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Clinical Genetics|November 10, 2022
Bridging clinical care and research in Ontario, Canada: Maximizing diagnoses from reanalysis of clinical exome sequencing dataTaila Hartley, Élisabeth Soubry, Meryl Acker, et al.Journal of Medical Genetics|December 18, 2013
A genome-wide copy number association study of osteoporotic fractures points to the 6p25.1 locusLing Oei, Yi-Hsiang Hsu, Unnur Styrkarsdottir, et al.Nature|May 13, 2026
An X-linked long non-coding RNA, PTCHD1-AS, and the core features of autismClarrisa A Bradley, Sangyoon Y Ko, Meng Tian, et al.Space Science Reviews|February 5, 2019
OSIRIS-REx Contamination Control Strategy and ImplementationJ P Dworkin, L A Adelman, T Ajluni, et al.Nature Neuroscience|March 7, 2017
Whole genome sequencing resource identifies 18 new candidate genes for autism spectrum disorderRyan K C Yuen, Daniele Merico, Matt Bookman, et al.Human Molecular Genetics|January 2, 2014
Disruption of the ASTN2/TRIM32 locus at 9q33.1 is a risk factor in males for autism spectrum disorders, ADHD and other neurodevelopmental phenotypesAnath C Lionel, Kristiina Tammimies, Andrea K Vaags, et al.Science (New York, N.Y.)|October 15, 2016
Positive biodiversity-productivity relationship predominant in global forestsJingjing Liang, Thomas W Crowther, Nicolas Picard, et al.Nature|November 4, 2014
Synaptic, transcriptional and chromatin genes disrupted in autismSilvia De Rubeis, Xin He, Arthur P Goldberg, et al.Cell|November 11, 2022
Genomic architecture of autism from comprehensive whole-genome sequence annotationBrett Trost, Bhooma Thiruvahindrapuram, Ada J S Chan, et al.American Journal of Human Genetics|April 29, 2014
Convergence of genes and cellular pathways dysregulated in autism spectrum disordersDalila Pinto, Elsa Delaby, Daniele Merico, et al.Pageof 201