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1. Full Text Identification of nine new susceptibility loci for endometrial cancer
by O’Mara, Tracy A and Glubb, Dylan M and Amant, Frederic and Annibali, Daniela and Ashton, Katie and Attia, John and Auer, Paul L and Beckmann, Matthias W and Black, Amanda and Bolla, Manjeet K and Brauch, Hiltrud and Brenner, Hermann and Brinton, Louise and Buchanan, Daniel D and Burwinkel, Barbara and Chang-Claude, Jenny and Chanock, Stephen J and Chen, Chu and Chen, Maxine M and Cheng, Timothy H. T and Clarke, Christine L and Clendenning, Mark and Cook, Linda S and Couch, Fergus J and Cox, Angela and Crous-Bous, Marta and Czene, Kamila and Day, Felix and Dennis, Joe and Depreeuw, Jeroen and Doherty, Jennifer Anne and Dörk, Thilo and Dowdy, Sean C and Dürst, Matthias and Ekici, Arif B and Fasching, Peter A and Fridley, Brooke L and Friedenreich, Christine M and Fritschi, Lin and Fung, Jenny and García-Closas, Montserrat and Gaudet, Mia M and Giles, Graham G and Goode, Ellen L and Gorman, Maggie and Haiman, Christopher A and Hall, Per and Hankison, Susan E and Healey, Catherine S and Hein, Alexander and Hillemanns, Peter and Hodgson, Shirley and Hoivik, Erling A and Holliday, Elizabeth G and Hopper, John L and Hunter, David J and Jones, Angela and Krakstad, Camilla and Kristensen, Vessela N and Lambrechts, Diether and Marchand, Loic Le and Liang, Xiaolin and Lindblom, Annika and Lissowska, Jolanta and Long, Jirong and Lu, Lingeng and Magliocco, Anthony M and Martin, Lynn and McEvoy, Mark and Meindl, Alfons and Michailidou, Kyriaki and Milne, Roger L and Mints, Miriam and Montgomery, Grant W and Nassir, Rami and Olsson, Håkan and Orlow, Irene and Otton, Geoffrey and Palles, Claire and Perry, John R. B and Peto, Julian and Pooler, Loreall and Prescott, Jennifer and Proietto, Tony and Rebbeck, Timothy R and Risch, Harvey A and Rogers, Peter A. W and Rübner, Matthias and Runnebaum, Ingo and Sacerdote, Carlotta and Sarto, Gloria E and Schumacher, Fredrick and Scott, Rodney J and Setiawan, V. Wendy and Shah, Mitul and Sheng, Xin and Shu, Xiao-Ou and Southey, Melissa C and Swerdlow, Anthony J and Tham, Emma and ... and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Ortopedi and Uppsala universitet and Institutionen för kirurgiska vetenskaper
Nature Communications, ISSN 2041-1723, 12/2018, Volume 9, Issue 1, pp. 3166 - 12
Endometrial cancer is the most commonly diagnosed cancer of the female reproductive tract in developed countries. Through genome-wide association studies... 
