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1. Full Text Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer
by Milne, Roger L and Kuchenbaecker, Karoline B and Michailidou, Kyriaki and Beesley, Jonathan and Kar, Siddhartha and Lindström, Sara and Hui, Shirley and Lemaçon, Auey and Soucy, Penny and Dennis, Joe and Jiang, Xia and Rostamianfar, Asha and Finucane, Hilary and Bolla, Manjeet K and McGuffog, Lesley and Wang, Qin and Aalfs, Cora M and Adams, Marcia and Adlard, Julian and Agata, Simona and Ahmed, Shahana and Ahsan, Habibul and Aittomäki, Kristiina and Al-Ejeh, Fares and Allen, Jamie and Ambrosone, Christine B and Amos, Christopher I and Anulis, Irene L and Anton-Culver, Hoda and Antonenkova, Natalia N and Arndt, Volker and Arnold, Norbert and Aronson, Kristan J and Auber, Bernd and Auer, Paul L and Ausems, Margreet G. E. M and Azzollini, Jacopo and Bacot, François and Balmaña, Judith and Barile, Monica and Barjhoux, Laure and Barkardottir, Rosa B and Barrdahl, Myrto and Barnes, Daniel and Barrowdale, Daniel and Baynes, Caroline and Beckmann, Matthias W and Benitez, Javier and Bermisheva, Marina and Bernstein, Leslie and Bignon, Yves-Jean and Blazer, Kathleen R and Blok, Marinus J and Blomqvist, Carl and Blot, William and Bobolis, Kristie and Boeckx, Bram and Bogdanova, Natalia V and Bojesen, Anders and Bojesen, Stig E and Bonanni, Bernardo and Børresen-Dale, Anne-Lise and Bozsik, Aniko and Bradbury, Angela R and Brand, Judith S and Brauch, Hiltrud and Brenner, Hermann and Bressac-de Paillerets, Brigitte and Brewer, Carole and Brinton, Louise and Broberg, Per and Brooks-Wilson, Angela and Brunet, Joan and Brüning, Thomas and Burwinkel, Barbara and Buys, Sauna S and Byun, Jinyoung and Cai, Qiuyin and Caldés, Trinidad and Caligo, Maria A and Campbell, Ian and Canzian, Federico and Caron, Olivier and Carracedo, Angel and Carter, Brian D and Castelao, J. Esteban and Castera, Laurent and Caux-Moncoutier, Virginie and Chan, Salina B and Chang-Claude, Jenny and Chanock, Stephen J and Chen, Xiaoqing and Cheng, Ting-Yuan David and Chiquette, Jocelyne and Christiansen, Hans and Claes, Kathleen B. M and Clarke, Christine L and Conner, Thomas and Conroy, Don M and Cook, Jackie and ... and ABCTB Investigators and HEBON and EMBRACE and GEMO Study Collaborators and kConFab AOCS Investigators and NBSC Collaborators and kConFab/AOCS Investigators and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Institutionen för immunologi, genetik och patologi and Medicinsk genetik och genomik and Ortopedi and Uppsala universitet and Institutionen för kirurgiska vetenskaper
Nature genetics, ISSN 1061-4036, 2017, Volume 49, Issue 12, pp. 1767 - 1778
Most common breast cancer susceptibility variants have been identified through genome-wide association studies (GWAS) of predominantly estrogen receptor... 
