Norman Kock

2.1k total citations
26 papers, 1.3k citations indexed

About

Norman Kock is a scholar working on Neurology, Cellular and Molecular Neuroscience and Molecular Biology. According to data from OpenAlex, Norman Kock has authored 26 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Neurology, 11 papers in Cellular and Molecular Neuroscience and 5 papers in Molecular Biology. Recurrent topics in Norman Kock's work include Neurological disorders and treatments (13 papers), Parkinson's Disease Mechanisms and Treatments (9 papers) and Genetic Neurodegenerative Diseases (9 papers). Norman Kock is often cited by papers focused on Neurological disorders and treatments (13 papers), Parkinson's Disease Mechanisms and Treatments (9 papers) and Genetic Neurodegenerative Diseases (9 papers). Norman Kock collaborates with scholars based in Germany, United States and Italy. Norman Kock's co-authors include Christine Klein, Birgitt Schüle, Jeremy C. Smith, Stacy R. Denison, Anne Grünewald, Laurie J. Ozelius, Fang Wang, Nicole A. Becker, Leslie A. Phillips and Xandra O. Breakefield and has published in prestigious journals such as Neurology, Oncogene and Annals of Neurology.

In The Last Decade

Norman Kock

26 papers receiving 1.3k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Norman Kock Germany 18 785 492 484 255 200 26 1.3k
Vı́ctor Volpini Spain 23 395 0.5× 605 1.2× 532 1.1× 94 0.4× 188 0.9× 45 1.2k
Oswaldo Lorenzo‐Betancor Spain 19 806 1.0× 357 0.7× 348 0.7× 132 0.5× 121 0.6× 36 1.1k
Shabnam Ghazi‐Noori United Kingdom 7 339 0.4× 782 1.6× 594 1.2× 82 0.3× 141 0.7× 7 1.2k
Hidetoshi Date Japan 14 424 0.5× 764 1.6× 546 1.1× 84 0.3× 113 0.6× 20 1.2k
Christopher M. Treleaven United States 16 641 0.8× 489 1.0× 298 0.6× 99 0.4× 145 0.7× 19 1.2k
Barbara Castellotti Italy 25 670 0.9× 987 2.0× 757 1.6× 41 0.2× 305 1.5× 65 1.8k
Rim Amouri Tunisia 24 541 0.7× 702 1.4× 667 1.4× 80 0.3× 124 0.6× 58 1.5k
Hiroyuki Morino Japan 20 494 0.6× 685 1.4× 564 1.2× 46 0.2× 124 0.6× 78 1.2k
Emilia Bellone Italy 24 787 1.0× 681 1.4× 1.0k 2.1× 50 0.2× 176 0.9× 100 1.8k
Coro Paisán‐Ruiz United States 19 472 0.6× 479 1.0× 322 0.7× 66 0.3× 237 1.2× 34 1.1k

Countries citing papers authored by Norman Kock

Since Specialization
Citations

This map shows the geographic impact of Norman Kock'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 Norman Kock with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Norman Kock more than expected).

Fields of papers citing papers by Norman Kock

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Norman Kock. 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 Norman Kock. The network helps show where Norman Kock may publish in the future.

