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The rate of unfavorable features is increased in association with increasing MYCN copy number in patients with neuroblastoma

MYCN Copy Number Tied to Poor Features in Neuroblastoma

Patients with MYCN gain had inferior outcomes, including lowest response rate after chemo
Germline deleterious mutations are enriched among men with prostate cancer and at least one additional primary cancer

Germline Mutations Up in Men With Prostate CA, One Other CA

However, most of these men do not meet current clinical criteria for germline testing
Whole-genome sequencing of healthy people reveals that while some are at risk for rare genetic diseases

Whole-Genome Sequencing of Uncertain Clinical Utility

Testing may prompt additional clinical actions of unclear value, researchers say
Plasma suPAR levels independently predict renal function decline in individuals with apolipoprotein L1 risk variants

suPAR Protein Levels Impact CKD Risk With APOL1 Variants

Risk reduced with lower levels of plasma suPAR, strengthened by higher levels
For patients with acute myeloid leukemia and a FLT3 mutation

Longer Survival for Midostaurin + Chemotherapy in AML With FLT3

Prolonged overall, event-free survival for patients with acute myeloid leukemia, FLT3 mutation
For patients undergoing outpatient colonoscopy

Family History Questionnaire Ups Genetic Counseling for CRC

Findings in patients who received family history questionnaire before outpatient colonoscopy
More than half of patients with advanced cancer who undergo tumor genomic profiling are interested in learning their secondary germline findings

Many With Advanced Cancer Want Secondary Germline Findings Info

Attitudes toward learning influenced by patients' personal disease experience, health status
The presence of clonal hematopoiesis of indeterminate potential is associated with coronary heart disease

Clonal Hematopoiesis Linked to Coronary Heart Disease

CHIP linked to coronary heart disease, myocardial infarction in humans; atherosclerosis in mice
Angiotensin I-converting enzyme gene rs4343 polymorphism is associated with the risk of migraine

Polymorphism in rs4343 of ACE Gene Linked to Migraine

Odds ratio of migraine 4.17 for G/G versus A/A, A/G polymorphism in angiotensin I converting enzyme
Breast cancer risk peaks around the 40s for BRCA1 mutation carriers and around the 50s for BRCA2 carriers

Family Hx, Mutation Position Key Variables in BRCA1/2 Cancer Risk

Study findings provide cancer risk patterns based on BRCA status using prospective data