World's Best Scientists 2026 revealed!
Jyoti Chattopadhyaya

Jyoti Chattopadhyaya

D-Index & Metrics

Chemistry

D-Index
53
Citations
10498
World Ranking
13035
National Ranking
194

Jyoti Chattopadhyaya 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 Jyoti Chattopadhyaya 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: 457 publications — 85th percentile

85% of scientists in this discipline score the same or lower.

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

Jyoti Chattopadhyaya 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 Jyoti Chattopadhyaya 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: 53 D-Index — 28th percentile

28% of scientists in this discipline score the same or lower.

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

Overview

Jyoti Chattopadhyaya is affiliated with Uppsala University in Sweden. Their academic profile does not currently include records of recent papers, co-authors, or frequent publication venues. Additionally, there are no listed book publications associated with their name.

Information regarding primary fields of study, subfields, and main research topics for Jyoti Chattopadhyaya is not available in the dataset. There is also no record of awards received during their career.

Despite the limited data on publications and research areas, the association with Uppsala University suggests involvement in a research environment known for diverse scientific activities and disciplines. Further data would be required to provide a more detailed overview of their specific contributions and areas of expertise.

Best Publications

  • A large-scale chemical modification screen identifies design rules to generate siRNAs with high activity, high stability and low toxicity

    Jesper B. Bramsen;Maria B. Laursen;Anne F. Nielsen;Thomas B. Hansen

  • How do the gauche and anomeric effects drive the pseudorotational equilibrium of the pentofuranose moiety of nucleosides

    Janez Plavec;Weimin Tong;Jyoti Chattopadhyaya

  • A screen of chemical modifications identifies position-specific modification by UNA to most potently reduce siRNA off-target effects

    Jesper B. Bramsen;Malgorzata M. Pakula;Thomas B. Hansen;Claus Bus

  • Structure and toxicity of a peptide hepatotoxin from the cyanobacterium Oscillatoria agardhii.

    J.A.O. Meriluoto;A. Sandström;J.E. Eriksson;G. Remaud

  • Fine tuning of electrostatics around the internucleotidic phosphate through incorporation of modified 2',4'-carbocyclic-LNAs and -ENAs leads to significant modulation of antisense properties.

    Chuanzheng Zhou;Yi Liu;Mounir Andaloussi;Naresh Badgujar

  • A New Generalized Karplus-Type Equation Relating Vicinal Proton-Fluorine Coupling Constants to H−C−C−F Torsion Angles

    Christophe Thibaudeau;Janez Plavec;Jyoti Chattopadhyaya

  • A critical survey of the structure-function of the antisense oligo/RNA heteroduplex as substrate for RNase H.

    Edouard Zamaratski;P.I. Pradeepkumar;Jyoti Chattopadhyaya

  • Design, synthesis, biological evaluation and molecular modelling studies of novel quinoline derivatives against Mycobacterium tuberculosis.

    Ram Shankar Upadhayaya;Jaya Kishore Vandavasi;Nageswara Rao Vasireddy;Vivek Sharma

  • Allele-selective inhibition of mutant huntingtin expression with antisense oligonucleotides targeting the expanded CAG repeat.

    Keith T. Gagnon;Hannah M. Pendergraff;Glen F. Deleavey;Eric E. Swayze

  • Five- and Six-Membered Conformationally Locked 2',4'-Carbocyclic ribo-Thymidines: Synthesis, Structure, and Biochemical Studies

    Puneet Srivastava;Jharna Barman;Wimal Pathmasiri;Oleksandr Plashkevych

  • The pKa's of 2‘-Hydroxyl Group in Nucleosides and Nucleotides

    Irina Velikyan;Sandipta Acharya;Anna Trifonova;and Andras Földesi

  • Inhibition of the reverse transcriptase from HIV by 3'-azido-3'-deoxythymidine triphosphate and its threo analogue.

    Lotta Vrang;Hervé Bazin;Gerald Remaud;Jyoti Chattopadhyaya

  • Rapid and quantitative recovery of DNA fragments from gels by displacement electrophoresis (isotachophoresis).

    Lars-Göran Öfverstedt;Karin Hammarström;Neil Balgobin;Stellan Hjertén

  • How Does the Electronegativity of the Substituent Dictate the Strength of the Gauche Effect

    C. Thibaudeau;J. Plavec;N. Garg;A. Papchikhin

  • Single-stranded adenine-rich DNA and RNA retain structural characteristics of their respective double-stranded conformations and show directional differences in stacking pattern.

    Johan Isaksson;Sandipta Acharya;Jharna Barman;Pradeep Cheruku

  • Chemical synthesis of a tridecanucleoside dodecaphosphate sequence of SV40 DNA

    J.B. Chattopadhyaya;C.B. Reese

  • How Does the 2'-Hydroxy Group Drive the Pseudorotational Equilibrium in Nucleoside and Nucleotide by the Tuning of the 3'-Gauche Effect?

    Janez Plavec;Christophe Thibaudeau;Jyoti Chattopadhyaya

  • Quantitation of the pD Dependent Thermodynamics of the N ⇄ S Pseudorotational Equilibrium of the Pentofuranose Moiety in Nucleosides Gives a Direct Measurement of the Strength of the Tunable Anomeric Effect and the pKa of the Nucleobase†

    C. Thibaudeau;J. Plavec;J. Chattopadhyaya

  • Conformationally constrained 2'-N,4'-C-ethylene-bridged thymidine (aza-ENA-T): synthesis, structure, physical, and biochemical studies of aza-ENA-T-modified oligonucleotides.

    Oommen P. Varghese;Jharna Barman;Wimal Pathmasiri;Oleksandr Plashkevych

  • Measurement of nucleobase pKa values in model mononucleotides shows RNA-RNA duplexes to be more stable than DNA-DNA duplexes

    P Acharya;P Cheruku;S Chatterjee;S Acharya

  • How do the energetics of the stereoelectronic gauche and anomeric effects modulate the conformation of nucleos(t)ides

    J. Plavec;C. Thibaudeau;Jyoti Chattopadhyaya

Frequent Co-Authors

Colin B. Reese
Colin B. Reese University of Cambridge
Christopher J. Welch
Christopher J. Welch Indiana Consortium for Analytical Science & Engineering
Ivar Ugi
Ivar Ugi Technical University of Munich
Harri Lönnberg
Harri Lönnberg University of Turku
Akira Matsuda
Akira Matsuda Juntendo University
Stephen Neidle
Stephen Neidle University College London
Masad J. Damha
Masad J. Damha McGill University
Eric E. Swayze
Eric E. Swayze Ionis Pharmaceuticals (United States)
Jussi Meriluoto
Jussi Meriluoto Åbo Akademi University
Olov Sterner
Olov Sterner Lund University

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