Wolfgang Berger

Overview

Best Publications

• The molecular basis of human retinal and vitreoretinal diseases.

  Wolfgang Berger;Barbara Kloeckener-Gruissem;Barbara Kloeckener-Gruissem;John Neidhardt

  716
  Citations

• Positional cloning of the gene for X-linked retinitis pigmentosa 2

  U. Schwahn;S. Lenzner;J Dong;S. Feil

  440
  Citations

• Opitz G/BBB syndrome, a defect of midline development, is due to mutations in a new RING finger gene on Xp22

  Nandita A. Quaderi;Susann Schweiger;Karin Gaudenz;Brunella Franco

  409
  Citations

• Isolation of a candidate gene for Norrie disease by positional cloning.

  Berger W;Meindl A;van de Pol Tj;Cremers Fp

  323
  Citations

• A functional genetic variation of adenosine deaminase affects the duration and intensity of deep sleep in humans

  J. V. Rétey;M. Adam;E. Honegger;R. Khatami

  321
  Citations

• A genetic variation in the adenosine A2A receptor gene (ADORA2A) contributes to individual sensitivity to caffeine effects on sleep.

  J. V. Retey;M. Adam;R. Khatami;U. F. O. Luhmann

  315
  Citations

• The complete form of X-linked congenital stationary night blindness is caused by mutations in a gene encoding a leucine-rich repeat protein

  Carsten M. Pusch;Christina Zeitz;Oliver Brandau;Katrin Pesch

  297
  Citations

• Functional implications of the spectrum of mutations found in 234 cases with X-linked juvenile retinoschisis (XLRS)

  J.T. Dendunnen;T. Kraayenbrink;T. Kraayenbrink;M. van Schooneveld;M. van Schooneveld;E. van de Vosse

  283
  Citations

• Panel-based next generation sequencing as a reliable and efficient technique to detect mutations in unselected patients with retinal dystrophies

  Nicola Glöckle;Susanne Kohl;Julia Mohr;Tim Scheurenbrand

  279
  Citations

• TRPM1 Is Mutated in Patients with Autosomal-Recessive Complete Congenital Stationary Night Blindness

  Isabelle Audo;Susanne Kohl;Bart P. Leroy;Francis L. Munier

  270
  Citations

• Positional cloning of the gene for x-linked retinitis pigmentosa 3: homology with the guanine-nucleotide-exchange factor RCC1

  R. Roepman;G. Van Duijnhoven;T. Rosenberg;A. J. L. G. Pinckers

  233
  Citations

• Mutations in CABP4, the gene encoding the Ca2+-binding protein 4, cause autosomal recessive night blindness.

  Christina Zeitz;Barbara Kloeckener-Gruissem;Ursula Forster;Susanne Kohl

  232
  Citations

• The retinitis pigmentosa GTPase regulator (RPGR) interacts with novel transport-like proteins in the outer segments of rod photoreceptors

  Ronald Roepman;Nathalie Bernoud-Hubac;Diana E. Schick;Alessandra Maugeri

  232
  Citations

• Full-Length Human L1 Insertions Retain the Capacity for High Frequency Retrotransposition in Cultured Cells

  Michelle L. Kimberland;Vladimir Divoky;Josef Prchal;Uwe Schwahn

  226
  Citations

• Norrie disease is caused by mutations in an extracellular protein resembling C-terminal globular domain of mucins.

  Meindl A;Berger W;Meitinger T;van de Pol D

  211
  Citations

• Specific genetic deficiencies of the A and B isoenzymes of monoamine oxidase are characterized by distinct neurochemical and clinical phenotypes.

  J. W. M. Lenders;G. Eisenhofer;N. G. G. M. Abeling;W. Berger

  204
  Citations

• RPGR Transcription Studies in Mouse and Human Tissues Reveal a Retina-Specific Isoform That Is Disrupted in a Patient With X-Linked Retinitis Pigmentosa

  Renate Kirschner;Thomas Rosenberg;Robert Schultz-Heienbrok;Steffen Lenzner

  193
  Citations

• Vascular Defects and Sensorineural Deafness in a Mouse Model of Norrie Disease

  Heidi L. Rehm;Duan-Sun Zhang;Duan-Sun Zhang;M. Christian Brown;M. Christian Brown;Barbara Burgess

  193
  Citations

• Mutations in the candidate gene for Norrie disease

  W Berger;D van de Pol;M Warburg;A Gal

  192
  Citations

• ZNF408 is mutated in familial exudative vitreoretinopathy and is crucial for the development of zebrafish retinal vasculature

  Rob W. J. Collin;Konstantinos Nikopoulos;Margo Dona;Christian Gilissen

  184
  Citations