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Filters

Elizabeth W Pugh

Showing results (1-10 of 44) with videos related to

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BMC Proceedings|December 19, 2009
Application of sex-specific single-nucleotide polymorphism filters in genome-wide association dataHua Ling, Kurt Hetrick, Joan E Bailey-Wilson, et al.
BMC Genetics|February 12, 2016
Filtering genetic variants and placing informative priors based on putative biological functionStefanie Friedrichs, Dörthe Malzahn, Elizabeth W Pugh, et al.
Genetic Epidemiology|December 13, 2005
Comparison of single-nucleotide polymorphisms and microsatellite markers for linkage analysis in the COGA and simulated data sets for Genetic Analysis Workshop 14: Presentation Groups 1, 2, and 3Marsha A Wilcox, Elizabeth W Pugh, Heping Zhang, et al.
BMC Genetics|February 21, 2004
Comparison of year-of-exam- and age-matched estimates of heritability in the Framingham Heart Study dataRasika A Mathias, Marie-Hélène Roy-Gagnon, Cristina M Justice, et al.
BMC Proceedings|December 17, 2016
Comparison of parametric and machine methods for variable selection in simulated Genetic Analysis Workshop 19 dataEmily R Holzinger, Silke Szymczak, James Malley, et al.
American Journal of Human Genetics|February 15, 2002
An autosomal recessive form of bilateral frontoparietal polymicrogyria maps to chromosome 16q12.2-21Xianhua Piao, Lina Basel-Vanagaite, Rachel Straussberg, et al.
G3 (Bethesda, Md.)|August 28, 2013
Imputation-based genomic coverage assessments of current human genotyping arraysSarah C Nelson, Kimberly F Doheny, Elizabeth W Pugh, et al.
American Journal of Medical Genetics. Part A|April 6, 2006
Linkage analysis of genetic loci for kyphoscoliosis on chromosomes 5p13, 13q13.3, and 13q32Nancy H Miller, Beth Marosy, Cristina M Justice, et al.
Human Genetics|November 6, 2008
Genomewide association study for susceptibility genes contributing to familial Parkinson diseaseNathan Pankratz, Jemma B Wilk, Jeanne C Latourelle, et al.
Genes & Development|September 7, 2019
<i>ZCCHC8</i>, the nuclear exosome targeting component, is mutated in familial pulmonary fibrosis and is required for telomerase RNA maturationDustin L Gable, Valeriya Gaysinskaya, Christine C Atik, et al.
Pageof 5

Showing results (1-10 of 44) with videos related to

Sort By:
Pageof 5
BMC Proceedings|December 19, 2009
Application of sex-specific single-nucleotide polymorphism filters in genome-wide association dataHua Ling, Kurt Hetrick, Joan E Bailey-Wilson, et al.
BMC Genetics|February 12, 2016
Filtering genetic variants and placing informative priors based on putative biological functionStefanie Friedrichs, Dörthe Malzahn, Elizabeth W Pugh, et al.
Genetic Epidemiology|December 13, 2005
Comparison of single-nucleotide polymorphisms and microsatellite markers for linkage analysis in the COGA and simulated data sets for Genetic Analysis Workshop 14: Presentation Groups 1, 2, and 3Marsha A Wilcox, Elizabeth W Pugh, Heping Zhang, et al.
BMC Genetics|February 21, 2004
Comparison of year-of-exam- and age-matched estimates of heritability in the Framingham Heart Study dataRasika A Mathias, Marie-Hélène Roy-Gagnon, Cristina M Justice, et al.
BMC Proceedings|December 17, 2016
Comparison of parametric and machine methods for variable selection in simulated Genetic Analysis Workshop 19 dataEmily R Holzinger, Silke Szymczak, James Malley, et al.
American Journal of Human Genetics|February 15, 2002
An autosomal recessive form of bilateral frontoparietal polymicrogyria maps to chromosome 16q12.2-21Xianhua Piao, Lina Basel-Vanagaite, Rachel Straussberg, et al.
G3 (Bethesda, Md.)|August 28, 2013
Imputation-based genomic coverage assessments of current human genotyping arraysSarah C Nelson, Kimberly F Doheny, Elizabeth W Pugh, et al.
American Journal of Medical Genetics. Part A|April 6, 2006
Linkage analysis of genetic loci for kyphoscoliosis on chromosomes 5p13, 13q13.3, and 13q32Nancy H Miller, Beth Marosy, Cristina M Justice, et al.
Human Genetics|November 6, 2008
Genomewide association study for susceptibility genes contributing to familial Parkinson diseaseNathan Pankratz, Jemma B Wilk, Jeanne C Latourelle, et al.
Genes & Development|September 7, 2019
<i>ZCCHC8</i>, the nuclear exosome targeting component, is mutated in familial pulmonary fibrosis and is required for telomerase RNA maturationDustin L Gable, Valeriya Gaysinskaya, Christine C Atik, et al.
Pageof 5