Paternal genetic variants and risk of obstructive heart defects: A parent-of-origin approach - Patel, Jenil; Bircan, Emine; Tang, Xinyu; Orloff, Mohammed; Hobbs, Charlotte A.; Browne, Marilyn L.; Botto, Lorenzo D.; Finnell, Richard H.; Jenkins, Mary M.; Olshan, Andrew; Romitti, Paul A.; Shaw, Gary M.; et al. (PLoS genetics, 2021)
Keywords: Adult; Age; Alleles; Analysis; Aorta; Biology and Life Sciences; Birth defects; Cardiomyopathy, Hypertrophic, Familial - genetics; Chromosome Mapping; Congenital defects; Congenital heart disease; Deoxyribonucleic acid; Diabetes; DNA; Epigenetic inheritance; Epigenetics; Etiology; Families & family life; Female; Folic acid; Genes; Genetic aspects; Genetic diversity; Genetic Predisposition to Disease; Genetic Variation; Genotype; Glutathione; Heart; Heart Defects, Congenital - epidemiology; Heart Defects, Congenital - genetics; Heart Defects, Congenital - metabolism; Homocysteine; Humans; Infants; Inheritance Patterns; Male; Medicine and Health Sciences; Middle Aged; Mothers; Odds Ratio; Paternity testing; People and Places; Phenotype; Polymorphism, Single Nucleotide; Pregnancy; Prevention; Risk Assessment; Risk factors; Single-nucleotide polymorphism; Smoking; Statistical analysis; Stenosis; Vitamin B; Young Adult; United States; United States--US