The American Society of Human Genetics (ASHG), founded in 1948, is the primary professional membership organization for specialists in human genetics worldwide. As of 2009, the organization had approximately 8,000 members. The Society's members include researchers, academicians, clinicians, laboratory practice professionals, genetic counselors, nurses, and others who have a special interest in the field of human genetics. ASHG serves research scientists, health professionals, and the general public by providing forums to: The ASHG Annual Meeting is the oldest and largest international human genetics conference worldwide. The Society's Annual Meeting is held each fall in a major U.S. or Canadian city and attracts about 6,000-7,000 attendees, plus exhibitors. The ASHG Annual Meeting features invited presentations from the world's leading geneticists, along with a variety of symposia, workshops, and other abstract-driven sessions focusing on the most important and recent developments in basic, translational, and clinical human genetics research and technology.
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The first evidence that the underlying genetic defect responsible for trisomy 21, also known as Down syndrome, can be suppressed in laboratory cultures of patient-derived stem cells was presented today (Oct. 22) at the American ...
Oct 22, 2013
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Scientists have adopted a novel laboratory approach for determining the effect of genetic variation on the efficiency of the biological process that translates a gene's DNA sequence into a protein, such as hemoglobin, according ...
Nov 6, 2012
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An international team of researchers who identified genetic variants associated with reproductive success say their findings could highlight mechanisms underlying fertility and infertility. In addition, their analyses detected ...
Oct 29, 2020
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Although a recent campaign by Cancer Research UK emphasized obesity as a risk factor for cancer on par with smoking, the scientific literature on the relationship between increased weight and cancer risk is not so clear. ...
Oct 26, 2020
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Researchers announce the first robust evidence for the role of the major histocompatibility complex gene HLA-B in penicillin allergy. To identify genetic risk factors for penicillin allergy, the international team of researchers ...
Oct 26, 2020
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Women with the onset of breast cancer over age 65 often do not qualify for genetic testing, yet little is known about the frequency of disease-causing mutations in breast cancer predisposition genes in this population. In ...
Oct 26, 2020
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Short fragments of cell-free DNA (cfDNA) that circulate in blood, urine, and other biofluids can offer an information-rich window into human physiology and disease. By looking at the methylation markers of cfDNA, researchers ...
Oct 26, 2020
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In research that helps scientists better understand and explore treatments for diseases like Alzheimer's, scientists have developed a line of mice in which the mouse version of the Alzheimer's-associated MAPT gene has been ...
Oct 17, 2019
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Researchers are exploring the cause and effect relationships between common health indicators and lifespan, by analyzing polygenic risk scores (PRS), a numerical score of a person's risk for disease based on multiple genetic ...
Oct 17, 2019
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Researchers have implicated 10 new genes in the development of schizophrenia using a method called whole exome sequencing, the analysis of the portion of DNA that codes for proteins. Working with a global consortium of schizophrenia ...
Oct 16, 2019
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