World's Best Scientists 2026 revealed!

D-Index & Metrics

Genetics

D-Index
70
Citations
22899
World Ranking
2248
National Ranking
34

Wim Van Hul publication distribution in Genetics in 2026

The chart shows the distribution of publications by all Research.com ranked scientists in the field of Genetics in 2026. The highlighted bar marks where Wim Van Hul sits on this spectrum.

45–54 publications: 6 scientists 55–64 publications: 10 scientists 65–74 publications: 35 scientists 75–84 publications: 84 scientists 85–94 publications: 102 scientists 95–104 publications: 151 scientists 105–114 publications: 175 scientists 115–124 publications: 203 scientists 125–134 publications: 217 scientists 135–144 publications: 205 scientists 145–154 publications: 193 scientists 155–164 publications: 188 scientists 165–174 publications: 170 scientists 175–184 publications: 178 scientists 185–194 publications: 164 scientists 195–204 publications: 173 scientists 205–214 publications: 159 scientists 215–224 publications: 134 scientists 225–234 publications: 143 scientists 235–244 publications: 105 scientists 245–254 publications: 114 scientists 255–264 publications: 92 scientists 265–274 publications: 88 scientists 275–284 publications: 87 scientists 285–294 publications: 80 scientists 295–304 publications: 62 scientists 305–314 publications: 75 scientists 315–324 publications: 67 scientists 325–334 publications: 60 scientists 335–344 publications: 52 scientists 345–354 publications: 40 scientists 355–364 publications: 48 scientists 365–374 publications: 47 scientists 375–384 publications: 46 scientists 385–394 publications: 31 scientists 395–404 publications: 27 scientists 405–414 publications: 40 scientists 415–424 publications: 30 scientists 425–434 publications: 43 scientists 435–444 publications: 29 scientists 445–454 publications: 14 scientists 455–464 publications: 28 scientists 465–474 publications: 21 scientists 475–484 publications: 21 scientists 485–494 publications: 22 scientists 495–504 publications: 17 scientists 505–514 publications: 12 scientists 515–524 publications: 11 scientists 525–534 publications: 8 scientists 535–544 publications: 8 scientists 545–554 publications: 14 scientists 555–564 publications: 4 scientists 565–574 publications: 11 scientists 575–584 publications: 5 scientists 585–594 publications: 11 scientists 595–604 publications: 12 scientists 605–614 publications: 7 scientists 615–624 publications: 6 scientists 625–634 publications: 10 scientists 635–644 publications: 9 scientists 645–654 publications: 10 scientists 655–664 publications: 6 scientists 665–674 publications: 6 scientists 675–684 publications: 6 scientists 685–694 publications: 4 scientists 695–702 publications: 6 scientists 703+ publications: 100 scientists
45 publications 703+

This scientist: 283 publications — 73rd percentile

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

The last bar groups every scientist with 703 publications or more.

Wim Van Hul D-index placement in Genetics in 2026

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

40–41 D-Index: 24 scientists 42–43 D-Index: 52 scientists 44–45 D-Index: 84 scientists 46–47 D-Index: 112 scientists 48–49 D-Index: 118 scientists 50–51 D-Index: 141 scientists 52–53 D-Index: 143 scientists 54–55 D-Index: 145 scientists 56–57 D-Index: 179 scientists 58–59 D-Index: 162 scientists 60–61 D-Index: 175 scientists 62–63 D-Index: 191 scientists 64–65 D-Index: 172 scientists 66–67 D-Index: 184 scientists 68–69 D-Index: 164 scientists 70–71 D-Index: 158 scientists 72–73 D-Index: 150 scientists 74–75 D-Index: 136 scientists 76–77 D-Index: 127 scientists 78–79 D-Index: 127 scientists 80–81 D-Index: 111 scientists 82–83 D-Index: 110 scientists 84–85 D-Index: 110 scientists 86–87 D-Index: 84 scientists 88–89 D-Index: 102 scientists 90–91 D-Index: 66 scientists 92–93 D-Index: 72 scientists 94–95 D-Index: 70 scientists 96–97 D-Index: 54 scientists 98–99 D-Index: 60 scientists 100–101 D-Index: 49 scientists 102–103 D-Index: 55 scientists 104–105 D-Index: 45 scientists 106–107 D-Index: 42 scientists 108–109 D-Index: 28 scientists 110–111 D-Index: 39 scientists 112–113 D-Index: 25 scientists 114–115 D-Index: 31 scientists 116–117 D-Index: 29 scientists 118–119 D-Index: 34 scientists 120–121 D-Index: 29 scientists 122–123 D-Index: 29 scientists 124–125 D-Index: 18 scientists 126–127 D-Index: 27 scientists 128–129 D-Index: 22 scientists 130–131 D-Index: 16 scientists 132–133 D-Index: 11 scientists 134–135 D-Index: 17 scientists 136–137 D-Index: 12 scientists 138–139 D-Index: 21 scientists 140–141 D-Index: 4 scientists 142–143 D-Index: 9 scientists 144–145 D-Index: 14 scientists 146–147 D-Index: 6 scientists 148–149 D-Index: 10 scientists 150–151 D-Index: 7 scientists 152–153 D-Index: 9 scientists 154–155 D-Index: 8 scientists 156–157 D-Index: 8 scientists 158–159 D-Index: 9 scientists 160+ D-Index: 96 scientists
40 D-Index 160+