FUNCTIONAL VARIANTS | COMMON VARIANTS | MODIFIERS | MUTATION CARRIERS | OVARIAN CANCERS | GENETICS & HEREDITY | SUSCEPTIBILITY LOCI | ENHANCER | CONFER SUSCEPTIBILITY | GENOME-WIDE ASSOCIATION | REVEALS | Breast cancer | Genetic aspects | Genetic variation | Health aspects | Risk factors | Disease | BRCA1 protein | Genes | Estrogens | Health risks | Estrogen receptors | Risk | Genomes | Carriers | Consortia | Cell cycle | Breast | Hormone replacement therapy | Mutation | Gene mapping | Health risk assessment | Bioinformatics | Cancer | Medical and Health Sciences | Medicin och hälsovetenskap
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2. Full Text Breast Cancer Risk and 6q22.33: Combined Results from Breast Cancer Association Consortium and Consortium of Investigators on Modifiers of BRCA1/2
by Kirchhoff, Tomas and Gaudet, Mia M and Antoniou, Antonis C and McGuffog, Lesley and Humphreys, Manjeet K and Dunning, Alison M and Bojesen, Stig E and Nordestgaard, Børge G and Flyger, Henrik and Kang, Daehee and Yoo, Keun-Young and Noh, Dong-Young and Ahn, Sei-Hyun and Dork, Thilo and Schürmann, Peter and Karstens, Johann H and Hillemanns, Peter and Couch, Fergus J and Olson, Janet and Vachon, Celine and Wang, Xianshu and Cox, Angela and Brock, Ian and Elliott, Graeme and Reed, Malcolm W. R and Burwinkel, Barbara and Meindl, Alfons and Brauch, Hiltrud and Hamann, Ute and Ko, Yon-Dschun and Broeks, Annegien and Schmidt, Marjanka K and van 't Veer, Laura J and Braaf, Linde M and Johnson, Nichola and Fletcher, Olivia and Gibson, Lorna and Peto, Julian and Turnbull, Clare and Seal, Sheila and Renwick, Anthony and Rahman, Nazneen and Wu, Pei-Ei and Yu, Jyh-Cherng and Hsiung, Chia-Ni and Shen, Chen-Yang and Southey, Melissa C and Hopper, John L and Hammet, Fleur and van Dorpe, Thijs and Dieudonne, Anne-Sophie and Hatse, Sigrid and Lambrechts, Diether and Anulis, Irene L and Bogdanova, Natalia and Antonenkova, Natalia and Rogov, Juri I and Prokofieva, Daria and Bermisheva, Marina and Khusnutdinova, Elza and van Asperen, Christi J and Tollenaar, Robert A. E. M and Hooning, Maartje J and Devilee, Peter and Margolin, Sara and Lindblom, Annika and Milne, Roger L and Arias, José Ignacio and Zamora, M. Pilar and Benítez, Javier and Severi, Gianluca and Baglietto, Laura and Giles, Graham G and Spurdle, Amanda B and Beesley, Jonathan and Chen, Xiaoqing and Holland, Helene and Healey, Sue and Wang-Gohrke, Shan and Chang-Claude, Jenny and Mannermaa, Arto and Kosma, Veli-Matti and Kauppinen, Jaana and Kataja, Vesa and Agnarsson, Bjarni A and Caligo, Maria A and Godwin, Anew K and Nevanlinna, Heli and Heikkinen, Tuomas and Fredericksen, Zachary and Lindor, Noralane and Nathanson, Katherine L and Domchek, Susan M and Loman, Niklas and Karlsson, Per and Stenmark Askmalm, Marie and Melin, Beatrice and von Wachenfeldt, Anna and Hogervorst, Frans B. L and Verheus, Martijn and ... and EMBRACE and BCAC-CIMBA and HEBON and kConFab and GENICA Network and AOCS Study Grp and SWE-BRCA and AOCS Study Group and BCAC/CIMBA and on behalf of BCAC/CIMBA and Linköpings universitet and Institutionen för klinisk och experimentell medicin and Diagnostikcentrum and Klinisk patologi och klinisk genetik and Östergötlands Läns Landsting and Onkologi and Hälsouniversitetet
PLoS ONE, ISSN 1932-6203, 2012, Volume 7, Issue 6, p. e35706
Recently, a locus on chromosome 6q22.33 (rs2180341) was reported to be associated with increased breast cancer risk in the Ashkenazi Jewish (AJ) population,... 
