Genetics News and Research

Latest Genetics News and Research

Researchers recruit 20,000th participant to landmark genetics study to improve risk prediction of coronary disease

A team of researchers from the University of Leicester and NIHR Leicester Cardiovascular Biomedical Research Unit (LCBRU) in conjunction with colleagues from Primary Care and Leicester and Leicestershire CCGs have recruited their 20,000th participant to a landmark genetics study.

24 Oct 2016

Congenica reports high diagnostic yields by Sapientia platform in UK 100,000 Genomes Project

Congenica, a clinical interpretation partner for the UK 100,000 Genomes Project, has announced that its whole genome analysis platform Sapientia™ is detecting clinically relevant variants in over 35% of diagnostics reports returned to the NHS Genomic Medicine Centres (GMCs) for the Pilot and Main Phase studies.

24 Oct 2016

Rare neurological syndromes linked to variations in ATAD3A gene

A team of scientists from a number of institutions around the world, including Baylor College of Medicine, has discovered that rare neurological syndromes for which there was no cause can be the result of variations in the gene ATAD3A.

21 Oct 2016

Scientists suggest potential approach of lowering tau levels to thwart Alzheimer's disease

Taking a pill that prevents the accumulation of toxic molecules in the brain might someday help prevent or delay Alzheimer's disease, according to scientists at Baylor College of Medicine, Texas Children's Hospital and Johns Hopkins University School of Medicine.

21 Oct 2016

UA neuroscientists receive $10.3 million grant to find cause for heightened risk of Alzheimer's in women

Why do more women than men get Alzheimer's disease? In their quest to find the answer, neuroscientist Roberta Diaz Brinton, PhD, and her collegues in the Center for Innovation in Brain Science at the University of Arizona Health Sciences, have been awarded a $10.3 million five-year Program Project Grant from the National Institute on Aging at the National Institutes of Health.

21 Oct 2016

Study provides novel insights into genetic factors linked to age-related hearing disorders

A study of patient electronic medical records and genome sequences from adults with age-related hearing impairment by researchers at UC San Francisco and Kaiser Permanente Northern California, identified two genetic variations linked to the hearing disorder.

21 Oct 2016

Researchers identify genomic regions linked to ulcerative colitis in African-Americans

In the first genome-wide association study of genetic risk factors for inflammatory bowel disease in African Americans, a research team has identified two regions of the genome (loci) associated with ulcerative colitis only in people of African descent.

20 Oct 2016

Scientists use male mice model to study how genes affect sequencing of vocal sounds

There's a particular order to the sounds of the ultrasonic song a male mouse performs to impress his potential mate.

20 Oct 2016

Cancer cell's shape may offer clues for precise prognosis

Doctors can sometimes use a cancer cell's genetics to predict how it will act - how dangerous it is and thus what treatments should be used against it.

20 Oct 2016

Gene deletion shows new way to treat influenza

Researchers at Houston Methodist kept mice from getting the flu by removing a gene that regulates their immune system.

19 Oct 2016

Signs and impact of hypos

Hypoglycemia, or hypos are the result of blood glucose levels falling too low (less than 4mmol/l). The symptoms and severity of hypoglycemia can differ for each patient. The symptoms can range from headaches, dizziness, irritability, hunger to...

19 Oct 2016

Molecular signaling pathway could be basis of potential new treatment for osteoporosis

A molecular signaling pathway identified by an international research team could be the basis of improved treatment for osteoporosis.

19 Oct 2016

Salk scientist receives NIH Pioneer Award to support innovative biomedical research

Salk Professor Juan Carlos Izpisua Belmonte has been awarded a 2016 National Institutes of Health Pioneer Award, a highly coveted grant that supports the most innovative biomedical research, for his work in stem cell biology and regeneration.

18 Oct 2016

Chemotherapy leads to drug-resistance in bladder cancer patients

Chemotherapy is indicated as the first line of treatment for advanced bladder cancer. New research by Weill Cornell Medicine and University of Trento scientists shows that while chemotherapy kills the most common type of bladder cancer, urothelial cancer, chemotherapy also shapes the genetic evolution of remaining urothelial cancer cell clones to become drug-resistant.

18 Oct 2016

NYU Langone's cancer researcher receives Outstanding Investigator Award from NCI

Throughout her distinguished career, cancer researcher Dafna Bar-Sagi, PhD, has made fundamental contributions to the understanding of the mechanisms that drive the disease.

18 Oct 2016

Sleep abnormality may play vital role in schizophrenia, say BIDMC experts

A sleep abnormality likely plays an important role in schizophrenia, according to sleep experts at Beth Israel Deaconess Medical Center.

18 Oct 2016

H3Africa Initiative selects Illumina to develop new array for genome-wide association studies

Driven by the need for a tool to address African genomic diversity, Illumina was selected to develop an array for genome-wide association studies (GWAS) by the Human Heredity and Health in Africa (H3Africa) Initiative, a partnership between NIH, the African Society of Human Genetics, and Wellcome Trust.

From Illumina, Inc. 17 Oct 2016

Study quantifies burden of adverse drug reactions in general adult population

In a study of 1000 adult patients with unplanned admission to a tertiary hospital in Singapore, the prevalence of adverse drug reactions (ADRs) at the time of admission was 12.4 percent, and the prevalence of ADRs causing admission to the hospital was 8.1 percent.

17 Oct 2016

Icelandic people more likely to carry novel rare genetic variant linked to risk of Alzheimer's disease

People with Icelandic heritage are more likely to carry a novel rare mutation in the TM2D3 gene, which leads to greater risk for Alzheimer's disease, based on a new study published October 14th, 2016 in PLOS Genetics by Johanna Jakobsdottir of the Icelandic Heart Association, Sven van der Lee of Erasmus University in Rotterdam, and colleagues.

17 Oct 2016

Immune system plays important role in Duchenne muscular dystrophy, research reveals

A new paper, co-written by faculty at Binghamton University, State University of New York, increases the understanding of Duchenne muscular dystrophy (DMD)—one of the most common lethal genetic disorders—and points to potential therapeutic approaches.

14 Oct 2016

Genetics News and Research

Latest Genetics News and Research

Researchers recruit 20,000th participant to landmark genetics study to improve risk prediction of coronary disease

Congenica reports high diagnostic yields by Sapientia platform in UK 100,000 Genomes Project

Rare neurological syndromes linked to variations in ATAD3A gene

Scientists suggest potential approach of lowering tau levels to thwart Alzheimer's disease

UA neuroscientists receive $10.3 million grant to find cause for heightened risk of Alzheimer's in women

Study provides novel insights into genetic factors linked to age-related hearing disorders

Researchers identify genomic regions linked to ulcerative colitis in African-Americans

Scientists use male mice model to study how genes affect sequencing of vocal sounds

Cancer cell's shape may offer clues for precise prognosis

Gene deletion shows new way to treat influenza

Signs and impact of hypos

Molecular signaling pathway could be basis of potential new treatment for osteoporosis

Salk scientist receives NIH Pioneer Award to support innovative biomedical research

Chemotherapy leads to drug-resistance in bladder cancer patients

NYU Langone's cancer researcher receives Outstanding Investigator Award from NCI

Sleep abnormality may play vital role in schizophrenia, say BIDMC experts

H3Africa Initiative selects Illumina to develop new array for genome-wide association studies

Study quantifies burden of adverse drug reactions in general adult population

Icelandic people more likely to carry novel rare genetic variant linked to risk of Alzheimer's disease

Immune system plays important role in Duchenne muscular dystrophy, research reveals

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