Adrien Georges

1.9k total citations
30 papers, 1.0k citations indexed

About

Adrien Georges is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Genetics. According to data from OpenAlex, Adrien Georges has authored 30 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Molecular Biology, 8 papers in Cardiology and Cardiovascular Medicine and 8 papers in Genetics. Recurrent topics in Adrien Georges's work include FOXO transcription factor regulation (9 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers) and Congenital heart defects research (4 papers). Adrien Georges is often cited by papers focused on FOXO transcription factor regulation (9 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers) and Congenital heart defects research (4 papers). Adrien Georges collaborates with scholars based in France, United States and Belgium. Adrien Georges's co-authors include Reiner A. Veitia, Anne‐Laure Todeschini, David L’Hôte, Bérénice A. Benayoun, Sandrine Caburet, Aurélie Auguste, Anne Vanet, Aurélie Dipietromaria, Angela M. Belcher and Ahmad S. Khalil and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nucleic Acids Research and PLoS ONE.

In The Last Decade

Adrien Georges

29 papers receiving 1.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Adrien Georges France 14 596 348 195 190 128 30 1.0k
Nicola Reynolds United Kingdom 18 1.2k 2.0× 321 0.9× 123 0.6× 111 0.6× 113 0.9× 26 1.5k
Brendan Doe United Kingdom 11 674 1.1× 304 0.9× 214 1.1× 240 1.3× 39 0.3× 16 1.2k
Natalie K. Ryan Australia 14 720 1.2× 181 0.5× 213 1.1× 153 0.8× 37 0.3× 20 1.4k
Chie Murata Japan 11 326 0.5× 168 0.5× 88 0.5× 72 0.4× 120 0.9× 21 771
Annekatrien Boel Belgium 18 479 0.8× 176 0.5× 182 0.9× 292 1.5× 47 0.4× 41 814
Yael Kalma Israel 15 1.1k 1.9× 205 0.6× 203 1.0× 211 1.1× 77 0.6× 36 1.5k
Dachang Tao China 18 623 1.0× 239 0.7× 215 1.1× 90 0.5× 38 0.3× 67 1000
Judith Reichmann United Kingdom 10 850 1.4× 228 0.7× 48 0.2× 116 0.6× 60 0.5× 12 1.0k
Taichi Noda Japan 22 593 1.0× 344 1.0× 554 2.8× 456 2.4× 55 0.4× 56 1.2k
Alphons P. M. Stassen Netherlands 17 681 1.1× 272 0.8× 69 0.4× 179 0.9× 33 0.3× 30 1.1k

