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Early puberty may increase risk of obesity in later life

The earlier girls start puberty, the greater their chances are of suffering from obesity in later life, according to a new study.

16 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

Researchers explore whether MERS-CoV is a threat for Africa

Middle East respiratory syndrome (MERS) is a lethal disease in humans, caused by a coronavirus (MERS-CoV). It was first identified in man in 2012, in the Arabian Peninsula.

15 Mar 2018

Artificial sweetener sucralose worsens gut inflammation in mice with Crohn's disease

In a study that has implications for humans with inflammatory diseases, researchers from Case Western Reserve University School of Medicine and colleagues have found that, given over a six-week period, the artificial sweetener sucralose, known by the brand name Splenda, worsens gut inflammation in mice with Crohn's-like disease, but had no substantive effect on those without the condition.

15 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

Researchers uncover link between Parkinson’s disease mutations and plaque formation in the brain

Working with lab-grown human brain cells, Johns Hopkins researchers report they have uncovered a much sought-after connection between one of the most common genetic mutations in Parkinson's disease and the formation of fatty plaques in the brain thought to contribute to the destruction of motor neurons that characterize the disease.

15 Mar 2018

Study shows feasibility of PerkinElmer's Vanadis NIPT assay for detection of fetal trisomy 21

PerkinElmer, Inc., a global leader committed to innovating for a healthier world, today announced the publication of a research study describing the technology behind the Vanadis NIPT system.

14 Mar 2018

MIT engineers develop new technology that could improve drug evaluation

MIT engineers have developed new technology that could be used to evaluate new drugs and detect possible side effects before the drugs are tested in humans.

14 Mar 2018

Researchers identify novel gene involved in familial breast cancer

An international research consortium led by Dr Jordi Surrallés, director of the Genetics Service at the Hospital de Sant Pau and professor of Genetics at the UAB, and by Dr Miquel Àngel Pujana, director of the ProCURE Research Programme of the Catalan Institute of Oncology, has identified a novel gene involved in this type of cancer, known as EDC4.

14 Mar 2018

NIH researchers explore genetic clocks to understand role of aging in neurodegeneration

To understand the link between aging and neurodegenerative disorders such as Alzheimer's disease, NIH scientists compared the genetic clocks that tick during the lives of normal and mutant flies.

14 Mar 2018

Common genetic variation shown to increase Alzheimer’s risk

A recent study has found that African Americans with a common genetic variation are at an increased risk for developing Alzheimer’s disease.

14 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 counseling missed by some breast cancer patients, study finds

As new genes are linked to breast cancer occurring in families and as genetic testing becomes more important in directing treatment for newly diagnosed patients, a substantial number of those at the highest risk are not getting tested.

14 Mar 2018

African Americans with thyroid gene variation more likely to develop Alzheimer's

African Americans with a common genetic variation are at increased risk for developing Alzheimer's disease, while European Americans with the same variation are not, according to a study led by researchers at Rush University Medical Center.

14 Mar 2018

New findings yield insights into factors that contribute to aggressive endometrial tumors

New research from Huntsman Cancer Institute at the University of Utah indicates steroid and hormone receptors are simultaneously active in many endometrial cancer tissues.

13 Mar 2018

New guidelines intend to provide template for optimal, most up-to-date DMD care

Diagnostic and treatment advances are helping patients with Duchenne muscular dystrophy - one of nine major types of muscular dystrophy that affects males - live into their 30s and beyond, raising challenges in such areas as education, vocation, levels of independence, personal relationships, emotional health, and intimacy.

13 Mar 2018

Genetic heart mutations account for fewer sudden and unexplained infant deaths

Researchers have discovered that heart disease caused by genetic mutations account for significantly fewer sudden and unexplained deaths of infants than previously reported.

13 Mar 2018

NIH-funded researchers use CRISPR to rapidly find new genetic suspects behind ALS, FTD

NIH-funded researchers at Stanford University used the gene editing tool CRISPR-Cas9 to rapidly identify genes in the human genome that might modify the severity of amyotrophic lateral sclerosis and frontotemporal dementia caused by mutations in a gene called C9orf72.

13 Mar 2018

Large number of genes associated with intelligence discovered

A large genome study by researchers at the University of Edinburgh and Harvard University has found over 500 genes that can be attributed to intelligence. The study was published in the latest issue of the journal Molecular Psychiatry.

13 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

Genetic News and Research

Early puberty may increase risk of obesity in later life

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

Researchers explore whether MERS-CoV is a threat for Africa

Artificial sweetener sucralose worsens gut inflammation in mice with Crohn's disease

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

Researchers uncover link between Parkinson’s disease mutations and plaque formation in the brain

Study shows feasibility of PerkinElmer's Vanadis NIPT assay for detection of fetal trisomy 21

MIT engineers develop new technology that could improve drug evaluation

Researchers identify novel gene involved in familial breast cancer

NIH researchers explore genetic clocks to understand role of aging in neurodegeneration

Common genetic variation shown to increase Alzheimer’s risk

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

Genetic counseling missed by some breast cancer patients, study finds

African Americans with thyroid gene variation more likely to develop Alzheimer's

New findings yield insights into factors that contribute to aggressive endometrial tumors

New guidelines intend to provide template for optimal, most up-to-date DMD care

Genetic heart mutations account for fewer sudden and unexplained infant deaths

NIH-funded researchers use CRISPR to rapidly find new genetic suspects behind ALS, FTD

Large number of genes associated with intelligence discovered

Genetic link to insomnia found

Sequencing & Genomics: Elevating Science and Healthcare eBook

Bringing real-time analytics to downstream bioprocess monitoring

Designing fluidic architecture for scalable diagnostic platforms

Evaluating new approaches for rare disease genomics

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