BREAST-CANCER | RISK LOCI | METAANALYSIS | VARIANTS | GENOTYPE IMPUTATION | MULTIDISCIPLINARY SCIENCES | BODY-MASS INDEX | MENDELIAN RANDOMIZATION | LD SCORE REGRESSION | FAMILY-HISTORY | GENOME-WIDE ASSOCIATION | Genetic Predisposition to Disease | Genome-Wide Association Study | Signal Transduction | Gene Frequency | Humans | Risk Factors | Genotype | Endometrial Neoplasms - genetics | Alleles | Female | Biomarkers, Tumor - genetics | Polymorphism, Single Nucleotide | Quantitative Trait Loci | Chromatin - chemistry | Developed countries | Regulators | Endometrial cancer | Genes | Colorectal carcinoma | Health risks | Risk | Genomes | Gene expression | Loci | Proteins | Quantitative trait loci | Signal transduction | Chromosome 12 | Hormone replacement therapy | Transduction | Reproductive system | Health risk assessment | Endometrium | Genotypes | Cancer | Medical and Health Sciences | Medicin och hälsovetenskap
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2. Full Text Identification of six new susceptibility loci for invasive epithelial ovarian cancer
by Kuchenbaecker, Karoline and Ramus, Susan and Tyrer, Jonathan and Lee, Anew and Shen, Howard C and Beesley, Jonathan and Lawrenson, Kate and McGuffog, Lesley and Healey, Sue and Lee, Janet M and Spindler, Tassja J and Lin, Yvonne G and Pejovic, Tanja and Bean, Yukie and Li, Qiyuan and Coetzee, Simon and Hazelett, Dennis and Miron, Alexander and Southey, Melissa and Terry, Mary Beth and Goldgar, David and Buys, Sauna and Janavicius, Ramunas and Dorfling, Cecilia and Rensburg, Elizabeth and Neuhausen, Susan and Ding, Yuan and Hansen, Thomas and Jønson, Lars and Gerdes, Anne-Marie and Ejlertsen, Bent and Barrowdale, Daniel and Dennis, Joe and Benítez, Javier and Osorio, Ana and Garcia, Maria Jose and Komenaka, Ian and Weitzel, Jeffrey and Ganschow, Pamela and Peterlongo, Paolo and Bernard, Loris and Viel, Alessana and Bonnani, Bernardo and Peissel, Bernard and Manoukian, Siranoush and Radice, Paolo and Papi, Laura and Ottini, Laura and Fostira, Florentia and Konstantopoulou, I and Garber, Judy and Frost, Debra and Perkins, Jo and Platte, Radka and Ellis, Steve and Godwin, Anew K and Schmutzler, Rita and Meindl, Alfons and Engel, Christoph and Sutter, Christian and Sinilnikova, Olga and Damiola, Francesca and Mazoyer, Sylvie and Stoppa-Lyonnet, Dominique and Claes, Kathleen B.M and De Leeneer, Kim and Kirk, Judy and Roiguez, Gustavo and Piedmonte, Marion and O'Malley, David M and Hoya, Miguel and Caldes, Trinidad and Aittomäki, Kristiina and Nevanlinna, Heli and Margriet, J. Collée and Rookus, Matti and Oosterwijk, Jan and Tihomirova, Laima and Tung, Nadine and Hamann, Ute and Isaccs, Claudine and Tischkowitz, Marc and Imyanitov, Evgeny and Caligo, Maria and Campbell, Ian and Hogervorst, Frans and Olah, E and Díez, Orland and Blanco, Ignacio and Brunet, Joan and Lazaro, Conxi and Pujana, Miguel and Jakubowska, Anna and Gronwald, Jacek and Lubinski, Jan and Sukiennicki, Grzegorz and Barkardottir, Rosa and Plante, Marie and Simard, Jacques and Soucy, Penny and ... and KConFab Investigators and EMBRACE and GEMO Study Collaborators and Breast Cancer Family Registry and Australian Ovarian Canc Study Grp and HEBON and Consortium Invest Modifiers BRCA1 and Australian Canc Study Ovarian Canc and Australian Cancer Study (Ovarian Cancer Investigators) and Australian Ovarian Cancer Study Group and Consortium of Investigators of Modifiers of BRCA1 and BRCA2 and the Consortium of Investigators of Modifiers of BRCA1 and BRCA2 and Region Östergötland and Linköpings universitet and Institutionen för klinisk och experimentell medicin and Diagnostikcentrum and Klinisk patologi och klinisk genetik and Avdelningen för kliniska vetenskaper and Hälsouniversitetet
Nature Genetics, ISSN 1061-4036, 01/2015, Volume 47, Issue 2, pp. 164 - 171
textabstractGenome-wide association studies (GWAS) have identified 12 epithelial ovarian cancer (EOC) susceptibility alleles. The pattern of association at... 
