Motor impairment and its relationship to fitness in children

por Morris, Martyn, Dawes, Helen, Howells, Ken, Janssen, Roel
Publicado 2013

MutationalPatterns: comprehensive genome-wide analysis of mutational processes

por Blokzijl, Francis, Janssen, Roel, van Boxtel, Ruben, Cuppen, Edwin
Publicado 2018

Cystic Adventitial Disease of the (ilio) Femoral Artery with a Connection to the Hip Joint: Case Report and a Review of the Literature

por Frenken, Misha R.M., Arnoldussen, Carsten W.K.P., Janssen, Roel J.L.
Publicado 2022

Twenty Years of Ferroportin Disease: A Review or An Update of Published Clinical, Biochemical, Molecular, and Functional Features

por Vlasveld, L. Tom, Janssen, Roel, Bardou-Jacquet, Edouard, Venselaar, Hanka, Hamdi-Roze, Houda, Drakesmith, Hal, Swinkels, Dorine W.
Publicado 2019

GRIDSS2: comprehensive characterisation of somatic structural variation using single breakend variants and structural variant phasing

por Cameron, Daniel L., Baber, Jonathan, Shale, Charles, Valle-Inclan, Jose Espejo, Besselink, Nicolle, van Hoeck, Arne, Janssen, Roel, Cuppen, Edwin, Priestley, Peter, Papenfuss, Anthony T.
Publicado 2021

Scalable Workflows and Reproducible Data Analysis for Genomics

por Strozzi, Francesco, Janssen, Roel, Wurmus, Ricardo, Crusoe, Michael R., Githinji, George, Di Tommaso, Paolo, Belhachemi, Dominique, Möller, Steffen, Smant, Geert, de Ligt, Joep, Prins, Pjotr
Publicado 2019

The mutational impact of culturing human pluripotent and adult stem cells

por Kuijk, Ewart, Jager, Myrthe, van der Roest, Bastiaan, Locati, Mauro D., Van Hoeck, Arne, Korzelius, Jerome, Janssen, Roel, Besselink, Nicolle, Boymans, Sander, van Boxtel, Ruben, Cuppen, Edwin
Publicado 2020

Publisher Correction: The mutational impact of culturing human pluripotent and adult stem cells

por Kuijk, Ewart, Jager, Myrthe, van der Roest, Bastiaan, Locati, Mauro D., Van Hoeck, Arne, Korzelius, Jerome, Janssen, Roel, Besselink, Nicolle, Boymans, Sander, van Boxtel, Ruben, Cuppen, Edwin
Publicado 2020

5-Fluorouracil treatment induces characteristic T>G mutations in human cancer

por Christensen, Sharon, Van der Roest, Bastiaan, Besselink, Nicolle, Janssen, Roel, Boymans, Sander, Martens, John W. M., Yaspo, Marie-Laure, Priestley, Peter, Kuijk, Ewart, Cuppen, Edwin, Van Hoeck, Arne
Publicado 2019

Deficiency of nucleotide excision repair is associated with mutational signature observed in cancer

por Jager, Myrthe, Blokzijl, Francis, Kuijk, Ewart, Bertl, Johanna, Vougioukalaki, Maria, Janssen, Roel, Besselink, Nicolle, Boymans, Sander, de Ligt, Joep, Pedersen, Jakob Skou, Hoeijmakers, Jan, Pothof, Joris, van Boxtel, Ruben, Cuppen, Edwin
Publicado 2019

Prioritization of genes driving congenital phenotypes of patients with de novo genomic structural variants

por Middelkamp, Sjors, Vlaar, Judith M., Giltay, Jacques, Korzelius, Jerome, Besselink, Nicolle, Boymans, Sander, Janssen, Roel, de la Fonteijne, Lisanne, van Binsbergen, Ellen, van Roosmalen, Markus J., Hochstenbach, Ron, Giachino, Daniela, Talkowski, Michael E., Kloosterman, Wigard P., Cuppen, Edwin
Publicado 2019

Optimizing Nanopore sequencing-based detection of structural variants enables individualized circulating tumor DNA-based disease monitoring in cancer patients

por Valle-Inclan, Jose Espejo, Stangl, Christina, de Jong, Anouk C., van Dessel, Lisanne F., van Roosmalen, Markus J., Helmijr, Jean C. A., Renkens, Ivo, Janssen, Roel, de Blank, Sam, de Witte, Chris J., Martens, John W. M., Jansen, Maurice P. H. M., Lolkema, Martijn P., Kloosterman, Wigard P.
Publicado 2021

Precancerous liver diseases do not cause increased mutagenesis in liver stem cells

por Nguyen, Luan, Jager, Myrthe, Lieshout, Ruby, de Ruiter, Petra E., Locati, Mauro D., Besselink, Nicolle, van der Roest, Bastiaan, Janssen, Roel, Boymans, Sander, de Jonge, Jeroen, IJzermans, Jan N. M., Doukas, Michail, Verstegen, Monique M. A., van Boxtel, Ruben, van der Laan, Luc J. W., Cuppen, Edwin, Kuijk, Ewart
Publicado 2021