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Abstract:
Genetic
mapping has been a very powerful tool for identifying human disease
genes. Family-based
linkage analysis has lead to mapping several hundreds of human diseases
to specific chromosomal
regions with nearly 100 genes being identified by positional cloning.
However, the success of the
linkage analysis has been mainly limited to rare disorders. Numerous
efforts of large-scale linkage
analysis have been attempted for mapping human common or complex
diseases, but only in a very
few cases has the linkage analysis been successful in identifying
the gene associated with the risk
for developing disease such as in Alzheimer’s and Crohn’s
diseases. Such a failure is likely due to the
pathogenic complexity of human common diseases, which is believed
to be influenced by both genetic
and non-genetic factors as well as their interaction. Recent progress
in genomics, especially the
development of high-throughput platform for lage-scale genotyping
analysis, has opened new avenues
for studying human complex disease. Due to its high power for detection,
association analysis has
emerged as a much more popular approach for mapping and identifying
genes for human complex
disease. In this presentation, genetic theories behind gene mapping
in human diseases will be discussed
briefly. Then, an example will be provided to demonstrate the difficulties
and challenges for studying
human complex diseases. At last, new strategies for identifying
genes for human common diseases,
especially those that can take an advantage of the rapid progress
in genomics, will be discussed.
Speaker
Dr.
Liu is currently a Senior Research Scientist in the population genetics
group at the Genome
Institute of Singapore (GIS) and an Adjunct Research Fellow in the
Centre for Molecular Epidemiology
at the National University of Singapore. Besides his academic appointments,
Dr. Liu is also a Member
of the Central, Sensory & Cellular Nervous System/Mental Health
Subcommittee and National Medical
Research Council of Singapore. Dr. Liu did his Ph.D. study in quantitative
genetics with Prof. Cathy Laurie
at the Duke University. After finishing his Ph.D. study, Dr. Liu
joined Prof. T. Conrad Gilliam’s laboratory
at the Columbia University Genome Center as a Postdoc Research Follow
to study the genetic bases of
human complex diseases. Before joining GIS in 2002, Dr. Liu was
a Research Scientist at the Columbia
University Genome Center (CGC) and led the large-scale genotyping
analysis effort at CGC. Dr. Liu’s main
research interest is to understand the genetic bases of human diseases
by using both genetic and genomic approaches.
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