World's Best Scientists 2026 revealed!

D-Index & Metrics

Chemistry

D-Index
70
Citations
16003
World Ranking
5920
National Ranking
149

Ole Hindsgaul 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 Ole Hindsgaul 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: 324 publications — 68th percentile

68% of scientists in this discipline score the same or lower.

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

Ole Hindsgaul 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 Ole Hindsgaul 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: 70 D-Index — 68th percentile

68% of scientists in this discipline score the same or lower.

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

Research.com Recognitions

  • 2001 - Fellow of the Royal Society of Canada Academy of Science

Overview

Ole Hindsgaul is affiliated with the University of Alberta in Canada and is recognized within the fields of Biochemistry, Genetics and Molecular Biology, as well as Chemistry. Their research contributions span across several subfields, including Molecular Biology and Organic Chemistry.

Hindsgaul's work has concentrated on topics such as Enzyme Catalysis and Immobilization, Carbohydrate Chemistry and Synthesis, and Porphyrin Metabolism and Disorders. These specialized areas reflect a focus on biochemical processes and chemical biology, intersecting both molecular mechanisms and synthetic chemistry.

The scientist has published research primarily in "The Journal of Organic Chemistry," with at least one known publication:

  • Raymond Urgel Lemieux (June 16, 1920-July 22, 2000): A Lifelong Love Affair with Sugar Chemistry, 2020, The Journal of Organic Chemistry

Frequent co-authorship collaborations are not documented in the available data, indicating either solo authorship or diverse collaboration patterns.

In recognition of scholarly contributions, Ole Hindsgaul was elected as a Fellow of the Royal Society of Canada in 2001, within the Academy of Science category.

Best Publications

  • The α(1,3)Fucosyltransferase Fuc-TVII Controls Leukocyte Trafficking through an Essential Role in L-, E-, and P-selectin Ligand Biosynthesis

    Petr Malý;Aron D Thall;Bronislawa Petryniak;Clare E Rogers

  • The α(1,3)fucosyltransferases FucT-IV and FucT-VII Exert Collaborative Control over Selectin-Dependent Leukocyte Recruitment and Lymphocyte Homing

    Jonathon W Homeister;Aron D Thall;Bronia Petryniak;Petr Malý

  • The use of hydrophobic synthetic glycosides as acceptors in glycosyltransferase assays

    Monica M Palcic;Louis D Heerze;Michael Pierce;Ole Hindsgaul

  • A hepatic reticuloendothelial cell receptor specific for SO4-4GalNAcβ1, 4GlcNAcβ1,2Manα that mediates rapid clearance of lutropin

    Dorothy Fiete;Vandana Srivastava;Ole Hindsgaul;Jacques U. Baenziger

  • Novel Sulfated Lymphocyte Homing Receptors and Their Control by a Core1 Extension β1,3-N-Acetylglucosaminyltransferase

    Jiunn-Chern Yeh;Nobuyoshi Hiraoka;Bronislawa Petryniak;Jun Nakayama

  • Synthesis of .beta.-mannopyranosides by intramolecular aglycon delivery

    Frank Barresi;Ole Hindsgaul

  • Synthesis of type 2 human blood-group antigenic determinants. The H, X, and Y haptens and variations of the H type 2 determinant as probes for the combining site of the lectin I of Ulex europaeus

    O Hindsgaul;T Norberg;J Le Pendu;R U Lemieux

  • Bovine α1,3‐galactosyltransferase catalytic domain structure and its relationship with ABO histo‐blood group and glycosphingolipid glycosyltransferases

    Louis N. Gastinel;Christophe Bignon;Anup K. Misra;Anup K. Misra;Ole Hindsgaul;Ole Hindsgaul

  • Acceptor-substrate recognition by N-acetylglucosaminyltransferase-V: Critical role of the 4″-hydroxyl group in β-d-GlcpNAc-(1 → 2)-α-d-Manp(1 → 6)-β-d-Glcp-OR

    Osamu Kanie;Suzanne C. Crawley;Monica M. Palcic;Ole Hindsgaul

  • Antibacterial agents that target lipid A biosynthesis in gram-negative bacteria. Inhibition of diverse UDP-3-O-(r-3-hydroxymyristoyl)-n-acetylglucosamine deacetylases by substrate analogs containing zinc binding motifs.

