Estelle Lopez

1.4k total citations
10 papers, 561 citations indexed

About

Estelle Lopez is a scholar working on Genetics, Molecular Biology and Immunology. According to data from OpenAlex, Estelle Lopez has authored 10 papers receiving a total of 561 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 5 papers in Molecular Biology and 2 papers in Immunology. Recurrent topics in Estelle Lopez's work include Craniofacial Disorders and Treatments (2 papers), Ocular Disorders and Treatments (2 papers) and Developmental Biology and Gene Regulation (2 papers). Estelle Lopez is often cited by papers focused on Craniofacial Disorders and Treatments (2 papers), Ocular Disorders and Treatments (2 papers) and Developmental Biology and Gene Regulation (2 papers). Estelle Lopez collaborates with scholars based in France, United States and Australia. Estelle Lopez's co-authors include Bryan L. Roth, Wesley K. Kroeze, Shamil Patel, Laurence Faivre, Christel Thauvin‐Robinet, Benoı̂t Arveiler, Didier Lacombe, Angèle Tingaud‐Sequeira, Caroline Rooryck and Bérénice Doray and has published in prestigious journals such as PLoS ONE, PLoS Biology and Cellular and Molecular Life Sciences.

In The Last Decade

Estelle Lopez

10 papers receiving 557 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Estelle Lopez France 7 328 216 132 91 54 10 561
Ritushree Kukreti India 14 175 0.5× 141 0.7× 38 0.3× 75 0.8× 46 0.9× 34 488
Meenal Gupta India 10 149 0.5× 130 0.6× 30 0.2× 53 0.6× 24 0.4× 18 433
Yangang Zhao China 15 182 0.6× 193 0.9× 21 0.2× 87 1.0× 25 0.5× 21 528
Julia Oosterom Netherlands 14 316 1.0× 56 0.3× 21 0.2× 168 1.8× 31 0.6× 16 900
Miquel Tuson Spain 10 571 1.7× 269 1.2× 15 0.1× 43 0.5× 93 1.7× 14 880
Diana Wu United States 7 361 1.1× 42 0.2× 48 0.4× 117 1.3× 100 1.9× 19 679
Frederick J. Troendle United States 7 220 0.7× 38 0.2× 33 0.3× 58 0.6× 66 1.2× 9 540
L. Michelle Lewis United States 13 584 1.8× 47 0.2× 32 0.2× 354 3.9× 47 0.9× 30 747
Jian‐Nong Ma United States 10 304 0.9× 66 0.3× 28 0.2× 232 2.5× 33 0.6× 17 452
Magnús Haraldsson Iceland 7 150 0.5× 78 0.4× 27 0.2× 14 0.2× 23 0.4× 17 337

Countries citing papers authored by Estelle Lopez

Since Specialization
Citations

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

Fields of papers citing papers by Estelle Lopez

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Estelle Lopez

This figure shows the co-authorship network connecting the top 25 collaborators of Estelle Lopez. A scholar is included among the top collaborators of Estelle Lopez 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 Estelle Lopez. Estelle Lopez 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.
Tingaud‐Sequeira, Angèle, Aurélien Trimouille, Rachel Stapleton, et al.. (2021). A recurrent missense variant in EYA3 gene is associated with oculo-auriculo-vertebral spectrum. Human Genetics. 140(6). 933–944. 16 indexed citations
2.
Tingaud‐Sequeira, Angèle, Aurélien Trimouille, Sandrine Marlin, et al.. (2020). Functional and genetic analyses of ZYG11B provide evidences for its involvement in OAVS. Molecular Genetics & Genomic Medicine. 8(10). e1375–e1375. 20 indexed citations
3.
Li, Chunmei, Victor L. Jensen, Kwangjin Park, et al.. (2016). MKS5 and CEP290 Dependent Assembly Pathway of the Ciliary Transition Zone. PLoS Biology. 14(3). e1002416–e1002416. 95 indexed citations
4.
Lopez, Estelle, Angèle Tingaud‐Sequeira, Sandrine Marlin, et al.. (2016). Mutations in MYT1, encoding the myelin transcription factor 1, are a rare cause of OAVS. Journal of Medical Genetics. 53(11). 752–760. 45 indexed citations
5.
Lopez, Estelle, et al.. (2013). Phosphorylated C/EBPβ Influences a Complex Network Involving YY1 and USF2 in Lung Epithelial Cells. PLoS ONE. 8(4). e60211–e60211. 6 indexed citations
6.
Lopez, Estelle, Patrick Callier, Valérie Cormier‐Daire, et al.. (2012). Search for a gene responsible for Floating‐Harbor syndrome on chromosome 12q15q21.1. American Journal of Medical Genetics Part A. 158A(2). 333–339. 6 indexed citations
7.
Courcet, Jean‐Benoît, Laurence Faivre, Perrine Malzac, et al.. (2012). The DYRK1A gene is a cause of syndromic intellectual disability with severe microcephaly and epilepsy. Journal of Medical Genetics. 49(12). 731–736. 80 indexed citations
8.
René, Céline, et al.. (2010). NF-E2-related factor 2, a key inducer of antioxidant defenses, negatively regulates the CFTR transcription. Cellular and Molecular Life Sciences. 67(13). 2297–2309. 23 indexed citations
9.
Lopez, Estelle, et al.. (2009). Evolución del diagnóstico prenatal delas anomalías cromosómicas en Asturias(España). Período 1990-2004. 2–7. 2 indexed citations
10.
Roth, Bryan L., Estelle Lopez, Shamil Patel, & Wesley K. Kroeze. (2000). The Multiplicity of Serotonin Receptors: Uselessly Diverse Molecules or an Embarrassment of Riches?. The Neuroscientist. 6(4). 252–262. 268 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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