Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Maranian Mel J"'
Autor:
Abraham Jean E, Maranian Mel J, Spiteri Inmaculada, Russell Roslin, Ingle Susan, Luccarini Craig, Earl Helena M, Pharoah Paul PD, Dunning Alison M, Caldas Carlos
Publikováno v:
BMC Medical Genomics, Vol 5, Iss 1, p 19 (2012)
Abstract Background The increasing trend for incorporation of biological sample collection within clinical trials requires sample collection procedures which are convenient and acceptable for both patients and clinicians. This study investigated the
Externí odkaz:
https://doaj.org/article/ec892ec30f254150b33d22483caacf3b
Autor:
Maranian, Mel J, Snead, Martin P
Publikováno v:
Eye. 37:388-390
The relationship between the vitreous body, posterior vitreous detachment (PVD) and retina has been the focus of much research for over a hundred years [1-10 and references therein] and yet in spite of such prolonged investigation, there is still muc
Autor:
Maranian, Mel J., Snead, Martin P.
Publikováno v:
Eye; February 2023, Vol. 37 Issue: 3 p388-390, 3p
Autor:
Thompson, Deborah J, O'Mara, Tracy A, Glubb, Dylan M, Painter, Jodie N, Cheng, Timothy, Folkerd, Elizabeth, Doody, Deborah, Dennis, Joe, Webb, Penelope M, Gorman, Maggie, Martin, Lynn, Hodgson, Shirley, Michailidou, Kyriaki, Tyrer, Jonathan P, Maranian, Mel J, Hall, Per, Czene, Kamila, Darabi, Hatef, Li, Jingmei, Fasching, Peter A, Hein, Alexander, Beckmann, Matthias W, Ekici, Arif B, Dörk, Thilo, Hillemanns, Peter, Dürst, Matthias, Runnebaum, Ingo, Zhao, Hui, Depreeuw, Jeroen, Schrauwen, Stefanie, Amant, Frederic, Goode, Ellen L, Fridley, Brooke L, Dowdy, Sean C, Winham, Stacey J, Salvesen, Helga B, Trovik, Jone, Njolstad, Tormund S, Werner, Henrica M J, Ashton, Katie, Proietto, Tony, Otton, Geoffrey, Carvajal-Carmona, Luis, Tham, Emma, Liu, Tao, Mints, Miriam, Scott, Rodney J, McEvoy, Mark, Attia, John, Holliday, Elizabeth G, Montgomery, Grant W, Martin, Nicholas G, Nyholt, Dale R, Henders, Anjali K, Hopper, John L, Traficante, Nadia, Ruebner, Matthias, Swerdlow, Anthony J, Burwinkel, Barbara, Brenner, Hermann, Meindl, Alfons, Brauch, Hiltrud, Lindblom, Annika, Lambrechts, Diether, Chang-Claude, Jenny, Couch, Fergus J, Giles, Graham G, Kristensen, Vessela N, Cox, Angela, Bolla, Manjeet K, Wang, Qin, Bojesen, Stig E, Shah, Mitul, Luben, Robert, Khaw, Kay-Tee, Pharoah, Paul D P, Dunning, Alison M, Tomlinson, Ian, Dowsett, Mitch, Easton, Douglas F, Spurdle, Amanda B
Publikováno v:
Endocrine-related cancer, 23(2), 77-91. Society for Endocrinology
Endocrine-Related Cancer
Endocrine-Related Cancer
Candidate gene studies have reported CYP19A1 variants to be associated with endometrial cancer and with estradiol (E2) concentrations. We analyzed 2937 single nucleotide polymorphisms (SNPs) in 6608 endometrial cancer cases and 37 925 controls and re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::b3c15d7543a25a173aee6b7b115afce8
https://lirias.kuleuven.be/handle/123456789/530065
https://lirias.kuleuven.be/handle/123456789/530065
Autor:
Thompson, Deborah J, O'Mara, Tracy A, Glubb, Dylan M, Painter, Jodie N, Cheng, Timothy, Folkerd, Elizabeth J, Doody, Deborah, Dennis, Joe, Webb, Penelope M, Gorman, Maggie, Martin, Lynn, Hodgson, Shirley, Michailidou, Kyriaki, Tyrer, Jonathan P, Maranian, Mel J, Hall, Per, Czene, Kamila, Darabi, Hatef, Li, Jingmei, Fasching, Peter A, Hein, Alexander, Beckmann, Matthias W, Ekici, Arif B, Doerk, Thilo, Hillemanns, Peter, Durst, Matthias, Runnebaum, Ingo, Zhao, Hui, Depreeuw, Jeroen, Schrauwen, Stefanie, Amant, Frederic, Goode, Ellen L, Fridley, Brooke L, Dowdy, Sean C, Winham, Stacey J, Salvesen, Helga