Patients’ experiences with pre-test genetic counseling provided by breast cancer healthcare professionals: Results from a large prospective multicenter study von Bokkers, K., Bleiker, E.M.A., Velthuizen, M.E., Koelemij, R., Burgmans, J.P.J., Klinkenbijl, J.H., Schouten van der Velden, A.P., Vermulst, N., Huizinga, B.F., Witkamp, A.J., Frakking, T., Brohet, R.M., Aalfs, C.M., Koole, W., Schoenmaeckers, E.J.P., Ausems, M.G.E.M.

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Polygenic risk scores for genetic counseling in psychiatry: Lessons learned from other fields of medicine von Eeltink, E., van der Horst, M.Z., Zinkstok, J.R., Aalfs, C.M., Luykx, J.J.

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Atypical progeroid syndrome: An unknown helicase gene defect? von Ruijs, M.W.G., van Andel, R.N.J., Oshima, J., Madan, K., Nieuwint, A.W.M., Aalfs, C.M.

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Informing relatives about their hereditary or familial cancer risk: study protocol for a randomized controlled trial von de Geus, E.D, Aalfs, C.M, Verdam, M.G.E, de Haes, J.C.J.M, Smets, E.M.A

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A scoping review of practice recommendations for clinicians' communication of uncertainty von Medendorp, N.M., Stiggelbout, A.M., Aalfs, C.M., Han, P.K.J., Smets, E.M.A., Hillen, M.A.

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Genetic Counselling for Familial Conditions during Pregnancy: A Review of the Literature Published during the Years 1989–2004 von Aalfs, C.M., Smets, E.M.A., Leschot, N.J.

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Uncertainty in consultations about genetic testing for cancer: an explorative observational study von Medendorp, N.M., Hillen, M.A., Murugesu, L., Aalfs, C.M., Stiggelbout, A.M., Smets, E.M.A.

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Prophylactic total pancreatectomy in individuals at high risk of pancreatic ductal adenocarcinoma (PROPAN): systematic review and shared decision-making programme using decision ta... von Scholten, L., Latenstein, A.E.J., Aalfs, C.M., Bruno, M.J., Busch, O.R., Bonsing, B.A., Koerkamp, B.G., Molenaar, I.Q., Ubbink, D.T., Hooft, J.E. van, Fockens, P., Glas, J., DeVries, J.H., Besselink, M.G.

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'We don't know for sure': discussion of uncertainty concerning multigene panel testing during initial cancer genetic consultations von Medendorp, N.M., Hillen, M.A., Maarschalkerweerd, P.E.A. van, Aalfs, C.M., Ausems, M.G.E.M., Verhoef, S., Kolk, L.E. van der, Berger, L.P.V., Wevers, M.R., Wagner, A., Caanen, B.A.H., Stiggelbout, A.M., Smets, E.M.A.

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Reproductive decision-making in the context of hereditary cancer: the effects of an online decision aid on informed decision-making von Reumkens, K., Tummers, M.H.E., Severijns, Y., Gietel-Habets, J.J.G., Kuijk, S.M.J. van, Aalfs, C.M., Asperen, C.J. van, Ausems, M.G.E.M., Collee, M., Dommering, C.J., Kets, M., Kolk, L.E. van der, Oosterwijk, J.C., Tjan-Heijnen, V.C.G., Weijden, T. van der, Die-Smulders, C.E.M. de, Osch, L.A.D.M. van

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Role of germline aberrations affecting CTNNA1, MAP3K6 and MYD88 in gastric cancer susceptibility von Weren, R.D.A., Post, R.S. van der, Vogelaar, I.P., Krieken, J.H. van, Spruijt, L., Lubinski, J., Jakubowska, A., Teodorczyk, U., Aalfs, C.M., Hest, L.P. van, Oliveira, C., Kamping, E.J., Schackert, H.K., Ranzani, G.N., Garcia, E.B.G., Hes, F.J., Holinski-Feder, E., Genuardi, M., Ausems, M.G.E.M., Sijmons, R.H., Wagner, A., Kolk, L.E. van der, Cats, A., Bjornevoll, I., Hoogerbrugge, N., Ligtenberg, M.J.L.

