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1. Full Text Reply
by Troisi, Rebecca and Hoover, Robert N
American Journal of Obstetrics and Gynecology, ISSN 0002-9378, 02/2017, Volume 216, Issue 2, p. 198
To link to full-text access for this article, visit this link: http://dx.doi.org/10.1016/j.ajog.2016.09.098 Byline: Rebecca Troisi, Robert N. Hoover Author... 
Social service | Epidemiology
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2. Full Text Reply
by Troisi, Rebecca and Hoover, Robert N
American Journal of Obstetrics and Gynecology, ISSN 0002-9378, 02/2017, Volume 216, Issue 2, p. 198
Social service | Epidemiology
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3. Full Text Reply
by Troisi, Rebecca and Hoover, Robert N
American Journal of Obstetrics and Gynecology, ISSN 0002-9378, 02/2017, Volume 216, Issue 2, p. 198
Social service | Epidemiology
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4. Full Text Reply
by Troisi, Rebecca and Hoover, Robert N and Hatch, Elizabeth E
American Journal of Obstetrics and Gynecology, ISSN 0002-9378, 02/2017, Volume 216, Issue 2, pp. 198 - 199
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5. Full Text Reply
by Troisi, Rebecca and Hoover, Robert N and Hatch, Elizabeth E
American Journal of Obstetrics and Gynecology, ISSN 0002-9378, 02/2017, Volume 216, Issue 2, pp. 198 - 199
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6. Full Text Reply
by Troisi, Rebecca and Hoover, Robert N and Hatch, Elizabeth E
American Journal of Obstetrics and Gynecology, ISSN 0002-9378, 02/2017, Volume 216, Issue 2, pp. 198 - 199
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7. 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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8. Full Text Genome-wide association studies identify four ER negative-specific breast cancer risk loci
by Garcia-Closas, Montserrat and Couch, Fergus J and Lindstrom, Sara and Michailidou, Kyriaki and Schmidt, Marjanka K and Brook, Mark N and Orr, Nick and Rhie, Suhn Kyong and Riboli, Elio and Feigelson, Heather S and Le Marchand, Loic and Buring, Julie E and Eccles, Diana and Miron, Penelope and Fasching, Peter A and Brauch, Hiltrud and Chang-Claude, Jenny and Carpenter, Jane and Godwin, Anew K and Nevanlinna, Heli and Giles, Graham G and Cox, Angela and Hopper, John L and Bolla, Manjeet K and Wang, Qin and Dennis, Joe and Dicks, Ed and Howat, Will J and Schoof, Nils and Bojesen, Stig E and Lambrechts, Diether and Broeks, Annegien and Anulis, Irene L and Guénel, Pascal and Burwinkel, Barbara and Sawyer, Elinor J and Hollestelle, Antoinette and Fletcher, Olivia and Winqvist, Robert and Brenner, Hermann and Mannermaa, Arto and Hamann, Ute and Meindl, Alfons and Lindblom, Annika and Zheng, Wei and Devillee, Peter and Goldberg, Mark S and Lubinski, Jan and Kristensen, Vessela and Swerdlow, Anthony and Anton-Culver, Hoda and Dörk, Thilo and Muir, Kenneth and Matsuo, Keitaro and Wu, Anna H and Radice, Paolo and teo, Soo Hwang and Shu, Xiao-Ou and Blot, William and Kang, Daehee and