Albert J. Poustka

6.5k total citations · 1 hit paper
48 papers, 3.0k citations indexed

About

Albert J. Poustka is a scholar working on Molecular Biology, Plant Science and Aquatic Science. According to data from OpenAlex, Albert J. Poustka has authored 48 papers receiving a total of 3.0k indexed citations (citations by other indexed papers that have themselves been cited), including 35 papers in Molecular Biology, 8 papers in Plant Science and 7 papers in Aquatic Science. Recurrent topics in Albert J. Poustka's work include Genomics and Phylogenetic Studies (10 papers), Developmental Biology and Gene Regulation (10 papers) and Marine Biology and Environmental Chemistry (7 papers). Albert J. Poustka is often cited by papers focused on Genomics and Phylogenetic Studies (10 papers), Developmental Biology and Gene Regulation (10 papers) and Marine Biology and Environmental Chemistry (7 papers). Albert J. Poustka collaborates with scholars based in Germany, United States and United Kingdom. Albert J. Poustka's co-authors include G. V. Panopoulou, Karlheinz Mann, Hans Lehrach, Matthias Mann, Ralf Herwig, Kevin J. Peterson, Detlef Groth, Konstanze Fischer, H. Döhner and Peter R. Galle and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and SHILAP Revista de lepidopterología.

In The Last Decade

Albert J. Poustka

45 papers receiving 2.9k citations

Hit Papers

p53 gene deletion predict... 1995 2026 2005 2015 1995 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Albert J. Poustka Germany 27 1.6k 490 435 367 358 48 3.0k
Zbyněk Kozmík Czechia 39 3.7k 2.3× 186 0.4× 325 0.7× 606 1.7× 207 0.6× 114 5.0k
Stefania Bortoluzzi Italy 31 2.2k 1.4× 95 0.2× 190 0.4× 374 1.0× 210 0.6× 102 3.4k
Franco Cotelli Italy 35 1.9k 1.2× 77 0.2× 138 0.3× 221 0.6× 45 0.1× 118 3.4k
Satoshi Nojima Japan 34 1.3k 0.8× 64 0.1× 280 0.6× 463 1.3× 121 0.3× 122 3.2k
Lorraine Robb Australia 39 3.5k 2.2× 182 0.4× 452 1.0× 1.8k 4.8× 129 0.4× 52 6.4k
Paul Moran United States 42 1.5k 0.9× 153 0.3× 273 0.6× 323 0.9× 81 0.2× 101 4.2k
Gerald H. Thomsen United States 30 5.8k 3.7× 102 0.2× 291 0.7× 215 0.6× 445 1.2× 48 6.7k
Christopher J. Lowe United States 36 2.4k 1.5× 52 0.1× 1.1k 2.4× 105 0.3× 28 0.1× 74 4.3k
Lynne M. Angerer United States 41 4.1k 2.6× 46 0.1× 655 1.5× 290 0.8× 36 0.1× 81 5.7k
Robert C. Angerer United States 39 3.7k 2.4× 44 0.1× 602 1.4× 292 0.8× 33 0.1× 77 5.4k

Countries citing papers authored by Albert J. Poustka

Since Specialization
Citations

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

Fields of papers citing papers by Albert J. Poustka

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Albert J. Poustka. 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 Albert J. Poustka. The network helps show where Albert J. Poustka may publish in the future.

