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1. 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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2. 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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3. Full Text Association analysis identifies 65 new breast cancer risk loci
by Michailidou, Kyriaki and Lindström, Sara and Dennis, Joe and Beesley, Jonathan and Hui, Shirley and Kar, Siddhartha and Lemaçon, Auey and Soucy, Penny and Glubb, Dylan and Rostamianfar, Asha and Bolla, Manjeet K and Wang, Qin and Tyrer, Jonathan and Dicks, Ed and Lee, Anew and Wang, Zhaoming and Allen, Jamie and Keeman, Renske and Eilber, Ursula and French, Juliet D and Qing Chen, Xiao and Fachal, Laura and McCue, Karen and McCart Reed, Amy E and Ghoussaini, Maya and Carroll, Jason S and Jiang, Xia and Finucane, Hilary and Adams, Marcia and Adank, Muriel A and Ahsan, Habibul and Aittomäki, Kristiina and Anton-Culver, Hoda and Antonenkova, Natalia N and Arndt, Volker and Aronson, Kristan J and Arun, Banu and Auer, Paul L and Bacot, François and Barrdahl, Myrto and Baynes, Caroline and Beckmann, Matthias W and Behrens, Sabine and Benitez, Javier and Bermisheva, Marina and Bernstein, Leslie and Blomqvist, Carl and Bogdanova, Natalia V and Bojesen, Stig E and Bonanni, Bernardo and Børresen-Dale, Anne-Lise and Brand, Judith S and Brauch, Hiltrud and Brennan, Paul and Brenner, Hermann and Brinton, Louise and Broberg, Per and Brock, Ian W and Broeks, Annegien and Brooks-Wilson, Angela and Brucker, Sara Y and Brüning, Thomas and Burwinkel, Barbara and Butterbach, Katja and Cai, Qiuyin and Cai, Hui and Caldés, Trinidad and Canzian, Federico and Carracedo, Angel and Carter, Brian D and Castelao, Jose E and Chan, Tsun L and David Cheng, Ting-Yuan and Seng Chia, Kee and Choi, Ji-Yeob and Christiansen, Hans and Clarke, Christine L and Collée, Margriet and Conroy, Don M and Cordina-Duverger, Emilie and Cornelissen, Sten and Cox, David G and Cox, Angela and Cross, Simon S and Cunningham, Julie M and Czene, Kamila and Daly, Mary B and Devilee, Peter and Doheny, Kimberly F and Dörk, Thilo and Dos-Santos-Silva, Isabel and Dumont, Martine and Durcan, Lorraine and Dwek, Miriam and Eccles, Diana M and Ekici, Arif B and Eliassen, A. Heather and Ellberg, Carolina and Elvira, Mingajeva and Engel, Christoph and ... and KConFab AOCS Investigators and ABCTB Investigators and NBCS Collaborators and ConFab/AOCS Investigators and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Ortopedi and Uppsala universitet and Institutionen för kirurgiska vetenskaper
Nature, ISSN 0028-0836, 2017, Volume 551, Issue 7678, pp. 92 - 94
Breast cancer risk is influenced by rare coding variants in susceptibility genes, such as BRCA1, and many common, mostly non-coding variants. However, much of... 
