Pages that link to "Q36661591"

The following pages link to Linkage to chromosome 1p36 for attention-deficit/hyperactivity disorder traits in school and home settings (Q36661591):

Displaying 27 items.

• The genetics of attention deficit/hyperactivity disorder in adults, a review (Q22251103) ‎ (← links)
• Genome-wide association scan of the time to onset of attention deficit hyperactivity disorder (Q24644291) ‎ (← links)
• The genetics of reading disabilities: from phenotypes to candidate genes (Q30459192) ‎ (← links)
• Genome-wide association scan of attention deficit hyperactivity disorder (Q33699542) ‎ (← links)
• The impact of study design and diagnostic approach in a large multi-centre ADHD study. Part 1: ADHD symptom patterns (Q33865138) ‎ (← links)
• A common haplotype of KIAA0319 contributes to the phonological awareness skill in Chinese children (Q33965244) ‎ (← links)
• Case-Control Genome-Wide Association Study of Attention-Deficit/Hyperactivity Disorder (Q34085418) ‎ (← links)
• Identifying loci for the overlap between attention-deficit/hyperactivity disorder and autism spectrum disorder using a genome-wide QTL linkage approach (Q34089144) ‎ (← links)
• Suggestive linkage of ADHD to chromosome 18q22 in a young genetically isolated Dutch population (Q34326731) ‎ (← links)
• Neuropsychological endophenotype approach to genome-wide linkage analysis identifies susceptibility loci for ADHD on 2q21.1 and 13q12.11. (Q36744642) ‎ (← links)
• Genome-wide association studies in ADHD. (Q37175234) ‎ (← links)
• Advances in genetic studies of attention-deficit/hyperactivity disorder (Q37419585) ‎ (← links)
• The molecular genetic architecture of attention deficit hyperactivity disorder. (Q38323555) ‎ (← links)
• Neuropsychological intra-individual variability explains unique genetic variance of ADHD and shows suggestive linkage to chromosomes 12, 13, and 17. (Q42631220) ‎ (← links)
• The NeuroIMAGE study: a prospective phenotypic, cognitive, genetic and MRI study in children with attention-deficit/hyperactivity disorder. Design and descriptives (Q42671533) ‎ (← links)
• ADHD in Dutch adults: heritability and linkage study (Q42688955) ‎ (← links)
• The role of cadherin genes in five major psychiatric disorders: A literature update. (Q47766376) ‎ (← links)
• Familial dyslexia in a large Swedish family: a whole genome linkage scan (Q48531897) ‎ (← links)
• Quantitative linkage for autism spectrum disorders symptoms in attention-deficit/hyperactivity disorder: significant locus on chromosome 7q11. (Q50342841) ‎ (← links)
• Genome-wide association study of motor coordination problems in ADHD identifies genes for brain and muscle function. (Q51873167) ‎ (← links)
• Epidemiology of Attention Deficit Hyperactivity Disorder (Q57399827) ‎ (← links)
• Neurobiology and neurogenetics of dyslexia (Q58227231) ‎ (← links)
• Dislexias evolutivas: qué pueden decirnos la neurología y la genética al respecto (Q58227234) ‎ (← links)
• A Cohort of Balanced Reciprocal Translocations Associated with Dyslexia: Identification of Two Putative Candidate Genes at DYX1 (Q58612547) ‎ (← links)
• Genomic evidence for MHC disassortative mating in humans (Q92484417) ‎ (← links)
• Single nucleotide polymorphism heritability and differential patterns of genetic overlap between inattention and four neurocognitive factors in youth (Q92778923) ‎ (← links)
• Wikidata:WikiProject Scholia/Listeria/topic/Works with many co-authors but no main subject ‎ (← links | edit)