Frank Mendrzyk

1.3k total citations
10 papers, 952 citations indexed

About

Frank Mendrzyk is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Frank Mendrzyk has authored 10 papers receiving a total of 952 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 6 papers in Genetics and 3 papers in Cancer Research. Recurrent topics in Frank Mendrzyk's work include Genomic variations and chromosomal abnormalities (6 papers), Genomics and Chromatin Dynamics (4 papers) and Cancer Genomics and Diagnostics (3 papers). Frank Mendrzyk is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), Genomics and Chromatin Dynamics (4 papers) and Cancer Genomics and Diagnostics (3 papers). Frank Mendrzyk collaborates with scholars based in Germany, United Kingdom and Russia. Frank Mendrzyk's co-authors include Peter Lichter, Bernhard Radlwimmer, Axel Benner, Grischa Toedt, Stefan M. Pfister, Andrey Korshunov, Daniel E. Stange, Stefan Joos, Guido Reifenberger and Andrea Wittmann and has published in prestigious journals such as Nucleic Acids Research, Journal of Clinical Oncology and Clinical Cancer Research.

In The Last Decade

Frank Mendrzyk

10 papers receiving 941 citations

Peers

Frank Mendrzyk

GENET

ONCOL

NEURO

Dorota Denkhaus Germany

Suzanne E. Little United Kingdom

Frauke Devens Germany

David Shih United States

Anke Waha Germany

Meryl E. Lusher United Kingdom

Bastien Job France

Sandra Boots‐Sprenger Netherlands

Jesse Chung‐Sean Pang Hong Kong

Nancy E. Hasselt Netherlands

Dorota Denkhaus Germany

Frank Mendrzyk

820 ×1.2

293 ×0.8

GENET

147 ×0.6

184 ×0.9

ONCOL

129 ×1.1

NEURO

Citations per year, relative to Frank Mendrzyk Frank Mendrzyk (= 1×) peers Dorota Denkhaus

Countries citing papers authored by Frank Mendrzyk

Since Specialization

Citations

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

Fields of papers citing papers by Frank Mendrzyk

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Frank Mendrzyk

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

All Works

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10 of 10 papers shown

Pfister, Stefan M., Marc Remke, Axel Benner, et al.. (2009). Outcome Prediction in Pediatric Medulloblastoma Based on DNA Copy-Number Aberrations of Chromosomes 6q and 17q and the MYC and MYCN Loci. Journal of Clinical Oncology. 27(10). 1627–1636. 198 indexed citations

Pfister, Stefan M., Frank Mendrzyk, Andrea Wittmann, et al.. (2007). Array-based profiling of reference-independent methylation status (aPRIMES) identifies frequent promoter methylation and consecutive downregulation of ZIC2 in pediatric medulloblastoma. Nucleic Acids Research. 35(7). e51–e51. 48 indexed citations

Pfister, Stefan M., Stephen Rea, Mikko Taipale, et al.. (2007). The histone acetyltransferase hMOF is frequently downregulated in primary breast carcinoma and medulloblastoma and constitutes a biomarker for clinical outcome in medulloblastoma. International Journal of Cancer. 122(6). 1207–1213. 126 indexed citations

Pfister, Stefan M., Marc Remke, Grischa Toedt, et al.. (2007). Supratentorial primitive neuroectodermal tumors of the central nervous system frequently harbor deletions of the CDKN2A locus and other genomic aberrations distinct from medulloblastomas. Genes Chromosomes and Cancer. 46(9). 839–851. 53 indexed citations

Mendrzyk, Frank, Andrey Korshunov, Grischa Toedt, et al.. (2006). Isochromosome breakpoints on 17p in medulloblastoma are flanked by different classes of DNA sequence repeats. Genes Chromosomes and Cancer. 45(4). 401–410. 31 indexed citations

Stange, Daniel E., Bernhard Radlwimmer, Falk Schubert, et al.. (2006). High-Resolution Genomic Profiling Reveals Association of Chromosomal Aberrations on 1q and 16p with Histologic and Genetic Subgroups of Invasive Breast Cancer. Clinical Cancer Research. 12(2). 345–352. 66 indexed citations

Mendrzyk, Frank, Andrey Korshunov, Axel Benner, et al.. (2006). Identification of Gains on 1q and Epidermal Growth Factor Receptor Overexpression as Independent Prognostic Markers in Intracranial Ependymoma. Clinical Cancer Research. 12(7). 2070–2079. 160 indexed citations

Toedt, Grischa, Frank Mendrzyk, Daniel E. Stange, et al.. (2005). Detection of chromosomal imbalances in retinoblastoma by matrix‐based comparative genomic hybridization. Genes Chromosomes and Cancer. 43(3). 294–301. 85 indexed citations

Mendrzyk, Frank, Bernhard Radlwimmer, Stefan Joos, et al.. (2005). Genomic and Protein Expression Profiling Identifies CDK6 As Novel Independent Prognostic Marker in Medulloblastoma. Journal of Clinical Oncology. 23(34). 8853–8862. 180 indexed citations

10.

Stange, Daniel E., Bernhard Radlwimmer, Falk Schubert, et al.. (2005). P42: High resolution genomic profiling reveals association of chromosomal aberrations on 1q and 16p with histological and genetic subgroups of invasive breast cancer. European Journal of Medical Genetics. 48(4). 506–507. 5 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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