COMPREHENSIVE MOLECULAR PORTRAITS | PROTEIN | ANNOTATION | MULTIDISCIPLINARY SCIENCES | SUSCEPTIBILITY LOCI | ARCHITECTURE | PATHWAY ANALYSIS | MUTATIONS | ENHANCERS | EXPRESSION | GENOME-WIDE ASSOCIATION | Multifactorial Inheritance - genetics | European Continental Ancestry Group - genetics | Genetic Predisposition to Disease - genetics | Genome-Wide Association Study | Risk Assessment | Humans | Regulatory Sequences, Nucleic Acid | Asia - ethnology | Asian Continental Ancestry Group - genetics | Binding Sites - genetics | Genetic Loci | Europe - ethnology | Transcription Factors - metabolism | Breast Neoplasms - genetics | Computer Simulation | Polymorphism, Single Nucleotide - genetics | Female | Breast Neoplasms - diagnosis | Quantitative trait loci | Breast cancer | Genetic aspects | Health aspects | Risk factors | Medical research | Transcription factors | BRCA1 protein | Genes | Health risks | Association analysis | Risk | Genomes | Biology | Single-nucleotide polymorphism | Regulatory sequences | Epidemiology | Loci | Medicine | Womens health | Breast | Genetics | Heritability | Health risk assessment | Binding sites | Tumors | Cancer | Medical and Health Sciences | Medicin och hälsovetenskap
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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 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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6. Full Text Shared heritability and functional enrichment across six solid cancers (vol 10, 431, 2019)
by Jiang, X and Finucane, HK and Schumacher, FR and Schmit, SL and Tyrer, JP and Han, Y and Michailidou, K and Lesseur, C and Kuchenbaecker, KB and Dennis, J and Conti, DV and Casey, G and Gaudet, MM and Huyghe, JR and Albanes, D and Aldrich, MC and Andrew, AS and Andrulis, IL and Anton-Culver, H and Antoniou, AC and Antonenkova, NN and Arnold, SM and Aronson, KJ and Arun, BK and Bandera, EV and Barkardottir, RB and Barnes, DR and Batra, J and Beckmann, MW and Benitez, J and Benlloch, S and Berchuck, A and Berndt, SI and Bickeboller, H and Bien, SA and Blomqvist, C and Boccia, S and Bogdanova, NV and Bojesen, SE and Bolla, MK and Brauch, H and Brenner, H and Brenton, JD and Brook, MN and Brunet, J and Brunnstrom, H and Buchanan, DD and Burwinkel, B and Butzow, R and Cadoni, G and Caldes, T and Caligo, MA and Campbell, I and Campbell, PT and Cancel-Tassin, G and Cannon-Albright, L and Campa, D and Caporaso, N and Carvalho, AL and Chan, AT and Chang-Claude, J and Chanock, SJ and Chen, C and Christiani, DC and Claes, KBM and Claessens, F and Clements, J and Collee, JM and Correa, MC and Couch, FJ and Cox, A and Cunningham, JM and Cybulski, C and Czene, K and Daly, MB and deFazio, A and Devilee, P and Diez, O and Gago-Dominguez, M and Donovan, JL and Dork, T and Duell, EJ and Dunning, AM and Dwek, M and Eccles, DM and Edlund, CK and Edwards, DRV and Ellberg, C and Evans, DG and Fasching, PA and Ferris, RL and Liloglou, T and Figueiredo, JC and Fletcher, O and Fortner, RT and Fostira, F and Franceschi, S and Friedman, E and Gallinger, SJ and Ganz, PA and ... and Institutionen för kliniska vetenskaper, Avdelningen för obstetrik och gynekologi and Sahlgrenska akademin and Göteborgs universitet and Gothenburg University and Institute of Clinical Sciences, Department of Obstetrics and Gynecology and Sahlgrenska Academy
NATURE COMMUNICATIONS, ISSN 2041-1723, 09/2019, Volume 10
Quantifying the genetic correlation between cancers can provide important insights into the mechanisms driving cancer etiology. Using genome-wide association... 
