Genomics

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Genetics plays major role in how infants visually explore social world, twin study reveals

New research has uncovered compelling evidence that genetics plays a major role in how children look at the world and whether they have a preference for gazing at people's eyes and faces or at objects.

12 Jul 2017

Variation in sleep patterns between age groups linked to evolutionary adaptation, study finds

A study conducted on the Hadza people in Tanzania suggests a natural variation in sleeping patterns among people living in groups, where there is rarely a moment when someone isn’t vigilant enough to raise an alarm.

12 Jul 2017

Researchers identify common genetic factors that influence muscle strength

Common genetic factors that influence muscle strength in humans have been identified for the first time in a study led by researchers from the University of Cambridge and published today in Nature Communications.

12 Jul 2017

Study shows potential of whole genome sequencing and AI to help clinicians scale precision oncology

In a study published today in the July 11, 2017 issue of Neurology Genetics, an official journal of the American Academy of Neurology, researchers at the New York Genome Center, The Rockefeller University and other NYGC member institutions, and IBM have illustrated the potential of IBM Watson for Genomics to analyze complex genomic data from state-of-the-art DNA sequencing of whole genomes.

11 Jul 2017

Researchers discover basic genetic mechanism that causes congenital myotonic dystrophy

For years, the underlying process that causes a debilitating muscle disorder in infants and young children has been largely unknown.

11 Jul 2017

Research provides new insight into biology of premature birth

Research carried out by the University of Kent with doctors on the neonatal unit at the William Harvey Hospital and Brunel University have provided further insight into the biology of premature birth, with findings that may have implications for treating premature babies.

11 Jul 2017

Synthetic compound that reads mitochondrial DNA could lead to treatments for nerve, muscle diseases

For the first time, a synthetic compound has been made that can bind to DNA in the cells' energy powerhouses, suppressing a gene associated with nerve and muscle disease.

11 Jul 2017

Scientists find single protein that controls genes essential for spermatogenesis

Scientists have found a single protein--Ptbp2--controls a network of over 200 genes central to how developing sperm move and communicate. The protein works by regulating how RNA is processed during each stage of sperm development.

10 Jul 2017

Study uncovers new genetic variants for lung cancer risk

A new study conducted by an international team of lung cancer researchers, including Professor John Field from the University of Liverpool, have identified new genetic variants for lung cancer risk.

10 Jul 2017

CHOP researchers pinpoint WDR26 haploinsufficiency as cause for rare genetic syndrome

Researchers have identified a rare genetic syndrome characterized by intellectual disability, seizures, an abnormal gait and distinctive facial features.

6 Jul 2017

Scientists show how muscles request more energy from fat storage tissues

Muscles require energy to perform all of the movements that we do in a day, and now, for the first time, researchers at the Texas A&M College of Medicine have shown how muscles "request" more energy from fat storage tissues in fruit fly models.

6 Jul 2017

Dmrta2 gene mutation can lead to abnormal brain development in unborn babies

Researchers from Cardiff University and Université Libre de Bruxelles have identified how the function of a key gene significantly impacts nerve stem cell growth, and how it can lead to abnormal brain development in unborn babies if the system goes awry.

6 Jul 2017

New research offers crucial step towards understanding cause of myopathy

Pioneering research using the tropical zebrafish could provide new insights into the genetic basis of myopathy, a type of human muscle disease.

6 Jul 2017

IRB Barcelona scientists reveal role of Dpp gene in wing growth of fruit flies

Researchers working in the Development and Growth Control Lab at IRB Barcelona reveal that the Dpp gene (BMP in humans) plays a double role in the structural organization and growth of the wings of the fruit fly Drosophila melanogaster.

5 Jul 2017

New technique can help predict and combat potential pandemic virus

By developing a new technique for labeling the gene segments of influenza viruses, researchers now know more about how influenza viruses enter the cell and establish cell co-infections - a major contributing factor to potential pandemic development.

5 Jul 2017

New molecular technique can clone thousands of long DNA sequences at the same time

Scientists at Johns Hopkins, Rutgers, the University of Trento in Italy, and Harvard Medical School report they have developed a new molecular technique called LASSO cloning, which can be used to isolate thousands of long DNA sequences at the same time, more than ever before possible.

5 Jul 2017

First systematic genomic analysis of patients with T-ALL may aid development of new therapies

A consortium including St. Jude Children's Research Hospital and the Children's Oncology Group has performed an unprecedented genomic sequencing analysis of hundreds of patients with T-lineage acute lymphoblastic leukemia (T-ALL).

4 Jul 2017

New technique to study genetic changes could enhance cancer diagnosis

Large-scale changes to the structure of the genome are often seen in cancer cells. Scientists at the Babraham Institute in Cambridge, UK, have found a way to detect these changes, which could enhance cancer diagnosis and aid the use of targeted treatments.

4 Jul 2017

Finnish mothers carry rare gene variants that protect them from pre-eclampsia, study finds

Researchers at the University of Helsinki, in cooperation with two research groups in the United States, have discovered that some Finnish mothers carry rare gene variants that protect them from pre-eclampsia, also known as toxaemia of pregnancy.

3 Jul 2017

Study indicates new element involved in genome instability

Genome instability is the main risk factor in the development of tumours in humans. Understanding how, where, when and why these mutations are produced in DNA is one of the great objectives of the global scientific community.

30 Jun 2017

Genomics

Genetics plays major role in how infants visually explore social world, twin study reveals

Variation in sleep patterns between age groups linked to evolutionary adaptation, study finds

Researchers identify common genetic factors that influence muscle strength

Study shows potential of whole genome sequencing and AI to help clinicians scale precision oncology

Researchers discover basic genetic mechanism that causes congenital myotonic dystrophy

Research provides new insight into biology of premature birth

Synthetic compound that reads mitochondrial DNA could lead to treatments for nerve, muscle diseases

Scientists find single protein that controls genes essential for spermatogenesis

Study uncovers new genetic variants for lung cancer risk

CHOP researchers pinpoint WDR26 haploinsufficiency as cause for rare genetic syndrome

Scientists show how muscles request more energy from fat storage tissues

Dmrta2 gene mutation can lead to abnormal brain development in unborn babies

New research offers crucial step towards understanding cause of myopathy

IRB Barcelona scientists reveal role of Dpp gene in wing growth of fruit flies

New technique can help predict and combat potential pandemic virus

New molecular technique can clone thousands of long DNA sequences at the same time

First systematic genomic analysis of patients with T-ALL may aid development of new therapies

New technique to study genetic changes could enhance cancer diagnosis

Finnish mothers carry rare gene variants that protect them from pre-eclampsia, study finds

Study indicates new element involved in genome instability

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