Nombre de documents

77

CV de Catalina Betancur


Article dans une revue74 documents

  • Anne Claire Richard, Anne Rovelet-Lecrux, Elsa Delaby, Camille Charbonnier, Bhooma Thiruvahindrapuram, et al.. The 22q11 PRODH/DGCR6 deletion is frequent in hyperprolinemic subjects but is not a strong risk factor for ASD.. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, Wiley, 2016, <10.1002/ajmg.b.32416>. <inserm-01289348>
  • Marion Pilorge, Coralie Fassier, Hervé Le Corronc, Anaïs Potey, Jing Bai, et al.. Genetic and functional analyses demonstrate a role for abnormal glycinergic signaling in autism. Molecular Psychiatry, Nature Publishing Group, 2016, 21 (7), pp.936-945 <10.1038/mp.2015.139>. <inserm-01211157>
  • Anne-Claude Tabet, Alain Verloes, Marion Pilorge, Elsa Delaby, Richard Delorme, et al.. Complex nature of apparently balanced chromosomal rearrangements in patients with autism spectrum disorder. Molecular Autism, BioMed Central, 2015, 6 (1), pp.19. <10.1186/s13229-015-0015-2>. <inserm-01181008>
  • Dalila Pinto, Elsa Delaby, Daniele Merico, Mafalda Barbosa, Alison Merikangas, et al.. Convergence of Genes and Cellular Pathways Dysregulated in Autism Spectrum Disorders.. American Journal of Human Genetics, Elsevier (Cell Press), 2014, 94 (5), pp.677-694. <10.1016/j.ajhg.2014.03.018>. <inserm-00986225>
  • Dexter Hadley, Zhi-Liang Wu, Charlly Kao, Akshata Kini, Alisha Mohamed-Hadley, et al.. The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism.. Nature Communications, Nature Publishing Group, 2014, 5, pp.4074. <10.1038/ncomms5074>. <inserm-01009668>
  • Claire Leblond, Caroline Nava, Anne Polge, Julie Gauthier, Guillaume Huguet, et al.. Meta-analysis of SHANK Mutations in Autism Spectrum Disorders: A Gradient of Severity in Cognitive Impairments.. PLoS Genetics, Public Library of Science, 2014, 10 (9), pp.e1004580. <10.1371/journal.pgen.1004580>. <inserm-01061498>
  • Uzoezi Ozomaro, Guiqing Cai, Yuji Kajiwara, Seungtai Yoon, Vladimir Makarov, et al.. Characterization of SLITRK1 Variation in Obsessive-Compulsive Disorder.. PLoS ONE, Public Library of Science, 2013, 8 (8), pp.e70376. <10.1371/journal.pone.0070376>. <inserm-00871302>
  • Catalina Betancur, Joseph Buxbaum. SHANK3 haploinsufficiency: a "common" but underdiagnosed highly penetrant monogenic cause of autism spectrum disorders.. Molecular Autism, BioMed Central, 2013, 4 (1), pp.17. <10.1186/2040-2392-4-17>. <inserm-00839363>
  • Latha Soorya, Alexander Kolevzon, Jessica Zweifach, Teresa Lim, Yuriy Dobry, et al.. Prospective investigation of autism and genotype-phenotype correlations in 22q13 deletion syndrome and SHANK3 deficiency.. Molecular Autism, BioMed Central, 2013, 4 (1), pp.18. <10.1186/2040-2392-4-18>. <inserm-00843238>
  • Hyun Ji Noh, Chris Ponting, Hannah Boulding, Stephen Meader, Catalina Betancur, et al.. Network topologies and convergent aetiologies arising from deletions and duplications observed in individuals with autism.. PLoS Genetics, Public Library of Science, 2013, 9 (6), pp.e1003523. <10.1371/journal.pgen.1003523>. <inserm-00834559>
  • Isabelle Scheid, Anna Maruani, Guillaume Huguet, Claire Leblond, Gudrun Nygren, et al.. Heterozygous FA2H mutations in autism spectrum disorders.. BMC Medical Genetics, BioMed Central, 2013, 14 (1), pp.124. <10.1186/1471-2350-14-124>. <inserm-00918083>