B, Trovik, Jone, Njolstad, Tormund S, Werner, Henrica M J, Ashton, Katie, Proietto, Tony, Otton, Geoffrey, Carvajal-carmona, Luis, Tham, Emma, Liu, Tao, Mints, Miriam, Scott, Rodney J, McEvoy, Mark G, Attia, John R, Holliday, Elizabeth G, Montgomery, Grant W., Martin, Nicholas G., Nyholt, Dale R, Henders, Anjali K, Hopper, John L, Traficante, Nadia, Ruebner, Matthias, Swerdlow, Anthony J, Burwinkel, Barbara, Brenner, Hermann, Meindl, Alfons, Brauch, Hiltrud, Lindblom, Annika, Lambrechts, Diether, Chang-Claude, Jenny, Couch, Fergus J, Giles, Graham, Kristensen, Vessela N, Cox, Angela, Bolla, Manjeet K, Wang, Qin, Bojesen, Stig E, Shah, Mitul, Luben, Robert, Khaw, Kay-Tee, Pharoah, Paul P D, Dunning, Alison M, Tomlinson, Ian, Dowsett, Mitch, Easton, Douglas F, Spurdle, Amanda B
Publikováno v:
Thompson, D J, O'Mara, T A, Glubb, D M, Painter, J N, Cheng, T, Folkerd, E J, Doody, D, Dennis, J, Webb, P M, Gorman, M, Martin, L, Hodgson, S, Michailidou, K, Tyrer, J P, Maranian, M J, Hall, P, Czene, K, Darabi, H, Li, J, Fasching, P A, Hein, A, Beckmann, M W, Ekici, A B, Doerk, T, Hillemanns, P, Durst, M, Runnebaum, I, Zhao, H, Depreeuw, J, Schrauwen, S, Amant, F, Goode, E L, Fridley, B L, Dowdy, S C, Winham, S J, Salvesen, H B, Trovik, J, Njolstad, T S, Werner, H M J, Ashton, K, Proietto, T, Otton, G, Carvajal-carmona, L, Tham, E, Liu, T, Mints, M, Scott, R J, McEvoy, M G, Attia, J R, Holliday, E G, Montgomery, G W, Martin, N G, Nyholt, D R, Henders, A K, Hopper, J L, Traficante, N, Ruebner, M, Swerdlow, A J, Burwinkel, B, Brenner, H, Meindl, A, Brauch, H, Lindblom, A, Lambrechts, D, Chang-Claude, J, Couch, F J, Giles, G, Kristensen, V N, Cox, A, Bolla, M K, Wang, Q, Bojesen, S E, Shah, M, Luben, R, Khaw, K-T, Pharoah, P P D, Dunning, A M, Tomlinson, I, Dowsett, M, Easton, D F & Spurdle, A B 2016, ' CYP19A1 fine-mapping and Mendelian randomization ', Endocrine-Related Cancer, vol. 23, pp. 77-91 . https://doi.org/10.1530/ERC-15-0386
Candidate gene studies have reported CYP19A1 variants to be associated with endometrial cancer and with estradiol (E2) concentrations. We analyzed 2937 single nucleotide polymorphisms (SNPs) in 6608 endometrial cancer cases and 37 925 controls and re
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2751::b9fff2f6f34608934378104e2ca23abe
https://curis.ku.dk/ws/files/179630304/77.full.pdf
https://curis.ku.dk/ws/files/179630304/77.full.pdf
Autor:
Michailidou, Kyriaki, Beesley, Jonathan, Lindstrom, Sara, Canisius, Sander, Dennis, Joe, Lush, Michael J., Maranian, Mel J., Bolla, Manjeet K., Wang, Qin, Shah, Mitul, Perkins, Barbara J., Czene, Kamila, Eriksson, Mikael, Darabi, Hatef, Brand, Judith S., Bojesen, Stig E., Nordestgaard, Borge G., Flyger, Henrik, Nielsen, Sune F., Rahman, Nazneen, Turnbull, Clare, Fletcher, Olivia, Peto, Julian, Gibson, Lorna, dos-Santos-Silva, Isabel, Chang-Claude, Jenny, Flesch-Janys, Dieter, Rudolph, Anja, Eilber, Ursula, Behrens, Sabine, Nevanlinna, Heli, Muranen, Taru A., Aittomaki, Kristiina, Blomqvist, Carl, Khan, Sofia, Aaltonen, Kirsimari, Ahsan, Habibul, Kibriya, Muhammad G., Whittemore, Alice S., John, Esther M., Malone, Kathleen E., Gammon, Marilie D., Santella, Regina M., Ursin, Giske, Makalic, Enes, Schmidt, Daniel F., Casey, Graham, Hunter, David J., van der Luijt, Rob B., Peeters, Petra, BOCS, KConFab Investigators, AOCS Grp, NBCS, GENICA Network
Genome-wide association studies (GWAS) and large-scale replication studies have identified common variants in 79 loci associated with breast cancer, explaining similar to 14% of the familial risk of the disease. To identify new susceptibility loci, w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_____10691::970bd07788c5264c61271499b0bc7ef0
