Britta Hasemeier

1.9k total citations
30 papers, 1.5k citations indexed

About

Britta Hasemeier is a scholar working on Molecular Biology, Hematology and Genetics. According to data from OpenAlex, Britta Hasemeier has authored 30 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 9 papers in Hematology and 8 papers in Genetics. Recurrent topics in Britta Hasemeier's work include Epigenetics and DNA Methylation (12 papers), Acute Myeloid Leukemia Research (8 papers) and Genetic Syndromes and Imprinting (6 papers). Britta Hasemeier is often cited by papers focused on Epigenetics and DNA Methylation (12 papers), Acute Myeloid Leukemia Research (8 papers) and Genetic Syndromes and Imprinting (6 papers). Britta Hasemeier collaborates with scholars based in Germany, Indonesia and Netherlands. Britta Hasemeier's co-authors include Ulrich Lehmann, Hans Kreipe, Florian Länger, Matthias Christgen, Elisa Schipper, Mirco Müller, Sumadi Lukman Anwar, Arndt Vogel, Till Krech and Henning Feist and has published in prestigious journals such as PLoS ONE, Human Molecular Genetics and American Journal Of Pathology.

In The Last Decade

Britta Hasemeier

30 papers receiving 1.5k citations

Peers

Britta Hasemeier
Uğur Gezer Türkiye
Seema Bhatlekar United States
Beth O. Van Emburgh United States
Musaffe Tuna United States
Saori Ushijima United Kingdom
Siân Rizzo United Kingdom
Britta Hasemeier
Citations per year, relative to Britta Hasemeier Britta Hasemeier (= 1×) peers Leonidas Benetatos

