Andreas Schedl

17.7k citations
116 papers · 13.4k indexed · 6 hit papers · h-index 52

Impact in

Papers in

    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 32
    • Animal Genetics and Reproduction 12
    • Genetic and Kidney Cyst Diseases 8
    • Renal and related cancers 51
    • Sexual Differentiation and Disorders 15
    • Pluripotent Stem Cells Research 13
    • Wnt/β-catenin signaling in development and cancer 8

Andreas Schedl

114 papers receiving 13.2k citations

Hit Papers

Visceral and subcutaneous fat have different origins and evidence supports a mesothelial source 2014 · 401 citations
40119972026200620164008001.2k

Peers

Andreas Schedl
Comparison fields: 5 of 148
  • Developmental Neuroscience 713
  • Genetics 4.3k
  • Molecular Biology 9.6k
  • Reproductive Medicine 1.0k
  • Cell Biology 1.8k
Replace Hannu Sariola with:
Hannu Sariola Finland
Thomas Doetschman United States
Andreas Kispert Germany
Pascal Dollé France
Brian D. Harfe United States
Jordan A. Kreidberg United States
Roger A. Pedersen United States
Jill A. McMahon United States
Thomas Gridley United States
Terry P. Yamaguchi United States
Andreas Schedl relative to Hannu Sariola Finland Hannu Sariola's profile →
Citations per field
00.5×10×
Hannu Sariola · 1×
Citations per year

Countries citing papers authored by Andreas Schedl

Since Specialization
Citations

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

Fields of papers citing papers by Andreas Schedl

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown
#Work
1 20250
2 20238
3 202320
4 20237
5 202031
6 202016
7 202022
8 202013
9 201810
10 201815
11 201538
12 2012168
13 200939
14 20081
15 2004450
16 200476
17
The Sox9 transcription factor determines glial fate choice in the developing spinal cord
Hit paper breakdown →
2003509
18
WT1 is a key regulator of podocyte function
20022
19 2002128
20 199834

About Andreas Schedl

Andreas Schedl is a scholar working on Genetics, Molecular Biology, Urology, Reproductive Medicine and Developmental Neuroscience, having authored 116 papers that have together received 13.4k indexed citations. Recurring topics across this work include Renal and related cancers (51 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (32 papers), Sexual Differentiation and Disorders (15 papers), Renal cell carcinoma treatment (14 papers), Pluripotent Stem Cells Research (13 papers), Animal Genetics and Reproduction (12 papers), Genetic and Kidney Cyst Diseases (8 papers) and Wnt/β-catenin signaling in development and cancer (8 papers). The work is most often cited by research in Developmental Neuroscience (713 citations), Genetics (4.3k citations), Molecular Biology (9.6k citations), Reproductive Medicine (1.0k citations) and Cell Biology (1.8k citations). Andreas Schedl has collaborated with scholars based in France, Germany and United Kingdom. Frequent co-authors include Marie‐Christine Chaboissier, Valérie Vidal, Haruhiko Akiyama, Benoît De Crombrugghe, James F. Martin, Dirk G. de Rooij, Nicholas D. Hastie, James Briscoe, Veronica van Heyningen and Kay‐Dietrich Wagner. Their work appears in journals such as Genes & Development, Development, Human Molecular Genetics, Kidney International and Cell Reports.

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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