https://dspace.library.uu.nl/handle/1874/331634
https://dspace.library.uu.nl/handle/1874/331634
Autor:
Glubb, Dylan M., Maranian, Mel J., Michailidou, Kyriaki, Pooley, Karen A., Meyer, Kerstin B., Kar, Siddhartha, Carlebur, Saskia, O'Reilly, Martin, Betts, Joshua A., Hillman, Kristine M., Kaufmann, Susanne, Beesley, Jonathan, Canisius, Sander, Hopper, John L., Southey, Melissa C., Tsimiklis, Helen, Apicella, Carmel, Schmidt, Marjanka K., Broeks, Annegien, Hogervorst, Frans B., van der Schoot, C. Ellen, Muir, Kenneth, Lophatananon, Artitaya, Stewart-Brown, Sarah, Siriwanarangsan, Pornthep, Fasching, Peter A., Ruebner, Matthias, Ekici, Arif B., Beckmann, Matthias W., Peto, Julian, Dos-Santos-Silva, Isabel, Fletcher, Olivia, Johnson, Nichola, Pharoah, Paul D. P., Bolla, Manjeet K., Wang, Qin, Dennis, Joe, Sawyer, Elinor J., Tomlinson, Ian, Kerin, Michael J., Miller, Nicola, Burwinkel, Barbara, Marme, Frederik, Yang, Rongxi, Surowy, Harald, Guenel, Pascal, Nevanlinna, Heli, Muranen, Taru A., Aittomäki, Kristiina, Blomqvist, Carl, GENICA Network, kConFab Investigators, Norwegian Breast Canc Study
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1593::6f6b9688c002c3f2b996d29ca366b078
http://hdl.handle.net/10138/203748
http://hdl.handle.net/10138/203748
Autor:
Glubb, Dylan M, Maranian, Mel J, Michailidou, Kyriaki, Pooley, Karen A, Meyer, Kerstin B, Kar, Siddhartha, Carlebur, Saskia, O'Reilly, Martin, Betts, Joshua A, Hillman, Kristine M, Orr, Nicholas
Publikováno v:
Glubb, D M, Maranian, M J, Michailidou, K, Pooley, K A, Meyer, K B, Kar, S, Carlebur, S, O'Reilly, M, Betts, J A, Hillman, K M & Orr, N 2015, ' Fine-Scale Mapping of the 5q11.2 Breast Cancer Locus Reveals at Least Three Independent Risk Variants Regulating MAP3K1 ', The American Journal of Human Genetics, vol. 96, no. 1, pp. 5-20 . https://doi.org/10.1016/j.ajhg.2014.11.009
Genome-wide association studies (GWASs) have revealed SNP rs889312 on 5q11.2 to be associated with breast cancer risk in women of European ancestry. In an attempt to identify the biologically relevant variants, we analyzed 909 genetic variants across
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2607::c1b22c94037a2714db3c8b616d4b0b9a
https://pure.qub.ac.uk/en/publications/finescale-mapping-of-the-5q112-breast-cancer-locus-reveals-at-least-three-independent-risk-variants-regulating-map3k1(5391af09-27e1-4464-8da6-9f4d80674c39).html
https://pure.qub.ac.uk/en/publications/finescale-mapping-of-the-5q112-breast-cancer-locus-reveals-at-least-three-independent-risk-variants-regulating-map3k1(5391af09-27e1-4464-8da6-9f4d80674c39).html
Autor:
Rahman, Nazneen, Lush, Michael J, Bojesen, Stig E, Wang, Qin, Nordestgaard, Børge G, Maranian, Mel J, Turnbull, Clare, Bolla, Manjeet K, Shah, Mitul, Brand, Judith S, Darabi, Hatef, Lindstrom, Sara, Eilber, Ursula, Perkins, Barbara J, Nevanlinna, Heli, Beesley, Jonathan, Dennis, Joe, Nielsen, Sune F, Behrens, Sabine, Michailidou, Kyriaki, Flesch-Janys, Dieter, dos-Santos-Silva, Isabel, Czene, Kamila, Flyger, Henrik, Muranen, Taru A, Canisius, Sander, Chang-Claude, Jenny, Fletcher, Olivia, Eriksson, Mikael, Gibson, Lorna, Peto, Julian, Rudolph, Anja
Genome wide association studies (GWAS) and large scale replication studies have identified common variants in 79 loci associated with breast cancer, explaining ~14% of the familial risk of the disease. To identify new susceptibility loci, we performe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e1063ebdd764232fa12685f160c0f18e
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