Zobrazeno 1 - 10
of 62
pro vyhledávání: '"Depreeuw J"'
Autor:
O'Mara, T, Glubb, D, Amant, F, Annibali, D, Ashton, K, Attia, J, Auer, P, Beckmann, M, Black, A, Humphreys, M, Brauch, H, Brenner, H, Brinton, L, Buchanan, D, Burwinkel, B, Chang-Claude, J, Chanock, S, Chen, C, Chen, M, Cheng, T, Clarke, C, Clendenning, M, Cook, L, Couch, F, Cox, A, Crous-Bou, M, Czene, K, Day, F, Dennis, J, Depreeuw, J, Doherty, JA, Dork, T, Dowdy, S, Dürst, M, Ekici, A, Fasching, P, Fridley, B, Friedenreich, C, Fritschi, L, Fung, J, Garcia-Closas, M, Gaudet, M, Giles, G, Goode, E, Gorman, M, Haiman, C, Hall, P, Hankinson, S, Healey, C, Hein, A, Hillemanns, P, Hodgson, S, Hoivik, E, Holliday, E, Hopper, J, Hunter, D, Jones, A, Krakstad, C, Kristensen, V, Lambrechts, D, Le Marchand, L, Liang, X, Lindblom, A, Lissowska, J, Long, J, Lu, L, Magliocco, A, Martin, L, McEvoy, M, Meindl, A, Michailidou, K, Milne, R, Mints, M, Montgomery, G, Nassir, R, Olsson, H, Orlow, I, Sacerdote, G, Sarto, G, Schumacher, F, Scott, R, Setiawan, VW, Shah, M, Sheng, M, Shu, X-O, Southey, M, Swerdlow, A, Tham, E, Trovik, J, Wolk, A, Xia, L, Xiang, YB, Yang, H, Yu, H, Zheng, W, Pharoah, P, Dunning, A, Kraft, P, De Vivo, I, Tomlinson, I, Easton, D, Spurdle, A, Thompson, D
Endometrial cancer is the most commonly diagnosed cancer of the female reproductive tract in developed countries. Through genome-wide association studies (GWAS), we have previously identified eight risk loci for endometrial cancer. Here, we present a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::1dfae1a85e0882274be821ef3eaf821d
https://openaccess.sgul.ac.uk/id/eprint/110042/1/s41467-018-05427-7.pdf
https://openaccess.sgul.ac.uk/id/eprint/110042/1/s41467-018-05427-7.pdf
Autor:
Temko, D., Gool, I.C. van, Rayner, E., Glaire, M., Makino, S., Brown, M., Chegwidden, L., Palles, C., Depreeuw, J., Beggs, A., Stathopoulou, C., Mason, J., Baker, A.M., Williams, M., Cerundolo, V., Rei, M., Taylor, J.C., Schuh, A., Ahmed, A., Amant, F., Lambrechts, D., Smit, V.T.H.B.M., Bosse, T., Graham, T.A., Church, D.N., Tomlinson, I.
Publikováno v:
Journal of Pathology, 245(3), 283-296
Journal of pathology, 245(3), 283-296. John Wiley and Sons Ltd
The Journal of Pathology
Temko, D, Van Gool, I C, Rayner, E, Glaire, M, Makino, S, Brown, M, Chegwidden, L, Palles, C, Depreeuw, J, Beggs, A, Stathopoulou, C, Mason, J, Baker, A-M, Williams, M, Cerundolo, V, Rei, M, Taylor, J C, Schuh, A, Ahmed, A, Amant, F, Lambrechts, D, Smit, V T, Bosse, T, Graham, T A, Church, D N & Tomlinson, I 2018, ' Somatic POLE exonuclease domain mutations are early events in sporadic endometrial and colorectal carcinogenesis, determining driver mutational landscape, clonal neoantigen burden and immune response ', The Journal of Pathology, vol. 245, no. 3, pp. 283-296 . https://doi.org/10.1002/path.5081
Journal of pathology, 245(3), 283-296. John Wiley and Sons Ltd
The Journal of Pathology
Temko, D, Van Gool, I C, Rayner, E, Glaire, M, Makino, S, Brown, M, Chegwidden, L, Palles, C, Depreeuw, J, Beggs, A, Stathopoulou, C, Mason, J, Baker, A-M, Williams, M, Cerundolo, V, Rei, M, Taylor, J C, Schuh, A, Ahmed, A, Amant, F, Lambrechts, D, Smit, V T, Bosse, T, Graham, T A, Church, D N & Tomlinson, I 2018, ' Somatic POLE exonuclease domain mutations are early events in sporadic endometrial and colorectal carcinogenesis, determining driver mutational landscape, clonal neoantigen burden and immune response ', The Journal of Pathology, vol. 245, no. 3, pp. 283-296 . https://doi.org/10.1002/path.5081