ALLELES | VARIANTS | GENE | MULTIDISCIPLINARY SCIENCES | SUSCEPTIBILITY LOCI | FGFR2 | GENOME-WIDE ASSOCIATION | Confidence Intervals | Genetic Predisposition to Disease | Receptors, Estrogen - genetics | Genetic Association Studies | Humans | Middle Aged | Risk Factors | Proportional Hazards Models | Chromosomes, Human, Pair 6 - genetics | BRCA1 Protein - genetics | Breast Neoplasms - genetics | Alleles | Polymorphism, Single Nucleotide - genetics | Female | Heterozygote | Odds Ratio | BRCA2 Protein - genetics | Gene mutations | Oncology, Experimental | Breast cancer | Genetic aspects | Research | Health aspects | Risk factors | Cancer | Physicians | Genes | Oncology | Biochemistry | Epidemiology | Medical schools | Ovarian cancer | Consortia | Surgery | Genetics | Public health | BRCA2 protein | Medical research | Clinics | BRCA1 protein | Invasiveness | Gynecology | Environmental health | Health risks | Chromosome 6 | Obstetrics | Primary care | Carriers | Medicine | Studies | Hospitals | Breast | Medical and Health Sciences | MEDICINE | Medicin och hälsovetenskap | MEDICIN
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3. Full Text Discontinuation of tyrosine kinase inhibitor therapy in chronic myeloid leukaemia (EURO-SKI): a prespecified interim analysis of a prospective, multicentre, non-randomised, trial
by Saussele, Susanne and Richter, Johan and Guilhot, Francois and Guilhot, Joelle and Gruber, Franz X and Hjorth-Hansen, Henrik and Almeida, Antonio and Janssen, Jeroen J W M and Mayer, Jiri and Koskenvesa, Perttu and Panayiotidis, Panayiotis and Olsson-Strömberg, Ulla and Martinez-Lopez, Joaquin and Rousselot, Philippe and Vestergaard, Hanne and Ehrencrona, Hans and Kairisto, Veli and Machová Poláková, Katerina and Müller, Martin C and Mustjoki, Satu and Berger, Marc G and Fabarius, Alice and Hofmann, Wolf-Karsten and Hochhaus, Andreas and Pfirrmann, Markus and Mahon, Francois-Xavier and Ossenkoppele, Gert and Pagoni, Maria N and Söderlund, Stina and Escoffre-Barbe, Martine and Etienne, Gabriel and Dengler, Jolanta and Huguet, Francoise and von Bubnoff, Nikolas and Klamova, Hana and Faber, Edgar and Lotfi, Kourosh and Rea, Delphine and Brümmendorf, Tim H and de Greef, Gorgine E and Stenke, Leif and Nicolini, Franck E and Legros, Laurence and Burchert, Andreas and Voglova, Jaroslava and Charbonnier, Aude and Gyan, Emmanuel and Kunzmann, Volker and Westerweel, Peter E and EURO-SKI Investigators and EURO-SKI investigators and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Uppsala universitet and Institutionen för medicinska vetenskaper and Hematologi
The Lancet Oncology, ISSN 1470-2045, 06/2018, Volume 19, Issue 6, pp. 747 - 757
Tyrosine kinase inhibitors (TKIs) have improved the survival of patients with chronic myeloid leukaemia. Many patients have deep molecular responses, a... 
SURVIVAL | MAJOR MOLECULAR RESPONSE | TREATMENT-FREE REMISSION | ONCOLOGY | IMATINIB DISCONTINUATION | DISEASE | FOLLOW-UP | DASATINIB | WITHDRAWAL SYNDROME | NILOTINIB | PHASE-2 TRIAL | Antimitotic agents | Tyrosine | Antineoplastic agents | Analysis | Life Sciences | Hematology | Human health and pathology | Clinical Medicine | Medical and Health Sciences | Cancer and Oncology | Klinisk medicin | Medicin och hälsovetenskap | Cancer och onkologi
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4. Full Text Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus
