Breast cancer risk in transgender people receiving hormone treatment: nationwide cohort study in the Netherlands
de Blok, Christel J M, Wiepjes, Chantal M, Nota, Nienke M, van Engelen, Klaartje, Adank, Muriel A, Dreijerink, Koen M A, Barbé, Ellis, Konings, Inge R H M, den Heijer, Martin
Published in BMJ (Online) (14.05.2019)
Published in BMJ (Online) (14.05.2019)
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CDC73-Related Disorders: Clinical Manifestations and Case Detection in Primary Hyperparathyroidism
van der Tuin, Karin, Tops, Carli M J, Adank, Muriel A, Cobben, Jan-Maarten, Hamdy, Neveen A T, Jongmans, Marjolijn C, Menko, Fred H, van Nesselrooij, Bernadette P M, Netea-Maier, Romana T, Oosterwijk, Jan C, Valk, Gerlof D, Wolffenbuttel, Bruce H R, Hes, Frederik J, Morreau, Hans
Published in The journal of clinical endocrinology and metabolism (01.12.2017)
Published in The journal of clinical endocrinology and metabolism (01.12.2017)
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The benefit of adding polygenic risk scores, lifestyle factors, and breast density to family history and genetic status for breast cancer risk and surveillance classification of unaffected women from germline CHEK2 c.1100delC families
Schreurs, Maartje A.C., Ramón y Cajal, Teresa, Adank, Muriel A., Collée, J. Margriet, Hollestelle, Antoinette, van Rooij, Jeroen, Schmidt, Marjanka K., Hooning, Maartje J.
Published in Breast (Edinburgh) (01.02.2024)
Published in Breast (Edinburgh) (01.02.2024)
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Cohort profile: a nationwide study in Dutch CHEK2 c.1100delC families using the infrastructure of the HEreditary Breast and Ovarian cancer study Netherlands – Hebon-CHEK2
Schreurs, Maartje A.C., Adank, Muriel A, Hollestelle, Antoinette, de Groot, Rosa, Stommel-Jenner, Denise J, Van Asperen, Christi J., Ausems, Margreet G.E.M., Berger, Lieke P V, Blok, Marinus J, van Engelen, Klaartje, Hogervorst, Frans B L, Geurts-Giele, Willemina, Gille, Johan J P, Wevers, Marijke R, Schmidt, Marjanka K, Hooning, Maartje J.
Published in BMJ open (09.10.2024)
Published in BMJ open (09.10.2024)
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Lack of large genomic deletions in BRIP1, PALB2, and FANCD2 genes in BRCA1/2 negative familial breast cancer
Ameziane, Najim, van den Ouweland, Ans M. W, Adank, Muriel A, Vijzelaar, Raymond N. C. P, Errami, Abdellatif, Dorsman, Josephine C, Joenje, Hans, Meijers-Heijboer, Hanne, Waisfisz, Quinten
Published in Breast cancer research and treatment (01.12.2009)
Published in Breast cancer research and treatment (01.12.2009)
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Cardiovascular disease risk after breast cancer treatment in patients with a BRCA1/2 pathogenic variant
Terra, Lara, Boekel, Naomi B, Hooning, Maartje H, Collee, Margriet, Schmidt, Marjanka K, Adank, Muriel A, Kok, Marleen, Aleman, Berthe M P, Jager, Agnes, Sattler, Margriet G A, Maas, Angela H E M, Schaapveld, Michael, van Leeuwen, Flora E
Published in Breast cancer research and treatment (31.10.2024)
Published in Breast cancer research and treatment (31.10.2024)
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Clinical applicability of the Polygenic Risk Score for breast cancer risk prediction in familial cases
Lakeman, Inge M M, Rodríguez-Girondo, Mar D M, Lee, Andrew, Celosse, Nandi, Braspenning, Merel E, van Engelen, Klaartje, van de Beek, Irma, van der Hout, Annemiek H, Gómez García, Encarna B, Mensenkamp, Arjen R, Ausems, Margreet G E M, Hooning, Maartje J, Adank, Muriel A, Hollestelle, Antoinette, Schmidt, Marjanka K, van Asperen, Christi J, Devilee, Peter
Published in Journal of medical genetics (01.04.2023)
Published in Journal of medical genetics (01.04.2023)
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Cancer risks by sex and variant type in PTEN hamartoma tumor syndrome