Genomic instability, which is a hallmark of cancer, is generally thought to occur in the middle to late stages of tumourigenesis, following the acquisition of permissive molecular aberrations such as TP53 mutation or whole genome doubling. Tumours wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::f2818dd8ec51574ecc992ecb4bb37de5
http://hdl.handle.net/1887/75545
http://hdl.handle.net/1887/75545
Autor:
Cheng, THT, Thompson, DJ, O'Mara, TA, Painter, JN, Glubb, DM, Flach, S, Lewis, A, French, JD, Freeman-Mills, L, Church, D, Gorman, M, Martin, L, National Study of Endometrial Cancer Genetics Group (NSECG), Hodgson, S, Webb, PM, Australian National Endometrial Cancer Study Group (ANECS), Attia, J, Holliday, EG, McEvoy, M, Scott, RJ, Henders, AK, Martin, NG, Montgomery, GW, Nyholt, DR, Ahmed, S, Healey, CS, Shah, M, Dennis, J, Fasching, PA, Beckmann, MW, Hein, A, Ekici, AB, Hall, P, Czene, K, Darabi, H, Li, J, Dörk, T, Dürst, M, Hillemanns, P, Runnebaum, I, Amant, F, Schrauwen, S, Zhao, H, Lambrechts, D, Depreeuw, J, Dowdy, SC, Goode, EL, Fridley, BL, Winham, SJ, Njølstad, TS, Salvesen, HB, Trovik, J, Werner, HMJ, Ashton, K, Otton, G, Proietto, T, Liu, T, Mints, M, Tham, E, RENDOCAS, CHIBCHA Consortium, Li, MJ, Yip, SH, Wang, J, Bolla, MK, Michailidou, K, Wang, Q, Tyrer, JP, Dunlop, M, Houlston, R, Palles, C, Hopper, JL, AOCS Group, Peto, J, Swerdlow, AJ, Burwinkel, B, Brenner, H, Meindl, A, Brauch, H, Lindblom, A, Chang-Claude, J, Couch, FJ, Giles, GG, Kristensen, VN, Cox, A, Cunningham, JM, Pharoah, PDP, Dunning, AM, Edwards, SL, Easton, DF, Tomlinson, I, Spurdle, AB
Publikováno v:
Nature Genetics
We conducted a meta-analysis of three endometrial cancer genome-wide association studies (GWAS) and two follow-up phases totaling 7,737 endometrial cancer cases and 37,144 controls of European ancestry. Genome-wide imputation and meta-analysis identi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::adc9037f5b68ccd4fb6d96ab697f2376
https://researchonline.lshtm.ac.uk/id/eprint/2551460/1/Cheng_etal_2016_Five_endometrial_cancer_risk_loci_identified_through_genome_wide_association_analysis.pdf
https://researchonline.lshtm.ac.uk/id/eprint/2551460/1/Cheng_etal_2016_Five_endometrial_cancer_risk_loci_identified_through_genome_wide_association_analysis.pdf
Autor:
Painter, J.N., O'Mara, T.A., Batra, J., Cheng, T., Lose, F.A., Dennis, J., Michailidou, K., Tyrer, J.P., Ahmed, S., Ferguson, K., Healey, C.S., Kaufmann, S., Hillman, K.M., Walpole, C., Moya, L., Pollock, P., Jones, A., Howarth, K., Martin, L., Gorman, M., Hodgson, S., Magdalena Echeverry De Polanco, M., Sans, M., Carracedo, A., Castellvi-Bel, S., Rojas-Martinez, A., Santos, E., Teixeira, M.R., Carvajal-Carmona, L., Shu, X-O., Long, J., Zheng, W., Xiang, Y-B., Montgomery, G.W., Webb, P.M., Scott, R.J., McEvoy, M., Attia, J., Holliday, E., Martin, N.G., Nyholt, D.R., Henders, A.K., Fasching, P.A., Hein, A., Beckmann, M.W., Renner, S.P., Doerk, T., Hillemanns, P., Duerst, M., Runnebaum, I., Lambrechts, D., Coenegrachts, L., Schrauwen, S., Amant, F., Winterhoff, B., Dowdy, S.C., Goode, E.L., Teoman, A., Salvesen, H.B., Trovik