المؤلفون: Svensson, Sara, Zagoras, Theofanis, Aravidis, Christos, Askmalm, Marie Stenmark, Björck, Erik, Borg, Åke, Kuchinskaya, Ekaterina, Nilbert, Mef, Nordling, Margareta, Rohlin, Anna, Silander, Gustav, Lagerstedt-Robinson, Kristina, Gebre-Medhin, Samuel

المصدر: Genes, Chromosomes and Cancer. 61(10):585-591

مصطلحات موضوعية: colorectal cancer, genetic testing, hereditary, polyposis, syndrome, variant classification

وصف الملف: electronic

الوصول الحر: https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-194893Test
https://doi.org/10.1002/gcc.23049Test
https://umu.diva-portal.org/smash/get/diva2:1665135/FULLTEXT02.pdfTest

المؤلفون: Lagerstedt-Robinson, Kristina, Baranowska Korberg, Izabella, Tsiaprazis, Stefanos, Bjorck, Erik, Tham, Emma, Poluha, Anna, Hellstrom Pigg, Maritta, Paulsson-Karlsson, Ylva, Nordenskjold, Magnus, Johansson-Soller, Maria, Aravidis, Christos

المصدر: PLOS ONE. 17(2)

وصف الملف: electronic

الوصول الحر: https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-472741Test
https://doi.org/10.1371/journal.pone.0264056Test
https://uu.diva-portal.org/smash/get/diva2:1652649/FULLTEXT01.pdfTest

المؤلفون: Jiao, Xiang, Aravidis, Christos, Marikkannu, Rajeshwari, Rantala, Johanna, Picelli, Simone, Adamovic, Tatjana, Liu, Tao, Maguire, Paula, Kremeyer, Barbara, Luo, Liping, von Holst, Susanna, Kontham, Vinaykumar, Thutkawkorapin, Jessada, Margolin, Sara, Du, Quan, Lundin, Johanna, Michailidou, Kyriaki, Bolla, Manjeet K, Wang, Qin, Dennis, Joe, Lush, Michael, Ambrosone, Christine B, Andrulis, Irene L, Anton-Culver, Hoda, Antonenkova, Natalia N, Arndt, Volker, Beckmann, Matthias W, Blomqvist, Carl, Blot, William, Boeckx, Bram, Bojesen, Stig E, Bonanni, Bernardo, Brand, Judith S, Brauch, Hiltrud, Brenner, Hermann, Broeks, Annegien, Brüning, Thomas, Burwinkel, Barbara, Cai, Qiuyin, Chang-Claude, Jenny, Couch, Fergus J, Cox, Angela, Cross, Simon S, Deming-Halverson, Sandra L, Devilee, Peter, dos-Santos-Silva, Isabel, Dörk, Thilo, Eriksson, Mikael, Fasching, Peter A, Figueroa, Jonine, Flesch-Janys, Dieter, Flyger, Henrik, Gabrielson, Marike, García-Closas, Montserrat, Giles, Graham G, González-Neira, Anna, Guénel, Pascal, Guo, Qi, Gündert, Melanie, Haiman, Christopher A, Hallberg, Emily, Hamann, Ute, Harrington, Patricia, Hooning, Maartje J, Hopper, John L, Huang, Guanmengqian, Jakubowska, Anna, Jones, Michael E, Kerin, Michael J, Kosma, Veli-Matti, Kristensen, Vessela N, Lambrechts, Diether, Le Marchand, Loic, Lubinski, Jan, Mannermaa, Arto, Martens, John WM, Meindl, Alfons, Milne, Roger L, Mulligan, Anna Marie, Neuhausen, Susan L, Nevanlinna, Heli, Peto, Julian, Pylkäs, Katri, Radice, Paolo, Rhenius, Valerie, Sawyer, Elinor J, Schmidt, Marjanka K, Schmutzler, Rita K, Seynaeve, Caroline, Shah, Mitul, Simard, Jacques, Southey, Melissa C, Swerdlow, Anthony J, Truong, Thérèse, Wendt, Camilla, Winqvist, Robert, Zheng, Wei, Benitez, Javier, Dunning, Alison M, Pharoah, Paul DP

المصدر: Oncotarget. 8(61)

مصطلحات موضوعية: Cancer, Prevention, Breast Cancer, Genetics, Human Genome, Genetic Testing, 2.1 Biological and endogenous factors, Aetiology, familial breast cancer, linkage analysis, risk haplotype, sequencing, NBCS Collaborators, kConFab/AOCS Investigators, Oncology and Carcinogenesis

وصف الملف: application/pdf

الوصول الحر: https://escholarship.org/uc/item/6gx4c4wcTest

المؤلفون: Bengtsson, Daniel, 1975, Joost, Patrick, Aravidis, Christos, Stenmark Askmalm, Marie, Backman, Ann-Sofie, Melin, Beatrice, von Salome, Jenny, Zagoras, Theofanis, Gebre-Medhin, Samuel, Burman, Pia

المصدر: Journal of Clinical Endocrinology and Metabolism. 102(11):3928-3932

وصف الملف: electronic

الوصول الحر: https://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-143246Test
https://liu.diva-portal.org/smash/get/diva2:1160429/FULLTEXT01.pdfTest

المؤلفون: Lagerstedt-Robinson, Kristina, Rohlin, Anna, Aravidis, Christos, Melin, Beatrice, Nordling, Margareta, Stenmark Askmalm, Marie, Lindblom, Annika, Nilbert, M. E. F.