This scientist: 70 D-Index — 49th percentile

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

The last bar groups every scientist with 160 D-Index or more.

Overview

Wim Van Hul is affiliated with the University of Antwerp in Belgium. Their research primarily spans the fields of Biochemistry, Genetics and Molecular Biology, and Medicine, with a particular focus on Genetics and Molecular Biology as key subfields. Additional areas of study include Oncology, Cell Biology, and Rheumatology.

The main topics of Van Hul's work include:

  • Bone health and treatments
  • Connective tissue disorders research
  • Bone Metabolism and Diseases
  • Dermatological and Skeletal Disorders
  • Wnt/β-catenin signaling in development and cancer
  • Genomics and Rare Diseases
  • Epigenetics and DNA Methylation

Van Hul has published extensively in several scientific venues. The most frequent publication forums are:

  • Frontiers in Endocrinology
  • Bone Reports
  • Calcified Tissue International
  • Bone
  • Genes

Among recent papers, notable titles include:

  • WNT Signaling and Bone: Lessons From Skeletal Dysplasias and Disorders, 2020, Frontiers in Endocrinology
  • Germline and Mosaic Variants in PRKACA and PRKACB Cause a Multiple Congenital Malformation Syndrome, 2020, The American Journal of Human Genetics
  • Insights into the multifactorial causation of obesity by integrated genetic and epigenetic analysis, 2020, Obesity Reviews
  • A Roadmap to Gene Discoveries and Novel Therapies in Monogenic Low and High Bone Mass Disorders, 2021, Frontiers in Endocrinology
  • Perspective of the GEMSTONE Consortium on Current and Future Approaches to Functional Validation for Skeletal Genetic Disease Using Cellular, Molecular and Animal-Modeling Techniques, 2021, Frontiers in Endocrinology

Van Hul collaborates frequently with a group of coauthors including:

  • Geert Mortier
  • Eveline Boudin
  • Yentl Huybrechts
  • Gretl Hendrickx
  • Ellen Steenackers

The researcher's work covers a range of genetic and molecular mechanisms underlying bone and connective tissue disorders, with an integrative approach that blends genetic discoveries with epigenetic and cellular analysis. This multidisciplinary expertise supports advances in understanding skeletal diseases and exploring potential therapeutic approaches.

Best Publications

  • Genome-wide meta-analysis identifies 56 bone mineral density loci and reveals 14 loci associated with risk of fracture

    Karol Estrada;Unnur Styrkarsdottir;Evangelos Evangelou;Yi-Hsiang Hsu

  • Presenile dementia and cerebral haemorrhage linked to a mutation at codon 692 of the β–amyloid precursor protein gene

    Lydia Hendriks;Cornelia M. van Duijn;Patrick Cras;Marc Cruts

  • TGF-Β1-induced migration of bone mesenchymal stem cells couples bone resorption with formation

    Yi Tang;Xiangwei Wu;Xiangwei Wu;Xiangwei Wu;Weiqi Lei;Lijuan Pang;Lijuan Pang

  • Transforming Growth Factor-β1 to the Bone

    Katrien Janssens;Peter ten Dijke;Sophie Janssens;Wim Van Hul

  • Extracellular regulation of BMP signaling in vertebrates: a cocktail of modulators.

