Marius Wöste

785 total citations
15 papers, 248 citations indexed

About

Marius Wöste is a scholar working on Molecular Biology, Genetics and Reproductive Medicine. According to data from OpenAlex, Marius Wöste has authored 15 papers receiving a total of 248 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 9 papers in Genetics and 4 papers in Reproductive Medicine. Recurrent topics in Marius Wöste's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers), Sperm and Testicular Function (4 papers) and Epigenetics and DNA Methylation (3 papers). Marius Wöste is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (5 papers), Sperm and Testicular Function (4 papers) and Epigenetics and DNA Methylation (3 papers). Marius Wöste collaborates with scholars based in Germany, United States and Netherlands. Marius Wöste's co-authors include Sabine Kliesch, Frank Tüttelmann, Martin Dugas, Corinna Friedrich, Albrecht Röpke, Elsa Leitão, Rolf Jessberger, Sandra Laurentino, Bernhard Horsthemke and Nina Neuhaus and has published in prestigious journals such as Bioinformatics, The Journal of Clinical Endocrinology & Metabolism and Human Reproduction.

In The Last Decade

Marius Wöste

14 papers receiving 248 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Marius Wöste Germany	10	160	102	95	63	38	15	248
Yaoting Gui China	11	191 1.2×	205 2.0×	104 1.1×	99 1.6×	43 1.1×	19	393
Pola Smirin‐Yosef Israel	10	178 1.1×	51 0.5×	160 1.7×	93 1.5×	26 0.7×	15	309
Bérangère Legois France	9	217 1.4×	157 1.5×	138 1.5×	113 1.8×	33 0.9×	12	359
Miaofei Xu China	10	173 1.1×	110 1.1×	140 1.5×	49 0.8×	85 2.2×	17	318
Irina Lagovsky Israel	8	122 0.8×	51 0.5×	118 1.2×	95 1.5×	15 0.4×	14	282
Yarui Du China	5	174 1.1×	54 0.5×	71 0.7×	56 0.9×	15 0.4×	12	258
Ahlem Amouri Tunisia	9	169 1.1×	35 0.3×	127 1.3×	24 0.4×	51 1.3×	27	257
Junshun Fang China	10	207 1.3×	74 0.7×	54 0.6×	107 1.7×	46 1.2×	24	384
Elizabeth P. Jeffries United States	5	213 1.3×	71 0.7×	170 1.8×	161 2.6×	30 0.8×	6	344
Hila Fridman Israel	7	104 0.7×	36 0.4×	130 1.4×	43 0.7×	18 0.5×	8	219

Countries citing papers authored by Marius Wöste

Since Specialization

Citations

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

Fields of papers citing papers by Marius Wöste

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marius Wöste

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

All Works

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15 of 15 papers shown

Krenz, Henrike, Tobias Tekath, Marius Wöste, et al.. (2022). Transcriptome analyses in infertile men reveal germ cell–specific expression and splicing patterns. Life Science Alliance. 6(2). e202201633–e202201633. 7 indexed citations

Schubert, Maria, Marius Wöste, Martin Dugas, et al.. (2022). A GWAS in Idiopathic/Unexplained Infertile Men Detects a Genomic Region Determining Follicle-Stimulating Hormone Levels. The Journal of Clinical Endocrinology & Metabolism. 107(8). 2350–2361. 7 indexed citations

Wyrwoll, Margot J., Albrecht Röpke, Marius Wöste, et al.. (2022). Analysis of copy number variation in men with non‐obstructive azoospermia. Andrology. 10(8). 1593–1604. 9 indexed citations

Persio, Sara Di, Elsa Leitão, Marius Wöste, et al.. (2021). Whole-genome methylation analysis of testicular germ cells from cryptozoospermic men points to recurrent and functionally relevant DNA methylation changes. Clinical Epigenetics. 13(1). 160–160. 14 indexed citations

Fernández, Lucia Torres, Sibylle Mitschka, Marius Wöste, et al.. (2021). TRIM71 Deficiency Causes Germ Cell Loss During Mouse Embryogenesis and Is Associated With Human Male Infertility. Frontiers in Cell and Developmental Biology. 9. 658966–658966. 18 indexed citations

Angenendt, Linus, Marius Wöste, Jan‐Henrik Mikesch, et al.. (2021). Calcitonin receptor-like (CALCRL) is a marker of stemness and an independent predictor of outcome in pediatric AML. Blood Advances. 5(21). 4413–4421. 14 indexed citations

Wyrwoll, Margot J., Geert Hamer, M. Mahdi Motazacker, et al.. (2021). Bi-allelic variants in DNA mismatch repair proteins MutS Homolog MSH4 and MSH5 cause infertility in both sexes. Human Reproduction. 37(1). 178–189. 29 indexed citations

Sandmann, Sarah, Stephanie Müller, Marius Wöste, et al.. (2020). Reconstructing clonal evolution in relapsed and non-relapsed Burkitt lymphoma. Leukemia. 35(2). 639–643. 13 indexed citations

Leitão, Elsa, Sara Di Persio, Sandra Laurentino, et al.. (2020). The sperm epigenome does not display recurrent epimutations in patients with severely impaired spermatogenesis. Clinical Epigenetics. 12(1). 61–61. 23 indexed citations

10.

Salas‐Huetos, Albert, Frank Tüttelmann, Margot J. Wyrwoll, et al.. (2020). Disruption of human meiotic telomere complex genes TERB1, TERB2 and MAJIN in men with non-obstructive azoospermia. Human Genetics. 140(1). 217–227. 32 indexed citations

11.

Wöste, Marius, Elsa Leitão, Sandra Laurentino, et al.. (2020). wg-blimp: an end-to-end analysis pipeline for whole genome bisulfite sequencing data. BMC Bioinformatics. 21(1). 169–169. 17 indexed citations

12.

Salas‐Huetos, Albert, Frank Tüttelmann, Margot J. Wyrwoll, et al.. (2020). Correction to: Disruption of human meiotic telomere complex genes TERB1, TERB2 and MAJIN in men with non-obstructive azoospermia. Human Genetics. 140(1). 229–229.

13.

Sandmann, Sarah, Marius Wöste, Aniek O. de Graaf, et al.. (2020). CopyDetective: Detection threshold–aware copy number variant calling in whole-exome sequencing data. GigaScience. 9(11). 3 indexed citations

14.

Röpke, Albrecht, Marius Wöste, Rolf Jessberger, et al.. (2019). Mutations in the stromal antigen 3 (STAG3) gene cause male infertility due to meiotic arrest. Human Reproduction. 34(11). 2112–2119. 58 indexed citations

15.

Wöste, Marius & Martin Dugas. (2018). VIPER: a web application for rapid expert review of variant calls. Bioinformatics. 34(11). 1928–1929. 4 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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