The importance for research and clinical utility of mutation databases, as well as the issues and difficulties entailed in their construction, is discussed within the Human Variome Project. While general principles and standards can apply to most human diseases, some specific questions arise when dealing with the nature of genetic neurological disorders. So far, publically accessible mutation databases exist for only about half of the genes causing neurogenetic disorders; and a considerable work is clearly still needed to optimize their content. The current landscape, main challenges, some potential solutions, and future perspectives on genetic databases for disorders of the nervous system are reviewed in this special issue of Human Mutatio...
ABSTRACT: The Alzheimer disease and frontotemporal dementia (AD&FTLD) and Parkinson disease (PD)...
Neurodevelopmental disorders (NDDs) represent a growing medical challenge in modern societies. Ever-...
The rate of DNA variation discovery has accelerated the need to collate, store and interpret the dat...
The importance for research and clinical utility of mutation databases, as well as the issues and di...
Tens of thousands of genetic association studies investigating the influence of common polymorphisms...
The need for Locus-Specific Databases, with disease-specific experts and curators, is an essential i...
The need for Locus-Specific Databases, with disease-specific experts and curators, is an essential i...
The need for Locus-Specific Databases, with disease-specific experts and curators, is an essential i...
Databases of mutations causing Mendelian disease play a crucial role in research, diagnostic and gen...
Although 20 years have elapsed since the first single basepair substitution underlying an inherited ...
The Human Gene Mutation Database (HGMD®) constitutes a comprehensive collection of published germlin...
AbstractBrain disorders remain one of the defining challenges of modern medicine and among the most ...
International audienceNew technologies, which constantly become available for mutation detection and...
AbstractThe knowledge of the human genome is in continuous progression: a large number of databases ...
The knowledge of the human genome is in continuous progression: a large number of databases have bee...
ABSTRACT: The Alzheimer disease and frontotemporal dementia (AD&FTLD) and Parkinson disease (PD)...
Neurodevelopmental disorders (NDDs) represent a growing medical challenge in modern societies. Ever-...
The rate of DNA variation discovery has accelerated the need to collate, store and interpret the dat...
The importance for research and clinical utility of mutation databases, as well as the issues and di...
Tens of thousands of genetic association studies investigating the influence of common polymorphisms...
The need for Locus-Specific Databases, with disease-specific experts and curators, is an essential i...
The need for Locus-Specific Databases, with disease-specific experts and curators, is an essential i...
The need for Locus-Specific Databases, with disease-specific experts and curators, is an essential i...
Databases of mutations causing Mendelian disease play a crucial role in research, diagnostic and gen...
Although 20 years have elapsed since the first single basepair substitution underlying an inherited ...
The Human Gene Mutation Database (HGMD®) constitutes a comprehensive collection of published germlin...
AbstractBrain disorders remain one of the defining challenges of modern medicine and among the most ...
International audienceNew technologies, which constantly become available for mutation detection and...
AbstractThe knowledge of the human genome is in continuous progression: a large number of databases ...
The knowledge of the human genome is in continuous progression: a large number of databases have bee...
ABSTRACT: The Alzheimer disease and frontotemporal dementia (AD&FTLD) and Parkinson disease (PD)...
Neurodevelopmental disorders (NDDs) represent a growing medical challenge in modern societies. Ever-...
The rate of DNA variation discovery has accelerated the need to collate, store and interpret the dat...