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1. Full Text Population‐based estimates of breast cancer risks associated with ATM gene variants c.7271T>G and c.1066–6T>G (IVS10–6T>G) from the Breast Cancer Family Registry
by Bernstein, J.L and Teraoka, S and Southey, M.C and Jenkins, M.A and Andrulis, I.L and Knight, J.A and John, E.M and Lapinski, R and Wolitzer, A.L and Whittemore, A.S and West, D and Seminara, D and Olson, E.R and Spurdle, A.B and Chenevix‐Trench, G and Giles, G.G and Hopper, J.L and Concannon, P
Human Mutation, ISSN 1059-7794, 11/2006, Volume 27, Issue 11, pp. 1122 - 1128
The ATM gene variants segregating in ataxia‐telangiectasia families are associated with increased breast cancer risk, but the contribution of specific variants... 
breast cancer | ATM | segregation analysis | gene variants | DNA damage | penetrance | Segregation analysis | Penetrance | Breast cancer | ATM gene variants | ATAXIA-TELANGIECTASIA FAMILIES | CONTRIBUTE | HETEROZYGOTES | SUSCEPTIBILITY | MISSENSE MUTATIONS | ALLELIC VARIANTS | FREQUENCY | GENETICS & HEREDITY | EARLY-ONSET | TRUNCATING MUTATIONS | HISTORY | Humans | Middle Aged | Case-Control Studies | Incidence | Genetic Variation | Registries - statistics & numerical data | Carcinoma - epidemiology | Tumor Suppressor Proteins - genetics | Cell Cycle Proteins - genetics | Adult | Female | Breast Neoplasms - epidemiology | Genetic Linkage | Genetics, Population | Genetic Predisposition to Disease | Risk Factors | Protein-Serine-Threonine Kinases - genetics | Ataxia Telangiectasia Mutated Proteins | DNA-Binding Proteins - genetics | Australia - epidemiology | Breast Neoplasms - genetics | Adolescent | Ontario - epidemiology | San Francisco - epidemiology | Carcinoma - genetics | Aged
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2. Full Text Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche
by Perry, John and Day, Felix and Elks, Cathy and Sulem, Patrick and Thompson, Deborah and Ferreira, Teresa and He, Chunyan and Chasman, Daniel and Esko, Tõnu and Thorleifsson, Gudmar and Albrecht, Eva and Ang, Wei and Corre, Tanguy and Cousminer, Diana and Feenstra, Bjarke and Franceschini, Nora and Ganna, Anea and Johnson, Anew and Kjellqvist, Sanela and Lunetta, Kathryn and Mcmahon, George and Nolte, Ilja and Paternoster, Lavinia and Porcu, Eleonora and Smith, G.D and Stolk, Lisette and Teumer, Alexander and Tsernikova, Natalia and Tikkanen, Emmi and Ulivi, Shelia and Wagner, Erin K and Amin, Najaf and Bierut, Laura and Byrne, Enda and Hottenga, Jouke Jan and Koller, Daniel and Mangino, Massimo and Pers, Tune and Yerges-Armstrong, Laura and Zhao, Jing Hua and Anulis, Irene and Anton-Culver, Hoda and Atsma, Femke and Bandinelli, Stefania and Beckmann, Matthias W and Benítez, Javier and Blomqvist, Carl and Bojesen, Stig and Bolla, Manjeet and Bonnani, Bernardo and Brauch, Hiltrud and Brenner, Hermann and Buring, Julie and Chang-Claude, Jenny and Chanock, Stephen and Chen, Jinhui and Chenevix-Trench, Georgia and Collee, Margriet and Couch, Fergus and Couper, David and Coviello, Anea and Cox, Angela and Czene, Kamila and Adamo, Pio and Vivo, Immaculata and Demerath, Ellen and Dennis, Joe and Devilee, Peter and Dieffenbach, Aida Karina and Dunning, Alison and Eiriksdottir, Gudny and Hagen, Knut and Fasching, Peter and Ferrucci, Luigi and Flesch-Janys, Dieter and Flyger, Henrik and Foroud, Tatiana and Franke, Lude and Garcia, Melissa and García-Closas, Montserrat and Geller, Frank and De Geus, Eco E. J and Giles, Graham and Gudbjartsson, Daniel and Gudnason, Vilmundur and Guénel, Pascal and Guo, Suiqun and Hall, Per and Hamann, Ute and Haring, Robin and Hartman, Catharina and Heath, Anew and Hofman, Albert and Hooning, Maartje and Hopper, John and Hu, Frank and Hunter, David and Karasik, David and Kiel, Douglas P and Knight, Julia and ... and kConFabt LifeLines Cohort Study and InterAct Consortium and Australian Ovarian Canc Study and Early Growth Genetics EGG Consorti and GENICA Network and Australian Ovarian Cancer Study and kConFab and LifeLines Cohort Study and Early Growth Genetics (EGG) Consortium and The GENICA Network and The InterAct Consortium and The LifeLines Cohort Study and Medicinska fakulteten and Science for Life Laboratory, SciLifeLab and Medicinska och farmaceutiska vetenskapsområdet and Uppsala universitet and Institutionen för medicinska vetenskaper and Molekylär epidemiologi
Nature: international weekly journal of science, ISSN 0028-0836, 10/2014, Volume 514, Issue 7520, pp. 92 - 97
textabstractAge at menarche is a marker of timing of puberty in females. It varies widely between individuals, is a heritable trait and is associated with... 
