World's Best Scientists 2026 revealed!

D-Index & Metrics

Genetics

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

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

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

Studying genetics in the USA opens doors to a variety of related healthcare careers, many of which can be started or advanced with online degrees. For those interested in the administrative side of healthcare, healthcare administration degrees and healthcare administration degree online programs offer flexible options to build leadership skills while balancing work and study.

Genetics students seeking alternative career paths may also consider programs like medical billing and coding courses, which train individuals to manage vital health information and support the efficiency of healthcare systems. For those drawn to patient care, some nursing colleges with high acceptance rates provide greater accessibility to nursing programs, allowing more students to pursue vital, hands-on healthcare roles.

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.

Best Scientists Citing Hannie Kremer

Trending Scientists

Recently Published Articles