Petra Laspe

818 total citations
19 papers, 564 citations indexed

About

Petra Laspe is a scholar working on Molecular Biology, Cancer Research and Physiology. According to data from OpenAlex, Petra Laspe has authored 19 papers receiving a total of 564 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 8 papers in Cancer Research and 5 papers in Physiology. Recurrent topics in Petra Laspe's work include DNA Repair Mechanisms (11 papers), Carcinogens and Genotoxicity Assessment (6 papers) and Erythrocyte Function and Pathophysiology (4 papers). Petra Laspe is often cited by papers focused on DNA Repair Mechanisms (11 papers), Carcinogens and Genotoxicity Assessment (6 papers) and Erythrocyte Function and Pathophysiology (4 papers). Petra Laspe collaborates with scholars based in Germany, United States and United Kingdom. Petra Laspe's co-authors include Steffen Emmert, Wilfried Kugler, Kai‐Martin Thoms, M. Lakomek, Lars Boeckmann, Sikandar G. Khan, Christiane Kuschal, Michael P. Schön, Kenneth H. Kraemer and Andreas Helmke and has published in prestigious journals such as Journal of Investigative Dermatology, Carcinogenesis and British Journal of Haematology.

In The Last Decade

Petra Laspe

19 papers receiving 556 citations

Peers

Petra Laspe
Maria Teresa Landi United States
Gregory Khitrov United States
Е А Комарова Russia
Hailong Pei China
Jim McBride United States
R G Wickremasinghe United Kingdom
Steven W. Remmenga United States
Nélida I. Noguera Italy
Ray A. Johnson United States
Cristina Morales Spain
Maria Teresa Landi United States
Petra Laspe
Citations per year, relative to Petra Laspe Petra Laspe (= 1×) peers Maria Teresa Landi

Countries citing papers authored by Petra Laspe

Since Specialization
Citations

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

Fields of papers citing papers by Petra Laspe

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Petra Laspe

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

All Works

19 of 19 papers shown
1.
Lehmann, Janin, Steffen Schubert, A Schäfer, et al.. (2014). A novel mutation in the XPA gene results in two truncated protein variants and leads to a severe XP/neurological symptoms phenotype. Journal of the European Academy of Dermatology and Venereology. 29(12). 2479–2482. 5 indexed citations
2.
Mertens, Nina, et al.. (2014). Inactivation of Microorganisms Using Cold Atmospheric Pressure Plasma with Different Temporal Discharge Characteristics. Plasma Processes and Polymers. 11(10). 910–920. 15 indexed citations
3.
Schubert, Steffen, Alexei Gratchev, Christina Seebode, et al.. (2013). Characterization of Three XPG-Defective Patients Identifies Three Missense Mutations that Impair Repair and Transcription. Journal of Investigative Dermatology. 133(7). 1841–1849. 20 indexed citations
4.
Hofmann, Lars, Alexei Gratchev, Petra Laspe, et al.. (2012). Molecular genetic analysis of 16 XP‐C patients from Germany: environmental factors predominately contribute to phenotype variations. Experimental Dermatology. 22(1). 24–29. 14 indexed citations
5.
Thoms, Kai‐Martin, Christiane Kuschal, E. Oetjen, et al.. (2011). Cyclosporin A, but not everolimus, inhibits DNA repair mediated by calcineurin: implications for tumorigenesis under immunosuppression. Experimental Dermatology. 20(3). 232–236. 38 indexed citations
6.
Kuschal, Christiane, Kai‐Martin Thoms, Lars Boeckmann, et al.. (2011). Cyclosporin A inhibits nucleotide excision repair via downregulation of the xeroderma pigmentosum group A and G proteins, which is mediated by calcineurin inhibition. Experimental Dermatology. 20(10). 795–799. 19 indexed citations
7.
Helmke, Andreas, Steffen Emmert, Petra Laspe, et al.. (2011). Physical and Microbiological Characterisation of Staphylococcus epidermidis Inactivation by Dielectric Barrier Discharge Plasma. Plasma Processes and Polymers. 8(4). 278–286. 55 indexed citations
8.
Kuschal, Christiane, Toshio Mori, Norio Kobayashi, et al.. (2009). Cyclosporin A, but not everolimus, inhibits DNA repair in human fibroblasts and lymphoblasts. International Journal of Clinical Pharmacology and Therapeutics. 47(1). 38–40. 7 indexed citations
9.
Boeckmann, Lars, Ralf Gutzmer, Cristina Has, et al.. (2009). Modulation of the efficacy of temozolomide and dacarbazine melanoma treatment by DNA-repair factors in vivo and in vitro. International Journal of Clinical Pharmacology and Therapeutics. 47(1). 33–35. 2 indexed citations
10.
Boeckmann, Lars, Markus Schirmer, Albert Rosenberger, et al.. (2009). Effect of DNA repair host factors on temozolomide or dacarbazine melanoma treatment in Caucasians. Pharmacogenetics and Genomics. 19(10). 760–769. 8 indexed citations
11.
Emmert, Steffen, Takahiro Ueda, Urs Zumsteg, et al.. (2008). Strict sun protection results in minimal skin changes in a patient with xeroderma pigmentosum and a novel c.2009delG mutation in XPD (ERCC2). Experimental Dermatology. 18(1). 64–68. 21 indexed citations
12.
Herrmann, Janne Rothmar, et al.. (2007). Functional DNA repair system analysis in haematopoietic progenitor cells using host cell reactivation. Scandinavian Journal of Clinical and Laboratory Investigation. 67(6). 580–588. 16 indexed citations
13.
Laspe, Petra, et al.. (2006). Nucleotide excision repair and cancer. Journal of Molecular Histology. 37(5-7). 225–238. 115 indexed citations
14.
König, Inke R., Petra Laspe, Kai‐Martin Thoms, et al.. (2005). Assessment of 3 xeroderma pigmentosum group C gene polymorphisms and risk of cutaneous melanoma: a case–control study. Carcinogenesis. 26(6). 1085–1090. 88 indexed citations
15.
König, Inke R., Petra Laspe, Kai‐Martin Thoms, et al.. (2004). No association between three xeroderma pigmentosum group C and one group G gene polymorphisms and risk of cutaneous melanoma. European Journal of Human Genetics. 13(2). 253–255. 35 indexed citations
16.
Kugler, Wilfried, Arnulf Pekrun, Petra Laspe, Bernhard Erdlenbruch, & M. Lakomek. (2001). Molecular basis of recessive congenital methemoglobinemia, types I and II: Exon skipping and three novel missense mutations in the NADH-cytochrome b5 reductase (diaphorase 1) gene. Human Mutation. 17(4). 348–348. 35 indexed citations
17.
Kugler, Wilfried, Andreas Ohlenbusch, Petra Laspe, et al.. (2000). Eight novel mutations and consequences on mRNA and protein level in pyruvate kinase-deficient patients with nonspherocytic hemolytic anemia. Human Mutation. 15(3). 261–272. 16 indexed citations
18.
Kugler, Wilfried, et al.. (1999). Identification of a novel promoter mutation in the human pyruvate kinase (PK) LR gene of a patient with severe haemolytic anaemia. British Journal of Haematology. 105(3). 596–598. 10 indexed citations
19.
Kugler, Wilfried, Petra Laspe, Hilary Muirhead, et al.. (1998). Molecular basis of neurological dysfunction coupled with haemolytic anaemia in human glucose-6-phosphate isomerase (GPI) deficiency. Human Genetics. 103(4). 450–454. 45 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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