Subcellular localization of MC4R with ADCY3 at neuronal primary cilia underlies a common pathway for genetic predisposition to obesity. Read more about Subcellular localization of MC4R with ADCY3 at neuronal primary cilia underlies a common pathway for genetic predisposition to obesity.
Evolution and clinical impact of co-occurring genetic alterations in advanced-stage EGFR-mutant lung cancers. Read more about Evolution and clinical impact of co-occurring genetic alterations in advanced-stage EGFR-mutant lung cancers.
Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology. Read more about Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology.
Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer. Read more about Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer.
Enhancer connectome in primary human cells identifies target genes of disease-associated DNA elements. Read more about Enhancer connectome in primary human cells identifies target genes of disease-associated DNA elements.
Lgr6 is a stem cell marker in mouse skin squamous cell carcinoma. Read more about Lgr6 is a stem cell marker in mouse skin squamous cell carcinoma.
Transcriptional risk scores link GWAS to eQTLs and predict complications in Crohn's disease. Read more about Transcriptional risk scores link GWAS to eQTLs and predict complications in Crohn's disease.
The genomic landscape of pediatric and young adult T-lineage acute lymphoblastic leukemia. Read more about The genomic landscape of pediatric and young adult T-lineage acute lymphoblastic leukemia.
Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors. Read more about Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors.
Biallelic mutations in human DCC cause developmental split-brain syndrome. Read more about Biallelic mutations in human DCC cause developmental split-brain syndrome.
