Stephan Niemann

2.6k total citations · 1 hit paper
26 papers, 1.6k citations indexed

About

Stephan Niemann is a scholar working on Cellular and Molecular Neuroscience, Neurology and Molecular Biology. According to data from OpenAlex, Stephan Niemann has authored 26 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Cellular and Molecular Neuroscience, 8 papers in Neurology and 7 papers in Molecular Biology. Recurrent topics in Stephan Niemann's work include Neurogenetic and Muscular Disorders Research (6 papers), Hereditary Neurological Disorders (6 papers) and Adrenal and Paraganglionic Tumors (6 papers). Stephan Niemann is often cited by papers focused on Neurogenetic and Muscular Disorders Research (6 papers), Hereditary Neurological Disorders (6 papers) and Adrenal and Paraganglionic Tumors (6 papers). Stephan Niemann collaborates with scholars based in Germany, United States and United Kingdom. Stephan Niemann's co-authors include Ulrich Müller, Dagmar Nolte, F Pascu, Ulrich Müller, Lee Niswander, Chengfeng Zhao, U. Stahl, James L. Weber, Dieter Engelhardt and Peter Lohse and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and Journal of Neuroscience.

In The Last Decade

Stephan Niemann

26 papers receiving 1.6k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Mutations in SDHC cause autosomal dominant paraganglioma, type 3

2000 689 citations Stephan Niemann, Ulrich Müller Nature Genetics profile →

Peers

Stephan Niemann

SURGE

EDM

NEURO

Francesca Boaretto Italy

Masahiko Tosaka Japan

Erika Peverelli Italy

Carles Gaston‐Massuet United Kingdom

Mabrouka Doghman France

Graeme R. Clark United Kingdom

M. Bassetti Italy

Jordan Jones Australia

Shirley Rainier United States

Lesley Tannahill United Kingdom

Francesca Boaretto Italy

Stephan Niemann

252 ×0.4

244 ×0.4

269 ×0.5

SURGE

230 ×0.5

EDM

136 ×0.5

NEURO

Citations per year, relative to Stephan Niemann Stephan Niemann (= 1×) peers Francesca Boaretto

Countries citing papers authored by Stephan Niemann

Since Specialization

Citations

This map shows the geographic impact of Stephan Niemann's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Stephan Niemann with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Stephan Niemann more than expected).

Fields of papers citing papers by Stephan Niemann

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Stephan Niemann. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Stephan Niemann. The network helps show where Stephan Niemann may publish in the future.

Co-authorship network of co-authors of Stephan Niemann

This figure shows the co-authorship network connecting the top 25 collaborators of Stephan Niemann. A scholar is included among the top collaborators of Stephan Niemann based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Stephan Niemann. Stephan Niemann is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Hartmann, Oliver, Frédérique Spyratos, Nadia Harbeck, et al.. (2008). DNA Methylation Markers Predict Outcome in Node-Positive, Estrogen Receptor-Positive Breast Cancer with Adjuvant Anthracycline-Based Chemotherapy. Clinical Cancer Research. 15(1). 315–323. 79 indexed citations

Landers, John E., Lijia Shi, Ting-Jan Cho, et al.. (2008). A common haplotype within the PON1 promoter region is associated with sporadic ALS. Amyotrophic Lateral Sclerosis. 9(5). 306–314. 33 indexed citations

Niemann, Stephan, Wendy Broom, & Robert Brown. (2007). Analysis of a genetic defect in the TATA box of the SOD1 gene in a patient with familial amyotrophic lateral sclerosis. Muscle & Nerve. 36(5). 704–707. 20 indexed citations

Niemann, Stephan, Hiroaki Kanki, Yasuyuki Fukui, et al.. (2007). Genetic ablation of NMDA receptor subunit NR3B in mouse reveals motoneuronal and nonmotoneuronal phenotypes. European Journal of Neuroscience. 26(6). 1407–1420. 39 indexed citations

Müller, Ulrich, Christian Troidl, & Stephan Niemann. (2005). SDHC mutations in hereditary paraganglioma/pheochromocytoma. Familial Cancer. 4(1). 9–12. 32 indexed citations

