Beatrice Schuster

1.4k total citations
6 papers, 639 citations indexed

About

Beatrice Schuster is a scholar working on Molecular Biology, Plant Science and Genetics. According to data from OpenAlex, Beatrice Schuster has authored 6 papers receiving a total of 639 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 3 papers in Plant Science and 1 paper in Genetics. Recurrent topics in Beatrice Schuster's work include DNA Repair Mechanisms (6 papers), CRISPR and Genetic Engineering (3 papers) and DNA and Nucleic Acid Chemistry (2 papers). Beatrice Schuster is often cited by papers focused on DNA Repair Mechanisms (6 papers), CRISPR and Genetic Engineering (3 papers) and DNA and Nucleic Acid Chemistry (2 papers). Beatrice Schuster collaborates with scholars based in Germany, United States and Netherlands. Beatrice Schuster's co-authors include Detlev Schindler, Martin A. Rooimans, Thomas Bettecken, Helmut Hanenberg, Johan P. de Winter, Chantal Stoepker, Katharina Eirich, Kornelia Neveling, Constanze Wiek and Marcel Freund and has published in prestigious journals such as Nature Genetics, Blood and PLoS ONE.

In The Last Decade

Beatrice Schuster

6 papers receiving 626 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Beatrice Schuster Germany	6	559	212	144	117	65	6	639
Daniela Endt Germany	5	473 0.8×	237 1.1×	139 1.0×	111 0.9×	46 0.7×	5	564
Scott Houghtaling United States	8	475 0.8×	96 0.5×	174 1.2×	110 0.9×	36 0.6×	11	544
Henri J. van de Vrugt Netherlands	12	819 1.5×	197 0.9×	247 1.7×	110 0.9×	99 1.5×	18	888
Ian Kesterton United Kingdom	6	352 0.6×	137 0.6×	128 0.9×	100 0.9×	38 0.6×	8	444
Chih‐Chao Liang United Kingdom	12	678 1.2×	98 0.5×	98 0.7×	126 1.1×	39 0.6×	15	715
Britta Wieland Germany	8	328 0.6×	136 0.6×	139 1.0×	133 1.1×	24 0.4×	9	453
Yu Zhi United States	10	682 1.2×	112 0.5×	245 1.7×	75 0.6×	85 1.3×	17	757
Suzanne A. Hartford United States	12	686 1.2×	206 1.0×	130 0.9×	117 1.0×	84 1.3×	16	833
Anita Cheng United States	8	1.0k 1.8×	92 0.4×	173 1.2×	350 3.0×	105 1.6×	8	1.1k

Countries citing papers authored by Beatrice Schuster

Since Specialization

Citations

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

Fields of papers citing papers by Beatrice Schuster

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Beatrice Schuster

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

All Works

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6 of 6 papers shown

1.

Knies, Kerstin, Beatrice Schuster, Najim Ameziane, et al.. (2012). Genotyping of Fanconi Anemia Patients by Whole Exome Sequencing: Advantages and Challenges. PLoS ONE. 7(12). e52648–e52648. 29 indexed citations

2.

Schuster, Beatrice, Kerstin Knies, Chantal Stoepker, et al.. (2012). Whole Exome Sequencing Reveals Uncommon Mutations in the Recently Identified Fanconi Anemia GeneSLX4/FANCP. Human Mutation. 34(1). 93–96. 20 indexed citations

3.

Trujillo‐Quintero, Juan Pablo, Leonardo Mina, Roser Pujol, et al.. (2012). On the role of FAN1 in Fanconi anemia. Blood. 120(1). 86–89. 27 indexed citations

4.

Stoepker, Chantal, Beatrice Schuster, Yvonne Hilhorst‐Hofstee, et al.. (2011). SLX4, a coordinator of structure-specific endonucleases, is mutated in a new Fanconi anemia subtype. Nature Genetics. 43(2). 138–141. 233 indexed citations

5.

Kopic, Sascha, Katharina Eirich, Beatrice Schuster, et al.. (2010). Hepatoblastoma in a 4‐year‐old girl with Fanconi anaemia. Acta Paediatrica. 100(5). 780–783. 20 indexed citations

6.

Hanenberg, Helmut, Beatrice Schuster, Karen Barker, et al.. (2010). Mutation of the RAD51C gene in a Fanconi anemia–like disorder. Nature Genetics. 42(5). 406–409. 310 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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