Author details

Full Name

Christine M Disteche

Affiliation

ORCID

Career Start Year

1971

Papers

244

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37419111	Spatial and temporal organization of the genome: Current state and future aims of the 4D nucleome project.	Mol Cell	2023
37905060	Cross-species imputation and comparison of single-cell transcriptomic profiles.	bioRxiv	2023
37645756	KDM6A facilitates Xist upregulation at the onset of X inactivation.		2023
36711823	Oligonucleotide-directed proximity-interactome mapping (O-MAP): A unified method for discovering RNA-interacting proteins, transcripts and genomic loci .		2023
37205597	CTCF-mediated insulation and chromatin environment modulate <i>Car5b</i> escape from X inactivation.	bioRxiv	2023
37192167	Aneuploidy effects on human gene expression across three cell types.	Proc Natl Acad Sci U S A	2023
37066300	A single-cell transcriptional timelapse of mouse embryonic development, from gastrula to pup.	bioRxiv	2023
36609876	In Memory of George M. Martin.	J Gerontol A Biol Sci Med Sci	2023
35288709	Systematic reconstruction of cellular trajectories across mouse embryogenesis.	Nat Genet	2022
35871105	Sex-biased and parental allele-specific gene regulation by KDM6A.	Biology of Sex Differences	2022
34387327	X-factors in human disease: impact of gene content and dosage regulation.	Human Molecular Genetics	2021
33171144	X-chromosome regulation and sex differences in brain anatomy.	Neuroscience and Biobehavioral Reviews	2021
34579774	Single-cell landscape of nuclear configuration and gene expression during stem cell differentiation and X inactivation.	Genome Biol	2021
31536770	Sci-Hi-C: A single-cell Hi-C method for mapping 3D genome organization in large number of single cells.	Methods	2020
32496026	Sex chromosome aneuploidies in 2020-The state of care and research in the world.	American Journal of Medical Genetics, Part C: Seminars in Medical Genetics	2020
33954299	Unsupervised manifold alignment for single-cell multi-omics data.	ACM BCB	2020
33247132	Trans- and cis-acting effects of Firre on epigenetic features of the inactive X chromosome.	Nat Commun	2020
31294511	Expanding phenotype with severe midline brain anomalies and missense variant supports a causal role for FOXA2 in 20p11.2 deletion syndrome.	Am J Med Genet A	2019
31632970	X Inactivation and Escape: Epigenetic and Structural Features.	Frontiers in Cell and Developmental Biology	2019
31582850	Rapid transcriptional bursts upregulate the X chromosome.	Nature Structural and Molecular Biology	2019
31495564	High-Throughput Single-Cell Sequencing with Linear Amplification.	Mol Cell	2019
29654302	Orientation-dependent Dxz4 contacts shape the 3D structure of the inactive X chromosome.	Nat Commun	2018
30218369	X-Chromosome Inactivation and Escape from X Inactivation in Mouse.	Methods in Molecular Biology	2018
30275051	Sexual Inequality in the Cancer Cell.	Cancer Research	2018
30078704	A Single-Cell Atlas of InÂ Vivo Mammalian Chromatin Accessibility.	Cell	2018
29382556	Using DNase Hi-C techniques to map global and local three-dimensional genome architecture at high resolution.	Methods	2018
28135255	Massively multiplex single-cell Hi-C.	Nat Methods	2017
28947656	Structural aspects of the inactive X chromosome.	Philosophical Transactions of the Royal Society B: Biological Sciences	2017
28320934	Allele-specific non-CG DNA methylation marks domains of active chromatin in female mouse brain.	Proc Natl Acad Sci U S A	2017
27685100	Mapping 3D genome architecture through in situ DNase Hi-C.	Nat Protoc	2016
27112542	Dosage compensation of the sex chromosomes and autosomes.	Seminars in Cell and Developmental Biology	2016
27421841	Patient Mutations of the Intellectual Disability Gene KDM5C Downregulate Netrin G2 and Suppress Neurite Growth in Neuro2a Cells.	Journal of Molecular Neuroscience	2016
26690513	X-chromosome inactivation and escape.	Journal of Genetics	2015
25887447	The lncRNA Firre anchors the inactive X chromosome to the nucleolus by binding CTCF and maintains H3K27me3 methylation.	Genome Biol	2015
25785854	Escape from X inactivation varies in mouse tissues.	PLoS Genet	2015
25437436	Fine-scale chromatin interaction maps reveal the cis-regulatory landscape of human lincRNA genes.	Nat Methods	2015
26248554	Bipartite structure of the inactive mouse X chromosome.	Genome Biol	2015
26693509	Identification of genes escaping X inactivation by allelic expression analysis in a novel hybrid mouse model.	Data Brief	2015
24733023	X chromosome regulation: diverse patterns in development, tissues and disease.	Nature Reviews Genetics	2014
25409824	A comparative encyclopedia of DNA elements in the mouse genome.	Nature	2014
23658530	Female bias in Rhox6 and 9 regulation by the histone demethylase KDM6A.	PLoS Genetics	2013
24080727	How to correct chromosomal trisomy.	Cell Research	2013
23523075	Mammalian X upregulation is associated with enhanced transcription initiation, RNA half-life, and MOF-mediated H4K16 acetylation.	Dev Cell	2013
22532833	Loss of maternal CTCF is associated with peri-implantation lethality of Ctcf null embryos.	PLoS ONE	2012
22974302	Dosage compensation of the sex chromosomes.	Annual Review of Genetics	2012
22019781	Evidence for compensatory upregulation of expressed X-linked genes in mammals, Caenorhabditis elegans and Drosophila melanogaster.	Nat Genet	2011
21282478	Clcn4-2 genomic structure differs between the X locus in Mus spretus and the autosomal locus in Mus musculus: AT motif enrichment on the X.	Genome Res	2011
21614513	Genes that escape from X inactivation.	Human Genetics	2011
20186268	Genomic responses to abnormal gene dosage: the X chromosome improved on a common strategy.	PLoS Biology	2010
20937776	Genome-wide distribution of macroH2A1 histone variants in mouse liver chromatin.	Molecular and Cellular Biology	2010