Tomasz Żemojtel

6.7k total citations
50 papers, 1.6k citations indexed

About

Tomasz Żemojtel is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, Tomasz Żemojtel has authored 50 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 17 papers in Genetics and 7 papers in Physiology. Recurrent topics in Tomasz Żemojtel's work include Genomics and Rare Diseases (10 papers), Genomics and Phylogenetic Studies (7 papers) and Nitric Oxide and Endothelin Effects (5 papers). Tomasz Żemojtel is often cited by papers focused on Genomics and Rare Diseases (10 papers), Genomics and Phylogenetic Studies (7 papers) and Nitric Oxide and Endothelin Effects (5 papers). Tomasz Żemojtel collaborates with scholars based in Germany, Poland and United States. Tomasz Żemojtel's co-authors include Peter N. Robinson, Marten Jäger, Sebastian Köhler, Martin Vingron, Melissa Haendel, Nicole Washington, Damian Smedley, Max Schubach, Mateusz Kolanczyk and Julius O.B. Jacobsen and has published in prestigious journals such as Journal of the American Chemical Society, Nucleic Acids Research and Journal of Biological Chemistry.

In The Last Decade

Tomasz Żemojtel

50 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Tomasz Żemojtel Germany 21 990 578 210 196 124 50 1.6k
Shaun S. Abeysinghe United Kingdom 8 1.4k 1.4× 845 1.5× 186 0.9× 185 0.9× 106 0.9× 8 2.1k
Jean McGowan‐Jordan Canada 15 690 0.7× 675 1.2× 208 1.0× 87 0.4× 108 0.9× 31 1.6k
Philip D. Cotter United States 26 1.3k 1.3× 994 1.7× 298 1.4× 318 1.6× 200 1.6× 95 2.4k
Barbara K. Goodman United States 25 811 0.8× 360 0.6× 146 0.7× 109 0.6× 193 1.6× 48 1.5k
Amy Tang United States 21 2.1k 2.1× 560 1.0× 301 1.4× 174 0.9× 197 1.6× 25 2.6k
Kyoichi Isono Japan 29 2.2k 2.2× 357 0.6× 170 0.8× 249 1.3× 202 1.6× 58 2.6k
G. Levan Sweden 25 1.1k 1.1× 588 1.0× 125 0.6× 187 1.0× 210 1.7× 99 1.8k
Andrei Kuzmichev United States 9 2.6k 2.6× 373 0.6× 264 1.3× 204 1.0× 209 1.7× 9 2.9k
Mihai Albu Canada 11 2.1k 2.1× 275 0.5× 342 1.6× 216 1.1× 201 1.6× 20 2.6k

