FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

André Hanauer

Research Profile

Anatomy

X Chromosome

Disorders

Chemicals & Drugs

Concepts & Ideas

Physiology

Genes & Molecular Sequences

Co-author Network

Publications

TOP 3
Anne Schneider; Raoul C M Hennekam; Saskia M Maas; André Hanauer
Identification of the first deep intronic mutation in the RPS6KA3 gene in a patient with a severe form of Coffin-Lowry syndrome.
Tahir Mehmood; Solange Pannetier; Anne Schneider; André Hanauer
Rsk2 Knockdown in PC12 Cells Results in Sp1 Dependent Increased Expression of the Gria2 Gene, Encoding the AMPA Receptor Subunit GluR2.
Emmanuel Darcq; Claire Gaveriaux-Ruff; André Hanauer; Pascale Koebel; Megan K Mahoney; Solange Pannetier; Katia Befort; Brigitte L Kieffer
RSK2 signaling in medial habenula contributes to acute morphine analgesia.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of André Hanauer (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2013: Anne Schneider; Raoul C M Hennekam; Saskia M Maas; André Hanauer
Identification of the first deep intronic mutation in the RPS6KA3 gene in a patient with a severe form of Coffin-Lowry syndrome.
European journal of medical genetics 2013;56(3):150-2.
2013: Tahir Mehmood; Solange Pannetier; Anne Schneider; André Hanauer
Rsk2 Knockdown in PC12 Cells Results in Sp1 Dependent Increased Expression of the Gria2 Gene, Encoding the AMPA Receptor Subunit GluR2.
International journal of molecular sciences 2013;14(2):3358-75.
2012: Emmanuel Darcq; Claire Gaveriaux-Ruff; André Hanauer; Pascale Koebel; Megan K Mahoney; Solange Pannetier; Katia Befort; Brigitte L Kieffer
RSK2 signaling in medial habenula contributes to acute morphine analgesia.
Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology 2012;37(5):1288-96.
2011: Anne Schneider; Tahir Mehmood; Solange Pannetier; André Hanauer
Altered ERK/MAPK signaling in the hippocampus of the mrsk2_KO mouse model of Coffin-Lowry syndrome.
Journal of neurochemistry 2011;119(3):447-59.
2011: Emmanuel Darcq; Carolina Del Boca; Jean-Marie Garnier; André Hanauer; Anne-Sophie Kirstetter; Pascale Koebel; Solange Pannetier; Katia Befort; Brigitte L Kieffer
RSK2 signaling in brain habenula contributes to place aversion learning.
Learning & memory (Cold Spring Harbor, N.Y.) 2011;18(9):574-8.
2011: Tahir Mehmood; Anne Schneider; Jérémie Sibille; Jérémie Sibillec; Patricia Marques Pereira; Solange Pannetier; Mohamed Raafet Ammar; Doulaye Dembele; Christelle Thibault-Carpentier; Nathalie Rouach; André Hanauer
Transcriptome profile reveals AMPA receptor dysfunction in the hippocampus of the Rsk2-knockout mice, an animal model of Coffin-Lowry syndrome.
Human genetics 2011;129(3):255-69.
2010: Patricia Marques Pereira; Anne Schneider; Solange Pannetier; Delphine Heron; André Hanauer
Coffin-Lowry syndrome.
European journal of human genetics : EJHG 2010;18(6):627-33.
2008: Patricia Marques Pereira; Michael Gruss; Katharina Braun; Nicolas Foos; Solange Pannetier; André Hanauer
Dopaminergic system dysregulation in the mrsk2_KO mouse, an animal model of the Coffin-Lowry syndrome.
Journal of neurochemistry 2008;107(5):1325-34.
2008: Maria Zeniou-Meyer; Yuanyuan Liu; Aurélie Béglé; Mary E Olanich; Mary Olanish; André Hanauer; Ute Becherer; Jens Rettig; Marie-France Bader; Nicolas Vitale
