Author details

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Full Name

Charlotte N Henrichsen

Affiliation

ORCID

Career Start Year

2001

Papers

19

H Index

16

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
34025350	Environmental Enrichment Induces Epigenomic and Genome Organization Changes Relevant for Cognition.	Front Mol Neurosci	2021
31776259	Sleep-wake-driven and circadian contributions to daily rhythms in gene expression and chromatin accessibility in the murine cortex.	Proc Natl Acad Sci U S A	2019
30091978	A systems genetics resource and analysis of sleep regulation in the mouse.	PLoS Biol	2018
26188006	Missense mutations in TENM4, a regulator of axon guidance and central myelination, cause essential tremor.	Hum Mol Genet	2015
24381371	DQB1 locus alone explains most of the risk and protection in narcolepsy with cataplexy in Europe.	Sleep	2014
21304579	Using transcription modules to identify expression clusters perturbed in Williams-Beuren syndrome.	PLoS Comput Biol	2011
21084671	Copy number variation modifies expression time courses.	Genome Research	2011
21267068	A high-resolution anatomical atlas of the transcriptome in the mouse embryo.	PLoS Biol	2011
20425838	A t(7;12) balanced translocation with breakpoints overlapping those of the Williams-Beuren and 12q14 microdeletion syndromes.	American Journal of Medical Genetics, Part A	2010
19270705	Segmental copy number variation shapes tissue transcriptomes.	Nat Genet	2009
19390049	The genome sequence of taurine cattle: a window to ruminant biology and evolution.	Science	2009
19297395	Copy number variants, diseases and gene expression.	Human Molecular Genetics	2009
17571346	Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project.	Nature	2007
17913489	Side effects of genome structural changes.	Current Opinion in Genetics and Development	2007
17567994	Prominent use of distal 5' transcription start sites and discovery of a large number of additional exons in ENCODE regions.	Genome Res	2007
16826523	Submicroscopic deletion in patients with Williams-Beuren syndrome influences expression levels of the nonhemizygous flanking genes.	American Journal of Human Genetics	2006
15231743	Gene expression from the aneuploid chromosome in a trisomy mouse model of down syndrome.	Genome Research	2004
15211637	No association between DUP25 and anxiety disorders.	Am J Med Genet B Neuropsychiatr Genet	2004
11707072	From PREDs and open reading frames to cDNA isolation: revisiting the human chromosome 21 transcription map.	Genomics	2001

1 - 19 of 19

Alexandre Reymond

Co-authored papers 12

Stylianos E Antonarakis

Co-authored papers 8

Jacqueline Chrast

Co-authored papers 5

Co-authored papers 4

Co-authored papers 4

Sylvain Pradervand

Co-authored papers 3

Jennifer Harrow

Co-authored papers 3

Universitat de Barcelona (UB)

Co-authored papers 3

Barcelona Institute of Science and Technology

Co-authored papers 3

Philipp Kapranov

Co-authored papers 2

Caroline Manzano

Co-authored papers 2

Richard A Gibbs

Baylor College of Medicine

Co-authored papers 2

Co-authored papers 2

Stephan Ossowski

Institute of Medical Genetics and Applied Genomics, University of Tubingen

Co-authored papers 2

Ioannis Xenarios

University of Lausanne

Co-authored papers 2

Erica Sodergren

The Genome Institute at Washington University

Co-authored papers 2

Richard M Myers

HudsonAlpha Institute for Biotechnology

Co-authored papers 2

George M Weinstock

The Genome Center at Washington University, Washington University School of Medicine

Co-authored papers 2

Magee-Womens Research Institute, University of Pittsburgh

Co-authored papers 2

Co-authored papers 2

Co-authored papers 2

Co-authored papers 2

Thomas R Gingeras

Stanley Institute for Cognitive Genomics

Co-authored papers 2

Baylor College of Medicine

Co-authored papers 2

Universitat Pompeu Fabra (UPF)

Co-authored papers 2

Baylor College of Medicine

Co-authored papers 2

The Wellcome Trust Sanger Institute

Co-authored papers 2

Co-authored papers 2

Co-authored papers 2

Co-authored papers 2

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