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Hanne Meijers-Heijboer

PROF.DR., (Principal Investigator)

 https://orcid.org/0000-0003-1169-3853
1991 …2023

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  • 2012

    Reproductive behavior of individuals with increased risk of having a child with retinoblastoma

    Dommering, C. J., Garvelink, M. M., Moll, A. C., van Dijk, J., Imhof, S., Meijers-Heijboer, E. J. & Henneman, L., 2012, In: Clinical genetics. 81, 3, p. 216-223

    Research output: Contribution to journal › Article › Academic › peer-review

    21 Citations (Scopus)

  • Supporting the generalist genes hypothesis for intellectual ability/disability: the case of SNAP25

    Rizzi, T. S., Beunders, G., Rizzu, P., Sistermans, E. A., Twisk, J. W. R., van Mechelen, W., Deijen, J. B., Meijers-Heijboer, H., Verhage, M., Heutink, P. & Posthuma, D., 2012, In: Genes, Brain and Behavior. 11, 7, p. 767-771

    Research output: Contribution to journal › Article › Academic › peer-review

    7 Citations (Scopus)
  • 2013

    Analysis of the Novel Fanconi Anemia Gene SLX4/FANCP in Familial Breast Cancer Cases

    Bakker, J. L., van Mil, S. E., Crossan, G., Sabbaghian, N., de Leeneer, K., Poppe, B., Adank, M., Gille, H., Verheul, H., Meijers-Heijboer, H., de Winter, J. P., Claes, K., Tischkowitz, M., Waisfisz, Q. & Gille, J. J. P., 2013, In: Human mutation. 34, 1, p. 70-73

    Research output: Contribution to journal › Article › Academic › peer-review

    19 Citations (Scopus)

  • Excess breast cancer risk in first degree relatives of CHEK2*1100delC positive familial breast cancer cases

    Adank, M. A., Verhoef, S., Oldenburg, R. A., Schmidt, M. K., Hooning, M. J., Martens, J. W. M., Broeks, A., Rookus, M., Waisfisz, Q., Witte, B. I., Jonker, M. A. & Meijers-Heijboer, H., 2013, In: European Journal of Cancer. 49, 8, p. 1993-1999

    Research output: Contribution to journal › Article › Academic › peer-review

    20 Citations (Scopus)

  • Exonic Deletions in AUTS2 Cause a Syndromic Form of Intellectual Disability and Suggest a Critical Role for the C Terminus

    Beunders, G., Voorhoeve, E., Golzio, C., Pardo, L. M., Rosenfeld, J. A., Talkowski, M. E., Simonic, I., Lionel, A. C., Vergult, S., Pyatt, R. E., van de Kamp, J. M., Nieuwint, A. W. M., Weiss, M. M., Rizzu, P., Verwer, L. E. N. I., van Spaendonk, R. M. L., Shen, Y. P., Wu, B. L., Yu, T. T., Yu, Y. G., & 43 othersChiang, C., Gusella, J. F., Lindgren, A. M., Morton, C. C., van Binsbergen, E., Bulk, S., van Rossem, E., Vanakker, O., Armstrong, R., Park, S. M., Greenhalgh, L., Maye, U., Neill, N. J., Abbott, K. M., Sell, S., Ladda, R., Farber, D. M., Bader, P. I., Cushing, T., Drautz, J. M., Konczal, L., Nash, P., de Los Reyes, E., Carter, M. T., Hopkins, E., Marshall, C. R., Osborne, L. R., Gripp, K. W., Thrush, D. L., Hashimoto, S., Gastier-Foster, J. M., Astbury, C., Ylstra, B., Meijers-Heijboer, E. J., Posthuma, D., Menten, B., Mortier, G., Scherer, S. W., Eichler, E. E., Girirajan, S., Katsanis, N., Groffen, A. J. A. & Sistermans, E. A., 7 Feb 2013, In: American journal of human genetics. 92, 2, p. 210-220 11 p.

    Research output: Contribution to journal › Article › Academic › peer-review

    Open Access
    118 Citations (Scopus)

  • Genome-wide association studies identify four ER negative-specific breast cancer risk loci

    Garcia-Closas, M., Couch, F. J., Lindstrom, S., Michailidou, K., Schmidt, M. K., Brook, M. N., Orr, N., Rhie, S. K., Riboli, E., Feigelson, H. S., Le Marchand, L., Buring, J. E., Eccles, D., Miron, P., Fasching, P. A., Brauch, H., Chang-Claude, J., Carpenter, J., Godwin, A. K., Nevanlinna, H., & 252 othersGiles, G. G., Cox, A., Hopper, J. L., Bolla, M. K., Wang, Q., Dennis, J., Dicks, E., Howat, W. J., Schoof, N., Bojesen, S. E., Lambrechts, D., Broeks, A., Andrulis, I. L., Guénel, P., Burwinkel, B., Sawyer, E. J., Hollestelle, A., Fletcher, O., Winqvist, R., Brenner, H., Mannermaa, A., Hamann, U., Meindl, A., Lindblom, A., Zheng, W., Devillee, P., Goldberg, M. S., Lubinski, J., Kristensen, V., Swerdlow, A., Anton-Culver, H., Dörk, T., Muir, K., Matsuo, K., Wu, A. H., Radice, P., teo, S. H., Shu, X-O., Blot, W., Kang, D., Hartman, M., Sangrajrang, S., Shen, C-Y., Southey, M. C., Park, D. J., Hammet, F., Stone, J., Veer, L. J. V., Rutgers, E. J., Lophatananon, A., Stewart-Brown, S., Siriwanarangsan, P., Peto, J., Schrauder, M. G., Ekici, A. B., Beckmann, M. W., dos Santos Silva, I., Johnson, N., Warren, H., Tomlinson, I., Kerin, M. J., Miller, N., Marme, F., Schneeweiss, A., Sohn, C., Truong, T., Laurent-Puig, P., Kerbrat, P., Nordestgaard, B. G., Nielsen, S. F., Flyger, H., Milne, R. L., Perez, J. I. A., Menéndez, P., Müller, H., Arndt, V., Stegmaier, C., Lichtner, P., Lochmann, M., Justenhoven, C., Ko, Y-D., Muranen, T. A., Aittomäki, K., Blomqvist, C., Greco, D., Heikkinen, T., Ito, H., Iwata, H., Yatabe, Y., Antonenkova, N. N., Margolin, S., Kataja, V., Kosma, V-M., Hartikainen, J. M., Balleine, R., Tseng, C-C., Berg, D. V. D., Stram, D. O., Neven, P., Dieudonné, A-S., Leunen, K., Rudolph, A., Nickels, S., Flesch-Janys, D., Peterlongo, P., Peissel, B., Bernard, L., Olson, J. E., Wang, X., Stevens, K., Severi, G., Baglietto, L., McLean, C., Coetzee, G. A., Feng, Y., Henderson, B. E., Schumacher, F., Bogdanova, N. V., Labrèche, F., Dumont, M., Yip, C. H., Taib, N. A. M., Cheng, C-Y., Shrubsole, M., Long, J., Pylkäs, K., Jukkola-Vuorinen, A., Kauppila, S., Knight, J. A., Glendon, G., Mulligan, A. M., Tollenaar, R. A. E. M., Seynaeve, C. M., Kriege, M., Hooning, M. J., van den Ouweland, A. M. W., van Deurzen, C. H. M., Lu, W., Gao, Y-T., Cai, H., Balasubramanian, S. P., Cross, S. S., Reed, M. W. R., Signorello, L., Cai, Q., Shah, M., Miao, H., Chan, C. W., Chia, K. S., Jakubowska, A., Jaworska, K., Durda, K., Hsiung, C-N., Wu, P-E., Yu, J-C., Ashworth, A., Jones, M., Tessier, D. C., González-Neira, A., Pita, G., Alonso, M. R., Vincent, D., Bacot, F., Ambrosone, C. B., Bandera, E. V., John, E. M., Chen, G. K., Hu, J. J., Rodriguez-Gil, J. L., Bernstein, L., Press, M. F., Ziegler, R. G., Millikan, R. M., Deming-Halverson, S. L., Nyante, S., Ingles, S. A., Waisfisz, Q., Tsimiklis, H., Makalic, E., Schmidt, D., Bui, M., Gibson, L., Müller-Myhsok, B., Schmutzler, R. K., Hein, R., Dahmen, N., Beckmann, L., Aaltonen, K., Czene, K., Irwanto, A., Liu, J., Turnbull, C., Rahman, N., Meijers-Heijboer, H., Uitterlinden, A. G., Rivadeneira, F., Olswold, C., Slager, S., Pilarski, R., Ademuyiwa, F., Konstantopoulou, I., Martin, N. G., Montgomery, G. W., Slamon, D. J., Rauh, C., Lux, M. P., Jud, S. M., Bruning, T., Weaver, J., Sharma, P., Pathak, H., Tapper, W., Gerty, S., Durcan, L., Trichopoulos, D., Tumino, R., Peeters, P. H., Kaaks, R., Campa, D., Canzian, F., Weiderpass, E., Johansson, M., Khaw, K-T., Travis, R., Clavel-Chapelon, F., Kolonel, L. N., Chen, C., Beck, A., Hankinson, S. E., Berg, C. D., Hoover, R. N., Lissowska, J., Figueroa, J. D., Chasman, D. I., Gaudet, M. M., Diver, W. R., Willett, W. C., Hunter, D. J., Simard, J., Benitez, J., Dunning, A. M., Sherman, M. E., Chenevix-Trench, G., Chanock, S. J., Hall, P., Pharoah, P. D. P., Vachon, C., Easton, D. F., Haiman, C. A., Kraft, P., Michailidouo, K. & Tomlins, I., 2013, In: Nature Genetics. 45, 4, p. 392-8, 398e1-2