The Coffin-Lowry syndrome-associated protein RSK2 is implicated in calcium-regulated exocytosis through the regulation of PLD1.
Proceedings of the National Academy of Sciences of the United States of America 2008;105(24):8434-9.
2007: Patricia Marques Pereira; Delphine Heron; André Hanauer
The first large duplication of the RSK2 gene identified in a Coffin-Lowry syndrome patient.
Human genetics 2007;122(5):541-3.
2007: Raphael Poirier; Sylvie Jacquot; Cyrille Vaillend; A A Soutthiphong; M Libbey; Sabrina Davis; Serge Laroche; André Hanauer; Hans Welzl; H-P Lipp; D P Wolfer
Deletion of the Coffin-Lowry syndrome gene Rsk2 in mice is associated with impaired spatial learning and reduced control of exploratory behavior.
Behavior genetics 2007;37(1):31-50.
2006: J P Delaunoy; A Dubos; Patricia Marques Pereira; André Hanauer
Identification of novel mutations in the RSK2 gene (RPS6KA3) in patients with Coffin-Lowry syndrome.
Clinical genetics 2006;70(2):161-6.
2006: Reetta Jalkanen; Ewa Pronicka; Henna Tyynismaa; André Hanauer; Roxanne Y Walder; Tiina Alitalo
Genetic background of HSH in three Polish families and a patient with an X;9 translocation.
European journal of human genetics : EJHG 2006;14(1):55-62.
2006: Olivier Hagens; Aline Dubos; fatima abidi; Gotthold Barbi; Laura Van Zutven; Maria Hoeltzenbein; Niels Tommerup; Claude Moraine; Jean-Pierre Fryns; Jamel Chelly; Hans van Bokhoven; Jozef Gécz; Hélène Dollfus; Hans-Hilger Ropers; Charles E Schwartz; Rita de Cassia Stocco Dos Santos; Vera Kalscheuer; André Hanauer
Disruptions of the novel KIAA1202 gene are associated with X-linked mental retardation.
Human genetics 2006;118(5):578-90.
2004: xiangli yang; Koichi Matsuda; Peter Bialek; Sylvie Jacquot; Howard C Masuoka; Thorsten Schinke; Lingzhen Li; Stefano Brancorsini; Paolo Sassone-Corsi; Tim M Townes; André Hanauer; Gerard Karsenty
ATF4 is a substrate of RSK2 and an essential regulator of osteoblast biology; implication for Coffin-Lowry Syndrome.
Cell 2004;117(3):387-98.
2004: Maria Zeniou; Renata Gattoni; André Hanauer; James Stévenin
Delineation of the mechanisms of aberrant splicing caused by two unusual intronic mutations in the RSK2 gene involved in Coffin-Lowry syndrome.
Nucleic acids research 2004;32(3):1214-23.
2002: Maria Zeniou; Thomas Ding; Elisabeth Trivier; André Hanauer
Expression analysis of RSK gene family members: the RSK2 gene, mutated in Coffin-Lowry syndrome, is prominently expressed in brain structures essential for cognitive function and learning.
Human molecular genetics 2002;11(23):2929-40.
2002: Maria Zeniou; Solange Pannetier; Jean-Pierre Fryns; André Hanauer
Unusual splice-site mutations in the RSK2 gene and suggestion of genetic heterogeneity in Coffin-Lowry syndrome.
American journal of human genetics 2002;70(6):1421-33.
2002: Renaud-Laurian Touraine; Maria Zeniou; André Hanauer
A syndromic form of X-linked mental retardation: the Coffin-Lowry syndrome.
European journal of pediatrics 2002;161(4):179-87.
2002: Sylvie Jacquot; Maria Zeniou; Renaud-Laurian Touraine; André Hanauer
X-linked Coffin-Lowry syndrome (CLS, MIM 303600, RPS6KA3 gene, protein product known under various names: pp90(rsk2), RSK2, ISPK, MAPKAP1).
European journal of human genetics : EJHG 2002;10(1):2-5.
2001: H Boeuf; Karine Merienne; Sylvie Jacquot; D Duval; Maria Zeniou; Charlotte Hauss; B Reinhardt; Yolande Huss-Garcia; Andrée Dierich; David A Frank; André Hanauer; Claude Kedinger