Hartman, Mikael and Sangrajrang, Suleeporn and Shen, Chen-Yang and Southey, Melissa C and Park, Daniel J and Hammet, Fleur and Stone, Jennifer and Veer, Laura J. Van't and Rutgers, Emiel J and Lophatananon, Artitaya and Stewart-Brown, Sarah and Siriwanarangsan, Pornthep and Peto, Julian and Schrauder, Michael G and Ekici, Arif B and Beckmann, Matthias W and dos Santos Silva, Isabel and Johnson, Nichola and Warren, Helen and Tomlinson, Ian and Kerin, Michael J and Miller, Nicola and Marme, Federick and Schneeweiss, Aneas and Sohn, Christof and Truong, Therese and Laurent-Puig, Pierre and Kerbrat, Pierre and Nordestgaard, Børge G and Nielsen, Sune F and Flyger, Henrik and Milne, Roger L and Perez, Jose Ignacio Arias and Menéndez, Primitiva and Müller, Heiko and Arndt, Volker and Stegmaier, Christa and Lichtner, Peter and Lochmann, Magdalena and Justenhoven, Christina and ... and KConFab Investigators and Gene ENvironm Interaction Breast and Familial Breast Canc Study FBCS and Australian Breast Canc Tissue Bank and kConFab Investigators and Familial Breast Cancer Study (FBCS) and Australian Breast Cancer Tissue Bank (ABCTB) Investigators and Gene ENvironmental Interaction and breast CAncer (GENICA) Network and The Gene ENvironmental Interaction and breast CAncer (GENICA) Network
Nature genetics, ISSN 1061-4036, 2013, Volume 45, Issue 4, pp. 392 - 398
Estrogen receptor (ER)-negative tumors represent 20-30% of all breast cancers, with a higher proportion occurring in younger women and women of African... 
ESTROGEN | GENE | COMMON VARIANT | EXPRESSION | SUSCEPTIBILITY | GENETICS & HEREDITY | Genetic Predisposition to Disease | Genome-Wide Association Study | Meta-Analysis as Topic | Receptors, Estrogen - metabolism | Receptors, Estrogen - genetics | Oligonucleotide Array Sequence Analysis | Humans | Risk Factors | Breast Neoplasms - etiology | Genetic Loci - genetics | Cooperative Behavior | Genotype | Case-Control Studies | Breast Neoplasms - metabolism | Breast Neoplasms - pathology | Polymorphism, Single Nucleotide - genetics | Female | Quantitative trait loci | Receptors | Estrogen | Physiological aspects | Breast cancer | Genetic aspects | Research | Identification and classification | Health aspects | Risk factors | Confidence intervals | Genealogy | Womens health | Cell cycle | African Americans | Genetics | Genomes | Family medical history | Tumors
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9. 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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10. Full Text Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci
