Joachim Nowock

2.3k total citations
30 papers, 1.9k citations indexed

About

Joachim Nowock is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Genetics. According to data from OpenAlex, Joachim Nowock has authored 30 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Molecular Biology, 14 papers in Cellular and Molecular Neuroscience and 9 papers in Genetics. Recurrent topics in Joachim Nowock's work include Neurobiology and Insect Physiology Research (8 papers), RNA Research and Splicing (8 papers) and Insect and Arachnid Ecology and Behavior (6 papers). Joachim Nowock is often cited by papers focused on Neurobiology and Insect Physiology Research (8 papers), RNA Research and Splicing (8 papers) and Insect and Arachnid Ecology and Behavior (6 papers). Joachim Nowock collaborates with scholars based in Germany, United States and Netherlands. Joachim Nowock's co-authors include Albrecht E. Sippel, Uwe Borgmeyer, Klaus‐Dieter Fischer, Georg Auburger, Richard J. Miksicek, Andreas W. Püschel, Ralph A.W. Rupp, Lawrence I. Gilbert, Franz Römer and Alexander Haese and has published in prestigious journals such as Nature, Cell and Nucleic Acids Research.

In The Last Decade

Joachim Nowock

30 papers receiving 1.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Joachim Nowock Germany 21 1.2k 616 536 206 188 30 1.9k
Kishan Agarwala Japan 14 718 0.6× 359 0.6× 324 0.6× 202 1.0× 51 0.3× 18 1.3k
Antonio A. Reyes United States 18 1.1k 0.9× 291 0.5× 184 0.3× 265 1.3× 37 0.2× 27 1.7k
Makoto Nakamura Japan 17 1.2k 1.0× 134 0.2× 345 0.6× 406 2.0× 180 1.0× 48 1.8k
J.H. Robbins United States 23 1.5k 1.2× 230 0.4× 310 0.6× 187 0.9× 24 0.1× 36 2.1k
Marianne Brown-Luedi Switzerland 20 996 0.8× 324 0.5× 155 0.3× 102 0.5× 36 0.2× 22 1.6k
Yavuz Ariyürek Netherlands 25 1.8k 1.5× 530 0.9× 93 0.2× 121 0.6× 46 0.2× 40 2.5k
Shirley Horn‐Saban Israel 12 1.6k 1.3× 383 0.6× 168 0.3× 149 0.7× 34 0.2× 18 2.1k
H. Steve Zhang United States 4 1.7k 1.3× 542 0.9× 141 0.3× 53 0.3× 62 0.3× 6 1.9k
Benjamin E. Housden United States 22 2.8k 2.2× 439 0.7× 323 0.6× 240 1.2× 235 1.3× 43 3.2k
Vaughn Cleghon United States 19 1.1k 0.9× 290 0.5× 176 0.3× 116 0.6× 18 0.1× 24 1.4k

