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1. Rare tandem repeat expansions associate with genes involved in synaptic and neuronal signaling functions in schizophrenia

3. Author Correction: Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia

4. Latin American Trans‐ancestry INitiative for OCD genomics (LATINO): Study protocol.

5. Characterization of Single Gene Copy Number Variants in Schizophrenia

6. Increased burden of ultra-rare structural variants localizing to boundaries of topologically associated domains in schizophrenia

7. Common-variant associations with fragile X syndrome

8. Latin American Trans-ancestry INitiative for OCD genomics (LATINO): Study Protocol

10. Rare tandem repeat expansions associate with genes involved in synaptic and neuronal signaling functions in schizophrenia

11. DIFFERENTIAL ISOFORM USAGE IN SCHIZOPHRENIA

13. 82. INCREASED BURDEN OF RARE TANDEM REPEAT EXPANSIONS IN SCHIZOPHRENIA

14. Correction: Common-variant associations with fragile X syndrome

15. Characterization of single gene copy number variants in schizophrenia

16. A CHROMATIN CATALOG FOR THE INTERPRETATION OF GENETIC ASSOCIATIONS OF PSYCHIATRIC DISORDERS

17. Common-variant associations with fragile X syndrome

18. Exploration of large, rare copy number variants associated with psychiatric and neurodevelopmental disorders in individuals with anorexia nervosa

19. Common Variant Associations with Fragile X Syndrome

22. Latin American Trans-ancestry INitiative for OCD genomics (LATINO): Study Protocol.

23. Exploration of large, rare copy number variants associated with psychiatric and neurodevelopmental disorders in individuals with anorexia nervosa.

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