by Schumacher, Fredrick R and Al Olama, Ali Amin and Berndt, Sonja I and Benlloch, Sara and Ahmed, Mahbubl and Saunders, Edward J and Dadaev, Tokhir and Leongamornlert, Daniel and Anokian, Ezequiel and Cieza-Borrella, Clara and Goh, Chee and Brook, Mark N and Sheng, Xin and Fachal, Laura and Dennis, Joe and Tyrer, Jonathan and Muir, Kenneth and Lophatananon, Artitaya and Stevens, Victoria L and Gapstur, Susan M and Carter, Brian D and Tangen, Catherine M and Goodman, Phyllis J and Thompson, Ian M and Batra, Jyotsna and Chambers, Suzanne and Moya, Leire and Clements, Judith and Horvath, Lisa and Tilley, Wayne and Risbridger, Gail P and Gronberg, Henrik and Aly, Markus and Nordström, Tobias and Pharoah, Paul and Pashayan, Nora and Schleutker, Johanna and Tammela, Teuvo L. J and Sipeky, Csilla and Auvinen, Anssi and Albanes, Demetrius and Weinstein, Stephanie and Wolk, Alicja and Håkansson, Niclas and West, Catharine M. L and Dunning, Alison M and Burnet, Neil and Mucci, Lorelei A and Giovannucci, Edward and Andriole, Gerald L and Cussenot, Olivier and Cancel-Tassin, Géraldine and Koutros, Stella and Beane Freeman, Laura E and Sorensen, Karina Dalsgaard and Orntoft, Torben Falck and Borre, Michael and Maehle, Lovise and Grindedal, Eli Marie and Neal, David E and Donovan, Jenny L and Hamdy, Freddie C and Martin, Richard M and Travis, Ruth C and Key, Tim J and Hamilton, Robert J and Fleshner, Neil E and Finelli, Antonio and Ingles, Sue Ann and Stern, Mariana C and Rosenstein, Barry S and Kerns, Sarah L and Ostrer, Harry and Lu, Yong-Jie and Zhang, Hong-Wei and Feng, Ninghan and Mao, Xueying and Guo, Xin and Wang, Guomin and Sun, Zan and Giles, Graham G and Southey, Melissa C and MacInnis, Robert J and Fitzgerald, Liesel M and Kibel, Adam S and Drake, Bettina F and Vega, Ana and Gómez-Caamaño, Antonio and Szulkin, Robert and Eklund, Martin and Kogevinas, Manolis and Llorca, Javier and Castaño-Vinyals, Gemma and Penney, Kathryn L and Stampfer, Meir and Park, Jong Y and Sellers, Thomas A and Lin, Hui-Yi and Stanford, Janet L and Cybulski, Cezary and ... and Profile Study and Canary PASS Investigators and Canc Prostate Sweden CAPS and IMPACT Study and Prostate Canc Genome-wide As and APCB and Breast Prostate Canc Cohort Consor and PRACTICAL Prostate Canc As and Genetic Assoc Mech Oncology GAME and Breast and Prostate Cancer Cohort Consortium (BPC3) and Prostate Cancer Genome-wide Association Study of Uncommon Susceptibility Loci (PEGASUS) and Australian Prostate Cancer BioResource (APCB) and Genetic Associations and Mechanisms in Oncology (GAME-ON)/Elucidating Loci Involved in Prostate Cancer Susceptibility (ELLIPSE) Consortium and Cancer of the Prostate in Sweden (CAPS) and PRACTICAL (Prostate Cancer Association Group to Investigate Cancer-Associated Alterations in the Genome) Consortium and The PRACTICAL (Prostate Cancer Association Group to Investigate Cancer-Associated Alterations in the Genome) Consortium and The IMPACT Study and The Profile Study and The Genetic Associations and Mechanisms in Oncology (GAME-ON)/Elucidating Loci Involved in Prostate Cancer Susceptibility (ELLIPSE) Consortium and Medicinska fakulteten and Medicinska och farmaceutiska vetenskapsområdet and Ortopedi and Uppsala universitet and Institutionen för kirurgiska vetenskaper
Nature Genetics, ISSN 1061-4036, 07/2018, Volume 50, Issue 7, pp. 928 - 936
Genome-wide association studies (GWAS) and fine-mapping efforts to date have identified more than 100 prostate cancer (PrCa)-susceptibility loci. We... 