Countries citing papers authored by Britta Hasemeier

Since Specialization
Citations

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

Fields of papers citing papers by Britta Hasemeier

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Britta Hasemeier

This figure shows the co-authorship network connecting the top 25 collaborators of Britta Hasemeier. A scholar is included among the top collaborators of Britta Hasemeier 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 Britta Hasemeier. Britta Hasemeier 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.
Sandbothe, Maria, Britta Hasemeier, Elisa Schipper, et al.. (2024). Diagnostic utility of ESR1 mutation detection in liquid biopsy of metastatic breast cancer patients. Archiv für Pathologische Anatomie und Physiologie und für Klinische Medicin. 487(4). 895–899. 2 indexed citations
2.
Bartels, Stephan, Britta Hasemeier, Elisa Schipper, et al.. (2020). Feasibility of Combined Detection of Gene Mutations and Fusion Transcripts in Bone Marrow Trephines from Leukemic Neoplasms. Journal of Molecular Diagnostics. 22(4). 591–598. 4 indexed citations
3.
Bartels, Stephan, Muhammad Salman Faisal, Guntram Büsche, et al.. (2020). Knochenmarkfibrose bei primärer Myelofibrose in Abhängigkeit von myelodysplasie- und altersassoziierten Mutationen der Hämatopoese. Der Pathologe. 41(S2). 124–128. 1 indexed citations
4.
Anwar, Sumadi Lukman, Britta Hasemeier, Elisa Schipper, et al.. (2019). LINE-1 hypomethylation in human hepatocellular carcinomas correlates with shorter overall survival and CIMP phenotype. PLoS ONE. 14(5). e0216374–e0216374. 15 indexed citations
5.
Bartels, Stephan, et al.. (2017). Molecular Analysis of Circulating Cell-Free DNA from Lung Cancer Patients in Routine Laboratory Practice. Journal of Molecular Diagnostics. 19(5). 722–732. 37 indexed citations
6.
Anwar, Sumadi Lukman, Till Krech, Britta Hasemeier, et al.. (2015). Loss of DNA methylation at imprinted loci is a frequent event in hepatocellular carcinoma and identifies patients with shortened survival. Clinical Epigenetics. 7(1). 110–110. 13 indexed citations
7.
Ammerpohl, Ole, Jana Gutwein, Doris Steinemann, et al.. (2014). The CpG Island Methylator Phenotype in Breast Cancer is Associated with the Lobular Subtype. Epigenomics. 7(2). 187–199. 21 indexed citations
8.
Hasemeier, Britta, et al.. (2013). Loss of imprinting and allelic switching at the DLK1-MEG3 locus in human hepatocellular carcinoma. Zeitschrift für Gastroenterologie. 51(1). 2 indexed citations
9.
Anwar, Sumadi Lukman, Till Krech, Britta Hasemeier, et al.. (2012). Loss of Imprinting and Allelic Switching at the DLK1-MEG3 Locus in Human Hepatocellular Carcinoma. PLoS ONE. 7(11). e49462–e49462. 113 indexed citations
10.
Ammerpohl, Ole, Jana Gutwein, Britta Hasemeier, et al.. (2012). Quantitative cross-validation and content analysis of the 450k DNA methylation array from Illumina, Inc.. BMC Research Notes. 5(1). 210–210. 85 indexed citations
11.
Potapova, Anna, Britta Hasemeier, Katrin Haeussler, et al.. (2011). Systematic cross-validation of 454 sequencing and pyrosequencing for the exact quantification of DNA methylation patterns with single CpG resolution. BMC Biotechnology. 11(1). 6–6. 41 indexed citations
12.
Lehmann, Ulrich, Thomas Streichert, Benjamin Otto, et al.. (2010). Identification of differentially expressed microRNAs in human male breast cancer. BMC Cancer. 10(1). 109–109. 105 indexed citations
13.
Potapova, Anna, Britta Hasemeier, Gudrun Göhring, et al.. (2009). Epigenetic inactivation of tumour suppressor gene KLF11 in myelodysplastic syndromes*. European Journal Of Haematology. 84(4). 298–303. 23 indexed citations
14.
Christgen, Matthias, Catarina Hadamitzky, Cornelia Rudolph, et al.. (2008). Comprehensive genetic and functional characterization of IPH‐926: a novel CDH1‐null tumour cell line from human lobular breast cancer. The Journal of Pathology. 217(5). 620–632. 27 indexed citations
15.
Hasemeier, Britta, Matthias Christgen, Hans Kreipe, & Ulrich Lehmann. (2008). Reliable microRNA profiling in routinely processed formalin-fixed paraffin-embedded breast cancer specimens using fluorescence labelled bead technology. BMC Biotechnology. 8(1). 90–90. 43 indexed citations
16.
Lehmann, Ulrich, Luzie U. Wingen, Kai Brakensiek, et al.. (2007). Epigenetic defects of hepatocellular carcinoma are already found in non-neoplastic liver cells from patients with hereditary haemochromatosis. Human Molecular Genetics. 16(11). 1335–1342. 38 indexed citations
17.
Tessema, Mathewos, Florian Länger, Oliver Bock, et al.. (2005). Down-regulation of the IGF-2/H19 locus during normal and malignant hematopoiesis is independent of the imprinting pattern. International Journal of Oncology. 26(2). 499–507. 18 indexed citations
18.
Lehmann, Ulrich, Florian Länger, Henning Feist, et al.. (2002). Quantitative Assessment of Promoter Hypermethylation during Breast Cancer Development. American Journal Of Pathology. 160(2). 605–612. 188 indexed citations
19.
Lehmann, Ulrich, Britta Hasemeier, Richard Lilischkis, & Hans Kreipe. (2001). Quantitative Analysis of Promoter Hypermethylation in Laser-Microdissected Archival Specimens. Laboratory Investigation. 81(4). 635–637. 38 indexed citations
20.
Hagting, Anja, Jan Knol, Britta Hasemeier, et al.. (1997). Amplified Expression, Purification and Functional Reconstitution of the Dipeptide and Tripeptide Transport Protein of Lactococcus Lactis. European Journal of Biochemistry. 247(2). 581–587. 20 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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