    Research output: Contribution to journal › Article › Academic › peer-review

    330 Citations (Scopus)

  • Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk

    Couch, F. J., Wang, X., McGuffog, L., Lee, A., Olswold, C., Kuchenbaecker, K. B., Soucy, P., Fredericksen, Z., Barrowdale, D., Dennis, J., Gaudet, M. M., Dicks, E., Kosel, M., Healey, S., Sinilnikova, O. M., Lee, A., Bacot, F., Vincent, D., Hogervorst, F. B. L., Peock, S., & 242 othersStoppa-Lyonnet, D., Jakubowska, A., Radice, P., Schmutzler, R. K., Domchek, S. M., Piedmonte, M., Singer, C. F., Friedman, E., Thomassen, M., Hansen, T. V. O., Neuhausen, S. L., Szabo, C. I., Blanco, I., Greene, M. H., Karlan, B. Y., Garber, J., Phelan, C. M., Weitzel, J. N., Montagna, M., Olah, E., Andrulis, I. L., Godwin, A. K., Yannoukakos, D., Goldgar, D. E., Caldes, T., Nevanlinna, H., Osorio, A., Terry, M. B., Daly, M. B., van Rensburg, E. J., Hamann, U., Ramus, S. J., Toland, A. E., Caligo, M. A., Olopade, O. I., Tung, N., Claes, K., Beattie, M. S., Southey, M. C., Imyanitov, E. N., Tischkowitz, M., Janavicius, R., John, E. M., Kwong, A., Diez, O., Balmaña, J., Barkardottir, R. B., Arun, B. K., Rennert, G., teo, S-H., Ganz, P. A., Campbell, I., van der Hout, A. H., van Deurzen, C. H. M., Seynaeve, C., Gómez Garcia, E. B., van Leeuwen, F. E., Meijers-Heijboer, H. E. J., Gille, J. J. P., Ausems, M. G. E. M., Blok, M. J., Ligtenberg, M. J. L., Rookus, M. A., Devilee, P., Verhoef, S., van Os, T. A. M., Wijnen, J. T., Frost, D., Ellis, S., Fineberg, E., Platte, R., Evans, D. G., Izatt, L., Eeles, R. A., Adlard, J., Eccles, D. M., Cook, J., Brewer, C., Douglas, F., Hodgson, S., Morrison, P. J., Side, L. E., Donaldson, A., Houghton, C., Rogers, M. T., Dorkins, H., Eason, J., Gregory, H., McCann, E., Murray, A., Calender, A., Hardouin, A., Berthet, P., Delnatte, C., Nogues, C., Lasset, C., Houdayer, C., Leroux, D., Rouleau, E., Prieur, F., Damiola, F., Sobol, H., Coupier, I., Venat-Bouvet, L., Castera, L., Gauthier-Villars, M., Léoné, M., Pujol, P., Mazoyer, S., Bignon, Y-J., Złowocka-Perłowska, E., Gronwald, J., Lubinski, J., Durda, K., Jaworska, K., Huzarski, T., Spurdle, A. B., Viel, A., Peissel, B., Bonanni, B., Melloni, G., Ottini, L., Papi, L., Varesco, L., Tibiletti, M. G., Peterlongo, P., Volorio, S., Manoukian, S., Pensotti, V., Arnold, N., Engel, C., Deissler, H., Gadzicki, D., Gehrig, A., Kast, K., Rhiem, K., Meindl, A., Niederacher, D., Ditsch, N., Plendl, H., Preisler-Adams, S., Engert, S., Sutter, C., Varon-Mateeva, R., Wappenschmidt, B., Weber, B. H. F., Arver, B., Stenmark-Askmalm, M., Loman, N., Rosenquist, R., Einbeigi, Z., Nathanson, K. L., Rebbeck, T. R., Blank, S. V., Cohn, D. E., Rodriguez, G. C., Small, L., Friedlander, M., Bae-Jump, V. L., Fink-Retter, A., Rappaport, C., Gschwantler-Kaulich, D., Pfeiler, G., tea, M-K., Lindor, N. M., Kaufman, B., Shimon Paluch, S., Laitman, Y., Skytte, A-B., Gerdes, A-M., Pedersen, I. S., Moeller, S. T., Kruse, T. A., Jensen, U. B., Vijai, J., Sarrel, K., Robson, M., Kauff, N., Mulligan, A. M., Glendon, G., Ozcelik, H., Ejlertsen, B., Nielsen, F. C., Jønson, L., Andersen, M. K., Ding, Y. C., Steele, L., Foretova, L., Teulé, A., Lazaro, C., Brunet, J., Pujana, M. A., Mai, P. L., Loud, J. T., Walsh, C., Lester, J., Orsulic, S., Narod, S. A., Herzog, J., Sand, S. R., Tognazzo, S., Agata, S., Vaszko, T., Weaver, J., Stavropoulou, A. V., Buys, S. S., Romero, A., de la Hoya, M., Aittomäki, K., Muranen, T. A., Duran, M., Chung, W. K., Lasa, A., Dorfling, C. M., Miron, A., Benitez, J., Senter, L., Huo, D., Chan, S. B., Sokolenko, A. P., Chiquette, J., Tihomirova, L., Friebel, T. M., Agnarsson, B. A., Lu, K. H., Lejbkowicz, F., James, P. A., Hall, P., Dunning, A. M., Tessier, D., Cunningham, J., Slager, S. L., Wang, C., Hart, S., Stevens, K., Simard, J., Pastinen, T., Pankratz, V. S., Offit, K., Easton, D. F., Chenevix-Trench, G. & Antoniou, A. C., 2013, In: PLoS genetics. 9, 3, p. e1003212 e1003212.

    Research output: Contribution to journal › Article › Academic › peer-review

    220 Citations (Scopus)

  • Identification of a BRCA2-Specific Modifier Locus at 6p24 Related to Breast Cancer Risk

    EMBRACE, HEBON, GENICA Network, GEMO Study, KConFab Investigators, Ontario Cancer Genetics Network, D'Andrea, E., Caldes, T., Nevanlinna, H., Osorio, A., van Rensburg, E. J., Arason, A., Rennert, G., van den Ouweland, A. M. W., van der Hout, A. H., Kets, C. M., Wijnen, J. T., Ausems, M. G. E. M., Frost, D., Ellis, S., & 74 othersFineberg, E., Platte, R., Evans, D. G., Jacobs, C., Adlard, J., Tischkowitz, M., Porteous, M. E., Damiola, F., Golmard, L., Barjhoux, L., Longy, M., Belotti, M., Ferrer, S. F., Mazoyer, S., Spurdle, A. B., Manoukian, S., Barile, M., Genuardi, M., Arnold, N., Meindl, A., Sutter, C., Wappenschmidt, B., Domchek, S. M., Pfeiler, G., Friedman, E., Jensen, U. B., Robson, M., Shah, S., Lazaro, C., Mai, P. L., Benitez, J., Southey, M. C., Schmidt, M. K., Fasching, P. A., Peto, J., Humphreys, M. K., Wang, Q., Michailidou, K., Sawyer, E. J., Burwinkel, B., Guénel, P., Bojesen, S. E., Milne, R. L., Brenner, H., Lochmann, M., Aittomäki, K., Dörk, T., Margolin, S., Mannermaa, A., Lambrechts, D., Chang-Claude, J., Radice, P., Giles, G. G., Haiman, C. A., Winqvist, R., Devillee, P., García-Closas, M., Schoof, N., Hooning, M. J., Cox, A., Pharoah, P. D. P., Jakubowska, A., Orr, N., González-Neira, A., Pita, G., Alonso, M. R., Hall, P., Couch, F. J., Simard, J., Altshuler, D., Easton, D. F., Chenevix-Trench, G., Antoniou, A. C. & Offit, K., 2013, In: PLoS genetics. 9, 3, p. e1003173 e1003173.

