Damien Haye

1.1k total citations
10 papers, 131 citations indexed

About

Damien Haye is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Damien Haye has authored 10 papers receiving a total of 131 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 4 papers in Genetics and 3 papers in Genetics. Recurrent topics in Damien Haye's work include RNA modifications and cancer (2 papers), Neurogenetic and Muscular Disorders Research (2 papers) and RNA Research and Splicing (2 papers). Damien Haye is often cited by papers focused on RNA modifications and cancer (2 papers), Neurogenetic and Muscular Disorders Research (2 papers) and RNA Research and Splicing (2 papers). Damien Haye collaborates with scholars based in France, United Kingdom and French Guiana. Damien Haye's co-authors include Alain Verloès, Jonathan Lévy, Brigitte Benzacken, Annick Toutain, Céline Dupont, Anne‐Claude Tabet, Eva Pipiras, N. Teissier, Cyril Mignot and Boris Keren and has published in prestigious journals such as Molecular Psychiatry, Cells and Human Genetics.

In The Last Decade

Damien Haye

10 papers receiving 128 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Damien Haye France 9 83 41 30 16 10 10 131
Marisol Mirabelli-Badenier Italy 10 104 1.3× 100 2.4× 29 1.0× 14 0.9× 13 1.3× 13 238
Janet Song United States 7 108 1.3× 43 1.0× 34 1.1× 12 0.8× 5 0.5× 11 200
Kristin D. Kernohan Canada 4 69 0.8× 38 0.9× 12 0.4× 9 0.6× 11 1.1× 4 112
Adel Qalieh United States 6 83 1.0× 14 0.3× 13 0.4× 20 1.3× 9 0.9× 6 135
D. G. Hernandez United Kingdom 3 67 0.8× 43 1.0× 45 1.5× 6 0.4× 6 0.6× 3 216
Selina Reich Germany 5 96 1.2× 24 0.6× 37 1.2× 20 1.3× 3 0.3× 8 127
Rafael E. Flores‐Obando United States 8 100 1.2× 33 0.8× 21 0.7× 11 0.7× 9 0.9× 18 198
Thuong Ha Australia 6 77 0.9× 47 1.1× 13 0.4× 16 1.0× 6 0.6× 13 136
Lauren Grote United States 6 105 1.3× 88 2.1× 36 1.2× 10 0.6× 12 1.2× 7 186
Lorida Llaci United States 8 95 1.1× 25 0.6× 13 0.4× 12 0.8× 11 1.1× 12 170

Countries citing papers authored by Damien Haye

Since Specialization
Citations

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

Fields of papers citing papers by Damien Haye

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Damien Haye

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

All Works

10 of 10 papers shown
1.
Désir, Julie, Damien Haye, Pauline Le Tanno, et al.. (2022). Perinatal presentations of non‐immune hydrops fetalis due to recessive PIEZO1 disease: A challenging fetal diagnosis. Clinical Genetics. 103(5). 560–565. 3 indexed citations
2.
Jeanne, Médéric, Marie‐Laure Vuillaume, Valerie E. Vancollie, et al.. (2021). Haploinsufficiency of the HIRA gene located in the 22q11 deletion syndrome region is associated with abnormal neurodevelopment and impaired dendritic outgrowth. Human Genetics. 140(6). 885–896. 14 indexed citations
3.
Khouri, Elma El, Jamal Ghoumid, Damien Haye, et al.. (2021). Wnt/β-catenin pathway and cell adhesion deregulation in CSDE1-related intellectual disability and autism spectrum disorders. Molecular Psychiatry. 26(7). 3572–3585. 11 indexed citations
4.
Vermehren‐Schmaedick, Anke, Sarah C. Reed, Gary A. Bellus, et al.. (2021). Characterization of PARP6 Function in Knockout Mice and Patients with Developmental Delay. Cells. 10(6). 1289–1289. 9 indexed citations
5.
Gaston, Véronique, Isabelle Meunier, Sabine Sigaudy, et al.. (2020). Confirmation of FZD5 implication in a cohort of 50 patients with ocular coloboma. European Journal of Human Genetics. 29(1). 131–140. 10 indexed citations
6.
Lévy, Jonathan, Damien Haye, Nicola Marziliano, et al.. (2018). EFNB2haploinsufficiency causes a syndromic neurodevelopmental disorder. Clinical Genetics. 93(6). 1141–1147. 19 indexed citations
7.
Lévy, Jonathan, Sarah Grotto, Cyril Mignot, et al.. (2018). NR4A2 haploinsufficiency is associated with intellectual disability and autism spectrum disorder. Clinical Genetics. 94(2). 264–268. 25 indexed citations
8.
Vial, Yoann, Damien Haye, Sandrine Passemard, et al.. (2017). Phosphoglycerate dehydrogenase (PHGDH) deficiency without epilepsy mimicking primary microcephaly. American Journal of Medical Genetics Part A. 173(7). 1936–1942. 8 indexed citations
9.
Haye, Damien, Jonathan Lévy, Véronique Lambert, et al.. (2016). Failure of ossification of the occipital bone in mandibuloacral dysplasia type B. American Journal of Medical Genetics Part A. 170(10). 2750–2755. 11 indexed citations
10.
Haye, Damien, et al.. (2014). Prenatal findings in carpenter syndrome and a novel mutation in RAB23. American Journal of Medical Genetics Part A. 164(11). 2926–2930. 21 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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