Zobrazeno 1 - 10
of 256
pro vyhledávání: '"Bickeböller, H."'
Autor:
Rosenberger, A., Tozzi, V., Bickeböller, H., Hung, R.J., Christiani, D.C., Caporaso, N.E., Liu, G., Bojesen, S.E., Le Marchand, L., Albanes, D., Aldrich, M.C., Tardon, A., Fernández-Tardón, G., Rennert, G., Field, J.K., Davies, M., Liloglou, T., Kiemeney, L.A., Lazarus, P., Haugen, A., Zienolddiny, S., Lam, S., Schabath, M.B., Andrew, A.S., Duell, E.J., Arnold, S.M., Brunnström, H., Melander, O., Goodman, G.E., Chen, C., Doherty, J.A., Teare, M.D., Cox, A., Woll, P.J., Risch, A., Muley, T.R., Johansson, M., Brennan, P., Landi, M.T., Shete, S.S., Amos, C.I.
Publikováno v:
BMC Bioinformatics
Background\ud \ud Imputation of untyped markers is a standard tool in genome-wide association studies to close the gap between directly genotyped and other known DNA variants. However, high accuracy with which genotypes are imputed is fundamental. Se
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::5a91c4c846bcd25f6c438ad49483ee79
https://eprints.whiterose.ac.uk/183287/1/s12859-022-04568-3.pdf
https://eprints.whiterose.ac.uk/183287/1/s12859-022-04568-3.pdf
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Background: Evidence from observational studies of telomere length (TL) has been conflicting regarding its direction of association with cancer risk. We investigated the causal relevance of TL for lung and head and neck cancers using Mendelian Random
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::b63c67ddb24d7ba9db9d22d624be9889
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3105943
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:3105943
Autor:
Zuber, V., Bettella, F., Witoelar, A.W., Andreassen, O.A., Mills, I.G., Urbanucci, A., Eeles, R.A., Easton, D.F., Kote-Jarai, Z., Al Olama, A.A., Benlloch, S., Muir, K., Giles, G.G., Wiklund, F., Grönberg, H., Haiman, C.A., Schleutker, J., Weischer, M., Travis, R.C., Neal, D., Pharoah, P., Khaw, K.T., Stanford, J.L., Blot, W.J., Thibodeau, S.N., Maier, C., Kibel, A.S., Cybulski, C., Cannon-Albright, L., Brenner, H., Park, J., Kaneva, R., Batra, J., Teixeira, M.R., Pandha, H., Chenevix-Trench, G., Humphreys, M.K., Hung, R.J., Han, Y., Brennan, P., Bickeböller, H., Rosenberger, A., Houlston, R.S., Caporaso, N., Landi, M.T., Heinrich, J., Risch, A., Wu, X., Ye, Y., Christiani, D.C., Amos, C.I., Michailidou, K., Bolla, M.K., Wang, Q., Berchuck, A., Antoniou, A.C., McGuffog, L., Couch, F.J., Offit, K., Dennis, J., Dunning, A.M., Lee, A., Dicks, E., Luccarini, C., Benítez, J., González-Neira, A., Simard, J., Tessier, D.C., Bacot, F., Vincent, D., Laboissiere, S.
