Jurgen Del-Favero

Overview

Best Publications

• Genome-wide association study identifies 30 loci associated with bipolar disorder

  Eli A. Stahl;Eli A. Stahl;Gerome Breen;Andreas J. Forstner;Andrew McQuillin

  1637
  Citations

• De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy.

  Lieve Claes;Jurgen Del-Favero;Berten Ceulemans;Lieven Lagae

  1536
  Citations

• VEGF is a modifier of amyotrophic lateral sclerosis in mice and humans and protects motoneurons against ischemic death

  Diether Lambrechts;Erik Storkebaum;Masafumi Morimoto;Jurgen Del-Favero

  1094
  Citations

• Thrombomodulin mutations in atypical hemolytic-uremic syndrome.

  Mieke Delvaeye;Marina Noris;Astrid De Vriese;Charles T. Esmon

  659
  Citations

• Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder.

  Ricardo Segurado;Sevilla D. Detera-Wadleigh;Douglas F. Levinson;Cathryn M. Lewis

  547
  Citations

• Meta-analyses of genetic studies on major depressive disorder.

  S López-León;A C J W Janssens;A M González-Zuloeta Ladd;J Del-Favero

  540
  Citations

• APP duplication is sufficient to cause early onset Alzheimer's dementia with cerebral amyloid angiopathy.

  Kristel Sleegers;Nathalie Brouwers;Ilse Gijselinck;Jessie Theuns

  459
  Citations

• Paroxysmal exercise-induced dyskinesia and epilepsy is due to mutations in SLC2A1, encoding the glucose transporter GLUT1.

  Arvid Suls;Peter Dedeken;Karolien Goffin;Hilde Van Esch

  392
  Citations

• novoSNP, a novel computational tool for sequence variation discovery

  Stefan Weckx;Jurgen Del-Favero;Rosa Rademakers;Lieve Claes

  312
  Citations

• Mutations in SEPT9 cause hereditary neuralgic amyotrophy.

  Gregor Kuhlenbäumer;Gregor Kuhlenbäumer;Mark C Hannibal;Eva Nelis;Anja Schirmacher

  292
  Citations

• Optimized filtering reduces the error rate in detecting genomic variants by short-read sequencing

  Joke Reumers;Joke Reumers;Peter De Rijk;Hui Zhao;Hui Zhao;Anthony Liekens

  272
  Citations

• De novo SCN1A mutations are a major cause of severe myoclonic epilepsy of infancy

  Lieve Claes;Berten Ceulemans;Dominique Audenaert;Katrien Smets

  265
  Citations

• Resequencing of positional candidates identifies low frequency IL23R coding variants protecting against inflammatory bowel disease

  Yukihide Momozawa;Myriam Mni;Kayo Nakamura;Wouter Coppieters

  213
  Citations

• Association between COMT (Val158Met) functional polymorphism and early onset in patients with major depressive disorder in a European multicenter genetic association study.

  I Massat;D Souery;J Del-Favero;M Nothen

  202
  Citations

• Clinical spectrum of early-onset epileptic encephalopathies associated with STXBP1 mutations

  Liesbet Deprez;Sarah Weckhuysen;Philip Holmgren;Arvid Suls

  197
  Citations

• Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis.

  Yurii S Aulchenko;Ilse A Hoppenbrouwers;Sreeram V Ramagopalan;Linda Broer

  191
  Citations

• Glucocorticoid receptor gene-based SNP analysis in patients with recurrent major depression

  Dirk Van West;Filip Van Den Eede;Jurgen Del-Favero;Daniel Souery

  183
  Citations

• High-density SNP haplotyping suggests altered regulation of tau gene expression in progressive supranuclear palsy

  Rosa Rademakers;Stacey Melquist;Marc Cruts;Jessie Theuns

  181
  Citations

• Short telomeres in depression and the general population are associated with a hypocortisolemic state.

  Mikael Wikgren;Martin Maripuu;Thomas Karlsson;Katarina Nordfjäll

  160
  Citations

• Paroxysmal exercise-induced dyskinesia and epilepsy due to mutations in SLC2A1, encoding the glucose transporter, Gluti

  David Cassiman;A Suls;P Dedeken;Karolien Goffin

  2
  Citations