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Diane E Dickel
Diane E Dickel
Head of Functional Genomics; Octant Bio
Verified email at octant.bio
Title
Cited by
Cited by
Year
Expanded encyclopaedias of DNA elements in the human and mouse genomes
JE Moore, MJ Purcaro, HE Pratt, CB Epstein, N Shoresh, J Adrian, T Kawli, ...
Nature 583 (7818), 699-710, 2020
11362020
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
8122009
A recurrent 16p12. 1 microdeletion supports a two-hit model for severe developmental delay
S Girirajan, JA Rosenfeld, GM Cooper, F Antonacci, P Siswara, A Itsara, ...
Nature genetics 42 (3), 203-209, 2010
6562010
Enhancer redundancy provides phenotypic robustness in mammalian development
M Osterwalder, I Barozzi, V Tissières, Y Fukuda-Yuzawa, BJ Mannion, ...
Nature 554 (7691), 239-243, 2018
5682018
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
3442017
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
3282006
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
3162019
Progressive loss of function in a limb enhancer during snake evolution
EZ Kvon, OK Kamneva, US Melo, I Barozzi, M Osterwalder, BJ Mannion, ...
Cell 167 (3), 633-642. e11, 2016
3152016
Single-nucleus analysis of accessible chromatin in developing mouse forebrain reveals cell-type-specific transcriptional regulation
S Preissl, R Fang, H Huang, Y Zhao, R Raviram, DU Gorkin, Y Zhang, ...
Nature neuroscience 21 (3), 432-439, 2018
3002018
An atlas of dynamic chromatin landscapes in mouse fetal development
DU Gorkin, I Barozzi, Y Zhao, Y Zhang, H Huang, AY Lee, B Li, J Chiou, ...
Nature 583 (7818), 744-751, 2020
291*2020
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
2172017
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
1862018
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
1312011
The changing mouse embryo transcriptome at whole tissue and single-cell resolution
P He, BA Williams, D Trout, GK Marinov, H Amrhein, L Berghella, ST Goh, ...
Nature 583 (7818), 760-767, 2020
1272020
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
1192007
Comprehensive in vivo interrogation reveals phenotypic impact of human enhancer variants
EZ Kvon, Y Zhu, G Kelman, CS Novak, I Plajzer-Frick, M Kato, TH Garvin, ...
Cell 180 (6), 1262-1271. e15, 2020
1122020
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
1112020
Genomic analyses implicate noncoding de novo variants in congenital heart disease
F Richter, SU Morton, SW Kim, A Kitaygorodsky, LK Wasson, KM Chen, ...
Nature genetics 52 (8), 769-777, 2020
1052020
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
1022016
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
1012010
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