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1. Full Text Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk
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
BRCA1-associated breast and ovarian cancer risks can be modified by common genetic variants. To identify further cancer risk-modifying loci, we performed a... 
CONSORTIUM | COMMON VARIANTS | POPULATION | INVESTIGATORS | MODIFIERS | SUBTYPES | SUSCEPTIBILITY ALLELES | GENETICS & HEREDITY | GENETIC-VARIANTS | SELECTION | ZNF365 | Genetic Predisposition to Disease | Genome-Wide Association Study | Prognosis | Humans | Middle Aged | Risk Factors | Ovarian Neoplasms - pathology | Genotype | Ovarian Neoplasms - genetics | BRCA1 Protein - genetics | Breast Neoplasms - genetics | Breast Neoplasms - pathology | Female | Heterozygote | Polymorphism, Single Nucleotide | Mutation | BRCA2 Protein - genetics | Gene mutations | Genomics | Physiological aspects | Breast cancer | Genetic aspects | Research | Risk factors | Ovarian cancer | Cancer | Càncer d'ovari | Càncer de mama | Malalties hereditàries | Genètica humana | Genetic diseases | Human genetics | Life Sciences | Medical and Health Sciences | Medicin och hälsovetenskap | Medical research
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2. Full Text Assessing associations between the AURKA-HMMR-TPX2-TUBG1 functional module and breast cancer risk in BRCA1/2 mutation carriers
by Blanco, Ignacio and Kuchenbaecker, Karoline and Cuaas, Daniel and Wang, Xianshu and Barrowdale, Daniel and de Garibay, Gorka Ruiz and Librado, Pablo and Sánchez-Gracia, Alejano and Rozas, Julio and Bonifaci, Núria and McGuffog, Lesley and Pankratz, Vernon S and Islam, Abul and Mateo, Francesca and Berenguer, Antoni and Petit, Anna and Català, Isabel and Brunet, Joan and Feliubadaló, Lidia and Tornero, Eva and Benítez, Javier and Osorio, Ana and Ramón Y Cajal, Teresa and Nevanlinna, Heli and Aittomäki, Kristiina and Arun, Banu K and Toland, Amanda E and Karlan, Beth Y and Walsh, Christine and Lester, Jenny and Greene, Mark H and Mai, Phuong L and Nussbaum, Robert L and Anulis, Irene L and Domchek, Susan M and Nathanson, Katherine L and Rebbeck, Timothy R and Barkardottir, Rosa B and Jakubowska, Anna and Lubinski, Jan and Durda, Katarzyna and Jaworska-Bieniek, Katarzyna and Claes, Kathleen and van Maerken, Tom and Díez, Orland and Hansen, Thomas V and Jønson, Lars and Gerdes, Anne-Marie and Ejlertsen, Bent and de la Hoya, Miguel and Caldés, Trinidad and Dunning, Alison M and Oliver, Clare and Fineberg, Elena and Cook, Margaret and Peock, Susan and McCann, Emma and Murray, Alex and Jacobs, Chris and Pichert, Gabriella and Lalloo, Fiona and Chu, Carol and Dorkins, Huw and Paterson, Joan and Ong, Kai-Ren and Teixeira, Manuel R and Hogervorst, Frans B. L and van der Hout, Annemarie H and Seynaeve, Caroline and van der Luijt, Rob B and Ligtenberg, Marjolijn J. L and Devilee, Peter and Wijnen, Juul T and Rookus, Matti A and Meijers-Heijboer, Hanne E. J and Blok, Marinus J and van den Ouweland, Ans M. W and Aalfs, Cora M and Roiguez, Gustavo C and Phillips, Kelly-Anne A and Piedmonte, Marion and Nerenstone, Stacy R and Bae-Jump, Victoria L and O'Malley, David M and Ratner, Elena S and Schmutzler, Rita K and Wappenschmidt, Barbara and Rhiem, Kerstin and Engel, Christoph and Meindl, Alfons and Ditsch, Nina and Arnold, Norbert and Plendl, Hansjoerg J and Niederacher, Dieter and Sutter, Christian and Wang-Gohrke, Shan and Steinemann, Doris and Preisler-Adams, Sabine and Kast, Karin and Varon-Mateeva, Raymonda and ... and KConFab Investigators and GEMO and BCFR and SWE-BRCA and kConFab Investigators and Teixeira 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
PLoS ONE, ISSN 1932-6203, 2015, Volume 10, Issue 4, pp. e0120020 - e0120020
While interplay between BRCA1 and AURKA-RHAMM-TPX2-TUBG1 regulates mammary epithelial polarization, common genetic variation in HMMR (gene product RHAMM) may... 
