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Daniel E Weeks

Showing results (31-40 of 183) with videos related to

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Human Heredity|July 8, 2011
Coordinated conditional simulation with SLINK and SUP of many markers linked or associated to a trait in large pedigreesAlejandro A Schäffer, Mathieu Lemire, Jürg Ott, et al.
Genetic Epidemiology|January 19, 2019
Spinning convincing stories for both true and false association signalsRichard J Biedrzycki, Ashley E Sier, Dongjing Liu, et al.
Plos One|May 22, 2008
C2 and CFB genes in age-related maculopathy and joint action with CFH and LOC387715 genesJohanna Jakobsdottir, Yvette P Conley, Daniel E Weeks, et al.
Plos Genetics|February 7, 2009
Interpretation of genetic association studies: markers with replicated highly significant odds ratios may be poor classifiersJohanna Jakobsdottir, Michael B Gorin, Yvette P Conley, et al.
Epigenetics Communications|January 27, 2022
Characterization of cerebrospinal fluid DNA methylation age during the acute recovery period following aneurysmal subarachnoid hemorrhageLacey W Heinsberg, Dongjing Liu, John R Shaffer, et al.
Biological Research for Nursing|August 27, 2022
Advancing Nursing Research Through Interactive Data Visualization With R ShinyLacey W Heinsberg, Theresa A Koleck, Mitali Ray, et al.
American Journal of Human Genetics|February 29, 2008
Robust score statistics for QTL linkage analysisSamsiddhi Bhattacharjee, Chia-Ling Kuo, Nandita Mukhopadhyay, et al.
Genome Research|March 5, 2002
A tale of two genotypes: consistency between two high-throughput genotyping centersDaniel E Weeks, Yvette P Conley, Robert E Ferrell, et al.
BMC Medical Genetics|January 21, 2011
Enhanced genetic maps from family-based disease studies: population-specific comparisonsChunsheng He, Daniel E Weeks, Steven Buyske, et al.
Scientific Reports|June 23, 2016
The impact of genotype calling errors on family-based studiesQi Yan, Rui Chen, James S Sutcliffe, et al.
Pageof 19

Showing results (31-40 of 183) with videos related to

Sort By:
Pageof 19
Human Heredity|July 8, 2011
Coordinated conditional simulation with SLINK and SUP of many markers linked or associated to a trait in large pedigreesAlejandro A Schäffer, Mathieu Lemire, Jürg Ott, et al.
Genetic Epidemiology|January 19, 2019
Spinning convincing stories for both true and false association signalsRichard J Biedrzycki, Ashley E Sier, Dongjing Liu, et al.
Plos One|May 22, 2008
C2 and CFB genes in age-related maculopathy and joint action with CFH and LOC387715 genesJohanna Jakobsdottir, Yvette P Conley, Daniel E Weeks, et al.
Plos Genetics|February 7, 2009
Interpretation of genetic association studies: markers with replicated highly significant odds ratios may be poor classifiersJohanna Jakobsdottir, Michael B Gorin, Yvette P Conley, et al.
Epigenetics Communications|January 27, 2022
Characterization of cerebrospinal fluid DNA methylation age during the acute recovery period following aneurysmal subarachnoid hemorrhageLacey W Heinsberg, Dongjing Liu, John R Shaffer, et al.
Biological Research for Nursing|August 27, 2022
Advancing Nursing Research Through Interactive Data Visualization With R ShinyLacey W Heinsberg, Theresa A Koleck, Mitali Ray, et al.
American Journal of Human Genetics|February 29, 2008
Robust score statistics for QTL linkage analysisSamsiddhi Bhattacharjee, Chia-Ling Kuo, Nandita Mukhopadhyay, et al.
Genome Research|March 5, 2002
A tale of two genotypes: consistency between two high-throughput genotyping centersDaniel E Weeks, Yvette P Conley, Robert E Ferrell, et al.
BMC Medical Genetics|January 21, 2011
Enhanced genetic maps from family-based disease studies: population-specific comparisonsChunsheng He, Daniel E Weeks, Steven Buyske, et al.
Scientific Reports|June 23, 2016
The impact of genotype calling errors on family-based studiesQi Yan, Rui Chen, James S Sutcliffe, et al.
Pageof 19