Géraldine Goudefroye

722 total citations
2 papers, 17 citations indexed

About

Géraldine Goudefroye is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Géraldine Goudefroye has authored 2 papers receiving a total of 17 indexed citations (citations by other indexed papers that have themselves been cited), including 1 paper in Molecular Biology, 1 paper in Genetics and 1 paper in Pediatrics, Perinatology and Child Health. Recurrent topics in Géraldine Goudefroye's work include Congenital heart defects research (1 paper), Genomic variations and chromosomal abnormalities (1 paper) and Tracheal and airway disorders (1 paper). Géraldine Goudefroye is often cited by papers focused on Congenital heart defects research (1 paper), Genomic variations and chromosomal abnormalities (1 paper) and Tracheal and airway disorders (1 paper). Géraldine Goudefroye collaborates with scholars based in France. Géraldine Goudefroye's co-authors include Heather Etchevers, Christelle Golzio, Michel Vekemans, Sophie Thomas, Tania Attié‐Bitach, Catherine Ozilou, N. Morichon-Delvallez, Fanny Bajolle, Véronique Abadie and Stanislas Lyonnet and has published in prestigious journals such as Prenatal Diagnosis and Archives of Cardiovascular Diseases Supplements.

In The Last Decade

Géraldine Goudefroye

1 paper receiving 6 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Géraldine Goudefroye France 1 14 9 4 3 1 2 17
Vinita Leedom United States 2 7 0.5× 6 0.7× 2 0.5× 5 1.7× 1 1.0× 5 12
Svetlana Kotzeva Italy 2 12 0.9× 4 0.4× 4 1.0× 7 2.3× 1 1.0× 3 19
Kimberly A. Schahl United States 2 23 1.6× 7 0.8× 2 0.7× 2 24
Marta Magno Italy 2 15 1.1× 5 0.6× 6 2.0× 1 1.0× 4 19
Shlomit Barzilai Israel 2 8 0.6× 8 0.9× 2 0.5× 11 3.7× 2 2.0× 4 26
Sandra Mercier France 2 14 1.0× 4 0.4× 3 1.0× 2 18
Tina K. Truong United States 2 18 1.3× 6 0.7× 1 0.3× 5 1.7× 3 24
Lucinda Antonacci-Fulton United States 2 13 0.9× 3 0.3× 2 0.5× 9 3.0× 2 15
Britta Schlott Kristiansen Denmark 2 7 0.5× 8 0.9× 4 1.3× 2 2.0× 4 12
Helen Coolican Australia 2 11 0.8× 3 0.3× 3 1.0× 3 15

Countries citing papers authored by Géraldine Goudefroye

Since Specialization
Citations

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

Fields of papers citing papers by Géraldine Goudefroye

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Géraldine Goudefroye

This figure shows the co-authorship network connecting the top 25 collaborators of Géraldine Goudefroye. A scholar is included among the top collaborators of Géraldine Goudefroye based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Géraldine Goudefroye. Géraldine Goudefroye is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

2 of 2 papers shown
1.
Parisot, Pauline, Fanny Bajolle, Tania Attié‐Bitach, et al.. (2010). 321 Congenital heart defects in CHARGE syndrome patients with CHD7 mutations. Archives of Cardiovascular Diseases Supplements. 2(1). 104–105.
2.
Golzio, Christelle, Catherine Ozilou, Sophie Thomas, et al.. (2006). Cytogenetic and histological features of a human embryo with homogeneous chromosome 8 trisomy. Prenatal Diagnosis. 26(13). 1201–1205. 17 indexed citations

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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