, J., Njolstad, T.S., Werner, H.M.J., Ashton, K., Proietto, T., Otton, G., Tzortzatos, G., Mints, M., Tham, E., Hall, P., Czene, K., Liu, J., Li, J., Hopper, J.L., Southey, M.C., Ekici, A.B., Ruebner, M., Johnson, N., Peto, J., Burwinkel, B., Marme, F., Brenner, H., Dieffenbach, A.K., Meindl, A., Brauch, H., Lindblom, A., Depreeuw, J., Moisse, M., Chang-Claude, J., Rudolph, A., Couch, F.J., Olson, J.E., Giles, G.G., Bruinsma, F., Cunningham, J.M., Fridley, B.L., Borresen-Dale, A-L., Kristensen, V.N., Cox, A., Swerdlow, A.J., Orr, N., Bolla, M.K., Wang, Q., Weber, R.P., Chen, Z., Shah, M., French, J.D., Pharoah, P.D.P., Dunning, A.M., Tomlinson, I., Easton, D.F., Edwards, S.L., Thompson, D.J., Spurdle, A.B., Canc, N.S.E., Consortium, CHIBCHA, Canc, ANE, RENDOCAS, AOCS, Network, GENICA
Common variants in the hepatocyte nuclear factor 1 homeobox B (HNF1B) gene are associated with the risk of type II diabetes and multiple cancers. Evidence to date indicates that cancer risk may be mediated via genetic or epigenetic effects on HNF1B g
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::052a12e5548d41409adf9220b74cb114
https://openaccess.sgul.ac.uk/id/eprint/107373/1/Fine_mapping_HNF1B_multicancer_locus_identifies_candidate_variants_mediate_endometrial_cancer_risk.pdf
https://openaccess.sgul.ac.uk/id/eprint/107373/1/Fine_mapping_HNF1B_multicancer_locus_identifies_candidate_variants_mediate_endometrial_cancer_risk.pdf
Autor:
Carvajal-Carmona, L.G., O'Mara, T.A., Painter, J.N.., Lose, F.A., Dennis, J., Michailidou, K., Tyrer, J.P., Ahmed, S., Ferguson, K., Healey, C.S., Pooley, K., Beesley, J., Cheng, T., Jones, A., Howarth, K., Martin, L., Gorman, M., Hodgson, S., Wentzensen, N., Fasching, P.A., Hein, A., Beckmann, M.W., Renner, S.P., Doerk, T., Hillemanns, P., Duerst, M., Runnebaum, I., Lambrechts, D., Coenegrachts, L., Schrauwen, S., Amant, F., Winterhoff, B., Dowdy, S.C., Goode, E.L., Teoman, A., Salvesen, H.B., Trovik, J., Njolstad, T.S., Werner, H.M.J., Scott, R.J., Ashton, K., Proietto, T., Otton, G., Wersaell, O., Mints, M., Tham, E., Hall, P., Czene, K., Liu, J., Li, J., Hopper, J.L., Southey, M.C., Ekici, A.B., Ruebner, M., Johnson, N., Peto, J., Burwinkel, B., Marme, F., Brenner, H., Dieffenbach, A.K., Meindl, A., Brauch, H., Lindblom, A., Depreeuw, J., Moisse, M., Chang-Claude, J., Rudolph, A., Couch, F.J., Olson, J.E., Giles, G.G., Bruinsma, F., Cunningham, J.M., Fridley, B.L., Borresen-Dale, A.-L., Kristensen, V.N., Cox, A., Swerdlow, A.J., Orr, N., Bolla, M.K., Wang, Q., Weber, R.P., Chen, Z., Shah, M., Pharoah, P.D.P., Dunning, A.M., Tomlinson, I., Easton, D.F., Spurdle, A.B., Thompson, D.J., NSECG, ANECS, RENDOCAS, AOCS, Network, GENICA
Publikováno v:
Human genetics, vol 134, iss 2
Several studies have reported associations between multiple cancer types and single-nucleotide polymorphisms (SNPs) on chromosome 5p15, which harbours TERT and CLPTM1L, but no such association has been reported with endometrial cancer. To evaluate th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::4220a523555e0091f274e13c67356620
Autor:
Church, D.N., Stelloo, E., Nout, R.A., Valtcheva, N., Depreeuw, J., Haar, N. ter, Noske, A., Amant, F., Tomlinson, I.P.M., Wild, P.J., Lambrechts, D., Jurgenliemk-Schulz, I.M., Jobsen, J.J., Smit, V.T.H.B.M., Creutzberg, C.L., Bosse, T.
