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Researchers discover a new molecular cause for aggressive leukemia in children

Around 600 children under the age of 15 are diagnosed with leukemia each year in Germany. The effects are especially dramatic if this severe illness develops at birth or shortly afterwards.

4 Apr 2018

DNA-mimicking synthetic molecule could lead to new HIV treatment

Researchers have developed a synthetic compound that mimics the surface of DNA and is able to inhibit several DNA-processing enzymes.

4 Apr 2018

UTA professor wins AHA grant to study biomechanical influences on ventricular development

A University of Texas at Arlington researcher is working to determine how blood flow and cardiac muscle contraction affects gene development that leads to ventricular chamber development in the heart.

31 Mar 2018

New model predicts impact of rare genetic variants on IQ

Researchers have developed a new model that can predict the effect of rare genetic variants on a person’s IQ.

30 Mar 2018

New model predicts impact of rare genetic variants on IQ

Researchers have developed a new model that can predict the effect of rare genetic variants on a person’s IQ.

30 Mar 2018

Scientists identify early markers of infection in nonhuman primates exposed to Ebola virus

Scientists have identified potential biomarkers in nonhuman primates exposed to Ebola virus (EBOV) that appeared up to four days before the onset of fever, according to research published today in the journal Science Translational Medicine.

28 Mar 2018

Briefing note examines ethical issues in whole genome sequencing of babies

The Nuffield Council on Bioethics has today published a briefing note that examines the ethical issues raised by whole genome sequencing of babies.

28 Mar 2018

Stigma associated with Alzheimer's may prevent people from getting early diagnosis, treatment

Stigma associated with Alzheimer's disease may be an obstacle for individuals to seek information about their risk of developing Alzheimer's disease and to participate in clinical studies that discover potential therapies.

27 Mar 2018

Researchers identify new treatment targets for lung diseases using big data

Every year, approximately 12 million adults in the U.S. are diagnosed with Chronic Obstructive Pulmonary Disease, and 120,000 die from it. For people with COPD, Haemophilus influenzae, a bacterium, can be particularly dangerous.

20 Mar 2018

Genomics England announces new partnership to improve efficiency of next-generation sequencing analysis

Today (8 January 2018) at the annual J.P. Morgan Healthcare Conference, Edico Genome and Genomics England announced a new partnership to strengthen the accuracy and consistency of next-generation sequencing data analysis in Genomics England’s Rare Disease Pilot.

From Genomics England 20 Mar 2018

‘Fast track’ project shows promising results in cancer whole genome analyses

One key aim of the 100,000 Genomes Project is to improve cancer care for NHS patients. Whole genome sequencing in cancer can enable clinicians to choose better treatments and improve outcomes for patients through personalized medicine.

From Genomics England 20 Mar 2018

Scotland study aims to offer precise diagnoses for people with rare genetic diseases

People in Scotland with rare genetic diseases are set to benefit from a DNA study that seeks to improve their diagnoses and treatments.

From Genomics England 20 Mar 2018

Researchers find way to identify undiagnosed genetic diseases in electronic health records

Patients diagnosed with heart failure, stroke, infertility and kidney failure could actually be suffering from rare and undiagnosed genetic diseases.

16 Mar 2018

UCLA-developed nanospears could make gene therapies safer, faster and more cost-effective

UCLA scientists have developed a new method that utilizes microscopic splinter-like structures called "nanospears" for the targeted delivery of biomolecules such as genes straight to patient cells. These magnetically guided nanostructures could enable gene therapies that are safer, faster and more cost-effective.

15 Mar 2018

Medical University of Vienna to partner with bio.logis GIM in pharmacogenetics

Within the framework of U-PGx, an EU project for promoting the use of pharmacogenetic insights in healthcare, the Medical University of Vienna will implement the Genetic Information Management Suite developed by bio.logis Genetic Information Management GmbH.

14 Mar 2018

Genetic link to insomnia found

A new study has found certain genes that predispose a person to develop insomnia or sleep problems. This was one of the largest genome wide studies undertaken on insomnia. The study led by psychiatrist Murray Stein from the University of California San Diego was published in the latest issue of the journal Molecular Psychiatry.

13 Mar 2018

Southern Research scientists target mutated protein to combat prostate cancer

Southern Research scientists are exploring how a mutated protein implicated in prostate cancer plays a role in the development of the disease and whether it holds a key to better treatment outcomes.

13 Mar 2018

Britain announces £300 million for its elderly population in a healthy aging initiative

Britain is embarking upon a multi-million government scheme that will develop products and services that allow the elderly to stay independently in their own homes for longer.

12 Mar 2018

Researchers report genomic sequencing of 250,000 developmental cells

Researchers from the global Human Cell Atlas Consortium report that they have sequenced a quarter of a million separate cells that are of importance for early development of organs such as the liver, skin and kidneys. Sten Linnarsson at Karolinska Institutet is participating in the project.

9 Mar 2018

TSRI researchers show path to developing treatments for Charcot-Marie-Tooth disease

Scientists at The Scripps Research Institute have now shown a path to developing treatments for disease subtype CMT2D.

8 Mar 2018

Genetic Information News and Research

Researchers discover a new molecular cause for aggressive leukemia in children

DNA-mimicking synthetic molecule could lead to new HIV treatment

UTA professor wins AHA grant to study biomechanical influences on ventricular development

New model predicts impact of rare genetic variants on IQ

New model predicts impact of rare genetic variants on IQ

Scientists identify early markers of infection in nonhuman primates exposed to Ebola virus

Briefing note examines ethical issues in whole genome sequencing of babies

Stigma associated with Alzheimer's may prevent people from getting early diagnosis, treatment

Researchers identify new treatment targets for lung diseases using big data

Genomics England announces new partnership to improve efficiency of next-generation sequencing analysis

‘Fast track’ project shows promising results in cancer whole genome analyses

Scotland study aims to offer precise diagnoses for people with rare genetic diseases

Researchers find way to identify undiagnosed genetic diseases in electronic health records

UCLA-developed nanospears could make gene therapies safer, faster and more cost-effective

Medical University of Vienna to partner with bio.logis GIM in pharmacogenetics

Genetic link to insomnia found

Southern Research scientists target mutated protein to combat prostate cancer

Britain announces £300 million for its elderly population in a healthy aging initiative

Researchers report genomic sequencing of 250,000 developmental cells

TSRI researchers show path to developing treatments for Charcot-Marie-Tooth disease

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