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.
The Journal of biological chemistry 2001;276(49):46204-11.
2001: J Delaunoy; fatima abidi; Maria Zeniou; Sylvie Jacquot; Karine Merienne; Solange Pannetier; M Schmitt; C Schwartz; André Hanauer
Mutations in the X-linked RSK2 gene (RPS6KA3) in patients with Coffin-Lowry syndrome.
Human mutation 2001;17(2):103-16.
2000: Jean-Pierre Fryns; Martine Borghgraef; T W Brown; Jamel Chelly; Gene S Fisch; Ben Hamel; André Hanauer; D Lacombe; L Luo; J N MacPherson; J L Mandel; Claude Moraine; John C Mulley; D Nelson; B Oostra; Michael Partington; G J Ramakers; Hans-Hilger Ropers; Francois Rousseau; C Schwartz; P Steinbach; claude stoll; L Tranebjaerg; Gillian Turner; Hans van Bokhoven; A Vianna-Morgante
9th international workshop on fragile X syndrome and X-linked mental retardation.
American journal of medical genetics 2000;94(5):345-60.
2000: K Mérienne; Sylvie Jacquot; Maria Zeniou; Solange Pannetier; Paolo Sassone-Corsi; André Hanauer
Activation of RSK by UV-light: phosphorylation dynamics and involvement of the MAPK pathway.
Oncogene 2000;19(37):4221-9.
1999: Sylvie MANOUVRIER; J Amiel; Sylvie Jacquot; Karine Merienne; Alexandre Moerman; A Coëslier; F Labarriere; Louis Vallée; Marie-Françoise Croquette; André Hanauer
Unreported RSK2 missense mutation in two male sibs with an unusually mild form of Coffin-Lowry syndrome.
Journal of medical genetics 1999;36(10):775-8.
1999: Paolo Sassone-Corsi; Craig A Mizzen; P Cheung; Claudia Crosio; Lucia Monaco; Sylvie Jacquot; André Hanauer; C David Allis
Requirement of Rsk-2 for epidermal growth factor-activated phosphorylation of histone H3.
Science (New York, N.Y.) 1999;285(5429):886-91.
1999: Sylvie Jacquot; Karine Merienne; Elisabeth Trivier; Maria Zeniou; Solange Pannetier; André Hanauer
Coffin-Lowry syndrome: current status.
American journal of medical genetics 1999;85(3):214-5.
1999: D Filisetti; G Ostermann; M von Bredow; T Strom; Guido Filler; J Ehrich; Solange Pannetier; J M Garnier; P Rowe; Fiona Francis; A Julienne; André Hanauer; Michael J Econs; Claudine Oudet
Non-random distribution of mutations in the PHEX gene, and under-detected missense mutations at non-conserved residues.
European journal of human genetics : EJHG 1999;7(5):615-9.
1999: Karine Merienne; Sylvie Jacquot; Solange Pannetier; Maria Zeniou; A Bankier; Jozef Gecz; Jean-Louis Mandel; John C Mulley; Paolo Sassone-Corsi; André Hanauer
A missense mutation in RPS6KA3 (RSK2) responsible for non-specific mental retardation.
Nature genetics 1999;22(1):13-4.
1999: Laurent Villard; M C Bonino; fatima abidi; Angela Ragusa; Jérôme Belougne; Anne-Marie Lossi; L Seaver; J P Bonnefont; Corrado Romano; Marco Fichera; D Lacombe; André Hanauer; Nicole Philip; C Schwartz; Michel Fontés
Evaluation of a mutation screening strategy for sporadic cases of ATR-X syndrome.
Journal of medical genetics 1999;36(3):183-6.
1999: fatima abidi; Sylvie Jacquot; C Lassiter; Elisabeth Trivier; André Hanauer; Charles E Schwartz
Novel mutations in Rsk-2, the gene for Coffin-Lowry syndrome (CLS).
European journal of human genetics : EJHG 1999;7(1):20-6.
1998: Sylvie Jacquot; Karine Merienne; Dario De Cesare; Solange Pannetier; Jean-Louis Mandel; Paolo Sassone-Corsi; André Hanauer
Mutation analysis of the RSK2 gene in Coffin-Lowry patients: extensive allelic heterogeneity and a high rate of de novo mutations.
