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Search Results to Cathy Barr

This is a "connection" page, showing the details of why an item matched the keywords from your search.

                     
                     

One or more keywords matched the following items that are connected to Barr, Cathy

Item TypeName
Concept Chromosomes, Human, Pair 15
Concept Sex Chromosome Aberrations
Concept Chromosomes, Human, X
Concept Chromosomes, Human, Pair 12
Concept Chromosomes, Human, Pair 16
Concept Chromosomes, Human, Pair 17
Concept Chromosomes, Human, Pair 11
Concept Chromosomes, Human, Pair 1
Concept Chromosomes, Human, Pair 4
Concept Chromosomes, Human, Pair 5
Concept Chromosome Mapping
Concept Chromosome Aberrations
Concept Chromosomes, Human, Pair 6
Concept Chromosomes, Human, Pair 13
Concept Chromosomes, Human, Pair 9
Concept Chromosome Disorders
Academic Article Linkage study between congenital cataracts and five crystallin loci.
Academic Article Glutamate receptor, ionotropic, N-methyl D-aspartate 2A (GRIN2A) gene as a positional candidate for attention-deficit/hyperactivity disorder in the 16p13 region.
Academic Article Support for EKN1 as the susceptibility locus for dyslexia on 15q21.
Academic Article Indications of linkage and association of Gilles de la Tourette syndrome in two independent family samples: 17q25 is a putative susceptibility region.
Academic Article The SNAP25 gene as a susceptibility gene contributing to attention-deficit hyperactivity disorder.
Academic Article Association study between Gilles de la Tourette Syndrome and two genes in the Robo-Slit pathway located in the chromosome 11q24 linked/associated region.
Academic Article GPR50 is not associated with childhood-onset mood disorders in a large sample of Hungarian families.
Academic Article Association study for genes at chromosome 5p13-q11 in attention deficit hyperactivity disorder.
Academic Article Association of the neurotrophic tyrosine kinase receptor 3 (NTRK3) gene and childhood-onset mood disorders.
Academic Article Chromosome 5 and Gilles de la Tourette syndrome: Linkage in a large pedigree and association study of six candidates in the region.
Academic Article Tagging SNP association study of the IL-1beta gene (IL1B) and childhood-onset mood disorders.
Academic Article Genome scan in sibling pairs with juvenile-onset mood disorders: Evidence for linkage to 13q and Xq.
Academic Article Association of ADHD and the Protogenin gene in the chromosome 15q21.3 reading disabilities linkage region.
Academic Article The KIAA0319-like (KIAA0319L) gene on chromosome 1p34 as a candidate for reading disabilities.
Academic Article Association of attention-deficit/hyperactivity disorder with a candidate region for reading disabilities on chromosome 6p.
Academic Article Association of reading disabilities with regions marked by acetylated H3 histones in KIAA0319.
Academic Article Genetic variation in the KIAA0319 5' region as a possible contributor to dyslexia.
Academic Article Genome-wide association study of Tourette's syndrome.
Academic Article (G)n-mononucleotide polymorphism in the human D4 dopamine receptor (DRD4) gene.
Academic Article Linkage study of a susceptibility locus for schizophrenia in the pseudoautosomal region.
Academic Article Alleles at the dopamine D4 receptor locus do not contribute to the genetic susceptibility to schizophrenia in a large Swedish kindred.
Academic Article Why two findings which were eventually refuted have been seminal for the field of psychiatric genetics.
Academic Article Genetic locus heterogeneity in Lafora's progressive myoclonus epilepsy.
Academic Article Genetics and sleep disorders.
Academic Article Evidence for the serotonin HTR2A receptor gene as a susceptibility factor in attention deficit hyperactivity disorder (ADHD).
Academic Article Attention-deficit hyperactivity disorder and the gene for the dopamine D5 receptor.
Academic Article Linkage study of polymorphisms in the gene for myelin oligodendrocyte glycoprotein located on chromosome 6p and attention deficit hyperactivity disorder.
Academic Article Linkage study in families with posterior helical ear pits and Wiedemann-Beckwith syndrome.
Academic Article Attention deficit hyperactivity disorder and the gene for dopamine Beta-hydroxylase.
Academic Article Genome-wide association study of word reading: Overlap with risk genes for neurodevelopmental disorders.

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  • Chromosomes