Patrick Frosk

2.0k citations
18 papers · 618 · h-index 10

Impact in

Papers in

    • RNA Research and Splicing 5
    • Muscle Physiology and Disorders 5
    • Nuclear Structure and Function 2
    • RNA and protein synthesis mechanisms 2
    • Genetics and Neurodevelopmental Disorders 3
    • Genomic variations and chromosomal abnormalities 2

Patrick Frosk

18 papers receiving 599 citations

Peers

Patrick Frosk
Comparison fields: 5 of 60
  • Molecular Biology 495
  • Cellular and Molecular Neuroscience 119
  • Cardiology and Cardiovascular Medicine 140
  • Genetics 59
  • Immunology 101
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Patrick Frosk relative to Edward Nylen Canada Edward Nylen's profile →
Citations per field
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Edward Nylen · 1×
Citations per year

Countries citing papers authored by Patrick Frosk

Since Specialization
Citations

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

Fields of papers citing papers by Patrick Frosk

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

18 of 18 papers shown
#Work
1 2002188
2 200481
3 200677
4 200571
5 200453
6 201735
7 201935
8 200522
9 201213
10 202110
11 20189
12 20159
13 20074
14 20203
15 20093
16 20242
17 20122
18 20161

About Patrick Frosk

Patrick Frosk is a scholar working on Molecular Biology, Genetics, Cellular and Molecular Neuroscience, Surgery and Cardiology and Cardiovascular Medicine, having authored 18 papers that have together received 618 indexed citations. Recurring topics across this work include RNA Research and Splicing (5 papers), Muscle Physiology and Disorders (5 papers), Genetic Neurodegenerative Diseases (3 papers), Genetics and Neurodevelopmental Disorders (3 papers), Nuclear Structure and Function (2 papers), RNA and protein synthesis mechanisms (2 papers), Vascular Malformations and Hemangiomas (2 papers) and Genomic variations and chromosomal abnormalities (2 papers). The work is most often cited by research in Molecular Biology (495 citations), Cellular and Molecular Neuroscience (119 citations), Cardiology and Cardiovascular Medicine (140 citations), Genetics (59 citations) and Immunology (101 citations). Patrick Frosk has collaborated with scholars based in Canada, United States and Germany. Frequent co-authors include Klaus Wrogemann, Cheryl R. Greenberg, Edward Nylen, Takuya Fujiwara, Kenneth Morgan, Tracey Weiler, Thangirala Sudha, Benedikt Schoser, Hanns Lochmüller and Andrew G. Engel. Their work appears in journals such as Journal of Child Neurology, Annals of Neurology, Human Molecular Genetics, European Journal of Human Genetics 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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