Genetics News and Research

Latest Genetics News and Research

Maternal folic acid intake round conception may reduce children's pesticide-related autism risk

Researchers at UC Davis and other institutions have shown that mothers who take recommended amounts of folic acid around conception might reduce their children's pesticide-related autism risk.

8 Sep 2017

UCLA awarded $8.4 million NIH grant to improve outcomes for liver transplant recipients

UCLA has received an $8.4 million grant from the National Institutes of Health to research ways to help donated livers last longer and improve outcomes for transplant recipients.

8 Sep 2017

Differentiating sepsis and systemic inflammatory response syndrome using biomarkers

Firstly, it is necessary to make a distinction between systemic inflammation and Systemic Inflammatory Response Syndrome (SIRS). SIRS consists of changes in clinical signs including an abnormal body temperature, increased heart rate, increased respiratory rate, an abnormal white cell count (either decreased or elevated), or an increase in band neutrophils.

7 Sep 2017

Coimbra Pediatric Hospital selects Congenica's Sapientia software platform for In2Genome project

Congenica, a global provider of clinical genomics interpretation software, today announced a new customer partnership with the Coimbra Paediatric Hospital, a leading paediatric hospital in Portugal and part of the Coimbra Hospital and University Centre.

7 Sep 2017

Myriad Genetics introduces new precision medicine tool to enhance myRisk Hereditary Cancer test

Myriad Genetics, Inc., a leader in molecular diagnostics and personalized medicine, announced today that it has launched riskScore, a new clinically validated precision medicine tool to enhance its myRisk Hereditary Cancer test. riskScore quantifies a woman's risk of developing breast cancer by combining genetic markers throughout the genome with her family and clinical history.

7 Sep 2017

Study identifies genes that regulate gestational length and likelihood of preterm delivery

The genes that regulate gestational length and the likelihood of preterm delivery, have been identified in a study involving more than 50,000 women. An article in the New England Journal of Medicine (NEJM) describes the scientific breakthrough that can lead to improved health and survival among children.

7 Sep 2017

Salk professor awarded $950,000 NSF grant to explore how the brain processes complex sounds

Salk Associate Professor Tatyana Sharpee has been awarded a grant of approximately $950,000 over 4 years by the National Science Foundation to study how the brain processes complex sounds. This grant is part of a multi-national project together with groups in France and Israel.

7 Sep 2017

Exploration of human genetics reveals new targets to combat heart disease

Again and again, it's the rare among humans that help the rest of us. The exploration of human genetics is revealing new targets to combat heart disease among atypical variants. Mutations in genes that play a role in heart health are the inspiration for a cluster of new heart drugs.

7 Sep 2017

Study reveals how changes in gene can lead to blindness in middle age

Blindness study shows how gene causes middle-age sight loss. Chemical changes in the eye that can lead to blindness have been identified by scientists, a conference has heard.

6 Sep 2017

Genetic risk for obesity influenced by lifestyle, study shows

The risk for developing obesity is influenced by our lifestyle as well as our genes. In a new study from Uppsala University, researchers show that our genetic risk for obesity is not static, but is influenced by our lifestyle. Results from the study have been published in the scientific journal PLOS Genetics.

6 Sep 2017

Study reveals link between increased height and blood clots in vein

A new study published in the Circulation: Cardiovascular Genetics – a journal of the American Heart Association – suggested that there is an increased probability of developing blood clots in the veins with an increase in height.

6 Sep 2017

Split-brain study using fruit fly provides better understanding of autism

A better understanding of the cause of autism may come from an unlikely source, neurological studies of the fruit fly.

6 Sep 2017

Novel, ultra-rare damaging genetic variants may contribute to eating disorders

By combining whole exome sequencing, machine learning, and network analysis, researchers have identified new, ultra-rare gene mutations within specific biological pathways that may contribute to eating disorders.

5 Sep 2017

Largest ever genetic study paves way for potential osteoporosis treatment

Scientists are honing in on a potential treatment for osteoporosis, after performing the largest ever genetic study of the common age-related bone-thinning disease.

5 Sep 2017

Researchers identify gene variants linked to both type 2 diabetes and CHD risk

Type 2 diabetes (T2D) has become a global epidemic affecting more than 380 million people worldwide; yet there are knowledge gaps in understanding the etiology of type-2 diabetes.

4 Sep 2017

Genetics of circadian rhythms found to have effect on migraine

People with a specific variation in the CLOCK gene have more migraines under financial stress. This work, the first time that the genetics of circadian rhythms has been shown to have an effect on migraine, is presented at the ECNP conference in Paris.

4 Sep 2017

Existing drug may one day protect premenopausal women from infertility after cancer treatments

An existing drug may one day protect premenopausal women from life-altering infertility that commonly follows cancer treatments, according to a new study.

1 Sep 2017

Mutations altering gene function play role in development of intellectual disabilities

Intellectual disabilities are often caused by a mutation that damages a gene, preventing the associated protein from functioning properly.

1 Sep 2017

Researchers perform first-ever clinical trial involving genetic screening for Parkinson’s disease

In the first ever clinical investigation involving genetic screening for Parkinson's disease, researchers are testing whether the presence of a specific genetic mutation identifies which patients are the best candidates for deep brain stimulation surgery, and whether neurologists should perform that procedure differently based on that genetic information.

1 Sep 2017

Scientists question CRISPR human embryo editing claims

A paper published in the journal Nature on the 2nd August described how a gene editing tool CRISPR could be used to correct a genetic mutation that leads to a heart condition. This team had performed the genetic editing on the gene sequences in dozens of viable human embryos to attempt to prevent a genetic heart condition called hypertrophic cardiomyopathy.

31 Aug 2017

Genetics News and Research

Latest Genetics News and Research

Maternal folic acid intake round conception may reduce children's pesticide-related autism risk

UCLA awarded $8.4 million NIH grant to improve outcomes for liver transplant recipients

Differentiating sepsis and systemic inflammatory response syndrome using biomarkers

Coimbra Pediatric Hospital selects Congenica's Sapientia software platform for In2Genome project

Myriad Genetics introduces new precision medicine tool to enhance myRisk Hereditary Cancer test

Study identifies genes that regulate gestational length and likelihood of preterm delivery

Salk professor awarded $950,000 NSF grant to explore how the brain processes complex sounds

Exploration of human genetics reveals new targets to combat heart disease

Study reveals how changes in gene can lead to blindness in middle age

Genetic risk for obesity influenced by lifestyle, study shows

Study reveals link between increased height and blood clots in vein

Split-brain study using fruit fly provides better understanding of autism

Novel, ultra-rare damaging genetic variants may contribute to eating disorders

Largest ever genetic study paves way for potential osteoporosis treatment

Researchers identify gene variants linked to both type 2 diabetes and CHD risk

Genetics of circadian rhythms found to have effect on migraine

Existing drug may one day protect premenopausal women from infertility after cancer treatments

Mutations altering gene function play role in development of intellectual disabilities

Researchers perform first-ever clinical trial involving genetic screening for Parkinson’s disease

Scientists question CRISPR human embryo editing claims

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

How GLP‑1 Agonists Are Shaping the Future of Obesity Treatment With Dr Bryony Henderson

Flow chemistry, AI, and NMR: A next-gen approach to scalable API production

Digital pathology and the PathoVerse: A conversation with Dr. Singh