Erik Fransen

Overview

Best Publications

• Graded persistent activity in entorhinal cortex neurons

  Alexei V. Egorov;Bassam N. Hamam;Erik Fransén;Michael E. Hasselmo

  947
  Citations

• Temporal Frequency of Subthreshold Oscillations Scales with Entorhinal Grid Cell Field Spacing

  Lisa M. Giocomo;Eric A. Zilli;Erik Fransén;Michael E. Hasselmo

  486
  Citations

• Properties and role of I(h) in the pacing of subthreshold oscillations in entorhinal cortex layer II neurons.

  Clayton T. Dickson;Jacopo Magistretti;Mark H. Shalinsky;Erik Fransén

  392
  Citations

• 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

  346
  Citations

• Mechanism of Graded Persistent Cellular Activity of Entorhinal Cortex Layer V Neurons

  Erik Fransén;Babak Tahvildari;Alexei V. Egorov;Michael E. Hasselmo

  331
  Citations

• Comparative analysis of dynamic cell viability, migration and invasion assessments by novel real-time technology and classic endpoint assays.

  Ridha Limame;An Wouters;Bea Pauwels;Erik Fransen

  330
  Citations

• Architecture of the Mouse Brain Synaptome

  Fei Zhu;Fei Zhu;Mélissa Cizeron;Mélissa Cizeron;Zhen Qiu;Ruth Benavides-Piccione

  296
  Citations

• L1 Knockout Mice Show Dilated Ventricles, Vermis Hypoplasia and Impaired Exploration Patterns

  Erik Fransen;Rudi D'Hooge;Guy Van Camp;Marleen Verhoye

  290
  Citations

• Positional Cloning of a Gene Involved in Hereditary Multiple Exostoses

  W. Wuyts;W. Van Hul;J. Wauters;M. Nemtsova

  279
  Citations

• L1-Associated Diseases: Clinical Geneticists Divide, Molecular Geneticists Unite

  Erik Fransen;Guy Van Camp;Lieve Vits;Patrick J. Willems

  275
  Citations

• CRASH syndrome: clinical spectrum of corpus callosum hypoplasia, retardation, adducted thumbs, spastic paraparesis and hydrocephalus due to mutations in one single gene, L1.

  E. Fransen;V. Lemmon;G. Van Camp;L. Vits

  263
  Citations

• A COMMON FOUNDER FOR THE 35DELG GJB2 GENE MUTATION IN CONNEXIN 26 HEARING IMPAIRMENT

  L Van Laer;P Coucke;R F Mueller;G Caethoven

  258
  Citations

• GRM7 variants confer susceptibility to age-related hearing impairment

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

  247
  Citations

• High Prevalence of Symptoms of Menière's Disease in three Families With a Mutation in the COCH Gene

  E. Fransen;M. Verstreken;W. I. M. Verhagen;F. L. Wuyts

  202
  Citations

• C-terminal neurogranin is increased in cerebrospinal fluid but unchanged in plasma in Alzheimer's disease

  Ann De Vos;Dirk Jacobs;Hanne Struyfs;Erik Fransen

  202
  Citations

• 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

  189
  Citations

• MASA syndrome is due to mutations in the neural cell adhesion gene L1CAM.

  Lieve Vits;Guy Van Camp;Paul Coucke;Erik Fransen

  187
  Citations

• BMI-related metabolic composition of the follicular fluid of women undergoing assisted reproductive treatment and the consequences for oocyte and embryo quality

  S D M Valckx;I De Pauw;Diane De Neubourg;I Inion

  178
  Citations

• A dominant-negative GFI1B mutation in the gray platelet syndrome

  Davide Monteferrario;Nikhita A Bolar;Anna E Marneth;Konnie M Hebeda

  176
  Citations

• Simulations of the role of the muscarinic-activated calcium-sensitive nonspecific cation current I-NCM in entorhinal neuronal activity during delayed matching tasks

  Erik Fransén;Angel A. Alonso;Michael E. Hasselmo

  172
  Citations