    Wendy Balemans;Wim Van Hul

  • Dysfunction of lipid sensor GPR120 leads to obesity in both mouse and human

    Atsuhiko Ichimura;Akira Hirasawa;Odile Poulain-Godefroy;Odile Poulain-Godefroy;Amélie Bonnefond;Amélie Bonnefond

  • Six Novel Missense Mutations in the LDL Receptor-Related Protein 5 (LRP5) Gene in Different Conditions with an Increased Bone Density

    Liesbeth Van Wesenbeeck;Erna Cleiren;Jeppe Gram;Rodney K. Beals

  • Loss-of-function mutations in LEMD3 result in osteopoikilosis, Buschke-Ollendorff syndrome and melorheostosis.

    Jan Hellemans;Olena Preobrazhenska;Andy Willaert;Philippe Debeer

  • Albers-Schönberg disease (autosomal dominant osteopetrosis, type II) results from mutations in the ClCN7 chloride channel gene

    Erna Cleiren;Olivier Bénichou;Els Van Hul;Jeppe Gram

  • Domain-specific mutations in sequestosome 1 (SQSTM1) cause familial and sporadic Paget's disease

    Lynne J. Hocking;Gavin J.A. Lucas;Anna Daroszewska;Jon Mangion

  • Mutations in the CCN gene family member WISP3 cause progressive pseudorheumatoid dysplasia.

    J R Hurvitz;W M Suwairi;W Van Hul;H El-Shanti

  • PPARα gene expression correlates with severity and histological treatment response in patients with non-alcoholic steatohepatitis

    Sven Francque;An Verrijken;Sandrine Caron;Janne Prawitt

  • Large-Scale Analysis of Association Between LRP5 and LRP6 Variants and Osteoporosis

    Joyce B J. van Meurs;Thomas A. Trikalinos;Thomas A. Trikalinos;Stuart H. Ralston;Susana Balcells

  • Bone Overgrowth-associated Mutations in the LRP4 Gene Impair Sclerostin Facilitator Function

    Olivier Leupin;Elke Piters;Christine Halleux;Shouih Hu

  • Reduced affinity to and inhibition by DKK1 form a common mechanism by which high bone mass-associated missense mutations in LRP5 affect canonical Wnt signaling.

    Minrong Ai;Sheri L. Holmen;Wim Van Hul;Bart O. Williams

  • A look behind the scenes: the risk and pathogenesis of primary osteoporosis

    Gretl Hendrickx;Eveline Boudin;Wim Van Hul

  • Molecular basis of multiple exostoses: mutations in the EXT1 and EXT2 genes.

    Wim Wuyts;Wim Van Hul

  • LRP5 and Wnt signaling: a union made for bone.

    Mark L Johnson;Kimberley Harnish;Roel Nusse;Wim Van Hul

  • EXT-mutation analysis and loss of heterozygosity in sporadic and hereditary osteochondromas and secondary chondrosarcomas.

    Judith V.M.G. Bovée;Anne-Marie Cleton-Jansen;Wim Wuyts;Goedele Caethoven

  • Involvement of PLEKHM1 in osteoclastic vesicular transport and osteopetrosis in incisors absent rats and humans

    Liesbeth Van Wesenbeeck;Paul R. Odgren;Fraser Coxon;Annalisa Frattini

Frequent Co-Authors

Luc Van Gaal
Luc Van Gaal University of Antwerp
Geert Mortier
Geert Mortier University of Antwerp
Wim Wuyts
Wim Wuyts University of Antwerp
Stuart H. Ralston
Stuart H. Ralston University of Edinburgh
Kim Brixen
Kim Brixen University of Southern Denmark
Jean-Pierre Devogelaer
Jean-Pierre Devogelaer Université Catholique de Louvain
Jens Bollerslev
Jens Bollerslev Oslo University Hospital
Erik Fransen
Erik Fransen University of Antwerp
Philippe Froguel
Philippe Froguel Imperial College London

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