Genome-Wide Analysis of Copy Number Variants in Attention Deficit Hyperactivity Disorder: The Role of Rare Variants and Duplications at 15q13.3Nigel Williams, Stephen V. Faraone, Michael J. Owen et al.|American Journal of Psychiatry|2011Cited by 303
Joint Analysis of the DRD5 Marker Concludes Association with Attention-Deficit/Hyperactivity Disorder Confined to the Predominantly Inattentive and Combined SubtypesNaomi Lowe, Michael Gill, Aiveen Kirley et al.|The American Journal of Human Genetics|2004Cited by 184
Integration of xeno-free single-cell cloning in CRISPR-mediated DNA editing of human iPSCs improves homogeneity and methodological efficiency of cellular disease modelingAtefeh Namipashaki, Ziarih Hawi|Stem Cell Reports|2023Cited by 3
Integration of Xeno-Free Single-cell Cloning in CRISPR-mediated DNA Editing of Human iPSCs Improves Homogeneity and Methodological Efficiency of Cellular Disease ModellingAtefeh Namipashaki, Ziarih Hawi|bioRxiv (Cold Spring Harbor Laboratory)|2022Cited by 0