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Genetic variation, environmental conditions can have significant impact on human health

Scientists at the Wayne State University School of Medicine's Center for Molecular Medicine and Genetics have shown for the first time the extent by which interactions between environmental exposures and genetic variation across individuals have a significant impact on human traits and diseases like diabetes, heart disease and obesity, strengthening the case for precision medicine initiatives.

4 Nov 2016

Problems with nuclear membrane play role in leukemia, heart disease and aging disorders

We put things into a container to keep them organized and safe. In cells, the nucleus has a similar role: keeping DNA protected and intact within an enveloping membrane.

2 Nov 2016

Illumina donates more than 95,000 human genetic variants to ClinVar database

Illumina, Inc. announced that it has contributed over 95,000 human genetic variants to ClinVar, a public database hosted by the National Center for Biotechnology Information (NCBI).

From Illumina, Inc. 1 Nov 2016

Study yields insights into shifts in epidemiology of multi-drug resistant organisms

A first-of-its-kind study of 900,000 hospital admissions from an integrated health system has yielded insights into shifts in the epidemiology of multi-drug resistant organisms (MDROs) in the community.

27 Oct 2016

Researchers developing guidelines on ethics and best practices for biorepositories

What if a patient gave permission to a researcher at her local hospital to use her blood or specimen for research, and later the researcher decided to share that sample with others?

27 Oct 2016

NIH researchers identify novel role for Hsp60 protein in tissue regeneration and wound healing

National Institutes of Health researchers have identified a novel role for a gene known as heat shock protein 60 (Hsp60), finding that it is critical in tissue regeneration and wound healing.

27 Oct 2016

Researchers identify existing drugs that appear to prevent aggressive subtype of pediatric brain tumors

More than 4,000 children and teens are diagnosed with brain cancer each year and the disease kills more children than any other cancer.

27 Oct 2016

Gene therapy may be effective method for treating Niemann-Pick disease, type C1

For the first time, National Institutes of Health researchers have demonstrated in mice that gene therapy may be the best method for correcting the single faulty gene that causes Niemann-Pick disease, type C1 (NPC1).

26 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

New study examines how tumor genome testing helps improve breast cancer treatment

A new study examines how one early example of precision medicine--tumor genome testing--is being used in women with breast cancer to reduce overtreatment and maximize the benefits of chemotherapy.

24 Oct 2016

New oncogene may contribute to high incidence of prostate cancer among African American men

A team of scientists has identified MNX1 as a new oncogene - a gene than can cause cancer - that is more active in African American prostate cancer than in European American prostate cancer.

21 Oct 2016

Sanford opens new immunotherapy study on colorectal cancer

Sanford Health has opened another clinical trial exploring the power of the body's immune system to fight cancer.

21 Oct 2016

Novel approach may speed up development of new drugs against skin disease

In an ideal world, the newest and most effective drugs for chronic inflammatory conditions would immediately help everyone who took them.

21 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

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

Yale researchers develop new mouse model to understand multiple myeloma

Understanding how multiple myeloma develops and responds to therapies may be easier using a new mouse model developed at Yale University School of Medicine.

21 Oct 2016

Gut microbes can modify our mood and behaviour, research reveals

If aliens were to examine a human, they would think we were just slavish organisms designed to feed microbes and carry them around.

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

NIH funds innovative study to examine use of text messaging in improving diabetes care

Scripps Whittier Diabetes Institute has received a five-year, $2.9 million grant from the National Institutes of Health to fund an innovative clinical trial that will use mHealth technology and text messaging to improve type 2 diabetes management among high-risk Hispanic patients in San Diego County.

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

Genomic News and Research

Genetic variation, environmental conditions can have significant impact on human health

Problems with nuclear membrane play role in leukemia, heart disease and aging disorders

Illumina donates more than 95,000 human genetic variants to ClinVar database

Study yields insights into shifts in epidemiology of multi-drug resistant organisms

Researchers developing guidelines on ethics and best practices for biorepositories

NIH researchers identify novel role for Hsp60 protein in tissue regeneration and wound healing

Researchers identify existing drugs that appear to prevent aggressive subtype of pediatric brain tumors

Gene therapy may be effective method for treating Niemann-Pick disease, type C1

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

New study examines how tumor genome testing helps improve breast cancer treatment

New oncogene may contribute to high incidence of prostate cancer among African American men

Sanford opens new immunotherapy study on colorectal cancer

Novel approach may speed up development of new drugs against skin disease

Rare neurological syndromes linked to variations in ATAD3A gene

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

Yale researchers develop new mouse model to understand multiple myeloma

Gut microbes can modify our mood and behaviour, research reveals

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

NIH funds innovative study to examine use of text messaging in improving diabetes care

Cancer cell's shape may offer clues for precise prognosis

Genetics & Genomics - Second Edition eBook

Achieving and maintaining ISO/IEC 27001 and BS 10012 certifications

Expanding research and clinical options for children with cancer

Examining how pain could play a direct protective role in the gut

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