Niemann, Stephan, Chengfeng Zhao, F Pascu, et al.. (2004). Homozygous WNT3 Mutation Causes Tetra-Amelia in a Large Consanguineous Family. The American Journal of Human Genetics. 74(3). 558–563. 225 indexed citations

Niemann, Stephan. (2004). Familial ALS in Germany: origin of the R115G SOD1 mutation by a founder effect. Journal of Neurology Neurosurgery & Psychiatry. 75(8). 1186–1188. 27 indexed citations

Evidente, Virgilio Gerald H., Dagmar Nolte, Stephan Niemann, et al.. (2004). Phenotypic and Molecular Analyses of X-linked Dystonia-Parkinsonism (“Lubag”) in Women. Archives of Neurology. 61(12). 1956–9. 50 indexed citations

Niemann, Stephan, Ulrich Müller, Dieter Engelhardt, & Peter Lohse. (2003). Autosomal dominant malignant and catecholamine-producing paraganglioma caused by a splice donor site mutation in SDHC. Human Genetics. 113(1). 92–94. 59 indexed citations

10.

Prudlo, Johannes, Burkhard Alber, Vera M. Kalscheuer, et al.. (2003). Chromosomal translocation t(18;21)(q23;q22.1) indicates novel susceptibility loci for frontotemporal dementia with ALS. Annals of Neurology. 55(1). 134–138. 4 indexed citations

11.

Nolte, Dagmar, Stephan Niemann, & Ulrich Müller. (2003). Specific sequence changes in multiple transcript system DYT3 are associated with X-linked dystonia parkinsonism. Proceedings of the National Academy of Sciences. 100(18). 10347–10352. 78 indexed citations

12.

Nolte, Dagmar, Juliane Ramser, Stephan Niemann, et al.. (2001). ACRC codes for a novel nuclear protein with unusual acidic repeat tract and maps to DYT3 (dystonia parkinsonism) critical interval in Xq13.1. Neurogenetics. 3(4). 207–213. 11 indexed citations

13.

Niemann, Stephan & Ulrich Müller. (2000). Mutations in SDHC cause autosomal dominant paraganglioma, type 3. Nature Genetics. 26(3). 268–270. 689 indexed citations breakdown →

14.

Niemann, Stephan, Nicole Sieweke, Horst Traupe, et al.. (2000). Assignment of PGL3 to chromosome 1 (q21-q23) in a family with autosomal dominant non-chromaffin paraganglioma. American Journal of Medical Genetics. 98(1). 32–36. 23 indexed citations

15.

Niemann, Stephan, Daniela Steinberger, & U. Müller. (1999). PGL3 , a third, not maternally imprinted locus in autosomal dominant paraganglioma. Neurogenetics. 2(3). 167–170. 42 indexed citations

16.

Niemann, Stephan, Michael W. Sereda, Moritz J. Rossner, et al.. (1999). The “CMT Rat”: Peripheral Neuropathy and Dysmyelination Caused by Transgenic Overexpression of PMP22. Annals of the New York Academy of Sciences. 883(1). 254–261. 19 indexed citations

17.

Németh, Andrea H., Dagmar Nolte, Eimear Dunne, et al.. (1999). Refined Linkage Disequilibrium and Physical Mapping of the Gene Locus for X-Linked Dystonia–Parkinsonism (DYT3). Genomics. 60(3). 320–329. 42 indexed citations

18.

Niemann, Stephan, Richard L. Sidman, & Klaus‐Armin Nave. (1998). Evidence against altered forms of MAG in the dysmyelinated mouse mutant claw paw. Mammalian Genome. 9(11). 903–904. 2 indexed citations

19.

Köster, Frank, et al.. (1998). Identification of shyc, a novel gene expressed in the murine developing and adult nervous system. Neuroscience Letters. 252(1). 69–71. 7 indexed citations

20.

Niemann, Stephan & Hubert Schaller. (1996). Head-activator and the neuroectodermal differentiation of P19 mouse embryonal carcinoma cells. Neuroscience Letters. 207(1). 49–52. 9 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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