Simone Heidemann

733 total citations
14 papers, 140 citations indexed

About

Simone Heidemann is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Simone Heidemann has authored 14 papers receiving a total of 140 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 8 papers in Pediatrics, Perinatology and Child Health and 5 papers in Molecular Biology. Recurrent topics in Simone Heidemann's work include Prenatal Screening and Diagnostics (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and BRCA gene mutations in cancer (4 papers). Simone Heidemann is often cited by papers focused on Prenatal Screening and Diagnostics (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and BRCA gene mutations in cancer (4 papers). Simone Heidemann collaborates with scholars based in Germany, Austria and Estonia. Simone Heidemann's co-authors include W. Jonat, Norbert Arnold, Almuth Caliebe, Reiner Siebert, Christoph Engel, Christel Eckmann-Scholz, Christine Fischer, Sandra C. Doelken, Nicola Dikow and Barbara Fischer and has published in prestigious journals such as SHILAP Revista de lepidopterología, PLoS ONE and The American Journal of Human Genetics.

In The Last Decade

Simone Heidemann

13 papers receiving 134 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Simone Heidemann Germany 7 96 66 35 25 16 14 140
Hélène Moirot France 9 119 1.2× 76 1.2× 59 1.7× 26 1.0× 12 0.8× 13 198
Margaret Harr United States 10 130 1.4× 79 1.2× 29 0.8× 12 0.5× 13 0.8× 16 194
Stacy J. Hines‐Dowell United States 7 109 1.1× 39 0.6× 57 1.6× 10 0.4× 13 0.8× 10 156
Kristen Rasmussen United States 8 163 1.7× 114 1.7× 33 0.9× 33 1.3× 22 1.4× 10 263
Alejandro Martin-Trujillo United States 8 145 1.5× 154 2.3× 73 2.1× 10 0.4× 4 0.3× 9 219
Ferdouse Begum United States 7 147 1.5× 103 1.6× 55 1.6× 5 0.2× 5 0.3× 13 231
Michiel Oorsprong Netherlands 2 54 0.6× 45 0.7× 18 0.5× 12 0.5× 6 0.4× 3 112
Francisco Álvarez‐Nava Venezuela 9 181 1.9× 145 2.2× 39 1.1× 6 0.2× 8 0.5× 25 254
Hannaleena Kokkonen Finland 8 173 1.8× 152 2.3× 83 2.4× 7 0.3× 9 0.6× 20 238
Kimberly Foss United States 7 83 0.9× 54 0.8× 14 0.4× 9 0.4× 7 0.4× 11 139

Countries citing papers authored by Simone Heidemann

Since Specialization
Citations

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

Fields of papers citing papers by Simone Heidemann

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Simone Heidemann

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

All Works

14 of 14 papers shown
1.
Schwaninger, Gunda, Simone Heidemann, Sabine Rudnik‐Schöneborn, & Johannes Zschocke. (2024). The current state of the genetic counselor profession in the German-speaking countries. SHILAP Revista de lepidopterología. 2(Suppl 2). 101849–101849.
2.
Schwaninger, Gunda, et al.. (2021). Prospects and challenges for the genetic counsellor profession in the German-speaking countries: report of a workshop. Medizinische Genetik. 33(1). 35–44. 3 indexed citations
3.
4.
Heidemann, Simone, et al.. (2017). CDH1 mutation screen in a BRCA1/2-negative familial breast-/ovarian cancer cohort. Archives of Gynecology and Obstetrics. 297(1). 147–152. 6 indexed citations
5.
Roos, Andreas, Constantin S. von Kaisenberg, Thomas Eggermann, et al.. (2013). Analysis of SYCP3 encoding synaptonemal complex protein 3 in human aneuploidies. Archives of Gynecology and Obstetrics. 288(5). 1153–1158. 5 indexed citations
6.
Eckmann-Scholz, Christel, Susanne Bens, Julia Kolarova, et al.. (2012). DNA-Methylation Profiling of Fetal Tissues Reveals Marked Epigenetic Differences between Chorionic and Amniotic Samples. PLoS ONE. 7(6). e39014–e39014. 24 indexed citations
7.
Heidemann, Simone, Christine Fischer, Christoph Engel, et al.. (2012). Double heterozygosity for mutations in BRCA1 and BRCA2 in German breast cancer patients: implications on test strategies and clinical management. Breast Cancer Research and Treatment. 134(3). 1229–1239. 43 indexed citations
8.
Eckmann-Scholz, Christel, Constantin S. von Kaisenberg, Norbert Arnold, et al.. (2012). Chromosomal mosaicisms in prenatal diagnosis: correlation with first trimester screening and clinical outcome. Journal of Perinatal Medicine. 40(3). 215–23. 9 indexed citations
9.
Weimer, Jörg, Simone Heidemann, Constantin S. von Kaisenberg, et al.. (2011). Isolated trisomy 7q21.2-31.31 resulting from a complex familial rearrangement involving chromosomes 7, 9 and 10. Molecular Cytogenetics. 4(1). 28–28. 6 indexed citations
10.
Fischer, Christine, Christoph Engel, Christian Sutter, et al.. (2011). BRCA1/2 testing: uptake, phenocopies, and strategies to improve detection rates in initially negative families. Clinical Genetics. 82(5). 478–483. 12 indexed citations
11.
Heidemann, Simone, et al.. (2011). Gendiagnostikgesetz : Kommentar für die Praxis. Medical Entomology and Zoology. 5 indexed citations
12.
13.
Muhle, Hiltrud, Sarah von Spiczak, André Franke, et al.. (2010). A duplication in 1q21.3 in a family with early onset and childhood absence epilepsy. Epilepsia. 51(12). 2453–2456. 11 indexed citations
14.
Liehr, Thomas, Victoria Bryant, John Barber, et al.. (2007). The Variant inv(2)(p11.2q13) Is a Genuinely Recurrent Rearrangement but Displays Some Breakpoint Heterogeneity. The American Journal of Human Genetics. 81(4). 847–856. 13 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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