Tops CM - Search Results

1

Colibactin mutational signatures in NTHL1 tumor syndrome and MUTYH associated polyposis patients.

Terlouw D, Boot A, Ducarmon QR, Nooij S, Jessurun MA, van Leerdam ME, Tops CM, Langers AMJ, Morreau H, van Wezel T, Nielsen M. Terlouw D, et al. Among authors: tops cm. Genes Chromosomes Cancer. 2024 Jan;63(1):e23208. doi: 10.1002/gcc.23208. Epub 2023 Oct 5. Genes Chromosomes Cancer. 2024. PMID: 37795928

2

Mapping of two new markers within the smallest interval harboring the spinal muscular atrophy locus by family and radiation hybrid analysis.

Brahe C, Velonà I, van der Steege G, Zappata S, van de Veen AY, Osinga J, Tops CM, Fodde R, Khan PM, Buys CH, et al. Brahe C, et al. Among authors: tops cm. Hum Genet. 1994 May;93(5):494-501. doi: 10.1007/BF00202811. Hum Genet. 1994. PMID: 8168823

3

MAX mutations cause hereditary and sporadic pheochromocytoma and paraganglioma.

Burnichon N, Cascón A, Schiavi F, Morales NP, Comino-Méndez I, Abermil N, Inglada-Pérez L, de Cubas AA, Amar L, Barontini M, de Quirós SB, Bertherat J, Bignon YJ, Blok MJ, Bobisse S, Borrego S, Castellano M, Chanson P, Chiara MD, Corssmit EP, Giacchè M, de Krijger RR, Ercolino T, Girerd X, Gómez-García EB, Gómez-Graña A, Guilhem I, Hes FJ, Honrado E, Korpershoek E, Lenders JW, Letón R, Mensenkamp AR, Merlo A, Mori L, Murat A, Pierre P, Plouin PF, Prodanov T, Quesada-Charneco M, Qin N, Rapizzi E, Raymond V, Reisch N, Roncador G, Ruiz-Ferrer M, Schillo F, Stegmann AP, Suarez C, Taschin E, Timmers HJ, Tops CM, Urioste M, Beuschlein F, Pacak K, Mannelli M, Dahia PL, Opocher G, Eisenhofer G, Gimenez-Roqueplo AP, Robledo M. Burnichon N, et al. Among authors: tops cm. Clin Cancer Res. 2012 May 15;18(10):2828-37. doi: 10.1158/1078-0432.CCR-12-0160. Epub 2012 Mar 27. Clin Cancer Res. 2012. PMID: 22452945

4

A novel nonsense B3GALTL mutation confirms Peters plus syndrome in a patient with multiple malformations and Peters anomaly.

Aliferis K, Marsal C, Pelletier V, Doray B, Weiss MM, Tops CM, Speeg-Schatz C, Lesnik SA, Dollfus H. Aliferis K, et al. Among authors: tops cm. Ophthalmic Genet. 2010 Dec;31(4):205-8. doi: 10.3109/13816810.2010.512355. Ophthalmic Genet. 2010. PMID: 21067481

5

Recurrence and variability of germline EPCAM deletions in Lynch syndrome.

Kuiper RP, Vissers LE, Venkatachalam R, Bodmer D, Hoenselaar E, Goossens M, Haufe A, Kamping E, Niessen RC, Hogervorst FB, Gille JJ, Redeker B, Tops CM, van Gijn ME, van den Ouweland AM, Rahner N, Steinke V, Kahl P, Holinski-Feder 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 JH, Schackert HK, Hoogerbrugge N, van Kessel AG, Ligtenberg MJ. Kuiper RP, et al. Among authors: tops cm. Hum Mutat. 2011 Apr;32(4):407-14. doi: 10.1002/humu.21446. Epub 2011 Mar 1. Hum Mutat. 2011. PMID: 21309036

6

[Genetics of colorectal cancer. II. Hereditary background of sporadic and familial colorectal cancer].

Menko FH, Griffioen G, Wijnen JT, Tops CM, Fodde R, Vasen HF. Menko FH, et al. Among authors: tops cm. Ned Tijdschr Geneeskd. 1999 Jun 5;143(23):1207-11. Ned Tijdschr Geneeskd. 1999. PMID: 10389535 Review. Dutch.

7

[Genetics of colorectal cancer. I. Non-polyposis and polyposis forms of hereditary colorectal cancer].

Menko FH, Griffioen G, Wijnen JT, Tops CM, Fodde R, Vasen HF. Menko FH, et al. Among authors: tops cm. Ned Tijdschr Geneeskd. 1999 Jun 5;143(23):1201-6. Ned Tijdschr Geneeskd. 1999. PMID: 10389534 Review. Dutch.

8

Long term follow-up of HNPCC gene mutation carriers: compliance with screening and satisfaction with counseling and screening procedures.

Wagner A, van Kessel I, Kriege MG, Tops CM, Wijnen JT, Vasen HF, van der Meer CA, van Oostrom II, Meijers-Heijboer H. Wagner A, et al. Among authors: tops cm. Fam Cancer. 2005;4(4):295-300. doi: 10.1007/s10689-005-0658-9. Fam Cancer. 2005. PMID: 16341806

9

[Increased sensitivity for detection of mutations in exon 15 of the APC gene in patients with familial adenomatous polyposis].

Konvalinka D, Bik EC, Tops CM, Bakker E, Singh AR, Vrtĕl R, Santavý J. Konvalinka D, et al. Among authors: tops cm. Cas Lek Cesk. 2004;143(8):543-6. Cas Lek Cesk. 2004. PMID: 15446460 Czech.

10

[From gene to disease; the APC gene and familial adenomatous polyposis coli].

van der Luijt RB, Tops CM, Vasen HF. van der Luijt RB, et al. Among authors: tops cm. Ned Tijdschr Geneeskd. 2000 Oct 14;144(42):2007-9. Ned Tijdschr Geneeskd. 2000. PMID: 11072519 Review. Dutch.

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