D-Index: 646 scientists 72–73 D-Index: 561 scientists 74–75 D-Index: 501 scientists 76–77 D-Index: 437 scientists 78–79 D-Index: 388 scientists 80–81 D-Index: 354 scientists 82–83 D-Index: 292 scientists 84–85 D-Index: 275 scientists 86–87 D-Index: 254 scientists 88–89 D-Index: 235 scientists 90–91 D-Index: 185 scientists 92–93 D-Index: 192 scientists 94–95 D-Index: 155 scientists 96–97 D-Index: 163 scientists 98–99 D-Index: 125 scientists 100–101 D-Index: 105 scientists 102–103 D-Index: 105 scientists 104–105 D-Index: 112 scientists 106–107 D-Index: 88 scientists 108–109 D-Index: 68 scientists 110–111 D-Index: 69 scientists 112–113 D-Index: 65 scientists 114–115 D-Index: 79 scientists 116–117 D-Index: 61 scientists 118–119 D-Index: 44 scientists 120–121 D-Index: 37 scientists 122–123 D-Index: 40 scientists 124–125 D-Index: 33 scientists 126–127 D-Index: 26 scientists 128–129 D-Index: 34 scientists 130–131 D-Index: 35 scientists 132–133 D-Index: 25 scientists 134–135 D-Index: 27 scientists 136–137 D-Index: 17 scientists 138–139 D-Index: 16 scientists 140–141 D-Index: 20 scientists 142–143 D-Index: 20 scientists 144–145 D-Index: 15 scientists 146–147 D-Index: 9 scientists 148–149 D-Index: 9 scientists 150–151 D-Index: 16 scientists 152–153 D-Index: 11 scientists 154–155 D-Index: 9 scientists 156–157 D-Index: 3 scientists 158 D-Index: 3 scientists 159+ D-Index: 98 scientists
40 D-Index 159+

This scientist: 60 D-Index — 47th percentile

47% of scientists in this discipline score the same or lower.

The last bar groups every scientist with 159 D-Index or more.

Overview

Marco Mor is affiliated with the University of Parma in Italy and has contributed extensively to the fields of biochemistry, genetics, and molecular biology, as well as medicine. Their research includes a significant focus on molecular biology, pharmacology, cellular and molecular neuroscience, organic chemistry, and oncology.

The scientist's work has been published in a range of scientific journals, with frequent appearances in the following venues:

  • European Journal of Medicinal Chemistry
  • Journal of Chemical Information and Modeling
  • Journal of Medicinal Chemistry
  • Blood
  • Biochemical Pharmacology

Marco Mor has coauthored numerous papers with several frequent collaborators. The most common coauthors include:

  • Laura Scalvini
  • Federica Vacondio
  • Alessio Lodola
  • Silvia Rivara
  • Francesca Ferlenghi

The scientist's research topics cover a wide spectrum. Major areas of focus are:

  • Cannabis and Cannabinoid Research
  • Pharmacological Receptor Mechanisms and Effects
  • Neuroscience and Neuropharmacology Research
  • Histone Deacetylase Inhibitors Research
  • Fibroblast Growth Factor Research
  • Circadian rhythm and melatonin
  • Gut microbiota and health

Selected recent publications by Marco Mor include:

  • N-Acylethanolamine Acid Amidase (NAAA): Structure, Function, and Inhibition, 2020, Journal of Medicinal Chemistry
  • FGF Trapping Inhibits Multiple Myeloma Growth through c-Myc Degradation-Induced Mitochondrial Oxidative Stress, 2020, Cancer Research
  • A sulfonyl fluoride derivative inhibits EGFRL858R/T790M/C797S by covalent modification of the catalytic lysine, 2021, European Journal of Medicinal Chemistry
  • NAAA-regulated lipid signaling governs the transition from acute to chronic pain, 2021, Science Advances
  • Steps towards sustainable solid phase peptide synthesis: use and recovery of N-octyl pyrrolidone, 2021, Green Chemistry

Best Publications

  • Modulation of anxiety through blockade of anandamide hydrolysis

    Daniele Piomelli;Andrea Duranti;Andrea Tontini;Marco Mor

  • Antidepressant-like activity and modulation of brain monoaminergic transmission by blockade of anandamide hydrolysis

    G. Gobbi;F. R. Bambico;R. Mangieri;M. Bortolato

  • Characterization of the fatty acid amide hydrolase inhibitor cyclohexyl carbamic acid 3'-carbamoyl-biphenyl-3-yl ester (URB597): effects on anandamide and oleoylethanolamide deactivation.

    Darren Fegley;Silvana Gaetani;Andrea Duranti;Andrea Tontini

  • Pharmacological profile of the selective FAAH inhibitor KDS-4103 (URB597).