Hendricks, Linda A J, Hoogerbrugge, Nicoline, Mensenkamp, Arjen R, Brunet, Joan, Lleuger-Pujol, Roser, Høberg-Vetti, Hildegunn, Tveit Haavind, Marianne, Innella, Giovanni, Turchetti, Daniela, Aretz, Stefan, Spier, Isabel, Tischkowitz, Marc, Jahn, Arne, Links, Thera P, Olderode-Berends, Maran J W, Blatnik, Ana, Leter, Edward M, Evans, D Gareth, Woodward, Emma R, Steinke-Lange, Verena, Anastasiadou, Violetta C, Colas, Chrystelle, Villy, Marie-Charlotte, Benusiglio, Patrick R, Gerasimenko, Anna, Barili, Valeria, Branchaud, Maud, Houdayer, Claude, Tesi, Bianca, Yazicioglu, M Omer, van der Post, Rachel S, Schuurs-Hoeijmakers, Janneke H M, Vos, Janet R
Published in JNCI : Journal of the National Cancer Institute (10.01.2023)
Published in JNCI : Journal of the National Cancer Institute (10.01.2023)
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Erratum to ‘The benefit of adding polygenic risk scores, lifestyle factors, and breast density to family history and genetic status for breast cancer risk and surveillance classification of unaffected women from germline CHEK2 c.1100delC families’ [The Breast 73 (2024) 103611]
Schreurs, Maartje A.C., Ramón y Cajal, Teresa, Adank, Muriel A., Collée, J. Margriet, Hollestelle, Antoinette, van Rooij, Jeroen, Schmidt, Marjanka K., Hooning, Maartje J.
Published in Breast (Edinburgh) (01.06.2024)
Published in Breast (Edinburgh) (01.06.2024)
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Journal Article
The benefit of adding polygenic risk scores, lifestyle factors, and breast density to family history and genetic status for breast cancer risk and surveillance classification of unaffected women from germline CHEK2 c.1100delC families
Schreurs, Maartje A.C., Ramón y Cajal, Teresa, Adank, Muriel A., Collée, J. Margriet, Hollestelle, Antoinette, van Rooij, Jeroen, Schmidt, Marjanka K., Hooning, Maartje J.
Published in Breast (Edinburgh) (01.06.2024)
Published in Breast (Edinburgh) (01.06.2024)
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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
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, Bent, Gerdes, Anne-Marie, Pedersen, Inge Søkilde, Caputo, Sandrine M, Couch, Fergus, Hallberg, Emily J, van den Ouweland, Ans MW, Collée, Margriet J, Teugels, Erik, Adank, Muriel A, van der Luijt, Rob B, Mensenkamp, Arjen R, Oosterwijk, Jan C, Blok, Marinus J, Janin, Nicolas, Claes, Kathleen BM, Tucker, Kathy, Viassolo, Valeria, Toland, Amanda Ewart, Eccles, Diana E, Devilee, Peter, Van Asperen, Christie J, Spurdle, Amanda B, Goldgar, David E, García, Encarna Gómez
Published in Journal of medical genetics (01.01.2018)
Published in Journal of medical genetics (01.01.2018)
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Challenges in breast cancer genetic testing. A call for novel forms of multidisciplinary care and long-term evaluation
Menko, Fred H., Monkhorst, Kim, Hogervorst, Frans B.L., Rosenberg, Efraim H., Adank, Muriël, Ruijs, Mariëlle W.G., Bleiker, Eveline M.A., Sonke, Gabe S., Russell, Nicola S., Oldenburg, Hester S.A., van der Kolk, Lizet E.
Published in Critical reviews in oncology/hematology (01.08.2022)
Published in Critical reviews in oncology/hematology (01.08.2022)
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Breast cancer genomes from CHEK2 c.1100delC mutation carriers lack somatic TP53 mutations and display a unique structural variant size distribution profile
Smid, Marcel, Schmidt, Marjanka K, Prager-van der Smissen, Wendy J C, Ruigrok-Ritstier, Kirsten, Schreurs, Maartje A C, Cornelissen, Sten, Garcia, Aida Marsal, Broeks, Annegien, Timmermans, A Mieke, Trapman-Jansen, Anita M A C, Collée, J Margriet, Adank, Muriel A, Hooning, Maartje J, Martens, John W M, Hollestelle, Antoinette
Published in Breast cancer research : BCR (09.05.2023)
Published in Breast cancer research : BCR (09.05.2023)
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Effects of chemotherapy on contralateral breast cancer risk in BRCA1 and BRCA2 mutation carriers: A nationwide cohort study
Akdeniz, Delal, van Barele, Mark, Heemskerk-Gerritsen, Bernadette A.M., Steyerberg, Ewout W., Hauptmann, Michael, van de Beek, Irma, van Engelen, Klaartje, Wevers, Marijke R., Gómez García, Encarnacion B., Ausems, Margreet G.E.M., Berger, Lieke P.V., van Asperen, Christi J., Adank, Muriel A., Collée, Margriet J., Stommel-Jenner, Denise J., Jager, Agnes, Schmidt, Marjanka K., Hooning, Maartje J.
