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113 results on '"Farh, Kai-How"'

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1. Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptions

2. Using brain cell-type-specific protein interactomes to interpret neurodevelopmental genetic signals in schizophrenia

3. Population‐based identity‐by‐descent mapping combined with exome sequencing to detect rare risk variants for schizophrenia

4. Genetic Risk Score for Intracranial Aneurysms: Prediction of Subarachnoid Hemorrhage and Role in Clinical Heterogeneity

5. Analysis of shared heritability in common disorders of the brain

6. Analysis of shared heritability in common disorders of the brain.

7. Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

8. Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores

9. Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common Diseases

10. Biological insights from 108 schizophrenia-associated genetic loci

11. Schizophrenia-associated somatic copy-number variants from 12,834 cases reveal recurrent NRXN1 and ABCB11 disruptions

12. A polygenic resilience score moderates the genetic risk for schizophrenia

13. Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants With Treatment Resistance in Schizophrenia

14. Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders

15. Migraine, inflammatory bowel disease and celiac disease: A Mendelian randomization study.

16. Sex-Dependent Shared and Nonshared Genetic Architecture Across Mood and Psychotic Disorders

17. A Comparison of Ten Polygenic Score Methods for Psychiatric Disorders Applied Across Multiple Cohorts

18. Integrative analysis of 111 reference human epigenomes

19. A Comparison of Ten Polygenic Score Methods for Psychiatric Disorders Applied Across Multiple Cohorts

20. Cerebral small vessel disease genomics and its implications across the lifespan

21. A genome-wide cross-phenotype meta-analysis of the association of blood pressure with migraine

22. Complement genes contribute sex-biased vulnerability in diverse disorders

23. Gene expression imputation across multiple brain regions provides insights into schizophrenia risk

24. Gene expression imputation across multiple brain regions provides insights into schizophrenia risk

25. Gene expression imputation across multiple brain regions provides insights into schizophrenia risk

26. Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof of concept

27. Molecular genetic overlap between migraine and major depressive disorder

28. A correction for sample overlap in genome-wide association studies in a polygenic pleiotropy-informed framework

29. Estimation of Genetic Correlation via Linkage Disequilibrium Score Regression and Genomic Restricted Maximum Likelihood

30. Age at first birth in women is genetically associated with increased risk of schizophrenia

31. Analysis of shared heritability in common disorders of the brain

32. A correction for sample overlap in genome-wide association studies in a polygenic pleiotropy-informed framework

33. Estimation of Genetic Correlation via Linkage Disequilibrium Score Regression and Genomic Restricted Maximum Likelihood

34. Analysis of shared heritability in common disorders of the brain

35. Habitual sleep disturbances and migraine: a Mendelian randomization study.

36. Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

37. Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

38. Estimation of Genetic Correlation via Linkage Disequilibrium Score Regression and Genomic Restricted Maximum Likelihood

39. Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

40. No Reliable Association between Runs of Homozygosity and Schizophrenia in a Well-Powered Replication Study

41. Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

42. Biological insights from 108 schizophrenia-associated genetic loci

43. Integrative analysis of 111 reference human epigenomes

44. Meta-analysis of 375,000 individuals identifies 38 susceptibility loci for migraine

45. Biological insights from 108 schizophrenia-associated genetic loci

46. Genetic correlation between amyotrophic lateral sclerosis and schizophrenia

47. Integrative analysis of 111 reference human epigenomes

48. Genetic influences on schizophrenia and subcortical brain volumes: large-scale proof of concept

49. No Reliable Association between Runs of Homozygosity and Schizophrenia in a Well-Powered Replication Study

50. Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common Diseases

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