    Research output: Contribution to journal › Article › Academic › peer-review

    Open Access
    95 Citations (Scopus)

  • Large-scale genotyping identifies 41 new loci associated with breast cancer risk

    Michailidou, K., Hall, P., Gonzalez-Neira, A., Ghoussaini, M., Dennis, J., Milne, R. L., Schmidt, M. K., Chang-Claude, J., Bojesen, S. E., Bolla, M. K., Wang, Q., Dicks, E., Lee, A., Turnbull, C., Rahman, N., Fletcher, O., Peto, J., Gibson, L., dos Santos Silva, I., Nevanlinna, H., & 201 othersMuranen, T. A., Aittomäki, K., Blomqvist, C., Czene, K., Irwanto, A., Liu, J., Waisfisz, Q., Meijers-Heijboer, H., Adank, M., van der Luijt, R. B., Hein, R., Dahmen, N., Beckman, L., Meindl, A., Schmutzler, R. K., Müller-Myhsok, B., Lichtner, P., Hopper, J. L., Southey, M. C., Makalic, E., Schmidt, D. F., Uitterlinden, A. G., Hofman, A., Hunter, D. J., Chanock, S. J., Vincent, D., Bacot, F., Tessier, D. C., Canisius, S., Wessels, L. F. A., Haiman, C. A., Shah, M., Luben, R., Brown, J., Luccarini, C., Schoof, N., Humphreys, K., Li, J., Nordestgaard, B. G., Nielsen, S. F., Flyger, H., Couch, F. J., Wang, X., Vachon, C., Stevens, K. N., Lambrechts, D., Moisse, M., Paridaens, R., Christiaens, M-R., Rudolph, A., Nickels, S., Flesch-Janys, D., Johnson, N., Aitken, Z., Aaltonen, K., Heikkinen, T., Broeks, A., van 't Veer, L. J., van der Schoot, C. E., Guénel, P., Truong, T., Laurent-Puig, P., Menegaux, F., Marme, F., Schneeweiss, A., Sohn, C., Burwinkel, B., Zamora, M. P., Perez, J. I. A., Pita, G., Alonso, M. R., Cox, A., Brock, I. W., Cross, S. S., Reed, M. W. R., Sawyer, E. J., Tomlinson, I., Kerin, M. J., Miller, N., Henderson, B. E., Schumacher, F., Le Marchand, L., Andrulis, I. L., Knight, J. A., Glendon, G., Mulligan, A. M., Lindblom, A., Margolin, S., Hooning, M. J., Hollestelle, A., van den Ouweland, A. M. W., Jager, A., Bui, Q. M., Stone, J., Dite, G. S., Apicella, C., Tsimiklis, H., Giles, G. G., Severi, G., Baglietto, L., Fasching, P. A., Haeberle, L., Ekici, A. B., Beckmann, M. W., Brenner, H., Müller, H., Arndt, V., Stegmaier, C., Swerdlow, A., Ashworth, A., Orr, N., Jones, M., Figueroa, J., Lissowska, J., Brinton, L., Goldberg, M. S., Labrèche, F., Dumont, M., Winqvist, R., Pylkäs, K., Jukkola-Vuorinen, A., Grip, M., Brauch, H., Hamann, U., Brüning, T., Radice, P., Peterlongo, P., Manoukian, S., Bonanni, B., Devilee, P., Tollenaar, R. A. E. M., Seynaeve, C., van Asperen, C. J., Jakubowska, A., Lubinski, J., Jaworska, K., Durda, K., Mannermaa, A., Kataja, V., Kosma, V-M., Hartikainen, J. M., Bogdanova, N. V., Antonenkova, N. N., Dörk, T., Kristensen, V. N., Anton-Culver, H., Slager, S., Toland, A. E., Edge, S., Fostira, F., Kang, D., Yoo, K-Y., Noh, D-Y., Matsuo, K., Ito, H., Iwata, H., Sueta, A., Wu, A. H., Tseng, C-C., van den Berg, D., Stram, D. O., Shu, X-O., Lu, W., Gao, Y-T., Cai, H., teo, S. H., Yip, C. H., Phuah, S. Y., Cornes, B. K., Hartman, M., Miao, H., Lim, W. Y., Sng, J-H., Muir, K., Lophatananon, A., Stewart-Brown, S., Siriwanarangsan, P., Shen, C-Y., Hsiung, C-N., Wu, P-E., Ding, S-L., Sangrajrang, S., Gaborieau, V., Brennan, P., McKay, J., Blot, W. J., Signorello, L. B., Cai, Q., Zheng, W., Deming-Halverson, S., Shrubsole, M., Long, J., Simard, J., Garcia-Closas, M., Pharoah, P. D. P., Chenevix-Trench, G., Dunning, A. M., Benitez, J., Easton, D. F., Aittomaki, K. & Burwinke, B., 2013, In: Nature Genetics. 45, 4, p. 353-61, 361e1-2

    Research output: Contribution to journal › Article › Academic › peer-review

    873 Citations (Scopus)

  • Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer

    Bojesen, S. E., Pooley, K. A., Johnatty, S. E., Beesley, J., Michailidou, K., Tyrer, J. P., Edwards, S. L., Pickett, H. A., Shen, H. C., Smart, C. E., Hillman, K. M., Mai, P. L., Lawrenson, K., Stutz, M. D., Lu, Y., Karevan, R., Woods, N., Johnston, R. L., French, J. D., Chen, X., & 419 othersWeischer, M., Nielsen, S. F., Maranian, M. J., Ghoussaini, M., Ahmed, S., Baynes, C., Bolla, M. K., Wang, Q., Dennis, J., McGuffog, L., Barrowdale, D., Lee, A., Healey, S., Lush, M., Tessier, D. C., Vincent, D., Bacot, F., Vergote, I., Lambrechts, S., Despierre, E., Risch, H. A., González-Neira, A., Rossing, M. A., Pita, G., Doherty, J. A., Alvarez, N., Larson, M. C., Fridley, B. L., Schoof, N., Chang-Claude, J., Cicek, M. S., Peto, J., Kalli, K. R., Broeks, A., Armasu, S. M., Schmidt, M. K., Braaf, L. M., Winterhoff, B., Nevanlinna, H., Konecny, G. E., Lambrechts, D., Rogmann, L., Guénel, P., Teoman, A., Milne, R. L., Garcia, J. J., Cox, A., Shridhar, V., Burwinkel, B., Marme, F., Hein, R., Sawyer, E. J., Haiman, C. A., Wang-Gohrke, S., Andrulis, I. L., Moysich, K. B., Hopper, J. L., Odunsi, K., Lindblom, A., Giles, G. G., Brenner, H., Simard, J., Lurie, G., Fasching, P. A., Carney, M. E., Radice, P., Wilkens, L. R., Swerdlow, A., Goodman, M. T., Brauch, H., Garcia-Closas, M., Hillemanns, P., Winqvist, R., Dürst, M., Devilee, P., Runnebaum, I., Jakubowska, A., Lubinski, J., Mannermaa, A., Butzow, R., Bogdanova, N. V., Dörk, T., Pelttari, L. M., Zheng, W., Leminen, A., Anton-Culver, H., Bunker, C. H., Kristensen, V., Ness, R. B., Muir, K., Edwards, R., Meindl, A., Heitz, F., Matsuo, K., du Bois, A., Wu, A. H., Harter, P., teo, S-H., Schwaab, I., Shu, X-O., Blot, W., Hosono, S., Kang, D., Nakanishi, T., Hartman, M., Yatabe, Y., Hamann, U., Karlan, B. Y., Sangrajrang, S., Kjaer, S. K., Gaborieau, V., Jensen, A., Eccles, D., Høgdall, E., Shen, C-Y., Brown, J., Woo, Y. L., Shah, M., Azmi, M. A. N., Luben, R., Omar, S. Z., Czene, K., Vierkant, R. A., Nordestgaard, B. G., Flyger, H., Vachon, C., Olson, J. E., Wang, X., Levine, D. A., Rudolph, A., Weber, R. P., Flesch-Janys, D., Iversen, E., Nickels, S., Schildkraut, J. M., Silva, I. D. S., Cramer, D. W., Gibson, L., Terry, K. L., Fletcher, O., Vitonis, A. F., van der Schoot, C. E., Poole, E. M., Hogervorst, F. B. L., Tworoger, S. S., Liu, J., Bandera, E. V., Li, J., Olson, S. H., Humphreys, K., Orlow, I., Blomqvist, C., Rodriguez-Rodriguez, L., Aittomäki, K., Salvesen, H. B., Muranen, T. A., Wik, E., Brouwers, B., Krakstad, C., Wauters, E., Halle, M. K., Wildiers, H., Kiemeney, L. A., Mulot, C., Aben, K. K., Laurent-Puig, P., Altena, A. M., Truong, T., Massuger, L. F. A. G., Benitez, J., Pejovic, T., Perez, J. I. A., Hoatlin, M., Zamora, M. P., Cook, L. S., Balasubramanian, S. P., Kelemen, L. E., Schneeweiss, A., Le, N. D., Sohn, C., Brooks-Wilson, A., Tomlinson, I., Kerin, M. J., Miller, N., Cybulski, C., Henderson, B. 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E., Caldes, T., Imyanitov, E. N., Tihomirova, L., Arun, B. K., Campbell, I., Mensenkamp, A. R., van Asperen, C. J., van Roozendaal, K. E. P., Meijers-Heijboer, H., Collée, J. M., Oosterwijk, J. C., Hooning, M. J., Rookus, M. A., van der Luijt, R. B., Os, T. A. M., Evans, D. G., Frost, D., Fineberg, E., Barwell, J., Walker, L., Kennedy, M. J., Platte, R., Davidson, R., Ellis, S. D., Cole, T., Bressac-de Paillerets, B., Buecher, B., Damiola, F., Faivre, L., Frenay, M., Sinilnikova, O. M., Caron, O., Giraud, S., Mazoyer, S., Bonadona, V., Caux-Moncoutier, V., Toloczko-Grabarek, A., Gronwald, J., Byrski, T., Spurdle, A. B., Bonanni, B., Zaffaroni, D., Giannini, G., Bernard, L., Dolcetti, R., Manoukian, S., Arnold, N., Engel, C., Deissler, H., Rhiem, K., Niederacher, D., Plendl, H., Sutter, C., Wappenschmidt, B., Borg, A., Melin, B., Rantala, J., Soller, M., Nathanson, K. L., Domchek, S. M., Rodriguez, G. C., Salani, R., Kaulich, D. G., tea, M-K., Paluch, S. S., Laitman, Y., Skytte, A-B., Kruse, T. A., Jensen, U. B., Robson, M., Gerdes, A-M., Ejlertsen, B., Foretova, L., Savage, S. A., Lester, J., Soucy, P., Kuchenbaecker, K. B., Olswold, C., Cunningham, J. M., Slager, S., Pankratz, V. S., Dicks, E., Lakhani, S. R., Couch, F. J., Hall, P., Monteiro, A. N. A., Gayther, S. A., Pharoah, P. D. P., Reddel, R. R., Goode, E. L., Greene, M. H., Easton, D. F., Berchuck, A., Antoniou, A. C., Chenevix-Trench, G., Dunning, A. M., Johnstonw, R. L. & Gonzaalez-Neira, A., 2013, In: Nature Genetics. 45, 4, p. 371-84, 384e1-2

