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1. Full Text Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer
by Bojesen, Stig E and Pooley, Karen A and Johnatty, Sharon E and Beesley, Jonathan and Michailidou, Kyriaki and Tyrer, Jonathan P and Edwards, Stacey L and Pickett, Hilda A and Shen, Howard C and Smart, Chanel E and Hillman, Kristine M and Mai, Phuong L and Lawrenson, Kate and Stutz, Michael D and Lu, Yi and Karevan, Rod and Woods, Nicholas and Johnston, Rebecca L and French, Juliet D and Chen, Xiaoqing and Weischer, Maren and Nielsen, Sune F and Maranian, Melanie J and Ghoussaini, Maya and Ahmed, Shahana and Baynes, Caroline and Bolla, Manjeet K and Wang, Qin and Dennis, Joe and McGuffog, Lesley and Barrowdale, Daniel and Lee, Anew and Healey, Sue and Lush, Michael and Tessier, Daniel C and Vincent, Daniel and Bacot, Françis and Vergote, Ignace and Lambrechts, Sanina and Despierre, Evelyn and Risch, Harvey A and González-Neira, Anna and Rossing, Mary Anne and Pita, Guillermo and Doherty, Jennifer A and Alvarez, Nuria and Larson, Melissa C and Fridley, Brooke L and Schoof, Nils and Chang-Claude, Jenny and Cicek, Mine S and Peto, Julian and Kalli, Kimberly R and Broeks, Annegien and Armasu, Sebastian M and Schmidt, Marjanka K and Braaf, Linde M and Winterhoff, Boris and Nevanlinna, Heli and Konecny, Gottfried E and Lambrechts, Diether and Rogmann, Lisa and Guénel, Pascal and Teoman, Attila and Milne, Roger L and Garcia, Joaquin J and Cox, Angela and Shridhar, Vijayalakshmi and Burwinkel, Barbara and Marme, Frederik and Hein, Rebecca and Sawyer, Elinor J and Haiman, Christopher A and Wang-Gohrke, Shan and Anulis, Irene L and Moysich, Kirsten B and Hopper, John L and Odunsi, Kunle and Lindblom, Annika and Giles, Graham G and Brenner, Hermann and Simard, Jacques and Lurie, Galina and Fasching, Peter A and Carney, Michael E and Radice, Paolo and Wilkens, Lynne R and Swerdlow, Anthony and Goodman, Marc T and Brauch, Hiltrud and Garcia-Closas, Montserrat and Hillemanns, Peter and Winqvist, Robert and Dürst, Matthias and Devilee, Peter and Runnebaum, Ingo and Jakubowska, Anna and Lubinski, Jan and Mannermaa, Arto and Butzow, Ralf and ... and Gene Environm Interactimi Breast and Kathleen Cuningham Fdn Consortium and Australian Ovarian Canc Study and Epidemiological Study BRCA1 and Hereditary Breast Ovarian Canc Res and Genetic Modifiers Canc Risk BRCA1 and Australian Canc Study and Swedish Breast Canc Study SWE-BRCA and Medicinska fakulteten and Umeå universitet and Institutionen för strålningsvetenskaper
Nature genetics, ISSN 1061-4036, 2013, Volume 45, Issue 4, pp. 371 - 384
TERT-locus SNPs and leukocyte telomere measures are reportedly associated with risks of multiple cancers. Using the Illumina custom genotyping array iCOGs, we... 
BUCCAL CELLS | GENETIC-VARIATION | COMMON VARIANTS | TERT-CLPTM1L LOCUS | REVERSE-TRANSCRIPTASE | SEQUENCE | GENETICS & HEREDITY | SUSCEPTIBILITY LOCI | POLYMORPHISM | FIBROBLASTS | GENOME-WIDE ASSOCIATION | Breast cancer | Genetic aspects | Research | Single nucleotide polymorphisms | Risk factors | Ovarian cancer | Genetics | Mutation | Càncer de mama | Càncer d'ovari | Telòmer | Telomere | Clinical Medicine | Medical and Health Sciences | Cancer and Oncology | Klinisk medicin | Medicin och hälsovetenskap | Cancer och onkologi
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2. Full Text Genome-wide association study identifies five new breast cancer susceptibility loci
by Turnbull, Clare and Ahmed, Shahana and Morrison, Jonathan and Pernet, David and Renwick, Anthony and Maranian, Mel and Seal, Sheila and Ghoussaini, Maya and Hines, Sarah and Healey, Catherine S and Hughes, Deborah and Warren-Perry, Margaret and Tapper, William and Eccles, Diana and Evans, D Gareth and Hooning, Maartje and Schutte, Mieke and Van Den Ouweland, Ans and Houlston, Richard and Ross, Gillian and Langford, Cordelia and Pharoah, Paul D.P and Stratton, Michael R and Dunning, Alison M and Rahman, Nazneen and Easton, Douglas F and Breast Canc Susceptibility and Breast Cancer Susceptibility Collaboration (UK) and The Breast Cancer Susceptibility Collaboration (UK)
Nature Genetics, ISSN 1061-4036, 06/2010, Volume 42, Issue 6, pp. 504 - 507
Breast cancer is the most common cancer in women in developed countries. To identify common breast cancer susceptibility alleles, we conducted a genome-wide... 
