Stefan Kirsch

3.8k citations
33 papers · 2.5k · 2 hit papers · h-index 15

Impact in

  • Genetics top 1%
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
    • Genomic variations and chromosomal abnormalities
    • Genetics and Neurodevelopmental Disorders
    • Sperm and Testicular Function

Papers in

    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 16
    • Genomic variations and chromosomal abnormalities 5
    • Genomics and Chromatin Dynamics 7
    • Sexual Differentiation and Disorders 5
    • Single-cell and spatial transcriptomics 2

Stefan Kirsch

33 papers receiving 2.5k citations

Hit Papers

Biology of interleukin-10 2010 · 806 citations
8060+9+19Years since publication250500750

Peers

Stefan Kirsch
Comparison fields: 5 of 121
  • Genetics 1.2k
  • Reproductive Medicine 292
  • Immunology 498
  • Molecular Biology 1.2k
  • Gender Studies 143
Replace Patricia Taillon‐Miller with:
Patricia Taillon‐Miller United States
Yvonne Boyd United Kingdom
Maris Laan Estonia
Landian Hu China
Dale E. Bockman United States
Carlos Alberto Moreira‐Filho Brazil
David W. Silversides Canada
Joshua Starmer United States
Michael Cheeseman United Kingdom
Jean‐Jacques Panthier France
Stefan Kirsch relative to Patricia Taillon‐Miller United States Patricia Taillon‐Miller's profile →
Citations per field
00.5×11.9×
Patricia Taillon‐Miller · 1×
Citations per year

Countries citing papers authored by Stefan Kirsch

Since Specialization
Citations

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

Fields of papers citing papers by Stefan Kirsch

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Stefan Kirsch, 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 Stefan Kirsch Line = papers co-authored together Stefan Kirsch links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 33 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Biology of interleukin-10
Hit paper breakdown →
2010806
2
Pseudoautosomal deletions encompassing a novel homeobox gene cause growth failure in idiopathic short stature and Turner syndrome
Hit paper breakdown →
1997701
3 1992177
4 2002166
5 2013108
6
The critical region of overlap defining the AZFa male infertility interval of proximal Yq contains three transcribed sequences.
199987
7 200085
8 200672
9 202161
10 200528
11 200826
12 200026
13 201526
14 199619
15 200416
16 200213
17 200213
18 200912
19 201512
20
The definition of the Y chromosome growth-control gene (GCY) critical region: relevance of terminal and interstitial deletions.
200211

About Stefan Kirsch

Stefan Kirsch is a scholar working on Genetics, Molecular Biology, Plant Science, Cancer Research and Reproductive Medicine, having authored 33 papers that have together received 2.5k indexed citations. Recurring topics across this work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (16 papers), Chromosomal and Genetic Variations (12 papers), Genomics and Chromatin Dynamics (7 papers), Sperm and Testicular Function (5 papers), Sexual Differentiation and Disorders (5 papers), Genomic variations and chromosomal abnormalities (5 papers), Cancer Genomics and Diagnostics (3 papers) and Single-cell and spatial transcriptomics (2 papers). The work is most often cited by research in Genetics (1.2k citations), Reproductive Medicine (292 citations), Immunology (498 citations), Molecular Biology (1.2k citations) and Gender Studies (143 citations). Stefan Kirsch has collaborated with scholars based in Germany, United States and Poland. Frequent co-authors include Ellen Witte, Katarzyna Warszawska, Robert Sabat, Kerstin Wolk, Jens Geginat, Gerald Grütz, Gudrun Rappold, Birgit Weiß, Maki Fukami and Beate Niesler. Their work appears in journals such as Cytogenetic and Genome Research, BMC Evolutionary Biology, Journal of Medical Genetics, Genome Research and Nature 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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