Solange Pannetier

2.6k total citations
22 papers, 1.0k citations indexed

About

Solange Pannetier is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Solange Pannetier has authored 22 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 17 papers in Genetics and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in Solange Pannetier's work include Genetics and Neurodevelopmental Disorders (15 papers), Chromatin Remodeling and Cancer (6 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers). Solange Pannetier is often cited by papers focused on Genetics and Neurodevelopmental Disorders (15 papers), Chromatin Remodeling and Cancer (6 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (6 papers). Solange Pannetier collaborates with scholars based in France, United States and Pakistan. Solange Pannetier's co-authors include André Hanauer, Paolo Sassone‐Corsi, Sylvie Jacquot, Karine Mérienne, Dario De Cesare, Jean‐Louis Mandel, Elisabeth Trivier, Ian Young, Elaine H. Zackai and Anne Schneider and has published in prestigious journals such as Nature, PLoS ONE and Molecular and Cellular Biology.

In The Last Decade

Solange Pannetier

22 papers receiving 1.0k citations

Peers

Countries citing papers authored by Solange Pannetier

Since Specialization

Citations

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

Fields of papers citing papers by Solange Pannetier

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Solange Pannetier

This figure shows the co-authorship network connecting the top 25 collaborators of Solange Pannetier. A scholar is included among the top collaborators of Solange Pannetier 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 Solange Pannetier. Solange Pannetier 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

