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pro vyhledávání: '"Melin, Beatrice S"'
Akademický článek
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Autor:
Andersson, Ulrika, Degerman, Sofie, Dahlin, Anna M., Wibom, Carl, Johansson, Gunnar, Bondy, Melissa L., Melin, Beatrice S.
Publikováno v:
Cancer Causes & Control, 2019 Feb 01. 30(2), 177-185.
Externí odkaz:
https://www.jstor.org/stable/48691285
Autor:
Rosenbaum, Adam, Dahlin, Anna M., Andersson, Ulrika, Björkblom, Benny, Wu, Wendy Yi-Ying, Hedman, Håkan, Wibom, Carl, Melin, Beatrice S.
Publikováno v:
Scientific Reports. 13
Genome-wide association studies (GWAS) have contributed to our understanding of glioma susceptibility. To date, 25 risk loci for development of any of the glioma subtypes are known. However, GWAS studies reveal little about the molecular processes th
Autor:
Choi, Dong-Joo, Armstrong, Georgina, Lozzi, Brittney, Vijayaraghavan, Prashanth, Plon, Sharon E., Wong, Terence C., Boerwinkle, Eric, Muzny, Donna M., Chen, Hsiao-Chi, Gibbs, Richard A., Ostrom, Quinn T., Melin, Beatrice S., Deneen, Benjamin, Bondy, Melissa L., Bainbridge, Matthew N.
Glioma is a rare brain tumor with a poor prognosis. Familial glioma is a subset of glioma with a strong genetic predisposition that accounts for approximately 5% of glioma cases. We performed whole-genome sequencing on an exploratory cohort of 203 in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______264::51991d9dde4bb09ff7c6aef567055565
http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-209881
http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-209881
Autor:
Sjöström, Sara, Hjalmars, Ulf, Juto, Per, Wadell, Göran, Hallmans, Göran, Tjönneland, Anne, Halkjaer, Jytte, Manjer, Jonas, Almquist, Martin, Melin, Beatrice S.
Publikováno v:
Cancer Causes & Control, 2011 Sep 01. 22(9), 1259-1266.
Externí odkaz:
https://www.jstor.org/stable/41485207
I och med utveckling inom storskalig analys av blodprover har man idag insett nyttan av att omvandla biobanker med lagrade humanprover till data-banker där forskare snabbt kan få tillgång till data för att svara på forsknings-frågor. Problemet
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od_______264::e9485366ebc1628082a99a3c217aef76
http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-201292
http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-201292
Autor:
Michaud, Dominique S, Gallo, Valentina, Schlehofer, Brigitte, Tjønneland, Anne, Olsen, Anja, Overvad, Kim, Dahm, Christina C, Teucher, Birgit, Lukanova, Annekatrin, Boeing, Heiner, Schütze, Madlen, Trichopoulou, Antonia, Lagiou, Pagona, Kyrozis, Andreas, Sacerdote, Carlotta, Krogh, Vittorio, Masala, Giovanna, Tumino, Rosario, Mattiello, Amalia, Bueno-de-Mesquita, H Bas, Ros, Martine M, Peeters, Petra HM, van Gils, Carla H, Skeie, Guri, Engeset, Dagrun, Parr, Christine L, Ardanaz, Eva, Chirlaque, Maria-Dolores, Dorronsoro, Miren, Sánchez, Maria José, Argüelles, Marcial, Jakszyn, Paula, Nilsson, Lena M, Melin, Beatrice S, Manjer, Jonas, Wirfält, Elisabet, Khaw, Kay-Tee, Wareham, Nick, Allen, Naomi E, Key, Timothy J, Romieu, Isabelle, Vineis, Paolo, Riboli, Elio
Publikováno v:
In The American Journal of Clinical Nutrition November 2010 92(5):1145-1150
Autor:
Saunders, Charlie N., Cornish, Alex J., Kinnersley, Ben, Law, Philip J., Houlston, Richard S., Claus, Elizabeth B., Il’yasova, Dora, Schildkraut, Joellen, Barnholtz-Sloan, Jill S., Olson, Sara H., Bernstein, Jonine L., Lai, Rose K., Chanock, Stephen, Rajaraman, Preetha, Johansen, Christoffer, Jenkins, Robert B., Melin, Beatrice S., Wrensch, Margaret R., Sanson, Marc, Bondy, Melissa L.
Publikováno v:
Saunders, C N, Cornish, A J, Kinnersley, B, Law, P J, Houlston, R S, Claus, E B, Il’yasova, D, Schildkraut, J, Barnholtz-Sloan, J S, Olson, S H, Bernstein, J L, Lai, R K, Chanock, S, Rajaraman, P, Johansen, C, Jenkins, R B, Melin, B S, Wrensch, M R, Sanson, M, Bondy, M L & Collaborators 2021, ' Searching for causal relationships of glioma : a phenome-wide Mendelian randomisation study ', British Journal of Cancer, vol. 124, no. 2, pp. 447-454 . https://doi.org/10.1038/s41416-020-01083-1
Background The aetiology of glioma is poorly understood. Summary data from genome-wide association studies (GWAS) can be used in a Mendelian randomisation (MR) phenome-wide association study (PheWAS) to search for glioma risk factors. Methods We perf
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e51cfdf11312d8939324d49af9854bc8
https://curis.ku.dk/portal/da/publications/searching-for-causal-relationships-of-glioma(2a649d26-9144-4cee-85f8-c309b2b9ad8c).html
https://curis.ku.dk/portal/da/publications/searching-for-causal-relationships-of-glioma(2a649d26-9144-4cee-85f8-c309b2b9ad8c).html
Autor:
Dahlin, Anna M., Wibom, Carl, Andersson, Ulrika, Bybjerg-Grauholm, Jonas, Deltour, Isabelle, Hougaard, David M., Scheurer, Michael E., Lau, Ching C., McKean-Cowdin, Roberta, Kennedy, Rebekah J., Hung, Long T., Yee, Janis, Margol, Ashley S., Barrington-Trimis, Jessica, Gauderman, W. James, Feychting, Maria, Schüz, Joachim, Röösli, Martin, Kjaerheim, Kristina, Prochazka, Michaela, Adel Fahmideh, Maral, Lannering, Birgitta, Schmidt, Lisbeth S., Johansen, Christoffer, Sehested, Astrid, Kuehni, Claudia, Grotzer, Michael, Tynes, Tore, Eggen, Tone, Klaeboe, Lars, Januszkiewicz-Lewandowska, Danuta, Fichna, Marta, Nowak, Jerzy, Searles Nielsen, Susan, Asgharzadeh, Shahab, Mirabello, Lisa, Hjalmars, Ulf, Melin, Beatrice S.
Publikováno v:
Journal of Neuro-Oncology
Introduction Medulloblastoma is a malignant embryonal tumor of the cerebellum that occurs predominantly in children. To find germline genetic variants associated with medulloblastoma risk, we conducted a genome-wide association study (GWAS) including
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40258d3b80392767e0934ec768326999
http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-168914
http://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-168914
Akademický článek
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