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NPJ Science of Learning|July 2, 2026
Shared genetic architecture of reading and attention disorders using genomic structural equation modelingShiying Wang, Joan Bosson-Heenan, Andrew Grotzinger, et al.The Journal of Pediatrics|September 21, 2010
The impact of environmental and genetic factors on neonatal late-onset sepsisMatthew J Bizzarro, Yuan Jiang, Naveed Hussain, et al.Human Molecular Genetics|September 1, 2007
Association of haplotypic variants in DRD2, ANKK1, TTC12 and NCAM1 to alcohol dependence in independent case control and family samplesBao-Zhu Yang, Henry R Kranzler, Hongyu Zhao, et al.Alcoholism, Clinical and Experimental Research|October 3, 2008
Haplotypic variants in DRD2, ANKK1, TTC12, and NCAM1 are associated with comorbid alcohol and drug dependenceBao-Zhu Yang, Henry R Kranzler, Hongyu Zhao, et al.Journal of Human Genetics|March 20, 2010
Functional impact of a single-nucleotide polymorphism in the OPRD1 promoter regionHuiping Zhang, Joel Gelernter, Jeffrey R Gruen, et al.Pediatrics|January 28, 2009
Genetic contribution to patent ductus arteriosus in the premature newbornVineet Bhandari, Gongfu Zhou, Matthew J Bizzarro, et al.Molecular and Cellular Biology|January 6, 2005
Prss16 is not required for T-cell developmentSaijai Cheunsuk, Zhe-Xiong Lian, Guo-Xiang Yang, et al.Psychiatric Genetics|September 2, 2011
DCDC2 genetic variants and susceptibility to developmental dyslexiaCecilia Marino, Haiying Meng, Sara Mascheretti, et al.The Journal of Clinical Endocrinology and Metabolism|December 24, 2010
A highly sensitive, high-throughput assay for the detection of Turner syndromeScott A Rivkees, Karl Hager, Seiyu Hosono, et al.Journal of Cognitive Neuroscience|September 24, 2025
Shared and Unique Connectivity Signatures of Reading and Language DeficitsMia C Daucourt, Matthew Rosenblatt, Jan C Frijters, et al.Pageof 9