Gesa Schwanitz

2.8k total citations
132 papers, 1.6k citations indexed

About

Gesa Schwanitz is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Gesa Schwanitz has authored 132 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 82 papers in Genetics, 50 papers in Molecular Biology and 41 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Gesa Schwanitz's work include Genomic variations and chromosomal abnormalities (64 papers), Prenatal Screening and Diagnostics (39 papers) and Chromosomal and Genetic Variations (36 papers). Gesa Schwanitz is often cited by papers focused on Genomic variations and chromosomal abnormalities (64 papers), Prenatal Screening and Diagnostics (39 papers) and Chromosomal and Genetic Variations (36 papers). Gesa Schwanitz collaborates with scholars based in Germany, Poland and Iran. Gesa Schwanitz's co-authors include Regine Schubert, Thomas Eggermann, Hartmut Engels, Markus Montag, Katrin van der Ven, Klaus Zerres, H.‐D. Rott, H. van der Ven, M. Hansmann and G. Lehnert and has published in prestigious journals such as Human Reproduction, Genomics and Journal of Medical Genetics.

In The Last Decade

Gesa Schwanitz

127 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Gesa Schwanitz Germany 22 1.1k 696 532 418 151 132 1.6k
M.J.W. Faed United Kingdom 22 711 0.7× 366 0.5× 664 1.2× 349 0.8× 192 1.3× 52 1.6k
Philippos C. Patsalis Cyprus 27 1.2k 1.1× 705 1.0× 1.0k 2.0× 266 0.6× 77 0.5× 100 2.0k
Avirachan T. Tharapel United States 19 976 0.9× 881 1.3× 443 0.8× 274 0.7× 125 0.8× 61 1.5k
Heinz-Ulrich Weier United States 13 658 0.6× 270 0.4× 1.1k 2.1× 363 0.9× 189 1.3× 16 1.8k
Josep Egozcue Spain 25 707 0.6× 473 0.7× 521 1.0× 347 0.8× 287 1.9× 61 1.4k
Thue Bryndorf Denmark 16 516 0.5× 445 0.6× 272 0.5× 217 0.5× 185 1.2× 29 997
M. Ray Canada 15 731 0.7× 377 0.5× 391 0.7× 292 0.7× 65 0.4× 36 1.1k
E. Boyd United Kingdom 22 804 0.7× 233 0.3× 623 1.2× 304 0.7× 49 0.3× 55 1.3k
M.A. Hultén United Kingdom 15 440 0.4× 324 0.5× 447 0.8× 263 0.6× 151 1.0× 20 930
Joseph Shen United States 16 598 0.5× 481 0.7× 678 1.3× 193 0.5× 223 1.5× 26 1.3k

Countries citing papers authored by Gesa Schwanitz

Since Specialization
Citations

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

Fields of papers citing papers by Gesa Schwanitz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gesa Schwanitz

This figure shows the co-authorship network connecting the top 25 collaborators of Gesa Schwanitz. A scholar is included among the top collaborators of Gesa Schwanitz 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 Gesa Schwanitz. Gesa Schwanitz 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.
2.
Gamerdinger, Ulrike, Thomas Eggermann, Regine Schubert, Gesa Schwanitz, & Martina Kreiß‐Nachtsheim. (2008). Rare interstitial deletion 9q31.2 to q33.1 de novo: Longitudinal study in a patient over a period of more than 20 years. American Journal of Medical Genetics Part A. 146A(9). 1180–1184. 10 indexed citations
3.
Roos, Andreas, Sabine Rudnik‐Schöneborn, Katja Eggermann, et al.. (2006). Submicroscopic unbalanced translocation resulting in del10p/dup13q detected by subtelomere FISH. European Journal of Medical Genetics. 49(6). 505–510. 5 indexed citations
4.
Schmidt‐Wolf, Ingo, Axel Glasmacher, Corinna Hahn‐Ast, et al.. (2006). Chromosomal aberrations in 130 patients with multiple myeloma studied by interphase FISH: diagnostic and prognostic relevance. Cancer Genetics and Cytogenetics. 167(1). 20–25. 19 indexed citations
5.
Zahn, Susanne, Kristin Bosse, Vera M. Kalscheuer, et al.. (2005). Further delineation of the phenotype maps for partial trisomy 16q24 and Jacobsen syndrome by a subtle familial translocation t(11;16)(q24.2;q24.1). American Journal of Medical Genetics Part A. 139A(1). 19–24. 15 indexed citations
6.
Eggermann, Thomas, Ulrike Gamerdinger, Kristin Bosse, et al.. (2005). Mosaic tetrasomy 14pter‐q13 due to a supernumerary isodicentric derivate of proximal chromosome 14q. American Journal of Medical Genetics Part A. 134A(3). 305–308. 7 indexed citations
7.
Schubert, Regine, et al.. (2002). Clinical, cytogenetic, and molecular findings in 45,X/47,XX,+18 mosaicism: Clinical report and review of the literature. American Journal of Medical Genetics. 110(3). 278–282. 16 indexed citations
8.
Haidl, Gerhard, et al.. (2000). Cytogenetic and andrological status and ICSI-results in couples with severe male factor infertility.. PubMed. 2(4). 293–6. 10 indexed citations
9.
Schubert, Regine, et al.. (2000). Combination of Hypospadias and Maldescended Testis as Cardinal Symptoms in Gonosomal Chromosome Aberrations*. European Journal of Pediatric Surgery. 10(4). 270–275. 6 indexed citations
10.
Ven, Katrin van der, et al.. (1998). Increased frequency of congenital chromosomal aberrations in female partners of couples undergoing intracytoplasmic sperm injection. Human Reproduction. 13(1). 48–54. 65 indexed citations
11.
Schubert, Regine, et al.. (1998). Maldescensus testis und Hypospadie bei Aberration der Geschlechtschromosomen. Klinische Pädiatrie. 210(6). 400–405. 3 indexed citations
12.
Montag, Markus, Katrin van der Ven, Andreas Schmutzler, et al.. (1997). Success of intracytoplasmic sperm injection in couples with male and/or female chromosome aberrations. Human Reproduction. 12(12). 2635–2640. 40 indexed citations
13.
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15.
Eiben, B., R. Goebel, Ulrike Gamerdinger, et al.. (1992). Prenatal diagnosis of monosomy 18 and ring chromosome 18 mosaicism. Prenatal Diagnosis. 12(11). 945–950. 10 indexed citations
16.
Schwanitz, Gesa, Max P. Baur, Carol M. Black, et al.. (1988). Family studies in scleroderma (systemic sclerosis) demonstrating an HLA-linked increased chromosomal breakage rate in cultured lymphocytes. Human Genetics. 81(1). 64–70. 22 indexed citations
17.
Bornkamm, Georg W., B. Kaduk, Ulf C. Schneider, et al.. (1980). Epstein-Barr virus-positive Burkitt's lymphoma in a german woman during pregnancy. Annals of Hematology. 40(3). 167–177. 55 indexed citations
18.
Rott, H.‐D., et al.. (1972). Chromosomenbefunde bei Ehepaaren mit geh�uften Aborten. Archives of Gynecology and Obstetrics. 213(2). 110–118. 10 indexed citations
19.
Becker, J., et al.. (1971). Kongenitale dyserythropoetische Anämie. Annals of Hematology. 23(6). 347–358. 4 indexed citations
20.
Schwanitz, Gesa, G. Lehnert, & E. Gebhart. (1970). Chromosomal injury due to occupational lead poisoning.. 15(12). 2 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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