BRCA1 and BRCA2 germline mutation spectrum and frequencies in Belgian breast/ovarian cancer families

by Claes, K, Poppe, B, Coene, I, Paepe, A De, Messiaen, L
Published 2004

Diabetic Muscle Infarction: A Rare Cause of Acute Limb Pain in Dialysis Patients

by De Vlieger, G., Bammens, B., Claus, F., Vos, R., Claes, K.
Published 2013

Chromosomal radiosensitivity in breast cancer patients with a known or putative genetic predisposition

by Baeyens, A, Thierens, H, Claes, K, Poppe, B, Messiaen, L, De Ridder, L, Vral, A
Published 2002

Benefit of anti-TNFα treatment for nephrotic syndrome in a patient with juvenile inflammatory bowel disease associated spondyloarthropathy complicated with amyloidosis and glomerul...

by Verschueren, P, Lensen, F, Lerut, E, Claes, K, De Vos, R, Van Damme, B, Westhovens, R
Published 2003

Genetic Counselling and Testing for Hereditary Breast and Ovarian Cancer: The Gent(le) Approach

by De Vos, M., Poppe, B., Delvaux, I., Mortier, G., Claes, K., Messiaen, L., De Paepe, A.
Published 1999

Impact of early parenteral nutrition on catabolism

by Gunst, J, Vanhorebeek, I, Casaer, MP, Hermans, G, Wouters, PJ, Dubois, J, Claes, K, Schetz, M, Van den Berghe, G
Published 2013

Next Generation Sequencing to Determine the Cystic Fibrosis Mutation Spectrum in Palestinian Population

by Essawi, O., Farraj, M., De Leeneer, K., Steyaert, W., De Pauw, K., De Paepe, A., Claes, K., Essawi, T., Coucke, P. J.
Published in Dis Markers (2015)

Questioning the Pathogenic Role of the GLA p.Ala143Thr “Mutation” in Fabry Disease: Implications for Screening Studies and ERT

by Terryn, W., Vanholder, R., Hemelsoet, D., Leroy, B. P., Van Biesen, W., De Schoenmakere, G., Wuyts, B., Claes, K., De Backer, J., De Paepe, G., Fogo, A., Praet, M., Poppe, B.
Published 2012

Mutation analysis of RAD51D in non-BRCA1/2 ovarian and breast cancer families

by Osher, D J, De Leeneer, K, Michils, G, Hamel, N, Tomiak, E, Poppe, B, Leunen, K, Legius, E, Shuen, A, Smith, E, Arseneau, J, Tonin, P, Matthijs, G, Claes, K, Tischkowitz, M D, Foulkes, W D
Published 2012

BRCA1, BRCA2 and PALB2 mutations and CHEK2 c.1100delC in different South African ethnic groups diagnosed with premenopausal and/or triple negative breast cancer

by Francies, F. Z., Wainstein, T., De Leeneer, K., Cairns, A., Murdoch, M., Nietz, S., Cubasch, H., Poppe, B., Van Maerken, T., Crombez, B., Coene, I., Kerr, R., Slabbert, J. P., Vral, A., Krause, A., Baeyens, A., Claes, K. B. M.
Published in BMC Cancer (2015)

IRF6 Screening of Syndromic and a priori Non-Syndromic Cleft Lip and Palate Patients: Identification of a New Type of Minor VWS Sign

by Desmyter, L., Ghassibe, M., Revencu, N., Boute, O., Lees, M., François, G., Verellen-Dumoulin, C., Sznajer, Y., Moncla, A., Benateau, H., Claes, K., Devriendt, K., Mathieu, M., Van Maldergem, L., Addor, M.-C., Drouin-Garraud, V., Mortier, G., Bouma, M., Dieux-Coeslier, A., Genevieve, D., Goldenberg, A., Gozu, A., Makrythanasis, P., McEntagart, U., Sanchez, A., Vilain, C., Vermeer, S., Connell, F., Verheij, J., Manouvrier, S., Pierquin, G., Odent, S., Holder-Espinasse, M., Vincent-Delorme, C., Gillerot, Y., Vanwijck, R., Bayet, B., Vikkula, M.
Published 2010

Breast-Cancer Risk in Families with Mutations in PALB2

by Antoniou, A.C., Casadei, S., Heikkinen, T., Barrowdale, D., Pylkäs, K., Roberts, J., Lee, A., Subramanian, D., De Leeneer, K., Fostira, F., Tomiak, E., Neuhausen, S.L., Teo, Z.L., Khan, S., Aittomäki, K., Moilanen, J.S., Turnbull, C., Seal, S., Mannermaa, A., Kallioniemi, A., Lindeman, G.J., Buys, S.S., Andrulis, I.L., Radice, P., Tondini, C., Manoukian, S., Toland, A.E., Miron, P., Weitzel, J.N., Domchek, S.M., Poppe, B., Claes, K.B.M., Yannoukakos, D., Concannon, P., Bernstein, J.L., James, P.A., Easton, D.F., Goldgar, D.E., Hopper, J.L., Rahman, N., Peterlongo, P., Nevanlinna, H., King, M.-C., Couch, F.J., Southey, M.C., Winqvist, R., Foulkes, W.D., Tischkowitz, M.
Published 2014