    Research output: Contribution to journal › Article › Academic › peer-review

    457 Citations (Scopus)

  • Novel strategies towards the use of anti-angiogenic agents in breast cancer

    Bakker, J. L., Meijers-Heijboer, H. & Verheul, H., 2013, In: European journal of pharmacology. 717, 1-3, p. 36-39

    Research output: Contribution to journal › Article › Academic › peer-review

    5 Citations (Scopus)

  • Phenotype and genotype in 101 males with X-linked creatine transporter deficiency

    van de Kamp, J. M., Betsalel, O. T., Mercimek-Mahmutoglu, S., Abulhoul, L., Grunewald, S., Anselm, I., Azzouz, H., Bratkovic, D., de Brouwer, A., Hamel, B., Kleefstra, T., Yntema, H., Campistol, J., Vilaseca, M. A., Cheillan, D., D'Hooghe, M., Diogo, L., Garcia, P., Valongo, C., Fonseca, M., & 40 othersFrints, S., Wilcken, B., Haar, S., Meijers-Heijboer, H. E., Hofstede, F., Johnson, D., Kant, S. G., Lion-Francois, L., Pitelet, G., Longo, N., Maat-Kievit, J. A., Monteiro, J. P., Munnich, A., Muntau, A. C., Nassogne, M. C., Osaka, H., Ounap, K., Pinard, J. M., Quijano-Roy, S., Poggenburg, I., Poplawski, N., Abdul-Rahman, O. A., Ribes, A., Arias, A., Yaplito-Lee, J., Schulze, A., Schwartz, C. E., Schwenger, S., Soares, G., Sznajer, Y., Valayannopoulos, V., Van Esch, H., Waltz, S., Wamelink, M. M. C., Pouwels, P. J. W., Errami, A., van der Knaap, M. S., Jakobs, C. A. J. M., Mancini, G. M. & Salomons, G. S., 2013, In: Journal of medical genetics. 50, 7, p. 463-472

    Research output: Contribution to journal › Article › Academic › peer-review

    108 Citations (Scopus)

  • PLS3 mutations in X-linked osteoporosis with fractures

    van Dijk, F. S., Zillikens, M. C., Micha, D., Riessland, M., Marcelis, C. L. M., de Die-Smulders, C. E., Milbradt, J., Franken, A. A., Harsevoort, A. J., Lichtenbelt, K. D., Pruijs, H. E., Rubio-Gozalbo, M. E., Zwertbroek, R., Moutaouakil, Y., Egthuijsen, J., Hammerschmidt, M., Bijman, R., Semeins, C. M., Bakker, A. D., Everts, V., & 13 othersKlein-Nulend, J., Campos-Obando, N., Hofman, A., te Meerman, G. J., Verkerk, A. J. M. H., Uitterlinden, A. G., Maugeri, A., Sistermans, E. A., Waisfisz, Q., Meijers-Heijboer, H., Wirth, B., Simon, M. E. H. & Pals, G., 2013, In: The New England journal of medicine. 369, 16, p. 1529-1536

    Research output: Contribution to journal › Article › Academic › peer-review

    161 Citations (Scopus)

  • Whole-genome sequencing in health care: recommendations of the European Society of Human Genetics

    van El, C. G., Cornel, M. C., Borry, P., Hastings, R. J., Fellmann, F., Hodgson, S. V., Howard, H. C., Cambon-Thomsen, A., Knoppers, B. M., Meijers-Heijboer, H., Scheffer, H., Tranebjaerg, L., Dondorp, W., de Wert, G. M. W. R. & Hodgson, SV., 2013, In: European journal of human genetics. 21, 6, p. 580-584

    Research output: Contribution to journal › Article › Academic › peer-review

    359 Citations (Scopus)
  • 2014

    A genome-wide association study of early-onset breast cancer identifies PFKM as a novel breast cancer gene and supports a common genetic spectrum for breast cancer at any age

    Ahsan, H., Halpern, J., Kibriya, M. G., Pierce, B. L., Tong, L., Gamazon, E., McGuire, V., Felberg, A., Shi, J., Jasmine, F., Roy, S., Brutus, R., Argos, M., Melkonian, S., Chang-Claude, J., Andrulis, I., Hopper, J. L., John, E. M., Malone, K., Ursin, G., & 57 othersGammon, M. D., Thomas, D. C., Seminara, D., Casey, G., Knight, J. A., Southey, M. C., Giles, G. G., Santella, R. M., Lee, E., Conti, D., Duggan, D., Gallinger, S., Haile, R., Jenkins, M., Lindor, N. M., Newcomb, P., Michailidou, K., Apicella, C., Park, D. J., Peto, J., Fletcher, O., dos Santos Silva, I., Lathrop, M., Hunter, D. J., Chanock, S. J., Meindl, A., Schmutzler, R. K., Müller-Myhsok, B., Lochmann, M., Beckmann, L., Hein, R., Makalic, E., Schmidt, D. F., Bui, Q. M., Stone, J., Flesch-Janys, D., Dahmen, N., Nevanlinna, H., Aittomäki, K., Blomqvist, C., Hall, P., Czene, K., Irwanto, A., Liu, J., Rahman, N., Turnbull, C., Dunning, A. M., Pharoah, P., Waisfisz, Q., Meijers-Heijboer, H., Uitterlinden, A. G., Rivadeneira, F., Nicolae, D., Easton, D. F., Cox, N. J., Whittemore, A. S. & Aittomaki, K., 2014, In: Cancer epidemiology, biomarkers & prevention. 23, 4, p. 658-669

    Research output: Contribution to journal › Article › Academic › peer-review

    77 Citations (Scopus)

  • A Novel Splice Site Mutation in the Noncoding Region of BRCA2: Implications for Fanconi Anemia and Familial Breast Cancer Diagnostics

    Bakker, J. L., Thirthagiri, E., van Mil, S. E., Adank, M. A., Ikeda, H., Verheul, H. M. W., Meijers-Heijboer, H., de Winter, J. P., Sharan, S. K. & Waisfisz, Q., 2014, In: Human mutation. 35, 4, p. 442-446

    Research output: Contribution to journal › Article › Academic › peer-review

    9 Citations (Scopus)

  • Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers

    AUTHOR GROUP, 2014, In: Breast Cancer Research. 16, 6, p. 3416

    Research output: Contribution to journal › Article › Academic › peer-review

    43 Citations (Scopus)

  • Breast and ovarian cancer risks in a large series of clinically ascertained families with a high proportion of BRCA1 and BRCA2 Dutch founder mutations

    AUTHOR GROUP, 2014, In: Journal of medical genetics. 51, 2, p. 98-107

    Research output: Contribution to journal › Article › Academic › peer-review

    66 Citations (Scopus)

  • Coregulation of FANCA and BRCA1 in human cells

    Haitjema, A., Mol, B. M., Kooi, E. I., Massink, M. P. G., Jorgensen, J. A. L., Rockx, D. A. P., Rooimans, M. A., de Winter, J. P., Meijers-Heijboer, H., Joenje, H. & Dorsman, J. C., 2014, In: SpringerPlus. 3, 381.

    Research output: Contribution to journal › Article › Academic › peer-review

    5 Citations (Scopus)

  • DNA glycosylases involved in base excision repair may be associated with cancer risk in BRCA1 and BRCA2 mutation carriers