American journal of human genetics 1998;63(6):1631-40.
1998: Sylvie Jacquot; Karine Merienne; Solange Pannetier; S Blumenfeld; A Schinzel; André Hanauer
Germline mosaicism in Coffin-Lowry syndrome.
European journal of human genetics : EJHG 1998;6(6):578-82.
1998: Karine Merienne; Sylvie Jacquot; Elisabeth Trivier; Solange Pannetier; A Rossi; C Scott; A Schinzel; C Castellan; W Kress; André Hanauer
Rapid immunoblot and kinase assay tests for a syndromal form of X linked mental retardation: Coffin-Lowry syndrome.
Journal of medical genetics 1998;35(11):890-4.
1998: Dario De Cesare; Sylvie Jacquot; André Hanauer; Paolo Sassone-Corsi
Rsk-2 activity is necessary for epidermal growth factor-induced phosphorylation of CREB protein and transcription of c-fos gene.
Proceedings of the National Academy of Sciences of the United States of America 1998;95(21):12202-7.
1997: Claudine Oudet; D Martin-Coignard; Solange Pannetier; E Praud; G Champion; André Hanauer
A second family with XLRH displays the mutation S244L in the CLCN5 gene.
Human genetics 1997;99(6):781-4.
1997: Peter S N Rowe; Claudine Oudet; Fiona Francis; Christiane Sinding; Solange Pannetier; Michael J Econs; Tim M Strom; Thomas Meitinger; M Garabedian; A David; M A Macher; E Questiaux; Ewa Popowska; Ewa Pronicka; A P Read; A Mokrzycki; Francis Glorieux; Marc K Drezner; André Hanauer; Hans Lehrach; J N Goulding; Jeffrey L H O'Riordan
Distribution of mutations in the PEX gene in families with X-linked hypophosphataemic rickets (HYP).
Human molecular genetics 1997;6(4):539-49.
1996: Elisabeth Trivier; Dario De Cesare; Sylvie Jacquot; Solange Pannetier; E Zackai; I Young; Jean-Louis Mandel; Paolo Sassone-Corsi; André Hanauer
Mutations in the kinase Rsk-2 associated with Coffin-Lowry syndrome.
Nature 1996;384(6609):567-70.
1996: Peter S N Rowe; J N Goulding; Fiona Francis; Claudine Oudet; Michael J Econs; André Hanauer; Hans Lehrach; A P Read; R C Mountford; T Summerfield; J Weissenbach; W Fraser; Marc K Drezner; Kay E Davies; Jeffrey L H O'Riordan
The gene for X-linked hypophosphataemic rickets maps to a 200-300kb region in Xp22.1, and is located on a single YAC containing a putative vitamin D response element (VDRE).
Human genetics 1996;97(3):345-52.
1995: V Dumur; Elisabeth Trivier; Bernard Puech; F Peugnet; X Zanlonghi; Jean-Claude Hache; André Hanauer
Genetic analysis of new French X-linked juvenile retinoschisis kindreds using microsatellite markers closely linked to the RS locus: further narrowing of the RS candidate region.
Human genetics 1995;96(1):79-82.
1995: C Piussan; André Hanauer; N Dahl; M Mathieu; C Kolski; Valérie Biancalana; S Heyberger; V Strunski
X-linked progressive mixed deafness: a new microdeletion that involves a more proximal region in Xq21.
American journal of human genetics 1995;56(1):224-30.
1994: Valérie Biancalana; Elisabeth Trivier; C Weber; J Weissenbach; Peter S N Rowe; Jeffrey L H O'Riordan; M W Partington; S Heyberger; Claudine Oudet; André Hanauer
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 1994;22(3):617-25.
1994: L J Hu; S Blumenfeld-Heyberger; André Hanauer; J Weissenbach; Jean-Louis Mandel
Non-specific X-linked mental retardation: linkage analysis in MRX2 and MRX4 families revisited.
American journal of medical genetics 1994;51(4):569-74.
