Hans Knoblauch

Mutability of Y-Chromosomal Microsatellites: Rates, Characteristics, Molecular Bases, and Forensic Implications

Kaye N. Ballantyne, Miriam Goedbloed, Rixun Fang et al. · The American Journal of Human Genetics · 2010 · 400 citations · Full text

Molecular diagnosis of the Prader-Willi and Angelman syndromes by detection of parent-of-origin specific DNA methylation in 15q11-13

B�rbel Dittrich, WendyP. Robinson, Hans Knoblauch et al. · Human Genetics · 1992 · 202 citations

Molecular Diagnosis, Mendelian Disorder, Genetic Disorder +11

Phenotypic variation and genetic heterogeneity in Léri-Weill syndrome

Simone Schiller, Stephanie Spranger, Birgit Schechinger et al. · European Journal of Human Genetics · 2000 · 138 citations · Full text

Allelic Variant, Genetic Disorder, Genetics +3

Haplotypes and SNPs in 13 lipid-relevant genes explain most of the genetic variance in high-density lipoprotein and low-density lipoprotein cholesterol

Hans Knoblauch · Human Molecular Genetics · 2004 · 101 citations

Phenotypic Variation, Genetics, Genetic Epidemiology +21

A Cholesterol-Lowering Gene Maps to Chromosome 13q

Hans Knoblauch, Bertram Müller‐Myhsok, Andreas Busjahn et al. · The American Journal of Human Genetics · 2000 · 94 citations · Full text

Chromatin, Genetics, Human Polymorphism +3