Constance Wells

489 total citations
11 papers, 124 citations indexed

About

Constance Wells is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Constance Wells has authored 11 papers receiving a total of 124 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 5 papers in Genetics and 2 papers in Surgery. Recurrent topics in Constance Wells's work include Genomic variations and chromosomal abnormalities (3 papers), Amino Acid Enzymes and Metabolism (1 paper) and Neonatal and fetal brain pathology (1 paper). Constance Wells is often cited by papers focused on Genomic variations and chromosomal abnormalities (3 papers), Amino Acid Enzymes and Metabolism (1 paper) and Neonatal and fetal brain pathology (1 paper). Constance Wells collaborates with scholars based in France, Netherlands and Australia. Constance Wells's co-authors include Guillaume Captier, E. Mousty, F. Fuchs, Pierre Boulot, M. Bigorre, Jean Michel Faure, Tania Attié‐Bitach, Alexia Savignoni, François Doz and J. Stirnemann and has published in prestigious journals such as The American Journal of Human Genetics, Investigative Ophthalmology & Visual Science and Prenatal Diagnosis.

In The Last Decade

Constance Wells

10 papers receiving 119 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Constance Wells France 7 61 49 23 20 15 11 124
Arjan Bouman Netherlands 8 73 1.2× 68 1.4× 21 0.9× 6 0.3× 16 1.1× 14 146
Becky Treacy United Kingdom 5 139 2.3× 60 1.2× 34 1.5× 8 0.4× 31 2.1× 5 195
Vyne van der Schoot Netherlands 8 98 1.6× 48 1.0× 56 2.4× 7 0.3× 12 0.8× 15 182
Maryam Rafati Iran 6 17 0.3× 45 0.9× 16 0.7× 11 0.6× 5 0.3× 22 90
Cathleen M. Cronin United States 5 51 0.8× 29 0.6× 33 1.4× 11 0.6× 12 0.8× 6 109
Anne‐Sophie Jourdain France 6 50 0.8× 99 2.0× 7 0.3× 6 0.3× 4 0.3× 9 154
Shamsa Anazi Saudi Arabia 5 68 1.1× 52 1.1× 26 1.1× 6 0.3× 49 3.3× 6 180
Rocío Mena Spain 7 75 1.2× 65 1.3× 32 1.4× 27 1.4× 2 0.1× 16 182
Richard Lao United States 4 68 1.1× 51 1.0× 4 0.2× 23 1.1× 13 0.9× 7 117
Ulrik Kristoffer Stoltze Denmark 8 55 0.9× 73 1.5× 39 1.7× 8 0.4× 2 0.1× 19 137

Countries citing papers authored by Constance Wells

Since Specialization
Citations

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

Fields of papers citing papers by Constance Wells

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Constance Wells

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

All Works

11 of 11 papers shown
1.
Fuchs, F., E. Mousty, Denis Morin, et al.. (2023). Postnatal outcome of children with antenatal colonic hyperechogenicity. Prenatal Diagnosis. 44(1). 28–34.
2.
Willems, Marjolaine, et al.. (2022). Hypolacrimia and Alacrimia as Diagnostic Features for Genetic or Congenital Conditions. Investigative Ophthalmology & Visual Science. 63(9). 3–3. 2 indexed citations
3.
Lamouroux, Audrey, Constance Wells, E. Mousty, et al.. (2022). Extending the prenatal Noonan's phenotype by review of ultrasound and autopsy data. Prenatal Diagnosis. 42(5). 574–582. 6 indexed citations
4.
Fuchs, F., E. Mousty, Estelle Morau, et al.. (2021). Use of Remifentanil Associated with Lidocaine for Feticides in Late Terminations of Pregnancy: A Randomized Clinical Trial. Fetal Diagnosis and Therapy. 48(11-12). 812–818. 1 indexed citations
5.
Faure, Jean Michel, E. Mousty, M. Bigorre, et al.. (2020). Prenatal ultrasound diagnosis of cleft palate without cleft lip, the new ultrasound semiology. Prenatal Diagnosis. 40(11). 1447–1458. 26 indexed citations
6.
Yauy, Kévin, Anouck Schneider, Bee Ling Ng, et al.. (2019). Disruption of chromatin organisation causes MEF2C gene overexpression in intellectual disability: a case report. BMC Medical Genomics. 12(1). 116–116. 8 indexed citations
7.
Thévenon, Julien, Yannis Duffourd, Sophie Nambot, et al.. (2018). TBL1XR1 mutations in Pierpont syndrome are not restricted to the recurrent p.Tyr446Cys mutation. American Journal of Medical Genetics Part A. 176(12). 2813–2818. 12 indexed citations
8.
Millot, Gaël A., Constance Wells, Hervé J. Brisse, et al.. (2018). Correlation between RB1germline mutations and second primary malignancies in hereditary retinoblastoma patients treated with external beam radiotherapy. European Journal of Medical Genetics. 62(3). 217–223. 23 indexed citations
9.
Cameron‐Christie, Sophia, Constance Wells, Marleen Simon, et al.. (2018). Recessive Spondylocarpotarsal Synostosis Syndrome Due to Compound Heterozygosity for Variants in MYH3. The American Journal of Human Genetics. 102(6). 1115–1125. 22 indexed citations
10.
Wells, Constance, Natalie Loundon, N Garabédian, et al.. (2016). A case of mild CHARGE syndrome associated with a splice site mutation in CHD7. European Journal of Medical Genetics. 59(4). 195–197. 6 indexed citations
11.
Wells, Constance, Emmanuel Spaggiari, Valérie Malan, et al.. (2015). First fetal case of the 8q24.3 contiguous genes syndrome. American Journal of Medical Genetics Part A. 170(1). 239–242. 18 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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