    Osorio, A., Milne, R. L., Kuchenbaecker, K., Vaclova, T., Pita, G., Alonso, R., Peterlongo, P., Blanco, I., de la Hoya, M., Duran, M., Diez, O., Ramon y Cajal, T., Konstantopoulou, I., Martinez-Bouzas, C., Andres Conejero, R., Soucy, P., McGuffog, L., Barrowdale, D., Lee, A., Swe-Brca, N. N., & 180 othersArver, B., Rantala, J., Loman, N., Ehrencrona, H., Olopade, O. I., Beattie, M. S., Domchek, S. M., Nathanson, K., Rebbeck, T. R., Arun, B. K., Karlan, B. Y., Walsh, C., Lester, J., John, E. M., Whittemore, A. S., Daly, M. B., Southey, M., Hopper, J., Terry, M. B., Buys, S. S., Janavicius, R., Dorfling, C. M., van Rensburg, E. J., Steele, L., Neuhausen, S. L., Ding, Y. C., Hansen, T. V. O., Jonson, L., Ejlertsen, B., Gerdes, A-M., Infante, M., Herraez, B., Moreno, L. T., Weitzel, J. N., Herzog, J., Weeman, K., Manoukian, S., Peissel, B., Zaffaroni, D., Scuvera, G., Bonanni, B., Mariette, F., Volorio, S., Viel, A., Varesco, L., Papi, L., Ottini, L., Tibiletti, M. G., Radice, P., Yannoukakos, D., Garber, J., Ellis, S., Frost, D., Platte, R., Fineberg, E., Evans, G., Lalloo, F., Izatt, L., Eeles, R., Adlard, J., Davidson, R., Cole, T., Eccles, D., Cook, J., Hodgson, S., Brewer, C., Tischkowitz, M., Douglas, F., Porteous, M., Side, L., Walker, L., Morrison, P., Donaldson, A., Kennedy, J., Foo, C., Godwin, A. K., Schmutzler, R. K., Wappenschmidt, B., Rhiem, K., Engel, C., Meindl, A., Ditsch, N., Arnold, N., Plendl, H. J., Niederacher, D., Sutter, C., Wang-Gohrke, S., Steinemann, D., Preisler-Adams, S., Kast, K., Varon-Mateeva, R., Gehrig, A., Stoppa-Lyonnet, D., Sinilnikova, O. M., Mazoyer, S., Damiola, F., Poppe, B., Claes, K., Piedmonte, M., Tucker, K., Backes, F., Rodriguez, G., Brewster, W., Wakeley, K., Rutherford, T., Caldes, T., Nevanlinna, H., Aittomaki, K., Rookus, M. A., van Os, T. A. M., van der Kolk, L., de Lange, J. L., Meijers-Heijboer, H. E. J., van der Hout, A. H., van Asperen, C. J., Gomez Garcia, E. B., Hoogerbrugge, N., Collee, J. M., van Deurzen, C. H. M., van der Luijt, R. B., Devilee, P., Hebon, N. N., Olah, E., Lazaro, C., Teule, A., Menendez, M., Jakubowska, A., Cybulski, C., Gronwald, J., Lubinski, J., Durda, K., Jaworska-Bieniek, K., Johannsson, O. T., Maugard, C., Montagna, M., Tognazzo, S., Teixeira, M. R., Healey, S., Investigators, KC., Olswold, C., Guidugli, L., Lindor, N., Slager, S., Szabo, C. I., Vijai, J., Robson, M., Kauff, N., Zhang, L., Rau-Murthy, R., Fink-Retter, A., Singer, C. F., Rappaport, C., Geschwantler Kaulich, D., Pfeiler, G., tea, M-K., Berger, A., Phelan, C. M., Greene, M. H., Mai, P. L., Lejbkowicz, F., Andrulis, I., Mulligan, A. M., Glendon, G., Toland, A. E., Bojesen, A., Pedersen, I. S., Sunde, L., Thomassen, M., Kruse, T. A., Jensen, U. B., Friedman, E., Laitman, Y., Shimon, S. P., Simard, J., Easton, D. F., Offit, K., Couch, F. J., Chenevix-Trench, G., Antoniou, A. C. & Benitez, J., 2014, In: PLoS genetics. 10, 4, p. e1004256 e1004256.

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    44 Citations (Scopus)

  • First steps in exploring prospective exome sequencing of consanguineous couples

    Teeuw, M. E., Waisfisz, Q., Zwijnenburg, P. J. G., Sistermans, E. A., Weiss, M. M., Henneman, L., ten Kate, L. P., Cornel, M. C. & Meijers-Heijboer, H., 2014, In: European journal of medical genetics. 57, 11-12, p. 613-616

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    11 Citations (Scopus)

  • High resolution SNP array profiling identifies variability in retinoblastoma genome stability

    Mol, B. M., Massink, M. P. G., van der Hout, A. H., Dommering, C. J., Zaman, J. M. A., Bosscha, M. I., Kors, W. A., Meijers-Heijboer, H. E., Kaspers, G. J. L., te Riele, H., Moll, A. C., Cloos, J. & Dorsman, J. C., 2014, In: Genes, Chromosomes and Cancer. 53, 1, p. 1-14

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    26 Citations (Scopus)

  • MicroRNA related polymorphisms and breast cancer risk

    Khan, S. M., Greco, D., Michailidou, K., Milne, R. L., Muranen, T. A., Heikkinen, T., Aaltonen, K., Dennis, J., Bolla, M. K., Liu, J., Hall, P., Irwanto, A., Humphreys, K., Li, J., Czene, K., Chang-Claude, J., Hein, R., Rudolph, A., Seibold, P., Flesch-Janys, D., & 81 othersFletcher, O., Peto, J., dos, S. S. . I., Johnson, N., Gibson, L., Aitken, Z., Hopper, J. L., Tsimiklis, H., Bui, M., Makalic, E., Schmidt, D. F., Southey, M. C., Apicella, C., Stone, J., Waisfisz, Q., Meijers-Heijboer, H. E., Adank, M. A., van der Luijt, R. B., Meindl, A., Schmutzler, R. K., Muller-Myhsok, B., Lichtner, P., Turnbull, C., Rahman, N., Chanock, S. J., Hunter, D. J., Cox, A., Cross, S. S., Reed, M. W., Schmidt, M. K., Broeks, A., van 't Veer, L. J., Hogervorst, FB., Fasching, P. A., Schrauder, M. G., Ekici, A. B., Beckmann, M. W., Bojesen, S. E., Nordestgaard, B. G., Nielsen, S. F., Flyger, H., Benitez, J., Zamora, P. M., Perez, J. I., Haiman, C. A., Henderson, B. E., Schumacher, F., Le, M. L., Pharoah, P. D., Dunning, A. M., Shah, M., Luben, R., Brown, J., Couch, F. J., Wang, X., Vachon, C., Olson, J. E., Lambrechts, D., Moisse, M., Paridaens, R., Christiaens, M. R., Guenel, P., Truong, T., Laurent-Puig, P., Mulot, C., Marme, F., Burwinkel, B., Schneeweiss, A., Sohn, C., Sawyer, E. J., Tomlinson, I., Kerin, M. J., Miller, N., Andrulis, I. L., Knight, J. A., Tchatchou, S., Mulligan, A. M., Dork, T., Bogdanova, N. V., Easton, D. F. & Nevanlinna, H., 2014, In: PLOS ONE. 9, 11, e109973.

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    38 Citations (Scopus)

  • Mutation frequency of PRKAR1B and the major familial dementia genes in a Dutch early onset dementia cohort

    Cohn-Hokke, P. E., Wong, T. H., Rizzu, P., Breedveld, G., van der Flier, W. M., Scheltens, P., Baas, F., Heutink, P., Meijers-Heijboer, E. J., van Swieten, J. C. & Pijnenburg, Y. A. L., 2014, In: Journal of neurology. 261, 11, p. 2085-2092

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    9 Citations (Scopus)

  • RB1 mutation spectrum in a comprehensive nationwide cohort of retinoblastoma patients

    Dommering, C. J., Mol, B. M., Moll, A. C., Burton, M., Cloos, J., Dorsman, J. C., Meijers-Heijboer, H. & van der Hout, A. H., 2014, In: Journal of medical genetics. 51, 6, p. 366-374

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    63 Citations (Scopus)

  • Relevance and efficacy of breast cancer screening in BRCA1 and BRCA2 mutation carriers above 60 years: A national cohort study

    Saadatmand, S., Vos, J. R., Hooning, M. J., Oosterwijk, J. C., Koppert, L. B., de Bock, G. H., Ausems, M. G., van Asperen, C. J., Aalfs, C. M., Gómez Garcia, E. B., Meijers-Heijboer, H., Hoogerbrugge, N., Piek, M., Seynaeve, C., Verhoef, C., Rookus, M. & Tilanus-Linthorst, M. M., 2014, In: International journal of cancer. Journal international du cancer. 135, 12, p. 2940-2949

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    13 Citations (Scopus)

  • Somatic mutations found in the healthy blood compartment of a 115-yr-old woman demonstrate oligoclonal hematopoiesis

    Holstege, H., Pfeiffer, W., Sie, D. L. S., Hulsman, M., Nicholas, T. J., Lee, C. C., Ross, T., Lin, J., Miller, M. A., Ylstra, B., Meijers-Heijboer, H. E., Brugman, M. H., Staal, F. J. T., Holstege, G., Reinders, M. J. T., Harkins, T. T., Levy, S. & Sistermans, E. A., 2014, In: Genome Research. 24, 5, p. 733-742

    Research output: Contribution to journal › Article › Academic › peer-review

    115 Citations (Scopus)

  • The value of DNA storage and pedigree analysis in rare diseases: a 17-year-old boy with X-linked lymphoproliferative disease (XLP) caused by a de novo SH2D1A mutation

    Overwater, E., Smulders, Y., van der Burg, M., Lombardi, M. P., Meijers-Heijboer, H. E., Kuijpers, T. W. & Houweling, A. C., 2014, In: European journal of pediatrics. 173, 12, p. 1695-1698

    Research output: Contribution to journal › Article › Academic › peer-review

    6 Citations (Scopus)

  • Variation in mutation spectrum partly explains regional differences in the breast cancer risk of female BRCA mutation carriers in the Netherlands

    AUTHOR GROUP, van der Kolk, DM. & Vasen, HF., 2014, In: Cancer epidemiology, biomarkers & prevention. 23, 11, p. 2482-2491