Published in Breast (Edinburgh) (01.02.2022)
Published in Breast (Edinburgh) (01.02.2022)
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Do BRCA1/2 mutation carriers have an earlier onset of natural menopause?
van Tilborg, Theodora C, Broekmans, Frank J, Pijpe, Anouk, Schrijver, Lieske H, Mooij, Thea M, Oosterwijk, Jan C, Verhoef, Senno, Gómez Garcia, Encarna B, van Zelst-Stams, Wendy A, Adank, Muriel A, van Asperen, Christi J, van Doorn, Helena C, van Os, Theo A, Bos, Anna M, Rookus, Matti A, Ausems, Margreet G
Published in Menopause (New York, N.Y.) (01.08.2016)
Published in Menopause (New York, N.Y.) (01.08.2016)
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CHEK21100delC homozygosity is associated with a high breast cancer risk in women
Adank, Muriel A, Jonker, Marianne A, Kluijt, Irma, van Mil, Saskia E, Oldenburg, Rogier A, Mooi, Wolter J, Hogervorst, Frans B L, van den Ouweland, Ans M W, Gille, Johan J P, Schmidt, Marjanka K, van der Vaart, Aad W, Meijers-Heijboer, Hanne, Waisfisz, Quinten
Published in Journal of medical genetics (01.12.2011)
Published in Journal of medical genetics (01.12.2011)
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Outcome of ovarian cancer after breast cancer in BRCA1 and BRCA2 mutation carriers
Zaaijer, Leendert H, van Doorn, Helena C, Mourits, Marian J E, van Beurden, Marc, de Hullu, Joanne A, Adank, Muriel A, van Lonkhuijzen, Luc R C W, Vasen, Hans F A, Slangen, Brigitte F M, Gaarenstroom, Katja N, Zweemer, Ronald P, Vencken, Peggy M L H, Seynaeve, Caroline, Kriege, Mieke
Published in British journal of cancer (08.11.2016)
Published in British journal of cancer (08.11.2016)
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Excess breast cancer risk in first degree relatives of CHEK2 ∗1100delC positive familial breast cancer cases
Adank, Muriel A, Verhoef, Senno, Oldenburg, Rogier A, Schmidt, Marjanka K, Hooning, Maartje J, Martens, John W.M, Broeks, Annegien, Rookus, Matti, Waisfisz, Quinten, Witte, Birgit I, Jonker, Marianne A, Meijers-Heijboer, Hanne
Published in European journal of cancer (1990) (01.05.2013)
Published in European journal of cancer (1990) (01.05.2013)
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Excess breast cancer risk in first degree relatives of CHEK21100delC positive familial breast cancer cases
ADANK, Muriel A, VERHOEF, Senno, JONKER, Marianne A, MEIJERS-HEIJBOER, Hanne, OLDENBURG, Rogier A, SCHMIDT, Marjanka K, HOONING, Maartje J, MARTENS, John W. M, BROEKS, Annegien, ROOKUS, Matti, WAISFISZ, Quinten, WITTE, Birgit I
Published in European journal of cancer (1990) (01.05.2013)
Published in European journal of cancer (1990) (01.05.2013)
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Evaluation of the association of heterozygous germline variants in NTHL1 with breast cancer predisposition: an international multi-center study of 47,180 subjects
Li, Na, Zethoven, Magnus, McInerny, Simone, Devereux, Lisa, Huang, Yu-Kuan, Thio, Niko, Cheasley, Dane, Gutiérrez-Enríquez, Sara, Moles-Fernández, Alejandro, Diez, Orland, Nguyen-Dumont, Tu, Southey, Melissa C., Hopper, John L., Simard, Jacques, Dumont, Martine, Soucy, Penny, Meindl, Alfons, Schmutzler, Rita, Schmidt, Marjanka K., Adank, Muriel A., Andrulis, Irene L., Hahnen, Eric, Engel, Christoph, Lesueur, Fabienne, Girard, Elodie, Neuhausen, Susan L., Ziv, Elad, Allen, Jamie, Easton, Douglas F., Scott, Rodney J., Gorringe, Kylie L., James, Paul A., Campbell, Ian G.
Published in NPJ breast cancer (12.05.2021)
Published in NPJ breast cancer (12.05.2021)
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