Sanne Janssen

456 total citations
9 papers, 282 citations indexed

About

Sanne Janssen is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Sanne Janssen has authored 9 papers receiving a total of 282 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 5 papers in Genetics and 2 papers in Cancer Research. Recurrent topics in Sanne Janssen's work include Epigenetics and DNA Methylation (7 papers), Genetic Syndromes and Imprinting (4 papers) and Cancer Genomics and Diagnostics (2 papers). Sanne Janssen is often cited by papers focused on Epigenetics and DNA Methylation (7 papers), Genetic Syndromes and Imprinting (4 papers) and Cancer Genomics and Diagnostics (2 papers). Sanne Janssen collaborates with scholars based in Canada, Netherlands and Israel. Sanne Janssen's co-authors include Matthew C. Lorincz, Tjitske Kleefstra, Kenjiro Shirane, Nael Nadif Kasri, Marco Benevento, Hans van Bokhoven, Kentaro Mochizuki, Aaron Bogutz, Haruhiko Koseki and Akihiko Okuda and has published in prestigious journals such as Nature Communications, Nature Reviews Genetics and Development.

In The Last Decade

Sanne Janssen

8 papers receiving 276 citations

Peers

Sanne Janssen

MB

GENET

CN

PPCH

CR

Michele Gabriele Italy

Ganka Douglas United States

Frédérique Sloan‐Béna Switzerland

Andrea K. Vaags Canada

Yukiko Kuroda Japan

Yiping Shen China

Irén Haltrich Hungary

Syed K. Rafi United States

Thomas Arbogast France

Alisdair McNeill United Kingdom

Michele Gabriele Italy

Sanne Janssen

482 ×2.2

MB

113 ×1.1

GENET

39 ×1.9

CN

9 ×0.5

PPCH

22 ×1.5

CR

Citations per year, relative to Sanne Janssen Sanne Janssen (= 1×) peers Michele Gabriele

Countries citing papers authored by Sanne Janssen

Since Specialization

Citations

This map shows the geographic impact of Sanne Janssen's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Sanne Janssen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Sanne Janssen more than expected).

Fields of papers citing papers by Sanne Janssen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Sanne Janssen. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Sanne Janssen. The network helps show where Sanne Janssen may publish in the future.

Co-authorship network of co-authors of Sanne Janssen

This figure shows the co-authorship network connecting the top 25 collaborators of Sanne Janssen. A scholar is included among the top collaborators of Sanne Janssen based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Sanne Janssen. Sanne Janssen is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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9 of 9 papers shown

1.

Gibson, William T., Sanne Janssen, B. Adair, et al.. (2025). Minimally Humanized Ezh2 Exon-18 Mouse Cell Lines Validate Preclinical CRISPR/Cas9 Approach to Treat Weaver Syndrome. Human Gene Therapy. 36(5-6). 618–627.

2.

Janssen, Sanne, et al.. (2023). BORIS / CTCFL ‐mediated chromatin accessibility alterations promote a pro‐invasive transcriptional signature in melanoma cells. Pigment Cell & Melanoma Research. 36(3-4). 299–313. 3 indexed citations

3.

Chan, Donovan, Kenjiro Shirane, Sanne Janssen, et al.. (2021). Paternal MTHFR deficiency leads to hypomethylation of young retrotransposons and reproductive decline across two successive generations. Development. 148(13). 15 indexed citations

4.

Mochizuki, Kentaro, Jafar Sharif, Kenjiro Shirane, et al.. (2021). Repression of germline genes by PRC1.6 and SETDB1 in the early embryo precedes DNA methylation-mediated silencing. Nature Communications. 12(1). 7020–7020. 39 indexed citations

5.

McCrum, Christopher, et al.. (2021). Sample size justifications in Gait & Posture. Gait & Posture. 92. 333–337. 13 indexed citations

6.

Janssen, Sanne & Matthew C. Lorincz. (2021). Interplay between chromatin marks in development and disease. Nature Reviews Genetics. 23(3). 137–153. 80 indexed citations

7.

Janssen, Sanne, Mounib Elchebly, Andreas I. Papadakis, et al.. (2020). BORIS/CTCFL promotes a switch from a proliferative towards an invasive phenotype in melanoma cells. Cell Death Discovery. 6(1). 1–1. 22 indexed citations

8.

Ansar, Muhammad, Astrid Oudakker, A. van Caam, et al.. (2013). Reduced Euchromatin histone methyltransferase 1 causes developmental delay, hypotonia, and cranial abnormalities associated with increased bone gene expression in Kleefstra syndrome mice. Developmental Biology. 386(2). 395–407. 55 indexed citations

9.

Kasri, Nael Nadif, Nurudeen O. Afinowi, Geert M. J. Ramakers, et al.. (2012). Hippocampal dysfunction in the Euchromatin histone methyltransferase 1 heterozygous knockout mouse model for Kleefstra syndrome. Human Molecular Genetics. 22(5). 852–866. 55 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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