1994: M Chery; Valérie Biancalana; C Philippe; G Malpuech; H Carla; S Gilgenkrantz; Jean-Louis Mandel; André Hanauer
Hypomagnesemia with secondary hypocalcemia in a female with balanced X;9 translocation: mapping of the Xp22 chromosome breakpoint.
Human genetics 1994;93(5):587-91.
1994: Peter S N Rowe; J Goulding; A Read; Hans Lehrach; Fiona Francis; André Hanauer; Claudine Oudet; Valérie Biancalana; S W Kooh; Kay E Davies
Refining the genetic map for the region flanking the X-linked hypophosphataemic rickets locus (Xp22.1-22.2).
Human genetics 1994;93(3):291-4.
1993: Peter S N Rowe; J Goulding; A Read; R Mountford; André Hanauer; Claudine Oudet; M P Whyte; S Meier-Ewert; Hans Lehrach; Kay E Davies
New markers for linkage analysis of X-linked hypophosphataemic rickets.
Human genetics 1993;91(6):571-5.
1993: C Weber; Claudine Oudet; S Johnson; G Pilia; David Schlessinger; André Hanauer
Dinucleotide repeat polymorphism close to IDS gene in Xq27.3-q28 (DXS1113).
Human molecular genetics 1993;2(5):612.
1993: C Weber; Claudine Oudet; S Johnson; G Pilia; David Schlessinger; André Hanauer
Dinucleotide repeat polymorphism at Xq26.1 (DXS1114).
Human molecular genetics 1993;2(5):612.
1993: Claudine Oudet; C Weber; J Kaplan; B Segues; Marie-Françoise Croquette; E O Roman; André Hanauer
Characterisation of a highly polymorphic microsatellite at the DXS207 locus: confirmation of very close linkage to the retinoschisis disease gene.
Journal of medical genetics 1993;30(4):300-3.
1992: Claudine Oudet; André Hanauer; P Clemens; T Caskey; Jean-Louis Mandel
Two hot spots of recombination in the DMD gene correlate with the deletion prone regions.
Human molecular genetics 1992;1(8):599-603.
1992: Valérie Biancalana; F Serville; J Pommier; J Julien; André Hanauer; Jean-Louis Mandel
Moderate instability of the trinucleotide repeat in spino bulbar muscular atrophy.
Human molecular genetics 1992;1(4):255-8.
1991: Valérie Biancalana; B Le Marec; S Odent; J A van den Hurk; André Hanauer
Oto-palato-digital syndrome type I: further evidence for assignment of the locus to Xq28.
Human genetics 1991;88(2):228-30.
1991: Claudine Oudet; R Heilig; André Hanauer; Jean-Louis Mandel
Nonradioactive assay for new microsatellite polymorphisms at the 5' end of the dystrophin gene, and estimation of intragenic recombination.
American journal of human genetics 1991;49(2):311-9.
1991: I Oberlé; Francois Rousseau; D Heitz; Christine Kretz; Didier Devys; André Hanauer; J Boué; M F Bertheas; Jean-Louis Mandel
Instability of a 550-base pair DNA segment and abnormal methylation in fragile X syndrome.
Science (New York, N.Y.) 1991;252(5009):1097-102.
1990: C de la Salle; Q Wu; M J Baas; André Hanauer; C Ruan; Jean-Pierre Cazenave
Common intragenic and extragenic polymorphisms of blood coagulation factors VIII and IX are different in Chinese and Caucasian populations.
Clinical genetics 1990;38(6):434-40.
1990: Massimo Pandolfo; Giorgio Sirugo; A Antonelli; L Weitnauer; L Ferretti; Maurizio Leone; I Dones; A Cerino; R Fujita; André Hanauer
Friedreich ataxia in Italian families: genetic homogeneity and linkage disequilibrium with the marker loci D9S5 and D9S15.
American journal of human genetics 1990;47(2):228-35.
1990: André Hanauer; C de la Salle
Direct detection of the deletion-insertion polymorphism of the factor IX gene by analysis of amplified DNA sequences (PCR).
Thrombosis research 1990;59(1):219-20.