    Research output: Contribution to journal › Article › Academic › peer-review

    9 Citations (Scopus)
  • 2015

    An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers

    Blein, S., Bardel, C., Danjean, V., McGuffog, L., Healey, S., Barrowdale, D., Lee, A., Dennis, J., Kuchenbaecker, K. B., Soucy, P., Terry, M. B., Chung, W. K., Goldgar, D. E., Buys, S. S., Janavicius, R., Tihomirova, L., Tung, N., Dorfling, C. M., van Rensburg, E. J., Neuhausen, S. L., & 186 othersDing, Y. C., Gerdes, A-M., Ejlertsen, B., Nielsen, F. C., Hansen, T. VO., Osorio, A., Benitez, J., Conejero, R. A., Segota, E., Weitzel, J. N., Thelander, M., Peterlongo, P., Radice, P., Pensotti, V., Dolcetti, R., Bonanni, B., Peissel, B., Zaffaroni, D., Scuvera, G., Manoukian, S., Varesco, L., Capone, G. L., Papi, L., Ottini, L., Yannoukakos, D., Konstantopoulou, I., Garber, J., Hamann, U., Donaldson, A., Brady, A., Brewer, C., Foo, C., Evans, D. G., Frost, D., Eccles, D., Douglas, F., Cook, J., Adlard, J., Barwell, J., Walker, L., Izatt, L., Side, L. E., Kennedy, M. J., Tischkowitz, M., Rogers, M. T., Porteous, M. E., Morrison, P. J., Platte, R., Eeles, R., Davidson, R., Hodgson, S., Cole, T., Godwin, A. K., Isaacs, C., Claes, K., de Leeneer, K., Meindl, A., Gehrig, A., Wappenschmidt, B., Sutter, C., Engel, C., Niederacher, D., Steinemann, D., Plendl, H., Kast, K., Rhiem, K., Ditsch, N., Arnold, N., Varon-Mateeva, R., Schmutzler, R. K., Preisler-Adams, S., Markov, N. B., Wang-Gohrke, S., de Pauw, A., Lefol, C., Lasset, C., Leroux, D., Rouleau, E., Damiola, F., Dreyfus, H., Barjhoux, L., Golmard, L., Uhrhammer, N., Bonadona, V., Sornin, V., Bignon, Y-J., Carter, J., van Le, L., Piedmonte, M., DiSilvestro, P. A., de la Hoya, M., Caldes, T., Nevanlinna, H., Aittomäki, K., Jager, A., van den Ouweland, A. M., Kets, C. M., Aalfs, C. M., van Leeuwen, F. E., Hogervorst, F. B., Meijers-Heijboer, H. E., Oosterwijk, J. C., van Roozendaal, K. E., Rookus, M. A., Devilee, P., van der Luijt, R. B., Olah, E., Diez, O., Teulé, A., Lazaro, C., Blanco, I., del Valle, J., Jakubowska, A., Sukiennicki, G., Gronwald, J., Lubinski, J., Durda, K., Jaworska-Bieniek, K., Agnarsson, B. A., Maugard, C., Amadori, A., Montagna, M., Teixeira, M. R., Spurdle, A. B., Foulkes, W., Olswold, C., Lindor, N. M., Pankratz, V. S., Szabo, C. I., Lincoln, A., Jacobs, L., Corines, M., Robson, M., Vijai, J., Berger, A., Fink-Retter, A., Singer, C. F., Rappaport, C., Kaulich, D. G., Pfeiler, G., tea, M-K., Greene, M. H., Mai, P. L., Rennert, G., Imyanitov, E. N., Mulligan, A. M., Glendon, G., Andrulis, I. L., Tchatchou, S., Toland, A. E., Pedersen, I. S., Thomassen, M., Kruse, T. A., Jensen, U. B., Caligo, M. A., Friedman, E., Zidan, J., Laitman, Y., Lindblom, A., Melin, B., Arver, B., Loman, N., Rosenquist, R., Olopade, O. I., Nussbaum, R. L., Ramus, S. J., Nathanson, K. L., Domchek, S. M., Rebbeck, T. R., Arun, B. K., Mitchell, G., Karlan, B. Y., Lester, J., Orsulic, S., Stoppa-Lyonnet, D., Thomas, G., Simard, J., Couch, F. J., Offit, K., Easton, D. F., Chenevix-Trench, G., Antoniou, A. C., Mazoyer, S., Phelan, C. M., Sinilnikova, O. M. & Cox, D. G., 2015, In: Breast Cancer Research. 17, 1, p. 61 61.

    Research output: Contribution to journal › Article › Academic › peer-review

    30 Citations (Scopus)

  • A novel Fanconi anaemia subtype associated with a dominant-negative mutation in RAD51

    Ameziane, N., May, P., Haitjema, A., van de Vrugt, H. J., van Rossum-Fikkert, S. E., Ristic, D., Williams, G. J., Balk, J., Rockx, D., Li, H., Rooimans, M. A., Oostra, A. B., Velleuer, E., Dietrich, R., Bleijerveld, O. B., Maarten Altelaar, A. F., Meijers-Heijboer, H., Joenje, H., Glusman, G., Roach, J., & 9 othersHood, L., Galas, D., Wyman, C., Balling, R., den Dunnen, J., de Winter, J. P., Kanaar, R., Gelinas, R. & Dorsman, J. C., 2015, In: Nature communications. 6, p. 8829 8829.

    Research output: Contribution to journal › Article › Academic › peer-review

    113 Citations (Scopus)

  • Assessing associations between the AURKA-HMMR-TPX2-TUBG1 functional module and breast cancer risk in BRCA1/2 mutation carriers

    AUTHOR GROUP, Aittomaki, K., Jonson, L., Ejlertsen, B., de la Hoya, M., Caldees, T., Dunning, A. M., Oliver, C., Fineberg, E., Cook, M., Peock, S., McCann, E., Murray, A., Jacobs, C., Pichert, G., Lalloo, F., Chu, C., Dorkins, H., Paterson, J., Ong, K. R., & 33 othersTeixeira, M. R., Hogervorst, F. B. L., van der Hout, A. H., Seynaeve, C., van der Luijt, R. B., Ligtenberg, M. J. L., Devilee, P., Wijnen, J. T., Rookus, M. A., Blok, M. J., van den Ouweland, A. M. W., Rodriguez, G. C., Phillips, K. A. A., Piedmonte, M., Nerenstone, S. R., Bae-Jump, V. L., O'Malley, D. M., Ratner, E. S., Schmutzler, R. K., Wappenschmidt, B., Rhiem, K., Engel, C., Meindl, A., Ditsch, N., Arnold, N., Plendl, H. J., Niederacher, D., Sutter, C., Wang-Gohrke, S., Steinemann, D., Preisler-Adams, S., Antoniou, A. C. & Pujana, M. A., 2015, In: PLOS ONE. 10, 4, p. e0120020 e0120020.

    Research output: Contribution to journal › Article › Academic › peer-review

    32 Citations (Scopus)

  • Beneficial Outcome of Losartan Therapy Depends on Type of FBN1 Mutation in Marfan Syndrome

    Franken, R., den Hartog, A. W., Radonic, T., Micha, D., Maugeri, A., van Dijk, F. S., Meijers-Heijboer, H. E., Timmermans, J., Scholte, A. J., van den Berg, M. P., Groenink, M., Mulder, B. J. M., Zwinderman, A. H., de Waard, V. & Pals, G., 2015, In: Circulation. Cardiovascular genetics. 8, 2, p. 383-388

    Research output: Contribution to journal › Article › Academic › peer-review

    132 Citations (Scopus)

  • Breast Cancer Risk After Salpingo-Oophorectomy in Healthy BRCA1/2 Mutation Carriers: Revisiting the Evidence for Risk Reduction

    AUTHOR GROUP, 2015, In: Journal of the National Cancer Institute. 107, 5, p. djv033 djv033.

    Research output: Contribution to journal › Article › Academic › peer-review

    150 Citations (Scopus)

  • Candidate genetic modifiers for breast and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers

    Peterlongo, P., Chang-Claude, J., Moysich, K. B., Rudolph, A., Schmutzler, R. K., Simard, J., Soucy, P., Eeles, R. A., Easton, D. F., Hamann, U., Wilkening, S., Chen, B., Rookus, M. A., Schmidt, M. K., van der Baan, F. H., Spurdle, A. B., Walker, L. C., Lose, F., Maia, A-T., Montagna, M., & 183 othersMatricardi, L., Lubinski, J., Jakubowska, A., Gómez Garcia, E. B., Olopade, O. I., Nussbaum, R. L., Nathanson, K. L., Domchek, S. M., Rebbeck, T. R., Arun, B. K., Karlan, B. Y., Orsulic, S., Lester, J., Chung, W. K., Miron, A., Southey, M. C., Goldgar, D. E., Buys, S. S., Janavicius, R., Dorfling, C. M., van Rensburg, E. J., Ding, Y. C., Neuhausen, S. L., Hansen, T. V. O., Gerdes, A-M., Ejlertsen, B., Jønson, L., Osorio, A., Martínez-Bouzas, C., Benitez, J., Conway, E. E., Blazer, K. R., Weitzel, J. N., Manoukian, S., Peissel, B., Zaffaroni, D., Scuvera, G., Barile, M., Ficarazzi, F., Mariette, F., Fortuzzi, S., Viel, A., Giannini, G., Papi, L., Martayan, A., Tibiletti, M. G., Radice, P., Vratimos, A., Fostira, F., Garber, J. E., Donaldson, A., Brewer, C., Foo, C., Evans, D. G. R., Frost, D., Eccles, D., Brady, A., Cook, J., Tischkowitz, M., Adlard, J., Barwell, J., Walker, L., Izatt, L., Side, L. E., Kennedy, M. J., Rogers, M. T., Porteous, M. E., Morrison, P. J., Platte, R., Davidson, R., Hodgson, S. V., Ellis, S., Cole, T., Godwin, A. K., Claes, K., van Maerken, T., Meindl, A., Gehrig, A., Sutter, C., Engel, C., Niederacher, D., Steinemann, D., Plendl, H., Kast, K., Rhiem, K., Ditsch, N., Arnold, N., Varon-Mateeva, R., Wappenschmidt, B., Wang-Gohrke, S., Bressac-de Paillerets, B., Buecher, B., Delnatte, C., Houdayer, C., Stoppa-Lyonnet, D., Damiola, F., Coupier, I., Barjhoux, L., Venat-Bouvet, L., Golmard, L., Boutry-Kryza, N., Sinilnikova, O. M., Caron, O., Pujol, P., Mazoyer, S., Belotti, M., Piedmonte, M., Friedlander, M. L., Rodriguez, G. C., Copeland, L. J., de la Hoya, M., Segura, P. P., Nevanlinna, H., Aittomäki, K., van Os, T. A. M., Meijers-Heijboer, H. E. J., van der Hout, A. H., Vreeswijk, M. P. G., Hoogerbrugge, N., Ausems, M. G. E. M., van Doorn, H. C., Collée, J. M., Olah, E., Diez, O., Blanco, I., Lazaro, C., Brunet, J., Feliubadalo, L., Cybulski, C., Gronwald, J., Durda, K., Jaworska-Bieniek, K., Sukiennicki, G., Arason, A., Chiquette, J., Teixeira, M. R., Olswold, C., Couch, F. J., Lindor, N. M., Wang, X., Szabo, C. I., Offit, K., Corines, M., Jacobs, L., Robson, M. E., Zhang, L., Joseph, V., Berger, A., Singer, C. F., Rappaport, C., Kaulich, D. G., Pfeiler, G., tea, M-K. M., Phelan, C. M., Greene, M. H., Mai, P. L., Rennert, G., Mulligan, A. M., Glendon, G., Tchatchou, S., Andrulis, I. L., Toland, A. E., Bojesen, A., Pedersen, I. S., Thomassen, M., Jensen, U. B., Laitman, Y., Rantala, J., von Wachenfeldt, A., Ehrencrona, H., Askmalm, M. S., Borg, Å., Kuchenbaecker, K. B., McGuffog, L., Barrowdale, D., Healey, S., Lee, A., Pharoah, P. D. P., Chenevix-Trench, G., Antoniou, A. C., Friedman, E., Jonson, L. & Hodgson, SV., 2015, In: Cancer epidemiology, biomarkers & prevention. 24, 1, p. 308-316

    Research output: Contribution to journal › Article › Academic › peer-review

    18 Citations (Scopus)

  • Effect of Comprehensive Oncogenetics Training Interventions for General Practitioners, Evaluated at Multiple Performance Levels

    Houwink, E. J. F., Muijtjens, A. M. M., van Teeffelen, S. R., Henneman, L., Rethans, J. J., Jacobi, F., van der Jagt, L., Stirbu, I., van Luijk, S. J., Stumpel, C. T. R., Meijers-Heijboer, H. E., van der Vleuten, C., Cornel, M. C. & Dinant, G. J., 2015, In: PLOS ONE. 10, 4, e0122648.

    Research output: Contribution to journal › Article › Academic › peer-review

    28 Citations (Scopus)

  • Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer

    Michailidou, K., Beesley, J., Lindstrom, S., Canisius, S., Dennis, J., Lush, M. J., Maranian, M. J., Bolla, M. K., Wang, Q., Shah, M., Perkins, B. J., Czene, K., Eriksson, M., Darabi, H., Brand, J. S., Bojesen, S. E., Nordestgaard, B. G., Flyger, H., Nielsen, S. F., Rahman, N., & 81 othersTurnbull, C., Fletcher, O., Peto, J., Gibson, L., dos-Santos-Silva, I., Chang-Claude, J., Flesch-Janys, D., Rudolph, A., Eilber, U., Behrens, S., Nevanlinna, H., Muranen, T. A., Aittomaki, K., Blomqvist, C., Khan, S. I., Aaltonen, K., Ahsan, H., Kibriya, M. G., Whittemore, A. S., John, E. M., Malone, K. E., Gammon, M. D., Santella, R. M., Ursin, G., Makalic, E., Schmidt, D. F., Casey, G., Hunter, D. J., Gapstur, S. M., Gaudet, M. M., Diver, W. R., Haiman, C. A., Schumacher, F., Henderson, B. E., Le Marchand, L., Berg, C. D., Chanock, S. J., Figueroa, J., Hoover, R. N., Lambrechts, D., Neven, P., Wildiers, H., van Limbergen, E., Schmidt, M. K., Broeks, A., Verhoef, S., Cornelissen, S., Couch, F. J., Olson, J. E., Hallberg, E., Vachon, C., Waisfisz, Q., Meijers-Heijboer, H., Adank, M. A., van der Luijt, R. B., Li, J. M., Liu, J. J., Humphreys, K., Kang, D., Choi, J. Y., Park, S. K., Yoo, K. Y., Matsuo, K., Ito, H., Iwata, H., Tajima, K., Guenel, P., Truong, T., Mulot, C., Sanchez, M., Burwinkel, B., Marme, F., Surowy, H., Sohn, C., Wu, A. H., Tseng, C. C., Berg, D., Stram, D. O., Gonzalez-Neira, A., Hall, P. & Easton, D. F., 2015, In: Nature Genetics. 47, 4, p. 373-380

    Research output: Contribution to journal › Article › Academic › peer-review

    442 Citations (Scopus)

  • Genomic profiling of CHEK2*1100delC-mutated breast carcinomas

    Massink, M. P. G., Kooi, I. E., Martens, J. W. M., Waisfisz, Q., Meijers-Heijboer, H. & Kooi, E. I., 2015, In: BMC Cancer. 15, p. 877 877.

    Research output: Contribution to journal › Article › Academic › peer-review

    38 Citations (Scopus)

  • Identification and characterization of novel associations in the CASP8/ALS2CR12 region on chromosome 2 with breast cancer risk

    Lin, W-Y., Camp, N. J., Ghoussaini, M., Beesley, J., Michailidou, K., Hopper, J. L., Apicella, C., Southey, M. C., Stone, J., Schmidt, M. K., Broeks, A., van't Veer, L. J., Th Rutgers, E. J., Muir, K., Lophatananon, A., Stewart-Brown, S., Siriwanarangsan, P., Fasching, P. A., Haeberle, L., Ekici, A. B., & 204 othersBeckmann, M. W., Peto, J., Dos-Santos-Silva, I., Fletcher, O., Johnson, N., Bolla, M. K., Wang, Q., Dennis, J., Sawyer, E. J., Cheng, T., Tomlinson, I., Kerin, M. J., Miller, N., Marmé, F., Surowy, H. M., Burwinkel, B., Guénel, P., Truong, T., Menegaux, F., Mulot, C., Bojesen, S. E., Nordestgaard, B. G., Nielsen, S. F., Flyger, H., Benitez, J., Zamora, M. P., Arias Perez, J. I., Menéndez, P., González-Neira, A., Pita, G., Alonso, M. R., Alvarez, N., Herrero, D., Anton-Culver, H., Brenner, H., Dieffenbach, A. K., Arndt, V., Stegmaier, C., Meindl, A., Lichtner, P., Schmutzler, R. K., Müller-Myhsok, B., Brauch, H., Brüning, T., Ko, Y-D., Tessier, D. C., Vincent, D., Bacot, F., Nevanlinna, H., Aittomäki, K., Blomqvist, C., Khan, S., Matsuo, K., Ito, H., Iwata, H., Horio, A., Bogdanova, N. V., Antonenkova, N. N., Dörk, T., Lindblom, A., Margolin, S., Mannermaa, A., Kataja, V., Kosma, V-M., Hartikainen, J. M., Wu, A. H., Tseng, C-C., van den Berg, D., Stram, D. O., Neven, P., Wauters, E., Wildiers, H., Lambrechts, D., Chang-Claude, J., Rudolph, A., Seibold, P., Flesch-Janys, D., Radice, P., Peterlongo, P., Manoukian, S., Bonanni, B., Couch, F. J., Wang, X., Vachon, C., Purrington, K., Giles, G. G., Milne, R. L., McLean, C., Haiman, C. A., Henderson, B. E., Schumacher, F., Le Marchand, L., Simard, J., Goldberg, M. S., Labrèche, F., Dumont, M., teo, S. H., Yip, C. H., Hassan, N., Vithana, E. N., Kristensen, V., Zheng, W., Deming-Halverson, S., Shrubsole, M. J., Long, J., Winqvist, R., Pylkäs, K., Jukkola-Vuorinen, A., Kauppila, S., Andrulis, I. L., Knight, J. A., Glendon, G., Tchatchou, S., Devilee, P., Tollenaar, R. A. E. M., Seynaeve, C., van Asperen, C. J., García-Closas, M., Figueroa, J., Lissowska, J., Brinton, L., Czene, K., Darabi, H., Eriksson, M., Brand, J. S., Hooning, M. J., Hollestelle, A., van den Ouweland, A. M. W., Jager, A., Li, J., Liu, J., Humphreys, K., Shu, X-O., Lu, W., Gao, Y-T., Cai, H., Cross, S. S., Reed, M. W. R., Blot, W., Signorello, L. B., Cai, Q., Pharoah, P. D. P., Perkins, B., Shah, M., Blows, F. M., Kang, D., Yoo, K-Y., Noh, D-Y., Hartman, M., Miao, H., Chia, K. S., Putti, T. C., Hamann, U., Luccarini, C., Baynes, C., Ahmed, S., Maranian, M., Healey, C. S., Jakubowska, A., Lubinski, J., Jaworska-Bieniek, K., Durda, K., Sangrajrang, S., Gaborieau, V., Brennan, P., McKay, J., Slager, S., Toland, A. E., Yannoukakos, D., Shen, C-Y., Hsiung, C-N., Wu, P-E., Ding, S-L., Ashworth, A., Jones, M., Orr, N., Swerdlow, A. J., Tsimiklis, H., Makalic, E., Schmidt, D. F., Bui, Q. M., Chanock, S. J., Hunter, D. J., Hein, R., Dahmen, N., Beckmann, L., Aaltonen, K., Muranen, T. A., Heikkinen, T., Irwanto, A., Rahman, N., Turnbull, C. A., Waisfisz, Q., Meijers-Heijboer, H. E. J., Adank, M. A., van der Luijt, R. B., Hall, P., Chenevix-Trench, G., Dunning, A., Easton, D. F., Cox, A., Herrera, D., Aittomaki, K. & Dork, T., 2015, In: Human Molecular Genetics. 24, 1, p. 285-298

    Research output: Contribution to journal › Article › Academic › peer-review

    37 Citations (Scopus)

  • Identification of a Dutch founder mutation in MUSK causing fetal akinesia deformation sequence.

