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1. A case-control collapsing analysis identifies epilepsy genes implicated in trio sequencing studies focused on de novo mutations

7. Association of IREB2 and CHRNA3 polymorphisms with airflow obstruction in severe alpha-1 antitrypsin deficiency

8. Comparative Anatomy of Chromosomal Domains with Imprinted and Non-Imprinted Allele-Specific DNA Methylation

14. Evidence-Based Assessment of Congenital Heart Disease Genes to Enable Returning Results in a Genomic Study

16. Gene-centric Meta-analysis in 87,736 Individuals of European Ancestry Identifies Multiple Blood-Pressure-Related Loci

17. Generalization of DNA microarray dispersion properties: microarray equivalent of t-distribution

20. Genome-Wide Association of Body Fat Distribution in African Ancestry Populations Suggests New Loci

21. Genome-wide association study of lung function and clinical implication in heavy smokers

24. Integration of Sequence Data from a Consanguineous Family with Genetic Data from an Outbred Population Identifies PLB1 as a Candidate Rheumatoid Arthritis Risk Gene

26. Large-Scale Genome-Wide Association Studies and Meta-Analyses of Longitudinal Change in Adult Lung Function

27. Lp-PLA2, scavenger receptor class B type I gene (SCARB1) rs10846744 variant, and cardiovascular disease

31. NPHS2 variation in focal and segmental glomerulosclerosis

36. Rare variants in SOX17 are associated with pulmonary arterial hypertension with congenital heart disease

39. Single-trait and multi-trait genome-wide association analyses identify novel loci for blood pressure in African-ancestry populations

41. The Congenital Heart Disease Genetic Network Study: Cohort description

43. Transcriptomic profiles of aging in purified human immune cells