CELLS | METAANALYSIS | VARIANTS | CENTRAL PRECOCIOUS PUBERTY | BREAST-CANCER RISK | MULTIDISCIPLINARY SCIENCES | DISEASE | GENE-EXPRESSION | HUMAN PREFRONTAL CORTEX | WIDE ASSOCIATION | REVEALS | Age Factors | Diabetes Mellitus, Type 2 - genetics | Humans | Genetic Loci - genetics | Parents | Male | Cardiovascular Diseases - genetics | Obesity - genetics | Europe - ethnology | Female | Ribonucleoproteins - genetics | Hypothalamo-Hypophyseal System - physiology | Child | Body Mass Index | Genome-Wide Association Study | Membrane Proteins - genetics | Menarche - genetics | Intercellular Signaling Peptides and Proteins - genetics | Potassium Channels, Tandem Pore Domain - genetics | Ovary - physiology | Receptors, Retinoic Acid - metabolism | Genomic Imprinting - genetics | Proteins - genetics | Breast Neoplasms - genetics | Adolescent | Alleles | Polymorphism, Single Nucleotide - genetics | Quantitative Trait Loci - genetics | Receptors, GABA-B - metabolism | Allelomorphism | Menarche | Physiological aspects | Genome-wide association studies | Genetic aspects | Vitamin A | Puberty | Menstruation | Acids | Genomes | Mutation | Chromosomes | Girls | Age | Hälsovetenskaper | Folkhälsovetenskap, global hälsa, socialmedicin och epidemiologi | Medical and Health Sciences | Medicin och hälsovetenskap | Public Health, Global Health, Social Medicine and Epidemiology | Health Sciences
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3. 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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4. 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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5. Full Text A comprehensive gene-environment interaction analysis in Ovarian Cancer using genome-wide significant common variants
: G x E analysis in ovarian cancer
by Kim, Sehee and Wang, Miao and Tyrer, Jonathan P and Jensen, Allan and Wiensch, Ashley and Liu, Gang and Lee, Alice W and Ness, Roberta B and Salvatore, Maxwell and Tworoger, Shelley S and Whittemore, Alice S and Anton-Culver, Hoda and Sieh, Weiva and Olson, Sara H and Berchuck, Andrew and Goode, Ellen L and Goodman, Marc T and Doherty, Jennifer Anne and Chenevix-Trench, Georgia and Rossing, Mary Anne and Webb, Penelope M and Giles, Graham G and Terry, Kathryn L and Ziogas, Argyrios and Fortner, Renée T and Menon, Usha and Gayther, Simon A and Wu, Anna H and Song, Honglin and Brooks-Wilson, Angela and Bandera, Elisa V and Cook, Linda S and Cramer, Daniel W and Milne, Roger L and Winham, Stacey J and Kjaer, Susanne K and Modugno, Francesmary and Thompson, Pamela J and Chang-Claude, Jenny and Harris, Holly R and Schildkraut, Joellen M and Le, Nhu D and Wentzensen, Nico and Trabert, Britton and Høgdall, Estrid and Huntsman, David and Pike, Malcolm C and Pharoah, Paul D.P and Pearce, Celeste Leigh and Mukherjee, Bhramar
International Journal of Cancer, ISSN 0020-7136, 05/2019, Volume 144, Issue 9, pp. 2192 - 2205
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6. 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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7. Full Text Genome-wide association study identifies novel breast cancer susceptibility loci
