Clemens R. Müller

Overview

Best Publications

• Association of Anxiety-Related Traits with a Polymorphism in the Serotonin Transporter Gene Regulatory Region

  Klaus-Peter Lesch;Dietmar Bengel;Armin Heils;Sue Z. Sabol

  6648
  Citations

• Mutations in VKORC1 cause warfarin resistance and multiple coagulation factor deficiency type 2

  Simone Rost;Andreas Fregin;Vytautas Ivaskevicius;Ernst Conzelmann

  1483
  Citations

• A novel functional polymorphism within the promoter of the serotonin transporter gene: possible role in susceptibility to affective disorders

  D. A. Collier;G. Stober;T. Li;A. Heils

  862
  Citations

• Mutations in the skeletal muscle α-actin gene in patients with actin myopathy and nemaline myopathy

  Kristen J. Nowak;Kristen J. Nowak;Duangrurdee Wattanasirichaigoon;Hans H. Goebel;Matthew Wilce

  453
  Citations

• DNA finger printing by oligonucleotide probes specific for simple repeats.

  S. Ali;C. R. Müller;J. T. Epplen

  425
  Citations

• The Genetic Basis of Resistance to Anticoagulants in Rodents

  Hans-Joachim Pelz;Simone Rost;Mirja Hünerberg;Andreas Fregin

  422
  Citations

• Laboratory guidelines for molecular diagnosis of Y-chromosomal microdeletions

  M Simoni;E Bakker;M C Eurlings;Gert Matthijs

  376
  Citations

• VKORC1 haplotypes and their impact on the inter-individual and inter-ethnical variability of oral anticoagulation

  Christof Geisen;Matthias Watzka;Katja Sittinger;Michael Steffens

  350
  Citations

• RYR1 mutations are a common cause of congenital myopathies with central nuclei

  J M Wilmshurst;S Lillis;H Zhou;K Pillay

  282
  Citations

• A standardized framework for the validation and verification of clinical molecular genetic tests

  Christopher J Mattocks;Michael A Morris;Gert Matthijs;Elfriede Swinnen

  228
  Citations

• Recognizing and managing a malignant hyperthermia crisis: guidelines from the European Malignant Hyperthermia Group

  K.P.E. Glahn;F.R. Ellis;P.J. Halsall;C.R. Müller

  219
  Citations

• Autosomal recessive inheritance of RYR1 mutations in a congenital myopathy with cores.

  H. Jungbluth;C.R. Muller;B. Halliger-Keller;M. Brockington

  217
  Citations

• European Malignant Hyperthermia Group guidelines for investigation of malignant hyperthermia susceptibility

  P M Hopkins;H Rüffert;M M Snoeck;T Girard

  204
  Citations

• Molecular mechanisms and phenotypic variation in RYR1-related congenital myopathies

  Haiyan Zhou;Heinz Jungbluth;Caroline A. Sewry;Lucy Feng

  197
  Citations

• Identification of four novel mutations in the C-terminal membrane spanning domain of the ryanodine receptor 1: association with central core disease and alteration of calcium homeostasis

  Nikola Tilgen;Francesco Zorzato;Birgit Halliger-Keller;Francesco Muntoni

  196
  Citations

• The spectrum of pathology in central core disease.

  C.A. Sewry;C. Muller;M. Davis;J.S.M. Dwyer

  189
  Citations

• Magnetic resonance imaging of muscle in congenital myopathies associated with RYR1 mutations

  Heinz Jungbluth;Heinz Jungbluth;Mark R. Davis;Clemens Müller;Serena Counsell

  189
  Citations

• Novel mutations in the VKORC1 gene of wild rats and mice – a response to 50 years of selection pressure by warfarin?

  Simone Rost;Hans Joachim Pelz;Sandra Menzel;Alan D. MacNicoll

  186
  Citations

• VKORC1: molecular target of coumarins

  J. Oldenburg;M. Watzka;S. Rost;C. R. Müller

  182
  Citations

• Assignment by deletion mapping of the steroid sulfatase X-linked ichthyosis locus to Xp223

  L. Tiepolo;Orsetta Zuffardi;M. Fraccaro;D. di Natale

  181
  Citations