by Lawrenson, Kate and Kar, Siddhartha and McCue, Karen and Kuchenbaeker, K and Michailidou, Kyriaki and Tyrer, Jonathan and Beesley, Jonathan and Ramus, Susan and Li, Q and Delgado, M.K and Lee, Janet M and Aittomäki, Kristiina and Anulis, Irene and Anton-Culver, Hoda and Arndt, V and Arun, Banu and Arver, Brita Wasteson and Bandera, Elisa and Barile, Monica and Barkardottir, R.B and Barrowdale, Daniel and Beckmann, Matthias and Benítez, Javier and Berchuck, Anew and Bisogna, Maria and Bjorge, Line and Blomqvist, Carl and Blot, William and Bogdanova, Natalia and Bojesen, A and Bojesen, Stig and Bolla, Manjeet K and Bonnani, Bernardo and Borresen-Dale, Anne-Lise and Brauch, Hiltrud and Brennan, Paul and Brenner, Hermann and Bruinsma, Fiona and Brunet, Joan and Buhari, Shaik Ahmad Bin Syed and Burwinkel, Barbara and Butzow, Ralf and Buys, Sauna and Cai, Qiuyin and Caldes, Trinidad and Campbell, Ian and Canniotto, R and Chang-Claude, Jenny and Chiquette, J and Choi, J.-Y and Claes, Kathleen B.M and Cook, Linda S and Cox, Angela and Cramer, Daniel and Cross, Simon and Cybulski, Cezary and Czene, Kamila and Daly, Mary B and Damiola, Francesca and Dansonka-Mieszkowska, Agnieszka and Darabi, Hatef and Dennis, Joe and Devilee, Peter and Díez, Orland and Doherty, Jennifer A and Domchek, Susan and Dorfling, Cecilia and Dörk, Thilo and Dumont, Martine and Ehrencrona, Hans and Ejlertsen, Bent and Ellis, Steve and Engel, Christoph and Lee, Eunjung and Evans, D.G and Fasching, Peter and Feliubadaló, L and Figueroa, Jonine and Flesch-Janys, Dieter and Fletcher, Olivia and Flyger, Henrik and Foretova, Lenka and Fostira, Florentia and Foulkes, William and Fridley, Brooke and Friedman, Eitan and Frost, Debra and Gambino, G and Ganz, Patricia A and Garber, Judy and García-Closas, Montserrat and Gentry-Maharaj, Aleksana and Ghoussaini, Maya and Giles, Graham and Glasspool, Rosalind and Godwin, Anew K and Goldberg, Mark and Goldgar, David and González-Neira, Anna and Goode, Ellen and ... and KConFab Investigators and Australian Ovarian Canc Study Grp and GEMO Study Collaborators and EMBRACE and Hereditary Breast & Ovarian Canc R and Australian Ovarian Cancer Study Group and Hereditary Breast and Ovarian Cancer Research Group Netherlands (HEBON) and The Hereditary Breast and Ovarian Cancer Research Group Netherlands (HEBON) and Medicinska fakulteten and Region Östergötland and Linköpings universitet and Institutionen för klinisk och experimentell medicin and Diagnostikcentrum and Klinisk patologi och klinisk genetik and Avdelningen för cellbiologi
Nature Communications, ISSN 2041-1723, 09/2016, Volume 7, Issue 1, p. 12675
textabstractA locus at 19p13 is associated with breast cancer (BC) and ovarian cancer (OC) risk. Here we analyse 438 SNPs in this region in 46,451 BC and... 
BRCA2 MUTATION CARRIERS | COMMON VARIANTS | IDENTIFIES 3 | GWAS | INVESTIGATORS | EPITHELIAL-CELLS | MODIFIERS | GENE | MULTIDISCIPLINARY SCIENCES | GENOME-WIDE ASSOCIATION | REVEALS | Genetic Predisposition to Disease | Genome-Wide Association Study | Humans | RNA, Messenger - genetics | Asian Continental Ancestry Group - genetics | Genotype | RNA, Messenger - metabolism | Ovarian Neoplasms - genetics | Chromosomes, Human, Pair 19 - genetics | Breast Neoplasms - genetics | Alleles | Female | Polymorphism, Single Nucleotide | African Continental Ancestry Group - genetics | Basic Medicine | Medical Genetics | Medicinsk genetik | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper
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5. Full Text DNA glycosylases involved in base excision repair may be associated with cancer risk in BRCA1 and BRCA2 mutation carriers
