Angela Nietzel

541 total citations
8 papers, 217 citations indexed

About

Angela Nietzel is a scholar working on Genetics, Plant Science and Molecular Biology. According to data from OpenAlex, Angela Nietzel has authored 8 papers receiving a total of 217 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 6 papers in Plant Science and 4 papers in Molecular Biology. Recurrent topics in Angela Nietzel's work include Genomic variations and chromosomal abnormalities (7 papers), Chromosomal and Genetic Variations (6 papers) and Genomics and Chromatin Dynamics (3 papers). Angela Nietzel is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Chromosomal and Genetic Variations (6 papers) and Genomics and Chromatin Dynamics (3 papers). Angela Nietzel collaborates with scholars based in Germany, Poland and India. Angela Nietzel's co-authors include Thomas Liehr, Heike Starke, Uwe Claussen, Anita Heller, Volkmar Beensen, Wolfgang Fiedler, Ivan Lončarević, Mariano Rocchi, Iwona Włodarska and Aïda Pujol and has published in prestigious journals such as Journal of Histochemistry & Cytochemistry, British Journal of Haematology and Human Genetics.

In The Last Decade

Angela Nietzel

8 papers receiving 207 citations

Peers

Countries citing papers authored by Angela Nietzel

Since Specialization

Citations

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

Fields of papers citing papers by Angela Nietzel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Angela Nietzel

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

All Works

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8 of 8 papers shown

#	Work	Indexed citations
1	Karyotyping of human synaptonemal complexes by cenM-FISH 2003 ·European Journal of Human Genetics ·M. Oliver‐Bonet, Thomas Liehr, Angela Nietzel, Anita Heller, Heike Starke, Uwe Claussen, M. Codina‐Pascual, Aïda Pujol, Carlos Abad, Josep Egozcue, J. Navarro, J. Benet	29
2	Characterization of Small Marker Chromosomes (SMC) by Recently Developed Molecular Cytogenetic Approaches. 2003 ·PubMed ·Thomas Liehr, Angela Nietzel, Heike Starke, Anita Heller, Anja Weise, A. Kuechler, Gabriele Senger, (unknown), Thomas Martin, Markus Stümm, (unknown), H. Tönnies, Christian Hoppe, U. Claussen, (unknown)	8
3	First patient with trisomy 21 accompanied by an additional der(4)(:p11 → q11:) plus partial uniparental disomy 4p15‐16 2002 ·American Journal of Medical Genetics Part A ·Heike Starke, Beate Mitulla, Angela Nietzel, Anita Heller, Volkmar Beensen, (unknown), Uwe Claussen, Ferdinand von Eggeling, Thomas Liehr	12
4	Suspension (S)-FISH, a New Technique for Interphase Nuclei 2002 ·Journal of Histochemistry & Cytochemistry ·(unknown), Heike Starke, Angela Nietzel, (unknown), (unknown), Uwe Claussen, Thomas Liehr	16
5	Molecular cytogenetic characterization of an acquired minute supernumerary marker chromosome as the sole abnormality in a case clinically diagnosed as atypical Philadelphia‐negative chronic myelogenous leukaemia 2001 ·British Journal of Haematology ·Heike Starke, Martin Kristian Raida, Vladimir A. Trifonov, Joachim H. Clement, Ivan Lončarević, Anita Heller, (unknown), Angela Nietzel, Н. Б. Рубцов, Uwe Claussen, Thomas Liehr	18
6	A new multicolor-FISH approach for the characterization of marker chromosomes: centromere-specific multicolor-FISH (cenM-FISH) 2001 ·Human Genetics ·Angela Nietzel, Mariano Rocchi, Heike Starke, Anita Heller, Wolfgang Fiedler, Iwona Włodarska, Ivan Lončarević, Volkmar Beensen, Uwe Claussen, Thomas Liehr	115
7	Molecular cytogenetic characterization of a prenatally detected supernumerary minute marker chromosome 8 1999 ·Prenatal Diagnosis ·Heike Starke, Isolde Schreyer, (unknown), Wolfgang Fiedler, Volkmar Beensen, Anita Heller, Angela Nietzel, Uwe Claussen, Thomas Liehr	2
8	Molecular cytogenetic characterization of a prenatally detected supernumerary minute marker chromosome 8 1999 ·Prenatal Diagnosis ·Heike Starke, Isolde Schreyer, (unknown), Wolfgang Fiedler, Volkmar Beensen, Anita Heller, Angela Nietzel, Uwe Claussen, Thomas Liehr	17

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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