CONSORTIUM | METAANALYSIS | GENE | VARIANTS | PATHWAY | GENETICS & HEREDITY | RISK | MULTIPLE LOCI | IDENTIFICATION | GENOME-WIDE ASSOCIATION | PREDICTION | Genetic Predisposition to Disease | Prostatic Neoplasms - genetics | Humans | Genotype | Male | Risk | Polymorphism, Single Nucleotide | Genetic Loci | Genome-Wide Association Study - methods | Case-Control Studies | Case studies | Genome-wide association studies | Usage | Men | Genetic aspects | Health aspects | Prostate cancer | Risk factors | Genealogy | Data processing | Genomes | Mapping | Biology | Family medical history | Loci | Meta-analysis | Confidence intervals | Consortia | Signal transduction | Software | Gene mapping | Health risk assessment | Prostate | Genotypes | Cancer | Basic Medicine | Medical Genetics | Medicinsk genetik | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper
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11. Full Text Detectable clonal mosaicism and its relationship to aging and cancer
by Jacobs, Kevin B and Yeager, Meredith and Zhou, Weiyin and Wacholder, Sholom and Wang, Zhaoming and Rodriguez-Santiago, Benjamin and Hutchinson, Amy and Deng, Xiang and Liu, Chenwei and Horner, Marie-Josephe and Cullen, Michael and Epstein, Caroline G and Burdett, Laurie and Dean, Michael C and Chatterjee, Nilanjan and Sampson, Joshua and Chung, Charles C and Kovaks, Joseph and Gapstur, Susan M and Stevens, Victoria L and Teras, Lauren T and Gaudet, Mia M and Albanes, Demetrius and Weinstein, Stephanie J and Virtamo, Jarmo and Taylor, Philip R and Freedman, Neal D and Abnet, Christian C and Goldstein, Alisa M and Hu, Nan and Yu, Kai and Yuan, Jian-Min and Liao, Linda and Ding, Ti and Qiao, You-Lin and Gao, Yu-Tang and Koh, Woon-Puay and Xiang, Yong-Bing and Tang, Ze-Zhong and Fan, Jin-Hu and Aldrich, Melinda C and Amos, Christopher and Blot, William J and Bock, Cathryn H and Gillanders, Elizabeth M and Harris, Curtis C and Haiman, Christopher A and Henderson, Brian E and Kolonel, Laurence N and Le Marchand, Loic and McNeill, Lorna H and Rybicki, Benjamin A and Schwartz, Ann G and Signorello, Lisa B and Spitz, Margaret R and Wiencke, John K and Wrensch, Margaret and Wu, Xifeng and Zanetti, Krista A and Ziegler, Regina G and Figueroa, Jonine D and Garcia-Closas, Montserrat and Malats, Nuria and Marenne, Gaelle and Prokunina-Olsson, Ludmila and Baris, Dalsu and Schwenn, Molly and Johnson, Alison and Landi, Maria Teresa and Goldin, Lynn and Consonni, Dario and Bertazzi, Pier Alberto and Rotunno, Melissa and Rajaraman, Preetha and Andersson, Ulrika and Freeman, Laura E. Beane and Berg, Christine D and Buring, Julie E and Butler, Mary A and Carreon, Tania and Feychting, Maria and Ahlbom, Anders and Gaziano, J Michael and Giles, Graham G and Hallmans, Goran and Hankinson, Susan E and Hartge, Patricia and Henriksson, Roger and Inskip, Peter D and Johansen, Christoffer and Landgren, Annelie and McKean-Cowdin, Roberta and Michaud, Dominique S and Melin, Beatrice S and Peters, Ulrike and Ruder, Avima M and Sesso, Howard D and Severi, Gianluca and Shu, Xiao-Ou and Visvanathan, Kala and ... and Medicinska fakulteten and Institutionen för folkhälsa och klinisk medicin and Institutionen för strålningsvetenskaper and Näringsforskning and Onkologi and Umeå universitet
Nature Genetics, ISSN 1061-4036, 06/2012, Volume 44, Issue 6, pp. 651 - 658
In an analysis of 31,717 cancer cases and 26,136 cancer-free controls from 13 genome-wide association studies, we observed large chromosomal abnormalities in a... 
MAFFUCCI SYNDROME | OLLIER DISEASE | ANEUPLOIDY | SUSCEPTIBILITY | GENETICS & HEREDITY | CHRONIC LYMPHOCYTIC-LEUKEMIA | MECHANISMS | MUTATIONS | GENOMIC IMBALANCES | ABERRATIONS | ASSOCIATION | Aging - genetics | Neoplasms - genetics | Humans | Middle Aged | Chromosome Aberrations | Female | Male | Mosaicism | Risk | Aged | Aging | Physiological aspects | Genetic aspects | Research | Cancer | Genotype & phenotype | Occupational safety | Bladder | Genomes | Mutation | Genetic testing | Chromosomes | Blood | Methods | Basic Medicine | Medical Genetics | Medicinsk genetik | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper
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