Angelika Köhler

Isolation, Characterization, and Organ-Specific Expression of Two Novel Human Zinc Finger Genes Related to theDrosophilaGenespalt

Jürgen Kohlhase, Reinhard Schuh, Gordon Dowe et al. · Genomics · 1996 · 145 citations

Life Sciences, Genetics, Molecular Genetics +7

Molecular Characterization of Breakpoints in Patients with Holoprosencephaly and Definition of the HPE2 Critical Region 2p21

Ute Schell, Johannes Wienberg, Angelika Köhler et al. · Human Molecular Genetics · 1996 · 60 citations

Life Sciences, Genetics, Molecular Genetics +12

Benign infantile convulsions (IC) and subsequent paroxysmal kinesigenic dyskinesia (PKD) in a patient with 16p11.2 microdeletion syndrome

Axel Weber, Angelika Köhler, Andreas Hahn et al. · Neurogenetics · 2013 · 36 citations

Medicine, Neurology, Neuroscience +14

Duplication or insertion in 15q11–13 associated with mental retardation ‐short stature and obesity ‐ Prader‐Willi or Cohen syndrome?

A Fuhrmann-Rieger, Angelika Köhler, Walter Fuhrmann · Clinical Genetics · 1984 · 27 citations

Life Sciences, Genetics, Cytogenetics +14

Plasmolipin: genomic structure, chromosomal localization, protein expression pattern, and putative association with Bardet-Biedl syndrome

Michael Hamacher, U. Pippirs, Angelika Köhler et al. · Mammalian Genome · 2001 · 22 citations

Life Sciences, Genetics, Molecular Genetics +9