COMMON VARIANTS | ALLELES | GLIOMA | GENETICS & HEREDITY | CONFER SUSCEPTIBILITY | RISK | 9P21 | Genetic Predisposition to Disease | Genome-Wide Association Study | Breast Neoplasms - genetics | Humans | Female | Genotype | Chromosomes, Human, Pair 11 | Chromosomes, Human, Pair 8 | Polymorphism, Single Nucleotide | Chromosomes, Human, Pair 9 | Chromosomes, Human, Pair 6 | Chromosomes, Human, Pair 10 | Gene mutations | Breast cancer | Genetic aspects | Disease susceptibility | Diagnosis | Research | Single nucleotide polymorphisms | Health aspects | Risk factors | Studies | Medical research | Genetics | Family medical history
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3. Full Text Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer
by Michailidou, Kyriaki and Beesley, Jonathan and Lindstrom, Stephen and Canisius, Sander and Dennis, Joe and Lush, Michael and Maranian, Melanie and Bolla, Manjeet and Wang, Qing and Shah, Mitul and Perkins, Barbara and Czene, Kamila and Eriksson, Mikael and Darabi, Hatef and Brand, Judith S and Bojesen, Stig and Nordestgaard, Børge and Flyger, Henrik and Nielsen, Sune and Rahman, Nazneen and Turnbull, Clare and Fletcher, Olivia and Peto, Julian and Gibson, Lorna and Santos Silva, Isabel and Chang-Claude, Jenny and Flesch-Janys, Dieter and Rudolph, Anja and Eilber, Ursula and Behrens, Timothy and Nevanlinna, Heli and Muranen, Taru and Aittomäki, Kristiina and Blomqvist, Carl and Khan, Sofia and Aaltonen, Kirsimari and Ahsan, Habibul and Kibriya, Muhammad and Whittemore, Alice S and John, Esther M and Malone, Kathleen E and Gammon, Marilie and Santella, Regina M and Ursin, Giske and Makalic, Enes and Schmidt, Daniel and Casey, Graham and Hunter, David J and Gapstur, Susan M and Gaudet, Mia and Diver, Ryan and Haiman, Christopher A and Schumacher, Freick and Henderson, Brian and Le Marchand, Loic and Berg, Christine and Chanock, Stephen and Figueroa, Jonine and Hoover, Robert N and Lambrechts, Diether and Neven, Patrick and Wildiers, Hans and Limbergen, Erik and Schmidt, Marjanka and Broeks, Annegien and Verhoef, S and Cornelissen, Sten and Couch, Fergus and Olson, Janet and Hallberg, Boubou and Vachon, Celine and Waisfisz, Quinten and Meijers-Heijboer, Hanne and Adank, Muriel and Luijt, Rob and Li, Jingmei and Liu, Jianjun and Humphreys, Manjeet and Kang, Daehee and Choi, Ji-Yeob and Park, Sue K and Yoo, K.Y and Matsuo, Keitaro and Ito, Hidemi and Iwata, Hiroji and Tajima, Kazuo and Guénel, Pascal and Truong, Thérèse and Mulot, Claire and Sanchez, Marie and Burwinkel, Barbara and Marme, Federick and Surowy, Harald and Sohn, Christof and Wu, Anna H and Tseng, Chiu-chen and Van Den Berg, David and Stram, Daniel O and González-Neira, Anna and Benítez, Javier and ... and KConFab Investigators and AOCS Grp and BOCS and NBCS and GENICA Network and kConFab Investigators and AOCS Group and Medicinska fakulteten and Kirurgi and Institutionen för kirurgisk och perioperativ vetenskap and Umeå universitet
Nature Genetics, ISSN 1061-4036, 04/2015, Volume 47, Issue 4, pp. 373 - 380
textabstractGenome-wide association studies (GWAS) and large-scale replication studies have identified common variants in 79 loci associated with breast... 