  • Hong Lee, Stephan Ripke, Benjamin Neale, Stephen Faraone, Shaun Purcell, et al.. Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs.. Nature Genetics, Nature Publishing Group, 2013, 45 (9), pp.984-94. <10.1038/ng.2711>. <inserm-00864642>
  • Anne-Claude Tabet, Marion Pilorge, Richard Delorme, Frédérique Amsellem, Jean-Marc Pinard, et al.. Autism multiplex family with 16p11.2p12.2 microduplication syndrome in monozygotic twins and distal 16p11.2 deletion in their brother.: Duplication 16p11.2p12.2 in twins with autism. European Journal of Human Genetics, Nature Publishing Group, 2012, 20 (5), pp.540-6. <10.1038/ejhg.2011.244>. <inserm-00661857>
  • Yan Kou, Catalina Betancur, Huilei Xu, Joseph Buxbaum, Avi Ma'Ayan. Network- and attribute-based classifiers can prioritize genes and pathways for autism spectrum disorders and intellectual disability.: Prioritizing genes in autism and related disorders. American Journal of Medical Genetics Part C: Seminars in Medical Genetics, Wiley, 2012, 160C (2), pp.130-42. <10.1002/ajmg.c.31330>. <inserm-00688142>
  • Richard Anney, Lambertus Klei, Dalila Pinto, Joana Almeida, Elena Bacchelli, et al.. Individual common variants exert weak effects on the risk for autism spectrum disorders.. Human Molecular Genetics, Oxford University Press (OUP), 2012, 21 (21), pp.4781-92. <10.1093/hmg/dds301>. <inserm-00723650>
  • Patrícia Celestino-Soper, Sara Violante, Emily Crawford, Rui Luo, Anath Lionel, et al.. A common X-linked inborn error of carnitine biosynthesis may be a risk factor for nondysmorphic autism.. Proceedings- National Academy of Sciences Usa, 2012, 109 (21), pp.7974-81. <10.1073/pnas.1120210109>. <inserm-00696112>
  • Pauline Chaste, Catalina Betancur, Marion Gérard-Blanluet, Anne Bargiacchi, Suzanne Kuzbari, et al.. High-functioning autism spectrum disorder and fragile X syndrome: report of two affected sisters.. Molecular Autism, BioMed Central, 2012, 3 (1), pp.5. <10.1186/2040-2392-3-5>. <inserm-00733073>
  • Joseph Buxbaum, Catalina Betancur, Ozlem Bozdagi, Nate Dorr, Gregory Elder, et al.. Optimizing the phenotyping of rodent ASD models: Enrichment analysis of mouse and human neurobiological phenotypes associated with high-risk autism genes identifies morphological, electrophysiological, neurological, and behavioral features.. Molecular Autism, BioMed Central, 2012, 3 (1), pp.1. <10.1186/2040-2392-3-1>. <inserm-00672942>
  • Claire Leblond, Jutta Heinrich, Richard Delorme, Christian Proepper, Catalina Betancur, et al.. Genetic and functional analyses of SHANK2 mutations suggest a multiple hit model of autism spectrum disorders.. PLoS Genetics, Public Library of Science, 2012, 8 (2), pp.e1002521. <10.1371/journal.pgen.1002521>. <inserm-00834560>
  • Benjamin Neale, Yan Kou, Li Liu, Avi Ma'Ayan, Kaitlin E Samocha, et al.. Patterns and rates of exonic de novo mutations in autism spectrum disorders.. Nature, Nature Publishing Group, 2012, 485 (7397), pp.242-5. <10.1038/nature11011>. <inserm-00939274>
  • Alistair Pagnamenta, Richard Holt, Mohammed Yusuf, Dalila Pinto, Kirsty Wing, et al.. A family with autism and rare copy number variants disrupting the Duchenne/Becker muscular dystrophy gene DMD and TRPM3.. Journal of Neurodevelopmental Disorders, BioMed Central, 2011, 3 (2), pp.124-31. <10.1007/s11689-011-9076-5>. <inserm-00598894>
  • Catalina Betancur. Etiological heterogeneity in autism spectrum disorders: more than 100 genetic and genomic disorders and still counting.. Brain Research, Elsevier, 2011, 1380, pp.42-77. <10.1016/j.brainres.2010.11.078>. <inserm-00549873>
