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André Hanauer

Observed names: A André Hanauer, A Hanauer, A. Hanauer, Andr Hanauer, André Hanauer, Andre Hanauer, Andre ́ Hanauer, André Hanauer, Andr� Hanauer, HANAUER, André, Hanauer, A, Hanauer, A.
Observed institutions: Hôpital Necker-Enfants Malades, Centre National de la Recherche Scientifique, University of Miami, Inserm, Centre Hospitalier Universitaire de Lille, Institut Necker Enfants Malades, Institut de génétique et de biologie moléculaire et cellulaire, Centre Hospitalier Régional et Universitaire de Nancy, Hôpital Roger Salengro, Hôpital Saint-Antoine, Hôpital Jeanne de Flandre, Centre Hospitalier Universitaire de Poitiers, Centre Hospitalier Universitaire d'Angers, Hôpital Edouard Herriot, Genethon (France), Hôpitaux Universitaires de Strasbourg, Greenwood Genetic Center, Institut de Biologie Moléculaire et Cellulaire, Hôpital Laennec, Hôpital de la Timone, University College London, Université de Strasbourg, UConn Health
OpenAlex ID: A5109969408
Instability of a 550-Base Pair DNA Segment and Abnormal Methylation in Fragile X Syndrome
1991 · I. Oberlé, F. Rousseau, et al. · Science · 1,499
A gene (PEX) with homologies to endopeptidases is mutated in patients with X–linked hypophosphatemic rickets
1995 · F. Francis, S. Hennig, et al. · Nature Genetics · 1,099
ATF4 Is a Substrate of RSK2 and an Essential Regulator of Osteoblast Biology
2004 · Xiangli Yang, Koichi Matsuda, et al. · Cell · 822
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Requirement of Rsk-2 for Epidermal Growth Factor-Activated Phosphorylation of Histone H3
1999 · Paolo Sassone-Corsi, Craig A. Mizzen, et al. · Science · 485
Mutations in the kinase Rsk-2 associated with Coffin-Lowry syndrome
1996 · Elisabeth Trivier, Dario De Cesare, et al. · Nature · 406
Rsk-2 activity is necessary for epidermal growth factor-induced phosphorylation of CREB protein and transcription of c- fos gene
1998 · Dario De Cesare, Sylvie Jacquot, et al. · Proceedings of the National Academy of Sciences · 309
The glyceraldehyde 3 phosphate dehydrogenase gene family: structure of a human cDNA and of an X chromosome linked pseudogene; amazing complexity of the gene family in mouse.
1984 · A. Hanauer, J.L. Mandel · The EMBO Journal · 172
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Coffin-Lowry syndrome: clinical and molecular features
2002 · A Hanauer, I D Young · Journal of Medical Genetics · 149
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A missense mutation in RPS6KA3 (RSK2) responsible for non-specific mental retardation
1999 · Karine Merienne, Sylvie Jacquot, et al. · Nature Genetics · 148
Coffin–Lowry syndrome
2009 · Patricia Marques Pereira, Anne Schneider, et al. · European Journal of Human Genetics · 137
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Moderate instability of the trinucleotide repeat in spino bulbar muscular atrophy
1992 · V. Biancalana, F. Serville, et al. · Human Molecular Genetics · 124
Two hot spots of recombination in the DMD gene correlate with the deletion prone regions
1992 · Claudine Oudet, André Hanauer, et al. · Human Molecular Genetics · 123
Isolation and characterization of cDNA clones for human skeletal muscle α actin
1983 · A. Hanauer, M. Levin, et al. · Nucleic Acids Research · 92
Mutations in the X-linked RSK2 gene (RPS6KA3) in patients with Coffin-Lowry syndrome
2001 · Jean-Pierre Delaunoy, Fatima Abidi, et al. · Human Mutation · 91
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Mutation Analysis of the RSK2 Gene in Coffin-Lowry Patients: Extensive Allelic Heterogeneity and a High Rate of De Novo Mutations
1998 · Sylvie Jacquot, Karine Merienne, et al. · The American Journal of Human Genetics · 88
Deletion of the Coffin–Lowry Syndrome Gene Rsk2 in Mice is Associated With Impaired Spatial Learning and Reduced Control of Exploratory Behavior
2006 · R. Poirier, S. Jacquot, et al. · Behavior Genetics · 87
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p90Rsk is not involved in cytostatic factor arrest in mouse oocytes
2005 · Julien Dumont, Muriel Umbhauer, et al. · The Journal of Cell Biology · 87
Confirmation of linkage of Friedreich ataxia to chromosome 9 and identification of a new closely linked marker
1989 · Ricardo Fujita, Yves Agid, et al. · Genomics · 76
Disruptions of the novel KIAA1202 gene are associated with X-linked mental retardation
2005 · Olivier Hagens, Aline Dubos, et al. · Human Genetics · 73
Non-random distribution of mutations in the PHEX gene, and under-detected missense mutations at non-conserved residues
1999 · Denis Filisetti, Georg Ostermann, et al. · European Journal of Human Genetics · 68
Conservation and reorganization of loci on the mammalian X chromosome: A molecular framework for the identification of homologous subchromosomal regions in man and mouse
1988 · Laurence C. Amar, Luisa Dandolo, et al. · Genomics · 65
Nonradioactive assay for new microsatellite polymorphisms at the 5' end of the dystrophin gene, and estimation of intragenic recombination.
1991 · C Oudet, R Heilig, et al. · Europe PMC (PubMed Central) · 61
Multipoint genetic mapping of the Xq26-q28 region in families with fragile X mental retardation and in normal families reveals tight linkage of markers in q26?q27
1987 · I. Oberl�, G. Camerino, et al. · Human Genetics · 61
The Ribosomal S6 Kinases, cAMP-responsive Element-binding, and STAT3 Proteins Are Regulated by Different Leukemia Inhibitory Factor Signaling Pathways in Mouse Embryonic Stem Cells
2001 · Helene Boeuf, Karine Merienne, et al. · Journal of Biological Chemistry · 59
The Coffin-Lowry Syndrome-Associated Protein RSK2 Regulates Neurite Outgrowth through Phosphorylation of Phospholipase D1 (PLD1) and Synthesis of Phosphatidic Acid
2013 · Mohamed-Raafet Ammar, Yann Humeau, et al. · Journal of Neuroscience · 58
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Works count: 125
Citation count: 8,451
H-index: 39
I10-index: 88
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