World's Best Scientists 2026 revealed!

D-Index & Metrics

Genetics

D-Index
74
Citations
19221
World Ranking
1967
National Ranking
70

Hannie Kremer 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 Hannie Kremer 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: 235 publications — 62nd percentile

62% of scientists in this discipline score the same or lower.

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

Hannie Kremer 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 Hannie Kremer 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: 74 D-Index — 56th percentile

56% of scientists in this discipline score the same or lower.

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

Overview

Hannie Kremer is affiliated with Radboud University in the Netherlands. The scientific work focuses primarily on the fields of Biochemistry, Genetics and Molecular Biology, with significant contributions in Neuroscience.

The research covers a broad range of subfields including Molecular Biology, Sensory Systems, Genetics, Cognitive Neuroscience, and Neurology. Key topics within this work include hearing, cochlea, tinnitus, genetics, retinal development and disorders, CRISPR and genetic engineering, RNA and protein synthesis mechanisms, vestibular and auditory disorders, advanced biosensing and bioanalysis techniques, and RNA regulation and disease.

The frequent co-authors collaborating with Hannie Kremer are:

  • Ronald J. E. Pennings
  • Erik de Vrieze
  • Erwin van Wijk
  • Cris Lanting
  • Jaap Oostrik

Publications appear predominantly in several venues where the researcher has multiple contributions:

  • Human Genetics
  • International Journal of Molecular Sciences
  • bioRxiv (Cold Spring Harbor Laboratory)
  • Molecular Therapy - Nucleic Acids
  • Genetics in Medicine

Recent papers associated with Hannie Kremer include:

  • Antisense oligonucleotide-based treatment of retinitis pigmentosa caused by USH2A exon 13 mutations (2021), published in Molecular Therapy
  • Structural Variants Create New Topological-Associated Domains and Ectopic Retinal Enhancer-Gene Contact in Dominant Retinitis Pigmentosa (2020), published in The American Journal of Human Genetics
  • Cochlear supporting cells require GAS2 for cytoskeletal architecture and hearing (2021), published in Developmental Cell
  • Disease-specific ACMG/AMP guidelines improve sequence variant interpretation for hearing loss (2021), published in Genetics in Medicine
  • Usher syndrome type IV: clinically and molecularly confirmed by novel ARSG variants (2022), published in Human Genetics

Best Publications

  • Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome.

    Marco Tartaglia;Marco Tartaglia;Ernest L. Mehler;Rosalie Goldberg;Giuseppe Zampino

  • SDH5, a Gene Required for Flavination of Succinate Dehydrogenase, Is Mutated in Paraganglioma

    Huai Xiang Hao;Oleh Khalimonchuk;Margit Schraders;Noah Dephoure

  • Localization of the gene for Cowden disease to chromosome 10q22-23

    M. R. Nelen;G. W. Padberg;E. A J Peeters;A. Y. Lin

  • Germline Mutations in the PTEN/MMAC1 Gene in Patients With Cowden Disease

    M. R. Nelen;W. C. G. Van Staveren;E. A. J. Peeters;Mohammed Ben Hassel

  • A post-hoc comparison of the utility of sanger sequencing and exome sequencing for the diagnosis of heterogeneous diseases

    Kornelia Neveling;Ilse Feenstra;Christian Gilissen;Lies H. Hoefsloot

  • Male pseudohermaphroditism due to a homozygous missense mutation of the luteinizing hormone receptor gene

    J.M.J. Kremer;R. Kraaij;S.P.A. Toledo;M. Post

  • Expert specification of the ACMG/AMP variant interpretation guidelines for genetic hearing loss.

    Andrea M Oza;Andrea M Oza;Marina T DiStefano;Marina T DiStefano;Sarah E Hemphill;Brandon J Cushman

  • Novel PTEN mutations in patients with Cowden disease: absence of clear genotype-phenotype correlations.

    M R Nelen;H Kremer;I B Konings;F Schoute

  • Occupational noise, smoking, and a high body mass index are risk factors for age-related hearing impairment and moderate alcohol consumption is protective: a European population-based multicenter study.

    Erik Fransen;Vedat Topsakal;Jan Jaap Hendrickx;Lut Van Laer

  • A novel Usher protein network at the periciliary reloading point between molecular transport machineries in vertebrate photoreceptor cells

    Tina Maerker;Erwin van Wijk;Nora Overlack;Ferry F.J. Kersten

  • Usher syndrome: molecular links of pathogenesis, proteins and pathways

    Hannie Kremer;Erwin van Wijk;Tina Märker;Uwe Wolfrum

  • Alterations in the ankyrin domain of TRPV4 cause congenital distal SMA, scapuloperoneal SMA and HMSN2C

    Michaela Auer-Grumbach;Andrea Olschewski;Lea Papić;Hannie Kremer

  • Identification of 51 Novel Exons of the Usher Syndrome Type 2A (USH2A) Gene That Encode Multiple Conserved Functional Domains and That Are Mutated in Patients with Usher Syndrome Type II

    Erwin van Wijk;Ronald J.E. Pennings;Heleen te Brinke;Annemarie Claassen

  • CDH23 Mutation and Phenotype Heterogeneity: A Profile of 107 Diverse Families with Usher Syndrome and Nonsyndromic Deafness

    L.M. Astuto;J.M. Bork;M.D. Weston;J.W. Askew

  • The DFNB31 gene product whirlin connects to the Usher protein network in the cochlea and retina by direct association with USH2A and VLGR1

    Erwin van Wijk;Bert van der Zwaag;Theo Peters;Ulrike Zimmermann

  • GRM7 variants confer susceptibility to age-related hearing impairment

    Rick A. Friedman;Lut Van Laer;Matthew J. Huentelman;Sonal S. Sheth

  • Scaffold protein harmonin (USH1C) provides molecular links between Usher syndrome type 1 and type 2

    Jan Reiners;Erwin van Wijk;Tina Märker;Ulrike Zimmermann

  • An organelle-specific protein landscape identifies novel diseases and molecular mechanisms

    Boldt K;van Reeuwijk J;Lu Q;Koutroumpas K

  • Cosegregation of missense mutations of the luteinizing hormone receptor gene with familial male-limited precocious puberty

    Hannie Kremer;Edwin Mariman;Barto J. Otten;George W. Moll

  • The grainyhead like 2 gene (GRHL2), alias TFCP2L3, is associated with age-related hearing impairment

    Lut Van Laer;Els Van Eyken;Erik Fransen;Jeroen R. Huyghe

Frequent Co-Authors

Cor W. R. J. Cremers
Cor W. R. J. Cremers Radboud University
Frans P.M. Cremers
Frans P.M. Cremers Radboud University
Lies H. Hoefsloot
Lies H. Hoefsloot Erasmus University Rotterdam
Ronald Roepman
Ronald Roepman Radboud University
Uwe Wolfrum
Uwe Wolfrum Johannes Gutenberg University of Mainz
Rob W.J. Collin
Rob W.J. Collin Radboud University
Guy Van Camp
Guy Van Camp University of Antwerp
Helger G. Yntema
Helger G. Yntema Radboud University
Han G. Brunner
Han G. Brunner Radboud University
marius ueffing
marius ueffing University of Tübingen

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Related Online Degrees & Career Pathways

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These pathways highlight the versatile opportunities within healthcare, allowing genetics graduates to expand their impact or shift their career focus, often by leveraging the convenience and affordability of online education.

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