  • Anne-Claude Tabet, Azzedine Aboura, Marion Gérard, Marion Pilorge, Céline Dupont, et al.. Molecular characterization of a de novo 6q24.2q25.3 duplication interrupting UTRN in a patient with arthrogryposis.. American Journal of Medical Genetics Part A, Wiley, 2010, 152A (7), pp.1781-8. <10.1002/ajmg.a.33433>. <inserm-00520796>
  • Richard Delorme, Catalina Betancur, Pauline Chaste, Solen Kernéis, Astrid Stopin, et al.. Reduced 3-O-methyl-dopa levels in OCD patients and their unaffected parents is associated with the low activity M158 COMT allele.. American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, Wiley, 2010, 153B (2), pp.542-8. <10.1002/ajmg.b.31016>. <inserm-00474052>
  • Françoise Devillard, Vincent Guinchat, Daniel Moreno-De-Luca, Anne-Claude Tabet, Nicolas Gruchy, et al.. Paracentric inversion of chromosome 2 associated with cryptic duplication of 2q14 and deletion of 2q37 in a patient with autism.. American Journal of Medical Genetics Part A, Wiley, 2010, 152A (9), pp.2346-54. <10.1002/ajmg.a.33601>. <inserm-00520816>
  • Richard Anney, Lambertus Klei, Dalila Pinto, Regina Regan, Judith Conroy, et al.. A genome-wide scan for common alleles affecting risk for autism.. Human Molecular Genetics, Oxford University Press (OUP), 2010, 19 (20), pp.4072-82. <10.1093/hmg/ddq307>. <inserm-00521391>
  • L Mcinnes, Alisa Nakamine, Marion Pilorge, Tracy Brandt, Patricia Jiménez González, et al.. A large-scale survey of the novel 15q24 microdeletion syndrome in autism spectrum disorders identifies an atypical deletion that narrows the critical region.. Molecular Autism, BioMed Central, 2010, 1 (5), 12 p. <10.1186/2040-2392-1-5>. <inserm-00622567>
  • Richard Delorme, Catalina Betancur, Isabelle Scheid, Henrik Anckarsäter, Pauline Chaste, et al.. Mutation screening of NOS1AP gene in a large sample of psychiatric patients and controls.. BMC Medical Genetics, BioMed Central, 2010, 11, pp.108. <10.1186/1471-2350-11-108>. <inserm-00533891>
  • Richard Delorme, Daniel Moreno-De-Luca, Aurélie Gennetier, Wolfgang Maier, Pauline Chaste, et al.. Search for copy number variants in chromosomes 15q11-q13 and 22q11.2 in obsessive compulsive disorder.. BMC Medical Genetics, BioMed Central, 2010, 11, pp.100. <10.1186/1471-2350-11-100>. <inserm-00520828>
  • Dalila Pinto, Alistair Pagnamenta, Lambertus Klei, Richard Anney, Daniele Merico, et al.. Functional impact of global rare copy number variation in autism spectrum disorders.. Nature, Nature Publishing Group, 2010, 466 (7304), pp.368-72. <10.1038/nature09146>. <inserm-00521387>
  • Christel Depienne, Daniel Moreno-De-Luca, Delphine Heron, Delphine Bouteiller, Aurélie Gennetier, et al.. Screening for genomic rearrangements and methylation abnormalities of the 15q11-q13 region in autism spectrum disorders.. Biological Psychiatry, Elsevier, 2009, 66 (4), pp.349-59. <10.1016/j.biopsych.2009.01.025>. <inserm-00369261>
  • Catalina Betancur, Takeshi Sakurai, Joseph D Buxbaum. The emerging role of synaptic cell-adhesion pathways in the pathogenesis of autism spectrum disorders.. Trends in Neurosciences, Elsevier, 2009, 32 (7), pp.402-412. <10.1016/j.tins.2009.04.003>. <inserm-00401195>
  • Xiaohong Gong, Richard Delorme, Fabien Fauchereau, Christelle Durand, Pauline Chaste, et al.. An investigation of ribosomal protein L10 gene in autism spectrum disorders.. BMC Medical Genetics, BioMed Central, 2009, 10, pp.7. <10.1186/1471-2350-10-7>. <inserm-00374531v2>
