World's Best Scientists 2026 revealed!

D-Index & Metrics

Chemistry

D-Index
51
Citations
6359
World Ranking
14207
National Ranking
3667

Roy L. Kisliuk 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 Roy L. Kisliuk 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: 204 publications — 34th percentile

34% of scientists in this discipline score the same or lower.

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

Roy L. Kisliuk 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 Roy L. Kisliuk 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: 51 D-Index — 23rd percentile

23% of scientists in this discipline score the same or lower.

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

Overview

Roy L. Kisliuk was affiliated with Tufts University in the United States. Their academic contributions do not include recent published papers, frequent co-authors, or documented publication venues based on the current available data.

There is no specific record of book publications or distinct main fields and subfields of study linked to their name in the accessible sources.

Similarly, no main topics of work or subject areas with associated publications have been identified for Roy L. Kisliuk.

There are no listed awards or honors recorded for this scientist in the presented data.

Overall, the information on Roy L. Kisliuk's career and research contributions is limited, and many typical academic metadata areas remain unspecified.

Best Publications

  • Design and synthesis of classical and nonclassical 6-arylthio-2,4-diamino-5-ethylpyrrolo[2,3-d]pyrimidines as antifolates.

    Aleem Gangjee;Yibin Zeng;Tina Talreja;John J. McGuire

  • Dihydrofolate reductase from Lactobacillus casei. X-ray structure of the enzyme methotrexate.NADPH complex.

    D A Matthews;R A Alden;J T Bolin;D J Filman

  • Polyglutamyl derivatives of folate as substrates and inhibitors of thymidylate synthetase.

    Roy L. Kisliuk;Yvette Gaumont;Charles M. Baugh

  • Syntheses and antifolate activity of 5-methyl-5-deaza analogues of aminopterin, methotrexate, folic acid, and N10-methylfolic acid.

    J R Piper;G S McCaleb;J A Montgomery;R L Kisliuk

  • 2,4-Diamino-5-deaza-6-substituted pyrido[2,3-d]pyrimidine antifolates as potent and selective nonclassical inhibitors of dihydrofolate reductases

    Aleem Gangjee;Anil Vasudevan;Sherry F. Queener;Roy L. Kisliuk

  • Properties of Thymidylate Synthetase from Dichloromethotrexate-resistant Lactobacillus casei

    Theodore C. Crusberg;Richard Leary;Roy L. Kisliuk

  • Studies on the mechanism of formaldehyde incorporation into serine

    Roy L. Kisliuk

  • Design, synthesis, and X-ray crystal structure of a potent dual inhibitor of thymidylate synthase and dihydrofolate reductase as an antitumor agent.

    Aleem Gangjee;Jianming Yu;John J. Mcguire;Vivian Cody

  • A study of the mechanism of serine biosynthesis.

    Roy L. Kisliuk;Warwick Sakami

  • Stereospecificity at carbon 6 of formyltetrahydrofolate as a competitive inhibitor of transport and cytotoxicity of methotrexate in vitro

    Francis M. Sirotnak;Paul L. Chello;Donna M. Moccio;Roy L. Kisliuk

  • Interaction of deoxyuridylate with thymidylate synthetase.

    R P Leary;N Beaudette;R L Kisliuk

  • Classical and nonclassical furo[2,3-d]pyrimidines as novel antifolates: synthesis and biological activities.

    Aleem Gangjee;Rajesh Devraj;John J. McGuire;Roy L. Kisliuk

  • Novel Boron-Containing, Nonclassical Antifolates: Synthesis and Preliminary Biological and Structural Evaluation.

    Robert C. Reynolds;Shiela R. Campbell;Ralph G. Fairchild;Roy L. Kisliuk

  • Absolute configuration of biological tetrahydrofolates. A crystallographic determination

    Juan C. Fontecilla-Camps;Charles E. Bugg;Carroll Temple;Jerry D. Rose

  • Synthesis of classical, three-carbon-bridged 5-substituted furo[2,3-d]pyrimidine and 6-substituted pyrrolo[2,3-d]pyrimidine analogues as antifolates.

    Aleem Gangjee;Yibin Zeng;John J. McGuire;Roy L. Kisliuk

  • Effect of bridge region variation on antifolate and antitumor activity of classical 5-substituted 2,4-diaminofuro[2,3-d]pyrimidines

    Aleem Gangjee;Rajesh Devraj;John J. McGuire;Roy L. Kisliuk

  • Synthesis, antifolate, and antitumor activities of classical and nonclassical 2-amino-4-oxo-5-substituted-pyrrolo[2,3-d]pyrimidines.

    Aleem Gangjee;Anup Vidwans;Elfatih Elzein;John J. Mcguire

  • Folate analogues. 35. Synthesis and biological evaluation of 1-deaza, 3-deaza, and bridge-elongated analogues of N10-propargyl-5,8-dideazafolic acid.

    Shu Wen Li;M. G. Nair;Donna M. Edwards;R. L. Kisliuk

  • Structure-based design and synthesis of lipophilic 2,4-diamino-6-substituted quinazolines and their evaluation as inhibitors of dihydrofolate reductases and potential antitumor agents.

    Aleem Gangjee;Anup P. Vidwans;Anil Vasudevan;Sherry F. Queener

  • THE STIMULATION OF SERINE BIOSYNTHESIS IN PIGEON LIVER EXTRACTS BY TETRAHYDROFOLIC ACID1

    Roy L. Kisliuk;Warwick Sakami

Frequent Co-Authors

Francis M. Sirotnak
Francis M. Sirotnak Memorial Sloan Kettering Cancer Center
Sherry F. Queener
Sherry F. Queener Indiana University
Larry H. Matherly
Larry H. Matherly Wayne State University
John A. Montgomery
John A. Montgomery University of Connecticut
Nathan O. Kaplan
Nathan O. Kaplan Harvard University
Juan C. Fontecilla-Camps
Juan C. Fontecilla-Camps Centre national de la recherche scientifique, CNRS
Eileen M. Lafer
Eileen M. Lafer The University of Texas Health Science Center at San Antonio
Joseph Kraut
Joseph Kraut University of California, San Diego

If you think any of the details on this page are incorrect, let us know.

Report an issue

We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below:

Related Online Degrees & Career Pathways

Pursuing a degree in Chemistry opens doors to various career paths beyond traditional lab roles. Many students explore specialized fields by combining their chemistry knowledge with complementary qualifications. For instance, those interested in the legal side of science can explore degrees for paralegals, which provide foundational skills for supporting legal processes related to chemical patents, compliance, and intellectual property.

Another promising option is entering the pharmaceutical industry. Becoming a pharmaceutical sales representative is a common career path for chemistry graduates, offering attractive earnings as outlined in the guide on drug rep salary. This role combines scientific knowledge with communication skills to promote medical products effectively.

For students aiming at advanced healthcare roles, understanding how much does it cost to become a pharmacist is essential. Pharmacists require extensive education and training but enjoy rewarding careers in medication management and patient care.

Lastly, chemistry graduates interested in forensic sciences might consider becoming a forensic autopsy technician. This pathway offers unique investigative work in forensic pathology, with insights on education, salary, and job outlook available through the forensic autopsy technician resource.

Best Scientists Citing Roy L. Kisliuk

Recently Published Articles