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Colorectal cancer risk variants at 8q23.3 and 11q23.1 are associated with disease phenotype in APC mutation carriers von Ghorbanoghli, Z., Nieuwenhuis, M.H., Houwing-Duistermaat, J.J., Jagmohan-Changur, S., Hes, F.J., Tops, C.M., Wagner, A., Aalfs, C.M., Verhoef, S., Garcia, E.B.G., Sijmons, R.H., Menko, F.H., Letteboer, T.G., Hoogerbrugge, N., Wezel, T. van, Vasen, H.F.A., Wijnen, J.T.

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Unraveling genetic predisposition to familial or early onset gastric cancer using germline whole-exome sequencing von Vogelaar, I.P., Post, R.S. van der, Krieken, J.H.J.M. van, Spruijt, L., Zelst-Stams, W.A.G. van, Kets, C.M., Lubinski, J., Jakubowska, A., Teodorczyk, U., Aalfs, C.M., Hest, L.P. van, Pinheiro, H., Oliveira, C., Jhangiani, S.N., Muzny, D.M., Gibbs, R.A., Lupski, J.R., Ligt, J. de, Vissers, L.E.L.M., Hoischen, A., Gilissen, C., Vorst, M. van de, Goeman, J.J., Schackert, H.K., Ranzani, G.N., Molinaro, V., Garcia, E.B.G., Hes, F.J., Holinski-Feder, E., Genuardi, M., Ausems, M.G.E.M., Sijmons, R.H., Wagner, A., Kolk, L.E. van der, Bjornevoll, I., Hoberg-Vetti, H., Kessel, A.G. van, Kuiper, R.P., Ligtenberg, M.J.L., Hoogerbrugge, N.

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The Influence of number and timing of pregnancies on breast cancer risk for women with BRCA1 or BRCA2 mutations von Kast, K., Antoniou, A.C., Mooij, T.M., Engel, C., Buecher, B., Mari, V., Moretta-Serra, J., Luporsi, E., Barrowdale, D., Frost, D., Brewer, C., Evans, D.G., Cook, J., Izatt, L., Dommering, C.J., Ausems, M.G.E.M., Kriege, M., John, E.M., Friedlander, M., Jakubowska, A., Singer, C.F., Tan, Y., Olah, E., Navratilova, M., Foretova, L., Arver, B., Olsson, H., Schmutzler, R.K., Hopper, J.L., Leeuwen, F.E. van, Milne, R.L., Evans, G., Adlard, J., Eeles, R., Davidson, R., Tischkowitz, M., Snape, K., Porteous, M., Morrison, P., Eason, J., Rogers, M., Brady, A., Kennedy, M.J., Pottinger, C., Murray, A., Angelakos, M., Dite, G., Tsimiklis, H., Breysse, E., Pontois, P., Stoppa-Lyonnet, D., Gauthier-Villars, M., Caron, O., Fourme-Mouret, E., Lasset, C., Bonadona, V., Fert-Ferrer, S., Gilbert-Dussardier, B., Faivre, L., Sobol, H., Eisinger, F., Longy, M., Dugast, C., Coupier, I., Corsini, C., Vennin, P., Adenis, C., Nguyen, T.D., Penet, C., Delnatte, C., Tinat, J., Tennevet, I., Limacher, J.M., Dreyfus, H., Cohen-Haguenauer, O., Leroux, D., Zattara-Cannoni, H., Bera, O., Adank, M.A., Jenner, D.J., Collee, J.M., Ouweland, A.M.W. van den, Hooning, M.J., Seynaeve, C.M., Deurzen, C.H.M. van, Obdeijn, I.M., Asperen, C.J. van, Devilee, P., Kets, C.M., Koudijs, M.J., Aalfs, C.M., Engelen, K. van, Gille, J.J.P., Gomez-Garcia, E.B., Blok, M.J., Hout, A.H. van der, Mourits, M.J., Bock, G.H. de, Siesling, S., Verloop, J.

