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BMC Bioinformatics|October 21, 2011
Mitochondrial genome sequence analysis: a custom bioinformatics pipeline substantially improves Affymetrix MitoChip v2.0 call rate and accuracyHongbo M Xie, Juan C Perin, Theodore G Schurr, et al.Nature Communications|September 20, 2017
Common variants in MMP20 at 11q22.2 predispose to 11q deletion and neuroblastoma riskXiao Chang, Yan Zhao, Cuiping Hou, et al.Molecular Autism|January 29, 2014
Identification of rare DNA sequence variants in high-risk autism families and their prevalence in a large case/control populationNori Matsunami, Charles H Hensel, Lisa Baird, et al.Biorxiv : the Preprint Server for Biology|November 24, 2025
Gram-positive bacterial cell wall components inhibit herpes simplex virus infectionAmanda N D Adams, Lauren E Griffin, Jonathan Burnie, et al.Nature|August 30, 2008
Identification of ALK as a major familial neuroblastoma predisposition geneYaël P Mossé, Marci Laudenslager, Luca Longo, et al.Plos One|February 2, 2012
Genome wide association identifies PPFIA1 as a candidate gene for acute lung injury risk following major traumaJason D Christie, Mark M Wurfel, Rui Feng, et al.Nature Genetics|March 9, 2010
Common variants at 5q22 associate with pediatric eosinophilic esophagitisMarc E Rothenberg, Jonathan M Spergel, Joseph D Sherrill, et al.Nature Genetics|May 5, 2009
Common variations in BARD1 influence susceptibility to high-risk neuroblastomaMario Capasso, Marcella Devoto, Cuiping Hou, et al.American Journal of Human Genetics|March 3, 2009
Diverse genome-wide association studies associate the IL12/IL23 pathway with Crohn DiseaseKai Wang, Haitao Zhang, Subra Kugathasan, et al.The New England Journal of Medicine|May 9, 2008
Chromosome 6p22 locus associated with clinically aggressive neuroblastomaJohn M Maris, Yael P Mosse, Jonathan P Bradfield, et al.Pageof 6