المصدر: Oncology Reports. 36(5):2823-2835

مصطلحات موضوعية: HNPCC, MLH1, MSH2, MSH6, EPCAM, hereditary colorectal cancer, Lynch syndrome

وصف الملف: electronic

الوصول الحر: https://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-132659Test
https://liu.diva-portal.org/smash/get/diva2:1048336/FULLTEXT01.pdfTest

المؤلفون: Olkinuora, Alisa, Nieminen, Taina T., Mårtensson, Emma, Rohlin, Anna, Ristimäki, Ari, Koskenvuo, Laura, Lepistö, Anna, Gebre-Medhin, Samuel, Nordling, Margareta, Peltomäki, Päivi, Silander, Gustav, Kuchinskaya, Ekaterina, Aravidis, Christos, Zagoras, Theofanis, Nilbert, Mef, Borg, Åke

المصدر: Genetics in Medicine ; volume 21, issue 8, page 1868-1873 ; ISSN 1098-3600

مصطلحات موضوعية: Genetics (clinical)

الإتاحة: https://doi.org/10.1038/s41436-018-0405-xTest
http://www.nature.com/articles/s41436-018-0405-x.pdfTest
http://www.nature.com/articles/s41436-018-0405-xTest
https://api.elsevier.com/content/article/PII:S1098360021016130?httpAccept=text/xmlTest
https://api.elsevier.com/content/article/PII:S1098360021016130?httpAccept=text/plainTest

المؤلفون: Karimi, Masoud, von Salome, Jenny, Aravidis, Christos, Silander, Gustav, Askmalm, Marie Stenmark, Henriksson, Isabelle, Gebre-Medhin, Samuel, Frodin, Jan-Erik, Bjorck, Erik, Lagerstedt-Robinson, Kristina, Lindblom, Annika, Tham, Emma

المصدر: Hereditary Cancer in Clinical Practice. 16

مصطلحات موضوعية: Lynch syndrome, MMR genes, Tumour spectrum, Extracolonic

وصف الملف: electronic

الوصول الحر: https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-369904Test
https://uu.diva-portal.org/smash/get/diva2:1272189/FULLTEXT01.pdfTest

المؤلفون: von Salomé, Jenny, Boonstra, Philip S., Karimi, Masoud, Silander, Gustav, Stenmark-Askmalm, Marie, Gebre-Medhin, Samuel, Aravidis, Christos, Nilbert, Mef, Lindblom, Annika, Lagerstedt-Robinson, Kristina

المصدر: PLoS Genetics EpiHealth: Epidemiology for Health BioCARE: Biomarkers in Cancer Medicine improving Health Care, Education and Innovation. 13(10)

مصطلحات موضوعية: Medicin och hälsovetenskap, Medicinska och farmaceutiska grundvetenskaper, Medicinsk genetik, Medical and Health Sciences, Basic Medicine, Medical Genetics, Klinisk medicin, Cancer och onkologi, Clinical Medicine, Cancer and Oncology

الوصول الحر: https://lup.lub.lu.se/record/a6f22508-a8dc-4a44-a9de-5a916fa1a29bTest
http://dx.doi.org/10.1371/journal.pgen.1007012Test

المؤلفون: Jiao, Xiang, Aravidis, Christos, Marikkannu, Rajeshwari, Rantala, Johanna, Picelli, Simone, Adamovic, Tatjana, Liu, Tao, Maguire, Paula, Kremeyer, Barbara, Luo, Liping, Von Holst, Susanna, Kontham, Vinaykumar, Thutkawkorapin, Jessada, Margolin, Sara, Du, Quan, Lundin, Johanna, Michailidou, Kyriaki, Bolla, Manjeet K., Wang, Qin, Dennis, Joe, Lush, Michael, Ambrosone, Christine B., Andrulis, Irene L., Anton-Culver, Hoda, Antonenkova, Natalia N., Arndt, Volker, Beckmann, Matthias W., Blomqvist, Carl, Blot, William, Boeckx, Bram, Bojesen, Stig E., Bonanni, Bernardo, Brand, Judith S., Brauch, Hiltrud, Brenner, Hermann, Broeks, Annegien, Bruning, Thomas, Burwinkel, Barbara, Cai, Qiuyin, Chang-Claude, Jenny, Couch, Fergus J., Cox, Angela, Cross, Simon S., Deming-Halverson, Sandra L., Devilee, Peter, dos-Santos-Silva, Isabel, Dork, Thilo, Eriksson, Mikael, Fasching, Peter A., Nevanlinna, Heli, NBCS Collaborators, kConFab-AOCS Investigators