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Oral contraceptive use and breast cancer risk: retrospective and prospective analyses from a BRCA1 and BRCA2 mutation carrier cohort study von Schrijver, L.H., Olsson, H., Phillips, K.A., Terry, M.B., Goldgar, D.E., Kast, K., Engel, C., Mooij, T.M., Adlard, J., Barrowdale, D., Davidson, R., Eeles, R., Ellis, S., Evans, D.G., Frost, D., Izatt, L., Porteous, M.E., Side, L.E., Walker, L., Berthet, P., Bonadona, V.E., Leroux, D., Mouret-Fourme, E., Venat-Bouvet, L., Buys, S.S., Southey, M.C., John, E.M., Chung, W.K., Daly, M.B., Bane, A., Asperen, C.J. van, Garcia, E.B.G., Mourits, M.J.E., Roos-Blom, M.J., Friedlander, M.L., McLachlan, S.A., Singer, C.F., Foretova, L., Gerdes, A.M., Caldes, T., Olah, E., Jakubowska, A., Nogues, C., Andrieu, N., Easton, D.F., Leeuwen, F.E. van, Hopper, J.L., Milne, R.L., Antoniou, A.C., Rookus, M.A., Hogervorst, F.B.L., Adank, M.A., Schmidt, M.K., Russell, N.S., Lange, J.L. de, Wijnands, R., Jenner, D.J., Collee, J.M., Ouweland, A.M.W. van den, Hooning, M.J., Seynaeve, C., Deurzen, C.H.M. van, Obdeijn, I.M., Wijnen, J.T., Tollenaar, R.A.E.M., Devilee, P., Cronenburg, T.C.T.E.F. van, Kets, C.M., Mensenkamp, A.R., Ausems, M.G.E.M., Luijt, R.B. van der, Pol, C.C. van der, Aalfs, C.M., Meijers-Heijboer, H.E.J., Os, T.A.M. van, Engelen, K. van, Gille, J.J.P., Waisfisz, Q., Gomez-Garcia, E.B., Blok, M.J., Oosterwijk, J.C., Hout, A.H. van der, Mourits, M.J., Bock, G.H. de, Siesling, S., Verloop, J., Overbeek, L.I.H.

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BRCA2 hypomorphic missense variants confer moderate risks of breast cancer von Shimelis, H, Mesman, R.L.S, Von Nicolai, C, Ehlen, A, Guidugli, L, Calleja, F.M.G.R, Meeks, H, Hallberg, E, Hinton, J, Lilyquist, J, Hu, C, Aalfs, C.M, Aittomaki, K, Andrulis, I.L, Arndt, V, Beckmann, M.W, Benitez, J.J, Bogdanova, N, Bojesen, S.E, Borresen-Dale, A.L, Brauch, H, Brennan, P, Broeks, A, Brouwers, B, Bruning, T, Burwinkel, B, Chang-Claude, J, Chenevix-Trench, G, Choi, J.Y, Collée, J.M, Cross, S.S, Czene, K, Dennis, J, Dork, T, dos Santos Silva, I, Dunning, A.M, Fasching, P.A, Figueroa, J.D, Flyger, H, Garcia-Closas, M, Glendon, G, Guenel, P, Haiman, C.A, Hamann, U, Hartman, M, Hogervorst, F.B.L, Hollestelle, A, Hopper, J.L, Kang, D, Kosma, V.M, Kristensen, V, Lai, K.N, Li, J, Lindblom, A, Lophatananon, A, Lubinski, J, Machackova, E, Mannermaa, A, Matsuo, K, Miao, H, Michailidou, K, Muir, K, Neuhausen, S.L, Nevanlinna, H, Olson, J.E, Olswold, C, Oosterwijk, J.C, Osorio, A, Peto, J, Pylkäs, K, Rashid, M.U, Rhenius, V, Sangrajrang, S, Sawyer, E.J, Schmidt, M.K, Seynaeve, C.M, Shen, C.Y, Shu, X.O, Slager, S.L, Southey, M.C, Stram, D.O, Swerdlow, A.J, Teo, S.H, Truong, T, van Asperen, C.J, van der Kolk, L.E, Wang, Q, Wu, A.H, Yu, J.C, Zheng, W, Zheng, Y, Leary, J, Walker, L.C, Varesco, L, Moghadasi, S, Easton, D.F, Spurdle, A.B, Devilee, P, Vrieling, H, Couch, F.J