A replication study confirms the association of TNFSF4 (OX40L) polymorphisms with Systemic Sclerosis in a large European cohort

by Airó P, Lie B A, Palm Ø, Nordin A, Padykov L, Claes K, Denton C, Fonseca C, Madhok R, Shiels P, Chee M M, Schuerwegh A J, Voskuyl A E, De Langhe E, Westhovens R, Smith V, De Keyser F, Houssiau F, Koeleman B P, Coenen MJH, Witte T, Riemekasten G, Hesselstrand R, González-Gay M A, Pros A, García de la Peña P, Follonosa V, Egurbide M V, Fernández-Nebro A, Gallego M, Castellví I, García-Hernández F J, Gómez-Gracia I, Román-Ivorra J A, Tolosa C, Rodríguez L, Vicente-Rabaneda E, González-Escribano M F, Navarrete N, Camps M T, Carreira P, Espinosa G, Ortego-Centeno N, Vonk M C, Beretta L, Simeon C P, Broen JCA, Bossini-Castillo L, Scorza R, van Laar J M, Hunzelmann N, Kreuter A, Herrick A, Worthington J, Radstake TRDJ, Martín J, Rueda B
Published 2010-11-01

A replication study confirms the association of TNFSF4 (OX40L) polymorphisms with Systemic Sclerosis in a large European cohort

by Bossini-Castillo, L, Broen, JCA, Simeon, C P, Beretta, L, Vonk, M C, Ortego-Centeno, N, Espinosa, G, Carreira, P, Camps, M T, Navarrete, N, González-Escribano, M F, Vicente-Rabaneda, E, Rodríguez, L, Tolosa, C, Román-Ivorra, J A, Gómez-Gracia, I, García-Hernández, F J, Castellví, I, Gallego, M, Fernández-Nebro, A, Egurbide, M V, Follonosa, V, García de la Peña, P, Pros, A, González-Gay, M A, Hesselstrand, R, Riemekasten, G, Witte, T, Coenen, MJH, Koeleman, B P, Houssiau, F, Smith, V, De Keyser, F, Westhovens, R, De Langhe, E, Voskuyl, A E, Schuerwegh, A J, Chee, M M, Madhok, R, Shiels, P, Fonseca, C, Denton, C, Claes, K, Padykov, L, Nordin, A, Palm, Ø, Lie, B A, Airó, P, Scorza, R, van Laar, J M, Hunzelmann, N, Kreuter, A, Herrick, A, Worthington, J, Radstake, TRDJ, Martín, J, Rueda, B
Published 2010

Evaluation of a candidate breast cancer associated SNP in ERCC4 as a risk modifier in BRCA1 and BRCA2 mutation carriers. Results from the Consortium of Investigators of Modifiers o...

by Osorio, A, Milne, R L, Pita, G, Peterlongo, P, Heikkinen, T, Simard, J, Chenevix-Trench, G, Spurdle, A B, Beesley, J, Chen, X, Healey, S, Neuhausen, S L, Ding, Y C, Couch, F J, Wang, X, Lindor, N, Manoukian, S, Barile, M, Viel, A, Tizzoni, L, Szabo, C I, Foretova, L, Zikan, M, Claes, K, Greene, M H, Mai, P, Rennert, G, Lejbkowicz, F, Barnett-Griness, O, Andrulis, I L, Ozcelik, H, Weerasooriya, N, Gerdes, A-M, Thomassen, M, Cruger, D G, Caligo, M A, Friedman, E, Kaufman, B, Laitman, Y, Cohen, S, Kontorovich, T, Gershoni-Baruch, R, Dagan, E, Jernström, H, Askmalm, M S, Arver, B, Malmer, B, Domchek, S M, Nathanson, K L, Brunet, J, Ramón y Cajal, T, Yannoukakos, D, Hamann, U, Hogervorst, F B L, Verhoef, S, García, EB Gómez, Wijnen, J T, van den Ouweland, A, Easton, D F, Peock, S, Cook, M, Oliver, C T, Frost, D, Luccarini, C, Evans, D G, Lalloo, F, Eeles, R, Pichert, G, Cook, J, Hodgson, S, Morrison, P J, Douglas, F, Godwin, A K, Sinilnikova, O M, Barjhoux, L, Stoppa-Lyonnet, D, Moncoutier, V, Giraud, S, Cassini, C, Olivier-Faivre, L, Révillion, F, Peyrat, J-P, Muller, D, Fricker, J-P, Lynch, H T, John, E M, Buys, S, Daly, M, Hopper, J L, Terry, M B, Miron, A, Yassin, Y, Goldgar, D, Singer, C F, Gschwantler-Kaulich, D, Pfeiler, G, Spiess, A-C, Hansen, Thomas v O, Johannsson, O T, Kirchhoff, T, Offit, K, Kosarin, K, Piedmonte, M, Rodriguez, G C, Wakeley, K, Boggess, J F, Basil, J, Schwartz, P E, Blank, S V, Toland, A E, Montagna, M, Casella, C, Imyanitov, E N, Allavena, A, Schmutzler, R K, Versmold, B, Engel, C, Meindl, A, Ditsch, N, Arnold, N, Niederacher, D, Deißler, H, Fiebig, B, Varon-Mateeva, R, Schaefer, D, Froster, U G, Caldes, T, de la Hoya, M, McGuffog, L, Antoniou, A C, Nevanlinna, H, Radice, P, Benítez, J
Published 2009