MULTIDISCIPLINARY SCIENCES | Andrew R.] Univ Bristol | 3400 Civ Ctr | risk-factors | England | Miranda] Univ Bristol | Clalit Natl Canc Control Ctr | Kenneth] Mem Sloan Kettering Canc Ctr | Kinghorn Canc Ctr | randomization | Pring | Div Populat Hlth Hlth Serv Res & Primary Care | Seattle | Upper Maudlin St | Stanford | Sch Womens & Childrens Hlth | Offit | Duarte | Ulrike | Susan J.] Garvan Inst Med Res | Sydney | Moreno | Plaseska-Karanfilska | Victor] Univ Barcelona | Warwick Med Sch | Dept | Lab Med Program | Wilbert H. M.] Radboud Univ Nijmegen | Elizabeth J.] Univ Pretoria | Anna Marie] Univ Hlth Network | Peters | Nielsen | Ness | 18 High St | lung-cancer | Lindstrom | 1275 York | Kenneth] Univ Warwick | Kari] Decode Genet | Blegdamsvej 9 | Harvey A.] Yale Sch Publ Hlth | Neal | Liene] Latvian Biomed Res & Study Ctr | Kirsten B.] Roswell Pk Canc Inst | Science & Technology - Other Topics | partitioning heritability | Dept Genet | Dept Res | Billrothstr11 | Bristol BS2 | Israel | Dept Obstet & Gynecol | Geert Grooteplein Zuid | Dept Canc Biol & Genet | Res Ctr Genet Engn & Biotechnol Georgi | Nussbaum | Iceland | WA 98195 USA | Haartmaninkatu 8 | Paolo] INT | Robert L.] Univ Calif San Francisco | NSW 2010 | Buffalo | 384 Victoria St | Rosenstein | cell-types | CT 06510 USA | Med Ctr | van Rensburg | Gad | Dept Urol | Angela] Salzburg Univ | Dept Chron Dis Epidemiol | Finn Cilius] Copenhagen Univ Hosp | Clin Genet Serv | Dijana] Macedonian Acad Sci & Arts | Nikitina-Zake | 200 Elizabeth St | Susan L.] Beckman Res Inst City Hope | Dept Genet & Genom Sci | Canc Ctr Cluster Salzburg | Muir | IS-101 Reykjavik | Risch | Div Hlth Sci | Sch Med | Canc Genet & Prevent Program | Wei] Vanderbilt Univ | New York | susceptibility loci | genetic architecture | 60 Coll St | Anna Marie] Univ Toronto | Avon | IBELL | Roobol | Dept Populat Sci | NL-3015 CN Rotterdam | Lower Maudlin St | 1275 York Ave | Div Epidemiol | Radice | Fdn IRCCS | Neuenheimer Feld 280 | breast-cancer | 1600 Div St | Wytemaweg 80 | Sturlugata 8 | Latvia | Helsinki Univ Hosp | Coventry CV4 7AL | W Midlands | Catalan Inst Oncol | Unit Mol Bases Genet Risk & Genet Testing | Leon | Lisa F.] Univ Washington | ON M5S | Skopje 1000 | Sch Publ Hlth | Dept Oncol | Susan J.] Univ NSW Sydney | 7 Michal St | Bristol Dent Sch | Cambridge CB1 8RN | NSW | New Haven | Raskin | Moysich | Ratsupites Str 1 | Ctr Genom Med | TLRC H | Toronto | Germany | David E.] Univ Cambridge | Dept Radiat Oncol | Dept Med | Elm & Carlton St | Addenbrookes Hosp | A-5020 | Stefansson | Div Epigen & Canc Risk Factors | Katherine L.] Univ Penn | Abramson Canc Ctr | Via Giacomo | South | Bristol BS1 2LY | Rennert | Spain | Rigshosp | Mulligan | Obstetrics, Gynecology and Reproductive Medicine | Perelman Sch Med | Sara] Univ Washington | Blvd Krste Petkov Misirkov | 1500 E Duarte | genome-wide association | 1 Kings Coll Circle | Dept Gastroenterol | 1425 Madison Ave | Fac Med | mendelian | ZA-0007 Arcadia | Hedy S.] Technion Fac Med | Barry S.] Icahn Sch Med Mt Sinai | Angela] German Ctr Lung Res DZL | Nathanson | Dept Lab Med & Pathobiol | Clin Genet Res Lab | Nevanlinna | Heli] Univ Helsinki | Amanda I | Private Bag X323 | Ramus | ON M5G 2C4 | DK-2100 | 97239 USA | Newcomb | Macedonia | IL-34362 Haifa | PLUS | Div Canc Prevent & Control | San | Janet L | D-69120 Heidelberg | Barcelona 08908 | Monique J.] Erasmus Univ | CA 91010 | Kenneth] Univ Manchester | LV-1067 Riga | Neuhausen | Dept Mol Biol | fremov | NIHR Bristol Biomed Res Ctr Nutr Theme | Hedy S.] Carmel Hosp | analyses identify | FIN | Vanderbilt Ingram Canc Ctr | Oxford Rd | Phipps | Zheng | Angela] DKFZ German Canc Res Ctr | Reproduktionsmedicin och gynekologi
