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| Microduplications of 16p11. 2 are associated with schizophrenia SE McCarthy, V Makarov, G Kirov, AM Addington, J McClellan, S Yoon, ... Nature genetics 41 (11), 1223-1227, 2009 | 814 | 2009 |
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| Genomic patterns of de novo mutation in simplex autism TN Turner, BP Coe, DE Dickel, K Hoekzema, BJ Nelson, MC Zody, ... Cell 171 (3), 710-722. e12, 2017 | 350 | 2017 |
| Association testing of the positional and functional candidate gene SLC1A1/EAAC1 in early-onset obsessive-compulsive disorder DE Dickel, J Veenstra-VanderWeele, NJ Cox, X Wu, DJ Fischer, ... Archives of general psychiatry 63 (7), 778-785, 2006 | 333 | 2006 |
| High-throughput single-cell transcriptome profiling of plant cell types CN Shulse, BJ Cole, D Ciobanu, J Lin, Y Yoshinaga, M Gouran, GM Turco, ... Cell reports 27 (7), 2241-2247. e4, 2019 | 325 | 2019 |
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| Germline Chd8 haploinsufficiency alters brain development in mouse AL Gompers, L Su-Feher, J Ellegood, NA Copping, MA Riyadh, ... Nature neuroscience 20 (8), 1062-1073, 2017 | 219 | 2017 |
| Ultraconserved enhancers are required for normal development DE Dickel, AR Ypsilanti, R Pla, Y Zhu, I Barozzi, BJ Mannion, YS Khin, ... Cell 172 (3), 491-499. e15, 2018 | 186 | 2018 |
| Reduced transcript expression of genes affected by inherited and de novo CNVs in autism AS Nord, W Roeb, DE Dickel, T Walsh, M Kusenda, KL O'connor, ... European Journal of Human Genetics 19 (6), 727-731, 2011 | 131 | 2011 |
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| Association studies of serotonin system candidate genes in early-onset obsessive-compulsive disorder DE Dickel, J Veenstra-VanderWeele, NC Bivens, X Wu, DJ Fischer, ... Biological psychiatry 61 (3), 322-329, 2007 | 119 | 2007 |
| Loss of extreme long-range enhancers in human neural crest drives a craniofacial disorder HK Long, M Osterwalder, IC Welsh, K Hansen, JOJ Davies, YE Liu, ... Cell Stem Cell 27 (5), 765-783. e14, 2020 | 113 | 2020 |
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| Genome-wide compendium and functional assessment of in vivo heart enhancers DE Dickel, I Barozzi, Y Zhu, Y Fukuda-Yuzawa, M Osterwalder, ... Nature communications 7 (1), 12923, 2016 | 103 | 2016 |
| Five novel loci for inherited hearing loss mapped by SNP-based homozygosity profiles in Palestinian families H Shahin, T Walsh, AA Rayyan, MK Lee, J Higgins, D Dickel, K Lewis, ... European Journal of Human Genetics 18 (4), 407-413, 2010 | 101 | 2010 |