Publikováno v:
JNCI: Journal of the National Cancer Institute, 107(1)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::4168e3a004407cb4ab0d171f41e131a5
https://hdl.handle.net/1887/102777
https://hdl.handle.net/1887/102777
Autor:
Cheng, T.H.T., Thompson, D., Painter, J., O'Mara, T., Gorman, M., Martin, L., Palles, C., Jones, A., Buchanan, D.D., Win, A.K., Hopper, J., Jenkins, M., Lindor, N.M., Newcomb, P.A., Gallinger, S., Conti, D., Schumacher, F., Casey, G., Giles, G.G., Pharoah, P., Peto, J., Cox, A., Swerdlow, A., Couch, F., Cunningham, J.M., Goode, E.L., Winham, S.J., Lambrechts, D., Fasching, P., Burwinkel, B., Brenner, H., Brauch, H., Chang-Claude, J., Salvesen, H.B., Kristensen, V., Darabi, H., Li, J., Liu, T., Lindblom, A., Hall, P., Echeverry de Polanco, M., Sans, M., Carracedo, A., Castellvi-Bel, S., Rojas-Martinez, A., Jr, A.S., Teixeira, M.R., Dunning, A.M., Dennis, J., Otton, G., Proietto, T., Holliday, E., Attia, J., Ashton, K., Scott, R.J., McEvoy, M., Dowdy, S.C., Fridley, B.L., Werner, H.M.J., Trovik, J., Njolstad, T.S., Tham, E., Mints, M., Runnebaum, I., Hillemanns, P., Doerk, T., Amant, F., Schrauwen, S., Hein, A., Beckmann, M.W., Ekici, A., Czene, K., Meindl, A., Bolla, M.K., Michailidou, K., Tyrer, J.P., Wang, Q., Ahmed, S., Healey, C.S., Shah, M., Annibali, D., Depreeuw, J., Al-Tassan, N.A., Harris, R., Meyer, B.F., Whiffin, N., Hosking, F.J., Kinnersley, B., Farrington, S.M., Timofeeva, M., Tenesa, A., Campbell, H., Haile, R.W., Hodgson, S., Carvajal-Carmona, L., Cheadle, J.P., Easton, D., Dunlop, M., Houlston, R., Spurdle, A., Tomlinson, I.
Publikováno v:
Scientific reports, 5. Nature Publishing Group
Scientific Reports
Cheng, T H, Thompson, D, Painter, J, O'Mara, T, Gorman, M, Martin, L, Palles, C, Jones, A, Buchanan, D D, Ko Win, A, Hopper, J, Jenkins, M, Lindor, N M, Newcomb, P A, Gallinger, S, Conti, D, Schumacher, F, Casey, G, Giles, G G, Pharoah, P, Peto, J, Cox, A, Swerdlow, A, Couch, F, Cunningham, J M, Goode, E L, Winham, S J, Lambrechts, D, Fasching, P, Burwinkel, B, Brenner, H, Brauch, H, Chang-Claude, J, Salvesen, H B, Kristensen, V, Darabi, H, Li, J, Liu, T, Lindblom, A, Hall, P, de Polanco, M E, Sans, M, Carracedo, A, Castellvi-Bel, S, Rojas-Martinez, A, Aguiar Jnr, S, Teixeira, M R, Dunning, A M, Dennis, J, Otton, G, Proietto, T, Holliday, E, Attia, J, Ashton, K, Scott, R J, McEvoy, M, Dowdy, S C, Fridley, B L, Werner, H M, Trovik, J, Njolstad, T S, Tham, E, Mints, M, Runnebaum, I, Hillemanns, P, Dörk, T, Amant, F, Schrauwen, S, Hein, A, Beckmann, M W, Ekici, A, Czene, K, Meindl, A, Bolla, M K, Michailidou, K, Tyrer, J P, Wang, Q, Ahmed, S, Healey, C S, Shah, M, Annibali, D, Depreeuw, J, Al-Tassan, N A, Harris, R, Meyer, B F, Whiffin, N, Hosking, F J, Kinnersley, B, Farrington, S M, Timofeeva, M, Tenesa, A, Campbell, H, Haile, R W, Hodgson, S, Carvajal-Carmona, L, Cheadle, J P, Easton, D, Dunlop, M, Houlston, R, Spurdle, A & Tomlinson, I 2015, ' Meta-analysis of genome-wide association studies identifies common susceptibility polymorphisms for colorectal and endometrial cancer near SH2B3 and TSHZ1 ', Scientific Reports, vol. 5, 17369 . https://doi.org/10.1038/srep17369