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Identification of a BRCA2-Specific Modifier Locus at 6p24 Related to Breast Cancer Risk von Gaudet, M.M, Klein, R.J, Kirchhoff, T, McGuffog, L, Dunning, A.M, Lee, A, Dennis, J, Healey, S, Dicks, E, Sinilnikova, O, Pankratz, V.S, Wang, X, Eldridge, R.C, Tessier, D.C, Bacot, F, Hogervorst, F.B.L, Peock, S, Stoppa-Lyonnet, D, Peterlongo, P, Schmutzler, R.K, Nathanson, K.L, Piedmonte, M, Singer, C.F, Hansen, T.V.O, Neuhausen, S.L, Garber, J, Weitzel, J.N, Andrulis, I.L, Goldgar, D.E, D'Andrea, E, Caldes, T, Nevanlinna, H, Osorio, A, van Rensburg, E.J, Arason, A, van den Ouweland, A.M.W, van der Hout, A.H, Kets, C.M, Wijnen, J.T, Ausems, M.G.E.M, Frost, D, Platte, R, Evans, D.G, Jacobs, C, Tischkowitz, M, Damiola, F, Golmard, L, Barjhoux, L, Belotti, M, Ferrer, S.F, Spurdle, A.B, Manoukian, S, Genuardi, M, Arnold, N, Sutter, C, Wappenschmidt, B, Pfeiler, G, Friedman, E, Jensen, U.B, Robson, M, Shah, S, Mai, P.L, Fasching, P.A, Peto, J, Humphreys, M.K, Michailidou, K, Sawyer, E.J, Burwinkel, B, Guenel, P, Milne, R.L, Brenner, H, Lochmann, M, Aittomaki, K, Doerk, T, Margolin, S, Mannermaa, A, Lambrechts, D, Chang-Claude, J, Radice, P, Giles, G.G, Winqvist, R, Garcia-Closas, M, Schoof, N, Hooning, M.J, Cox, A, Jakubowska, A, Orr, N, Pita, G, Rosario Alonso, M, Hall, P, Couch, F.J, Simard, J, Altshuler, D, Chenevix-Trench, G, Antoniou, A.C, Offit, K, HEBON, EMBRACE, Collaborators, GEMOS, Network, GENICA

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Breast Cancer Risk and 6q22.33: Combined Results from Breast Cancer Association Consortium and Consortium of Investigators on Modifiers of BRCA1/2 von Kirchhoff, T, Gaudet, M.M, Antoniou, A.C, Dunning, A.M, Flyger, H, Yoo, K-Y, Noh, D-Y, Ahn, S-H, Dork, T, Karstens, J.H, Hillemanns, P, Olson, J, Vachon, C, Wang, X, Elliott, G, Reed, M.W.R, Burwinkel, B, Brauch, H, Hamann, U, Ko, Y-D, Schmidt, M.K, Van 't Veer, L.J, Braaf, L.M, Fletcher, O, Peto, J, Turnbull, C, Seal, S, Renwick, A, Rahman, N, Yu, J-C, Hsiung, C-N, Southey, M.C, Hopper, J.L, Hammet, F, Van Dorpe, T, Hatse, S, Andrulis, I.L, Bogdanova, N, Rogov, J.I, Prokofieva, D, Khusnutdinova, E, van Asperen, C.J, Devilee, P, Margolin, S, Milne, R.L, Pilar Zamora, M, Benitez, J, Severi, G, Giles, G.G, Spurdle, A.B, Beesley, J, Holland, H, Healey, S, Wang-Gohrke, S, Mannermaa, A, Kosma, V-M, Kauppinen, J, Kataja, V, Agnarsson, B.A, Caligo, M.A, Godwin, A.K, Nevanlinna, H, Heikkinen, T, Lindor, N, Nathanson, K.L, Domchek, S.M, Loman, N, Karlsson, P, Askmalm, M.S, von Wachenfeldt, A, Verheus, M, Rookus, M.A, Oldenburg, R.A, Ligtenberg, M.J, Ausems, M.G.E.M, Aalfs, C.M, Garcia, E.B.G, Peock, S, Cook, M, Frost, D, Pichert, G, Davidson, R, Chu, C, Eccles, D, Ong, K-R, Douglas, F, Hodgson, S, Evans, D.G, Eeles, R, Pharoah, P.D.P, Offit, K, Chenevix-Trench, G, Easton, D.F, Network, GENICA, kConFab, Grp, AOCSS, SWE-BRCA, HEBON, EMBRACE, BCAC-CIMBA

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Atypical progeroid syndrome: An unknown helicase gene defect? von Ruijs, M.W.G., van Andel, R.N.J., Oshima, J., Madan, K., Nieuwint, A.W.M., Aalfs, C.M.

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Posterior tibial and sural nerve somatosensory evoked potentials: a study in spastic paraparesis and spinal cord lesions von Aalfs, C.M., Koelman, J.H.T.M., Meyjes, F.E.Posthumus, de Visser, B.W.Ongerboer

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