COMMON VARIANTS | ALLELES | METAANALYSIS | GENOTYPE IMPUTATION | GENETICS & HEREDITY | ESTROGEN | CONFER SUSCEPTIBILITY | RISK | OVARIAN-CANCER | BRCA1 | CHEK2-ASTERISK-1100DELC | Genetic Predisposition to Disease | Genome-Wide Association Study | Meta-Analysis as Topic | Breast Neoplasms - genetics | Microarray Analysis | Humans | Female | Polymorphism, Single Nucleotide | Genetic Loci | Case-Control Studies | Cohort Studies | Quantitative trait loci | Genetic susceptibility | Genetic research | Breast cancer | Genetic aspects | Research | Identification and classification | Risk factors | Studies | Datasets | Genealogy | Disease | Womens health | Genes | Genomes | Index Medicus | Clinical Medicine | Medical and Health Sciences | Cancer and Oncology | Klinisk medicin | Medicin och hälsovetenskap | Cancer och onkologi
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4. Full Text Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2
by Yoo, Keun-Young and Nordestgaard, Børge G and Peto, Julian and Schmidt, Marjanka K and Bojesen, Stig and Seynaeve, Caroline and Humphreys, Manjeet K and Bogdanova, Natalia V and Meindl, Alfons and Berg, Christine D and Burwinkel, Barbara and van Asperen, Christi J and Hamann, Ute and van Hien, Richard R and Benitez, Javier and Brinton, Louise and Reed, Malcolm W R and Ghoussaini, Maya and English, Dallas R and Peplonska, Beata and Bermisheva, Marina and Hein, Rebecca and Severi, Gianluca and Fredericksen, Zachary and Prentice, Ross and Brauch, Hiltrud and Anton-Culver, Hoda and Lissowska, Jolanta and Luben, Robert and Smith, Letitia and Fedorova, Sardana and Liu, Jianjun and Fletcher, Olivia and Zalutsky, Iosif V and Hankinson, Susan E and Heikkinen, Tuomas and Mannermaa, Arto and Dörk, Thilo and Li, Yuqing and Chang-Claude, Jenny and Hall, Per and McCarty, Catherine A and Ziogas, Argyrios and Schmutzler, Rita K and Calle, Eugenia E and Milne, Roger L and Olson, Janet E and Sigurdson, Alice and Anderson, Garnet L and Doody, Michele and Kumle, Merethe and Rajkovic, Aleksandar and Karstens, Johann H and Elliott, Graeme and Chanock, Stephen J and Knight, Julia A and Flyger, Henrik and Thomas, Gilles and Goode, Ellen L and Oldenburg, Rogier A and van den Ouweland, Ans M W and Jacobs, Kevin and Vatten, Lars J and Ahmed, Shahana and Thun, Michael J and Beesley, Jonathan and Ziegler, Regina G and Morrison, Jonathan and Kang, Daehee and Pooley, Karen A and Brock, Ian and Kosma, Veli-Matti and Aittomäki, Kristiina and Platte, Radka and Kataja, Vesa and Bartram, Claus R and Cox, David G and Giles, Graham G and Diver, W Ryan and Southey, Melissa C and Maranian, Melanie and Rahman, Nazneen and Couch, Fergus and Chenevix-Trench, Georgia and Wang-Gohrke, Shan and Schutte, Mieke and Johnson, Nichola and Healey, Catherine S and Antonenkova, Natalia N and Garcia-Closas, Montserrat and Bhatti, Parveen and Broeks, Annegien and Chen, Shou-Tung and Hillemanns, Peter and Andrulis, Irene L and Ponder, Bruce A J and Feigelson, Heather Spencer and Ahn, Sei-Hyun and Devilee, Peter and Spurdle, Amanda B and ... and GENICA Consortium and KConFab and Australian Ovarian Cancer Study and SEARCH and Australian Ovarian Cancer Study Group and kConFab and The GENICA Consortium and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Institutionen för onkologi, radiologi och klinisk immunologi and Uppsala universitet and Enheten för onkologi
Nature Genetics, ISSN 1061-4036, 05/2009, Volume 41, Issue 5, pp. 585 - 590
Genome-wide association studies (GWAS) have identified seven breast cancer susceptibility loci, but these explain only a small fraction of the familial risk of... 
