Search

Your search keyword '"Francks, C"' showing total 474 results

Search Constraints

Start Over You searched for: Author "Francks, C" Remove constraint Author: "Francks, C"
474 results on '"Francks, C"'

Search Results

1. Large-scale analysis of structural brain asymmetries during neurodevelopment : Associations with age and sex in 4265 children and adolescents.

2. Genetic architecture of the white matter connectome of the human brain.

3. Author Correction: Discovery of 42 genome-wide significant loci associated with dyslexia

4. Large-scale analysis of structural brain asymmetries in schizophrenia via the ENIGMA consortium.

5. Large- scale analysis of structural brain asymmetries in schizophrenia via the ENIGMA consortium

6. Tracing the development and lifespan change of population-level structural asymmetry in the cerebral cortex

7. Tracing the development and lifespan change of population-level structural asymmetry in the cerebral cortex

8. Exome-wide analysis implicates rare protein-altering variants in human handedness

9. Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities

10. Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people

11. Reproducibility in the absence of selective reporting: An illustration from large‐scale brain asymmetry research

12. Mapping brain asymmetry in health and disease through the ENIGMA consortium

13. Consortium neuroscience of attention deficit/hyperactivity disorder and autism spectrum disorder: The ENIGMA adventure

14. Reproducibility in the absence of selective reporting: An illustration from large-scale brain asymmetry research

15. Inherited variants in CHD3 show variable expressivity in Snijders Blok-Campeau syndrome

16. Topographic divergence of atypical cortical asymmetry and atrophy patterns in temporal lobe epilepsy

17. Reproducibility in the absence of selective reporting: An illustration from large-scale brain asymmetry research

18. Topographic divergence of atypical cortical asymmetry and atrophy patterns in temporal lobe epilepsy

19. An overview of the first 5 years of the ENIGMA obsessive-compulsive disorder working group: The power of worldwide collaboration

20. Mapping brain asymmetry in health and disease through the ENIGMA consortium

21. Consortium neuroscience of attention deficit/hyperactivity disorder and autism spectrum disorder: The ENIGMA adventure

24. Subtly altered topological asymmetry of brain structural covariance networks in autism spectrum disorder across 43 datasets from the ENIGMA consortium

25. Discovery of 42 genome-wide significant loci associated with dyslexia

26. Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people

27. Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities

29. In the News

31. Large-scale phenomic and genomic analysis of brain asymmetrical skew

32. Analysis of structural brain asymmetries in attention-deficit/hyperactivity disorder in 39 datasets

34. The genetic architecture of structural left-right asymmetry of the human brain

36. Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia

37. Whole-genome sequencing identifies functional noncoding variation in SEMA3C that cosegregates with dyslexia in a multigenerational family

38. Analysis of structural brain asymmetries in attention-deficit/hyperactivity disorder in 39 datasets

41. Large-scale phenomic and genomic analysis of brain asymmetrical skew

42. Copy number variations of chromosome 16p13.1 region associated with schizophrenia

49. LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia

Catalog

Books, media, physical & digital resources