BRCA2 MUTATION CARRIERS | BREAST-CANCER | COMMON VARIANTS | METAANALYSIS | HIGH-RISK | MYOPODIN | GENETICS & HEREDITY | HUMAN ELG1 | ABO BLOOD-GROUP | SINGLE NUCLEOTIDE POLYMORPHISMS | GENOME-WIDE ASSOCIATION | Genetic Predisposition to Disease | Humans | Genotype | Risk | Ovarian Neoplasms - genetics | Young Adult | BRCA1 Protein - genetics | Neoplasms, Glandular and Epithelial - genetics | Adolescent | Alleles | Carcinoma, Ovarian Epithelial | Adult | Female | Heterozygote | Polymorphism, Single Nucleotide | Mutation | Genome-Wide Association Study - methods | Quantitative Trait Loci | BRCA2 Protein - genetics | Genes, Reporter | Quantitative trait loci | Genetic aspects | Identification and classification | Health aspects | Ovarian cancer | Haplotypes | Accuracy | Population | Hormone replacement therapy | Genomes | Meta-analysis | Cèl·lules epitelials | Càncer d'ovari | Developmental genetics | Human genome | Epithelial cells | Genètica del desenvolupament | Nucleotides | Genoma humà | Nucleòtids | Clinical Medicine | Medical and Health Sciences | Klinisk medicin | Medicin och hälsovetenskap
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3. Full Text A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24
by Goode, E.L and Chenevix-Trench, G and Song, H and Ramus, S.J and Notaridou, M and Lawrenson, K and Widschwendter, M and Vierkant, R.A and Larson, M.C and Kjaer, S.K and Birrer, M.J and Berchuck, A and Schildkraut, J and Tomlinson, I.P and Kiemeney, L.A.L.M and Cook, L.S and Gronwald, J and Garcia-Closas, M and Gore, M.E and Campbell, I and Whittemore, A.S and Sutphen, R and Phelan, C.M and Anton-Culver, H and Pearce, C.L and Lambrechts, D and Rossing, M.A and Chang-Claude, J and Moysich, K.B and Goodman, M.T and Dork, T and Nevanlinna, H and Ness, R.B and Rafnar, T and Hogdall, E and Fridley, B.L and Cunningham, J.M and Sieh, W and McGuire, V and Godwin, A.K and Cramer, D.W and Hernandez, D and Levine, D and Lu, K and Iversen, E.S and Palmieri, R.T and Houlston, R.S and Altena, A.M. van and Aben, K.K.H and Massuger, L.F.A.G and Brooks-Wilson, A and Kelemen, L.E and Le, N.D and Jakubowska, A and Lubinski, J and Meek, K and Stafford, A and Easton, D.F and Tyrer, J.P and Bolton, K.L and Harrington, P and Eccles, D and Chen, A and Molina, A.N and Davila, B.N and Arango, H and Tsai, Y.Y and Chen, Z and Risch, H.A and McLaughlin, J and Narod, S and Ziogas, A and Brewster, W and Gentry-Maharaj, A and Menon, U and Wu, A.H and Stram, D.O and Pike, M.C and Beesley, J and Webb, P.M and Chen, X and Ekici, A.B and Thiel, F.C and Beckmann, M.W and Yang, H and Wentzensen, N and Lissowska, J and Fasching, P.A and Despierre, E and Amant, F and Vergote, I and Doherty, J and Hein, R and Wang-Gohrke, S and Lurie, G and Carney, M.E and Thompson, P and OCAC and Wellcome Trust Case-Control Conso and Australian Ovarian Canc Study Grp and Australian Canc Study Ovarian Canc and Australian Ovarian Cancer Study Group and Wellcome Trust Case-Control Consortium and Australian Cancer Study (Ovarian Cancer) and Ovarian Cancer Association Consortium (OCAC) and the Ovarian Cancer Association Consortium (OCAC) and The Wellcome Trust Case-Control Consortium and The Australian Ovarian Cancer Study Group and The Australian Cancer Study (Ovarian Cancer)
Nature Genetics, ISSN 1061-4036, 2010, Volume 42, Issue 10, pp. 874 - 879
Ovarian cancer accounts for more deaths than all other gynecological cancers combined. To identify common low-penetrance ovarian cancer susceptibility genes,... 
