Human molecular genetics
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A multi-ancestry genome-wide study incorporating gene-smoking interactions identifies multiple new loci for pulse pressure and mean arterial pressure.
GWAS meta-analysis of 16,852 women identifies new susceptibility locus for endometrial cancer.
Shared genetics underlying epidemiological association between endometriosis and ovarian cancer.
Epigenome-wide ovarian cancer analysis identifies a methylation profile differentiating clear-cell histology with epigenetic silencing of the HERG K+ channel.
Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error.
Inhibition of GSK3β improves hippocampus-dependent learning and rescues neurogenesis in a mouse model of fragile X syndrome.
Npc1 haploinsufficiency promotes weight gain and metabolic features associated with insulin resistance.
A set of differentially expressed miRNAs, including miR-30a-5p, act as post-transcriptional inhibitors of BDNF in prefrontal cortex.
The loss of methyl-CpG binding protein 1 leads to autism-like behavioral deficits.