Date |
Lecture |
Speaker |
Topic |
2007-03-07 |
1 |
孫孝芳(成大分醫所) |
Basic concepts of linkage analysis |
2007-03-14 |
2 |
林秀娟(成醫小兒科) |
Collection of clinical data for genetic studies |
2007-03-21 |
3 |
孫孝芳(成大分醫所) |
Determining the genetic component of a disease |
2007-03-28 |
4 |
孫孝芳(成大分醫所) |
Positional cloning |
2007-04-11 |
5 |
孫孝芳(成大分醫所) |
Alternative study designs (Sib-pair analysis and homozygosity mapping) |
2007-04-18 |
6 |
呂政展(成大病理部) |
Allelic association and Transmission Disequilibrium Test |
2007-04-25 |
7 |
張志欽(成大環醫所) |
Genetic epidemiology |
2007-05-02 |
8 |
孫孝芳(成大分醫所) |
Midterm examine |
2007-05-09 |
9 |
王憶卿(成大藥理所) |
Gene mapping by genetic and epigenetic approaches in cancer |
2007-05-16 |
10 |
張堯(NHRI臨床研究組) |
Transforming genes of EBV in related human malignancies |
2007-05-23 |
11 |
孫孝芳(成大分醫所) |
Methods in identification of sequence variants |
2007-05-30 |
12 |
郭保麟(成大婦產科) |
Identification of genes involved in male infertility |
2007-06-06 |
13 |
孫孝芳(成大分醫所) |
Paper discussion Autosomal recessive ichthyosis with hypotrichosis caused by a mutation in ST14, encoding type II transmembrane serine protease matriptase.A genome-wide association study identifies novel risk loci for type 2 diabetes. |
2007-06-13 |
14 |
孫孝芳(成大分醫所) |
Paper discussion Mutations in STRA6 cause a broad spectrum of malformations including anophthalmia, congenital heart defects, diaphragmatic hernia, alveolar capillary dysplasia, lung hypoplasia, and mental retardation. A nonsynonymous SNP in PRKCH (protein kinase C eta) increases the risk of cerebral infarction. |
2007-06-20 |
15 |
孫孝芳(成大分醫所) |
Paper discussion Familial chilblain lupus, a monogenic form of cutaneous lupus erythematosus, maps to chromosome 3p.Identification of genetic loci for basal cell nevus syndrome and inflammatory bowel disease in a single large pedigree. |
2007-06-27 |
16 |
孫孝芳(成大分醫所) |
Paper discussion A novel human primary immunodeficiency syndrome caused by deficiency of the endosomal adaptor protein p14.Functional variants in the promoter region of Chitinase 3-like 1 (CHI3L1) and susceptibility to schizophrenia. |