| Title | Author(s) | Year | View Count |
 | Risk of colorectal and endometrial cancers in EPCAM deletion-positive Lynch syndrome: A cohort study | Kempers, MJE; Kuiper, RP; Ockeloen, CW; Chappuis, PO; Hutter, P; Rahner, N; Schackert, HK; Steinke, V; HolinskiFeder, E; Morak, M; Kloor, M; Büttner, R; Verwiel, ETP; van Krieken, JH; Nagtegaal, ID; Goossens, M; van der Post, RS; Niessen, RC; Sijmons, RH; Kluijt, I; Hogervorst, FBL; Leter, EM; Gille, JJP; Aalfs, CM; Redeker, EJW; Hes, FJ; Tops, CMJ; van Nesselrooij, BPM; van Gijn, ME; García, EBG; Eccles, DM; Bunyan, DJ; Syngal, S; Stoffel, EM; Culver, JO; Palomares, MR; Graham, T; Velsher, L; Papp, J; Oláh, E; Chan, TL; Leung, SY; van Kessel, AG; Kiemeney, LALM; Hoogerbrugge, N; Ligtenberg, MJL | 2011 | 319 |
| Recurrence and variability of germline EPCAM deletions in Lynch syndrome | Kuiper, RP; Vissers, LELM; Venkatachalam, R; Bodmer, D; Hoenselaar, E; Goossens, M; Haufe, A; Kamping, E; Niessen, RC; Hogervorst, FBL; Gille, JJP; Redeker, B; Tops, CMJ; van Gijn, ME; van den Ouweland, AMW; Rahner, N; Steinke, V; Kahl, P; HolinskiFeder, E; Morak, M; Kloor, M; Stemmler, S; Betz, B; Hutter, P; Bunyan, DJ; Syngal, S; Culver, JO; Graham, T; Chan, TL; Nagtegaal, ID; van Krieken, JHJM; Schackert, HK; Hoogerbrugge, N; van Kessel, AG; Ligtenberg, MJL | 2011 | 101 |
| Heritable somatic methylation and inactivation of MSH2 in families with Lynch syndrome due to deletion of the 3′ exons of TACSTD1 | Ligtenberg, MJL; Kuiper, RP; Chan, TL; Goossens, M; Hebeda, KM; Voorendt, M; Lee, TYH; Bodmer, D; Hoenselaar, E; HendriksCornelissen, SJB; Tsui, WY; Kong, CK; Brunner, HG; Van Kessel, AG; Yuen, ST; Van Krieken, JHJM; Leung, SY; Hoogerbrugge, N | 2009 | 65 |
| The molecular genetic analysis of hemophilia A: A directed search strategy for the detection of point mutations in the human factor VIII gene | Pattinson, JK; Millar, DS; Mcvey, JH; Grundy, CB; Wieland, K; Mibashan, RS; Martinowitz, U; TanUn, K; Vidaud, M; Goossens, M; Sampietro, M; Mannucci, PM; Krawczak, M; Reiss, J; Zoll, B; Whitmore, D; Bowcock, S; Wensley, R; Ajani Et Al, A | 1990 | 52 |
| Unusual segregation of cystic fibrosis alleles [6] | Kitzis, A; Chomel, JC; Haliassos, A; Tesson, L; Kaplan, JC; Feingold, J; Giraud, G; Labbe, A; Dastugue, B; Dumur, V; Farriaux, JP; Roussel, P; Ferrec, C; Vidaud, M; Goossens, M; Bozon, D; Auvinet, M; Chambon, V; Andre, J; Lissens, W; Bonduelle, M; Liebaers, I; Cochaux, P; Vassart, G; Willems, P; DuckworthRaysiecki, G; Kerem, BS; Tsui, LC; Ray, PN; Krawczak, M; Schmidtke, J; Novelli, G; Dallapiccola, B; Gasparni, G; Pignatti, PP; Seia, M; Ferrari, M; Devoto, M; Romeo, G; Schwarz, M; Super, M; Ivinson, A; Read, AP; Meredith, L; Curtis, A; Williamson, R; Beaudet, AL; Feldman, GL; O'Brien, WE; Bowcock, AM; CavalliSforza, LL; Gilbert, F; Braman, J; King, MC | 1988 | 93 |
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