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Public Health Genomics
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November 30, 2016
The Rise and Rise of Exome Sequencing
Chee-Seng Ku, David N Cooper, George P Patrinos
Journal of Medical Genetics
|
February 12, 2013
From the periphery to centre stage: de novo single nucleotide variants play a key role in human genetic disease
Chee-Seng Ku, Eng King Tan, David N Cooper
Expert Review of Molecular Diagnostics
|
May 24, 2012
The 'sequence everything' approach and personalized clinical decision challenges
Chee-Seng Ku, David N Cooper, Dimitrios H Roukos
Human Genetics
|
November 25, 2010
Regions of homozygosity and their impact on complex diseases and traits
Chee Seng Ku, Nasheen Naidoo, Shu Mei Teo, et al.
Journal of Human Genetics
|
March 20, 2010
The pursuit of genome-wide association studies: where are we now?
Chee Seng Ku, En Yun Loy, Yudi Pawitan, et al.
The Lancet. Oncology
|
April 3, 2010
Molecular epidemiology and its current clinical use in cancer management
Mikael Hartman, En Yun Loy, Chee Seng Ku, et al.
Human Genomics
|
December 14, 2011
Human genetics and genomics a decade after the release of the draft sequence of the human genome
Nasheen Naidoo, Yudi Pawitan, Richie Soong, et al.
Journal of Human Genetics
|
May 21, 2010
The discovery of human genetic variations and their use as disease markers: past, present and future
Chee Seng Ku, En Yun Loy, Agus Salim, et al.
Bioinformatics (Oxford, England)
|
September 4, 2012
Statistical challenges associated with detecting copy number variations with next-generation sequencing
Shu Mei Teo, Yudi Pawitan, Chee Seng Ku, et al.
International Journal of Hematology
|
November 16, 2004
Genetic polymorphism of the CYP2C9 subfamily of 3 different races in warfarin maintenance dose
Gin Gin Gan, Maude Elvira Phipps, Chee Seng Ku, et al.
Page
of 3
Search research articles
Search
Showing results (11-20 of 29) with videos related to
Sort By:
Page
of 3
Public Health Genomics
|
November 30, 2016
The Rise and Rise of Exome Sequencing
Chee-Seng Ku, David N Cooper, George P Patrinos
Journal of Medical Genetics
|
February 12, 2013
From the periphery to centre stage: de novo single nucleotide variants play a key role in human genetic disease
Chee-Seng Ku, Eng King Tan, David N Cooper
Expert Review of Molecular Diagnostics
|
May 24, 2012
The 'sequence everything' approach and personalized clinical decision challenges
Chee-Seng Ku, David N Cooper, Dimitrios H Roukos
Human Genetics
|
November 25, 2010
Regions of homozygosity and their impact on complex diseases and traits
Chee Seng Ku, Nasheen Naidoo, Shu Mei Teo, et al.
Journal of Human Genetics
|
March 20, 2010
The pursuit of genome-wide association studies: where are we now?
Chee Seng Ku, En Yun Loy, Yudi Pawitan, et al.
The Lancet. Oncology
|
April 3, 2010
Molecular epidemiology and its current clinical use in cancer management
Mikael Hartman, En Yun Loy, Chee Seng Ku, et al.
Human Genomics
|
December 14, 2011
Human genetics and genomics a decade after the release of the draft sequence of the human genome
Nasheen Naidoo, Yudi Pawitan, Richie Soong, et al.
Journal of Human Genetics
|
May 21, 2010
The discovery of human genetic variations and their use as disease markers: past, present and future
Chee Seng Ku, En Yun Loy, Agus Salim, et al.
Bioinformatics (Oxford, England)
|
September 4, 2012
Statistical challenges associated with detecting copy number variations with next-generation sequencing
Shu Mei Teo, Yudi Pawitan, Chee Seng Ku, et al.
International Journal of Hematology
|
November 16, 2004
Genetic polymorphism of the CYP2C9 subfamily of 3 different races in warfarin maintenance dose
Gin Gin Gan, Maude Elvira Phipps, Chee Seng Ku, et al.
Page
of 3