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European Journal of Human Genetics, ISSN 1018-4813, 01/2016, Volume 24, Issue 1, pp. 99 - 105
Journal Article
by Antoniou, Antonis C and Wang, Xianshu and Fredericksen, Zachary S and McGuffog, Lesley and Tarrell, Robert and Sinilnikova, Olga M and Healey, Sue and Morrison, Jonathan and Kartsonaki, Christiana and Lesnick, Timothy and Ghoussaini, Maya and Barrowdale, Daniel and Peock, Susan and Cook, Margaret and Oliver, Clare and Frost, Debra and Eccles, Diana and Evans, D. Gareth and Eeles, Ros and Izatt, Louise and Chu, Carol and Douglas, Fiona and Paterson, Joan and Stoppa-Lyonnet, Dominique and Houdayer, Claude and Mazoyer, Sylvie and Giraud, Sophie and Lasset, Christine and Remenieras, Auey and Caron, Olivier and Hardouin, Agnès and Berthet, Pascaline and Hogervorst, Frans B. L and Rookus, Matti A and Jager, Agnes and van den Ouweland, Ans and Hoogerbrugge, Nicoline and van der Luijt, Rob B and Meijers-Heijboer, Hanne and Gómez García, Encarna B and Devilee, Peter and Vreeswijk, Maaike P. G and Lubinski, Jan and Jakubowska, Anna and Gronwald, Jacek and Huzarski, Tomasz and Byrski, Tomasz and Górski, Bohdan and Cybulski, Cezary and Spurdle, Amanda B and Holland, Helene and Goldgar, David E and John, Esther M and Hopper, John L and Southey, Melissa and Buys, Sauna S and Daly, Mary B and Terry, Mary-Beth and Schmutzler, Rita K and Wappenschmidt, Barbara and Engel, Christoph and Meindl, Alfons and Preisler-Adams, Sabine and Arnold, Norbert and Niederacher, Dieter and Sutter, Christian and Domchek, Susan M and Nathanson, Katherine L and Rebbeck, Timothy and Blum, Joanne L and Piedmonte, Marion and Roiguez, Gustavo C and Wakeley, Katie and Boggess, John F and Basil, Jack and Blank, Stephanie V and Friedman, Eitan and Kaufman, Bella and Laitman, Yael and Milgrom, Roni and Anulis, Irene L and Glendon, Gord and Ozcelik, Hilmi and Kirchhoff, Tomas and Vijai, Joseph and Gaudet, Mia M and Altshuler, David and Guiducci, Candace and Loman, Niklas and Harbst, Katja and Rantala, Johanna and Ehrencrona, Hans and Gerdes, Anne-Marie and Thomassen, Mads and Sunde, Lone and Peterlongo, Paolo and Manoukian, Siranoush and Bonanni, Bernardo and Viel, Alessana and Radice, Paolo and ... and KConFab and EMBRACE and GEMO Study Collaborators and GENICA and MOD SQUAD and HEBON and SWE-BRCA and kConFab and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Institutionen för genetik och patologi and Uppsala universitet
Nature genetics, ISSN 1061-4036, 2010, Volume 42, Issue 10, pp. 885 - 892
Journal Article
by Couch, Fergus J and Wang, Xianshu and McGuffog, Lesley and Lee, Anew and Olswold, Curtis and Kuchenbaecker, Karoline B and Soucy, Penny and Fredericksen, Zachary and Barrowdale, Daniel and Dennis, Joe and Gaudet, Mia M and Dicks, Ed and Kosel, Matthew and Healey, Sue and Sinilnikova, Olga M and Lee, Adam and Bacot, François and Vincent, Daniel and Hogervorst, Frans B. L and Peock, Susan and Stoppa-Lyonnet, Dominique and Jakubowska, Anna and Radice, Paolo and Schmutzler, Rita Katharina and Domchek, Susan M and Piedmonte, Marion and Singer, Christian F and Friedman, Eitan and Thomassen, Mads and Hansen, Thomas V. O and Neuhausen, Susan L and Szabo, Csilla I and Blanco, Ignacio and Greene, Mark H and Karlan, Beth Y and Garber, Judy and Phelan, Catherine M and Weitzel, Jeffrey N and Montagna, Marco and Olah, Edith and Anulis, Irene L and Godwin, Anew K and Yannoukakos, koulis and Goldgar, David E and Caldes, Trinidad and Nevanlinna, Heli and Osorio, Ana and Terry, Mary Beth and Daly, Mary B and van Rensburg, Elizabeth J and Hamann, Ute and Ramus, Susan J and Toland, Amanda Ewart and Caligo, Maria A and Olopade, Olufunmilayo I and Tung, Nadine and Claes, Kathleen and Beattie, Mary S and Southey, Melissa C