by Osorio, Ana and Milne, Roger L and Kuchenbaecker, Karoline and Vaclova, Tereza and Pita, Guillermo and Alonso, Rosario and Peterlongo, Paolo and Blanco, Ignacio and de la Hoya, Miguel and Duran, Mercedes and Diez, Orland and Ramon y Cajal, Teresa and Konstantopoulou, Irene and Martinez-Bouzas, Cristina and Anes Conejero, Raquel and Soucy, Penny and McGuffog, Lesley and Barrowdale, Daniel and Lee, Anew and Swe-Brca, N. N and Arver, Brita and Rantala, Johanna and Loman, Niklas and Ehrencrona, Hans and Olopade, Olufunmilayo I and Beattie, Mary S and Domchek, Susan M and Nathanson, Katherine and Rebbeck, Timothy R and Arun, Banu K and Karlan, Beth Y and Walsh, Christine and Lester, Jenny and John, Esther M and Whittemore, Alice S and Daly, Mary B and Southey, Melissa and Hopper, John and Terry, Mary B and Buys, Sauna S and Janavicius, Ramunas and Dorfling, Cecilia M and van Rensburg, Elizabeth J and Steele, Linda and Neuhausen, Susan L and Ding, Yuan Chun and Hansen, Thomas V. O and Jonson, Lars and Ejlertsen, Bent and Gerdes, Anne-Marie and Infante, Mar and Herraez, Belen and Moreno, Leticia Thais and Weitzel, Jeffrey N and Herzog, Josef and Weeman, Kisa and Manoukian, Siranoush and Peissel, Bernard and Zaffaroni, Daniela and Scuvera, Giulietta and Bonanni, Bernardo and Mariette, Frederique and Volorio, Sara and Viel, Alessana and Varesco, Liliana and Papi, Laura and Ottini, Laura and Tibiletti, Maria Grazia and Radice, Paolo and Yannoukakos, koulis and Garber, Judy and Ellis, Steve and Frost, Debra and Platte, Radka and Fineberg, Elena and Evans, Gareth and Lalloo, Fiona and Izatt, Louise and Eeles, Ros and Adlard, Julian and Davidson, Rosemarie and Cole, Trevor and Eccles, Diana and Cook, Jackie and Hodgson, Shirley and Brewer, Carole and Tischkowitz, Marc and Douglas, Fiona and Porteous, Mary and Side, Lucy and Walker, Lisa and Morrison, Patrick and Donaldson, Alan and Kennedy, John and Foo, Claire and Godwin, Anew K and Schmutzler, Rita Katharina and Wappenschmidt, Barbara and Rhiem, Kerstin and Engel, Christoph and ... and KConFab Investigators and HEBON and SWE-BRCA and Onkologi och Patologi, MV and Lund University and Division of Clinical Genetics and Oncology and Pathology, MV and Avdelningen för klinisk genetik and BioCARE: Biomarkers in Cancer Medicine improving Health Care, Education and Innovation and Lunds universitet
PLoS genetics, ISSN 1553-7390, 2014, Volume 10, Issue 4, p. e1004256
Single Nucleotide Polymorphisms (SNPs) in genes involved in the DNA Base Excision Repair (BER) pathway could be associated with cancer risk in carriers of... 
BREAST-CANCER | CONSORTIUM | COMMON VARIANTS | GENETIC MODIFIERS | NEIL2 | INVESTIGATORS | OGG1 | GENETICS & HEREDITY | OVARIAN-CANCER | SINGLE-NUCLEOTIDE POLYMORPHISMS | DAMAGE | Genetic Predisposition to Disease | Humans | Middle Aged | DNA Glycosylases - genetics | Genotype | Risk | DNA Repair - genetics | Ovarian Neoplasms - genetics | BRCA1 Protein - genetics | Breast Neoplasms - genetics | Adolescent | Aged, 80 and over | Polymorphism, Single Nucleotide - genetics | Adult | Female | Aged | BRCA2 Protein - genetics | Gene mutations | Oncology, Experimental | Genetic research | Research | Nucleotide sequencing | DNA repair | DNA sequencing | Cancer | Genetics | Càncer d'ovari | Genètica | Ovarian cancer | Medicinsk genetik | Basic Medicine | Medical Genetics | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper | Medical research | Breast cancer | Mutation | Genes
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6. Full Text Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170
