André Hanauer

8.1k total citations · 2 hit papers
86 papers, 5.5k citations indexed

About

André Hanauer is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, André Hanauer has authored 86 papers receiving a total of 5.5k indexed citations (citations by other indexed papers that have themselves been cited), including 68 papers in Molecular Biology, 50 papers in Genetics and 12 papers in Cellular and Molecular Neuroscience. Recurrent topics in André Hanauer's work include Genetics and Neurodevelopmental Disorders (42 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (15 papers) and Chromatin Remodeling and Cancer (9 papers). André Hanauer is often cited by papers focused on Genetics and Neurodevelopmental Disorders (42 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (15 papers) and Chromatin Remodeling and Cancer (9 papers). André Hanauer collaborates with scholars based in France, United States and United Kingdom. André Hanauer's co-authors include Jean‐Louis Mandel, Sylvie Jacquot, Paolo Sassone‐Corsi, I. Oberlé, M. F. Bertheas, Didier Devys, Dominique Heitz, F. Rousseau, J Boué and Christine Kretz and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

André Hanauer

86 papers receiving 5.4k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Instability of a 550-Base Pair DNA Segment and Abnormal Methylation in Fragile X Syndrome

1991 1.2k citations I. Oberlé, André Hanauer et al. Science profile →
ATF4 Is a Substrate of RSK2 and an Essential Regulator of Osteoblast Biology

2004 653 citations Sylvie Jacquot, Paolo Sassone‐Corsi et al. profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
André Hanauer France	35	4.0k	2.5k	771	657	532	86	5.5k
Melanie Pritchard Australia	36	2.9k 0.7×	2.2k 0.9×	554 0.7×	780 1.2×	321 0.6×	77	4.8k
Vera M. Kalscheuer Germany	45	4.4k 1.1×	3.6k 1.4×	586 0.8×	407 0.6×	405 0.8×	152	6.7k
Helger G. Yntema Netherlands	35	2.7k 0.7×	2.6k 1.0×	372 0.5×	401 0.6×	399 0.8×	100	4.9k
Aimee K. Ryan Canada	22	4.0k 1.0×	1.9k 0.7×	556 0.7×	204 0.3×	351 0.7×	48	5.7k
Tjitske Kleefstra Netherlands	38	3.4k 0.8×	3.7k 1.4×	483 0.6×	696 1.1×	446 0.8×	131	5.7k
Fred A. Pereira United States	31	2.3k 0.6×	919 0.4×	558 0.7×	385 0.6×	370 0.7×	65	3.9k
Hilde Van Esch Belgium	40	3.5k 0.9×	3.5k 1.4×	338 0.4×	682 1.0×	352 0.7×	148	5.6k
Chérif Beldjord France	30	2.5k 0.6×	1.3k 0.5×	686 0.9×	266 0.4×	698 1.3×	59	4.3k
Dietrich Stephan United States	32	2.3k 0.6×	812 0.3×	520 0.7×	371 0.6×	334 0.6×	78	3.9k
Pierre Billuart France	30	2.4k 0.6×	1.1k 0.4×	887 1.2×	229 0.3×	769 1.4×	63	3.8k

Countries citing papers authored by André Hanauer

Since Specialization

Citations

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

Fields of papers citing papers by André Hanauer

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of André Hanauer

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

All Works

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20 of 20 papers shown

Hanauer, André, et al.. (2018). Selective alteration of adult hippocampal neurogenesis and impaired spatial pattern separation performance in the RSK2-deficient mouse model of Coffin-Lowry syndrome. Neurobiology of Disease. 115. 69–81. 11 indexed citations

Mehmood, Tahir, Anne Schneider, Jérémie Sibille, et al.. (2010). Transcriptome profile reveals AMPA receptor dysfunction in the hippocampus of the Rsk2-knockout mice, an animal model of Coffin–Lowry syndrome. Human Genetics. 129(3). 255–269. 18 indexed citations

Fischer, Matthias, Patricia Marques Pereira, Bettina Holtmann, et al.. (2009). P90 Ribosomal s6 kinase 2 negatively regulates axon growth in motoneurons. Molecular and Cellular Neuroscience. 42(2). 134–141. 15 indexed citations

Dumont, Julien, Muriel Umbhauer, Pascale Rassinier, André Hanauer, & Marie‐Hélène Verlhac. (2005). p90Rsk is not involved in cytostatic factor arrest in mouse oocytes. The Journal of Cell Biology. 169(2). 227–231. 64 indexed citations

