Fabienne Parente

578 citations
12 papers · 174 · h-index 8

Impact in

    • Metabolism and Genetic Disorders
    • Genomic variations and chromosomal abnormalities
    • Genomics and Rare Diseases
    • Genetics and Neurodevelopmental Disorders

Papers in

    • RNA and protein synthesis mechanisms 2
    • Congenital heart defects research 1
    • Genomic variations and chromosomal abnormalities 4
    • Genetics and Neurodevelopmental Disorders 2

Fabienne Parente

12 papers receiving 173 citations

Peers

Fabienne Parente
Comparison fields: 5 of 49
  • Clinical Biochemistry 15
  • Genetics 60
  • Cancer Research 29
  • Gastroenterology 8
  • Hematology 14
Replace Elisabeth Steichen with:
Elisabeth Steichen Austria
Kelly Kyker‐Snowman United States
Gaia Roversi Italy
Silvia Lechner Austria
Rosaria Polci Italy
Rini Rossanti Japan
Merlin Airik United States
Shouyue Sun China
Omid Omrani Germany
Fabienne Parente relative to Elisabeth Steichen Austria Elisabeth Steichen's profile →
Citations per field
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Citations per year

Countries citing papers authored by Fabienne Parente

Since Specialization
Citations

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

Fields of papers citing papers by Fabienne Parente

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

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

All Works

12 of 12 papers shown
#Work
1 199945
2 200932
3 199729
4 201822
5 199910
6 20219
7 20149
8 20167
9 19977
10 20152
11 20241
12 20241

About Fabienne Parente

Fabienne Parente is a scholar working on Molecular Biology, Genetics, Clinical Biochemistry, Surgery and Pulmonary and Respiratory Medicine, having authored 12 papers that have together received 174 indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (4 papers), Genomic variations and chromosomal abnormalities (4 papers), RNA and protein synthesis mechanisms (2 papers), Genetics and Neurodevelopmental Disorders (2 papers), Liver Disease and Transplantation (1 paper), Pancreatic function and diabetes (1 paper), Congenital heart defects research (1 paper) and Lysosomal Storage Disorders Research (1 paper). The work is most often cited by research in Clinical Biochemistry (15 citations), Genetics (60 citations), Cancer Research (29 citations), Gastroenterology (8 citations) and Hematology (14 citations). Fabienne Parente has collaborated with scholars based in Canada, France and United States. Frequent co-authors include Claude Turc‐Carel, Josiane Grosgeorge, Brian M. Gilfix, Nicholas Ah Mew, Philippe Terrier, Jean‐Michel Coindre, Jaak Jaeken, Georges F. Carle, Patrick Gaudray and Laura Russell. Their work appears in journals such as Clinica Chimica Acta, Frontiers in Pediatrics, Molecular Genetics and Metabolism, Journal of Biological Chemistry 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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