by Dunning, Alison and Michailidou, Kyriaki and Kuchenbaecker, Karoline and Thompson, Deborah and French, Juliet and Beesley, Jonathan and Healey, Sue and Kar, Siddhartha and Pooley, Karen and Lopez-Knowles, Elena and Dicks, Ed and Barrowdale, Daniel and Sinnott-Armstrong, Nicholas A and Sallari, Richard C and Hillman, Kristine and Kaufmann, Susanne and Sivakumaran, Haran and Marjaneh, Mahdi Moradi and Lee, Jason S and Hills, Margaret and Jarosz, Monika and ry, Suzie and Canisius, Sander and KBolla, Manjeet and Dennis, Joe and Wang, Qin and LHopper, John and Southey, Mellissa C and Broeks, Annegien and Schmidt, Marjanka K and Lophatananon, Artitaya and Muir, K and Beckmann, Matthias W and Fasching, Peter and Santos Silva, Isabel and Peto, Julian and Sawyer, Elinor and Tomlinson, Ian and Burwinkel, Barbara and Marme, Federick and Guénel, Pascal and Truong, Thérèse and Bojesen, Stig and Flyger, Henrik and Gonzlez-Neira, Anna and Perez, Jose I.A and Anton-Culver, Hoda and Eunjung, Lee and Arndt, Volker and Brenner, Hermann and Meindl, Alfons and Schmutzler, Rita and Brauch, Hiltrud and Hamann, Ute and Aittomki, Kristiina and Blomqvist, Carl and Ito, Hidemi and Matsuo, Keitaro and Bogdanova, Natalia and Dörk, Thilo and Lindblom, Annika and Margolin, Sara and Kosma, Veli-Matti and Mannermaa, Arto and Tseng, Chiu-Chen and Wu, Anna and Lambrechts, Diether and Wildiers, Hans and Chang-Claude, Jenny and Rudolph, Anja and Peterlongo, Paolo and Radice, Paolo and EOlson, Janet and GGiles, Graham and Milne, Roger L and Haiman, Christopher A and Henderson, Brian and Goldberg, Mark and Teo, Soo Hwang and Yip, Cheng Har and Nord, Silje and Borresen-Dale, Anne-Lise and Kristensen, Vessela and Long, Jirong and Zheng, Wei and Pylks, Katri and Winqvist, Robert and Anulis, Irene and Knight, Julia A and Devilee, Peter and Seynaeve, Caroline and Figueroa, Jonine and Sherman, Mark and Czene, Kamila and Darabi, Hatef and Hollestelle, Antoinette and Ouweland, Ans and Humphreys, Keith and Gao, Yu-Tang and Shu, Xiao-Ou and ... and KConFab Investigators and HEBON and EMBRACE and GEMO Study Collaborators and kConFab Investigators and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Institutionen för immunologi, genetik och patologi and Uppsala universitet
Nature Genetics, ISSN 1061-4036, 03/2016, Volume 48, Issue 4, pp. 374 - 386
textabstractWe analyzed 3,872 common genetic variants across the ESR1 locus (encoding estrogen receptor α) in 118,816 subjects from three international... 
BRCA2 MUTATION CARRIERS | MAMMOGRAPHIC DENSITY | WOMEN | METAANALYSIS | BONE-MINERAL DENSITY | MODIFIERS | DISEASE | GENETICS & HEREDITY | SUSCEPTIBILITY LOCUS | GENOME-WIDE ASSOCIATION | REVEALS | Gene Expression | Genetic Predisposition to Disease | Genetic Association Studies | Humans | Risk Factors | Cell Cycle Proteins - metabolism | Gene Expression Regulation, Neoplastic | Chromosomes, Human, Pair 6 - genetics | Breast Neoplasms - metabolism | Carrier Proteins - genetics | Phenotype | Breast Neoplasms - genetics | Carrier Proteins - metabolism | Estrogen Receptor alpha - genetics | Base Sequence | Cell Cycle Proteins - genetics | Protein Binding | Estrogen Receptor alpha - metabolism | Female | Polymorphism, Single Nucleotide | Genetic variation | Breast cancer | Genetic aspects | Gene expression | Properties | Health aspects | Identification and classification | Risk factors | Basic Medicine | Medical Genetics | Medicinsk genetik | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper
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7. Full Text Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer
by Couch, Fergus and Kuchenbaecker, Karoline and Michailidou, Kyriaki and Mendoza-Fandino, Gustavo A and Nord, Silje and Lilyquist, Janna and Olswold, Curtis and Hallberg, Boubou and Agata, Simona and Ahsan, Habibul and Aittomäki, Kristiina and Ambrosone, Christine and Anulis, Irene and Anton-Culver, Hoda and Arndt, Volker and Arun, Banu and Arver, Brita Wasteson and Barile, Monica and Barkardottir, Rosa and Barrowdale, Daniel and Beckmann, Lars and Beckmann, Matthias and Benítez, Javier and Blank, Stephanie and Blomqvist, Carl and Bogdanova, Natalia and Bojesen, Stig and Bolla, Manjeet and Bonnani, Bernardo and Brauch, Hiltrud and Brenner, Hermann and Burwinkel, Barbara and Buys, Sauna S and Caldes, Trinidad and Caligo, Maria and Canzian, Federico and Carpenter, Aian and Chang-Claude, Jenny and Chanock, Stephen J and Chung, Wendy K and Claes, Kathleen B.M and Cox, Angela and Cross, Simon and Cunningham, Julie and Czene, Kamila and Daly, Mary B and Damiola, Francesca and Darabi, Hatef and Hoya, Miguel and Devilee, Peter and Díez, Orland and Ding, Yuan and Dolcetti, Riccardo and Domchek, Susan and Dorfling, Cecilia and Santos Silva, Isabel and Dumont, Martine and Dunning, Alison and Eccles, Diana and Ehrencrona, Hans and Ekici, Arif and Eliassen, Heather and Ellis, Steve and Fasching, Peter and Figueroa, Jonine and Flesch-Janys, Dieter and Försti, Asta and Fostira, Florentia and Foulkes, William and Friebel, Mark and Friedman, Eitan and Frost, Debra and Gabrielson, Marike and Gammon, Marilie and Ganz, Patricia A and Gapstur, Susan M and Garber, Judy and Gaudet, Mia and Gayther, Simon and Gerdes, Anne-Marie and Ghoussaini, Maya and Giles, Graham and Glendon, Gord and Godwin, Anew K and Goldberg, Mark and Goldgar, David and González-Neira, Anna and Greene, Mark H and Gronwald, Jacek and Guénel, Pascal and Gunter, Marc J and Haeberle, Lothar and Haiman, Christopher A and Hamann, Ute and Hansen, Thomas and Hart, Stewart and Healey, Sue and Heikkinen, Tuomas and Henderson, Brian and Herzog, Josef and ... and Medicinska fakulteten and Region Östergötland and Linköpings universitet and Institutionen för klinisk och experimentell medicin and Diagnostikcentrum and Klinisk patologi och klinisk genetik and Avdelningen för cellbiologi
Nature Communications, ISSN 2041-1723, 04/2016, Volume 7, Issue 1, p. 11375
textabstractCommon variants in 94 loci have been associated with breast cancer including 15 loci with genome-wide significant associations (P<5 × 10-8) with... 
BRCA2 MUTATION CARRIERS | CONSORTIUM | COMMON VARIANTS | IDENTIFY | INVESTIGATORS | METAANALYSIS | MULTIDISCIPLINARY SCIENCES | GENE-EXPRESSION | RISK | GENOME-WIDE ASSOCIATION | TELOMERE LENGTH | Genetic Predisposition to Disease - genetics | Receptors, Estrogen - genetics | Humans | Risk Factors | Genotype | Cyclophilins - genetics | BRCA1 Protein - genetics | Chromosomes, Human, Pair 2 - genetics | Breast Neoplasms - genetics | tRNA Methyltransferases | Female | Heterozygote | Polymorphism, Single Nucleotide | Mutation | Genome-Wide Association Study - methods | Samfunnsmedisin, sosialmedisin: 801 | Community medicine, Social medicine: 801 | VDP | Helsefag: 800 | Klinisk medisinske fag: 750 | Onkologi: 762 | Oncology: 762 | Health sciences: 800 | Medisinske Fag: 700 | Clinical medical disciplines: 750 | Medical disciplines: 700 | Clinical Medicine | Medical and Health Sciences | Cancer and Oncology | Klinisk medicin | Medicin och hälsovetenskap | Cancer och onkologi
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