American Society of Human Genetics

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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Novel type 2 diabetes genetic study involves five major ancestry groups

A consortium of scientists who are taking a novel approach in their research to detect the genetic variations that predispose individuals to type 2 diabetes provided an update of their findings at the American Society of ...

Genetics created Nov 08, 2012 | popularity 5 / 5 (1) | comments 0

Unexplained intellectual disability explained by state-of-the-art genetic analysis

A research team reported that next generation sequencing of the exome, the 1 to 2% of the DNA containing the genes that code for proteins, enabled the identification of the genetic causes of unexplained intellectual disability ...

Genetics created Nov 08, 2012 | popularity 4 / 5 (3) | comments 0

Significant relationship between mortality and telomere length discovered

A team of researchers at Kaiser Permanente and the University of California, San Francisco (UCSF) has identified a significant relationship between mortality and the length of telomeres, the stretches of DNA that protect ...

Genetics created Nov 08, 2012 | popularity 4.5 / 5 (2) | comments 0 | with audio podcast

Exome sequencing: Potential diagnostic assay for unexplained intellectual disability

Research findings confirming that de novo mutations represent a major cause of previously unexplained intellectual disability were presented on Nov. 8 at the American Society of Human Genetics 2012 meeting in San Francisco.

Genetics created Nov 08, 2012 | popularity 5 / 5 (1) | comments 0

DNA variants explain over 10 percent of inherited genetic risk for heart disease

About 10.6% of the inherited genetic risk for developing coronary artery disease (CAD) can be explained by specific DNA variations, according to research reported today at the American Society of Human Genetics 2012 meeting.

Genetics created Nov 08, 2012 | popularity 5 / 5 (1) | comments 0

Whole genome sequencing of de novo balanced rearrangements in prenatal diagnosis

Whole genome sequencing of the DNA code of three prenatal samples provided a detailed map of the locations of their chromosomal abnormalities in 14 days, scientists reported today at the American Society of Human Genetics ...

Genetics created Nov 07, 2012 | popularity 5 / 5 (1) | comments 0 | with audio podcast

DNA sequencing of infants and children with anatomical defects of unknown causes

A presentation at the American Society of Human Genetics 2012 meeting updated genetics experts about a one-year-old research initiative that brought together researchers, clinicians and policy experts to tackle the challenges ...

Genetics created Nov 06, 2012 | popularity not rated yet | comments 0

New method helps link genomic variation to protein production

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 ...

Genetics created Nov 06, 2012 | popularity 4.3 / 5 (3) | comments 0 | with audio podcast

Surprising findings from Exome Sequencing Project reported

A multi-institutional team of researchers has sequenced the DNA of 6,700 exomes, the portion of the genome that contains protein-coding genes, as part of the National Heart, Lung and Blood Institute (NHLBI)-funded Exome Sequencing ...

Genetics created Nov 06, 2012 | popularity 4 / 5 (1) | comments 0