Countries citing papers authored by Adrien Georges

Since Specialization
Citations

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

Fields of papers citing papers by Adrien Georges

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Adrien Georges

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

All Works

20 of 20 papers shown
1.
Liu, Yingwei, et al.. (2024). LRP1 Repression by SNAIL Results in ECM Remodeling in Genetic Risk for Vascular Diseases. Circulation Research. 135(11). 1084–1097. 2 indexed citations
2.
Yu, Mengyao, Catherine Tcheandjieu, Adrien Georges, et al.. (2022). Computational estimates of annular diameter reveal genetic determinants of mitral valve function and disease. JCI Insight. 7(3). 6 indexed citations
3.
Jouve, Charlène, et al.. (2022). Epigenetic regulation at LRP1 risk locus for cardiovascular diseases and assessment of cellular function in hiPSC derived smooth muscle cells. Cardiovascular Research. 118(Supplement_1). 1 indexed citations
4.
Kyryachenko, Sergiy, Adrien Georges, Mengyao Yu, et al.. (2021). Chromatin Accessibility of Human Mitral Valves and Functional Assessment of MVP Risk Loci. Circulation Research. 128(5). e84–e101. 12 indexed citations
5.
Ait‐Oufella, Hafid, Mengyao Yu, Salma Kotti, et al.. (2021). Plasma and genetic determinants of soluble TREM-1 and major adverse cardiovascular events in a prospective cohort of acute myocardial infarction patients. Results from the FAST-MI 2010 study. International Journal of Cardiology. 344. 213–219. 6 indexed citations
6.
Georges, Adrien, Juliette Albuisson, Aurélien Lorthioir, et al.. (2020). Rare loss-of-function mutations of PTGIR identified in fibromuscular dysplasia and spontaneous coronary artery dissection. Archives of Cardiovascular Diseases Supplements. 12(2-4). 216–216. 1 indexed citations
7.
Job, Sylvie, Adrien Georges, Nelly Burnichon, et al.. (2019). Transcriptome Analysis of lncRNAs in Pheochromocytomas and Paragangliomas. The Journal of Clinical Endocrinology & Metabolism. 105(3). 898–907. 13 indexed citations
8.
Georges, Adrien, et al.. (2019). Functional interplay between Mediator and RNA polymerase II in Rad2/XPG loading to the chromatin. Nucleic Acids Research. 47(17). 8988–9004. 12 indexed citations
9.
Georges, Adrien & Nabila Bouatia‐Naji. (2019). La génétique établit le lien entre plusieurs maladies cardiovasculaires affectant préférentiellement les femmes. médecine/sciences. 35(8-9). 605–607.
10.
Yu, Mengyao, Adrien Georges, Nathan R. Tucker, et al.. (2019). Genome-Wide Association Study–Driven Gene-Set Analyses, Genetic, and Functional Follow-Up Suggest GLIS1 as a Susceptibility Gene for Mitral Valve Prolapse. Circulation Genomic and Precision Medicine. 12(5). e002497–e002497. 22 indexed citations
11.
Monaco, Silvia Di, Adrien Georges, Jean‐Philippe Lengelé, Miikka Vikkula, & Alexandre Persu. (2018). Genomics of Fibromuscular Dysplasia. International Journal of Molecular Sciences. 19(5). 1526–1526. 24 indexed citations
12.
Anttonen, Mikko, Marjut Pihlajoki, Noora Andersson, et al.. (2014). FOXL2, GATA4, and SMAD3 Co-Operatively Modulate Gene Expression, Cell Viability and Apoptosis in Ovarian Granulosa Cell Tumor Cells. PLoS ONE. 9(1). e85545–e85545. 49 indexed citations
13.
Todeschini, Anne‐Laure, Adrien Georges, & Reiner A. Veitia. (2014). Transcription factors: specific DNA binding and specific gene regulation. Trends in Genetics. 30(6). 211–219. 144 indexed citations
14.
Georges, Adrien, et al.. (2013). FOXL2: a central transcription factor of the ovary. Journal of Molecular Endocrinology. 52(1). R17–R33. 132 indexed citations
15.
Georges, Adrien, et al.. (2013). Interaction with the Yes‐associated protein (YAP) allows TEAD1 to positively regulate NAIP expression. FEBS Letters. 587(19). 3216–3223. 11 indexed citations
16.
L’Hôte, David, Adrien Georges, Anne‐Laure Todeschini, et al.. (2012). Discovery of novel protein partners of the transcription factor FOXL2 provides insights into its physiopathological roles. Human Molecular Genetics. 21(14). 3264–3274. 39 indexed citations
17.
Benayoun, Bérénice A., Adrien Georges, David L’Hôte, et al.. (2011). Transcription factor FOXL2 protects granulosa cells from stress and delays cell cycle: role of its regulation by the SIRT1 deacetylase. Human Molecular Genetics. 20(9). 1673–1686. 77 indexed citations
18.
Todeschini, Anne‐Laure, Aurélie Dipietromaria, David L’Hôte, et al.. (2011). Mutational probing of the forkhead domain of the transcription factor FOXL2 provides insights into the pathogenicity of naturally occurring mutations. Human Molecular Genetics. 20(17). 3376–3385. 16 indexed citations
19.
Caburet, Sandrine, Adrien Georges, David L’Hôte, et al.. (2011). The transcription factor FOXL2: At the crossroads of ovarian physiology and pathology. Molecular and Cellular Endocrinology. 356(1-2). 55–64. 67 indexed citations
20.
Benayoun, Bérénice A., Sandrine Caburet, Aurélie Dipietromaria, et al.. (2010). Functional Exploration of the Adult Ovarian Granulosa Cell Tumor-Associated Somatic FOXL2 Mutation p.Cys134Trp (c.402C>G). PLoS ONE. 5(1). e8789–e8789. 64 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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