Yannis Duffourd

2.3k total citations
8 papers, 266 citations indexed

About

Yannis Duffourd is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Yannis Duffourd has authored 8 papers receiving a total of 266 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 7 papers in Genetics and 1 paper in Surgery. Recurrent topics in Yannis Duffourd's work include Genomics and Rare Diseases (2 papers), Genetic Syndromes and Imprinting (2 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Yannis Duffourd is often cited by papers focused on Genomics and Rare Diseases (2 papers), Genetic Syndromes and Imprinting (2 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Yannis Duffourd collaborates with scholars based in France, United States and India. Yannis Duffourd's co-authors include Julien Thévenon, Judith St‐Onge, Laurence Faivre, Alice Masurel‐Paulet, Mathilde Lefebvre, Patrick Callier, Jean‐Baptiste Rivière, Frédéric Huet, Christel Thauvin‐Robinet and François Feillet and has published in prestigious journals such as Human Reproduction, British Journal of Dermatology and Clinical Genetics.

In The Last Decade

Yannis Duffourd

8 papers receiving 263 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yannis Duffourd France 7 201 125 38 15 14 8 266
Benjamin Kamien Australia 9 128 0.6× 124 1.0× 42 1.1× 14 0.9× 10 0.7× 19 228
Tracy Dudding‐Byth Australia 10 146 0.7× 147 1.2× 37 1.0× 24 1.6× 9 0.6× 18 272
Érika L. Freitas Brazil 10 122 0.6× 112 0.9× 32 0.8× 6 0.4× 18 1.3× 16 260
Yukiko Kuroda Japan 11 178 0.9× 127 1.0× 31 0.8× 16 1.1× 12 0.9× 40 271
Laurence Faivre France 6 188 0.9× 117 0.9× 27 0.7× 6 0.4× 14 1.0× 7 252
Mary Willis United States 10 197 1.0× 200 1.6× 55 1.4× 7 0.5× 9 0.6× 17 361
Juliette Piard France 10 121 0.6× 151 1.2× 16 0.4× 16 1.1× 10 0.7× 24 253
Lee Zellmer United States 7 203 1.0× 88 0.7× 32 0.8× 8 0.5× 39 2.8× 8 257
Dingge Ying Hong Kong 9 147 0.7× 156 1.2× 25 0.7× 29 1.9× 11 0.8× 16 313
Dhanya Lakshmi Narayanan India 10 88 0.4× 135 1.1× 22 0.6× 8 0.5× 13 0.9× 42 261

Countries citing papers authored by Yannis Duffourd

Since Specialization
Citations

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

Fields of papers citing papers by Yannis Duffourd

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yannis Duffourd

This figure shows the co-authorship network connecting the top 25 collaborators of Yannis Duffourd. A scholar is included among the top collaborators of Yannis Duffourd 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 Yannis Duffourd. Yannis Duffourd is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

8 of 8 papers shown
1.
Bonnet, Céline, Virginie Roth, Yannis Duffourd, et al.. (2024). Patient with a heterozygous pathogenic variant in CSNK2A1 gene: A new case to update the Okur–Chung neurodevelopmental syndrome. American Journal of Medical Genetics Part A. 194(9). e63642–e63642. 1 indexed citations
2.
Barberet, Julie, Christine Binquet, Cécile Choux, et al.. (2020). Do assisted reproductive technologies andin vitroembryo culture influence the epigenetic control of imprinted genes and transposable elements in children?. Human Reproduction. 36(2). 479–492. 26 indexed citations
3.
Thévenon, Julien, Laurence Duplomb, Shubha R. Phadke, et al.. (2016). Autosomal recessive IFT57 hypomorphic mutation cause ciliary transport defect in unclassified oral–facial–digital syndrome with short stature and brachymesophalangia. Clinical Genetics. 90(6). 509–517. 18 indexed citations
4.
Kuentz, Paul, Sylvie Fraïtag, M. Gonzalés, et al.. (2016). Mosaic‐activating FGFR2 mutation in two fetuses with papillomatous pedunculated sebaceous naevus. British Journal of Dermatology. 176(1). 204–208. 11 indexed citations
5.
Allou, Lila, Sophie Julia, Daniel Amsallem, et al.. (2016). Rett‐like phenotypes: expanding the genetic heterogeneity to the KCNA2 gene and first familial case of CDKL5‐related disease. Clinical Genetics. 91(3). 431–440. 33 indexed citations
6.
Bruel, Ange‐Line, Alice Masurel‐Paulet, Jean‐Baptiste Rivière, et al.. (2016). Autosomal recessive truncating MAB21L1 mutation associated with a syndromic scrotal agenesis. Clinical Genetics. 91(2). 333–338. 13 indexed citations
7.
Lefebvre, Mathilde, Yannis Duffourd, Charlotte Pöe, et al.. (2016). Autosomal recessive variations of TBX6, from congenital scoliosis to spondylocostal dysostosis. Clinical Genetics. 91(6). 908–912. 26 indexed citations
8.
Thévenon, Julien, Yannis Duffourd, Alice Masurel‐Paulet, et al.. (2016). Diagnostic odyssey in severe neurodevelopmental disorders: toward clinical whole‐exome sequencing as a first‐line diagnostic test. Clinical Genetics. 89(6). 700–707. 138 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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