  • Susanne Henningsson, Lina Jonsson, Elin Ljunggren, Lars Westberg, Carina Gillberg, et al.. Possible association between the androgen receptor gene and autism spectrum disorder.: Association between androgen receptor gene and autism. Psychoneuroendocrinology, Elsevier, 2009, 34 (5), pp.752-61. <10.1016/j.psyneuen.2008.12.007>. <inserm-00390382>
  • Alireza Kashani, Eve Lepicard, Odile Poirel, Catherine Videau, Jean Philippe David, et al.. Loss of VGLUT1 and VGLUT2 in the prefrontal cortex is correlated with cognitive decline in Alzheimer disease.. Neurobiol Aging, 2008, 29 (11), pp.1619-30. <10.1016/j.neurobiolaging.2007.04.010>. <inserm-00166908>
  • Xiaohong Gong, Elena Bacchelli, Francesca Blasi, Claudio Toma, Catalina Betancur, et al.. Analysis of X chromosome inactivation in autism spectrum disorders.. American Journal of Medical Genetics Part B Neuropsychiatric Genetics, 2008, 147B (6), pp.830-5. <10.1002/ajmg.b.30688>. <inserm-00276460>
  • Guiqing Cai, Lisa Edelmann, Juliet Goldsmith, Ninette Cohen, Alisa Nakamine, et al.. Multiplex ligation-dependent probe amplification for genetic screening in autism spectrum disorders: Efficient identification of known microduplications and identification of a novel microduplication in ASMT.. BMC Medical Genomics, BioMed Central, 2008, 1, pp.50. <10.1186/1755-8794-1-50>. <inserm-00375019v2>
  • Jonas Melke, Hany Goubran-Botros, Pauline Chaste, Catalina Betancur, Gudrun Nygren, et al.. Abnormal melatonin synthesis in autism spectrum disorders.: Abnormal melatonin synthesis in autism. Molecular Psychiatry, Nature Publishing Group, 2008, 13 (1), pp.90-8. <10.1038/sj.mp.4002016>. <inserm-00166901>
  • Pauline Chaste, Gudrun Nygren, Henrik Anckarsäter, Maria Råstam, Mary Coleman, et al.. Mutation screening of the ARX gene in patients with autism.. Am J Med Genet B Neuropsychiatr Genet, 2007, 144 (2), pp.228-30. <10.1002/ajmg.b.30440>. <inserm-00109595>
  • Richard Delorme, Véronique Goussé, Isabelle Roy, Anca Trandafir, Flavie Mathieu, et al.. Shared executive dysfunctions in unaffected relatives of patients with autism and obsessive-compulsive disorder.: Executive dysfunctions in autism and OCD. European Psychiatry, Elsevier, 2007, 22 (1), pp.32-8. <10.1016/j.eurpsy.2006.05.002>. <inserm-00125292>
  • Joseph Buxbaum, Guiqing Cai, Pauline Chaste, Gudrun Nygren, Juliet Goldsmith, et al.. Mutation screening of the PTEN gene in patients with autism spectrum disorders and macrocephaly.: PTEN mutation screening in autism. Am J Med Genet B Neuropsychiatr Genet., 2007, 144 (4), pp.484-91. <10.1002/ajmg.b.30493>. <inserm-00125293>
  • Alireza Kashani, Catalina Betancur, Bruno Giros, Etienne Hirsch, Salah El Mestikawy. Altered expression of vesicular glutamate transporters VGLUT1 and VGLUT2 in Parkinson disease.. Neurobiol Aging, 2007, 28 (4), pp.568-78. <10.1016/j.neurobiolaging.2006.02.010>. <inserm-00154872>
  • Christel Depienne, Delphine Héron, Catalina Betancur, Baya Benyahia, Oriane Trouillard, et al.. Autism, language delay and mental retardation in a patient with 7q11 duplication.. Journal of Medical Genetics, BMJ Publishing Group, 2007, 44 (7), pp.452-8. <10.1136/jmg.2006.047092>. <inserm-00166907>
