Genomics News and Research

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Genomics is the study of the complete genetic material, including genes and their functions, of an organism.

Study reveals molecular architecture of fungal cell walls and structural responses to stress

In a new study published in Nature Communications, Associate Professor Tuo Wang and his research team from the Department of Chemistry at Louisiana State University revealed the molecular architecture of fungal cell walls and the structural responses to stresses, aiding the development of antifungal drugs targeting cell wall components.

21 Nov 2021

Researchers use embryonic stem cell model to study genetic architecture in the hypothalamus

A study led by researchers at Children's Hospital of Philadelphia has implicated several genes involved in a variety of bodily functions associated with the hypothalamus, a notoriously difficult-to-study region of the brain.

21 Nov 2021

Sharing large-scale health data to drive forward precision medicine

Precision medicine requires big data. In order to improve the treatment of individuals with cancer, or to understand rare diseases, scientists and clinicians, as well as AI technologies require access to larger sets of health research data that covers diverse populations and wide ranges of conditions.

20 Nov 2021

New study highlights the important role of rare genomic differences in OCD risk

Both rare and commonly observed differences in the DNA letters strung along a person's chromosomes can explain about a third of the risk for being diagnosed with obsessive-compulsive disorder (OCD), according to a new study led by scientists at the Icahn School of Medicine at Mount Sinai.

18 Nov 2021

Experts debate whether whole genome sequencing is necessary for all newborn babies

Genomics England, a government owned company, recently announced a pilot programme of whole genome sequencing to screen for genetic diseases in 200,000 healthy seeming newborns.

18 Nov 2021

Experts develop a functional precision medicine approach to assign therapies to cancer patients

A functional precision medicine study conducted in Finland demonstrates that treatment selection based on results from drug sensitivity testing of patients' cells can be clinically useful in patients with aggressive hematological cancers.

18 Nov 2021

Scientists discover the genes used by bacteria to live within complex communities

Scientists from the Quadram Institute at the Norwich Research Park have made an important discovery into the workings of bacterial communities.

18 Nov 2021

Young adults with cancer may require different treatments than older patients

Not all tumors are alike. Young adults who are diagnosed with skin, colon, and other cancer types may require different treatments than older patients receive.

16 Nov 2021

Study provides a new target for therapeutic intervention in Parkinson's disease

In an unexpected discovery, Georgetown University Medical Center researchers have identified what appears to be a significant vascular defect in patients with moderately severe Parkinson's disease.

14 Nov 2021

Scientists develop a single-cell chromatin atlas for the human genome

Researchers at University of California San Diego have produced a single-cell chromatin atlas for the human genome.

14 Nov 2021

New study challenges the popular belief that gut microbiome drives autism

A new Australian collaborative Autism CRC study, led by Mater Research and The University of Queensland, has challenged the growing popular belief that the gut microbiome drives autism.

12 Nov 2021

Johns Hopkins receives $20 million grant to develop technologies for healthy aging

Johns Hopkins has received a $20 million grant from the National Institute on Aging that will spur the development of artificial intelligence devices (AI) to improve the health of older adults and help them live independently for longer — a relatively untapped use of this technology.

11 Nov 2021

Whole senome sequencing can effectively secure a diagnosis for people with rare diseases

A world-first scientific study, published today in the New England Journal of Medicine, has shown that whole genome sequencing can uncover new diagnoses for people across the broadest range of rare diseases investigated to date and could deliver enormous benefits across the NHS.

10 Nov 2021

Retinoid therapy improves vision in mice with Usher syndrome

Using data generated from patients and mice with genetic mutation for the disorder Usher syndrome, researchers from the University of Maryland School of Medicine, the National Institutes of Health's National Eye Institute, and National Institute on Deafness and Other Communication Disorders, documented the natural history of vision impairment in patients and identified the cell mechanism behind progressive vision loss.

9 Nov 2021

Scientists discover gene responsible for doubling the risk of respiratory failure from COVID-19

Scientists at Oxford University have identified the gene responsible for doubling the risk of respiratory failure from COVID-19.

9 Nov 2021

Milestone study uncovers genetic risk factors for spine osteoarthritis

Scientists from the LKS Faculty of Medicine, The University of Hong Kong (HKUMed), contributing as part of the 'Genetics of Osteoarthritis (GO)' consortium to the world's largest study of over 800,000 individuals, have identified genetic risk factors - variants associated with SOX5 and CHST3 genes, key regulators of the development of the intervertebral discs, to be implicated in spine osteoarthritis (OA).

8 Nov 2021

Genomics News and Research

Further Reading

Study reveals molecular architecture of fungal cell walls and structural responses to stress

Researchers use embryonic stem cell model to study genetic architecture in the hypothalamus

Sharing large-scale health data to drive forward precision medicine

New study highlights the important role of rare genomic differences in OCD risk

Experts debate whether whole genome sequencing is necessary for all newborn babies

Experts develop a functional precision medicine approach to assign therapies to cancer patients

Scientists discover the genes used by bacteria to live within complex communities

Young adults with cancer may require different treatments than older patients

Study provides a new target for therapeutic intervention in Parkinson's disease

Scientists develop a single-cell chromatin atlas for the human genome

New study challenges the popular belief that gut microbiome drives autism

Johns Hopkins receives $20 million grant to develop technologies for healthy aging

Whole senome sequencing can effectively secure a diagnosis for people with rare diseases

Retinoid therapy improves vision in mice with Usher syndrome

Scientists discover gene responsible for doubling the risk of respiratory failure from COVID-19

Milestone study uncovers genetic risk factors for spine osteoarthritis

Washington University School of Medicine receives $17 million to address disparities in cancers

Genomic characterization of SARS-CoV-2 gamma variant in Brazil

Transmission of COVID-19 from pet parent to pet documented for first time in the U.S.

The impact of SARS-CoV-2 variants on the COVID-19 epidemic in South Africa

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