    Daniele Piomelli;Giorgio Tarzia;Andrea Duranti;Andrea Tontini

  • Antidepressant-like activity of the fatty acid amide hydrolase inhibitor URB597 in a rat model of chronic mild stress.

    Marco Bortolato;Regina A. Mangieri;Jin Fu;Janet H. Kim

  • Cyclohexylcarbamic acid 3'- or 4'-substituted biphenyl-3-yl esters as fatty acid amide hydrolase inhibitors: synthesis, quantitative structure-activity relationships, and molecular modeling studies.

    Marco Mor;Silvia Rivara;Alessio Lodola;Pier Vincenzo Plazzi

  • Selective N-acylethanolamine-hydrolyzing acid amidase inhibition reveals a key role for endogenous palmitoylethanolamide in inflammation

    Carlos Solorzano;Chenggang Zhu;Natalia Battista;Giuseppe Astarita

  • A catalytically silent FAAH-1 variant drives anandamide transport in neurons

    Jin Fu;Giovanni Bottegoni;Oscar Sasso;Rosalia Bertorelli

  • Design, synthesis, and structure-activity relationships of alkylcarbamic acid aryl esters, a new class of fatty acid amide hydrolase inhibitors.

    Giorgio Tarzia;Andrea Duranti;Andrea Tontini;Giovanni Piersanti

  • The Fatty Acid Amide Hydrolase Inhibitor URB597 (Cyclohexylcarbamic Acid 3′-Carbamoylbiphenyl-3-yl Ester) Reduces Neuropathic Pain after Oral Administration in Mice

    Roberto Russo;Jesse LoVerme;Giovanna La Rana;Timothy R. Compton

  • The Hippo Pathway and YAP/TAZ–TEAD Protein–Protein Interaction as Targets for Regenerative Medicine and Cancer Treatment

    Matteo Santucci;Tatiana Vignudelli;Stefania Ferrari;Marco Mor

  • Promotion of Non-Rapid Eye Movement Sleep and Activation of Reticular Thalamic Neurons by a Novel MT2 Melatonin Receptor Ligand

    Rafael Ochoa-Sanchez;Stefano Comai;Baptiste Lacoste;Francis Rodriguez Bambico

  • Synthesis and characterization of a peripherally restricted CB1 cannabinoid antagonist, URB447, that reduces feeding and body-weight gain in mice.

    Jesse LoVerme;Andrea Duranti;Andrea Tontini;Gilberto Spadoni

  • 5-benzylidene-hydantoins as new EGFR inhibitors with antiproliferative activity.

    Caterina Carmi;Andrea Cavazzoni;Valentina Zuliani;Alessio Lodola

  • URB602 inhibits monoacylglycerol lipase and selectively blocks 2-arachidonoylglycerol degradation in intact brain slices.

    Alvin R. King;Andrea Duranti;Andrea Tontini;Silvia Rivara

  • 2-[N-Acylamino(C1-C3)alkyl]indoles as MT1 melatonin receptor partial agonists, antagonists, and putative inverse agonists.

    G Spadoni;C Balsamini;A Bedini;G Diamantini

  • Discovery of Potent and Reversible Monoacylglycerol Lipase Inhibitors

    Alvin R. King;Emmanuel Y. Dotsey;Alessio Lodola;Kwang Mook Jung

  • Pharmacological characterization of hydrolysis-resistant analogs of oleoylethanolamide with potent anorexiant properties

    Giuseppe Astarita;Barbara Di Giacomo;Silvana Gaetani;Fariba Oveisi

  • Melatonin Receptor Ligands: Synthesis of New Melatonin Derivatives and Comprehensive Comparative Molecular Field Analysis (CoMFA) Study

    Marco Mor;Silvia Rivara;Claudia Silva;Fabrizio Bordi

  • Clinical perspectives for irreversible tyrosine kinase inhibitors in cancer

    Caterina Carmi;Marco Mor;Pier Giorgio Petronini;Roberta R. Alfieri

  • A critical cysteine residue in monoacylglycerol lipase is targeted by a new class of isothiazolinone‐based enzyme inhibitors

    A R King;A Lodola;C Carmi;J Fu

Frequent Co-Authors

Giorgio Tarzia
Giorgio Tarzia University of Urbino
Daniele Piomelli
Daniele Piomelli University of California, Irvine
Marco Presta
Marco Presta University of Brescia
Adrian J. Mulholland
Adrian J. Mulholland University of Bristol
Andrea Ardizzoni
Andrea Ardizzoni University of Bologna
Andrea Cavalli
Andrea Cavalli Italian Institute of Technology
Giuseppe Astarita
Giuseppe Astarita Georgetown University
Giovanni Casiraghi
Giovanni Casiraghi University of Parma
Antonino Neri
Antonino Neri University of Milan
Marco Bortolato
Marco Bortolato University of Florida

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