POLY(ADP-RIBOSE) POLYMERASE | CELLS | MULTIPLE LOCI | GENE | VARIANTS | GENETICS & HEREDITY | Chromosomes, Human, Pair 8 - genetics | Genetic Predisposition to Disease | Genome-Wide Association Study | Ovary - pathology | Humans | Proto-Oncogene Proteins c-myb - genetics | Genotype | Phosphoproteins - genetics | DNA-Binding Proteins - genetics | Case-Control Studies | Homeodomain Proteins - genetics | Ovarian Neoplasms - genetics | Chromosomes, Human, Pair 2 - genetics | Polymorphism, Single Nucleotide - genetics | Female | Biomarkers, Tumor - genetics | Genome, Human | Clinical Trials, Phase I as Topic | Clinical Trials, Phase II as Topic | Ovary - metabolism | Prevention | Evaluation | Genetic susceptibility | Genomics | Oncology, Experimental | Genetic aspects | Genomes | Research | Risk factors | Cancer | Ovarian cancer | Studies | Medical research | Hospitals | Biomedical research | Councils | Health services | Family medical history | Public health
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4. Full Text Beta HPV38 oncoproteins act with a hit-and-run mechanism in ultraviolet radiation-induced skin carcinogenesis in mice
by Viarisio, Daniele and Müller-Decker, Karin and Accardi, Rosita and Robitaille, Alexis and Dürst, Matthias and Beer, Katrin and Jansen, Lars and Flechtenmacher, Christa and Bozza, Matthias and Harbottle, Richard and Voegele, Catherine and Ardin, Maude and Zavadil, Jiri and Caldeira, Sandra and Gissmann, Lutz and Tommasino, Massimo
PLoS Pathogens, ISSN 1553-7366, 01/2018, Volume 14, Issue 1, pp. e1006783 - e1006783
Cutaneous beta human papillomavirus (HPV) types are suspected to be involved, together with ultraviolet (UV) radiation, in the development of non-melanoma skin... 
ACTIVATION | P53 FUNCTIONS | CANCER GENOME | MICROBIOLOGY | HUMAN-PAPILLOMAVIRUS | REPLICATION | VIROLOGY | SQUAMOUS-CELL CARCINOMA | LANDSCAPES | DIFFERENTIATION | EXPRESSION | PARASITOLOGY | TRANSGENIC MICE | Betapapillomavirus - metabolism | Receptors, Notch - metabolism | Skin - metabolism | Tumor Burden - radiation effects | Receptors, Notch - genetics | Neoplasm Proteins - metabolism | Viral Proteins - metabolism | Carcinogenesis - radiation effects | Mutagenesis - radiation effects | Gene Deletion | Female | Oncogene Proteins, Viral - genetics | Neoplasm Proteins - genetics | Neoplasms, Radiation-Induced - pathology | Skin - pathology | Oncogene Proteins, Viral - metabolism | Recombinant Proteins - metabolism | Skin Neoplasms - pathology | Epidermis - metabolism | Epidermis - pathology | Epidermis - radiation effects | Viral Proteins - genetics | Mice, Transgenic | Neoplasms, Radiation-Induced - metabolism | Ultraviolet Rays - adverse effects | Skin Neoplasms - metabolism | Animals | Genes, p53 - radiation effects | Skin - radiation effects | Mice | Skin Neoplasms - etiology | Mutation | Oncology, Experimental | Genes | Research | Carcinogenesis | Epidemiology | Skin cancer | Ultraviolet radiation | Gene mutations | Analysis | Genetic engineering | Skin | Tumor proteins | Papillomavirus infections | Cancer | Genetically modified mice | Papillomaviruses | Models | Genetic aspects | Gene expression | Oncogenes | Animal models | Recombination | p53 Protein | Transgenic | Carcinogens | Human papillomavirus | Clonal deletion | Deletion | Skin diseases | Lesions | Deoxyribonucleic acid--DNA | Radiation effects | U.V. radiation | Melanoma | Epidermis | Liquid oxygen | Irradiation | In vivo methods and tests | Notch protein | Tumors | Index Medicus | Deoxyribonucleic acid | DNA
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5. Full Text A genome-wide association study identifies a new ovarian cancer susceptibility locus on 9p22.2
