(Medical Xpress) -- Research co-led by Radboud University Nijmegen Medical Centre and the Wellcome Trust Sanger Institute has revealed gene mutations that account for 15 per cent of all babies born with Walker-Warburg ...
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A consortium led by scientists at the University of Oxford and Harvard Medical School has constructed the world's most detailed genetic map.
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While autism clearly runs in some families, few inherited genetic causes have been found. A major reason is that these causes are so varied that it's hard to find enough people with a given mutation to establish a clear pattern. ...
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Too often, newborns die of genetic diseases before doctors even know what is to blame. Now scientists have found a way to decode those babies' DNA in just days instead of weeks, moving gene-mapping closer to routine medical ...
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While your DNA is unique, it also tells the tale of your family line. It carries the genetic history of your ancestors down through the generations. Now, says a Tel Aviv University researcher, it's also possible ...
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With a 95 percent genomic similarity to humans, mice have long been used to learn about the genetic causes of human disease. Once researchers can shine a light on the genetic factors that cause disease in mice, they can start ...
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Gene scans for everyone? Not so fast. New research suggests that for the average person, decoding your own DNA may not turn out to be a really useful crystal ball for future health.
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Three new locations for Crohn's Disease genes have been uncovered by scientists at UCL using a novel gene mapping approach.
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A new study involving Canada's Centre for Addiction and Mental Health (CAMH) has found a gene connected with a type of intellectual disability called Joubert syndrome.
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New hope has arrived for migraine sufferers following a Griffith University study with the people of Norfolk Island.
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Researchers at the Centre for Addiction and Mental Health (CAMH) led a study discovering a gene for a new form of intellectual disability, as well as how it likely affects cognitive development by disrupting neuron functioning.
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(Medical Xpress) -- A new technique is helping researchers to pinpoint genetic information that contributes to cancer development.
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Uncovering the origin of illness is like finding a needle in a haystack, but that search is getting easier with the help of powerful tools like genetic analysis and satellite data.
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Alzheimer's disease (AD) is a common problem that is becoming progressively burdensome throughout the world. A new supplement to the Journal of Alzheimer's Disease, Imaging the Alzheimer Brain, clearly shows that multiple imagin ...
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An international team of researchers has identified two new genes connected with hereditary renal diseases.
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