by Easton, Douglas F and Pooley, Karen A and Dunning, Alison M and Pharoah, Paul D. P and Thompson, Deborah and Ballinger, Dennis G and Struewing, Jeffery P and Morrison, Jonathan and Field, Helen and Luben, Robert and Wareham, Nicholas and Ahmed, Shahana and Healey, Catherine S and Bowman, Richard and Meyer, Kerstin B and Haiman, Christopher A and Kolonel, Laurence K and Henderson, Brian E and Le Marchand, Loic and Brennan, Paul and Sangrajrang, Suleeporn and Gaborieau, Valerie and Odefrey, Fabrice and Shen, Chen-Yang and Wu, Pei-Ei and Wang, Hui-Chun and Eccles, Diana and Evans, D. Gareth and Peto, Julian and Fletcher, Olivia and Johnson, Nichola and Seal, Sheila and Stratton, Michael R and Rahman, Nazneen and Chenevix-Trench, Georgia and Bojesen, Stig E and Nordestgaard, Børge G and Axelsson, Christen K and Garcia-Closas, Montserrat and Brinton, Louise and Chanock, Stephen and Lissowska, Jolanta and Peplonska, Beata and Nevanlinna, Heli and Fagerholm, Rainer and Eerola, Hannaleena and Kang, Daehee and Yoo, Keun-Young and Noh, Dong-Young and Ahn, Sei-Hyun and Hunter, David J and Hankinson, Susan E and Cox, David G and Hall, Per and Ween, Sara and Liu, Jianjun and Low, Yen-Ling and Bogdanova, Natalia and Schürmann, Peter and Dörk, Thilo and Tollenaar, Rob A. E. M and Jacobi, Catharina E and Devilee, Peter and Klijn, Jan G. M and Sigurdson, Alice J and Doody, Michele M and Alexander, Bruce H and Zhang, Jinghui and Cox, Angela and Brock, Ian W and MacPherson, Gordon and Reed, Malcolm W. R and Couch, Fergus J and Goode, Ellen L and Olson, Janet E and Meijers-Heijboer, Hanne and van den Ouweland, Ans and Uitterlinden, Ané and Rivadeneira, Fernando and Milne, Roger L and Ribas, Gloria and Gonzalez-Neira, Anna and Benitez, Javier and Hopper, John L and McCredie, Margaret and Southey, Melissa and Giles, Graham G and Schroen, Chris and Justenhoven, Christina and Brauch, Hiltrud and Hamann, Ute and Ko, Yon-Dschun and Spurdle, Amanda B and Beesley, Jonathan and Chen, Xiaoqing and Mannermaa, Arto and Kosma, Veli-Matti and Kataja, Vesa and Hartikainen, Jaana and Day, Nicholas E and ... and kConFab and AOCS Management Grp and SEARCH Collaborators and AOCS Management Group and SEARCH collaborators and The SEARCH collaborators
Nature, ISSN 0028-0836, 2007, Volume 447, Issue 7148, pp. 1087 - 1093
Breast cancer exhibits familial aggregation, consistent with variation in genetic susceptibility to the disease. Known susceptibility genes account for less... 
BRCA2 MUTATIONS | GENE | DATABASE | MULTIDISCIPLINARY SCIENCES | DISEASE | GROWTH-FACTOR RECEPTOR-2 | POPULATIONS | PATTERNS | OVARIAN-CANCER | VARIANT | CHEK2-ASTERISK-1100DELC | Genetic Predisposition to Disease - genetics | Humans | Genotype | Receptors, Progesterone - genetics | North America | Case-Control Studies | Europe - ethnology | Genome, Human - genetics | Asia, Southeastern | Breast Neoplasms - genetics | Alleles | Polymorphism, Single Nucleotide - genetics | Female | MAP Kinase Kinase Kinase 1 - genetics | Australia | Odds Ratio | Microfilament Proteins - genetics | Receptor, Fibroblast Growth Factor, Type 2 - genetics | Breast cancer | Genetic aspects | Research | Genetic susceptibility | Risk factors | Medical research | Genomics | Polymorphism | Genes | Control equipment | Breast | Risk | Genetics | Nucleotides | Loci | Cancer
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