Publications by authors named "Sander Bollen"

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Association between a 46-SNP Polygenic Risk Score and melanoma risk in Dutch patients with familial melanoma.
Thomas P Potjer, Tara W J van der Grinten, Inge M M Lakeman, Sander H Bollen, Mar Rodríguez-Girondo

J Med Genet· November 2021

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Repurposing of Diagnostic Whole Exome Sequencing Data of 1,583 Individuals for Clinical Pharmacogenetics.
Maaike van der Lee, William G Allard, Sander Bollen, Gijs W E Santen, Claudia A L Ruivenkamp

Clin Pharmacol Ther· March 2020

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Multigene panel sequencing of established and candidate melanoma susceptibility genes in a large cohort of Dutch non-CDKN2A/CDK4 melanoma families.
Thomas P Potjer, Sander Bollen, Anneliese J E M Grimbergen, Remco van Doorn, Nelleke A Gruis

Int J Cancer· May 2019

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Origin and clinical relevance of chromosomal aberrations other than the common trisomies detected by genome-wide NIPS: results of the TRIDENT study.
Diane Van Opstal, Merel C van Maarle, Klaske Lichtenbelt, Marjan M Weiss, Heleen Schuring-Blom, Sander Bollen

Genet Med· April 2018

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CAFE: an R package for the detection of gross chromosomal abnormalities from gene expression microarray data.
Sander Bollen, Mathias Leddin, Miguel A Andrade-Navarro, Nancy Mah

Bioinformatics· May 2014

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CRISPR immunity relies on the consecutive binding and degradation of negatively supercoiled invader DNA by Cascade and Cas3.
Edze R Westra, Paul B G van Erp, Tim Künne, Shi Pey Wong, Raymond H J Staals, Sander Bollen

Mol Cell· June 2012

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