Florida International University
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GENETICS IN MEDICINE
publication venue for
2022 Association of Professors of Human and Medical Genetics (APHMG) consensus-based update of the core competencies for undergraduate medical education in genetics and genomics
Online interactive genetics education during internal medicine clinical clerkship
Recommendations from the EGAPP Working Group: does the use of Oncotype DX tumor gene expression profiling to guide treatment decisions improve outcomes in patients with breast cancer?
Recommendations from the EGAPP Working Group: does PCA3 testing for the diagnosis and management of prostate cancer improve patient health outcomes?
Recommendations from the EGAPP Working Group: does genomic profiling to assess type 2 diabetes risk improve health outcomes?
Recommendations from the EGAPP Working Group: Can testing of tumor tissue for mutations in EGFR pathway downstream effector genes in patients with metastatic colorectal cancer improve health outcomes by guiding decisions regarding anti-EGFR therapy?
Selection of family members for communication of cancer risk and barriers to this communication before and after genetic cancer risk assessment
Quantity versus quality: Optimal methods for cell-free DNA isolation from plasma of pregnant women
Ovarian Cancer Screening in Women from Hereditary Breast/Ovarian Cancer Families
Klinefelter syndrome: Expanding the phenotype and identifying new research directions
The EGAPP initiative: lessons learned
Recommendations from the EGAPP Working Group: Can tumor gene expression profiling improve outcomes in patients with breast cancer?
Recommendations from the EGAPP Working Group: Genetic testing strategies in newly diagnosed individuals with colorectal cancer aimed at reducing morbidity and mortality from Lynch syndrome in relatives
Recommendations from the EGAPP working group: Can UCT1A1 genotyping reduce morbidity and mortality in patients with metastatic colorectal cancer treated with irinotecan?
Recommendations from the EGAPP Working Group: Testing for cytochrome P450 polymorphisms in adults with nonpsychotic depression treated with selective serotonin reuptake inhibitors
Gender verification of female athletes
Developing medical genetics interest and literacy through student interest groups: The why, the how, and the challenges
Developing a national collaborative study system for rare genetic diseases
Erratum: Selection of family members for communication of cancer risk and barriers to this communication before and after genetic cancer risk assessment (Genetics in Medicine (2007) 9:5 (275-282))
GENETICS & HEREDITY
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