Wolfgang Berger

Wolfgang Berger publication distribution in Genetics in 2026

The chart shows the distribution of publications by all Research.com ranked scientists in the field of Genetics in 2026. The highlighted bar marks where Wolfgang Berger sits on this spectrum.

Wolfgang Berger D-index placement in Genetics in 2026

The chart shows the D-index (discipline H-index) distribution of Genetics scientists ranked by Research.com in 2026. The highlighted bar marks where Wolfgang Berger sits on this spectrum.

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