1990: André Hanauer; R Fujita; Paul Trouillas; C Tommasi-Davenas; Yves Agid; A Seck; Jean-Louis Mandel
Prenatal diagnosis of Friedreich ataxia.
Lancet 1990;335(8697):1102.
1990: T Léveillard; Giorgio Sirugo; André Hanauer; Richard Sesboüé; Jeannette Bourguignon; Maryam Diarra-Mehrpour; Jean-Philippe Salier; Jean-Pierre Martin
An hypervariable polymorphism detected in the human inter-alpha-trypsin inhibitor heavy chain gene ITIH2.
Nucleic acids research 1990;18(5):1319.
1990: R Fujita; André Hanauer; Giorgio Sirugo; R Heilig; Jean-Louis Mandel
Additional polymorphisms at marker loci D9S5 and D9S15 generate extended haplotypes in linkage disequilibrium with Friedreich ataxia.
Proceedings of the National Academy of Sciences of the United States of America 1990;87(5):1796-800.
1990: André Hanauer; M Chery; R Fujita; A J Driesel; S Gilgenkrantz; Jean-Louis Mandel
The Friedreich ataxia gene is assigned to chromosome 9q13-q21 by mapping of tightly linked markers and shows linkage disequilibrium with D9S15.
American journal of human genetics 1990;46(1):133-7.
1989: A Vincent; Niklas Dahl; I Oberlé; André Hanauer; Jean-Louis Mandel; H Malmgren; Ulf Pettersson
The polymorphic marker DXS304 is within 5 centimorgans of the fragile X locus.
Genomics 1989;5(4):797-801.
1989: R Fujita; Yves Agid; Paul Trouillas; A Seck; C Tommasi-Davenas; A J Driesel; K Olek; K H Grzeschik; Y Nakamura; Jean-Louis Mandel; André Hanauer
Confirmation of linkage of Friedreich ataxia to chromosome 9 and identification of a new closely linked marker.
Genomics 1989;4(1):110-1.
1988: André Hanauer; Y Alembik; B Arveiler; L Formiga; S Gilgenkrantz; Jean-Louis Mandel
Genetic mapping of anhidrotic ectodermal dysplasia: DXS159, a closely linked proximal marker.
Human genetics 1988;80(2):177-80.
1988: B Arveiler; Y Alembik; André Hanauer; P Jacobs; L Tranebjaerg; M Mikkelsen; H Puissant; L L Piet; Jean-Louis Mandel
Linkage analysis suggests at least two loci for X-linked non-specific mental retardation.
American journal of medical genetics 1988;30(1-2):473-83.
1988: R Heilig; I Oberlé; B Arveiler; André Hanauer; M Vidaud; Jean-Louis Mandel
Improved DNA markers for efficient analysis of fragile X families.
American journal of medical genetics 1988;30(1-2):543-50.
1988: T Léveillard; Jeannette Bourguignon; Richard Sesboüé; André Hanauer; Jean-Philippe Salier; Maryam Diarra-Mehrpour; Jean-Pierre Martin
BstXI RFLP in the human inter-alpha-trypsin inhibitor light chain gene.
Nucleic acids research 1988;16(6):2744.
1987: I Oberlé; G Camerino; Klaus Wrogemann; B Arveiler; André Hanauer; E Raimondi; Jean-Louis Mandel
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.
Human genetics 1987;77(1):60-5.
1986: Jean-Louis Mandel; B Arveiler; G Camerino; André Hanauer; R Heilig; M Koenig; I Oberlé
Genetic mapping of the human X chromosome: linkage analysis of the q26-q28 region that includes the fragile X locus and isolation of expressed sequences.
Cold Spring Harbor symposia on quantitative biology 1986;51 Pt 1():195-203.
1984: R Heilig; André Hanauer; K H Grzeschik; M C Hors-Cayla; J L Mandel
Actin-like sequences are present on human X and Y chromosomes.
The EMBO journal 1984;3(8):1803-7.
1983: André Hanauer; M Levin; R Heilig; D Daegelen; A Kahn; J L Mandel
Isolation and characterization of cDNA clones for human skeletal muscle alpha actin.
Nucleic acids research 1983;11(11):3503-16.