Aline Dubos

430 total citations
11 papers, 249 citations indexed

About

Aline Dubos is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Aline Dubos has authored 11 papers receiving a total of 249 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 8 papers in Genetics and 2 papers in Cell Biology. Recurrent topics in Aline Dubos's work include Genetics and Neurodevelopmental Disorders (8 papers), Congenital heart defects research (3 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers). Aline Dubos is often cited by papers focused on Genetics and Neurodevelopmental Disorders (8 papers), Congenital heart defects research (3 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers). Aline Dubos collaborates with scholars based in France, Netherlands and United States. Aline Dubos's co-authors include Bernadett Boda, André Hanauer, Dominique Müller, Patricia Marques Pereira, Solange Pannetier, Hans van Bokhoven, Yann Hérault, Hubert Gaertner, Yann Bernardinelli and Oliver Hartley and has published in prestigious journals such as Nucleic Acids Research, Journal of Neuroscience and Scientific Reports.

In The Last Decade

Aline Dubos

10 papers receiving 248 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Aline Dubos France	8	162	131	54	27	27	11	249
M. Reza Jabalameli United Kingdom	10	147 0.9×	82 0.6×	65 1.2×	16 0.6×	30 1.1×	18	312
Sébastien Moutton France	12	212 1.3×	211 1.6×	64 1.2×	26 1.0×	45 1.7×	17	367
Manuela Loi Italy	12	190 1.2×	151 1.2×	39 0.7×	31 1.1×	18 0.7×	21	297
Lynne M. Overman United States	5	175 1.1×	104 0.8×	51 0.9×	59 2.2×	25 0.9×	6	273
Laura Gennaccaro Italy	12	168 1.0×	202 1.5×	46 0.9×	41 1.5×	12 0.4×	14	286
Susanna Raitano Belgium	7	148 0.9×	86 0.7×	56 1.0×	50 1.9×	20 0.7×	8	267
Margot R.F. Reijnders Netherlands	5	130 0.8×	110 0.8×	24 0.4×	24 0.9×	39 1.4×	5	204
Micaela Lasser United States	6	119 0.7×	59 0.5×	42 0.8×	22 0.8×	66 2.4×	8	216
Hyojin Kim United States	9	128 0.8×	94 0.7×	40 0.7×	36 1.3×	23 0.9×	14	231
Roberta De Filippis Italy	7	151 0.9×	118 0.9×	21 0.4×	55 2.0×	11 0.4×	11	256

Countries citing papers authored by Aline Dubos

Since Specialization

Citations

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

Fields of papers citing papers by Aline Dubos

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Aline Dubos

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

All Works

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11 of 11 papers shown

Hinckelmann, María-Victoria, Aline Dubos, Gabrielle Rudolf, et al.. (2025). Interneuron migration defects during corticogenesis contribute to Dyrk1a haploinsufficiency syndrome pathogenesis. Molecular Psychiatry. 30(11). 5227–5244.

Méziane, Hamid, Marie‐Christine Birling, Olivia Wendling, et al.. (2022). Large-Scale Functional Assessment of Genes Involved in Rare Diseases with Intellectual Disabilities Unravels Unique Developmental and Behaviour Profiles in Mouse Models. Biomedicines. 10(12). 3148–3148. 1 indexed citations

Dubos, Aline, Hamid Méziane, Giovanni Iacono, et al.. (2018). A new mouse model of ARX dup24 recapitulates the patients’ behavioral and fine motor alterations. Human Molecular Genetics. 27(12). 2138–2153. 14 indexed citations

Iacono, Giovanni, Aline Dubos, Hamid Méziane, et al.. (2018). Increased H3K9 methylation and impaired expression of Protocadherins are associated with the cognitive dysfunctions of the Kleefstra syndrome. Nucleic Acids Research. 46(10). 4950–4965. 31 indexed citations

Wendling, Olivia, Marie‐France Champy, Guillaume Pavlovic, et al.. (2017). Atp6ap2 ablation in adult mice impairs viability through multiple organ deficiencies. Scientific Reports. 7(1). 9618–9618. 21 indexed citations

Iacono, Giovanni, Marco Benevento, Aline Dubos, et al.. (2017). Integrated transcriptional analysis unveils the dynamics of cellular differentiation in the developing mouse hippocampus. Scientific Reports. 7(1). 18073–18073. 7 indexed citations

Dubos, Aline, Yann Bernardinelli, Jean‐Vianney Barnier, et al.. (2012). Alteration of Synaptic Network Dynamics by the Intellectual Disability Protein PAK3. Journal of Neuroscience. 32(2). 519–527. 38 indexed citations

Boda, Bernadett, Aline Dubos, & Dominique Müller. (2010). Signaling mechanisms regulating synapse formation and function in mental retardation. Current Opinion in Neurobiology. 20(4). 519–527. 41 indexed citations

Dubos, Aline, Solange Pannetier, & André Hanauer. (2008). Inactivation of the CDKL3 gene at 5q31.1 by a balanced t(X;5) translocation associated with nonspecific mild mental retardation. American Journal of Medical Genetics Part A. 146A(10). 1267–1279. 18 indexed citations

10.

Dubos, Aline, et al.. (2006). Identification of novel mutations in the RSK2 gene (RPS6KA3) in patients with Coffin–Lowry syndrome. Clinical Genetics. 70(2). 161–166. 33 indexed citations

11.

Dubos, Aline, Fatima Abidi, Gotthold Barbi, et al.. (2005). Disruptions of the novel KIAA1202 gene are associated with X-linked mental retardation. Human Genetics. 118(5). 578–590. 45 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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