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Jessica X Chong

Showing results (1-10 of 94) with videos related to

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American Journal of Human Genetics|September 7, 2019
Mendelian Gene Discovery: Fast and Furious with No End in SightMichael J Bamshad, Deborah A Nickerson, Jessica X Chong
American Journal of Human Genetics|February 11, 2014
Solving glycosylation disorders: fundamental approaches reveal complicated pathwaysHudson H Freeze, Jessica X Chong, Michael J Bamshad, et al.
American Journal of Human Genetics|September 18, 2012
A population-based study of autosomal-recessive disease-causing mutations in a founder populationJessica X Chong, Rebecca Ouwenga, Rebecca L Anderson, et al.
BMC Bioinformatics|February 27, 2024
GPAD: a natural language processing-based application to extract the gene-disease association discovery information from OMIMK M Tahsin Hassan Rahit, Vladimir Avramovic, Jessica X Chong, et al.
Genetic Epidemiology|March 31, 2012
Accurate imputation of rare and common variants in a founder population from a small number of sequenced individualsLawrence H Uricchio, Jessica X Chong, Kevin D Ross, et al.
HGG Advances|January 20, 2022
Centering Equity in <i>Human Genetics and Genomics Advances</i>Jennifer K Wagner, Joon-Ho Yu, Jessica X Chong, et al.
Thyroid : Official Journal of the American Thyroid Association|November 9, 2016
DUOX2 Gene Mutation Manifesting as Resistance to Thyrotropin PhenotypePanudda Srichomkwun, Junta Takamatsu, Deborah A Nickerson, et al.
European Journal of Human Genetics : EJHG|May 26, 2011
A common spinal muscular atrophy deletion mutation is present on a single founder haplotype in the US HutteritesJessica X Chong, A Afşin Oktay, Zunyan Dai, et al.
Circulation. Cardiovascular Genetics|July 19, 2013
Homozygous founder mutation in desmocollin-2 (DSC2) causes arrhythmogenic cardiomyopathy in the Hutterite populationBrenda Gerull, Florian Kirchner, Jessica X Chong, et al.
American Journal of Medical Genetics. Part A|April 24, 2013
Practices and policies of clinical exome sequencing providers: analysis and implicationsSeema M Jamal, Joon-Ho Yu, Jessica X Chong, et al.
Pageof 10

Showing results (1-10 of 94) with videos related to

Sort By:
Pageof 10
American Journal of Human Genetics|September 7, 2019
Mendelian Gene Discovery: Fast and Furious with No End in SightMichael J Bamshad, Deborah A Nickerson, Jessica X Chong
American Journal of Human Genetics|February 11, 2014
Solving glycosylation disorders: fundamental approaches reveal complicated pathwaysHudson H Freeze, Jessica X Chong, Michael J Bamshad, et al.
American Journal of Human Genetics|September 18, 2012
A population-based study of autosomal-recessive disease-causing mutations in a founder populationJessica X Chong, Rebecca Ouwenga, Rebecca L Anderson, et al.
BMC Bioinformatics|February 27, 2024
GPAD: a natural language processing-based application to extract the gene-disease association discovery information from OMIMK M Tahsin Hassan Rahit, Vladimir Avramovic, Jessica X Chong, et al.
Genetic Epidemiology|March 31, 2012
Accurate imputation of rare and common variants in a founder population from a small number of sequenced individualsLawrence H Uricchio, Jessica X Chong, Kevin D Ross, et al.
HGG Advances|January 20, 2022
Centering Equity in <i>Human Genetics and Genomics Advances</i>Jennifer K Wagner, Joon-Ho Yu, Jessica X Chong, et al.
Thyroid : Official Journal of the American Thyroid Association|November 9, 2016
DUOX2 Gene Mutation Manifesting as Resistance to Thyrotropin PhenotypePanudda Srichomkwun, Junta Takamatsu, Deborah A Nickerson, et al.
European Journal of Human Genetics : EJHG|May 26, 2011
A common spinal muscular atrophy deletion mutation is present on a single founder haplotype in the US HutteritesJessica X Chong, A Afşin Oktay, Zunyan Dai, et al.
Circulation. Cardiovascular Genetics|July 19, 2013
Homozygous founder mutation in desmocollin-2 (DSC2) causes arrhythmogenic cardiomyopathy in the Hutterite populationBrenda Gerull, Florian Kirchner, Jessica X Chong, et al.
American Journal of Medical Genetics. Part A|April 24, 2013
Practices and policies of clinical exome sequencing providers: analysis and implicationsSeema M Jamal, Joon-Ho Yu, Jessica X Chong, et al.
Pageof 10