17 results on '"Francks C"'
Search Results
2. Next-gen sequencing identifies non-coding variation disrupting miRNA-binding sites in neurological disorders
3. Evaluation of results from genome-wide studies of language and reading in a novel independent dataset
4. A genome‐wide search for quantitative trait loci affecting the cortical surface area and thickness of Heschl's gyrus
5. Genome-wide association study of recurrent major depressive disorder in two European case–control cohorts
6. Population-based linkage analysis of schizophrenia and bipolar case–control cohorts identifies a potential susceptibility locus on 19q13
7. GENOMIC FINDINGS IN SCHIZOPHRENIA, ANIMAL MODELS AND INTERMEDIATE PHENOTYPES
8. 174 – Genomic findings in schizophrenia, animal models and intermediate phenotypes
9. α-5/α-3 nicotinic receptor subunit alleles increase risk for heavy smoking
10. LRRTM1 protein is located in the endoplasmic reticulum (ER) in mammalian cells
11. LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia
12. Genes, cognition and dyslexia: learning to read the genome
13. Pooled genome-wide linkage data on 424 ADHD ASPs suggests genetic heterogeneity and a common risk locus at 5p13
14. Bivariate linkage scan for reading disability and attention‐deficit/hyperactivity disorder localizes pleiotropic loci
15. Genome-wide scan of reading ability in affected sibling pairs with attention-deficit/hyperactivity disorder: unique and shared genetic effects
16. Parent-of-origin effects on handedness and schizophrenia susceptibility on chromosome 2p12-q11
17. A sibling-pair based approach for mapping genetic loci that influence quantitative measures of reading disability
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