and Imyanitov, Evgeny N and Tischkowitz, Marc and Janavicius, Ramunas and John, Esther M and Kwong, Ava and Diez, Orland and Balmaña, Judith and Barkardottir, Rosa B and Arun, Banu K and Rennert, Gad and teo, Soo-Hwang and Ganz, Patricia A and Campbell, Ian and van der Hout, Annemarie H and van Deurzen, Carolien H. M and Seynaeve, Caroline and Gómez Garcia, Encarna B and van Leeuwen, Flora E and Meijers-Heijboer, Hanne E. J and Gille, Johannes J. P and Ausems, Margreet G. E. M and Blok, Marinus J and Ligtenberg, Marjolijn J. L and Rookus, Matti A and Devilee, Peter and Verhoef, Senno and van Os, Theo A. M and Wijnen, Juul T and Frost, Debra and Ellis, Steve and Fineberg, Elena and Platte, Radka and Evans, D. Gareth and Izatt, Louise and Eeles, Rosalind A and Adlard, Julian and Eccles, Diana M and Cook, Jackie and Brewer, Carole and Douglas, Fiona and Hodgson, Shirley and ... and KConFab Investigators and Ontario Canc Genetics Network and EMBRACE and GEMO Study Collaborators and CIMBA and HEBON and BCFR and SWE-BRCA and Ontario Cancer Genetics Network and kConFab Investigators and on behalf of CIMBA and Linköpings universitet and Institutionen för klinisk och experimentell medicin and Onkologi and Hälsouniversitetet
PLoS genetics, ISSN 1553-7390, 2013, Volume 9, Issue 3, p. e1003212
Journal Article
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 10/2011, Volume 19, Issue 10, pp. 1052 - 1058
Journal Article
Journal Article
by Thion, Morgane Sonia and Tézenas Du Montcel, Sophie and Golmard, Jean-Louis and Vacher, Sophie and Barjhoux, Laure and Sornin, Valérie and Cazeneuve, Cécile and Bièche, Ivan and Sinilnikova, Olga and Stoppa-Lyonnet, Dominique and Durr, Alexandra and Humbert, Sandrine and Sinilnikova, Olga and Mazoyer, Sylvie and Damiola, Francesca and Barjhoux, Laure and Verny-Pierre, Carole and Calender, Alain and Giraud, Sophie and Léone, Mélanie and Stoppa-Lyonnet, Dominique and Gauthier-Villars, Marion and Buecher, Bruno and Houdayer, Claude and Moncoutier, Virginie and Belotti, Muriel and Tirapo, Carole and De Pauw, Antoine and Bressac-De-Paillerets, Brigitte and Caron, Olivier and Bignon, Yves-Jean and Uhrhammer, Nancy and Lasset, Christine and Bonadona, Valérie and Handallou, Sandrine and Hardouin, Agnès and Berthet, Pascaline and Sobol, Hagay and Bourdon, Violaine and Noguchi, Tetsuro and Remenieras, Audrey and Eisinger, François and Coupier, Isabelle and Pujol, Pascal and Peyrat, Jean-Philippe and Fournier, Joëlle and Révillion, Françoise and Vennin, Philippe and Adenis, Claude and Rouleau, Etienne and Lidereau, Rosette and Demange, Liliane and Nogues, Catherine and Muller, Danièle and Fricker, Jean-Pierre and Barouk-Simonet, Emmanuelle and Bonnet, Françoise and Bubien, Virginie and Sevenet, Nicolas and Longy, Michel and Toulas, Christine and Guimbaud, Rosine and Gladieff, Laurence and Feillel, Viviane and Leroux, Dominique and Dreyfus, Hélène and Rebischung, Christine and Peysselon, Magalie and Coron, Fanny and Faivre, Laurence and Prieur, Fabienne and Lebrun, Marine and Kientz, Caroline and Ferrer, Sandra Fert and Frénay, Marc and Vénat-Bouvet, Laurence and Delnatte, Capucine and Mortemousque, Isabelle and Coulet, Florence and Colas, Chrystelle and Soubrier, Florent and Sokolowska, Johanna and Bronner, Myriam and Collonge-Rame, Marie-Agnès and Damette, Alexandre and Lynch, Henry T and Snyder, Carrie L and GEMO and for GEMO
European Journal of Human Genetics, ISSN 1018-4813, 08/2016, Volume 24, Issue 9, pp. 1310 - 1315
Journal Article