    Tan-Sindhunata, M. B., Matthijssen, I. B., Smit, M., Baas, F., de Vries, J. I. P., van der Voorn, J. P., Kluijt, I., Hagen, M. A., Blom, E. W., Sistermans, E. A., Heijboer-Meijers, J. E., Waisfisz, Q., Weiss, M. M., Groffen, A. J. A. & Mathijssen, I. B., 14 Sept 2015, In: European journal of human genetics. 23, 9, p. 1151-1157 7 p.

    Research output: Contribution to journal › Article › Academic › peer-review

    Open Access
    34 Citations (Scopus)

  • Improved overall survival after contralateral risk-reducing mastectomy in BRCA1/2 mutation carriers with a history of unilateral breast cancer: a prospective analysis

    AUTHOR GROUP, 2015, In: International journal of cancer. Journal international du cancer. 136, 3, p. 668-677

    Research output: Contribution to journal › Article › Academic › peer-review

    163 Citations (Scopus)

  • Loss of photoreceptorness and gain of genomic alterations in retinoblastoma reveal tumor progression

    Kooi, I. E., Mol, B. M., Moll, A. C., van der Valk, P., de Jong, M. C., de Graaf, P., van Mil, S. E., Schouten-van Meeteren, A. Y. N., Meijers-Heijboer, H., Kaspers, G. L., te Riele, H., Cloos, J., Dorsman, J. C. & Kooi, E. I., 2015, In: eBioMedicine. 2, 7, p. 660-670

    Research output: Contribution to journal › Article › Academic › peer-review

    52 Citations (Scopus)

  • Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores

    AUTHOR GROUP, Schizophrenia Working Group of the Psychiatric Genomics Consortium, Psychosis Endophenotypes International Consortium, Wellcome Trust Case-Control Consortium, Discovery, Biology, and Risk of Inherited Variants in Breast Cancer (DRIVE) study & Hereditary Breast and Ovarian Cancer Research Group Netherlands (HEBON), 2015, In: American journal of human genetics. 97, 4, p. 576-592 17 p.

    Research output: Contribution to journal › Article › Academic › peer-review

    Open Access
    783 Citations (Scopus)

  • Proper genomic profiling of (BRCA1-mutated) basal-like breast carcinomas requires prior removal of tumor infiltrating lymphocytes

    Massink, M. P. G., Kooi, I. E., van Mil, S. E., Jordanova, E. S., Ameziane, N., Dorsman, J. C., van Beek, D. M., van der Voorn, J. P., Sie, D., Ylstra, B., van Deurzen, C. H. M., Martens, J. W., Smid, M., Sieuwerts, A. M., de Weerd, V., Foekens, J. A., van den Ouweland, A. M. W., van Dyk, E., Nederlof, P. M., Waisfisz, Q., & 2 othersMeijers-Heijboer, H. & Kooi, E. I., 2015, In: Molecular Oncology. 9, 4, p. 877-888

    Research output: Contribution to journal › Article › Academic › peer-review

    15 Citations (Scopus)

  • Targeted carrier screening for four recessive disorders: High detection rate within a founder population

    Mathijssen, I. B., Henneman, L., van Eeten-Nijman, J. M. C., Lakeman, P., Ottenheim, C. P. E., Redeker, E. J. W., Ottenhof, W., Meijers-Heijboer, H. & van Maarle, M. C., 2015, In: European journal of medical genetics. 58, 3, p. 123-128

    Research output: Contribution to journal › Article › Academic › peer-review

    24 Citations (Scopus)

  • Two male adults with pathogenic AUTS2 variants, including a two-base pair deletion, further delineate the AUTS2 syndrome

    Beunders, G., De Munnik, S. A., Van Der Aa, N., Ceulemans, B., Voorhoeve, E., Groffen, A. J., Nillesen, W. M., Meijers-Heijboer, E. J., Frank Kooy, R., Yntema, H. G., Sistermans, E. A. & Kooy, F. R., 15 Jun 2015, In: European journal of human genetics. 23, 6, p. 803-807 5 p.

    Research output: Contribution to journal › Article › Academic › peer-review

    Open Access
    24 Citations (Scopus)

  • What is the benefit of treatment with multiple lines of chemotherapy for patients with metastatic breast cancer? A retrospective cohort study

    Bakker, J. L., Wever, K., van Waesberghe, J. H. T. M., Beeker, A., Meijers-Heijboer, H., Konings, I. R. H. M. & Verheul, H. M. W., 2015, In: Cancer epidemiology. 39, 6, p. 848-853

    Research output: Contribution to journal › Article › Academic › peer-review

    8 Citations (Scopus)
  • 2016

    A detailed clinical analysis of 13 patients with AUTS2 syndrome further delineates the phenotypic spectrum and underscores the behavioural phenotype

    Beunders, G., van de Kamp, J., Vasudevan, P., Morton, J., Smets, K., Kleefstra, T., de Munnik, S. A., Schuurs-Hoeijmakers, J., Ceulemans, B., Zollino, M., Hoffjan, S., Wieczorek, S., So, J., Mercer, L., Walker, T., Velsher, L., Parker, M. J., Magee, A. C., Elffers, B., Frank Kooy, R., & 4 othersYntema, H. G., Meijers-Heijboer, E. J., Sistermans, E. A. & The DDD study, DDD. S., 1 Aug 2016, In: Journal of medical genetics. 53, 8, p. 523-532 10 p.

    Research output: Contribution to journal › Article › Academic › peer-review

    37 Citations (Scopus)

  • Age- and Tumor Subtype Specific Breast Cancer Risk Estimates for CHEK2*1100delC Carriers

    Schmidt, M. K., Hogervorst, F., van Hien, R., Cornelissen, S., Broeks, A., Adank, M. A., Meijers, H., Waisfisz, Q., Hollestelle, A., Schutte, M., van den Ouweland, A., Hooning, M., Andrulis, I. L., Anton-Culver, H., Antonenkova, N. N., Antoniou, A. C., Arndt, V., Bermisheva, M., Bogdanova, N. V., Bolla, M. K., & 64 othersBrauch, H., Brenner, H., Bruning, T., Burwinkel, B., Chang-Claude, J., Chenevix-Trench, G., Couch, F. J., Cox, A., Cross, S. S., Czene, K., Dunning, A. M., Fasching, P. A., Figueroa, J., Fletcher, O., Flyger, H., Galle, E., Garcia-Closas, M., Giles, G. G., Haeberle, L., Hall, P., Hillemanns, P., Hopper, J. L., Jakubowska, A., John, E. M., Jones, M., Khusnutdinova, E., Knight, J. A., Kosma, V-M., Kristensen, V., Lee, A., Lindblom, A., Lubinski, J., Mannermaa, A., Margolin, S., Meindl, A., Milne, R. L., Muranen, T. A., Newcomb, P. A., Offit, K., Park-Simon, T-W., Peto, J., Pharoah, P. D. P., Robson, M., Rudolph, A., Sawyer, E. J., Schmutzler, R. K., Seynaeve, C., Soens, J., Southey, M. C., Spurdle, A. B., Surowy, H., Swerdlow, A., Tollenaar, R. A. E. M., Tomlinson, I., Trentham-Dietz, A., Vachon, C., Wang, Q., Whittemore, A. S., Ziogas, A., van der Kolk, L., Nevanlinna, H., Doerk, T., Bojesen, S. & Easton, D. F., 10 Aug 2016, In: Journal of clinical oncology. 34, 23, p. 2750-+

    Research output: Contribution to journal › Article › Academic › peer-review

    135 Citations (Scopus)

  • A Meta-Analysis of Retinoblastoma Copy Numbers Refines the List of Possible Driver Genes Involved in Tumor Progression

    Kooi, I. E., Mol, B. M., Massink, M. P. G., de Jong, M. C., de Graaf, P., van der Valk, P., Meijers-Heijboer, H., Kaspers, G. J. L., Moll, A. C., te Riele, H., Cloos, J. & Dorsman, J. C., 26 Apr 2016, In: PLOS ONE. 11, 4

    Research output: Contribution to journal › Article › Academic › peer-review

    58 Citations (Scopus)