Gesa Schwanitz

2.8k citations
145 papers · 1.9k · h-index 24

Impact in

  • Genetics top 1%
    • Genomic variations and chromosomal abnormalities
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
    • Genetic Syndromes and Imprinting
    • Prenatal Screening and Diagnostics

Papers in

    • Genomic variations and chromosomal abnormalities 73
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 9
    • Genetic Syndromes and Imprinting 7
    • Sexual Differentiation and Disorders 8

Gesa Schwanitz

136 papers receiving 1.6k citations

Peers

Gesa Schwanitz
Comparison fields: 5 of 95
  • Genetics 1.1k
  • Pediatrics, Perinatology and Child Health 681
  • Developmental Biology 55
  • Reproductive Medicine 126
  • Plant Science 400
Replace M.J.W. Faed with:
M.J.W. Faed United Kingdom
K. Madan Netherlands
Noreen L. Rudd Canada
M. Ray Canada
PatriciaA. Jacobs United Kingdom
S Armendares Mexico
E. Boyd United Kingdom
Susana Kofman‐Alfaro Mexico
O.S. Alfi United States
Kiran Kucheria India
Gesa Schwanitz relative to M.J.W. Faed United Kingdom M.J.W. Faed's profile →
Citations per field
00.5×3.9×
M.J.W. Faed · 1×
Citations per year

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-authors

The 25 scholars most cited alongside Gesa Schwanitz, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Gesa Schwanitz Line = papers co-authored together Gesa Schwanitz links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 145 papers — load more, or switch the sort, to bring in the rest.

#Work
1 1999126
2 199882
3 200272
4 200865
5 198057
6 197053
7 199745
8 199945
9 199645
10 199741
11 199639
12 200438
13 200036
14 199735
15 198528
16 199428
17 199327
18
Klinefelter's syndrome and mitral valve prolapse. an echocardiographic study in twenty-two patients.
198427
19 201226
20 197226

About Gesa Schwanitz

Gesa Schwanitz is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Plant Science and Surgery, having authored 145 papers that have together received 1.9k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (73 papers), Prenatal Screening and Diagnostics (41 papers), Chromosomal and Genetic Variations (38 papers), Congenital limb and hand anomalies (11 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (9 papers), Congenital Anomalies and Fetal Surgery (9 papers), Sexual Differentiation and Disorders (8 papers) and Genetic Syndromes and Imprinting (7 papers). The work is most often cited by research in Genetics (1.1k citations), Pediatrics, Perinatology and Child Health (681 citations), Developmental Biology (55 citations), Reproductive Medicine (126 citations) and Plant Science (400 citations). Gesa Schwanitz has collaborated with scholars based in Germany, Poland and Iran. Frequent co-authors include Regine Schubert, Thomas Eggermann, Hartmut Engels, Katrin van der Ven, Markus Montag, Klaus Zerres, H.‐D. Rott, H. van der Ven, G. Lehnert and M. Hansmann. Their work appears in journals such as Human Genetics, Prenatal Diagnosis, Clinical Genetics, Human Reproduction and Journal of Medical Genetics.

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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