Countries citing papers authored by Joachim Nowock

Since Specialization
Citations

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

Fields of papers citing papers by Joachim Nowock

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Joachim Nowock

This figure shows the co-authorship network connecting the top 25 collaborators of Joachim Nowock. A scholar is included among the top collaborators of Joachim Nowock 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 Joachim Nowock. Joachim Nowock 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.
Lastres‐Becker, Isabel, David Nonis, Joachim Nowock, & Georg Auburger. (2019). New alternative splicing variants of the ATXN2 transcript. SHILAP Revista de lepidopterología. 1(1). 22–22. 12 indexed citations
2.
Nonis, David, Ewa Damrath, E. R. Brunt, et al.. (2013). Ataxin-2 Modulates the Levels of Grb2 and Src but Not Ras Signaling. Journal of Molecular Neuroscience. 51(1). 68–81. 45 indexed citations
3.
Damrath, Ewa, Suzana Gispert, Mekhman Azizov, et al.. (2012). ATXN2-CAG42 Sequesters PABPC1 into Insolubility and Induces FBXW8 in Cerebellum of Old Ataxic Knock-In Mice. PLoS Genetics. 8(8). e1002920–e1002920. 71 indexed citations
4.
Lastres‐Becker, Isabel, Susanne Brodesser, Dieter Lütjohann, et al.. (2008). Insulin receptor and lipid metabolism pathology in ataxin-2 knock-out mice. Human Molecular Genetics. 17(10). 1465–1481. 104 indexed citations
5.
Loo, Simone van de, et al.. (2008). Ataxin-2 associates with rough endoplasmic reticulum. Experimental Neurology. 215(1). 110–118. 67 indexed citations
6.
Nonis, David, Mirko H. H. Schmidt, Simone van de Loo, et al.. (2008). Ataxin-2 associates with the endocytosis complex and affects EGF receptor trafficking. Cellular Signalling. 20(10). 1725–1739. 87 indexed citations
7.
Wiedemeyer, Ruprecht, et al.. (2003). Ataxin-2 promotes apoptosis of human neuroblastoma cells. Oncogene. 22(3). 401–411. 48 indexed citations
8.
9.
Fischer, Klaus‐Dieter, Alexander Haese, & Joachim Nowock. (1993). Cooperation of GATA-1 and Sp1 can result in synergistic transcriptional activation or interference.. Journal of Biological Chemistry. 268(32). 23915–23923. 108 indexed citations
10.
Fischer, Klaus‐Dieter, Markus Stoffel, Joachim Nowock, et al.. (1992). The Gene for Erythropoietin Receptor Is Expressed in Multipotential Hematopoietic and Embryonal Stem Cells: Evidence for Differentiation Stage-Specific Regulation. Molecular and Cellular Biology. 12(4). 1815–1826. 24 indexed citations
11.
Fischer, Klaus‐Dieter, Markus Stoffel, Joachim Nowock, et al.. (1992). The gene for erythropoietin receptor is expressed in multipotential hematopoietic and embryonal stem cells: evidence for differentiation stage-specific regulation.. Molecular and Cellular Biology. 12(4). 1815–1826. 74 indexed citations
12.
Grez, Manuel, et al.. (1991). A single point mutation activates the Moloney murine leukemia virus long terminal repeat in embryonal stem cells. Journal of Virology. 65(9). 4691–4698. 53 indexed citations
13.
Fischer, Klaus‐Dieter & Joachim Nowock. (1990). The T→C substitution at -198 of the Aγ-globin gene associated with the British form of HPFH generates overlapping recognition sites for two DNA-binding proteins. Nucleic Acids Research. 18(19). 5685–5693. 32 indexed citations
14.
Nowock, Joachim, Uwe Borgmeyer, Andreas W. Püschel, Ralph A.W. Rupp, & Albrecht E. Sippel. (1985). The TGGCA protein binds to the MMTV-LTR, the adenovirus origin of replication, and the BK virus enhancer. Nucleic Acids Research. 13(6). 2045–2061. 189 indexed citations
15.
Igo‐Kemenes, Tibor, et al.. (1984). Alternative sets of DNase I-hypersensitive sites characterize the various functional states of the chicken lysozyme gene. Nature. 311(5982). 163–165. 126 indexed citations
16.
Nowock, Joachim & Albrecht E. Sippel. (1982). Specific protein-DNA interaction at four sites flanking the chicken lysozyme gene. Cell. 30(2). 607–615. 64 indexed citations
17.
Nowock, Joachim. (1973). Der Einflu\ von Farnesylmethyl�ther auf die H�utungsfolge und die Hodenentwicklung beiEphestia k�hniella. Untersuchungen in vivo und in vitro. Development Genes and Evolution. 172(4). 303–316. 3 indexed citations
18.
Nowock, Joachim. (1973). Growth and metamorphosis in the testes of Ephestia kühniella in vitro. Journal of Insect Physiology. 19(4). 941–949. 17 indexed citations
19.
Nowock, Joachim. (1972). Induction of imaginal differentiation by ecdysone in the testes of Ephestia kühniella. Journal of Insect Physiology. 18(9). 1699–1704. 19 indexed citations
20.
Nowock, Joachim. (1971). Die humorale Kontrolle der Hodenentwicklung vonEphestia k�hniella in der Metamorphose. Development Genes and Evolution. 168(1). 20–38. 6 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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