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A new test can predict the course of inflammatory bowel disease in patients

Biomarker Test Predicts Mild, Serious IBD in Newly Diagnosed

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Test based on genetic signature of CD8 T cells during active disease
Progress has been made toward developing diagnostic criteria for limbic-predominant age-related TDP-43 encephalopathy

Diagnostic Criteria Proposed for Advanced-Age Proteinopathy

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Gaps remain in understanding of limbic-predominant age-related TDP-43 encephalopathy
Rare variants have been identified in the DENND1A gene that are associated with hormonal traits of polycystic ovary syndrome

Rare Variants Identified in DENND1A Gene in PCOS

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Variants are associated with reproductive and metabolic traits in PCOS families
A machine learning process and clinical natural language processing can rapidly diagnose rare genetic diseases

Machine Learning Can Speed Diagnosis of Genetic Diseases in Children

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Automated, retrospective diagnoses concurred well with expert manual interpretation
Guidance has been updated for the health supervision of children with neurofibromatosis type 1

AAP Updates Guidance for Care in Neurofibromatosis Type 1

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Report describes criteria for diagnosis, role of genetic testing, possible health manifestations
Personalizing breast cancer treatment based on Oncotype DX recurrence scores could result in small decreases in costs in the initial 12 months of care

Personalizing Breast Cancer Tx Could Cut Initial Costs of Care

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Small decline seen in costs in first 12 months of care with personalized treatment based on recurrence scores
Genomic recurrence score testing using a 21-gene assay is associated with decreased cancer care costs in real-world practice among certain patients with breast cancer who would otherwise receive standard chemotherapy

Recurrence Score May Cut Costs for High-Risk Breast Cancer Care

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Testing with 21-gene assay linked to lower relative, absolute costs among high-risk patients
Only one-quarter of those with breast cancer and one-third with ovarian cancer undergo genetic testing

Genetic Testing Underused in Breast, Ovarian Cancer

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Pathogenic variants ID'd in 7.8 percent of patients with breast cancer, 14.5 percent with ovarian cancer
In certain cases

Genetic Research Results May Warrant Updates to Participants

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Participants should be recontacted in some cases of new information about variant, newly ID'd variants
For patients with FMS-like tyrosine kinase 3 mutations who have relapsed or refractory acute myeloid leukemia

AACR: Longer Survival With Gilteritinib in FLT3mut+ AML

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Longer overall survival, better remission rates seen for patients receiving gilteritinib versus salvage chemo