Genetics News and Research

Latest Genetics News and Research

Study shows how errors in specific gene can cause growth defects linked to dwarfism

A new study shows how errors in a specific gene can cause growth defects associated with a rare type of dwarfism.

13 Feb 2017

Study finds link between depression and initiation of e-cigarette use among college students

The emergence of e-cigarettes as a nicotine product has left scientists with many questions about their impact on health, including how the product interacts with depression.

13 Feb 2017

High-pressure culture of sports could increase risk of substance addiction among athletes, study finds

As she was planning her study to look into the role physical activity and sport play in the development of substance addiction, Laurie de Grace was forewarned that she may have trouble finding any recovering addicts with a sporting background to speak with.

13 Feb 2017

Scientists identify new biomarkers that could guide bowel cancer treatment

Colorectal carcinomas arise in different forms, so all treatments do not work for all patients. OncoTrack, a public-private consortium supported by the Innovative Medicines Initiative Joint Undertaking, has conducted one of Europe's largest collaborative academic-industry research projects to develop and assess novel approaches for identification of new markers for colon cancer.

13 Feb 2017

Duke Health researchers identify potential new drug target for Huntington's disease

The loss of motor function and mental acuity associated with Huntington's disease might be treatable by restoring a cellular quality control process, which Duke Health researchers have identified as a key factor in the degenerative illness.

13 Feb 2017

Defective brain cells disposing toxic proteins may be linked to neurodegenerative diseases

Rutgers scientists say neurodegenerative diseases like Alzheimer's and Parkinson's may be linked to defective brain cells disposing toxic proteins that make neighboring cells sick.

10 Feb 2017

Research suggests new type of congenital muscular dystrophy

A newly discovered mutation in the INPP5K gene, which leads to short stature, muscle weakness, intellectual disability, and cataracts, suggests a new type of congenital muscular dystrophy.

10 Feb 2017

Salk study finds similar algorithm governing the brain and Internet

Although we spend a lot of our time online nowadays--streaming music and video, checking email and social media, or obsessively reading the news--few of us know about the mathematical algorithms that manage how our content is delivered.

10 Feb 2017

Study discovers new form of congenital muscular dystrophy caused by faulty INPP5K gene

A new form of congenital muscular dystrophy has been discovered which is caused by mutations in a previously un-linked gene.

9 Feb 2017

Scientists identify gene variants that predispose children to developing Kawasaki disease

Kawasaki disease (KD) is the most common acquired heart disease in children. Untreated, roughly one-quarter of children with KD develop coronary artery aneurysms -- balloon-like bulges of heart vessels -- that may ultimately result in heart attacks, congestive heart failure or sudden death.

9 Feb 2017

Researchers uncover key molecular pathways behind gut bacterial imbalance during inflammation

A study led by UT Southwestern Medical Center researchers has uncovered key molecular pathways behind the disruption of the gut's delicate balance of bacteria during episodes of inflammatory disease.

8 Feb 2017

Wills Eye expert discusses what patients need to know about Age-Related Macular Degeneration

Carl D. Regillo, MD Chief of the Wills Eye Hospital Retina Service discusses what patients need to know about Age-Related Macular Degeneration.

8 Feb 2017

Genetic variant encoded in NCF1 linked to increased risk for autoimmune diseases, study shows

Investigators at the Medical University of South Carolina report pre-clinical research showing that a genetic variant encoded in neutrophil cystolic factor 1 (NCF1) is associated with increased risk for autoimmune diseases, including systemic lupus erythematosus (SLE), rheumatoid arthritis, and Sjögren's syndrome, in the January 2017 issue of Nature Genetics.

8 Feb 2017

Geneticists use evolutionary history to shine light on plethora of neurodevelopmental disorders

Geneticists from Trinity College Dublin have used our evolutionary history to shine light on a plethora of neurodevelopmental disorders and diseases.

8 Feb 2017

UCLA researchers identify drug combinations that may be successful in reducing growth of bacteria

A landmark report by the World Health Organization in 2014 observed that antibiotic resistance -- long thought to be a health threat of the future -- had finally become a serious threat to public health around the world.

8 Feb 2017

MGH researchers develop novel approach to analyze brainwave activity during sleep

Massachusetts General Hospital investigators have developed a novel approach to analyze brainwaves during sleep, which promises to give a more detailed and accurate depiction of neurophysiological changes than provided by a traditional sleep study.

8 Feb 2017

New study uncovers important links between glioblastoma and epileptic seizures

Detecting brain tumors at the earliest possible stage and eliminating them before seizures begin might be possible one day, according to research by scientists at Baylor College of Medicine and Texas Children's Hospital.

7 Feb 2017

Studies open new windows into understanding untreatable group of common genetic disorders

Two Princeton University studies are opening important new windows into understanding an untreatable group of common genetic disorders known as RASopathies that are characterized by distinct facial features, developmental delays, cognitive impairment and heart problems.

7 Feb 2017

Scientists use brain organoids to identify root causes of Miller-Dieker syndrome

Research led by scientists at UC San Francisco and Case Western Reserve University School of Medicine has used brain "organoids" — tiny 3D models of human organs that scientists grow in a dish to study disease — to identify root causes of Miller-Dieker Syndrome (MDS), a rare genetic disorder that causes fatal brain malformations.

7 Feb 2017

Patients with early, severe depression symptoms have increased genetic risk for psychiatric disorders

Clinical features of major depressive disorder (MDD) may help identify specific subgroups of depressed patients based on associations with genetic risk for major psychiatric disorders, reports a study in Biological Psychiatry.

7 Feb 2017

Genetics News and Research

Latest Genetics News and Research

Study shows how errors in specific gene can cause growth defects linked to dwarfism

Study finds link between depression and initiation of e-cigarette use among college students

High-pressure culture of sports could increase risk of substance addiction among athletes, study finds

Scientists identify new biomarkers that could guide bowel cancer treatment

Duke Health researchers identify potential new drug target for Huntington's disease

Defective brain cells disposing toxic proteins may be linked to neurodegenerative diseases

Research suggests new type of congenital muscular dystrophy

Salk study finds similar algorithm governing the brain and Internet

Study discovers new form of congenital muscular dystrophy caused by faulty INPP5K gene

Scientists identify gene variants that predispose children to developing Kawasaki disease

Researchers uncover key molecular pathways behind gut bacterial imbalance during inflammation

Wills Eye expert discusses what patients need to know about Age-Related Macular Degeneration

Genetic variant encoded in NCF1 linked to increased risk for autoimmune diseases, study shows

Geneticists use evolutionary history to shine light on plethora of neurodevelopmental disorders

UCLA researchers identify drug combinations that may be successful in reducing growth of bacteria

MGH researchers develop novel approach to analyze brainwave activity during sleep

New study uncovers important links between glioblastoma and epileptic seizures

Studies open new windows into understanding untreatable group of common genetic disorders

Scientists use brain organoids to identify root causes of Miller-Dieker syndrome

Patients with early, severe depression symptoms have increased genetic risk for psychiatric disorders

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