    Jane E. Jackman;Carol A. Fierke;L.Nathan Tumey;Michael Pirrung

  • Increased UDP-GlcNAc:Gal beta 1-3GaLNAc-R (GlcNAc to GaLNAc) beta-1, 6-N-acetylglucosaminyltransferase activity in metastatic murine tumor cell lines. Control of polylactosamine synthesis.

    S. Yousefi;E. Higgins;Zhuang Daoling;A. Pollex-Kruger

  • High-performance anion-exchange chromatography of oligosaccharides using pellicular resins and pulsed amperometric detection.

    R.Reid Townsend;Mark R. Hardy;Ole Hindsgaul;Yuan Chuan Lee

  • Proton NMR and fast-atom bombardment mass spectrometry analysis of the melanoma-associated ganglioside 9-O-acetyl-GD3.

    J Thurin;M Herlyn;O Hindsgaul;N Strömberg

  • Micro-Scale Frontal Affinity Chromatography with Mass Spectrometric Detection: A New Method for the Screening of Compound Libraries.

    David C. Schriemer;David R. Bundle;Liang Li;Ole Hindsgaul

  • Enzymic synthesis of oligosaccharides terminating in the tumor-associated sialyl-Lewis-a determinant.

    Palcic Mm;Venot Ap;Ratcliffe Rm;Hindsgaul O

  • The pili of Pseudomonas aeruginosa strains PAK and PAO bind specifically to the carbohydrate sequence beta GalNAc(1-4)beta Gal found in glycosphingolipids asialo-GM1 and asialo-GM2.

    H. B. Sheth;K. K. Lee;W. Y. Wong;G. Srivastava

  • Use of diethyl squarate for the coupling of oligosaccharide amines to carrier proteins and characterization of the resulting neoglycoproteins by MALDI-TOF mass spectrometry*

    Vivekanand P. Kamath;Paul Diedrich;Ole Hindsgaul

  • A bisubstrate analog inhibitor for alpha(1----2)-fucosyltransferase.

    M M Palcic;L D Heerze;O P Srivastava;O Hindsgaul

  • 6'-Sulfo sialyl Lex but not 6-sulfo sialyl Lex expressed on the cell surface supports L-selectin-mediated adhesion.

    Shigeru Tsuboi;Yukihiro Isogai;Noriyasu Hada;Jennifer K. King

  • Differential Biosynthesis of Polysialic Acid on Neural Cell Adhesion Molecule (NCAM) and Oligosaccharide Acceptors by Three Distinct α2,8-Sialyltransferases, ST8Sia IV (PST), ST8Sia II (STX), and ST8Sia III

    Kiyohiko Angata;Misa Suzuki;Joseph McAuliffe;Yili Ding

  • Evaluation of deoxygenated oligosaccharide acceptor analogs as specific inhibitors of glycosyltransferases.

    O Hindsgaul;K J Kaur;G Srivastava;M Blaszczyk-Thurin

  • Flexibility in the donor substrate specificity of β 1,4-galactosyltransferase: application in the synthesis of complex carbohydrates

    Monica M. Palcic;Ole Hindsgaul

  • Chemical cytometry: fluorescence-based single-cell analysis.

    Daniella Cohen;Jane A Dickerson;Colin D Whitmore;Emily H Turner

  • Structure of the LpxC deacetylase with a bound substrate-analog inhibitor.

    Brian E Coggins;Xuechen Li;Amanda L McClerren;Ole Hindsgaul

Frequent Co-Authors

Monica M. Palcic
Monica M. Palcic Carlsberg Laboratory
Norman J. Dovichi
Norman J. Dovichi University of Notre Dame
David R. Bundle
David R. Bundle University of Alberta
Ulf J. Nilsson
Ulf J. Nilsson Lund University
Todd L. Lowary
Todd L. Lowary University of Alberta
Christian R. H. Raetz
Christian R. H. Raetz Duke University
Morten Meldal
Morten Meldal University of Copenhagen
Robert S. Hodges
Robert S. Hodges University of Colorado Denver
Ronald L. Schnaar
Ronald L. Schnaar Johns Hopkins University School of Medicine
Jacques U. Baenziger
Jacques U. Baenziger Washington University in St. Louis

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