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Samuel G Younkin

Showing results (1-10 of 12) with videos related to

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Journal of Transport & Health|October 25, 2024
The Health-Oriented Transportation Model: Estimating the health benefits of active transportationSamuel G Younkin, Henry C Fremont, Jonathan A Patz
Frontiers in Genetics|January 1, 2014
On multi-marker tests for association in case-control studiesMargaret A Taub, Holger R Schwender, Samuel G Younkin, et al.
Biometrical Journal. Biometrische Zeitschrift|August 16, 2014
Analytic power and sample size calculation for the genotypic transmission/disequilibrium test in case-parent trio studiesChristoph Neumann, Margaret A Taub, Samuel G Younkin, et al.
BMC Bioinformatics|December 14, 2012
Fast detection of de novo copy number variants from SNP arrays for case-parent triosRobert B Scharpf, Terri H Beaty, Holger Schwender, et al.
Genetic Epidemiology|July 23, 2014
Detecting disease variants in case-parent trio studies using the bioconductor software package trioHolger Schwender, Qing Li, Christoph Neumann, et al.
BMC Genetics|February 18, 2014
A genome-wide study of de novo deletions identifies a candidate locus for non-syndromic isolated cleft lip/palate riskSamuel G Younkin, Robert B Scharpf, Holger Schwender, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|March 18, 2015
A genome-wide study of inherited deletions identified two regions associated with nonsyndromic isolated oral cleftsSamuel G Younkin, Robert B Scharpf, Holger Schwender, et al.
Bioinformatics (Oxford, England)|April 18, 2014
Inferring rare disease risk variants based on exact probabilities of sharing by multiple affected relativesAlexandre Bureau, Samuel G Younkin, Margaret M Parker, et al.
Human Molecular Genetics|December 11, 2007
Sex-dependent association of a common low-density lipoprotein receptor polymorphism with RNA splicing efficiency in the brain and Alzheimer's diseaseFanggeng Zou, Rangaraj K Gopalraj, Johann Lok, et al.
Nature Genetics|January 13, 2009
Genetic variation in PCDH11X is associated with susceptibility to late-onset Alzheimer's diseaseMinerva M Carrasquillo, Fanggeng Zou, V Shane Pankratz, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Journal of Transport & Health|October 25, 2024
The Health-Oriented Transportation Model: Estimating the health benefits of active transportationSamuel G Younkin, Henry C Fremont, Jonathan A Patz
Frontiers in Genetics|January 1, 2014
On multi-marker tests for association in case-control studiesMargaret A Taub, Holger R Schwender, Samuel G Younkin, et al.
Biometrical Journal. Biometrische Zeitschrift|August 16, 2014
Analytic power and sample size calculation for the genotypic transmission/disequilibrium test in case-parent trio studiesChristoph Neumann, Margaret A Taub, Samuel G Younkin, et al.
BMC Bioinformatics|December 14, 2012
Fast detection of de novo copy number variants from SNP arrays for case-parent triosRobert B Scharpf, Terri H Beaty, Holger Schwender, et al.
Genetic Epidemiology|July 23, 2014
Detecting disease variants in case-parent trio studies using the bioconductor software package trioHolger Schwender, Qing Li, Christoph Neumann, et al.
BMC Genetics|February 18, 2014
A genome-wide study of de novo deletions identifies a candidate locus for non-syndromic isolated cleft lip/palate riskSamuel G Younkin, Robert B Scharpf, Holger Schwender, et al.
Birth Defects Research. Part A, Clinical and Molecular Teratology|March 18, 2015
A genome-wide study of inherited deletions identified two regions associated with nonsyndromic isolated oral cleftsSamuel G Younkin, Robert B Scharpf, Holger Schwender, et al.
Bioinformatics (Oxford, England)|April 18, 2014
Inferring rare disease risk variants based on exact probabilities of sharing by multiple affected relativesAlexandre Bureau, Samuel G Younkin, Margaret M Parker, et al.
Human Molecular Genetics|December 11, 2007
Sex-dependent association of a common low-density lipoprotein receptor polymorphism with RNA splicing efficiency in the brain and Alzheimer's diseaseFanggeng Zou, Rangaraj K Gopalraj, Johann Lok, et al.
Nature Genetics|January 13, 2009
Genetic variation in PCDH11X is associated with susceptibility to late-onset Alzheimer's diseaseMinerva M Carrasquillo, Fanggeng Zou, V Shane Pankratz, et al.
Pageof 2