  • Joseph Buxbaum, Guiqing Cai, Gudrun Nygren, Pauline Chaste, Richard Delorme, et al.. Mutation analysis of the NSD1 gene in patients with autism spectrum disorders and macrocephaly.. BMC Medical Genetics, BioMed Central, 2007, 8, pp.68. <10.1186/1471-2350-8-68>. <inserm-00276438>
  • Elise Morice, Jean-Marie Billard, Cécile Denis, Flavie Mathieu, Catalina Betancur, et al.. Parallel Loss of Hippocampal LTD and Cognitive Flexibility in a Genetic Model of Hyperdopaminergia.: Synaptic and cognitive flexibility in DAT-KO mice. Neuropsychopharmacology, Nature Publishing Group, 2007, 32 (10), pp.2108-16. <10.1038/sj.npp.1301354>. <inserm-00166900>
  • Peter Szatmari, Andrew Paterson, Lonnie Zwaigenbaum, Wendy Roberts, Jessica Brian, et al.. Mapping autism risk loci using genetic linkage and chromosomal rearrangements.. Nature Genetics, Nature Publishing Group, 2007, 39 (3), pp.319-28. <10.1038/ng1985>. <inserm-00937094>
  • Christelle Durand, Catalina Betancur, Tobias Boeckers, Juergen Bockmann, Pauline Chaste, et al.. Mutations in the gene encoding the synaptic scaffolding protein SHANK3 are associated with autism spectrum disorders.. Nature Genetics, Nature Publishing Group, 2007, 39 (1), pp.25-7. <10.1038/ng1933>. <inserm-00126175v2>
  • Christelle Durand, Caroline Kappeler, Catalina Betancur, Richard Delorme, Hélène Quach, et al.. Expression and genetic variability of PCDH11Y, a gene specific to Homo sapiens and candidate for susceptibility to psychiatric disorders.. Am J Med Genet B Neuropsychiatr Genet, 2006, 141 (1), pp.67-70. <10.1002/ajmg.b.30229>. <inserm-00124745>
  • Richard Delorme, Christelle Durand, Catalina Betancur, Michael Wagner, Stephan Ruhrmann, et al.. No human tryptophan hydroxylase-2 gene R441H mutation in a large cohort of psychiatric patients and control subjects.. Biological Psychiatry, Elsevier, 2006, 60 (2), pp.202-3. <10.1016/j.biopsych.2005.12.014>. <inserm-00124742>
  • Malin Melin, Birgit Carlsson, Henrik Anckarsäter, Maria Rastam, Catalina Betancur, et al.. Constitutional downregulation of SEMA5A expression in autism.. Neuropsychobiology, Karger, 2006, 54 (1), pp.64-9. <10.1159/000096040>. <inserm-00124743>
  • Richard Delorme, Arnaud Bille, Catalina Betancur, Flavie Mathieu, Nadia Chabane, et al.. Exploratory analysis of obsessive compulsive symptom dimensions in children and adolescents: a prospective follow-up study.. BMC Psychiatry, BioMed Central, 2006, 6, pp.1. <10.1186/1471-244X-6-1>. <inserm-00089240>
  • Grazyna Biala, Catalina Betancur, Isabelle Mansuy, Bruno Giros. The reinforcing effects of chronic D-amphetamine and morphine are impaired in a line of memory-deficient mice overexpressing calcineurin.: Role of calcineurin in the effects of drugs of abuse. European Journal of Neuroscience, Wiley, 2005, 21 (11), pp.3089-96. <10.1111/j.1460-9568.2005.04132.x>. <inserm-00276426>
  • Richard Delorme, Catalina Betancur, Michael Wagner, Marie-Odile Krebs, Philip Gorwood, et al.. Support for the association between the rare functional variant I425V of the serotonin transporter gene and susceptibility to obsessive compulsive disorder.. Mol Psychiatry, 2005, 10 (12), pp.1059-61. <10.1038/sj.mp.4001728>. <inserm-00125111>
  • Richard Delorme, Catalina Betancur, Jacques Callebert, Nadia Chabane, Jean-Louis Laplanche, et al.. Platelet serotonergic markers as endophenotypes for obsessive-compulsive disorder.: Serotonergic endophenotypic markers in OCD. Neuropsychopharmacology, Nature Publishing Group, 2005, 30 (8), pp.1539-47. <10.1038/sj.npp.1300752>. <inserm-00109585>