CHIP-SEQ | SURVIVAL | ELEMENTS | GENETIC INTERACTION NETWORKS | MODIFIERS | MULTIDISCIPLINARY SCIENCES | SUSCEPTIBILITY LOCI | POLYMORPHISM | EXPRESSION SIGNATURE | CELL | GENOME-WIDE ASSOCIATION | Genetic Predisposition to Disease - genetics | Microtubule-Associated Proteins - genetics | Extracellular Matrix Proteins - genetics | Humans | Carcinogenesis - genetics | Genetic Loci - genetics | Tubulin - genetics | Mammary Glands, Human - metabolism | Hyaluronan Receptors - genetics | Breast Neoplasms - enzymology | Likelihood Functions | Breast Neoplasms - genetics | Breast Neoplasms - pathology | Cell Cycle Proteins - genetics | Genes, BRCA2 | Estrogen Receptor alpha - metabolism | Female | Polymorphism, Single Nucleotide | Retrospective Studies | Genes, BRCA1 | Mutation | Nuclear Proteins - genetics | Aurora Kinase A - genetics | Evolution, Molecular | Gene mutations | Genes | Breast cancer | Genetic aspects | Single nucleotide polymorphisms | Health aspects | Risk factors | Cancer | Biomedical research | Laboratories | Oncology | Genomes | Biology | Single-nucleotide polymorphism | Epidemiology | Carcinogenesis | Confidence intervals | Carcinogens | Risk assessment | Cell cycle | Bioinformatics | Public health | BRCA2 protein | BRCA1 protein | Health risks | Genetic diversity | Mammals | Primary care | Biological diversity | Carriers | Medicine | Pathology | Hospitals | Womens health | Alleles | Breast | Genetic engineering | Evolution & development | Tumors | Index Medicus | Càncer d'ovari | Càncer de mama | Mutació (Biologia) | Amino acid sequence | Seqüència d'aminoàcids | Mutation (Biology) | Ovarian cancer | Clinical Medicine | Medical and Health Sciences | Cancer and Oncology | Klinisk medicin | Medicin och hälsovetenskap | Cancer och onkologi
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3. Full Text Common Genetic Variants and Modification of Penetrance of BRCA2-Associated Breast Cancer
by Gaudet, Mia and Kircchoff, Tomas and Green, Todd and Vijai, Joseph and Korn, Joshua and Guiducci, Candace and Segrè, Ayellet and McGee, Kate and McGuffog, Lesley and Kartsonaki, Christiana and Morrison, Jonathan and Healey, Sue and Sinilnikova, Olga and Stoppa-Lyonnet, Dominique and Mazoyer, Sylvie and Gauthier-Villars, Marion and Sobol, Hagay and Longy, Michel and Frenay, Marc and Hogervorst, Frans and Rookus, Matti and Collée, Margriet and Hoogerbrugge, Nicoline and Roozendaal, Kees and Piedemonte, Marion and Rubinstein, Wendy and Nerenstone, Stacy and Le, Linda and Blank, Stephanie and Caldes, Trinidad and Hoya, Miguel and Nevanlinna, Heli and Aittomäki, Kristiina and Lazaro, Conxi and Blanco, Ignacio and Arason, Adalgeir and Johannson, Oskar and Barkardottir, Rosa and Devilee, Peter and Olopade, Olofunmilayo and Neuhausen, Susan and Wang, Xianshu and Fredericksen, Zachary and Peterlongo, Paolo and Manoukian, Siranoush and Barile, Monica and Viel, Alessana and Radice, Paolo and Phelan, Catherine and Narod, Steven and Rennert, Gad and Lejbkowicz, Flavio and Flugelman, Anath and Anulis, Irene and Glendon, Gord and Ozcelik, Hilmi and Toland, Amanda and Montagna, Marco and D'Anea, Emma and Friedman, Eitan and Laitman, Yael and Borg, Åke and Beattie, Mary and Ramus, Susan and Domchek, Susan and Nathanson, Katherine and Rebbeck, Timothy and Spurdle, Amanda and Chen, Xiaoqing and Holland, Helene and John, Esther and Hopper, John and Buys, Sauna and Daly, Mary and Southey, Melissa and Terry, Mary-beth and Tung, Nadine and Hansen, Thomas and Nielsen, Finn and Greene, Mark and Mai, Phuong and Osorio, Ana and Duran, M and Anes, Raquel and Benítez, Javier and Weitzel, Jeffrey and Garber, Judy and Hamann, Ute and Peock, Susan and Cook, Margaret and Oliver, Clare and Frost, Debra and Platte, Radka and Evans, Gareth and Lalloo, Fiona and Eeles, Rosalind and Izatt, Louise and Walker, Lisa and Eason, Jacqueline and Barwell, Julian and ... and HEBON Study Collaborators and GEMO Study Collaborators and kConFab and OCGN and EMBRACE and Onkologi och Patologi, MV and Lund University and Oncology and Pathology, MV and Lunds universitet
P L o S Genetics (Print), ISSN 1553-7390, 10/2010, Volume 6, Issue 10, pp. 1 - 12
textabstractThe considerable uncertainty regarding cancer risks associated with inherited mutations of BRCA2 is due to unknown factors. To investigate whether... 
