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Theodore Chiang

Showing results (1-10 of 20) with videos related to

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European Journal of Human Genetics : EJHG|April 29, 2010
A pure likelihood approach to the analysis of genetic association data: an alternative to Bayesian and frequentist analysisLisa J Strug, Susan E Hodge, Theodore Chiang, et al.
Bioinformatics (Oxford, England)|April 16, 2014
Association analysis using next-generation sequence data from publicly available control groups: the robust variance score statisticAndriy Derkach, Theodore Chiang, Jiafen Gong, et al.
Epigenetics|February 24, 2011
Assessment of methylation level prediction accuracy in methyl-DNA immunoprecipitation and sodium bisulfite based microarray platformsRageen Rajendram, Jose Carlos Ferreira, Daria Grafodatskaya, et al.
Human Genetics|September 24, 2013
Unraveling the complex genetic model for cystic fibrosis: pleiotropic effects of modifier genes on early cystic fibrosis-related morbiditiesWeili Li, David Soave, Melissa R Miller, et al.
Plos One|July 21, 2012
The genetics of reading disability in an often excluded sample: novel loci suggested for reading disability in Rolandic epilepsyLisa J Strug, Laura Addis, Theodore Chiang, et al.
American Journal of Medical Genetics. Part A|June 3, 2016
CRIPT exonic deletion and a novel missense mutation in a female with short stature, dysmorphic features, microcephaly, and pigmentary abnormalitiesMagalie S Leduc, Zhiyv Niu, Weimin Bi, et al.
European Journal of Human Genetics : EJHG|January 29, 2009
Centrotemporal sharp wave EEG trait in rolandic epilepsy maps to Elongator Protein Complex 4 (ELP4)Lisa J Strug, Tara Clarke, Theodore Chiang, et al.
Nucleic Acids Research|December 17, 2016
Homozygous and hemizygous CNV detection from exome sequencing data in a Mendelian disease cohortTomasz Gambin, Zeynep C Akdemir, Bo Yuan, et al.
Plos One|October 23, 2010
Specific variants in the MLH1 gene region may drive DNA methylation, loss of protein expression, and MSI-H colorectal cancerMiralem Mrkonjic, Nicole M Roslin, Celia M Greenwood, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 25, 2020
CNVs cause autosomal recessive genetic diseases with or without involvement of SNV/indelsBo Yuan, Lei Wang, Pengfei Liu, et al.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
European Journal of Human Genetics : EJHG|April 29, 2010
A pure likelihood approach to the analysis of genetic association data: an alternative to Bayesian and frequentist analysisLisa J Strug, Susan E Hodge, Theodore Chiang, et al.
Bioinformatics (Oxford, England)|April 16, 2014
Association analysis using next-generation sequence data from publicly available control groups: the robust variance score statisticAndriy Derkach, Theodore Chiang, Jiafen Gong, et al.
Epigenetics|February 24, 2011
Assessment of methylation level prediction accuracy in methyl-DNA immunoprecipitation and sodium bisulfite based microarray platformsRageen Rajendram, Jose Carlos Ferreira, Daria Grafodatskaya, et al.
Human Genetics|September 24, 2013
Unraveling the complex genetic model for cystic fibrosis: pleiotropic effects of modifier genes on early cystic fibrosis-related morbiditiesWeili Li, David Soave, Melissa R Miller, et al.
Plos One|July 21, 2012
The genetics of reading disability in an often excluded sample: novel loci suggested for reading disability in Rolandic epilepsyLisa J Strug, Laura Addis, Theodore Chiang, et al.
American Journal of Medical Genetics. Part A|June 3, 2016
CRIPT exonic deletion and a novel missense mutation in a female with short stature, dysmorphic features, microcephaly, and pigmentary abnormalitiesMagalie S Leduc, Zhiyv Niu, Weimin Bi, et al.
European Journal of Human Genetics : EJHG|January 29, 2009
Centrotemporal sharp wave EEG trait in rolandic epilepsy maps to Elongator Protein Complex 4 (ELP4)Lisa J Strug, Tara Clarke, Theodore Chiang, et al.
Nucleic Acids Research|December 17, 2016
Homozygous and hemizygous CNV detection from exome sequencing data in a Mendelian disease cohortTomasz Gambin, Zeynep C Akdemir, Bo Yuan, et al.
Plos One|October 23, 2010
Specific variants in the MLH1 gene region may drive DNA methylation, loss of protein expression, and MSI-H colorectal cancerMiralem Mrkonjic, Nicole M Roslin, Celia M Greenwood, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 25, 2020
CNVs cause autosomal recessive genetic diseases with or without involvement of SNV/indelsBo Yuan, Lei Wang, Pengfei Liu, et al.
Pageof 2