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Common vitamin D pathway gene variants reveal contrasting effects on serum vitamin D levels in African Americans and European Americans
CREM Variants rs4934540 and rs2295415 Conferred Susceptibility to Non-Obstructive Azoospermia Risk in the Chinese Population
Cuba: Exploring the History of Admixture and the Genetic Basis of Pigmentation Using Autosomal and Uniparental Mark
Detection of Copy Number Variation (CNV) by SNP-Allelotyping
Determinants Of Oral corticosteroid Responsiveness in Wheezing Asthmatic Youth (DOORWAY
Digital Genotyping of Macrosatellites and Multicopy Genes Reveals Novel Biological Functions Associated with Copy Number Variation of Large Tandem Repeats
Distribution and Medical Impact of Loss-of-Function Variants in the Finnish Founder Population
Clinical and non-targeted metabolomic profiling of homozygous carriers of Transcription Factor 7-like 2 variant rs7903146
Combination of hearing screening and genetic screening for deafness-susceptibility genes in newborns
Blood cis-eQTL Analysis Fails to Identify Novel Association Signals among Sub-Threshold Candidates from Genome-Wide Association Studies in Restless Legs Syndrome