Stephan Niemann - Concepedia

Concepedia

Author

Stephan Niemann

Justus-Liebig-Universität Gießen

Also Known As

S Niemann, S. Niemann, STEPHAN NIEMANN, Stephan Niemann

38

Publications

2.6K

Citations

19

H-Index

40

Concepts

All Affiliations

Justus-Liebig-Universität Gießen Harvard University Massachusetts General Hospital Max Planck Institute for Molecular Genetics University of Glasgow

SN

About

Stephan Niemann is an author at Justus-Liebig-Universität Gießen specializing in medicine, genetics, and tumor biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	13	14	2.2K
2	Cell Biology	2	2	146
3	Engineering	1	1	31
4	Biology	1	1	310
5	Microbiology	1	1	24

Stephan Niemann

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20

Publications

2.6K

Citations

18

H-Index

	Year	Citations
Mutations in SDHC cause autosomal dominant paraganglioma, type 3 Stephan Niemann, Ulrich Müller Nature Genetics Genetic DisorderMedicinePathologyCancer GeneticsType 3	2000	878
An immunohistochemical procedure to detect patients with paraganglioma and phaeochromocytoma with germline SDHB, SDHC, or SDHD gene mutations: a retrospective and prospective analysis Francien H. van Nederveen, José Gaal, Judith Favier, The Lancet Oncology Lymphoid NeoplasiaTumoral PathologyMedicineGermline SdhbPathology	2009	529
Homozygous WNT3 Mutation Causes Tetra-Amelia in a Large Consanguineous Family Stephan Niemann, Chengfeng Zhao, F Pascu, The American Journal of Human Genetics BiologyMendelian DisorderGenetic DisorderGeneticsHomozygous Wnt3 Mutation	2004	310
Specific sequence changes in multiple transcript system <i>DYT3</i> are associated with X-linked dystonia parkinsonism Dagmar Nolte, Stephan Niemann, Ulrich Müller Proceedings of the National Academy of Sciences GeneticsDisease GeneClinical NeuroscienceDisease Gene IdentificationSpecific Sequence Changes	2003	133
DNA Methylation Markers Predict Outcome in Node-Positive, Estrogen Receptor-Positive Breast Cancer with Adjuvant Anthracycline-Based Chemotherapy Oliver Hartmann, Frédérique Spyratos, Nadia Harbeck, Clinical Cancer Research	2008	105
Autosomal dominant malignant and catecholamine-producing paraganglioma caused by a splice donor site mutation in SDHC Stephan Niemann, Ulrich Müller, Dieter Engelhardt, Human Genetics Catecholamine-producing ParagangliomaPathologyMedicineRadiation OncologyTumor Biology	2003	74
Phenotypic and Molecular Analyses of X-linked Dystonia-Parkinsonism (“Lubag”) in Women Virgilio Gerald H. Evidente, Dagmar Nolte, Stephan Niemann, Archives of Neurology	2004	73
Uncoupling of Myelin Assembly and Schwann Cell Differentiation by Transgenic Overexpression of Peripheral Myelin Protein 22 Stephan Niemann, Michael W. Sereda, Ueli Suter, Journal of Neuroscience	2000	71
Refined Linkage Disequilibrium and Physical Mapping of the Gene Locus for X-Linked Dystonia–Parkinsonism (DYT3) Andrea H. Németh, Dagmar Nolte, Eimear Dunne, Genomics Gene LocusNeurodegenerative DiseasesLinkage DisequilibriumGenetic DisorderX-linked Dystonia–parkinsonism	1999	55
PGL3 , a third, not maternally imprinted locus in autosomal dominant paraganglioma Stephan Niemann, Daniela Steinberger, U. Müller Neurogenetics Imprinted LocusGenetic DisorderGeneticsPathologyAutosomal Dominant Paraganglioma	1999	50

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