Leslie Ratié

402 total citations
10 papers, 221 citations indexed

About

Leslie Ratié is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Leslie Ratié has authored 10 papers receiving a total of 221 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 5 papers in Genetics and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in Leslie Ratié's work include Hedgehog Signaling Pathway Studies (6 papers), Mitochondrial Function and Pathology (3 papers) and Developmental Biology and Gene Regulation (3 papers). Leslie Ratié is often cited by papers focused on Hedgehog Signaling Pathway Studies (6 papers), Mitochondrial Function and Pathology (3 papers) and Developmental Biology and Gene Regulation (3 papers). Leslie Ratié collaborates with scholars based in France, Spain and United Kingdom. Leslie Ratié's co-authors include Valérie Dupé, Véronique David, Isabelle Gicquel, Sylvie Odent, Sandrine Humbert, Christèle Dubourg, Sandra Mercier, Laurent Pasquier, Claude Bendavid and Alain Buisson and has published in prestigious journals such as Science, Development and The Journal of Clinical Endocrinology & Metabolism.

In The Last Decade

Leslie Ratié

10 papers receiving 220 citations

Peers

Leslie Ratié

MB

GENET

CMN

PPCH

DN

Victoria‐Elisabeth Gruber Austria

Carissa Adams United States

Suzanne F. C. Miller-Delaney Ireland

Satoshi Miyashita Japan

Silvia Marenna Italy

Jacqueline A.C. Goos Netherlands

Beatriz R. Versiani Brazil

Blandine Esteva France

Yongjin Yoo South Korea

Tyrone DeSpenza United States

Victoria‐Elisabeth Gruber Austria

Leslie Ratié

118 ×0.7

MB

50 ×0.6

GENET

56 ×1.1

CMN

19 ×0.6

PPCH

29 ×1.5

DN

Citations per year, relative to Leslie Ratié Leslie Ratié (= 1×) peers Victoria‐Elisabeth Gruber

Countries citing papers authored by Leslie Ratié

Since Specialization

Citations

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

Fields of papers citing papers by Leslie Ratié

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Leslie Ratié

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

All Works

Sort: Min cites: Since: Top N: Style:

10 of 10 papers shown

1.

Ratié, Leslie & Sandrine Humbert. (2024). A developmental component to Huntington's disease. Revue Neurologique. 180(5). 357–362. 8 indexed citations

2.

Braz, Barbara Y., Leslie Ratié, Jean‐Christophe Deloulme, et al.. (2022). Treating early postnatal circuit defect delays Huntington’s disease onset and pathology in mice. Science. 377(6613). eabq5011–eabq5011. 49 indexed citations

3.

Hamdi‐Rozé, Houda, Leslie Ratié, Wilfrid Carré, et al.. (2020). Disrupted Hypothalamo-Pituitary Axis in Association With Reduced SHH Underlies the Pathogenesis of NOTCH-Deficiency. The Journal of Clinical Endocrinology & Metabolism. 105(9). e3183–e3196. 9 indexed citations

4.

Ratié, Leslie, Fernando García‐Moreno, Anna Hoerder‐Suabedissen, et al.. (2019). Loss of Dmrt5 Affects the Formation of the Subplate and Early Corticogenesis. Cerebral Cortex. 30(5). 3296–3312. 9 indexed citations

5.

Vézain, Myriam, Marina Rubio, Valérie Dupé, et al.. (2018). A de novo variant in ADGRL2 suggests a novel mechanism underlying the previously undescribed association of extreme microcephaly with severely reduced sulcation and rhombencephalosynapsis. Acta Neuropathologica Communications. 6(1). 109–109. 16 indexed citations

6.

Ratié, Leslie, Frédérique Barloy-Hubler, Isabelle Gicquel, et al.. (2013). Novel genes upregulated when NOTCH signalling is disrupted during hypothalamic development. Neural Development. 8(1). 25–25. 26 indexed citations

7.

Démurger, Florence, Laurent Pasquier, Christèle Dubourg, et al.. (2013). Array-CGH Analysis Suggests Genetic Heterogeneity in Rhombencephalosynapsis. Molecular Syndromology. 4(6). 267–272. 11 indexed citations

8.

Mercier, Sandra, Véronique David, Leslie Ratié, et al.. (2013). NODAL and SHH dose-dependent double inhibition promotes an HPE-like phenotype in chick embryos. Development. 140(5). e506–e506. 4 indexed citations

9.

Mercier, Sandra, Véronique David, Leslie Ratié, et al.. (2012). NODAL and SHH dose-dependent double inhibition promotes an HPE-like phenotype in chick embryos. Disease Models & Mechanisms. 6(2). 537–43. 16 indexed citations

10.

Mercier, Sandra, Christèle Dubourg, Nicolas Garcelon, et al.. (2011). New findings for phenotype–genotype correlations in a large European series of holoprosencephaly cases. Journal of Medical Genetics. 48(11). 752–760. 73 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.

Explore authors with similar magnitude of impact