Scientific Reports
Cheng, T H, Thompson, D, Painter, J, O'Mara, T, Gorman, M, Martin, L, Palles, C, Jones, A, Buchanan, D D, Ko Win, A, Hopper, J, Jenkins, M, Lindor, N M, Newcomb, P A, Gallinger, S, Conti, D, Schumacher, F, Casey, G, Giles, G G, Pharoah, P, Peto, J, Cox, A, Swerdlow, A, Couch, F, Cunningham, J M, Goode, E L, Winham, S J, Lambrechts, D, Fasching, P, Burwinkel, B, Brenner, H, Brauch, H, Chang-Claude, J, Salvesen, H B, Kristensen, V, Darabi, H, Li, J, Liu, T, Lindblom, A, Hall, P, de Polanco, M E, Sans, M, Carracedo, A, Castellvi-Bel, S, Rojas-Martinez, A, Aguiar Jnr, S, Teixeira, M R, Dunning, A M, Dennis, J, Otton, G, Proietto, T, Holliday, E, Attia, J, Ashton, K, Scott, R J, McEvoy, M, Dowdy, S C, Fridley, B L, Werner, H M, Trovik, J, Njolstad, T S, Tham, E, Mints, M, Runnebaum, I, Hillemanns, P, Dörk, T, Amant, F, Schrauwen, S, Hein, A, Beckmann, M W, Ekici, A, Czene, K, Meindl, A, Bolla, M K, Michailidou, K, Tyrer, J P, Wang, Q, Ahmed, S, Healey, C S, Shah, M, Annibali, D, Depreeuw, J, Al-Tassan, N A, Harris, R, Meyer, B F, Whiffin, N, Hosking, F J, Kinnersley, B, Farrington, S M, Timofeeva, M, Tenesa, A, Campbell, H, Haile, R W, Hodgson, S, Carvajal-Carmona, L, Cheadle, J P, Easton, D, Dunlop, M, Houlston, R, Spurdle, A & Tomlinson, I 2015, ' Meta-analysis of genome-wide association studies identifies common susceptibility polymorphisms for colorectal and endometrial cancer near SH2B3 and TSHZ1 ', Scientific Reports, vol. 5, 17369 . https://doi.org/10.1038/srep17369
High-risk mutations in several genes predispose to both colorectal cancer (CRC) and endometrial cancer (EC). We therefore hypothesised that some lower-risk genetic variants might also predispose to both CRC and EC. Using CRC and EC genome-wide associ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::5b75206639aba75ebc46825f9288911c
https://pure.amc.nl/en/publications/metaanalysis-of-genomewide-association-studies-identifies-common-susceptibility-polymorphisms-for-colorectal-and-endometrial-cancer-near-sh2b3-and-tshz1(6d4040ab-1937-4431-9398-05908d4da84c).html
https://pure.amc.nl/en/publications/metaanalysis-of-genomewide-association-studies-identifies-common-susceptibility-polymorphisms-for-colorectal-and-endometrial-cancer-near-sh2b3-and-tshz1(6d4040ab-1937-4431-9398-05908d4da84c).html
Autor:
Church, D., Stelloo, E., Nout, R.A., Valtcheva, N., Depreeuw, J., Haar, N. ter, Amant, F., Tomlinson, I.P.M., Wild, P., Smit, V., Creutzberg, C.L., Bosse, T.
Publikováno v:
Publons
International Journal of Gynecological Cancer, 24(9), 1601-1602
International Journal of Gynecological Cancer, 24(9), 1601-1602
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::7e070245aaaf3a0045371826eb1e24fc
https://hdl.handle.net/1887/104600
https://hdl.handle.net/1887/104600
Akademický článek
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Akademický článek
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