World's Best Scientists 2026 revealed!
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Lak Shin Jeong

D-Index & Metrics

Chemistry

D-Index
47
Citations
8026
World Ranking
15639
National Ranking
299

Lak Shin Jeong 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 Lak Shin Jeong 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: 353 publications — 73rd percentile

73% of scientists in this discipline score the same or lower.

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

Lak Shin Jeong 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 Lak Shin Jeong 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: 47 D-Index — 14th percentile

14% of scientists in this discipline score the same or lower.

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

Overview

Lak Shin Jeong is affiliated with Seoul National University in South Korea and has contributed extensively to the fields of Biochemistry, Genetics and Molecular Biology, as well as Medicine. Their research encompasses several subfields, including Molecular Biology, Physiology, Organic Chemistry, Infectious Diseases, and Materials Chemistry.

The main topics of Lak Shin Jeong's research include:

  • Adenosine and Purinergic Signaling
  • Ubiquitin and proteasome pathways
  • Microtubule and mitosis dynamics
  • HIV/AIDS drug development and treatment
  • Click Chemistry and Applications
  • Synthesis and Biological Evaluation
  • Crystallization and Solubility Studies

Frequent collaborators in their work include Dnyandev B. Jarhad, Gibae Kim, Hongseok Choi, Vikas R. Aswar, and Minjae Kim, indicating a network of co-author relationships across multiple publications.

Lak Shin Jeong has published frequently in journals such as:

  • Journal of Medicinal Chemistry
  • ACS Medicinal Chemistry Letters
  • The Cambridge Structural Database
  • Pharmaceuticals
  • Bioorganic Chemistry

Selected recent papers authored or co-authored by Lak Shin Jeong include:

  • "<scp>UBC12</scp>-mediated <scp>SREBP</scp>-1 neddylation worsens metastatic tumor prognosis," 2020, International Journal of Cancer
  • "6'-β-Fluoro-Homoaristeromycin and 6'-Fluoro-Homoneplanocin A Are Potent Inhibitors of Chikungunya Virus Replication through Their Direct Effect on Viral Nonstructural Protein 1," 2020, Antimicrobial Agents and Chemotherapy
  • "A Novel cytarabine analog evokes synthetic lethality by targeting MK2 in p53-deficient cancer cells," 2020, Cancer Letters
  • "GPCR Agonist-to-Antagonist Conversion: Enabling the Design of Nucleoside Functional Switches for the A2A Adenosine Receptor," 2022, Journal of Medicinal Chemistry
  • "Discovery and Structure-Activity Relationships of Novel Template, Truncated 1'-Homologated Adenosine Derivatives as Pure Dual PPARγ/δ Modulators," 2020, Journal of Medicinal Chemistry

Best Publications

  • Activities of the four optical isomers of 2',3'-dideoxy-3'-thiacytidine (BCH-189) against human immunodeficiency virus type 1 in human lymphocytes.

    R F Schinazi;C K Chu;A Peck;A McMillan

  • Deoxycytidine deaminase-resistant stereoisomer is the active form of (+/-)-2',3'-dideoxy-3'-thiacytidine in the inhibition of hepatitis B virus replication.

    C.N. Chang;S.L. Doong;J.H. Zhou;J.W. Beach

  • Synthesis of enantiomerically pure (2'R,5'S)-(-)-1-(2-hydroxymethyloxathiolan-5-yl)cytosine as a potent antiviral agent against hepatitis B virus (HBV) and human immunodeficiency virus (HIV)

    J. Warren Beach;Lak S. Jeong;Antonio J. Alves;Douglas Pohl

  • Asymmetric synthesis and biological evaluation of beta-L-(2R,5S)- and alpha-L-(2R,5R)-1,3-oxathiolane-pyrimidine and -purine nucleosides as potential anti-HIV agents.

