Stefanie Engert

2.0k total citations
5 papers, 345 citations indexed

About

Stefanie Engert is a scholar working on Molecular Biology, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Stefanie Engert has authored 5 papers receiving a total of 345 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 3 papers in Genetics and 1 paper in Cardiology and Cardiovascular Medicine. Recurrent topics in Stefanie Engert's work include BRCA gene mutations in cancer (2 papers), RNA and protein synthesis mechanisms (2 papers) and RNA Research and Splicing (2 papers). Stefanie Engert is often cited by papers focused on BRCA gene mutations in cancer (2 papers), RNA and protein synthesis mechanisms (2 papers) and RNA Research and Splicing (2 papers). Stefanie Engert collaborates with scholars based in Germany, France and United States. Stefanie Engert's co-authors include Alfons Meindl, Juliane Ramser, Herbert A. Lubs, C Lenski, Geneviève Nguyen, Céline Burcklé, Helga V. Toriello, Fatima Abidi, Roger E. Stevenson and Gaiping Wen and has published in prestigious journals such as Nature Genetics, PLoS ONE and Human Molecular Genetics.

In The Last Decade

Stefanie Engert

5 papers receiving 341 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Stefanie Engert Germany	5	231	145	81	59	45	5	345
Yu Ding China	12	219 0.9×	170 1.2×	20 0.2×	55 0.9×	35 0.8×	38	359
Jesung Moon United States	9	254 1.1×	96 0.7×	83 1.0×	18 0.3×	18 0.4×	12	424
Luca Mariani Italy	11	155 0.7×	104 0.7×	32 0.4×	48 0.8×	54 1.2×	28	396
Erasmo M. Perera United States	10	228 1.0×	178 1.2×	33 0.4×	95 1.6×	22 0.5×	12	353
Shakila Abdul-Majeed United States	9	196 0.8×	215 1.5×	30 0.4×	18 0.3×	28 0.6×	10	347
N. Weinberg Israel	7	281 1.2×	334 2.3×	62 0.8×	24 0.4×	69 1.5×	8	512
Johannes Weigel Germany	11	279 1.2×	179 1.2×	21 0.3×	196 3.3×	35 0.8×	15	512
JJ Kopchick United States	6	180 0.8×	98 0.7×	44 0.5×	234 4.0×	36 0.8×	8	398
Ahmed Alfares Saudi Arabia	11	234 1.0×	209 1.4×	13 0.2×	23 0.4×	45 1.0×	38	474
Farhad Dehkhoda Australia	6	165 0.7×	41 0.3×	19 0.2×	124 2.1×	48 1.1×	9	355

Countries citing papers authored by Stefanie Engert

Since Specialization

Citations

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

Fields of papers citing papers by Stefanie Engert

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stefanie Engert

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

All Works

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5 of 5 papers shown

1.

Meindl, Alfons, Katharina Eirich, Stefanie Engert, et al.. (2012). Germline RAD51C mutations confer susceptibility to ovarian cancer. Nature Genetics. 44(5). 476–476. 5 indexed citations

2.

Wappenschmidt, Barbara, Alexandra Becker, Jan Hauke, et al.. (2012). Analysis of 30 Putative BRCA1 Splicing Mutations in Hereditary Breast and Ovarian Cancer Families Identifies Exonic Splice Site Mutations That Escape In Silico Prediction. PLoS ONE. 7(12). e50800–e50800. 41 indexed citations

3.

Engert, Stefanie, Barbara Wappenschmidt, Beate Betz, et al.. (2008). MLPA screening in theBRCA1gene from 1,506 German hereditary breast cancer cases: novel deletions, frequent involvement of exon 17, and occurrence in single early-onset cases. Human Mutation. 29(7). 948–958. 74 indexed citations

4.

Sadr‐Nabavi, Ariane, Juliane Ramser, Jens Volkmann, et al.. (2008). Decreased expression of angiogenesis antagonist EFEMP1 in sporadic breast cancer is caused by aberrant promoter methylation and points to an impact of EFEMP1 as molecular biomarker. International Journal of Cancer. 124(7). 1727–1735. 79 indexed citations

5.

Ramser, Juliane, Fatima Abidi, Céline Burcklé, et al.. (2005). A unique exonic splice enhancer mutation in a family with X-linked mental retardation and epilepsy points to a novel role of the renin receptor. Human Molecular Genetics. 14(8). 1019–1027. 146 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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