  • Christine Roubert, Cécile Spielewoy, Philippe Soubrié, Michel Hamon, Bruno Giros, et al.. Altered neurotensin mrna expression in mice lacking the dopamine transporter.. Neuroscience, Elsevier - International Brain Research Organization, 2004, 123 (2), pp.537-46. <inserm-00069638>
  • Marlene Lauritsen, Mette Nyegaard, Catalina Betancur, Catherine Colineaux, Trine Josiassen, et al.. Analysis of transmission of novel polymorphisms in the somatostatin receptor 5 (SSTR5) gene in patients with autism.: Analysis of SSTR5 gene polymorphisms in autism. Am J Med Genet B Neuropsychiatr Genet, 2003, 121 (1), pp.100-4. <10.1002/ajmg.b.20050>. <inserm-00124740>
  • Stéphane Jamain, Catalina Betancur, Bruno Giros, Marion Leboyer, Thomas Bourgeron. [Genetics of autism: from genome scans to candidate genes]. médecine/sciences, EDP Sciences, 2003, 19 (11), pp.1081-90. <inserm-00125099>
  • Stéphane Jamain, Hélène Quach, Catalina Betancur, Maria Råstam, Catherine Colineaux, et al.. Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism.. Nature Genetics, Nature Publishing Group, 2003, 34 (1), pp.27-9. <10.1038/ng1136>. <inserm-00124744>
  • Marlene Lauritsen, Anders Børglum, Catalina Betancur, Anne Philippe, Torben Kruse, et al.. Investigation of two variants in the DOPA decarboxylase gene in patients with autism.. Am J Med Genet, 2002, 114 (4), pp.466-70. <10.1002/ajmg.10379>. <inserm-00124738>
  • Catalina Betancur, Marion Leboyer, Christopher Gillberg. Increased rate of twins among affected sibling pairs with autism.. American Journal of Human Genetics, Elsevier (Cell Press), 2002, 70 (5), pp.1381-3. <10.1086/340364>. <inserm-00276423>
  • Stéphane Jamain, Hélène Quach, Luis Quintana-Murci, Catalina Betancur, Anne Philippe, et al.. Y chromosome haplogroups in autistic subjects: Y chromosome in autistic subjects. Molecular Psychiatry, Nature Publishing Group, 2002, 7 (2), pp.217-219. <10.1038/sj.mp.4000968>. <inserm-00124377>
  • Marie-Odile Krebs, Catalina Betancur, Sophie Leroy, Marie-Chantal Bourdel, Christopher Gillberg, et al.. Absence of association between a polymorphic GGC repeat in the 5' untranslated region of the reelin gene and autism. Molecular Psychiatry, Nature Publishing Group, 2002, 7 (7), pp.801. <inserm-00124376>
  • Stéphane Jamain, Catalina Betancur, Hélène Quach, Anne Philippe, Marc Fellous, et al.. Linkage and association of the glutamate receptor 6 gene with autism.. Molecular Psychiatry, Nature Publishing Group, 2002, 7 (3), pp.302-10. <10.1038/sj.mp.4000979>. <inserm-00125097>
  • Catalina Betancur, Marylis Corbex, Cécile Spielewoy, Anne Philippe, Jean-Louis Laplanche, et al.. Serotonin transporter gene polymorphisms and hyperserotonemia in autistic disorder.: Serotonin transporter gene, hyperserotonemia and autism. Molecular Psychiatry, Nature Publishing Group, 2002, 7 (1), pp.67. <inserm-00124375>
  • Cécile Spielewoy, Grazyna Biala, Christine Roubert, Michel Hamon, Catalina Betancur, et al.. Hypolocomotor effects of acute and daily d-amphetamine in mice lacking the dopamine transporter.: d-amphetamine-induced hypolocomotion in DAT-/- mice. Psychopharmacology (Berl), 2001, 159 (1), pp.2-9. <10.1007/s002130100901>. <inserm-00126158>