    L. S. Jeong;R. F. Schinazi;J. W. Beach;H. O. Kim

  • Overactivated Neddylation Pathway as a Therapeutic Target in Lung Cancer

    Lihui Li;Mingsong Wang;Guangyang Yu;Ping Chen;Ping Chen

  • c-Cbl-Mediated Neddylation Antagonizes Ubiquitination and Degradation of the TGF-β Type II Receptor

    Wei Zuo;Fei Huang;Y. Jeffrey Chiang;Meng Li

  • L-.beta.-(2S,4S)- and L-.alpha.-(2S,4R)-dioxolanyl nucleosides as potential anti-HIV agents: asymmetric synthesis and structure-activity relationships

    H. O. Kim;R. F. Schinazi;Kirupathevy Shanmuganathan;L. S. Jeong

  • Improved and alternative synthesis of d- and l-cyclopentenone derivatives, the versatile intermediates for the synthesis of carbocyclic nucleosides

    Hyung Ryong Moon;Won Jun Choi;Hea Ok Kim;Lak Shin Jeong

  • Potent anti-HIV and anti-HBV activities of (−)-L-β-dioxolane-C and (+)-L-β-dioxolane-T and their asymmetric syntheses.

    Hea O. Kim;Kirupathevy Shanmuganathan;Antonio J. Alves;Lak S. Jeong

  • Discovery of a new nucleoside template for human A3 adenosine receptor ligands: D-4'-thioadenosine derivatives without 4'-hydroxymethyl group as highly potent and selective antagonists.

    Lak Shin Jeong;Seung Ah Choe;Prashantha Gunaga;Hea Ok Kim

  • Dual-Specificity Tyrosine Phosphorylation-Regulated Kinase 1A (DYRK1A) Inhibitors as Potential Therapeutics

    Dnyandev B Jarhad;Karishma K Mashelkar;Hong-Rae Kim;Minsoo Noh

  • A highly stereoselective synthesis of anti-HIV 2',3'-dideoxy- and 2',3'-didehydro-2',3'-dideoxynucleosides

    J. Warren Beach;Hea O. Kim;Lak S. Jeong;Satyanarayana Nampalli

  • Enantiomeric synthesis of (+)-BCH-189 [(+)-(2S,5R)-1-[2-(hydroxymethyl)-1,3-oxathiolan-5-yl]cytosine] from D-mannose and its anti-HIV activity

    Chung K. Chu;J. Warren Beach;Lak S. Jeong;Bo G. Choi

  • N6-substituted D-4'-thioadenosine-5'-methyluronamides: potent and selective agonists at the human A3 adenosine receptor.

    Lak Shin Jeong;Dong Zhe Jin;Hea Ok Kim;Dae Hong Shin

  • Structure-activity relationships of .beta.-D-(2S,5R)- and .alpha.-D-(2S,5S)-1,3-oxathiolanyl nucleosides as potential anti-HIV agents

    L. S. Jeong;R. F. Schinazi;J. W. Beach;H. O. Kim

  • Preparative and stereoselective synthesis of the versatile intermediate for carbocyclic nucleosides: effects of the bulky protecting groups to enforce facial selectivity.

    Won Jun Choi;Hyung Ryong Moon;Hea Ok Kim;Byul Nae Yoo

  • Design, Synthesis, and Biological Evaluation of Fluoroneplanocin A as the Novel Mechanism-Based Inhibitor of S-Adenosylhomocysteine Hydrolase

    Lak Shin Jeong;Su Jeong Yoo;Kang Man Lee;Mi Jeong Koo

  • Recent Advances in the Synthesis of the Carbocyclic Nucleosides as Potential Antiviral Agents

    Lak Shin Jeong;Jeong A Lee

  • Structure-activity relationships of 2-chloro-N6-substituted-4'-thioadenosine-5'-uronamides as highly potent and selective agonists at the human A3 adenosine receptor.

    Lak Shin Jeong;Hyuk Woo Lee;Kenneth A. Jacobson;Hea Ok Kim

  • Syntheses of D- and L-cyclopentenone derivatives using ring-closing metathesis: versatile intermediates for the synthesis of D- and L-carbocyclic nucleosides.

