13(th) General Meeting of The Breast Cancer Linkage Consortium, November 29-December 1, 1999, Amsterdam, The Netherlands

por Devilee, Peter
Publicado 2000

Hypothesis: Why Different Types of SDH Gene Variants Cause Divergent Tumor Phenotypes

por Bayley, Jean-Pierre, Devilee, Peter
Publicado 2022

The SDH mutation database: an online resource for succinate dehydrogenase sequence variants involved in pheochromocytoma, paraganglioma and mitochondrial complex II deficiency

por Bayley, Jean-Pierre, Devilee, Peter, Taschner, Peter EM
Publicado 2005

Inhibition of succinate dehydrogenase dysregulates histone modification in mammalian cells

por Cervera, Ana M, Bayley, Jean-Pierre, Devilee, Peter, McCreath, Kenneth J
Publicado 2009

BRCA1 Mutation Analysis in a Portuguese Population with Early-Onset Breast and/or Ovarian Cancer

por Soares, Raquel, van Eijk, Ronald, Dias, Aureliano, Botelho, Mónica, Costa, Carla, Amendoeira, Isabel, Lopes, Carlos, Devilee, Peter, Schmitt, Fernando
Publicado 1999

BRCA2 Heterozygosity Delays Cytokinesis in Primary Human Fibroblasts

por Jonsdottir, Asta Björk, Vreeswijk, Maaike P. G., Wolterbeek, Ron, Devilee, Peter, Tanke, Hans J., Eyfjörd, Jorunn E., Szuhai, Karoly
Publicado 2009

Long-term in vitro 2D-culture of SDHB and SDHD-related human paragangliomas and pheochromocytomas

por Bayley, Jean-Pierre, Rebel, Heggert G., Scheurwater, Kimberly, Duesman, Dominique, Zhang, Juan, Schiavi, Francesca, Korpershoek, Esther, Jansen, Jeroen C., Schepers, Abbey, Devilee, Peter
Publicado 2022

Similar gene expression profiles of sporadic, PGL2-, and SDHD-linked paragangliomas suggest a common pathway to tumorigenesis

por Hensen, Erik F, Goeman, Jelle J, Oosting, Jan, Van der Mey, Andel GL, Hogendoorn, Pancras CW, Cremers, Cor WRJ, Devilee, Peter, Cornelisse, Cees J
Publicado 2009

Splicing analysis for exonic and intronic mismatch repair gene variants associated with Lynch syndrome confirms high concordance between minigene assays and patient RNA analyses

por van der Klift, Heleen M, Jansen, Anne M L, van der Steenstraten, Niki, Bik, Elsa C, Tops, Carli M J, Devilee, Peter, Wijnen, Juul T
Publicado 2015

Correction: Alternative mRNA splicing can attenuate the pathogenicity of presumed loss-of-function variants in BRCA2

por Mesman, Romy L. S., Calléja, Fabienne M. G. R., de la Hoya, Miguel, Devilee, Peter, van Asperen, Christi J., Vrieling, Harry, Vreeswijk, Maaike P. G.
Publicado 2020

Alternative mRNA splicing can attenuate the pathogenicity of presumed loss-of-function variants in BRCA2

por Mesman, Romy L. S., Calléja, Fabienne M. G. R., de la Hoya, Miguel, Devilee, Peter, van Asperen, Christi J., Vrieling, Harry, Vreeswijk, Maaike P. G.
Publicado 2020

Multi-gene panel testing and association analysis in Cypriot breast cancer cases and controls

por Zanti, Maria, Loizidou, Maria A., O’Mahony, Denise G., Dorling, Leila, Dennis, Joe, Devilee, Peter, Easton, Douglas F., Panayiotidis, Mihalis I., Hadjisavvas, Andreas, Michailidou, Kyriaki
Publicado 2023

Psychosocial problems in women attending French, German and Spanish genetics clinics before and after targeted or multigene testing results: an observational prospective study

por Brédart, Anne, Kop, Jean-Luc, Dick, Julia, Cano, Alejandra, De Pauw, Antoine, Anota, Amélie, Brunet, Joan, Devilee, Peter, Stoppa-Lyonnet, Dominique, Schmutzler, Rita, Dolbeault, Sylvie
Publicado 2019

Assessment of psychosocial difficulties by genetic clinicians and distress in women at high risk of breast cancer: a prospective study

por Brédart, Anne, Kop, Jean-Luc, Tüchler, Anja, De Pauw, Antoine, Cano, Alejandra, Dick, Julia, Rhiem, Kerstin, Devilee, Peter, Schmutzler, Rita, Stoppa-Lyonnet, Dominique, Dolbeault, Sylvie
Publicado 2022

The functional impact of variants of uncertain significance in BRCA2

por Mesman, Romy L. S., Calléja, Fabienne M. G. R., Hendriks, Giel, Morolli, Bruno, Misovic, Branislav, Devilee, Peter, van Asperen, Christi J., Vrieling, Harry, Vreeswijk, Maaike P. G.
Publicado 2018

Information needs on breast cancer genetic and non-genetic risk factors in relatives of women with a BRCA1/2 or PALB2 pathogenic variant

por Brédart, Anne, De Pauw, Antoine, Anota, Amélie, Tüchler, Anja, Dick, Julia, Müller, Anita, Kop, Jean-Luc, Rhiem, Kerstin, Schmutzler, Rita, Devilee, Peter, Stoppa-Lyonnet, Dominique, Dolbeault, Sylvie
Publicado 2021

Clustering of known low and moderate risk alleles rather than a novel recessive high‐risk gene in non‐BRCA1/2 sib trios affected with breast cancer

por Hilbers, Florentine S., van ‘t Hof, Peter J., Meijers, Caro M., Mei, Hailiang, Michailidou, Kyriaki, Dennis, Joe, Hogervorst, Frans B. L., Nederlof, Petra M., van Asperen, Christi J., Devilee, Peter
Publicado 2020

Exome Sequencing of Germline DNA from Non-BRCA1/2 Familial Breast Cancer Cases Selected on the Basis of aCGH Tumor Profiling

por Hilbers, Florentine S., Meijers, Caro M., Laros, Jeroen F. J., van Galen, Michiel, Hoogerbrugge, Nicoline, Vasen, Hans F. A., Nederlof, Petra M., Wijnen, Juul T., van Asperen, Christi J., Devilee, Peter
Publicado 2013

LncRNA LITATS1 suppresses TGF‐β‐induced EMT and cancer cell plasticity by potentiating TβRI degradation

por Fan, Chuannan, Wang, Qian, Kuipers, Thomas B, Cats, Davy, Iyengar, Prasanna Vasudevan, Hagenaars, Sophie C, Mesker, Wilma E, Devilee, Peter, Tollenaar, Rob A E M, Mei, Hailiang, ten Dijke, Peter
Publicado 2023

Sdhd and Sdhd/H19 Knockout Mice Do Not Develop Paraganglioma or Pheochromocytoma

por Bayley, Jean-Pierre, van Minderhout, Ivonne, Hogendoorn, Pancras C. W., Cornelisse, Cees J., van der Wal, Annemieke, Prins, Frans A., Teppema, Luc, Dahan, Albert, Devilee, Peter, Taschner, Peter E. M.
Publicado 2009