A transition zone complex regulates mammalian ciliogenesis and ciliary membrane composition. Read more about A transition zone complex regulates mammalian ciliogenesis and ciliary membrane composition.
The nuclear deubiquitinase BAP1 is commonly inactivated by somatic mutations and 3p21.1 losses in malignant pleural mesothelioma. Read more about The nuclear deubiquitinase BAP1 is commonly inactivated by somatic mutations and 3p21.1 losses in malignant pleural mesothelioma.
Genome-wide association study of prostate cancer in men of African ancestry identifies a susceptibility locus at 17q21. Read more about Genome-wide association study of prostate cancer in men of African ancestry identifies a susceptibility locus at 17q21.
Ancestry and pharmacogenomics of relapse in acute lymphoblastic leukemia. Read more about Ancestry and pharmacogenomics of relapse in acute lymphoblastic leukemia.
Common variants in P2RY11 are associated with narcolepsy. Read more about Common variants in P2RY11 are associated with narcolepsy.
A genome-wide association study of Hodgkin's lymphoma identifies new susceptibility loci at 2p16.1 (REL), 8q24.21 and 10p14 (GATA3). Read more about A genome-wide association study of Hodgkin's lymphoma identifies new susceptibility loci at 2p16.1 (REL), 8q24.21 and 10p14 (GATA3).
Mutations in WDR62, encoding a centrosome-associated protein, cause microcephaly with simplified gyri and abnormal cortical architecture. Read more about Mutations in WDR62, encoding a centrosome-associated protein, cause microcephaly with simplified gyri and abnormal cortical architecture.
Germline CBL mutations cause developmental abnormalities and predispose to juvenile myelomonocytic leukemia. Read more about Germline CBL mutations cause developmental abnormalities and predispose to juvenile myelomonocytic leukemia.
Genome-wide association study of follicular lymphoma identifies a risk locus at 6p21.32. Read more about Genome-wide association study of follicular lymphoma identifies a risk locus at 6p21.32.