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7. Full Text Mutational spectrum in a worldwide study of 29,700 families with BRCA1 or BRCA2 mutations
by Rebbeck, Timothy R and Friebel, Tara M and Friedman, Eitan and Hamann, Ute and Huo, Dezheng and Kwong, Ava and Olah, Edith and Olopade, Olufunmilayo I and Solano, Angela R and Teo, Soo‐Hwang and Thomassen, Mads and Weitzel, Jeffrey N and Chan, TL and Couch, Fergus J and Goldgar, David E and Kruse, Torben A and Palmero, Edenir Inêz and Park, Sue Kyung and Torres, Diana and Rensburg, Elizabeth J and McGuffog, Lesley and Parsons, Michael T and Leslie, Goska and Aalfs, Cora M and Abugattas, Julio and Adlard, Julian and Agata, Simona and Aittomäki, Kristiina and Andrews, Lesley and Andrulis, Irene L and Arason, Adalgeir and Arnold, Norbert and Arun, Banu K and Asseryanis, Ella and Auerbach, Leo and Azzollini, Jacopo and Balmaña, Judith and Barile, Monica and Barkardottir, Rosa B and Barrowdale, Daniel and Benitez, Javier and Berger, Andreas and Berger, Raanan and Blanco, Amie M and Blazer, Kathleen R and Blok, Marinus J and Bonadona, Valérie and Bonanni, Bernardo and Bradbury, Angela R and Brewer, Carole and Buecher, Bruno and Buys, Saundra S and Caldes, Trinidad and Caliebe, Almuth and Caligo, Maria A and Campbell, Ian and Caputo, Sandrine M and Chiquette, Jocelyne and Chung, Wendy K and Claes, Kathleen B.M and Collée, J. Margriet and Cook, Jackie and Davidson, Rosemarie and la Hoya, Miguel and Leeneer, Kim and Pauw, Antoine and Delnatte, Capucine and Diez, Orland and Ding, Yuan Chun and Ditsch, Nina and Domchek, Susan M and Dorfling, Cecilia M and Velazquez, Carolina and Dworniczak, Bernd and Eason, Jacqueline and Easton, Douglas F and Eeles, Ros and Ehrencrona, Hans and Ejlertsen, Bent and Engel, Christoph and Engert, Stefanie and Evans, D. Gareth and Faivre, Laurence and Feliubadaló, Lidia and Ferrer, Sandra Fert and Foretova, Lenka and Fowler, Jeffrey and Frost, Debra and Galvão, Henrique C. R and Ganz, Patricia A and Garber, Judy and Gauthier‐Villars, Marion and Gehrig, Andrea and Gerdes, Anne‐Marie and Gesta, Paul and Giannini, Giuseppe and Giraud, Sophie and Glendon, Gord and Godwin, Andrew K and Greene, Mark H and ... and KConFab Investigators and HEBON and EMBRACE and GEMO Study Collaborators
Human Mutation, ISSN 1059-7794, 05/2018, Volume 39, Issue 5, pp. 593 - 620
The prevalence and spectrum of germline mutations in BRCA1 and BRCA2 have been reported in single populations, with the majority of reports focused on White in... 
mutation | ethnicity | ovarian cancer | geography | breast cancer | BRCA1 | BRCA2 | GENE-MUTATIONS | HEREDITARY BREAST | 185DELAG MUTATION | FOUNDER MUTATIONS | RECURRENT BRCA1 | HAPLOTYPE ANALYSIS | PHENOTYPE ANALYSIS | HIGH-RISK | GENETICS & HEREDITY | BREAST-CANCER PATIENTS | GERMLINE MUTATIONS | Genetic aspects | BRCA mutations | Genetic screening | Singers | Ovarian cancer | BRCA2 protein | Mutation | Genotyping | BRCA1 protein | Minority & ethnic groups | Life Sciences | Genetics | Human genetics | Geography | Basic Medicine | Medical and Health Sciences | Medicin och hälsovetenskap | Breast cancer | Medicinsk genetik | Medical Genetics | Ethnicity | Medicinska och farmaceutiska grundvetenskaper
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