Personal information

Epigenetics
Canada, Netherlands

Activities

Employment (1)

University of British Columbia: Vancouver, British Columbia, CA

2020-03-02 to present | Postdoctoral Researcher (Medical Genetics)
Employment
Source: Self-asserted source
Sanne Janssen

Works (8)

BORIS/CTCFL‐mediated chromatin accessibility alterations promote a pro‐invasive transcriptional signature in melanoma cells

Pigment Cell & Melanoma Research
2023-05 | Journal article
Contributors: Roy Moscona; Sanne Marlijn Janssen; Mounib Elchebly; Andreas Ioannis Papadakis; Eitan Rubin; Alan Spatz
Source: check_circle
Crossref

BORIS/CTCFL-mediated chromatin accessibility alterations promote a pro-invasive transcriptional signature in melanoma cells

bioRxiv
2022-08-06 | Preprint
Contributors: Roy Moscona; Sanne Janssen; Mounib Elchebly; Andreas Ioannis Papadakis; Eitan Rubin; Alan Spatz
Source: Self-asserted source
Sanne Janssen

Interplay between chromatin marks in development and disease

Nature Reviews Genetics
2022-03 | Journal article
Contributors: Sanne M. Janssen; Matthew C. Lorincz
Source: check_circle
Crossref

Repression of germline genes by PRC1.6 and SETDB1 in the early embryo precedes DNA methylation-mediated silencing

Nature Communications
2021-12-02 | Journal article
Contributors: Kentaro Mochizuki; Jafar Sharif; Kenjiro Shirane; Kousuke Uranishi; Aaron B. Bogutz; Sanne M. Janssen; Ayumu Suzuki; Akihiko Okuda; Haruhiko Koseki; Matthew C. Lorincz
Source: check_circle
Crossref

Paternal MTHFR deficiency leads to hypomethylation of young retrotransposons and reproductive decline across two successive generations

Development
2021-07-15 | Journal article
Part of ISSN: 0950-1991
Part of ISSN: 1477-9129
Contributors: Gurbet Karahan; Donovan Chan; Kenjiro Shirane; Taylor McClatchie; Sanne Janssen; Jay M. Baltz; Matthew Lorincz; Jacquetta Trasler
Source: Self-asserted source
Sanne Janssen

BORIS/CTCFL promotes a switch from a proliferative towards an invasive phenotype in melanoma cells

Cell Death Discovery
2020-01-02 | Journal article
Contributors: Sanne Marlijn Janssen; Roy Moscona; Mounib Elchebly; Andreas Ioannis Papadakis; Margaret Redpath; Hangjun Wang; Eitan Rubin; Léon Cornelis van Kempen; Alan Spatz
Source: check_circle
Crossref

Reduced Euchromatin histone methyltransferase 1 causes developmental delay, hypotonia, and cranial abnormalities associated with increased bone gene expression in Kleefstra syndrome mice

Developmental Biology
2014-02 | Journal article
Part of ISSN: 0012-1606
Source: Self-asserted source
Sanne Janssen

Hippocampal dysfunction in the Euchromatin histone methyltransferase 1 heterozygous knockout mouse model for Kleefstra syndrome

Human Molecular Genetics
2013-03-01 | Journal article
Part of ISSN: 0964-6906
Part of ISSN: 1460-2083
Source: Self-asserted source
Sanne Janssen