Nature Genetics
hideNature Genetics is a scientific journal concerning genetics. It is published by Nature Publishing Group, and was founded in 1992. The 2008 impact factor is 30.259. Its sister journal is Nature Reviews Genetics.
For more information about Nature Genetics, read the full article at
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News tagged with nature genetics
Researchers Identify Gene Mutations Underlying Risk for Most Common Form of Parkinson's Disease
Nov 17, 2009 |
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(PhysOrg.com) -- Two genes containing mutations known to cause rare familial forms of parkinsonism are also associated with the more common, sporadic form of the disease where there is no family history, researchers have ...
For the first time, scientists discover causative gene of a rare disorder by exome sequencing
Nov 17, 2009 |
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(PhysOrg.com) -- UW researchers have successfully used a method called exome sequencing to quickly discover a previously unknown gene responsible for a rare disorder. The finding demonstrates the usefulness ...
Largest gene study of childhood IBD identifies 5 new genes
Nov 15, 2009 |
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In the largest, most comprehensive genetic analysis of childhood-onset inflammatory bowel disease (IBD), an international research team has identified five new gene regions, including one involved in a biological pathway ...
Deepening the search for clues to rheumatoid arthritis
Nov 09, 2009 |
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(PhysOrg.com) -- The gnawing pain of rheumatoid arthritis is a signal that the body’s immune system has hit the wrong target: its own cartilage and bone.
Developmental delay could stem from nicotinic receptor deletion
Nov 08, 2009 |
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The loss of a gene through deletion of genetic material on chromosome 15 is associated with significant abnormalities in learning and behavior, said a consortium of researchers led by Baylor College of Medicine in a report ...
Cucumber genome published
Nov 02, 2009 |
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The genome of the cucumber has been sequenced by an international consortium lead by Chinese and U.S. institutions. The annotated genome is published online Nov. 1 by the journal Nature Genetics.
The entwined destinies of mankind and leprosy bacteria
Nov 02, 2009 |
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Leprosy still affects hundreds of thousands of people today throughout the entire world. An international team headed by EPFL professor Stewart Cole has traced the history of the disease from ancient Egypt to today and in ...
Testicular tumors may explain why some diseases are more common in children of older fathers
Oct 25, 2009 |
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A rare form of testicular tumour has provided scientists with new insights into how genetic changes (mutations) arise in our children. The research, funded by the Wellcome Trust and the Danish Cancer Society, could explain ...
Rare mutation dramatically increasing schizophrenia risk
Oct 25, 2009 |
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An international team of researchers led by geneticist Jonathan Sebat, Ph.D., of Cold Spring Harbor Laboratory (CSHL), has identified a mutation on human chromosome 16 that substantially increases risk for schizophrenia.
New chromosomal abnormality identified in leukemia associated with Down syndrome
Oct 18, 2009 |
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Researchers identified a new chromosomal abnormality in acute lymphoblastic leukemia (ALL) that appears to work in concert with another mutation to give rise to cancer. This latest anomaly is particularly common in children ...
Loss of Tumor-Suppressor and DNA-Maintenance Proteins Causes Tissue Demise, Study Finds
Oct 15, 2009 |
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(PhysOrg.com) -- A study published in the October issue of Nature Genetics demonstrates that loss of the tumor-suppressor protein p53, coupled with elimination of the DNA-maintenance protein ATR, severely disrup ...
Common gene variant found to regulate iron levels
Oct 13, 2009 |
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(PhysOrg.com) -- An international research team including researchers at UQ's Diamantina Institute and the Queensland Institute of Medical Research has identified a new variant of a gene that helps to regulate iron and haemoglobin ...
Ironing out the genetic cause of hemoglobin problems
Oct 11, 2009 |
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(PhysOrg.com) -- A gene with a significant effect on regulating hemoglobin in the body has been identified as part of a genome-wide association study, which looked at the link between genes and hemoglobin ...
Blood counts are clues to human disease
Oct 11, 2009 |
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(PhysOrg.com) -- A new genome-wide association study published today in Nature Genetics begins to uncover the basis of genetic variations in eight blood measurements and the impact those variants can have o ...
New type of genetic change identified in inherited cancer
Oct 04, 2009 |
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Duke University Medical Center and National Cancer Institute scientists have discovered that a novel genetic alteration - a second copy of an entire gene - is a cause of familial chordoma, an uncommon form of cancer arising ...
