Author details

Full Name

Diane E Dickel

Affiliation

ORCID

Career Start Year

2006

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37425940	Combinatorial transcription factor binding encodes cis-regulatory wiring of forebrain GABAergic neurogenesis.	bioRxiv	2023
37968388	Single-cell, whole-embryo phenotyping of mammalian developmental disorders.	Nature	2023
37081156	Topologically associating domain boundaries are required for normal genome function.	Commun Biol	2023
37425964	Cell Type- and Tissue-specific Enhancers in Craniofacial Development.	bioRxiv	2023
34764456	Perfect and imperfect views of ultraconserved sequences.	Nat Rev Genet	2022
35649376	Differential Etv2 threshold requirement for endothelial and erythropoietic development.	Cell Rep	2022
35474001	Author Correction: Expanded encyclopaedias of DNA elements in the human and mouse genomes.	Nature	2022
34913122	Characterization of Mammalian In Vivo Enhancers Using Mouse Transgenesis and CRISPR Genome Editing.	Methods Mol Biol	2022
34385583	Plant single-cell solutions for energy and the environment.	Commun Biol	2021
33910599	Deletion of a non-canonical regulatory sequence causes loss of Scn1a expression and epileptic phenotypes in mice.	Genome Med	2021
33782603	Ultraconserved enhancer function does not require perfect sequence conservation.	Nat Genet	2021
34256850	Coding and noncoding variants in EBF3 are involved in HADDS and simplex autism.	Hum Genomics	2021
33398137	Author Correction: An atlas of dynamic chromatin landscapes in mouse fetal development.	Nature	2021
34921112	Transcriptional network orchestrating regional patterning of cortical progenitors.	Proc Natl Acad Sci U S A	2021
32728242	Spatiotemporal DNA methylome dynamics of the developing mouse fetus.	Nature	2020
32169219	Comprehensive InÂ Vivo Interrogation Reveals Phenotypic Impact of Human Enhancer Variants.	Cell	2020
32991838	Loss of Extreme Long-Range Enhancers in Human Neural Crest Drives a Craniofacial Disorder.	Cell Stem Cell	2020
32601476	Genomic analyses implicate noncoding de novo variants in congenital heart disease.	Nat Genet	2020
33037424	Author Correction: An atlas of dynamic chromatin landscapes in mouse fetal development.	Nature	2020
32737473	Supervised enhancer prediction with epigenetic pattern recognition and targeted validation.	Nat Methods	2020
32728249	Expanded encyclopaedias of DNA elements in the human and mouse genomes.	Nature	2020
32728245	The changing mouse embryo transcriptome at whole tissue and single-cell resolution.	Nature	2020
31217582	Noncoding deletions reveal a gene that is critical for intestinal function.	Nature	2019
31291572	Molecular Mechanisms Driving Switch Behavior in Xylem Cell Differentiation.	Cell Rep	2019
31091459	High-Throughput Single-Cell Transcriptome Profiling of Plant Cell Types.	Cell Rep	2019
31080136	Cardiac Reprogramming Factors Synergistically Activate Genome-wide Cardiogenic Stage-Specific Enhancers.	Cell Stem Cell	2019
31433982	Genomic Resolution of DLX-Orchestrated Transcriptional Circuits Driving Development of Forebrain GABAergic Neurons.	Cell Rep	2019
29497140	Author Correction: Single-nucleus analysis of accessible chromatin in developing mouse forebrain reveals cell-type-specific transcriptional regulation.	Nat Neurosci	2018
30503521	Parkinson-Associated SNCA Enhancer Variants Revealed by Open Chromatin in Mouse Dopamine Neurons.	Am J Hum Genet	2018
29358049	Ultraconserved Enhancers Are Required for Normal Development.	Cell	2018
29266543	Relationship between genetic variation at PPP1R3B and levels of liver glycogen and triglyceride.	Hepatology	2018
29434377	Single-nucleus analysis of accessible chromatin in developing mouse forebrain reveals cell-type-specific transcriptional regulation.	Nat Neurosci	2018
29420474	Enhancer redundancy provides phenotypic robustness in mammalian development.	Nature	2018
28193886	Improved regulatory element prediction based on tissue-specific local epigenomic signatures.	Proc Natl Acad Sci U S A	2017
28351867	Cooperative activation of cardiac transcription through myocardin bridging of paired MEF2 sites.	Development	2017
28671691	Germline Chd8 haploinsufficiency alters brain development in mouse.	Nat Neurosci	2017
28965761	Genomic Patterns of De Novo Mutation in Simplex Autism.	Cell	2017
28827824	Limb-Enhancer Genie: An accessible resource of accurate enhancer predictions in the developing limb.	PLoS Comput Biol	2017
27768887	Progressive Loss of Function in a Limb Enhancer during Snake Evolution.	Cell	2016
27220646	Fishing for Function in the Human Gene Pool.	Trends in Genetics	2016
27703156	Genome-wide compendium and functional assessment of in vivo heart enhancers.	Nat Commun	2016
27863237	The Ties That Bind: Mapping the Dynamic Enhancer-Promoter Interactome.	Cell	2016
24658141	Function-based identification of mammalian enhancers using site-specific integration.	Nat Methods	2014
23650633	Functional anatomy of distant-acting mammalian enhancers.	Philos Trans R Soc Lond B Biol Sci	2013
24244860	Single site-specific integration targeting coupled with embryonic stem cell differentiation provides a high-throughput alternative to in vivo enhancer analyses.	Biol Open	2013
21448237	Reduced transcript expression of genes affected by inherited and de novo CNVs in autism.	Eur J Hum Genet	2011
20154674	A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay.	Nat Genet	2010
19888295	Five novel loci for inherited hearing loss mapped by SNP-based homozygosity profiles in Palestinian families.	Eur J Hum Genet	2010
19855392	Microduplications of 16p11.2 are associated with schizophrenia.	Nat Genet	2009
17241828	Association studies of serotonin system candidate genes in early-onset obsessive-compulsive disorder.	Biological Psychiatry	2007