Karl-Heinz Grzeschik

Overview

Best Publications

• The precursor of Alzheimer's disease amyloid A4 protein resembles a cell-surface receptor

  Jie Kang;H.-G. Lemaire;A. Unterbeck;J. M. Salbaum

  6153
  Citations

• GLI3 zinc-finger gene interrupted by translocations in Greig syndrome families

  Andrea Vortkamp;Manfred Gessler;Karl-Heinz Grzeschik

  659
  Citations

• Hepatitis B virus DNA integration in a sequence homologous to v-erb-A and steroid receptor genes in a hepatocellular carcinoma.

  Anne Dejean;Lydie Bougueleret;Karl-Heinz Grzeschik;Pierre Tiollais

  554
  Citations

• Chromosome localization in normal human cells and neuroblastomas of a gene related to c- myc

  Manfred Schwab;Harold E. Varmus;J. Michael Bishop;Karl Heinz Grzeschik

  419
  Citations

• Mutations in the NSDHL gene, encoding a 3β-hydroxysteroid dehydrogenase, cause CHILD syndrome

  Arne König;Rudolf Happle;Dorothea Bornholdt;Hartmut Engel

  377
  Citations

• Simple repeat sequences on the human Y chromosome are equally polymorphic as their autosomal counterparts.

  L Roewer;J Arnemann;N K Spurr;K H Grzeschik

  357
  Citations

• Point Mutations in Human GLI3 Cause Greig Syndrome

  Anja Wild;Martha Kalff-Suske;Andrea Vortkamp;Dorothea Bornholdt

  242
  Citations

• The Phenotypic Spectrum of GLI3 Morphopathies Includes Autosomal Dominant Preaxial Polydactyly Type-IV and Postaxial Polydactyly Type-A/B; No Phenotype Prediction from the Position of GLI3 Mutations

  Uppala Radhakrishna;Dorothea Bornholdt;Hamish S. Scott;Uday C. Patel

  236
  Citations

• THIK-1 and THIK-2, a novel subfamily of tandem pore domain K+ channels.

  Sindhu Rajan;Erhard Wischmeyer;Christine Karschin;Regina Preisig-Müller

  232
  Citations

• Mutation in GLI3 in postaxial polydactyly type A

  Uppala Radhakrishna;Anja Wild;Karl-Heinz Grzeschik;Stylianos E. Antonarakis

  207
  Citations

• Mutations in bone morphogenetic protein receptor 1B cause brachydactyly type A2.

  Katarina Lehmann;Petra Seemann;Sigmar Stricker;Marai Sammar

  196
  Citations

• Regional localization on the human X chromosome and polymorphism of the coagulation factor IX gene (hemophilia B locus)

  G Camerino;K H Grzeschik;M Jaye

  186
  Citations

• Expression pattern in brain of TASK-1, TASK-3, and a tandem pore domain K(+) channel subunit, TASK-5, associated with the central auditory nervous system.

  Christine Karschin;Erhard Wischmeyer;Regina Preisig-Müller;Sindhu Rajan

  185
  Citations

• Molecular Characterization of Human Zyxin

  Teresita Macalma;Jürgen Otte;Mary E. Hensler;Susanne M. Bockholt

  181
  Citations

• Point Mutations Throughout the GLI3 Gene Cause Greig Cephalopolysyndactyly Syndrome

  Martha Kalff-Suske;Anja Wild;Juliane Topp;Martina Wessling

  175
  Citations

• Mutations in the Gene Encoding the Inwardly-Rectifying Renal Potassium Channel, ROMK, Cause the Antenatal Variant of Bartter Syndrome: Evidence for Genetic Heterogeneity

  Lothar Károlyi;Martin Konrad;Arnold Köckerling;Andreas Ziegler

  172
  Citations

• Localization of the human beta-catenin gene (CTNNB1) to 3p21: a region implicated in tumor development.

  Cornelia Kraus;Thomas Liehr;Jörg Hülsken;Jürgen Behrens

  170
  Citations

• Chromosome assignment of genes encoding the alpha and beta subunits of glycoprotein hormones in man and mouse.

  Susan L. Naylor;William W. Chin;William W. Chin;Howard M. Goodman;Peter A. Lalley

  166
  Citations

• IFAP Syndrome Is Caused by Deficiency in MBTPS2, an Intramembrane Zinc Metalloprotease Essential for Cholesterol Homeostasis and ER Stress Response

  Frank Oeffner;Gayle Fischer;Rudolf Happle;Arne König

  163
  Citations

• Serotonin transporter gene-linked polymorphic region: Allele distributions in relationship to body weight and in anorexia nervosa

  A. Hinney;N. Barth;A. Ziegler;S. Von Prittwitz

  155
  Citations