Lut Van Laer

Overview

Best Publications

• Mutations in the human |[alpha]|-tectorin gene cause autosomal dominant non-syndromic hearing impairment

  Kristien Verhoeven;Lut Van Laer;Karin Kirschhofer;P Kevin Legan

  469
  Citations

• Loss-of-function mutations in TGFB2 cause a syndromic presentation of thoracic aortic aneurysm

  Mark E. Lindsay;Dorien Schepers;Nikhita Ajit Bolar;Jefferson J. Doyle

  467
  Citations

• Nonsyndromic hearing impairment is associated with a mutation in DFNA5

  Lut Van Laer;Egbert H Huizing;Margriet Verstreken;Diederick van Zuijlen

  417
  Citations

• Mutations in the gene encoding pejvakin, a newly identified protein of the afferent auditory pathway, cause DFNB59 auditory neuropathy

  Sedigheh Delmaghani;Francisco J del Castillo;Vincent Michel;Michel Leibovici

  413
  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

• Mutations in the novel protocadherin PCDH15 cause Usher syndrome type 1F

  Kumar N. Alagramam;Huijun Yuan;Markus H. Kuehn;Crystal L. Murcia

  336
  Citations

• Mutations in a TGF-β ligand, TGFB3, cause syndromic aortic aneurysms and dissections.

  Aida M. Bertoli-Avella;Elisabeth Gillis;Hiroko Morisaki;Judith M A Verhagen

  306
  Citations

• Mutations in the TGF-β repressor SKI cause Shprintzen-Goldberg syndrome with aortic aneurysm.

  Alexander J Doyle;Alexander J Doyle;Alexander J Doyle;Jefferson J Doyle;Seneca L Bessling;Samantha Maragh;Samantha Maragh

  284
  Citations

• Phenotypic spectrum of the SMAD3-related aneurysms–osteoarthritis syndrome

  Ingrid M B H van de Laar;Denise van der Linde;Edwin H G Oei;Pieter K Bos

  274
  Citations

• Loeys-Dietz Syndrome

  Lut Van Laer;Harry C Dietz;Bart Loeys

  269
  Citations

• Differences in manifestations of Marfan syndrome, Ehlers-Danlos syndrome, and Loeys-Dietz syndrome.

  Josephina A. N. Meester;Aline Verstraeten;Dorien Schepers;Maaike Alaerts

  268
  Citations

• GRM7 variants confer susceptibility to age-related hearing impairment

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

  247
  Citations

• Clinical Validity of Genes for Heritable Thoracic Aortic Aneurysm and Dissection

  Marjolijn Renard;Catherine Francis;Rajarshi Ghosh;Alan F. Scott

  236
  Citations

• Genetics of Thoracic Aortic Aneurysm At the Crossroad of Transforming Growth Factor-β Signaling and Vascular Smooth Muscle Cell Contractility

  Elisabeth Gillis;Lut Van Laer;Bart L. Loeys

  231
  Citations

• GJB2 deafness gene shows a specific spectrum of mutations in Japan, including a frequent founder mutation

  Akihiro Ohtsuka;Isamu Yuge;Shinobu Kimura;Atsushi Namba

  218
  Citations

• Mutations in KIF11 Cause Autosomal-Dominant Microcephaly Variably Associated with Congenital Lymphedema and Chorioretinopathy

  Pia Ostergaard;Michael A Simpson;Antonella Mendola;Pradeep Vasudevan

  189
  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

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

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

  176
  Citations

• Marfan Syndrome and Related Disorders: 25 Years of Gene Discovery.

  Aline Verstraeten;Maaike Alaerts;Lut Van Laer;Bart Loeys;Bart Loeys

  170
  Citations

• Genetic studies on noise-induced hearing loss: a review.

  Annelies Konings;Lut Van Laer;Guy Van Camp

  159
  Citations