Stephanie Schubert

821 total citations
32 papers, 563 citations indexed

About

Stephanie Schubert is a scholar working on Molecular Biology, Genetics and Reproductive Medicine. According to data from OpenAlex, Stephanie Schubert has authored 32 papers receiving a total of 563 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 17 papers in Genetics and 8 papers in Reproductive Medicine. Recurrent topics in Stephanie Schubert's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (11 papers), Sperm and Testicular Function (8 papers) and Sexual Differentiation and Disorders (4 papers). Stephanie Schubert is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (11 papers), Sperm and Testicular Function (8 papers) and Sexual Differentiation and Disorders (4 papers). Stephanie Schubert collaborates with scholars based in Germany, United States and Italy. Stephanie Schubert's co-authors include Jörg Schmidtke, Andreas Meinhardt, Wolfgang Engel, Ibrahim M. Adham, Britta Skawran, Lyora A. Cohen, Yael Leichtmann‐Bardoogo, Avital Weiss, Esther G. Meyron‐Holtz and Manfred Stuhrmann and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and Molecular and Cellular Biology.

In The Last Decade

Stephanie Schubert

32 papers receiving 560 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Stephanie Schubert Germany 14 261 222 130 81 71 32 563
Dijana Plaseska‐Karanfilska North Macedonia 14 311 1.2× 262 1.2× 177 1.4× 71 0.9× 55 0.8× 102 805
Nicolas Richard France 16 446 1.7× 353 1.6× 237 1.8× 95 1.2× 49 0.7× 44 901
Kenneth Y. Ilio United States 10 282 1.1× 112 0.5× 144 1.1× 177 2.2× 46 0.6× 12 566
Tiangang Zhuang United States 16 495 1.9× 132 0.6× 133 1.0× 50 0.6× 42 0.6× 18 744
Toshina Oonuma Japan 8 116 0.4× 132 0.6× 90 0.7× 78 1.0× 30 0.4× 10 398
Kuniko Nakajima Japan 12 489 1.9× 150 0.7× 64 0.5× 24 0.3× 47 0.7× 19 580
Niema Ibrahim Saudi Arabia 17 411 1.6× 257 1.2× 57 0.4× 43 0.5× 97 1.4× 22 767
Maï Thu Vu Hai France 8 180 0.7× 201 0.9× 155 1.2× 117 1.4× 26 0.4× 9 552
Firdous Abdulwahab Saudi Arabia 14 412 1.6× 238 1.1× 95 0.7× 34 0.4× 73 1.0× 30 729
Jitendra Badhai Sweden 13 323 1.2× 145 0.7× 33 0.3× 130 1.6× 40 0.6× 24 581

