Rita Exeler

512 total citations
12 papers, 245 citations indexed

About

Rita Exeler is a scholar working on Molecular Biology, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, Rita Exeler has authored 12 papers receiving a total of 245 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Molecular Biology, 4 papers in Pediatrics, Perinatology and Child Health and 4 papers in Genetics. Recurrent topics in Rita Exeler's work include Reproductive System and Pregnancy (4 papers), Prenatal Screening and Diagnostics (3 papers) and Immune Cell Function and Interaction (3 papers). Rita Exeler is often cited by papers focused on Reproductive System and Pregnancy (4 papers), Prenatal Screening and Diagnostics (3 papers) and Immune Cell Function and Interaction (3 papers). Rita Exeler collaborates with scholars based in Germany, Poland and United States. Rita Exeler's co-authors include Stephan Braune, Volker Senner, Werner Paulus, Christian Rickert, Peter Miny, Siu Li Yong, Sylvie Langlois, Wendy P. Robinson, Dagmar K. Kalousek and Irene Barrett and has published in prestigious journals such as Human Reproduction, Journal of Immunological Methods and Frontiers in Oncology.

In The Last Decade

Rita Exeler

12 papers receiving 232 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Rita Exeler Germany 7 105 104 74 44 34 12 245
Laura J. C. M. van Zutven Netherlands 11 76 0.7× 113 1.1× 192 2.6× 26 0.6× 55 1.6× 19 351
Carole Goumy France 11 100 1.0× 185 1.8× 125 1.7× 17 0.4× 16 0.5× 36 324
An Ping China 5 108 1.0× 157 1.5× 246 3.3× 26 0.6× 20 0.6× 8 381
G R Jalali United Kingdom 9 54 0.5× 163 1.6× 213 2.9× 77 1.8× 125 3.7× 13 431
N. Logghe Belgium 9 37 0.4× 85 0.8× 104 1.4× 48 1.1× 31 0.9× 14 243
G. Reza Jalali United Kingdom 13 103 1.0× 132 1.3× 191 2.6× 57 1.3× 210 6.2× 16 456
Susan L. Halloran United States 6 91 0.9× 163 1.6× 145 2.0× 8 0.2× 59 1.7× 9 350
H. Tönnies Germany 9 63 0.6× 126 1.2× 110 1.5× 94 2.1× 6 0.2× 21 330
Francesca Cioppi Italy 10 27 0.3× 113 1.1× 140 1.9× 16 0.4× 78 2.3× 20 294
Mahmut Selman Yıldırım Türkiye 10 39 0.4× 67 0.6× 92 1.2× 19 0.4× 13 0.4× 44 226

Countries citing papers authored by Rita Exeler

Since Specialization
Citations

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

Fields of papers citing papers by Rita Exeler

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Rita Exeler

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

All Works

12 of 12 papers shown
1.
Thiele, Sebastian, Jörg Gromoll, Stefan Schlatt, et al.. (2023). Deep learning predicts therapy-relevant genetics in acute myeloid leukemia from Pappenheim-stained bone marrow smears. Blood Advances. 8(1). 70–79. 10 indexed citations
2.
Sandmann, Sarah, Peter Bartel, Rita Exeler, et al.. (2022). The Role of Clonal Evolution on Progression, Blood Parameters, and Response to Therapy in Multiple Myeloma. Frontiers in Oncology. 12. 919278–919278. 4 indexed citations
3.
Bogdanova, Nadia, U. Siebers, Reinhard Kelsch, et al.. (2010). Blood chimerism in a girl with Down syndrome and possible freemartin effect leading to aplasia of the Mullerian derivatives. Human Reproduction. 25(5). 1339–1343. 22 indexed citations
4.
Langlois, Sylvie, Paul J. Yong, Siu Li Yong, et al.. (2006). Postnatal follow‐up of prenatally diagnosed trisomy 16 mosaicism. Prenatal Diagnosis. 26(6). 548–558. 53 indexed citations
5.
Senner, Volker, et al.. (2005). Establishment of a benign meningioma cell line by hTERT-mediated immortalization. Laboratory Investigation. 85(9). 1163–1171. 79 indexed citations
6.
7.
Kennerknecht, Ingo, Rita Exeler, J. Horst, et al.. (2004). Mild phenotype in two unrelated patients with a partial deletion of 21q22.2‐q22.3 defined by FISH and molecular studies. American Journal of Medical Genetics Part A. 131A(3). 265–372. 27 indexed citations
8.
Brune, Thomas, Felix G. Riepe, Henk Garritsen, et al.. (2003). The Cellular Immune Response of Children is Specifically Decreased Against their Parents but not Vice versa, Independent of Pregnancy, age, or HLA or HY Antigens. American Journal of Reproductive Immunology. 49(5). 255–260. 4 indexed citations
9.
10.
Brune, Thomas, et al.. (2002). Differentiation of single populations in a bidirectional mixed lymphocyte culture using X and Y chromosome-specific FiSH markers. Journal of Immunological Methods. 266(1-2). 105–110. 4 indexed citations
11.
Meschede, Dieter, et al.. (1998). Submicroscopic deletion in 14q32.3 through a de novo tandem translocation between 14q and 21p. American Journal of Medical Genetics. 80(5). 443–447. 15 indexed citations
12.
Miny, Peter, Bernd Dworniczak, Nadia Bogdanova, et al.. (1995). Parental origin of the extra haploid chromosome set in triploidies diagnosed prenatally. American Journal of Medical Genetics. 57(1). 102–106. 23 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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