Co-authorship network of co-authors of Albert J. Poustka

This figure shows the co-authorship network connecting the top 25 collaborators of Albert J. Poustka. A scholar is included among the top collaborators of Albert J. Poustka 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 Albert J. Poustka. Albert J. Poustka 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.
Brachmann, Andreas, Kevin M. Kocot, Francesca Leasi, et al.. (2024). Complementing aculiferan mitogenomics: comparative characterization of mitochondrial genomes of Solenogastres (Mollusca, Aplacophora). SHILAP Revista de lepidopterología. 24(1). 128–128.
2.
Hogan, John D., Lingqi Luo, Jonas Ibn-Salem, et al.. (2019). The developmental transcriptome for Lytechinus variegatus exhibits temporally punctuated gene expression changes. Developmental Biology. 460(2). 139–154. 14 indexed citations
3.
Grau, José Horacio, Albert J. Poustka, M. Meixner, & Jörg Plötner. (2014). LTR retroelements are intrinsic components of transcriptional networks in frogs. BMC Genomics. 15(1). 626–626. 5 indexed citations
4.
Philippe, Hervé, Henner Brinkmann, Richard R. Copley, et al.. (2011). Acoelomorph flatworms are deuterostomes related to Xenoturbella. Nature. 470(7333). 255–258. 318 indexed citations
5.
Mann, Karlheinz, Albert J. Poustka, & Matthias Mann. (2010). Phosphoproteomes of Strongylocentrotus purpuratus shell and tooth matrix: identification of a major acidic sea urchin tooth phosphoprotein, phosphodontin. Proteome Science. 8(1). 6–6. 28 indexed citations
6.
Hufton, Andrew L., Susanne Mathia, Hans Lehrach, et al.. (2009). Deeply conserved chordate noncoding sequences preserve genome synteny but do not drive gene duplicate retention. Genome Research. 19(11). 2036–2051. 41 indexed citations
7.
Wierling, Christoph, Alexander Kühn, Edda Klipp, et al.. (2009). Monte Carlo analysis of an ODE Model of the Sea Urchin Endomesoderm Network. BMC Systems Biology. 3(1). 83–83. 13 indexed citations
8.
Davis, Lianne C., Anthony J. Morgan, Margarida Ruas, et al.. (2008). Ca2+ Signaling Occurs via Second Messenger Release from Intraorganelle Synthesis Sites. Current Biology. 18(20). 1612–1618. 55 indexed citations
9.
Kühn, Alexander, et al.. (2007). Modeling development: spikes of the sea urchin.. PubMed. 18. 75–84. 2 indexed citations
10.
Lapraz, François, Éric Röttinger, Véronique Duboc, et al.. (2006). RTK and TGF-β signaling pathways genes in the sea urchin genome. Developmental Biology. 300(1). 132–152. 130 indexed citations
11.
Hecht, Jochen, Heiner Kuhl, Stefan A. Haas, et al.. (2006). Gene identification and analysis of transcripts differentially regulated in fracture healing by EST sequencing in the domestic sheep. BMC Genomics. 7(1). 172–172. 23 indexed citations
12.
Panopoulou, G. V. & Albert J. Poustka. (2005). Timing and mechanism of ancient vertebrate genome duplications – the adventure of a hypothesis. Trends in Genetics. 21(10). 559–567. 175 indexed citations
13.
Takacs, Carter M., Gabriele Amore, Paola Oliveri, et al.. (2004). Expression of an NK2 homeodomain gene in the apical ectoderm defines a new territory in the early sea urchin embryo. Developmental Biology. 269(1). 152–164. 44 indexed citations
14.
Poustka, Albert J., et al.. (2004). Nodal/activin signaling establishes oral–aboral polarity in the early sea urchin embryo. Developmental Dynamics. 231(4). 727–740. 61 indexed citations
15.
Panopoulou, G. V., Steffen Hennig, Detlef Groth, et al.. (2003). New Evidence for Genome-Wide Duplications at the Origin of Vertebrates Using an Amphioxus Gene Set and Completed Animal Genomes. Genome Research. 13(6a). 1056–1066. 140 indexed citations
16.
Poustka, Albert J.. (2003). Generation, Annotation, Evolutionary Analysis, and Database Integration of 20,000 Unique Sea Urchin EST Clusters. Genome Research. 13(12). 2736–2746. 38 indexed citations
17.
Rast, Jonathan P., R. Andrew Cameron, Albert J. Poustka, & Eric H. Davidson. (2002). brachyury Target Genes in the Early Sea Urchin Embryo Isolated by Differential Macroarray Screening. Developmental Biology. 246(1). 191–208. 72 indexed citations
18.
Poustka, Albert J., Ralf Herwig, Antje Krause, et al.. (1999). Toward the Gene Catalogue of Sea Urchin Development: The Construction and Analysis of an Unfertilized Egg cDNA Library Highly Normalized by Oligonucleotide Fingerprinting. Genomics. 59(2). 122–133. 32 indexed citations
19.
Sedláček, Zdeněk, Roman Kodet, E Seemanová, et al.. (1998). Two Li-Fraumeni syndrome families with novel germline p53 mutations: loss of the wild-type p53 allele in only 50% of tumours. British Journal of Cancer. 77(7). 1034–1039. 35 indexed citations
20.
Delius, Hajo, et al.. (1996). Isolation, differential splicing and protein expression of a DNase on the human X chromosome.. PubMed. 3(2). 199–206. 19 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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