Co-authorship network of co-authors of Norman Kock

This figure shows the co-authorship network connecting the top 25 collaborators of Norman Kock. A scholar is included among the top collaborators of Norman Kock 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 Norman Kock. Norman Kock is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Raković, Aleksandar, Anne Grünewald, Philip Seibler, et al.. (2010). Effect of endogenous mutant and wild-type PINK1 on Parkin in fibroblasts from Parkinson disease patients. Human Molecular Genetics. 19(16). 3124–3137. 103 indexed citations
2.
Grünewald, Anne, Matthew E. Gegg, Jan‐Willem Taanman, et al.. (2009). Differential effects of PINK1 nonsense and missense mutations on mitochondrial function and morphology. Experimental Neurology. 219(1). 266–273. 86 indexed citations
3.
König, Inke R., Norbert Brüggemann, Norman Kock, et al.. (2009). MDR1 variants and risk of Parkinson disease. Journal of Neurology. 256(1). 115–120. 42 indexed citations
4.
Raymond, Deborah, Rachel Saunders‐Pullman, Patrícia de Carvalho Aguiar, et al.. (2008). Phenotypic spectrum and sex effects in eleven myoclonus‐dystonia families with ε‐sarcoglycan mutations. Movement Disorders. 23(4). 588–592. 35 indexed citations
5.
Kock, Norman, et al.. (2008). Betreuung medizinischer Doktoranden im interuniversitären Vergleich - Sollte das Promotionsverfahren geändert werden?. DMW - Deutsche Medizinische Wochenschrift. 125(23). 724–728. 2 indexed citations
6.
Reetz, Kathrin, Rebekka Lencer, Susanne Steinlechner, et al.. (2008). Limbic and Frontal Cortical Degeneration Is Associated with Psychiatric Symptoms in PINK1 Mutation Carriers. Biological Psychiatry. 64(3). 241–247. 42 indexed citations
7.
Kock, Norman, Randa Kasmieh, Ralph Weissleder, & Khalid Shah. (2007). Tumor Therapy Mediated by Lentiviral Expression of shBcl-2 and S-TRAIL. Neoplasia. 9(5). 435–442. 60 indexed citations
8.
Kostić, Vladimir, Marina Svetel, Kemal Kabakci, et al.. (2006). Intrafamilial phenotypic and genetic heterogeneity of dystonia. Journal of the Neurological Sciences. 250(1-2). 92–96. 9 indexed citations
9.
Kock, Norman, Teresa V. Naismith, Heather Boston, et al.. (2006). Effects of genetic variations in the dystonia protein torsinA: identification of polymorphism at residue 216 as protein modifier. Human Molecular Genetics. 15(8). 1355–1364. 79 indexed citations
10.
Kock, Norman, Andrew Allchorne, Miguel Sena‐Esteves, Clifford J. Woolf, & Xandra O. Breakefield. (2005). RNAi blocks DYT1 mutant torsinA inclusions in neurons. Neuroscience Letters. 395(3). 201–205. 12 indexed citations
11.
Klein, Christine, Ana Djarmati, Katja Hedrich, et al.. (2005). PINK1, Parkin, and DJ-1 mutations in Italian patients with early-onset parkinsonism. European Journal of Human Genetics. 13(9). 1086–1093. 92 indexed citations
12.
Dragašević, Nataša, Biljana Čuljković, Christine Klein, et al.. (2005). Frequency analysis and clinical characterization of different types of spinocerebellar ataxia in Serbian patients. Movement Disorders. 21(2). 187–191. 18 indexed citations
13.
Djarmati, Ana, Kemal Kabakci, Irene Pichler, et al.. (2005). Co‐occurrence of restless legs syndrome and Parkin mutations in two families. Movement Disorders. 21(2). 258–263. 26 indexed citations
14.
Bragg, D. Cristopher, et al.. (2004). Inhibition of N-linked glycosylation prevents inclusion formation by the dystonia-related mutant form of torsinA. Molecular and Cellular Neuroscience. 27(4). 417–426. 23 indexed citations
15.
Denison, Stacy R., Jinping Lai, Norman Kock, et al.. (2004). Parkin gene alterations in hepatocellular carcinoma. Genes Chromosomes and Cancer. 40(2). 85–96. 101 indexed citations
16.
Kock, Norman, Meike Kasten, Birgitt Schüle, et al.. (2003). Clinical and genetic features of myoclonus–dystonia in 3 cases: A video presentation. Movement Disorders. 19(2). 231–234. 11 indexed citations
17.
Denison, Stacy R., Fang Wang, Nicole A. Becker, et al.. (2003). Alterations in the common fragile site gene Parkin in ovarian and other cancers. Oncogene. 22(51). 8370–8378. 188 indexed citations
18.
Müller, B., Katja Hedrich, Norman Kock, et al.. (2002). Evidence That Paternal Expression of the ε-Sarcoglycan Gene Accounts for Reduced Penetrance in Myoclonus-Dystonia. The American Journal of Human Genetics. 71(6). 1303–1311. 102 indexed citations
19.
Klein, Christine, Liu Liu, Dana Doheny, et al.. (2002). ε‐sarcoglycan mutations found in combination with other dystonia gene mutations. Annals of Neurology. 52(5). 675–679. 69 indexed citations
20.
Müller‐Steinhardt, Michael, Norman Kock, Christoph Härtel, Holger Kirchner, & Jürgen Steinhoff. (2001). Production of monokines in patients under polysulphone haemodiafiltration is influenced by the ultrafiltration flow rate. Nephrology Dialysis Transplantation. 16(9). 1830–1837. 11 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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