by Sellers, Thomas and Giles, Graham and Gentry-Maharaj, Aleksandra and Carney, Michael E and Hogdall, Estrid and Fasching, Peter A and Schildkraut, Joellen M and Kjaer, Susanne Krüger and Yang, Hannah and Jacobs, Ian J and Song, Honglin and Ziogas, Argyrios and Ness, Roberta B and Easton, Douglas F and Van Den Berg, David J and Lubi ski, Jan and Wilkens, Lynne R and Webb, Penelope M and Goode, Ellen L and McLaughlin, John and Tsai, Ya-Yu and Vierkant, Robert A and Lissowska, Jolanta and Risch, Harvey and Cramer, Daniel W and Beesley, Jonathan and Ekici, Arif B and Li, Dong and Goodman, Marc T and Narod, Steven and Wang-Gohrke, Shan and Gronwald, Jacek and Pearce, Celeste Leigh and Runnebaum, Ingo B and Bolton, Kelly L and Cunningham, Julie M and Whittemore, Alice S and Blaakaer, Jan and Chen, Zhihua and Lurie, Galina and M drek, Krzysztof and Chang-Claude, Jenny and Pharoah, Paul D P and Phelan, Catherine and Fridley, Brooke L and DiCioccio, Richard and Doherty, Jennifer A and Wu, Anna H and Pye, Carole and Tworoger, Shelley S and Gayther, Simon A and Anton-Culver, Hoda and Severi, Gianluca and Houlston, Richard and Jakubowska, Anna and Terry, Kathryn L and Gore, Martin E and Rossing, Mary Anne and Hillemanns, Peter and Thiel, Falk C and Berchuck, Andrew and Baglietto, Laura and Ponder, Bruce A J and Tomlinson, Ian and Fenstermacher, David and Stram, Daniel O and De Vivo, Immaculata and Dörk, Thilo and Southey, Melissa and Iversen, Edwin S and Moysich, Kirsten and Menon, Usha and Beckmann, Matthias W and Brewster, Wendy and Hogdall, Claus and Tyrer, Jonathan and Moorman, Patricia G and Garcia-Closas, Montserrat and Wozniak, Eva and Chenevix-Trench, Georgia and McGuire, Valerie and Dicks, Ed and Dürst, Matthias and Ramus, Susan J and Chanock, Stephen and Australian Ovarian Canc Study Grp and Ovarian Canc Assoc Consortium and Australian Canc Ovarian Study and Australian Ovarian Cancer Study Group and Australian Cancer (Ovarian) Study and Ovarian Cancer Association Consortium and The Australian Ovarian Cancer Study Group and The Ovarian Cancer Association Consortium
Nature Genetics, ISSN 1061-4036, 09/2009, Volume 41, Issue 9, pp. 996 - 1000
Epithelial ovarian cancer has a major heritable component, but the known susceptibility genes explain less than half the excess familial risk. We performed a... 
BREAST-CANCER | INVASIVE OVARIAN | CANDIDATE SNPS | COLORECTAL-CANCER | BASAL-CELL CARCINOMA | PROSTATE-CANCER | GENETICS & HEREDITY | RISK | MULTIPLE LOCI | PARP INHIBITORS | SINGLE NUCLEOTIDE POLYMORPHISMS | Haplotypes | Confidence Intervals | United States | Humans | Ovarian Neoplasms - pathology | Molecular Sequence Data | Case-Control Studies | Ovarian Neoplasms - genetics | Base Sequence | Female | Odds Ratio | European Continental Ancestry Group - genetics | Genetic Predisposition to Disease | Genome-Wide Association Study | Europe | Gene Frequency | Risk Factors | European Continental Ancestry Group - statistics & numerical data | Genotype | Chromosome Mapping | Chromosomes, Human, Pair 9 | Linkage Disequilibrium | Homozygote | Alleles | Heterozygote | Polymorphism, Single Nucleotide | Australia | BRCA mutations | Genetic aspects | Disease susceptibility | Research | Health aspects | Risk factors | Ovarian cancer | Studies | Medical research | Genotype & phenotype | Data analysis | Inflation | Biomedical research | Quality control
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6. Full Text Identification of 12 new susceptibility loci for different histotypes of epithelial ovarian cancer
