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Study identifies genetic factors linked to severity of acute viral bronchiolitis

A scientific study conducted at the State University of Campinas (UNICAMP) in São Paulo State, Brazil, has identified genetic factors associated with the severity of acute viral bronchiolitis. The study was supported by the Sao Paulo Research Foundation - FAPESP. Its results were published in the journal Gene.

27 Mar 2018

Researchers develop comprehensive map of genetic risk factors for stroke

Stroke is a serious disease affecting blood flow to and from the brain, and is the second leading cause of death worldwide. Stroke is characterized by a sudden onset of neurological dysfunction, caused by a blood clot or hemorrhage in a cerebral artery. While many genetic variants and lifestyle behaviors have been identified as risk factors for stroke, the genetic basis for the disease is unknown.

26 Mar 2018

Increasing prevalence of functional mitral regurgitation related to severity of heart failure

One potential therapeutic concept for treating heart failure besides guideline directed medical therapy, is to correct any concomitant severe mitral valve insufficiency (mitral regurgitation). Despite numerous treatment options being available, it is still not clear which patients will benefit most from such an intervention.

26 Mar 2018

Research provides better understanding of how some cancer cells resist treatment

An international team of researchers led by Lucio Miele, MD, PhD, Professor and Chair of Genetics at LSU Health New Orleans School of Medicine, and Justin Stebbing, BM BCh MA, PhD, Professor of Cancer Medicine and Medical Oncology at Imperial College of Medicine in London, has found new genetic mutations that promote the survival of cancer cells.

23 Mar 2018

Pittcon 2018 ends in Orlando with $23 million economic impact

Pittcon 2018, the 69th Conference and Exposition for Analytical Chemistry and Applied Spectroscopy, ended on March 1, in Orlando, Florida with an economic impact to the city estimated at $23 million. This global event brought together approximately 11,415 conferees and exhibitor personnel (official numbers to be released at the end of March).

From Pittcon 23 Mar 2018

New computational method helps to identify tumor cell mutations with greater accuracy

A new computational method developed by researchers at the New York Genome Center allows scientists to identify rare gene mutations in cancer cells with greater accuracy and sensitivity than currently available approaches.

22 Mar 2018

Agendia receives CE mark for MammaPrint BluePrint Breast Cancer Recurrence and Molecular Subtyping Kit

Agendia, Inc., a world leader in personalized medicine and molecular cancer diagnostics, today announces that its next-generation sequencing-based MammaPrint BluePrint Breast Cancer Recurrence and Molecular Subtyping Kit is now CE marked, enabling the Company to commercialize the device in Europe.

22 Mar 2018

Neuroscientists move closer to developing tools for deciphering brain function

A team of University of Missouri neuroscientists are inching closer to developing the tools needed to decipher the brain.

21 Mar 2018

Protein profiling reveals new prostate cancer mechanisms

A study by the University of Tampere in Finland used protein profiling to find new prostate cancer mechanisms that are not shown by aberrations at the genomic level. Several new potential biomarkers of prostate cancer were also found.

21 Mar 2018

Researchers discover 'missing mutation' in severe infant epilepsy

Researchers have discovered a "missing mutation" in severe infant epilepsy--long-suspected genetic changes that might trigger overactive, brain-damaging electrical signaling leading to seizures.

20 Mar 2018

Wales participates in the 100,000 Genomes Project

Wales has joined the 100,000 Genomes Project, the Welsh Government announced today. The project, now a UK-wide initiative, seeks to transform patient care, encourage genomic discovery and drive a thriving genomics sector.

From Genomics England 20 Mar 2018

Genomics England announces new partnership to improve efficiency of next-generation sequencing analysis

Today (8 January 2018) at the annual J.P. Morgan Healthcare Conference, Edico Genome and Genomics England announced a new partnership to strengthen the accuracy and consistency of next-generation sequencing data analysis in Genomics England’s Rare Disease Pilot.

From Genomics England 20 Mar 2018

‘Fast track’ project shows promising results in cancer whole genome analyses

One key aim of the 100,000 Genomes Project is to improve cancer care for NHS patients. Whole genome sequencing in cancer can enable clinicians to choose better treatments and improve outcomes for patients through personalized medicine.

From Genomics England 20 Mar 2018

Northwestern scientists bring precision medicine to rheumatoid arthritis

Scientists are bringing precision medicine to rheumatoid arthritis for the first time by using genetic profiling of joint tissue to see which drugs will work for which patients, reports a new Northwestern Medicine multi-site study.

19 Mar 2018

Researchers find way to identify undiagnosed genetic diseases in electronic health records

Patients diagnosed with heart failure, stroke, infertility and kidney failure could actually be suffering from rare and undiagnosed genetic diseases.

16 Mar 2018

Medical University of Vienna to partner with bio.logis GIM in pharmacogenetics

Within the framework of U-PGx, an EU project for promoting the use of pharmacogenetic insights in healthcare, the Medical University of Vienna will implement the Genetic Information Management Suite developed by bio.logis Genetic Information Management GmbH.

14 Mar 2018

Precision Medicine News and Research

Study identifies genetic factors linked to severity of acute viral bronchiolitis

Researchers develop comprehensive map of genetic risk factors for stroke

Increasing prevalence of functional mitral regurgitation related to severity of heart failure

Research provides better understanding of how some cancer cells resist treatment

Pittcon 2018 ends in Orlando with $23 million economic impact

New computational method helps to identify tumor cell mutations with greater accuracy

Agendia receives CE mark for MammaPrint BluePrint Breast Cancer Recurrence and Molecular Subtyping Kit

Neuroscientists move closer to developing tools for deciphering brain function

Protein profiling reveals new prostate cancer mechanisms

Researchers discover 'missing mutation' in severe infant epilepsy

Wales participates in the 100,000 Genomes Project

Genomics England announces new partnership to improve efficiency of next-generation sequencing analysis

‘Fast track’ project shows promising results in cancer whole genome analyses

Northwestern scientists bring precision medicine to rheumatoid arthritis

Researchers find way to identify undiagnosed genetic diseases in electronic health records

Medical University of Vienna to partner with bio.logis GIM in pharmacogenetics

Precision oncology may improve overall survival, lower healthcare costs for advanced cancer patients

Southern Research scientists target mutated protein to combat prostate cancer

Scientists discover 36 previously unknown genes implicated in heart failure

Study identifies genetic defect linked to heart failure in African Americans

Event guide: The 4th Precision Medicine in Inflammatory Bowel Disease Summit eBook

Advancing Neuroscience Research Through Collaboration and Patient-Centered Innovation

The impact of vibration on microscopy

How Omics Technologies Are Transforming Biological Research and Drug Discovery

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