Erwin Petek

2.7k citations
69 papers · 2.2k · h-index 24

Impact in

Papers in

    • Genomic variations and chromosomal abnormalities 30
    • Genetics and Neurodevelopmental Disorders 7
    • Genomics and Rare Diseases 6
    • Genetic Associations and Epidemiology 4
    • Prenatal Screening and Diagnostics 6

Erwin Petek

68 papers receiving 2k citations

Peers

Erwin Petek
Comparison fields: 5 of 87
  • Genetics 599
  • Developmental Biology 40
  • Cellular and Molecular Neuroscience 294
  • Biochemistry 87
  • Pediatrics, Perinatology and Child Health 137
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Countries citing papers authored by Erwin Petek

Since Specialization
Citations

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

Fields of papers citing papers by Erwin Petek

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

20 of 20 papers shown

Showing the 20 most-cited of 69 papers — load more, or switch the sort, to bring in the rest.

#Work
1 2004320
2 2003166
3 2001153
4 2013127
5 2008121
6 201494
7 201567
8 200255
9 201853
10 200652
11 200350
12 201648
13 200147
14 200142
15 201642
16 200241
17 200140
18 200837
19 200333
20 200027

About Erwin Petek

Erwin Petek is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Reproductive Medicine, Developmental Biology and Cognitive Neuroscience, having authored 69 papers that have together received 2.2k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (30 papers), Genetics and Neurodevelopmental Disorders (7 papers), Genomics and Rare Diseases (6 papers), Prenatal Screening and Diagnostics (6 papers), Reproductive Biology and Fertility (4 papers), Genetic Associations and Epidemiology (4 papers), Autism Spectrum Disorder Research (4 papers) and Obsessive-Compulsive Spectrum Disorders (3 papers). The work is most often cited by research in Genetics (599 citations), Developmental Biology (40 citations), Cellular and Molecular Neuroscience (294 citations), Biochemistry (87 citations) and Pediatrics, Perinatology and Child Health (137 citations). Erwin Petek has collaborated with scholars based in Austria, Canada and Germany. Frequent co-authors include Christian Windpassinger, Klaus Wagner, Peter M. Kroisel, Stephen W. Scherer, Thomas Schwarzbraun, John B. Vincent, Joseph Cheung, Michaela Auer‐Grumbach, Omar Josef Shebl and Thomas Ebner. Their work appears in journals such as Cytogenetic and Genome Research, Clinical Genetics, Genomics, Journal of Medical Genetics and Gene.

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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