DNA hypomethylation within specific transposable element families associates with tissue-specific enhancer landscape. Read more about DNA hypomethylation within specific transposable element families associates with tissue-specific enhancer landscape.
A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry. Read more about A meta-analysis identifies new loci associated with body mass index in individuals of African ancestry.
Turning of COGS moves forward findings for hormonally mediated cancers. Read more about Turning of COGS moves forward findings for hormonally mediated cancers.
Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer. Read more about Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer.
Genome-wide association studies identify four ER negative-specific breast cancer risk loci. Read more about Genome-wide association studies identify four ER negative-specific breast cancer risk loci.
The genomic landscape of hypodiploid acute lymphoblastic leukemia. Read more about The genomic landscape of hypodiploid acute lymphoblastic leukemia.
A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9. Read more about A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9.
Inhibition of RNA lariat debranching enzyme suppresses TDP-43 toxicity in ALS disease models. Read more about Inhibition of RNA lariat debranching enzyme suppresses TDP-43 toxicity in ALS disease models.
CHMP1A encodes an essential regulator of BMI1-INK4A in cerebellar development. Read more about CHMP1A encodes an essential regulator of BMI1-INK4A in cerebellar development.
Genome-wide association study identifies a common variant in RAD51B associated with male breast cancer risk. Read more about Genome-wide association study identifies a common variant in RAD51B associated with male breast cancer risk.