Pronicka, Ewa, et al.. (2005). Genetic background of HSH in three Polish families and a patient with an X;9 translocation. European Journal of Human Genetics. 14(1). 55–62. 11 indexed citations

Jacquot, Sylvie, Maria Zeniou, Renaud Touraine, & André Hanauer. (2002). X-linked Coffin-Lowry syndrome (CLS, MIM 303600, RPS6KA3 gene, protein product known under various names: pp90rsk2, RSK2, ISPK, MAPKAP1). European Journal of Human Genetics. 10(1). 2–5. 18 indexed citations

Hanauer, André, et al.. (2002). Coffin-Lowry syndrome: clinical and molecular features. Journal of Medical Genetics. 39(10). 705–713. 118 indexed citations

Sassone‐Corsi, Paolo, Craig A. Mizzen, Peter Cheung, et al.. (1999). Requirement of Rsk-2 for Epidermal Growth Factor-Activated Phosphorylation of Histone H3. Science. 285(5429). 886–891. 408 indexed citations

Manouvrier‐Hanu, Sylvie, Jeanne Amiel, Sylvie Jacquot, et al.. (1999). Unreported RSK2 missense mutation in two male sibs with an unusually mild form of Coffin-Lowry syndrome. Journal of Medical Genetics. 36(10). 775–778. 22 indexed citations

10.

Jacquot, Sylvie, Karine Mérienne, Dario De Cesare, et al.. (1998). Mutation Analysis of the RSK2 Gene in Coffin-Lowry Patients: Extensive Allelic Heterogeneity and a High Rate of De Novo Mutations. The American Journal of Human Genetics. 63(6). 1631–1640. 68 indexed citations

11.

Vosse, Esther van de, Brunella Franco, Eugenio Montini, et al.. (1997). Exclusion of PPEF as the gene causing X-linked juvenile retinoschisis. Human Genetics. 101(2). 235–237. 3 indexed citations

12.

Trivier, Elisabeth, Dario De Cesare, Sylvie Jacquot, et al.. (1996). Mutations in the kinase Rsk-2 associated with Coffin-Lowry syndrome. Nature. 384(6609). 567–570. 319 indexed citations

13.

Hanauer, André, et al.. (1995). X-linked progressive mixed deafness: a new microdeletion that involves a more proximal region in Xq21.. HAL (Le Centre pour la Communication Scientifique Directe). 20 indexed citations

14.

Rowe, Peter, J.N. Goulding, Andrew Read, et al.. (1994). Refining the genetic map for the region flanking the X-linked hypophosphataemic rickets locus (Xp22.1?22.2). Human Genetics. 93(3). 291–294. 18 indexed citations

15.

Biancalana, Valérie, Elisabeth Trivier, C. R. Weber, et al.. (1994). Construction of a High-Resolution Linkage Map for Xp22.1-p22.2 and Refinement of the Genetic Localization of the Coffin-Lowry Syndrome Gene. Genomics. 22(3). 617–625. 32 indexed citations

16.

Oudet, C, André Hanauer, Paula R. Clemens, T. Caskey, & Jean‐Louis Mandel. (1992). Two hot spots of recombination in the DMD gene correlate with the deletion prone regions. Human Molecular Genetics. 1(8). 599–603. 97 indexed citations

17.

Fujita, Ricardo, André Hanauer, Anne Vincent, Jean‐Louis Mandel, & Michel Kœnig. (1991). Physical mapping of two loci (D9S5 and D9S15) tightly linked to Friedreich ataxia locus (FRDA) and identification of nearby CpG islands by pulse-field gel electrophoresis. Genomics. 10(4). 915–920. 18 indexed citations

18.

Frédéric, Florence, Dominique Simon, Jean‐Louis Guénet, et al.. (1990). Glutamate Dehydrogenase in Cerebellar Mutant Mice: Gene Localization and Enzyme Activity in Different Tissues. Journal of Neurochemistry. 54(1). 23–29. 9 indexed citations

19.

Vincent, Anne, Niklas Dahl, I. Oberlé, et al.. (1989). The polymorphic marker DXS304 is within 5 centimorgans of the fragile X locus. Genomics. 5(4). 797–801. 19 indexed citations

20.

Heilig, Roland, I. Oberlé, Benoı̂t Arveiler, et al.. (1988). Improved DNA markers for efficient analysis of fragile X families. American Journal of Medical Genetics. 30(1-2). 543–550. 35 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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