المساهمون: Department of Oncology, Clinicum, University of Helsinki, HUS Gynecology and Obstetrics, Department of Obstetrics and Gynecology, HUS Comprehensive Cancer Center

مصطلحات موضوعية: familial breast cancer, linkage analysis, risk haplotype, sequencing, DNA-SEQUENCING DATA, WIDE LINKAGE SCAN, GENOME, MUTATIONS, FAMILIES, GENE, ASSOCIATION, EXPRESSION, LOCALIZATION, DISCOVERY, 3122 Cancers, 3123 Gynaecology and paediatrics

وصف الملف: application/pdf

العلاقة: The study was supported by grants provided by the Swedish Cancer Society (Cancerfonden), the Stockholm County Council (ALF project), the Swedish Research Council (Vetenskapsradet), the Stockholm Cancer Society (Radiumhemsfonderna) and Bert von Kantzows and Nilsson-Ehle's foundations. BCAC is funded by Cancer Research UK (C1287/A16563, C1287/A10118), the European Union's Horizon 2020 Research and Innovation Programme (grant numbers 634935 and 633784 for BRIDGES and B-CAST respectively), and by the European Community's Seventh Framework Programme under grant agreement number 223175 (grant number HEALTH-F2-2009-223175) (COGS). Funding for the iCOGS infrastructure came from: the European Community's Seventh Framework Programme under grant agreement no 223175 (HEALTH-F2-2009-223175) (COGS), Cancer Research UK (C1287/A10118, C1287/A10710, C12292/A11174, C1281/A12014, C5047/A8384, C5047/A15007, C5047/A10692, C8197/A16565), the National Institutes of Health (CA128978) and Post-Cancer GWAS initiative (1U19 CA148537, 1U19 CA148065 and 1U19 CA148112 - the GAME-ON initiative), the Department of Defence (W81XWH-10-1-0341), the Canadian Institutes of Health Research (CIHR) for the CIHR Team in Familial Risks of Breast Cancer, Komen Foundation for the Cure, the Breast Cancer Research Foundation, and the Ovarian Cancer Research Fund. Funding of individual BCAC studies is listed in the Supplemental Note.; Jiao , X , Aravidis , C , Marikkannu , R , Rantala , J , Picelli , S , Adamovic , T , Liu , T , Maguire , P , Kremeyer , B , Luo , L , Von Holst , S , Kontham , V , Thutkawkorapin , J , Margolin , S , Du , Q , Lundin , J , Michailidou , K , Bolla , M K , Wang , Q , Dennis , J , Lush , M , Ambrosone , C B , Andrulis , I L , Anton-Culver , H , Antonenkova , N N , Arndt , V , Beckmann , M W , Blomqvist , C , Blot , W , Boeckx , B , Bojesen , S E , Bonanni , B , Brand , J S , Brauch , H , Brenner , H , Broeks , A , Bruning , T , Burwinkel , B , Cai , Q , Chang-Claude , J , Couch , F J , Cox , A , Cross , S S , Deming-Halverson , S L , Devilee , P , dos-Santos-Silva , I , Dork , T , Eriksson , M , Fasching , P A , Nevanlinna , H , NBCS Collaborators & kConFab-AOCS Investigators 2017 , ' PHIP - a novel candidate breast cancer susceptibility locus on 6q14.1 ' , Oncotarget , vol. 8 , no. 61 , pp. 102769-102782 . https://doi.org/10.18632/oncotarget.21800Test; 85035357496; 50e98fd9-61b9-46ec-892d-48cbe5ec266b; http://hdl.handle.net/10138/232516Test; 000419562500006

الإتاحة: http://hdl.handle.net/10138/232516Test

المؤلفون: Kruszka, Paul, Addissie, Yonit A., Yarnell, Colin M. P., Hadley, Donald W., Guillen Sacoto, Maria J., Platte, Petra, Paelecke, Yvonne, Collmann, Hartmut, Snow, Nicole, Schweitzer, Tilmann, Boyadjiev, Simeon A., Aravidis, Christos, Hall, Samantha E., Mulliken, John B., Roscioli, Tony, Muenke, Maximilian

المصدر: American Journal of Medical Genetics. Part A. 170(4):918-929

مصطلحات موضوعية: Muenke syndrome, FGFR3-related craniosynostosis, craniosynostosis

وصف الملف: print

الوصول الحر: https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-307991Test