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Genome-wide association study of bone mineral density in premenopausal European-American women and replication in African-American women
High-throughput analysis of candidate imprinted genes and allele-specific gene expression in the human term placenta
Haplotype analysis reveals a possible founder effect of RET mutation R114H for HirschsprungÂ´s disease in the Chinese population
Targeted genome-wide investigation identifies novel SNPs associated with diabetic nephropathy
Gender-specific association of galanin polymorphisms with HPA-axis dysregulation, symptom severity, and antidepressant treatment response
A genetic marker at the OLIG3/TNFAIP3 locus associated with methotrexate continuation in early inflammatory polyarthritis: results from the Norfolk Arthritis Register
Genome-wide Association Study identifies ALDH7A1 as a Novel Susceptibility Gene for Osteoporosis
Combined iPLEX and TaqMan assays to screen for 45 common mutations in Lynch syndrome and FAP patients
Genetic variability in the MTHFR gene and colorectal cancer risk using the colorectal cancer family registry
Genome-wide Association Study in a High-Risk Isolate for Multiple Sclerosis Reveals Associated Variants in STAT3 Gene