Catalina Betancur chercheuse
Betancur, Catalina, 19..-....
![Sudoc [ABES], France](/viaf/images/flags/SUDOC.png "Sudoc [ABES], France")
VIAF ID: 310753970 (Personal)
Permalink: http://viaf.org/viaf/310753970
Preferred Forms
4xx's: Alternate Name Forms (4)
Works
| Title | Sources |
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| Association between left-handedness and allergy: A reappraisal |
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| Autism multiplex family with 16p11.2p12.2 microduplication syndrome in monozygotic twins and distal 16p11.2 deletion in their brother |
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| A balanced reciprocal translocation t |
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| Caractérisation des CNV dans les troubles du spectre autistique : identification de nouveaux gènes et analyses fonctionnelles |
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| Characterization of the CNV in the autism spectrum disorders : identification of new genes and functional analysis. |
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| Chronic cocaine increases neurotensin gene expression in the shell of the nucleus accumbens and in discrete regions of the striatum |
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| Clinical utility gene card for: deletion 22q13 syndrome |
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| Complex nature of apparently balanced chromosomal rearrangements in patients with autism spectrum disorder |
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| Constitutional downregulation of SEMA5A expression in autism |
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| Contributors |
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| Cytokine Regulation of Corticosteroid Receptors in the Rat Hippocampus: Effects of Interleukin-1, Interleukin-6, Tumor Necrosis Factor and Lipopolysaccharide |
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| Delineation of the genetic and clinical spectrum of Phelan-McDermid syndrome caused by SHANK3 point mutations. |
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| Dissection of the genetic architecture of the autism by analysis of the variations of the number of copies of genes. |
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| The emerging role of synaptic cell-adhesion pathways in the pathogenesis of autism spectrum disorders |
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| Endogenous neurotensin regulates hypothalamic-pituitary-adrenal axis activity and peptidergic neurons in the rat hypothalamic paraventricular nucleus. |
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| Etiological heterogeneity in autism spectrum disorders: More than 100 genetic and genomic disorders and still counting |
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| Évaluation du récepteur cannabinoïde CB1 comme cible thérapeutique dans un modèle d'autisme et du syndrome de Phelan-McDermid des souris déficientes pour Shank3. |
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| Exploratory analysis of obsessive compulsive symptom dimensions in children and adolescents: a prospective follow-up study |
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| Expression and genetic variability of PCDH11Y, a gene specific to Homo sapiens and candidate for susceptibility to psychiatric disorders |
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| A framework for an evidence-based gene list relevant to autism spectrum disorder |
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| Functional brain asymmetry and lymphocyte proliferation in female mice: effects of right and left cortical ablation |
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| Functional brain asymmetry and murine systemic lupus erythematosus |
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| Genetic and functional analyses demonstrate a role for abnormal glycinergic signaling in autism |
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| Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs |
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| Genetics of autism: from genome scans to candidate genes |
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| Génétique et physiopathologie du syndrome de Lowe, analyse des aspects neurologiques |
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| A genome-wide scan for common alleles affecting risk for autism |
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| High-functioning autism spectrum disorder and fragile X syndrome: report of two affected sisters |
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| Hypolocomotor effects of acute and daily d-amphetamine in mice lacking the dopamine transporter |
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| Increased rate of twins among affected sibling pairs with autism |
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| Increased rewarding properties of morphine in dopamine-transporter knockout mice |
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| Individual common variants exert weak effects on the risk for autism spectrum disorders |
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| Introduction |
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| La latéralisation cérébrale comme source de différences interindividuelles dans la réponse immunitaire |
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| Loss of VGLUT1 and VGLUT2 in the prefrontal cortex is correlated with cognitive decline in Alzheimer disease |
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| Magnetic field effects on stress-induced analgesia in mice: modulation by light |
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| Mapping autism risk loci using genetic linkage and chromosomal rearrangements |
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| Molecular characterization of a de novo 6q24.2q25.3 duplication interrupting UTRN in a patient with arthrogryposis. |
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| Mutation screening of the ARX gene in patients with autism |
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| Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism |
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| Natural killer cell activity is associated with brain asymmetry in male mice |
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| Network- and attribute-based classifiers can prioritize genes and pathways for autism spectrum disorders and intellectual disability |
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| Network topologies and convergent aetiologies arising from deletions and duplications observed in individuals with autism |
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| Neuropsychiatric decompensation in adolescents and adults with Phelan-McDermid syndrome: a systematic review of the literature |
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| Neurotensin gene expression and behavioral responses following administration of psychostimulants and antipsychotic drugs in dopamine D(3) receptor deficient mice |
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| No human tryptophan hydroxylase-2 gene R441H mutation in a large cohort of psychiatric patients and control subjects |
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| Nonpeptide antagonists of neuropeptide receptors: tools for research and therapy. |
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| Novel genes for autism implicate both excitatory and inhibitory cell lineages in risk |
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| 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 |
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| Paracentric inversion of chromosome 2 associated with cryptic duplication of 2q14 and deletion of 2q37 in a patient with autism. |
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| Parallel loss of hippocampal LTD and cognitive flexibility in a genetic model of hyperdopaminergia |
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| Patterns and rates of exonic de novo mutations in autism spectrum disorders |
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| Platelet serotonergic markers as endophenotypes for obsessive-compulsive disorder |
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| Possible association between the androgen receptor gene and autism spectrum disorder |
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| Prospective investigation of autism and genotype-phenotype correlations in 22q13 deletion syndrome and SHANK3 deficiency |
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| Reduced 3-O-methyl-dopa levels in OCD patients and their unaffected parents is associated with the low activity M158 COMT allele |
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| Regulation of the neurotensin NT(1) receptor in the developing rat brain following chronic treatment with the antagonist SR 48692 |
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| The reinforcing effects of chronic D-amphetamine and morphine are impaired in a line of memory-deficient mice overexpressing calcineurin |
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| Repeated administration of the neurotensin receptor antagonist SR 48692 differentially regulates mesocortical and mesolimbic dopaminergic systems. |
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| Response to Visscher. |
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| Rigor in science and science reporting: updated guidelines for submissions to |
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| Role of dopamine D3 receptors in thermoregulation: a reappraisal |
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| Role of endogenous neurotensin in the behavioral and neuroendocrine effects of cocaine |
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| Screening for genomic rearrangements and methylation abnormalities of the 15q11-q13 region in autism spectrum disorders |
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| Search for copy number variants in chromosomes 15q11-q13 and 22q11.2 in obsessive compulsive disorder |
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| Serotonin transporter gene polymorphisms and hyperserotonemia in autistic disorder |
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| SHANK3 haploinsufficiency: a "common" but underdiagnosed highly penetrant monogenic cause of autism spectrum disorders |
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| Shared executive dysfunctions in unaffected relatives of patients with autism and obsessive-compulsive disorder |
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| Steroid effects on brain functions: an example of the action of glucocorticoids on central dopaminergic and neurotensinergic systems. |
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| Strain and sex differences in the degree of paw preference in mice |
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| Support for the association between the rare functional variant I425V of the serotonin transporter gene and susceptibility to obsessive compulsive disorder |
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| Tissue distribution and cellular localization of the levocabastine-sensitive neurotensin receptor mRNA in adult rat brain |
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| Use of nonpeptide antagonists to explore the physiological roles of neurotensin. Focus on brain neurotensin/dopamine interactions. |
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| Viral vector-mediated Cre recombinase expression in substantia nigra induces lesions of the nigrostriatal pathway associated with perturbations of dopamine-related behaviors and hallmarks of programmed cell death |
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| Y chromosome haplogroups in autistic subjects |
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| ভূমিকা |
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