BRCA2 MUTATION CARRIERS | RECURRENT BRCA1 | PREDISPOSITION | SUSCEPTIBILITY | FREQUENCY | GENETICS & HEREDITY | PHENOTYPE | RISK | MODEL | ASSOCIATION | Haplotypes | European Continental Ancestry Group - genetics | Genetic Predisposition to Disease - genetics | Gene Frequency | Humans | Middle Aged | Risk Factors | Penetrance | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Linkage Disequilibrium | Breast Neoplasms - genetics | Adult | Female | Heterozygote | Polymorphism, Single Nucleotide | Mutation | Chromosomes, Human, Pair 20 | Genome-Wide Association Study - methods | Chromosomes, Human, Pair 10 | BRCA2 Protein - genetics | Receptor, Fibroblast Growth Factor, Type 2 - genetics | Càncer de mama | Breast cancer | Clinical Medicine | Medical and Health Sciences | Klinisk medicin | Cancer and Oncology | Medicin och hälsovetenskap | Cancer och onkologi | Confidence intervals | Medical research | Genealogy | Quality control | Population | Genomes | Chromosomes
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4. Full Text Laparoscopy Compared With Laparotomy for Comprehensive Surgical Staging of Uterine Cancer: Gynecologic Oncology Group Study LAP2
by Joan L. Walker and Marion R. Piedmonte and Nick M. Spirtos and Scott M. Eisenkop and John B. Schlaerth and Robert S. Mannel and Gregory Spiegel and Richard Barakat and Michael L. Pearl and Sudarshan K. Sharma
Journal of Clinical Oncology, ISSN 0732-183X, 11/2009, Volume 27, Issue 32, pp. 5331 - 5336
Purpose The objective was to compare laparoscopy versus laparotomy for comprehensive surgical staging of uterine cancer. Patients and Methods Patients with... 
PHASE-III TRIAL | SURGERY | VAGINAL HYSTERECTOMY | ONCOLOGY | ADENOCARCINOMA | PELVIC LYMPHADENECTOMY | CYTOREDUCTION | SURVIVAL COMPARISONS | CARCINOMA | ENDOMETRIAL CANCER | RADIATION-THERAPY | Length of Stay | Outcome Assessment (Health Care) | Uterine Neoplasms - pathology | Humans | Middle Aged | Abscess - etiology | Neoplasm Staging - methods | Laparoscopy - methods | Uterine Neoplasms - surgery | Laparoscopy - adverse effects | Laparotomy - methods | Intraoperative Complications - etiology | Urinary Tract Infections - etiology | Fever - etiology | Female | Aged | Laparotomy - adverse effects | Original Reports | Gync9
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5. Full Text Recurrence and Survival After Random Assignment to Laparoscopy Versus Laparotomy for Comprehensive Surgical Staging of Uterine Cancer: Gynecologic Oncology Group LAP2 Study
by Joan L. Walker and Marion R. Piedmonte and Nick M. Spirtos and Scott M. Eisenkop and John B. Schlaerth and Robert S. Mannel and Richard Barakat and Michael L. Pearl and Sudarshan K. Sharma
Journal of Clinical Oncology, ISSN 0732-183X, 03/2012, Volume 30, Issue 7, pp. 695 - 700
Purpose The primary objective was to establish noninferiority of laparoscopy compared with laparotomy for recurrence after surgical staging of uterine cancer.... 
