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BMC Genetics|December 17, 2008
Imputation of missing genotypes: an empirical evaluation of IMPUTEZhenming Zhao, Nadia Timofeev, Stephen W Hartley, et al.American Journal of Hematology|July 22, 2014
The genetics of hemoglobin A2 regulation in sickle cell anemiaPaula J Griffin, Paola Sebastiani, Heather Edward, et al.Neurobiology of Aging|January 21, 2014
Search for age-related macular degeneration risk variants in Alzheimer disease genes and pathwaysMark W Logue, Matthew Schu, Badri N Vardarajan, et al.European Journal of Human Genetics : EJHG|December 4, 2002
Is DFNA5 a susceptibility gene for age-related hearing impairment?Lut Van Laer, Anita L DeStefano, Richard H Myers, et al.Human Genetics|November 5, 2014
Genetic variation of the transthyretin gene in wild-type transthyretin amyloidosis (ATTRwt)Jacquelyn L Sikora, Mark W Logue, Gloria G Chan, et al.American Journal of Respiratory and Critical Care Medicine|March 19, 2002
Genetic loci influencing lung function: a genome-wide scan in the Framingham StudyOscar Joost, Jemma B Wilk, L Adrienne Cupples, et al.Plos One|September 24, 2013
Genome-wide meta-analysis of systolic blood pressure in children with sickle cell diseasePallav Bhatnagar, Emily Barron-Casella, Christopher J Bean, et al.Neurobiology of Aging|March 31, 2009
Association of TTR polymorphisms with hippocampal atrophy in Alzheimer disease familiesKaren T Cuenco, Robert Friedland, Clinton T Baldwin, et al.Journal of Alzheimer'S Disease : JAD|November 25, 2010
Identification of novel candidate genes for Alzheimer's disease by autozygosity mapping using genome wide SNP dataRichard Sherva, Clinton T Baldwin, Rivka Inzelberg, et al.Blood Cells, Molecules & Diseases|May 7, 2011
Ancestry of African Americans with sickle cell diseaseNadia Solovieff, Stephen W Hartley, Clinton T Baldwin, et al.Pageof 7