Genetics News and Research

Latest Genetics News and Research

Study identifies 22 locations in the human genome that cause schizophrenia

A new genome-wide association study estimates the number of different places in the human genome that are involved in schizophrenia.

26 Aug 2013

Model including dozens of mutations helps clarify genetic factors involved in Crohn's disease

A statistical model accounting for dozens of different genes in combination-and the interactions between them-is an important step forward in understanding the genetic factors affecting the risk of Crohn's disease (CD), reports a study in Inflammatory Bowel Diseases, official journal of the Crohn's & Colitis Foundation of America (CCFA). The journal is published by Lippincott Williams & Wilkins, a part of Wolters Kluwer Health.

26 Aug 2013

Glutathione peroxidase activity protects against symptoms of Huntington's disease

Leicester geneticists have discovered a potential defence against Huntington's disease - a fatal neurodegenerative disorder which currently has no cure.

26 Aug 2013

DeNovoGear software uses statistical probabilities to help identify genetic mutations

Concealed within the vastness of the human genome, (comprised of some 3 billion base pairs), mutations are commonplace. While the majority of these appear to have neutral effect on human health, many others are associated with diseases and disease susceptibility.

26 Aug 2013

Challenges of studying health and mortality risks of obesity

Researchers from the Perelman School of Medicine point out that the body mass index, based on the weight and height, is not an accurate measure of body fat content and does not account for critical factors that contribute to health or mortality, such as fat distribution, proportion of muscle to fat, and the sex and racial differences in body composition.

23 Aug 2013

Understanding genetic factors that affect Crohn's disease risk

A statistical model accounting for dozens of different genes in combination—and the interactions between them—is an important step forward in understanding the genetic factors affecting the risk of Crohn's disease, reports a study in Inflammatory Bowel Diseases, official journal of the Crohn's & Colitis Foundation of America.

23 Aug 2013

Aging Gene Tied To Myeloma

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22 Aug 2013

Clinical study to investigate effects of prenatal chromosomal abnormalities through microarray analysis

Reproductive genetics researchers at Columbia University Medical Center (CUMC) are leading a multicenter prospective clinical study investigating the effects of chromosomal abnormalities (duplicative or missing material) found prenatally through microarray analysis.

22 Aug 2013

Majority of Alzheimer's researchers support disclosure of results to study participants

A leading group of Alzheimer's researchers contends that, as biomarkers to detect signals of the disease improve at providing clinically meaningful information, researchers will need guidance on how to constructively disclose test results and track how disclosure impacts both patients and the data collected in research studies.

22 Aug 2013

Researchers report overall increase in use of tPA to dissolve clots blocking arteries

Use of the "clot-busting" drug tissue plasminogen activator to treat patients with strokes caused by a blockage of blood flow nearly doubled between 2003 and 2011.

22 Aug 2013

HIV prevention program at UCLA may reduce unprotected sex among bisexual black men

A culturally tailored HIV prevention program developed and tested by investigators at UCLA and the Charles R. Drew University of Medicine and Science has been shown to significantly reduce unprotected sex among bisexual black men.

22 Aug 2013

Oxford Gene Technology releases next generation sequencing survey results

Oxford Gene Technology, provider of innovative genetics research and biomarker solutions to advance molecular medicine, has released the results from a recent survey of researchers using next generation sequencing.

From Oxford Gene Technology 21 Aug 2013

Researchers identify gene that contributes to development of acute myeloid leukemia

Researchers at the University of Chicago Medicine Comprehensive Cancer Center (UCCCC) have identified a gene that contributes to the development of acute myeloid leukemia (AML). This pivotal finding follows 40 years of University of Chicago research that has slowly unraveled the genetic basis of leukemia.

21 Aug 2013

Genetics may play role in how people's taste receptors send signals

Genetics may play a role in how people's taste receptors send signals, leading to a wide spectrum of taste preferences, according to Penn State food scientists. These varied, genetically influenced responses may mean that food and drink companies will need a range of artificial sweeteners to accommodate different consumer tastes.