PHASE-III TRIAL | SURGERY | IRRADIATION | ADVANCED ENDOMETRIAL CARCINOMA | CISPLATIN | ONCOLOGY | DOXORUBICIN | Lymph Node Excision | Ovariectomy - adverse effects | Recurrence | Prospective Studies | Uterine Neoplasms - pathology | Humans | Middle Aged | Hysterectomy - methods | Survival Rate | Ovariectomy - methods | Neoplasm Recurrence, Local - pathology | Young Adult | Laparoscopy - methods | Uterine Neoplasms - surgery | Laparoscopy - adverse effects | Laparotomy - methods | Aged, 80 and over | Adult | Female | Hysterectomy - adverse effects | Aged | Neoplasm Staging | Laparotomy - adverse effects | Original Reports | Gync10 | Gync9
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6. Full Text Identification of a BRCA2-specific modifier locus at 6p24 related to breast cancer risk
by Gaudet, Mia M and Kuchenbaecker, Karoline B and Vijai, Joseph and Klein, Robert J and Kirchhoff, Tomas and McGuffog, Lesley and Barrowdale, Daniel and Dunning, Alison M and Lee, Anew and Dennis, Joe and Healey, Sue and Dicks, Ed and Soucy, Penny and Sinilnikova, Olga M and Pankratz, Vernon S and Wang, Xianshu and Elidge, Ronald C and Tessier, Daniel C and Vincent, Daniel and Bacot, Francois and Hogervorst, Frans B. L and Peock, Susan and Stoppa-Lyonnet, Dominique and Peterlongo, Paolo and Schmutzler, Rita K and Nathanson, Katherine L and Piedmonte, Marion and Singer, Christian F and Thomassen, Mads and Hansen, Thomas v O and Neuhausen, Susan L and Blanco, Ignacio and Greene, Mark H and Garber, Judith and Weitzel, Jeffrey N and Anulis, Irene L and Goldgar, David E and D'Anea, Emma and Caldes, Trinidad and Nevanlinna, Heli and Osorio, Ana and van Rensburg, Elizabeth J and Arason, Adalgeir and Rennert, Gad and van den Ouweland, Ans M. W and van der Hout, Annemarie H and Kets, Carolien M and Aalfs, Cora M and Wijnen, Juul T and Ausems, Margreet G. E. M and Frost, Debra and Ellis, Steve and Fineberg, Elena and Platte, Radka and Evans, D. Gareth and Jacobs, Chris and Adlard, Julian and Tischkowitz, Marc and Porteous, Mary E and Damiola, Francesca and Golmard, Lisa and Barjhoux, Laure and Longy, Michel and Belotti, Muriel and Ferrer, Sana Fert and Mazoyer, Sylvie and Spurdle, Amanda B and Manoukian, Siranoush and Barile, Monica and Genuardi, Maurizio and Arnold, Norbert and Meindl, Alfons and Sutter, Christian and Wappenschmidt, Barbara and Domchek, Susan M and Pfeiler, Georg and Friedman, Eitan and Jensen, Uffe Birk and Robson, Mark and Shah, Sohela and Lazaro, Conxi and Mai, Phuong L and Benitez, Javier and Southey, Melissa C and Schmidt, Marjanka K and Fasching, Peter A and Peto, Julian and Humphreys, Manjeet K and Wang, Qin and Michailidou, Kyriaki and Sawyer, Elinor J and Burwinkel, Barbara and Guénel, Pascal and Bojesen, Stig E and Milne, Roger L and Brenner, Hermann and Lochmann, Magdalena and Aittomäki, Kristiina and Dörk, Thilo and Margolin, Sara and ... and KConFab Investigators and Ontario Canc Genetics Network and HEBON and EMBRACE and GEMO Study Collaborators and GENICA Network and Ontario Cancer Genetics Network and The GENICA Network
PLoS genetics, ISSN 1553-7390, 2013, Volume 9, Issue 3, p. e1003173
Common genetic variants contribute to the observed variation in breast cancer risk for BRCA2 mutation carriers; those known to date have all been found through... 
