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Genetic risk factors influence nighttime blood pressure and related cardiovascular complications in patients with coronary heart disease
No association between 5 new GWAS-linked loci in Parkinson’s disease and multiple system atrophy in a Chinese population
Single nucleotide polymorphisms in asthma candidate genes TBXA2R, ADAM33 FCER1B and ORMDL3 in Pakistani asthmatics a case control study
Allelic variation in dopamine D2 receptor gene is associated with attentional impulsiveness on the Barratt Impulsiveness Scale (BIS-11)
Genome-wide association study identifies a new locus at 7q21. 13 associated with hepatitis B virus–related hepatocellular carcinoma
Matrix‐assisted laser desorption/ionization time‐of‐flight mass spectrometry analysis of 36 blood group alleles among 396 T hai samples reveals region‐specific …
Replication Study Confirms the Association of the Common rs1800629 Variant of the TNFα Gene with Postmenopausal Osteoporosis Susceptibility in the Han …
Genetic variation in the von Willebrand factor gene in Swedish von Willebrand disease patients
Exome sequencing study in patients with multiple sclerosis reveals variants associated with disease course
Quantitative Measurement of PARD3 Copy Number Variations in Human Neural Tube Defects