    Won Jun Choi;Jae Gyu Park;Su Jeong Yoo;Hea Ok Kim

  • Asymmetric synthesis of enantiomerically pure (−)-(1′R,4′R)-dioxolane-thymine and its anti-HIV activity.

    Chung K. Chu;Soon K. Ahn;H.O. Kim;J.Warren Beach

  • A highly stereoselective glycosylation of 2-(phenylselenenyl)-2,3-dideoxyribose derivative with thymine: synthesis of 3'-deoxy-2',3'-didehydrothymidine and 3'-deoxythymidine

    Chung K. Chu;J. Ramesh Babu;J. Warren Beach;Soon K. Ahn

Frequent Co-Authors

Kenneth A. Jacobson
Kenneth A. Jacobson National Institutes of Health
Sang Kook Lee
Sang Kook Lee Seoul National University
Zhan-Guo Gao
Zhan-Guo Gao National Institutes of Health
Yong Chul Kim
Yong Chul Kim Gwangju Institute of Science and Technology
Chung K. Chu
Chung K. Chu University of Georgia
Robert M. Hoffman
Robert M. Hoffman AntiCancer (United States)
Yoongho Lim
Yoongho Lim Konkuk University
Yiwei Chu
Yiwei Chu Fudan University
Sanghee Kim
Sanghee Kim Seoul National University
Eric J. Snijder
Eric J. Snijder Leiden University Medical Center

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Related Online Degrees & Career Pathways

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Pursuing these degrees opens doors to various professions in forensic science, where competitive roles are reflected in the forensic scientist salary data, which underscores the financial viability of this career path. Overall, combining chemistry with forensic science education equips students with impactful skills for dynamic, rewarding careers.

Best Scientists Citing Lak Shin Jeong

Kenneth A. Jacobson

Kenneth A. Jacobson

National Institutes of Health

Publications: 71

Zhan-Guo Gao

Zhan-Guo Gao

National Institutes of Health

Publications: 43

Ronald S. Duman

Ronald S. Duman

Yale University

Publications: 41

Yi Sun

Yi Sun

Zhejiang University

Publications: 40

Chung K. Chu

Chung K. Chu

University of Georgia

Publications: 35

Raymond F. Schinazi

Raymond F. Schinazi

Emory University

Publications: 33

Etienne Sibille

Etienne Sibille

University of Toronto

Publications: 25

Pier Andrea Borea

Pier Andrea Borea

University of Ferrara

Publications: 25

Katia Varani

Katia Varani

University of Ferrara

Publications: 24

In Su Kim

In Su Kim

Sungkyunkwan University

Publications: 20

Yung-Chi Cheng

Yung-Chi Cheng

Yale University

Publications: 16

Stefania Gessi

Stefania Gessi

University of Ferrara

Publications: 15

Felicita Pedata

Felicita Pedata

University of Florence

Publications: 14

Daniela Salvemini

Daniela Salvemini

Saint Louis University

Publications: 13

Godefridus J. Peters

Godefridus J. Peters

Gdańsk Medical University

Publications: 13

Jan Balzarini

Jan Balzarini

KU Leuven

Publications: 12

Trending Scientists

Gabriel Cornic

Gabriel Cornic

University of Paris-Saclay

Niko Münzenrieder

Niko Münzenrieder

Free University of Bozen-Bolzano

Dimitrios Hatzinakos

Dimitrios Hatzinakos

University of Toronto

Jon Kabat-Zinn

Jon Kabat-Zinn

University of Massachusetts Chan Medical School

Stephen E. G. Lea

Stephen E. G. Lea

University of Exeter

Amy H. Butler

Amy H. Butler

National Oceanic and Atmospheric Administration

Shan Lu

Shan Lu

University of Massachusetts Chan Medical School

Rubens Maciel Filho

Rubens Maciel Filho

State University of Campinas

Marie-Francine Moens

Marie-Francine Moens

KU Leuven

Manuel Wimmer

Manuel Wimmer

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Harjinder Singh

Harjinder Singh

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Jaume Veciana

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Ajay Goel

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