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1. Fine-mapping across diverse ancestries drives the discovery of putative causal variants underlying human complex traits and diseases

2. Shared genetic architectures of educational attainment in East Asian and European populations

3. Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease

7. Plasma lipidomics profile in pregnancy and gestational diabetes risk: a prospective study in a multiracial/ethnic cohort

8. Evidence in the UK Biobank for the underdiagnosis of erythropoietic protoporphyria

9. Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders

10. Global Biobank analyses provide lessons for developing polygenic risk scores across diverse cohorts

12. Meta-analysis fine-mapping is often miscalibrated at single-variant resolution

13. Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals

17. Development and validation of a trans-ancestry polygenic risk score for type 2 diabetes in diverse populations

19. Genome-Wide Association Study of Treatment-Resistant Depression: Shared Biology With Metabolic Traits

20. Can polygenic scores enhance the predictive performance of clinical risk models for suicide attempts in a psychiatric emergency room setting? (Preprint)

25. Meta-Analyses of Genome-Wide Association Studies for Postpartum Depression

26. A second update on mapping the human genetic architecture of COVID-19

27. Global Biobank analyses provide lessons for developing polygenic risk scores across diverse cohorts

28. Global Biobank Meta-analysis Initiative: Powering genetic discovery across human disease

31. Global Biobank analyses provide lessons for developing polygenic risk scores across diverse cohorts

33. Investigating the genetic relationship between Alzheimer’s disease and cancer using GWAS summary statistics

35. NOVEL LOCI AND TARGET GENES INFLUENCING FUNCTIONAL SEIZURES IDENTIFIED IN A MULTI-SITE GENOME-WIDE ASSOCIATION STUDY META-ANALYSIS IN A SAMPLE OF 570,460 PATIENTS

39. Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals.

40. The role of common genetic variation in presumed monogenic epilepsies

41. Genome-wide association study of treatment resistant depression highlights shared biology with metabolic traits

43. The role of common genetic variation in presumed monogenic epilepsies

44. The role of common genetic variation in presumed monogenic epilepsies

45. Global Biobank Meta-analysis Initiative:Powering genetic discovery across human disease

46. Genome-wide risk prediction of common diseases across ancestries in one million people

48. Additional file 1 of Development and validation of a trans-ancestry polygenic risk score for type 2 diabetes in diverse populations

49. Additional file 1 of Psychiatric manifestations of rare variation in medically actionable genes: a PheWAS approach

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