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Author/Creator Devilee, Peter

41. Splicing predictions, minigene analyses, and ACMG‐AMP clinical classification of 42 germline PALB2 splice‐site variants. Issue 3 (28th December 2021)

Authors:
Valenzuela‐Palomo, Alberto; Bueno‐Martínez, Elena; Sanoguera‐Miralles, Lara; Lorca, Víctor; Fraile‐Bethencourt, Eugenia; Esteban‐Sánchez, Ada; Gómez‐Barrero, Susana; Carvalho, Sara; Allen, Jamie; García‐Álvarez, Alicia; Pérez‐Segura, Pedro; Dorling, Leila; Easton, Douglas F; Devilee, Peter; Vrees...
Journal:
Journal of pathology
Issue:
Volume 256:Issue 3(2022)
Page Start:
321
Record Type:
Journal Article
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42. The "Psychosocial Aspects in Hereditary Cancer" questionnaire in women attending breast cancer genetic clinics: Psychometric validation across French‐, German‐ and Spanish‐language versions. (30th September 2019)

Authors:
Brédart, Anne; Anota, Amélie; Dick, Julia; Cano, Alejandra; De Pauw, Antoine; Kop, Jean‐Luc; Aaronson, Neil K.; Bleiker, Eveline M.; Brunet, Joan; Devilee, Peter; Stoppa‐Lyonnet, Dominique; Schmutzler, Rita; Dolbeault, Sylvie
Journal:
European journal of cancer care
Issue:
Volume 29:Number 1(2020)
Page Start:
n/a
Record Type:
Journal Article
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43. The BRCA1 c. 5096G>A p.Arg1699Gln (R1699Q) intermediate risk variant: breast and ovarian cancer risk estimation and recommendations for clinical management from the ENIGMA consortium. Issue 1 (10th May 2017)

Authors:
Moghadasi, Setareh; Meeks, Huong D; Vreeswijk, Maaike PG; Janssen, Linda AM; Borg, Åke; Ehrencrona, Hans; Paulsson-Karlsson, Ylva; Wappenschmidt, Barbara; Engel, Christoph; Gehrig, Andrea; Arnold, Norbert; Hansen, Thomas Van Overeem; Thomassen, Mads; Jensen, Uffe Birk; Kruse, Torben A; Ejlertsen,...
Journal:
Journal of medical genetics
Issue:
Volume 55:Issue 1(2018)
Page Start:
15
Record Type:
Journal Article
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44. The BRCA2 c.68‐7T > A variant is not pathogenic: A model for clinical calibration of spliceogenicity. Issue 5 (6th April 2018)

Authors:
Colombo, Mara; Lòpez‐Perolio, Irene; Meeks, Huong D.; Caleca, Laura; Parsons, Michael T.; Li, Hongyan; De Vecchi, Giovanna; Tudini, Emma; Foglia, Claudia; Mondini, Patrizia; Manoukian, Siranoush; Behar, Raquel; Garcia, Encarna B. Gómez; Meindl, Alfons; Montagna, Marco; Niederacher, Dieter; Schmid...
Journal:
Human mutation
Issue:
Volume 39:Issue 5(2018)
Page Start:
729
Record Type:
Journal Article
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45. Transcriptome‐wide association study of breast cancer risk by estrogen‐receptor status. Issue 5 (1st March 2020)

Authors:
Feng, Helian; Gusev, Alexander; Pasaniuc, Bogdan; Wu, Lang; Long, Jirong; Abu‐full, Zomoroda; Aittomäki, Kristiina; Andrulis, Irene L.; Anton‐Culver, Hoda; Antoniou, Antonis C.; Arason, Adalgeir; Arndt, Volker; Aronson, Kristan J.; Arun, Banu K.; Asseryanis, Ella; Auer, Paul L.; Azzollini, Jacopo...
Journal:
Genetic epidemiology
Issue:
Volume 44:Issue 5(2020)
Page Start:
442
Record Type:
Journal Article
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46. Variant type is associated with disease characteristics in SDHB, SDHC and SDHD-linked phaeochromocytoma–paraganglioma. Issue 2 (6th September 2019)

Authors:
Bayley, Jean Pierre; Bausch, Birke; Rijken, Johannes Adriaan; van Hulsteijn, Leonie Theresia; Jansen, Jeroen C; Ascher, David; Pires, Douglas Eduardo Valente; Hes, Frederik J; Hensen, Erik F; Corssmit, Eleonora P M; Devilee, Peter; Neumann, Hartmut P H
Journal:
Journal of medical genetics
Issue:
Volume 57:Issue 2(2020)
Page Start:
96
Record Type:
Journal Article
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