Stephan Niemann
Epigenomics (Germany)(DE)
Publications by Year
Research Areas
Adrenal and Paraganglionic Tumors, Neurogenetic and Muscular Disorders Research, Cancer, Hypoxia, and Metabolism, Hereditary Neurological Disorders, Amyotrophic Lateral Sclerosis Research
Most-Cited Works
- → Mutations in SDHC cause autosomal dominant paraganglioma, type 3(2000)879 cited
- → An immunohistochemical procedure to detect patients with paraganglioma and phaeochromocytoma with germline SDHB, SDHC, or SDHD gene mutations: a retrospective and prospective analysis(2009)530 cited
- → Homozygous WNT3 Mutation Causes Tetra-Amelia in a Large Consanguineous Family(2004)311 cited
- → Specific sequence changes in multiple transcript system DYT3 are associated with X-linked dystonia parkinsonism(2003)137 cited
- → DNA Methylation Markers Predict Outcome in Node-Positive, Estrogen Receptor-Positive Breast Cancer with Adjuvant Anthracycline-Based Chemotherapy(2008)106 cited
- → Autosomal dominant malignant and catecholamine-producing paraganglioma caused by a splice donor site mutation in SDHC(2003)74 cited
- → Phenotypic and Molecular Analyses of X-linked Dystonia-Parkinsonism (“Lubag”) in Women(2004)73 cited
- → Uncoupling of Myelin Assembly and Schwann Cell Differentiation by Transgenic Overexpression of Peripheral Myelin Protein 22(2000)71 cited
- → Refined Linkage Disequilibrium and Physical Mapping of the Gene Locus for X-Linked Dystonia–Parkinsonism (DYT3)(1999)59 cited
- → PGL3 , a third, not maternally imprinted locus in autosomal dominant paraganglioma(1999)50 cited