21 Aug 2013

RI-CART receives $1.2M grant to create confidential registry of every individual diagnosed with autism

The Rhode Island Consortium for Autism Research and Treatment (RI-CART), a group of the state's leading experts on autism research, education, health and services, has received a $1.2 million grant to create a first-of-its-kind confidential registry of every individual diagnosed with autism in Rhode Island.

20 Aug 2013

New data analyzing technique via MR imaging identify tumors' response to anti-angiogenesis therapy

A new way of analyzing data acquired in MR imaging appears to be able to identify whether or not tumors are responding to anti-angiogenesis therapy, information that can help physicians determine the most appropriate treatments and discontinue ones that are ineffective.

20 Aug 2013

Research may shed light on what causes people to suffer from life-threatening anxiety disorders

New research at Rutgers University may help shed light on how and why nervous system changes occur and what causes some people to suffer from life-threatening anxiety disorders while others are better able to cope.

20 Aug 2013

Study examines ASDs recurrence risk for full and half-siblings

A Danish study of siblings suggests the recurrence risks for autism spectrum disorders (ASDs) varied from 4.5 percent to 10.5 percent depending on the birth years, which is higher than the ASD risk of 1.18 percent in the overall Danish population, according to a study published by JAMA Pediatrics, a JAMA Network publication.

20 Aug 2013

Study shows complement activation plays an important role in inherited macular degeneration

In a study published on line this week in the journal Human Molecular Genetics, Drs. Donita Garland, Rosario Fernandez-Godino, and Eric Pierce of the Ocular Genomics Institute at the Massachusetts Eye and Ear, Harvard Medical School, along with their colleagues, reported the unexpected finding that in mice genetically engineered to have an inherited form of macular degeneration, turning off the animals' complement system, a part of the immune system, prevented the disease.

20 Aug 2013

Illumina announces availability of its newest reagent kits for MiSeq benchtop sequencer

Illumina, Inc. today announced the availability of its newest reagent kits for the MiSeq, the industry's most accurate and easiest-to-use benchtop sequencer. The improved chemistry doubles sequencing output to 15 gigabases (Gb) by increasing the number of sequencing reads (up to 25 million reads) and overall read length (up to 2x300 base pairs). These innovations enable researchers to perform new applications including exome sequencing on the MiSeq.

From Illumina, Inc. 19 Aug 2013

Genetics News and Research

Latest Genetics News and Research

Study identifies 22 locations in the human genome that cause schizophrenia

Model including dozens of mutations helps clarify genetic factors involved in Crohn's disease

Glutathione peroxidase activity protects against symptoms of Huntington's disease

DeNovoGear software uses statistical probabilities to help identify genetic mutations

Challenges of studying health and mortality risks of obesity

Understanding genetic factors that affect Crohn's disease risk

Aging Gene Tied To Myeloma

Clinical study to investigate effects of prenatal chromosomal abnormalities through microarray analysis

Majority of Alzheimer's researchers support disclosure of results to study participants

Researchers report overall increase in use of tPA to dissolve clots blocking arteries

HIV prevention program at UCLA may reduce unprotected sex among bisexual black men

Oxford Gene Technology releases next generation sequencing survey results

Researchers identify gene that contributes to development of acute myeloid leukemia

Genetics may play role in how people's taste receptors send signals

RI-CART receives $1.2M grant to create confidential registry of every individual diagnosed with autism

New data analyzing technique via MR imaging identify tumors' response to anti-angiogenesis therapy

Research may shed light on what causes people to suffer from life-threatening anxiety disorders

Study examines ASDs recurrence risk for full and half-siblings

Study shows complement activation plays an important role in inherited macular degeneration

Illumina announces availability of its newest reagent kits for MiSeq benchtop sequencer

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