Genetics News and Research

Latest Genetics News and Research

Babies cry more in Britain, Canada and Italy than rest of the world, research reveals

Babies cry more in Britain, Canada and Italy, than the rest of the world -- according to new research by the University of Warwick.

3 Apr 2017

Amgen, UCB present romosozumab Phase 2 results at ENDO 2017

Amgen and UCB today announced results from the fourth year of a Phase 2 study showing the efficacy and safety of a second course of treatment with EVENITY™* (romosozumab), an investigational agent for postmenopausal women with osteoporosis.

3 Apr 2017

Flavors in e-cigarettes linked to increasing use among youth and young adults

Flavored e-cigarettes and e-cigarette marketing could be increasing e-cigarette use among youth and young adults, according to researchers from the Michael & Susan Dell Center for Healthy Living at The University of Texas Health Science Center at Houston School of Public Health in Austin.

2 Apr 2017

Discovery of new genes linked to Erdheim-Chester disease provides hope for improving diagnoses

National Human Genome Research Institute researchers have identified new genes associated with the Erdheim-Chester disease and some possible new therapies. Findings on this ultra-rare disease, found in approximately 600 people in the world, were published in Blood Advances.

31 Mar 2017

Feinstein Institute professor develops new tool to evaluate quality of eHealth applications

Feinstein Institute for Medical Research Assistant Professor Amit Baumel, PhD, has developed Enlight, a tool to evaluate the quality and therapeutic potential of computer and mobile-based eHealth applications.

31 Mar 2017

Research finds link between insomnia and increased risk of heart attack, stroke

Insomnia is associated with increased risk of heart attack and stroke, according to research published today in the European Journal of Preventive Cardiology.

31 Mar 2017

Clinical research trial investigates new treatment approach for early-stage eye melanoma

A first-of-its-kind, potentially groundbreaking new option for treating a form of eye cancer is now in its first phase-1 clinical research trial at Wills Eye Hospital in Philadelphia.

30 Mar 2017

Researchers use stem cells to model different genetic scenarios that underlie neurologic disease

Researchers at Case Western Reserve University School of Medicine have successfully grown stem cells from children with a devastating neurological disease to help explain how different genetic backgrounds can cause common symptoms.

30 Mar 2017

Researchers discover how epigenetic lesion can lead to T-cell acute lymphoblastic leukemia

Researchers from the Epigenetics and Cancer Biology Program led by Dr. Manel Esteller at the Bellvitge Biomedical Research Institute have discovered how an epigenetic lesion can lead to T-cell acute lymphoblastic leukemia.

30 Mar 2017

Rare ‘beneficial’ genetic mutations may provide clues to preventing heart attacks

Natural genetic changes can put some people at high risk of certain conditions, such as breast cancer, Alzheimer's disease or high blood pressure. But in rare cases, genetic errors also can have the opposite effect, protecting individuals with these helpful genetic mistakes from developing common diseases.

30 Mar 2017

Study identifies specific genetic risk factors that increase susceptibility to gliomas

A massive new study involving blood samples from over 30,000 individuals has identified 13 new genetic risk factors for glioma, the most common type of malignant brain tumor in adults

29 Mar 2017

New study identifies early vulnerability brain marker for psychosis

A new study has identified an early vulnerability brain marker for psychosis. A research team led by University of Montreal and Sainte-Justine University Hospital Research Center shows that an exaggerated emotional response from the brain to non-threatening and non-emotional cues predicts the emergence of the first signs of psychotic symptoms in late adolescence.

29 Mar 2017

Rarely studied faulty USF3 gene may predispose individuals to thyroid cancer

Charis Eng, M.D., Ph.D., of Cleveland Clinic and her team have discovered that a faulty, rarely studied gene called USF3 may predispose individuals to thyroid cancer. They recently published this discovery in Human Molecular Genetics.

29 Mar 2017

Researchers identify new gene mutation that leads to infertility in women

It has been estimated that more than 80 million people in the world have an unfulfilled desire to have children. But for every 10th couple, the reasons therefor remain unclear.

28 Mar 2017

Study shows how epigenetic randomness helps cancer cells proliferate

In a research effort that merged genetics, physics and information theory, a team at the schools of medicine and engineering at The Johns Hopkins University has added significantly to evidence that large regions of the human genome have built-in variability in reversible epigenetic modifications made to their DNA.

27 Mar 2017

Genetics News and Research

Latest Genetics News and Research

Babies cry more in Britain, Canada and Italy than rest of the world, research reveals

Amgen, UCB present romosozumab Phase 2 results at ENDO 2017

Flavors in e-cigarettes linked to increasing use among youth and young adults

Discovery of new genes linked to Erdheim-Chester disease provides hope for improving diagnoses

Feinstein Institute professor develops new tool to evaluate quality of eHealth applications

Research finds link between insomnia and increased risk of heart attack, stroke

Clinical research trial investigates new treatment approach for early-stage eye melanoma

Researchers use stem cells to model different genetic scenarios that underlie neurologic disease

Researchers discover how epigenetic lesion can lead to T-cell acute lymphoblastic leukemia

Rare ‘beneficial’ genetic mutations may provide clues to preventing heart attacks

Study identifies specific genetic risk factors that increase susceptibility to gliomas

New study identifies early vulnerability brain marker for psychosis

Rarely studied faulty USF3 gene may predispose individuals to thyroid cancer

Researchers identify new gene mutation that leads to infertility in women

Study shows how epigenetic randomness helps cancer cells proliferate

New research shows how molecular motors are transported into cilia

Study shows existence of numerous, varied genetic syndromes linked to obesity than previously thought

New UBC research reveals clues to how bacteria proliferates in lungs of cystic fibrosis patients

New genetic test may give men better view on how to deal with prostate cancer risk

Study identifies correlations between gene data and brain activity during memory processing

eBook: Using iPSCs models for human disease research and drug discovery eBook

Real-time Raman monitoring for pharmaceutical hot melt extrusion

Synthetic Psychedelics: A Growing Public Health Concern

How the Vutara VXL simplifies single-molecule imaging