  • Catalina Betancur, Isabelle Lépée-Lorgeoux, Michèle Cazillis, Domenico Accili, Sara Fuchs, et al.. Neurotensin gene expression and behavioral responses following administration of psychostimulants and antipsychotic drugs in dopamine D(3) receptor deficient mice.. Neuropsychopharmacology, Nature Publishing Group, 2001, 24 (2), pp.170-82. <10.1016/S0893-133X(00)00179-2>. <inserm-00125114>
  • Cécile Spielewoy, François Gonon, Christine Roubert, Valérie Fauchey, Mohamed Jaber, et al.. Increased rewarding properties of morphine in dopamine-transporter knockout mice.: Increased morphine reward in DAT-/- mice. European Journal of Neuroscience, Wiley, 2000, 12 (5), pp.1827-37. <inserm-00126167>
  • Cécile Spielewoy, Christine Roubert, Michel Hamon, Marika Nosten, Catalina Betancur, et al.. Behavioural disturbances associated with hyperdopaminergia in dopamine-transporter knockout mice.: Behavioral phenotype of DAT-/- mice. Behavioural Pharmacology, Lippincott, Williams & Wilkins, 2000, 11 (3-4), pp.279-90. <inserm-00126162>
  • Isabelle Lépée-Lorgeoux, Catalina Betancur, Frédérique Souazé, William Rostène, Anne Bérod, et al.. Regulation of the neurotensin NT(1) receptor in the developing rat brain following chronic treatment with the antagonist SR 48692.: Regulation of NT1 receptors in the developing rat brain. Journal of Neuroscience Research, Wiley, 2000, 60 (3), pp.362-9. <inserm-00126155>
  • Catalina Betancur, Maryse Canton, Alain Burgos, Bernard Labeeuw, Danielle Gully, et al.. Characterization of binding sites of a new neurotensin receptor antagonist, [3H]SR 142948A, in the rat brain.. European Journal of Pharmacology, Elsevier, 1998, 343 (1), pp.67-77. <inserm-00276332>
  • Catalina Betancur, Ricardo Cabrera, E. Ronald De Kloet, Didier Pélaprat, William Rostène. Role of endogenous neurotensin in the behavioral and neuroendocrine effects of cocaine.. Neuropsychopharmacology, Nature Publishing Group, 1998, 19 (4), pp.322-32. <10.1016/S0893-133X(98)00028-1>. <inserm-00276405>
  • Catalina Betancur, Mounia Azzi, William Rostène. Nonpeptide antagonists of neuropeptide receptors: tools for research and therapy.. Trends in Pharmacological Sciences, Elsevier, 1997, 18 (10), pp.372-86. <inserm-00276481>
  • Catalina Betancur, William Rostène, Anne Bérod. Chronic cocaine increases neurotensin gene expression in the shell of the nucleus accumbens and in discrete regions of the striatum.. Molecular Brain Research, Elsevier, 1997, 44 (2), pp.334-40. <inserm-00276420>
  • Catalina Betancur, Maryse Canton, Danielle Gully, Gema Vela, Didier Pélaprat, et al.. Characterization and distribution of binding sites for a new neurotensin receptor antagonist ligand, [3H]SR 48692, in the guinea pig brain.. Journal of Pharmacology and Experimental Therapeutics, American Society for Pharmacology and Experimental Therapeutics, 1995, 273 (3), pp.1450-8. <inserm-00276482>

Chapitre d'ouvrage3 documents

  • Catalina Betancur, Kevin Mitchell. Synaptic disorders. Kevin J. Mitchell. The Genetics of Neurodevelopmental Disorders, Wiley Blackwell, pp.195-238, 2015, 978-1-118-52488-6. <inserm-01181037>
  • Catalina Betancur, Mary Coleman. Etiological heterogeneity in autism spectrum disorders: role of rare variants. Joseph D. Buxbaum, Patrick R. Hof. The Neuroscience of Autism Spectrum Disorders, Academic Press, pp.113-144, 2013. <inserm-00968357>
  • Mary Coleman, Catalina Betancur. Chapter 1 - Introduction. The Neurology of Autism, edited by Mary Coleman. Mary Coleman. The Neurology of Autism, Oxford University Press, pp.3-39, 2005. <inserm-00968329>