by Antoniou, Antonis C and Beesley, Jonathan and McGuffog, Lesley and Sinilnikova, Olga M and Healey, Sue and Neuhausen, Susan L and Ding, Yuan Chun and Rebbeck, Timothy R and Weitzel, Jeffrey N and Lynch, Henry T and Isaacs, Claudine and Ganz, Patricia A and Tomlinson, Gail and Olopade, Olufunmilayo I and Couch, Fergus J and Wang, Xianshu and Lindor, Noralane M and Pankratz, Vernon S and Radice, Paolo and Manoukian, Siranoush and Peissel, Bernard and Zaffaroni, Daniela and Barile, Monica and Viel, Alessana and Allavena, Anna and Dall'olio, Valentina and Peterlongo, Paolo and Szabo, Csilla I and Zikan, Michal and Claes, Kathleen and Poppe, Bruce and Foretova, Lenka and Mai, Phuong L and Greene, Mark H and Rennert, Gad and Lejbkowicz, Flavio and Glendon, Gord and Ozcelik, Hilmi and Anulis, Irene L and Thomassen, Mads and Gerdes, Anne-Marie and Sunde, Lone and Cruger, Dorthe and Birk Jensen, Uffe and Caligo, Maria and Friedman, Eitan and Kaufman, Bella and Laitman, Yael and Milgrom, Roni and Dubrovsky, Maya and Cohen, Shimrit and Borg, Ake and Jernström, Helena and Lindblom, Annika and Rantala, Johanna and Stenmark-Askmalm, Marie and Melin, Beatrice and Nathanson, Kate and Domchek, Susan and Jakubowska, Ania and Lubinski, Jan and Huzarski, Tomasz and Osorio, Ana and Lasa, Aiana and Durán, Mercedes and Tejada, Maria-Isabel and Godino, Javier and Benitez, Javier and Hamann, Ute and Kriege, Mieke and Hoogerbrugge, Nicoline and Luijt, Rob B. van der and Asperen, Christi J. van and Devilee, Peter and Meijers-Heijboer, E. J and Blok, Marinus J and Aalfs, Cora M and Hogervorst, Frans and Rookus, Matti and Cook, Margaret and Oliver, Clare and Frost, Debra and Conroy, Don and Evans, D. Gareth and Lalloo, Fiona and Pichert, Gabriella and Davidson, Rosemarie and Cole, Trevor and Cook, Jackie and Paterson, Joan and Hodgson, Shirley and Morrison, Patrick J and Porteous, Mary E and Walker, Lisa and Kennedy, M. John and Dorkins, Huw and Peock, Susan and Godwin, Anew K and Stoppa-Lyonnet, Dominique and Pauw, Antoine de and ... and Ontario Canc Genetics Network and EMBRACE and CIMBA and GEMO and HEBON and Breast Canc Family Registry and kConFab and SWE-BRCA and Ontario Cancer Genetics Network and Breast Cancer Family Registry and for kConFab and for EMBRACE and for HEBON and for SWE-BRCA and for GEMO and on behalf of CIMBA and for the Ontario Cancer Genetics Network and for the Breast Cancer Family Registry
Cancer research, ISSN 0008-5472, 2010, Volume 70, Issue 23, pp. 9742 - 9754
The known breast cancer susceptibility polymorphisms in FGFR2, TNRC9/TOX3, MAP3K1, LSP1, and 2q35 confer increased risks of breast cancer for BRCA1 or BRCA2... 
LOCI | VARIANTS | ONCOLOGY | ESTROGEN-RECEPTOR | GENOME-WIDE ASSOCIATION | Genetic Predisposition to Disease - genetics | Risk Assessment | Humans | Middle Aged | Risk Factors | Sodium-Bicarbonate Symporters - genetics | Vesicular Transport Proteins - genetics | Genotype | Receptors, Progesterone - genetics | BRCA1 Protein - genetics | Breast Neoplasms - genetics | Breast Neoplasms - pathology | Alleles | Survival Analysis | Aged, 80 and over | Adult | Female | Heterozygote | Aged | Polymorphism, Single Nucleotide | Mutation | BRCA2 Protein - genetics | genetic counseling | genome-wide association study | penetrance | common variant | BRCA1 | BRCA2 | genetic modifier | risk assessment | Medical and Health Sciences | Medicin och hälsovetenskap | single nucleotide polymorphism | major clinical study | attributable risk | Klinisk medicin | clinical evaluation | heterozygote | Breast Neoplasms | Single Nucleotide | follow up | 80 and over | Receptors | priority journal | female | human | tumor suppressor gene | Vesicular Transport Proteins | BRCA2 protein | Genetic Predisposition to Disease | cancer susceptibility | BRCA1 protein | gene mutation | probability | aged | breast cancer | article | gene frequency | genotype | Clinical Medicine | controlled study | cancer risk | Progesterone | Cancer and Oncology | adult | Sodium-Bicarbonate Symporters | Cancer och onkologi | Polymorphism
Journal Article