Heide Ritter

Heterozygous mutations in ANKH, the human ortholog of the mouse progressive ankylosis gene, result in craniometaphyseal dysplasia

Peter Nürnberg, Hölger Thiele, David Chandler et al. · Nature Genetics · 2001 · 240 citations

Developmental Anomaly, Developmental Biology, Mendelian Disorder +10

Loss of chondroitin 6-<i>O</i>-sulfotransferase-1 function results in severe human chondrodysplasia with progressive spinal involvement

Hölger Thiele, Masahiro Sakano, Hiroshi Kitagawa et al. · Proceedings of the National Academy of Sciences · 2004 · 187 citations · Full text

Bioorganic Chemistry, Delta Hexa-galnac, Glycobiology +21

Evaluation of a potential epigenetic biomarker by quantitative methyl‐single nucleotide polymorphism analysis

Karen Uhlmann, Anja Brinckmann, Mohammad R. Toliat et al. · Electrophoresis · 2002 · 172 citations

Epigenetic Change, Genetics, Dna Methylation +21

Chromosome 18 replaced by two ring chromosomes of chromosome 18 origin

Konstantin Miller, Brigitte Pabst, Heide Ritter et al. · Human Genetics · 2003 · 54 citations

Chromatin, Genetics, Chromosome Biology +5

Identification of highly polymorphic microsatellites in the rhesus macaque <i>Macaca mulatta</i> by cross‐species amplification

Manfred Kayser, Heide Ritter, Fred B. Bercovitch et al. · Molecular Ecology · 1996 · 51 citations

Biology, Genetic Diversity, Molecular Ecology +9