Countries citing papers authored by Tomasz Żemojtel

Since Specialization
Citations

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

Fields of papers citing papers by Tomasz Żemojtel

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tomasz Żemojtel

This figure shows the co-authorship network connecting the top 25 collaborators of Tomasz Żemojtel. A scholar is included among the top collaborators of Tomasz Żemojtel 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 Tomasz Żemojtel. Tomasz Żemojtel 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.
Badura‐Stronka, Magdalena, et al.. (2021). CLN8 Mutations Presenting with a Phenotypic Continuum of Neuronal Ceroid Lipofuscinosis—Literature Review and Case Report. Genes. 12(7). 956–956. 6 indexed citations
2.
Zehtabian, Amin, Marten Jäger, Silke Reischl, et al.. (2021). Live-cell imaging of circadian clock protein dynamics in CRISPR-generated knock-in cells. Nature Communications. 12(1). 3796–3796. 42 indexed citations
3.
Budny, Bartłomiej, et al.. (2020). Copy Number Variants Contributing to Combined Pituitary Hormone Deficiency. International Journal of Molecular Sciences. 21(16). 5757–5757. 9 indexed citations
4.
Dietz, Steffen, Petros Christopoulos, Lisa Gu, et al.. (2019). Serial liquid biopsies for detection of treatment failure and profiling of resistance mechanisms in KLC1–ALK-rearranged lung cancer. Molecular Case Studies. 5(6). a004630–a004630. 17 indexed citations
5.
Budny, Bartłomiej, Ewelina Szczepanek‐Parulska, Tomasz Żemojtel, et al.. (2017). Mutations in proteasome-related genes are associated with thyroid hemiagenesis. Endocrine. 56(2). 279–285. 16 indexed citations
6.
Bukowska‐Olech, Ewelina, Tomasz Żemojtel, Anna Sowińska‐Seidler, et al.. (2016). Identification of a molecular defect in a stillborn fetus with perinatal lethal hypophosphatasia using a disease-associated genome sequencing approach. Polish Journal of Pathology. 1(1). 78–83. 4 indexed citations
7.
Horn, Denise, Bernhard Weschke, Ellen Knierim, et al.. (2016). BRAT1 mutations are associated with infantile epileptic encephalopathy, mitochondrial dysfunction, and survival into childhood. American Journal of Medical Genetics Part A. 170(9). 2274–2281. 21 indexed citations
8.
Kassner, Ursula, Bastian Salewsky, Adrian Rosada, et al.. (2016). Clinical characterization and mutation spectrum of German patients with familial hypercholesterolemia. Atherosclerosis. 253. 88–93. 35 indexed citations
9.
Jamsheer, Aleksander, Ewelina Bukowska‐Olech, K. Kozlowski, et al.. (2016). Exome sequencing reveals two novel compound heterozygous XYLT1 mutations in a Polish patient with Desbuquois dysplasia type 2 and growth hormone deficiency. Journal of Human Genetics. 61(7). 577–583. 15 indexed citations
10.
Smedley, Damian, Julius O.B. Jacobsen, Marten Jäger, et al.. (2015). Next-generation diagnostics and disease-gene discovery with the Exomiser. Nature Protocols. 10(12). 2004–2015. 228 indexed citations
11.
Groza, Tudor, Sebastian Köhler, Nicole Vasilevsky, et al.. (2015). The Human Phenotype Ontology: Semantic Unification of Common and Rare Disease. The American Journal of Human Genetics. 97(1). 111–124. 150 indexed citations
12.
Żemojtel, Tomasz, Jochen Hecht, Peter Krawitz, et al.. (2014). Somatic neurofibromatosis type 1 (NF1) inactivation events in cutaneous neurofibromas of a single NF1 patient. European Journal of Human Genetics. 23(6). 870–873. 16 indexed citations
13.
Jamsheer, Aleksander, Tomasz Żemojtel, Mateusz Kolanczyk, et al.. (2013). Whole exome sequencing identifies FGF16 nonsense mutations as the cause of X-linked recessive metacarpal 4/5 fusion. Journal of Medical Genetics. 50(9). 579–584. 25 indexed citations
14.
Sun, Ruping, Michael I. Love, Tomasz Żemojtel, et al.. (2012). Breakpointer: using local mapping artifacts to support sequence breakpoint discovery from single-end reads. Bioinformatics. 28(7). 1024–1025. 15 indexed citations
15.
Żemojtel, Tomasz & Martin Vingron. (2012). P53 Binding Sites in Transposons. Frontiers in Genetics. 3. 40–40. 4 indexed citations
16.
Żemojtel, Tomasz, Szymon M. Kiełbasa, Peter F. Arndt, et al.. (2011). CpG Deamination Creates Transcription Factor–Binding Sites with High Efficiency. Genome Biology and Evolution. 3. 1304–1311. 42 indexed citations
17.
Żemojtel, Tomasz, Marlena Duchniewicz, Zhongchun Zhang, et al.. (2010). Retrotransposition and mutation events yield Rap1 GTPases with differential signalling capacity. BMC Evolutionary Biology. 10(1). 55–55. 6 indexed citations
18.
Lin, Shen, Stefan A. Haas, Tomasz Żemojtel, et al.. (2010). Genome-wide comparison of cyanobacterial transposable elements, potential genetic diversity indicators. Gene. 473(2). 139–149. 48 indexed citations
19.
20.
Scheele, Jürgen, Eric L. Bruner, Tomasz Żemojtel, et al.. (2001). Kinetics of CO and NO Ligation with the Cys331 → Ala Mutant of Neuronal Nitric-oxide Synthase. Journal of Biological Chemistry. 276(7). 4733–4736. 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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