#	Work	Indexed citations
1	RSK2 Is a Modulator of Craniofacial Development 2014 ·PLoS ONE ·Virginie Laugel-Haushalter, Marie Paschaki, Pauline Marangoni, (unknown), (unknown), (unknown), (unknown), (unknown), Philippe Choquet, André Constantinesco, Fabien Bornert, Matthieu Schmittbuhl, Solange Pannetier, Laurent Viriot, André Hanauer, Pascal Dollé, Agnès Bloch‐Zupan	19
2	Rsk2 Knockdown in PC12 Cells Results in Sp1 Dependent Increased Expression of the Gria2 Gene, Encoding the AMPA Receptor Subunit GluR2 2013 ·International Journal of Molecular Sciences ·Tahir Mehmood, Anne Schneider, Solange Pannetier, André Hanauer	6
3	Defective synaptic transmission and structure in the dentate gyrus and selective fear memory impairment in the Rsk2 mutant mouse model of Coffin–Lowry syndrome 2013 ·Neurobiology of Disease ·Élise Morice, Séverine Farley, Roseline Poirier, Glenn Dallérac, Carine Chagneau, Solange Pannetier, André Hanauer, Sabrina Davis, Cyrille Vaillend, Serge Laroche	25
4	RSK2 Signaling in Medial Habenula Contributes to Acute Morphine Analgesia 2012 ·Neuropsychopharmacology ·Emmanuel Darcq, Katia Befort, Pascale Koebel, Solange Pannetier, (unknown), Claire Gavériaux‐Ruff, André Hanauer, Brigitte Kieffer	27
5	RSK2 signaling in brain habenula contributes to place aversion learning 2011 ·Learning & Memory ·Emmanuel Darcq, Pascale Koebel, (unknown), Solange Pannetier, (unknown), Jean‐Marie Garnier, André Hanauer, Katia Befort, Brigitte L. Kieffer	17
6	Altered ERK/MAPK signaling in the hippocampus of the mrsk2_KO mouse model of Coffin‐Lowry syndrome 2011 ·Journal of Neurochemistry ·Anne Schneider, Tahir Mehmood, Solange Pannetier, André Hanauer	25
7	Transcriptome profile reveals AMPA receptor dysfunction in the hippocampus of the Rsk2-knockout mice, an animal model of Coffin–Lowry syndrome 2010 ·Human Genetics ·Tahir Mehmood, Anne Schneider, Jérémie Sibille, Patricia Marques Pereira, Solange Pannetier, (unknown), Doulaye Dembélé, Christelle Thibault-Carpentier, Nathalie Rouach, André Hanauer	18
8	Coffin–Lowry syndrome 2009 ·European Journal of Human Genetics ·Patricia Marques Pereira, Anne Schneider, Solange Pannetier, Delphine Héron, André Hanauer	97
9	Inactivation of the CDKL3 gene at 5q31.1 by a balanced t(X;5) translocation associated with nonspecific mild mental retardation 2008 ·American Journal of Medical Genetics Part A ·Aline Dubos, Solange Pannetier, André Hanauer	18
10	Dopaminergic system dysregulation in the mrsk2_KO mouse, an animal model of the Coffin‐Lowry syndrome 2008 ·Journal of Neurochemistry ·Patricia Marques Pereira, Michael Gruß, Katharina Braun, (unknown), Solange Pannetier, André Hanauer	14
11	Unusual Splice-Site Mutations in the RSK2 Gene and Suggestion of Genetic Heterogeneity in Coffin-Lowry Syndrome 2002 ·The American Journal of Human Genetics ·Maria Zeniou, Solange Pannetier, Jean‐Pierre Fryns, André Hanauer	25
12	Mutations in the X-linked RSK2 gene (RPS6KA3) in patients with Coffin-Lowry syndrome 2001 ·Human Mutation ·Jean‐Pierre Delaunoy, Fatima Abidi, Maria Zeniou, Sylvie Jacquot, Karine Mérienne, Solange Pannetier, (unknown), Charles E. Schwartz, (unknown)	72
13	Activation of RSK by UV-light: phosphorylation dynamics and involvement of the MAPK pathway 2000 ·Oncogene ·Karine Mérienne, Sylvie Jacquot, Maria Zeniou, Solange Pannetier, Paolo Sassone‐Corsi, André Hanauer	41
14	Coffin‐Lowry syndrome: Current status 1999 ·American Journal of Medical Genetics ·Sylvie Jacquot, Karine Mérienne, Elisabeth Trivier, Maria Zeniou, Solange Pannetier, André Hanauer	2
15	Non-random distribution of mutations in the PHEX gene, and under-detected missense mutations at non-conserved residues 1999 ·European Journal of Human Genetics ·Denis Filisetti, Georg Ostermann, (unknown), Tim M. Strom, Guido Filler, (unknown), Solange Pannetier, Jean‐Marie Garnier, Peter Rowe, Fiona Francis, (unknown), André Hanauer, Michael J. Econs, C Oudet	54
16	Mutation Analysis of the RSK2 Gene in Coffin-Lowry Patients: Extensive Allelic Heterogeneity and a High Rate of De Novo Mutations 1998 ·The American Journal of Human Genetics ·Sylvie Jacquot, Karine Mérienne, Dario De Cesare, Solange Pannetier, Jean‐Louis Mandel, Paolo Sassone‐Corsi, André Hanauer	68
17	Germline mosaicism in Coffin-Lowry syndrome 1998 ·European Journal of Human Genetics ·Sylvie Jacquot, Karine Mérienne, Solange Pannetier, (unknown), Albert Schinzel, André Hanauer	15
18	Rapid immunoblot and kinase assay tests for a syndromal form of X linked mental retardation: Coffin-Lowry syndrome. 1998 ·Journal of Medical Genetics ·Karine Mérienne, Sylvie Jacquot, Elisabeth Trivier, Solange Pannetier, Antonio Rossi, C. Ronald Scott, Albert Schinzel, Claudio Castellan, (unknown), André Hanauer	25
19	A second family with XLRH displays the mutation S244L in the CLCN5 gene 1997 ·Human Genetics ·C Oudet, Dominique Martin‐Coignard, Solange Pannetier, (unknown), Gérard Champion, (unknown)	24
20	Mutations in the kinase Rsk-2 associated with Coffin-Lowry syndrome 1996 ·Nature ·Elisabeth Trivier, Dario De Cesare, Sylvie Jacquot, Solange Pannetier, Elaine H. Zackai, Ian Young, Jean‐Louis Mandel, Paolo Sassone‐Corsi, André Hanauer	319

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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