BRCA2 MUTATION CARRIERS | CONSORTIUM | COMMON VARIANTS | POPULATION | SUBTYPES | SUSCEPTIBILITY ALLELES | GENETICS & HEREDITY | OVARIAN-CANCER | TRANSCRIPTION FACTOR AP-2 | GENOME-WIDE ASSOCIATION | ZNF365 | Genetic Predisposition to Disease | Genome-Wide Association Study | Humans | Middle Aged | Risk Factors | Genotype | Chromosomes, Human, Pair 6 - genetics | BRCA1 Protein - genetics | Breast Neoplasms - genetics | Breast Neoplasms - pathology | Alleles | Adult | Female | Heterozygote | Aged | Polymorphism, Single Nucleotide | Mutation | BRCA2 Protein - genetics | Gene mutations | Genetic variation | Physiological aspects | Breast cancer | Genetic aspects | Research | Risk factors | Cancer | Human genome | Càncer de mama | Cromosomes humans | Malalties hereditàries | Human chromosomes | Genetic diseases | Genoma humà | Medical research | Womens health
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7. 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 The Hereditary Breast and Ovarian Cancer Research Group Netherlands (HEBON) and Genetic Modifiers of Cancer Risk in BRCA1/2 Mutation Carriers (GEMO) and Gene Environment Interaction and Breast Cancer (GENICA) and Swedish Breast Cancer Study (SWE-BRCA) and Epidemiological study of BRCA1 & BRCA2 Mutation Carriers (EMBRACE) and Australian Ovarian Cancer Study and Australian Cancer Study and Kathleen Cuningham Foundation Consortium for Research into Familial Breast Cancer (kConFab) 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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8. Full Text Fine-Scale Mapping at 9p22.2 Identifies Candidate Causal Variants That Modify Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers
by Vigorito, E and Kuchenbaecker, K.B and Beesley, J and Adlard, J and Agnarsson, B.A and Anulis, I.L and Arun, B.K and Barjhoux, L and Belotti, M and Benitez, J and Berger, A and Bojesen, A and Bonanni, B and Brewer, C and Caldes, T and Caligo, M.A and Campbell, I and Chan, S.B and Claes, K.B and Cohn, D.E and Cook, J and Daly, M.B and Damiola, F and Davidson, R and Pauw, A. de and Delnatte, C and Diez, O and Domchek, S.M and Dumont, M and Durda, K and Dworniczak, B and Easton, D.F and Eccles, D and Edwinsdotter Ardnor, C and Eeles, R and Ejlertsen, B and Ellis, S and Evans, D.G and Feliubadalo, L and Fostira, F and Foulkes, W.D and Friedman, E and Frost, D and Gaddam, P and Ganz, P.A and Garber, J and Garcia-Barberan, V and Gauthier-Villars, M and Gehrig, A and Gerdes, A.M and Giraud, S and Godwin, A.K and Goldgar, D.E and Hake, C.R and Hansen, T.V and Healey, S and Hodgson, S and Hogervorst, F.B and Houdayer, C and Hulick, P.J and Imyanitov, E.N and Isaacs, C and Izatt, L and Izquierdo, A and Jacobs, L and Jakubowska, A and Janavicius, R and Jaworska-Bieniek, K and Jensen, U.B and John, E.M and Vijai, J and Karlan, B.Y and Kast, K and Khan, S and Kwong, A and Laitman, Y and Lester, J and Lesueur, F and Liljegren, A and Lubinski, J and Mai, P.L and Manoukian, S and Mazoyer, S and Meindl, A and Mensenkamp, A.R and Montagna, M and Nathanson, K.L and Neuhausen, S.L and Nevanlinna, H and Niederacher, D and Olah, E and Olopade, O.I and Ong, K.R and Osorio, A and Park, S.K and Paulsson-Karlsson, Y and Pedersen, I.S and Peissel, B and Peterlongo, P and et al and Kconfab Investigators and Medicinska fakulteten and Institutionen för strålningsvetenskaper and Onkologi and Umeå universitet
Plos One, ISSN 1932-6203, 2016, Volume 11, Issue 7, p. e0158801
Population-based genome wide association studies have identified a locus at 9p22.2 associated with ovarian cancer risk, which also modifies ovarian cancer risk... 
CONSORTIUM | INVESTIGATORS | MULTIDISCIPLINARY SCIENCES | SUSCEPTIBILITY LOCI | PATHOLOGY | CENTLEIN | BREAST | GENOME-WIDE ASSOCIATION | Ovarian Neoplasms - genetics | Genetic Predisposition to Disease | Humans | Genes, BRCA2 | Female | Chromosome Mapping | Polymorphism, Single Nucleotide | Chromosomes, Human, Pair 9 | Genes, BRCA1 | Genetic Carrier Screening | Physiological aspects | Genetic aspects | Research | BRCA mutations | Risk factors | Ovarian cancer | BRCA2 protein | Ovarian carcinoma | Transcription | BRCA1 protein | Health risks | Upstream | Risk | Breast cancer | Genomes | Mapping | Single-nucleotide polymorphism | Loci | Carriers | Mutation | Gene mapping | Health risk assessment | Genotypes | Cancer | Clinical Medicine | Medical and Health Sciences | Cancer and Oncology | Klinisk medicin | Medicin och hälsovetenskap | Cancer och onkologi
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