COMMON VARIANTS | CONFER SUSCEPTIBILITY | GENETICS & HEREDITY | GENOME-WIDE ASSOCIATION | Genetic Predisposition to Disease - genetics | Breast Neoplasms - genetics | Breast Neoplasms - pathology | Humans | Disease Susceptibility - metabolism | Female | Genotype | Chromosome Mapping | Genome, Human | Chromosomes, Human, Pair 17 - genetics | Chromosomes, Human, Pair 3 - genetics | Breast cancer | Genetic aspects | Disease susceptibility | Research | Single nucleotide polymorphisms | Risk factors | Medical research | Genetic markers | Gene loci | Hospitals | Regression analysis | chromosome 3 | Medical and Health Sciences | MEDICINE | Medicin och hälsovetenskap | MEDICIN
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5. 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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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 Genome-wide association study identifies novel breast cancer susceptibility loci
by Easton, Douglas F and Pooley, Karen A and Dunning, Alison M and Pharoah, Paul D. P and Thompson, Deborah and Ballinger, Dennis G and Struewing, Jeffery P and Morrison, Jonathan and Field, Helen and Luben, Robert and Wareham, Nicholas and Ahmed, Shahana and Healey, Catherine S and Bowman, Richard and Meyer, Kerstin B and Haiman, Christopher A and Kolonel, Laurence K and Henderson, Brian E and Le Marchand, Loic and Brennan, Paul and Sangrajrang, Suleeporn and Gaborieau, Valerie and Odefrey, Fabrice and Shen, Chen-Yang and Wu, Pei-Ei and Wang, Hui-Chun and Eccles, Diana and Evans, D. Gareth and Peto, Julian and Fletcher, Olivia and Johnson, Nichola and Seal, Sheila and Stratton, Michael R and Rahman, Nazneen and Chenevix-Trench, Georgia and Bojesen, Stig E and Nordestgaard, Børge G and Axelsson, Christen K and Garcia-Closas, Montserrat and Brinton, Louise and Chanock, Stephen and Lissowska, Jolanta and Peplonska, Beata and Nevanlinna, Heli and Fagerholm, Rainer and Eerola, Hannaleena and Kang, Daehee and Yoo, Keun-Young and Noh, Dong-Young and Ahn, Sei-Hyun and Hunter, David J and Hankinson, Susan E and Cox, David G and Hall, Per and Ween, Sara and Liu, Jianjun and Low, Yen-Ling and Bogdanova, Natalia and Schürmann, Peter and Dörk, Thilo and Tollenaar, Rob A. E. M and Jacobi, Catharina E and Devilee, Peter and Klijn, Jan G. M and Sigurdson, Alice J and Doody, Michele M and Alexander, Bruce H and Zhang, Jinghui and Cox, Angela and Brock, Ian W and MacPherson, Gordon and Reed, Malcolm W. R and Couch, Fergus J and Goode, Ellen L and Olson, Janet E and Meijers-Heijboer, Hanne and van den Ouweland, Ans and Uitterlinden, Ané and Rivadeneira, Fernando and Milne, Roger L and Ribas, Gloria and Gonzalez-Neira, Anna and Benitez, Javier and Hopper, John L and McCredie, Margaret and Southey, Melissa and Giles, Graham G and Schroen, Chris and Justenhoven, Christina and Brauch, Hiltrud and Hamann, Ute and Ko, Yon-Dschun and Spurdle, Amanda B and Beesley, Jonathan and Chen, Xiaoqing and Mannermaa, Arto and Kosma, Veli-Matti and Kataja, Vesa and Hartikainen, Jaana and Day, Nicholas E and ... and kConFab and AOCS Management Grp and SEARCH Collaborators and AOCS Management Group and SEARCH collaborators and The SEARCH collaborators
Nature, ISSN 0028-0836, 2007, Volume 447, Issue 7148, pp. 1087 - 1093
Breast cancer exhibits familial aggregation, consistent with variation in genetic susceptibility to the disease. Known susceptibility genes account for less... 
BRCA2 MUTATIONS | GENE | DATABASE | MULTIDISCIPLINARY SCIENCES | DISEASE | GROWTH-FACTOR RECEPTOR-2 | POPULATIONS | PATTERNS | OVARIAN-CANCER | VARIANT | CHEK2-ASTERISK-1100DELC | Genetic Predisposition to Disease - genetics | Humans | Genotype | Receptors, Progesterone - genetics | North America | Case-Control Studies | Europe - ethnology | Genome, Human - genetics | Asia, Southeastern | Breast Neoplasms - genetics | Alleles | Polymorphism, Single Nucleotide - genetics | Female | MAP Kinase Kinase Kinase 1 - genetics | Australia | Odds Ratio | Microfilament Proteins - genetics | Receptor, Fibroblast Growth Factor, Type 2 - genetics | Breast cancer | Genetic aspects | Research | Genetic susceptibility | Risk factors | Medical research | Genomics | Polymorphism | Genes | Control equipment | Breast | Risk | Genetics | Nucleotides | Loci | Cancer
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