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Event
Join us on Wednesday, May 25, as scholars and scientists answer audience questions and address the complexities surrounding historical and present-day eugenics and scientific racism in the context of existing and developing genetic and genomic screening technologies.
… cost-effective, minimal-risk options for prenatal genetic screening and diagnosis for various conditions (variations) … potential benefits than established prenatal and newborn screening programs. Although the individual and public … are clear, scholars have long debated whether screening and sequencing technologies also perpetuate …
For Patients and Families
​Genetic tests may be used to identify increased risks of health problems, to choose treatments, or to assess responses to treatments.
… help identify fetuses that have certain diseases. Newborn screening is used to test babies one or two days after birth … assess responses to treatments. … Genetic Testing, Newborn Screening, Diagnosing A Genetic Condition, Genetic Disease … …
Health
Genomic medicine involves using genomic information as part of clinical care and the health outcomes and policy implications of that clinical use.
… and genomic markers are increasingly included in cancer screening, and to guide tailored treatment strategies. … It … Genomics In The Clinic, Genetics, Genetic Testing, Newborn Screening, Privacy In Genomics, Genomic Technology … Genomic …
Genetic Disorders
Phenylketonuria is an inherited disorder of metabolism that causes an increase in the blood of a chemical known as phenylalanine.
… disability and other serious problems. Women who have high levels of phenylalanine during pregnancy are at high risk for having babies born with mental disability, … in 1 in 10,000 to 1 in 15,000 newborn babies. Newborn screening has been used to detect PKU since the 1960's. As a …
Healthcare Provider Genomics Education Resource
Genomics plays a role in every area of nursing, whether nurses are at the bedside providing one-on-one care, treating entire populations, teaching the next generation of nurses, or making discoveries in the lab.
…  Obtain a family history to assist with early screening detection of genetic conditions or health habits …  Identify risk for asymptomatic individuals with high risk for hereditary cancers.  Advocate for … and email subscriptions. GenomeEd : a repository of high-quality genomic resources for interprofessional members …
Event
On November 1-5, 2023, the National Human Genome Research Institute (NHGRI) will participate in the ASHG Annual Meeting - the world's largest human genetics and genomics meeting and exposition.  The annual meeting provides a forum for the presentation and discussion of cutting-edge science in all areas of human genetics.Â
… Petcharat Leoyklang Cell-based functional assays for screening of drug candidates for Free Sialic Acid Storage …
For Health Professionals
Essential genomics competencies, practice guidelines, and curricular resources for a variety of health professions.
… in a Caucasian male: Jeff with wife Maria Colon cancer screening in a Hispanic male: Luis Familial adenomatous … polyposis testing in an Ashkenazi Jewish male: Gabe Cancer screening incidental findings in an African American male … Puerto Rican female: Peggy  Reproductive Issues: Newborn screening in an older pregnant Asian female: Dai Cystic …
Healthcare Provider Genomics Education Resource
Genomics plays a role in every area of nursing, whether nurses are at the bedside providing one-on-one care, treating entire populations, teaching the next generation of nurses, or making discoveries in the lab.
… and family risk information.  Follow risk-based screening guidelines. Nurse practitioners may also request … if an individual is at risk of developing a condition.  Screening to identify the need for preventive therapy.  … for patient health.  Improving health outcomes (determine screening timing and intervals).  Maintaining and …
Genetic Disorders
Severe Combined Immunodeficiency is a severe, genetic condition of the immune system.
… to individual blood samples and take hours to prepare. The high cost of current testing has prohibited newborn screening on a population-wide basis. To make screening for all newborns affordable, an automated screening …
Genetic Disorders
Factor V Leiden thrombophilia is an inherited disorder of blood clotting.
… of venous thrombosis. The diagnosis is made using a screening test called a coagulation screening test or by … with an anticoagulant during periods of particularly high risk, such as major surgery. Factor V Leiden increases … Having two copies of the mutation may raise the risk as high as 1 in 12. Additional Resources for Factor V Leiden …