Countries citing papers authored by Stephanie Schubert

Since Specialization
Citations

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

Fields of papers citing papers by Stephanie Schubert

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stephanie Schubert

This figure shows the co-authorship network connecting the top 25 collaborators of Stephanie Schubert. A scholar is included among the top collaborators of Stephanie Schubert 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 Stephanie Schubert. Stephanie Schubert 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.
Evans, T., et al.. (2024). Occurrence of ceramides in the Acidobacterium Solibacter usitatus: implications for bacterial physiology and sphingolipids in soils. SHILAP Revista de lepidopterología. 2. 3 indexed citations
2.
Schubert, Stephanie, Christopher Werlein, Helge Stark, et al.. (2021). The Challenge of Long-Term Cultivation of Human Precision-Cut Lung Slices. American Journal Of Pathology. 192(2). 239–253. 25 indexed citations
3.
Ackermann, Maximilian, Helge Stark, Lavinia Neubert, et al.. (2019). Morphomolecular motifs of pulmonary neoangiogenesis in interstitial lung diseases. European Respiratory Journal. 55(3). 1900933–1900933. 41 indexed citations
4.
Schubert, Stephanie, Gunnar Schmidt, Winfried Hofmann, et al.. (2019). From a variant of unknown significance to pathogenic: Reclassification of a large novel duplication in BRCA2 by high‐throughput sequencing. Molecular Genetics & Genomic Medicine. 8(9). e1045–e1045. 3 indexed citations
5.
Penkert, Judith, Gunnar Schmidt, Winfried Hofmann, et al.. (2018). Breast cancer patients suggestive of Li-Fraumeni syndrome: mutational spectrum, candidate genes, and unexplained heredity. Breast Cancer Research. 20(1). 87–87. 6 indexed citations
6.
Schubert, Stephanie, Noel F.C.C. de Miranda, Dina Ruano, et al.. (2018). PO-059 Cancer-predisposing variants in alternatively spliced TP53 exons. ESMO Open. 3. A249–A250. 1 indexed citations
7.
Schubert, Stephanie, Tim Ripperger, Winfried Hofmann, et al.. (2017). GT198 (PSMC3IP) germline variants in early-onset breast cancer patients from hereditary breast and ovarian cancer families. Genes & Cancer. 8(1-2). 472–483. 5 indexed citations
8.
Brand, Frank, Anna‐Carina Weiss, Martin Kreuzer, et al.. (2017). Mutations in the leukemia inhibitory factor receptor (LIFR) gene and Lifr deficiency cause urinary tract malformations. Human Molecular Genetics. 26(9). 1716–1731. 28 indexed citations
9.
Schubert, Stephanie, Cordula Haas, Christine Bärtsch, et al.. (2014). Variants in TSPYL1 are not associated with sudden infant death syndrome in a cohort of deceased infants from Switzerland. Molecular and Cellular Probes. 29(1). 31–34. 5 indexed citations
10.
Schubert, Stephanie, Frank Traub, Kai Brakensiek, et al.. (2014). CFTR, SPINK1, PRSS1, and CTRC Mutations Are Not Associated With Pancreatic Cancer in German Patients. Pancreas. 43(7). 1078–1082. 34 indexed citations
11.
Smits, Bart M. G., Stephanie Schubert, Heike Nave, et al.. (2011). A Mutation in Myo15 Leads to Usher-Like Symptoms in LEW/Ztm-ci2 Rats. PLoS ONE. 6(3). e15669–e15669. 6 indexed citations
12.
Stuhrmann, Manfred, et al.. (2011). Should TSPYL1 mutation screening be included in routine diagnostics of male idiopathic infertility?. Fertility and Sterility. 97(2). 402–406. 6 indexed citations
13.
Kido, Tatsuo, Stephanie Schubert, Jörg Schmidtke, & Yun‐Fai Chris Lau. (2011). Expression of the human TSPY gene in the brains of transgenic mice suggests a potential role of this Y chromosome gene in neural functions. Journal of genetics and genomics. 38(5). 181–191. 9 indexed citations
14.
Schubert, Stephanie & Jörg Schmidtke. (2010). Transgenic Mouse Studies to Understand the Regulation, Expression and Function of the Testis-Specific Protein Y-Encoded (TSPY) Gene. Genes. 1(2). 244–262. 3 indexed citations
15.
Adham, Ibrahim M., et al.. (2010). Partial Rescue of the KIT-Deficient Testicular Phenotype in KitW‑v/KitW‑v Tg(TSPY) Mice1. Biology of Reproduction. 83(1). 20–26. 11 indexed citations
16.
Schubert, Stephanie, Kenji Kamino, Detlef Böhm, et al.. (2008). TSPY Expression Is Variably Altered in Transgenic Mice with Testicular Feminization1. Biology of Reproduction. 79(1). 125–133. 7 indexed citations
17.
Kovac, Judit, et al.. (2006). Tspy is nonfunctional in the Mongolian gerbil but functional in the Syrian hamster. Genomics. 88(1). 65–73. 4 indexed citations
18.
Schubert, Stephanie, Britta Skawran, Heinz Winking, et al.. (2000). Silencing of the Y-chromosomal gene tspy during murine evolution. Mammalian Genome. 11(4). 288–291. 13 indexed citations
19.
Schubert, Stephanie, et al.. (1998). Organization and expression of rat <i>Tspy</i>. Cytogenetic and Genome Research. 83(3-4). 270–274. 16 indexed citations
20.
Schubert, Stephanie, Franco Laccone, & I. Hansmann. (1994). Towards positional cloning of the locus for benign neonatal epilepsy (EBN1) on chromosome 20. The American Journal of Human Genetics. 55. 1 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Dijana Plaseska‐Karanfilska Breakdown of academic impact, for papers by Nicolas Richard Breakdown of academic impact, for papers by Kenneth Y. Ilio Breakdown of academic impact, for papers by Tiangang Zhuang Breakdown of academic impact, for papers by Toshina Oonuma Breakdown of academic impact, for papers by Kuniko Nakajima Breakdown of academic impact, for papers by Niema Ibrahim Breakdown of academic impact, for papers by Maï Thu Vu Hai Breakdown of academic impact, for papers by Firdous Abdulwahab Breakdown of academic impact, for papers by Jitendra Badhai
Rankless by CCL
2026