Publikováno v:
Zuber, V, Bettella, F, Witoelar, A, Andreassen, O A, Mills, I G, Urbanucci, A & PRACTICAL Consortium 2017, ' Bromodomain protein 4 discriminates tissue-specific super-enhancers containing disease-specific susceptibility loci in prostate and breast cancer ', BMC Genomics, vol. 18, no. 1, pp. 270 . https://doi.org/10.1186/s12864-017-3620-y
BMC Genomics 18:270 (2017)
BMC Genomics
BMC Genomics 18:270 (2017)
BMC Genomics
Background Epigenetic information can be used to identify clinically relevant genomic variants single nucleotide polymorphisms (SNPs) of functional importance in cancer development. Super-enhancers are cell-specific DNA elements, acting to determine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::133f15c80a2e8e02e0caa94528d115e8
https://doi.org/10.1186/s12864-017-3620-y
https://doi.org/10.1186/s12864-017-3620-y
Autor:
Zuber, V, Bettella, F, Witoelar, A, Andreassen, OA, Mills, IG, Urbanucci, A, Eeles, R, Easton, D, Kote-Jarai, Z, Al Olama, AA, Benlloch, S, Muir, K, Giles, GG, Wiklund, F, Gronberg, H, Haiman, CA, Schleutker, J, Weischer, M, Travis, RC, Neal, D, Pharoah, P, Khaw, KT, Stanford, JL, Blot, WJ, Thibodeau, S, Maier, C, Kibel, AS, Cybulski, C, Cannon-Albright, L, Brenner, H, Park, J, Kaneva, R, Batra, J, Teixeira, MR, Pandha, H, Chenevix-Trench, G, Humphreys, M, Hung, RJ, Han, Y, Brennan, P, Bickeböller, H, Rosenberger, A, Houlston, RS, Caporaso, N, Landi, MT, Heinrich, J, Risch, A, Wu, X, Ye, Y, Christiani, DC, Amos, CI, Easton, DF, Michailidou, K, Bolla, MK, Wang, Q, Berchuck, A, Antoniou, A, McGuffog, L, Couch, F, Offit, K, Dennis, J, Dunning, AM, Lee, A, Dicks, E, Luccarini, C, Benitez, J, Gonzalez-Neira, A, Simard, J, Tessier, DC, Bacot, F, Vincent, D, LaBoissière, S
$\textbf{Background:}$ Epigenetic information can be used to identify clinically relevant genomic variants single nucleotide polymorphisms (SNPs) of functional importance in cancer development. Super-enhancers are cell-specific DNA elements, acting t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f1ebeb9ef5f9a7b2e84b1f49a6e746d
Autor:
Zuber, Verena, Bettella, Francesco, Witoelar, Aree, Andreassen, Ole A., Mills, Ian G., Urbanucci, Alfonso, Eeles, Rosalind, Easton, Doug, Kote-Jarai, Zsofia, Al Olama, Ali Amin, Benlloch, Sara, Muir, Kenneth, Giles, Graham G., Wiklund, Fredrik, Gronberg, Henrik, Haiman, Christopher A., Schleutker, Johanna, Weischer, Maren, Travis, Ruth C., Neal, David, Pharoah, Paul, Khaw, Kay Tee, Stanford, Janet L., Blot, William J., Thibodeau, Stephen, Maier, Christiane, Kibel, Adam S., Cybulski, Cezary, Cannon-Albright, Lisa, Brenner, Hermann, Park, Jong, Kaneva, Radka, Batra, Jyotsna, Teixeira, Manuel R., Pandha, Hardev, Chenevix-Trench, Georgia, Humphreys, Manjeet, Hung, R. J., Han, Y., Brennan, P., Bickeböller, H., Rosenberger, A., Houlston, R. S., Caporaso, N., Landi, M. T., Wu, X., Wang, Qin, Bojesen, Stig E., Nielsen, Sune F., Nordestgaard, Borge G.