by Phelan, Catherine M and Kuchenbaecker, Karoline B and Tyrer, Jonathan P and Kar, Siddhartha P and Lawrenson, Kate and Winham, Stacey J and Dennis, Joe and Pirie, Ailith and Riggan, Marjorie J and Chornokur, Ganna and Earp, Madalene A and Lyra, Paulo C and Lee, Janet M and Coetzee, Simon and Beesley, Jonathan and McGuffog, Lesley and Soucy, Penny and Dicks, Ed and Lee, Anew and Barrowdale, Daniel and Lecarpentier, Julie and Leslie, Goska and Aalfs, Cora M and Aben, Katja K. H and Adams, Marcia and Adlard, Julian and Anulis, Irene L and Anton-Culver, Hoda and Antonenkova, Natalia and Aravantinos, Gerasimos and Arnold, Norbert and Arun, Banu K and Arver, Brita and Azzollini, Jacopo and Balmaña, Judith and Banerjee, Susana N and Barjhoux, Laure and Barkardottir, Rosa B and Bean, Yukie and Beckmann, Matthias W and Beeghly-Fadiel, Alicia and Benitez, Javier and Bermisheva, Marina and Bernardini, Marcus Q and Birrer, Michael J and Bjorge, Line and Black, Amanda and Blankstein, Kenneth and Blok, Marinus J and Bodelon, Clara and Bogdanova, Natalia and Bojesen, Anders and Bonanni, Bernardo and Borg, Åke and Bradbury, Angela R and Brenton, James D and Brewer, Carole and Brinton, Louise and Broberg, Per and Brooks-Wilson, Angela and Bruinsma, Fiona and Brunet, Joan and Buecher, Bruno and Butzow, Ralf and Buys, Sauna S and Caldes, Trinidad and Caligo, Maria A and Campbell, Ian and Cannioto, Rikki and Carney, Michael E and Cescon, Terence and Chan, Salina B and Chang-Claude, Jenny and Chanock, Stephen and Chen, Xiao Qing and Chiew, Yoke-Eng and Chiquette, Jocelyne and Chung, Wendy K and Claes, Kathleen B. M and Conner, Thomas and Cook, Linda S and Cook, Jackie and Cramer, Daniel W and Cunningham, Julie M and D'Aloisio, Aimee A and Daly, Mary B and Damiola, Francesca and Damirovna, Sakaeva Dina and Dansonka-Mieszkowska, Agnieszka and Dao, Fanny and Davidson, Rosemarie and Defazio, Anna and Delnatte, Capucine and Doheny, Kimberly F and Diez, Orland and Ding, Yuan Chun and Doherty, Jennifer Anne and Domchek, Susan M and Dorfling, Cecilia M and Dörk, Thilo and ... and KConFab Investigators and EMEMBRACE Study and GEMO Study Collaborators and OPAL Study Grp and AOCS Study Grp and HEBON Study and AOCS study group and EMBRACE Study and OPAL study group and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Ortopedi and Uppsala universitet and Institutionen för kirurgiska vetenskaper
Nature genetics, ISSN 1061-4036, 2017, Volume 49, Issue 5, pp. 680 - 691
To identify common alleles associated with different histotypes of epithelial ovarian cancer (EOC), we pooled data from multiple genome-wide genotyping... 
BREAST-CANCER | COMMON VARIANTS | METAANALYSIS | CLEAR-CELL | ALGORITHM | GENETICS & HEREDITY | RISK | ASSOCIATION | CARCINOMA | ENDOMETRIOSIS | TELOMERE LENGTH | Neoplasms, Glandular and Epithelial - pathology | Genetic Predisposition to Disease - genetics | Genome-Wide Association Study | Meta-Analysis as Topic | Humans | Risk Factors | Genetic Loci - genetics | Ovarian Neoplasms - pathology | Genotype | Ovarian Neoplasms - genetics | BRCA1 Protein - genetics | Neoplasms, Glandular and Epithelial - genetics | Telomere-Binding Proteins - genetics | Alleles | Carcinoma, Ovarian Epithelial | Female | Polymorphism, Single Nucleotide | Mutation | BRCA2 Protein - genetics | Genetic susceptibility | Physiological aspects | Genetic aspects | Single nucleotide polymorphisms | Identification and classification | Health aspects | Risk factors | Ovarian cancer | Carriers | Medical research | Ovarian carcinoma | Genes | Gene regulation | Genomes | Breast cancer | Loci | Cancer | Life Sciences | Human health and pathology | Genetics | Medical and Health Sciences | Medicin och hälsovetenskap
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