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Chromosome 6p22 was identified recently as a neuroblastoma susceptibility locus, but its mechanistic contributions to… Expand We conducted a SNP-based genome-wide association study (GWAS) focused on the high-risk subset of neuroblastoma. As our previous… Expand BACKGROUND
Neuroblastoma is a malignant condition of the developing sympathetic nervous system that most commonly affects young… Expand Objective: To identify genes whose expression is most characteristic of chronic rhinosinusitis and aspirin‐sensitive asthma… Expand Dyslexia is one of the most prevalent childhood cognitive disorders, affecting approximately 5% of school-age children. We have… Expand To identify gene(s) targeted by 6p22 genomic gain, present in more than 50% retinoblastoma tumors, we used real‐time RT‐PCR to… Expand DYX2 on 6p22 is the most replicated reading disability (RD) locus. By saturating a previously identified peak of association with… Expand We demonstrate that, in human bladder cancer, amplification of the E2F3 gene, located at 6p22, is associated with overexpression… Expand Little is known about the genetic changes underlying invasive tumor growth in bladder cancer. Because alterations that are linked… Expand The influence of genetic factors in schizophrenia has been convincingly demonstrated by family, twin and adoption studies1–3, but… Expand