Publikováno v:
Zuber, V, Bettella, F, Witoelar, A, Andreassen, O A, Mills, I G, Urbanucci, A, Eeles, R, Easton, D, Kote-Jarai, Z, Al Olama, A A, Benlloch, S, Muir, K, Giles, G G, Wiklund, F, Gronberg, H, Haiman, C A, Schleutker, J, Weischer, M, Travis, R C, Neal, D, Pharoah, P, Khaw, K T, Stanford, J L, Blot, W J, Thibodeau, S, Maier, C, Kibel, A S, Cybulski, C, Cannon-Albright, L, Brenner, H, Park, J, Kaneva, R, Batra, J, Teixeira, M R, Pandha, H, Chenevix-Trench, G, Humphreys, M, Hung, R J, Han, Y, Brennan, P, Bickeböller, H, Rosenberger, A, Houlston, R S, Caporaso, N, Landi, M T, Wu, X, Wang, Q, Bojesen, S E, Nielsen, S F, Nordestgaard, B G & the PRACTICAL Consortium, the COGS-CRUK GWAS, the BCAC Consortium, the TRICL Consortium 2017, ' Bromodomain protein 4 discriminates tissue-specific super-enhancers containing disease-specific susceptibility loci in prostate and breast cancer ', BMC Genomics, vol. 18, 270 . https://doi.org/10.1186/s12864-017-3620-y
Background: Epigenetic information can be used to identify clinically relevant genomic variants single nucleotide polymorphisms (SNPs) of functional importance in cancer development. Super-enhancers are cell-specific DNA elements, acting to determine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2751::8a71837b67e1f9184628fb7a4cdaa450
https://curis.ku.dk/portal/da/publications/bromodomain-protein-4-discriminates-tissuespecific-superenhancers-containing-diseasespecific-susceptibility-loci-in-prostate-and-breast-cancer(00cec9f4-a609-4444-80a8-ec33d2d98e63).html
https://curis.ku.dk/portal/da/publications/bromodomain-protein-4-discriminates-tissuespecific-superenhancers-containing-diseasespecific-susceptibility-loci-in-prostate-and-breast-cancer(00cec9f4-a609-4444-80a8-ec33d2d98e63).html
Autor:
Li, Y., Xiao, X., Han, Y., Gorlova, O., Qian, D., Leigh, N., Johansen, J.S., Barnett, M., Chen, C., Goodman, G., Cox, A., Taylor, F., Woll, P., Wichmann, H.E., Manz, J., Muley, T., Risch, A., Rosenberger, A., Arnold, S.M., Haura, E.B., Bolca, C., Holcatova, I., Janout, V., Kontic, M., Lissowska, J., Mukeria, A., Ognjanovic, S., Orlowski, T.M., Scelo, G., Swiatkowska, B., Zaridze, D., Bakke, Per S., Skaug, Vidar, Zienolddiny, Shanbeh, Duell, E.J., Butler, L.M., Houlston, R., Artigas, M.S., Grankvist, K., Johansson, M., Shepherd, F.A., Marcus, M.W., Brunnström, H., Manjer, J., Melander, O., Muller, D.C., Overvad, K., Trichopoulou, A., Tumino, R., Liu, G., Bojesen, S.E., Wu, X., Le Marchand, L., Albanes, D., Bickeböller, H., Aldric, M.C., Bush, W.S., Tardon, A., Rennert, G., Teare, M.D., Field, J.K., Kiemeney, L.A., Lazarus, P., Haugen, Aage, Lam, S., Scabath, M.B., Andrew, A.S., Bertazzi, P.A., Pesatori, A.C., Christiani, D.C., Caporaso, N., McKay, J.D., Brennan, P., Hung, R.J., Amos, C.I.
Externí odkaz:
https://hdl.handle.net/11250/3149616
Autor:
Malzahn, D., Müller-Nurasyid, M., Heid, I.M., Wichmann, H.-E., Bickeböller, H., KORA Study Group (Gieger, C., Grallert, H., Heinrich, J., Holle, R., Leidl, R., Meisinger, C., Peters, A., Strauch, K.)
Publikováno v:
Eur. J. Hum. Genet. 22, 1217-1224 (2014)
Among the single-nucleotide polymorphisms (SNPs) previously reported to be associated with body mass index (BMI) and obesity, we focus on a common risk variant rs7566605 upstream of the insulin-induced gene 2 (INSIG2) gene and a rare protective varia
Autor:
Fischer, C.1 cfischer@uni-hd.de, Bickeböller, H.2
Publikováno v:
Medizinische Genetik. Jun2007, Vol. 19 Issue 2, p245-249. 5p.
Autor:
Köhler, K.1 karola.koehler@medizin.uni-goettingen.de, Bickeböller, H.1
Publikováno v:
Annals of Human Genetics. Jan2006, Vol. 70 Issue 1, p98-115. 18p. 4 Charts, 3 Graphs.