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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 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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3. Full Text Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
by Lee, Shermin and Ripke, S and Neale, B.M and Faraone, S.V and Purcell, S.M and Perlis, R.H and Mowry, B.J and Thapar, A and Goddard, M.E and Witte, J.S and Absher, D and Agartz, I and Akil, H and Amin, F and Aneassen, O.A and Anjorin, A and Anney, R and Anttila, V and Arking, D.E and Asherson, P and Azevedo, M.H and Backlund, L and Badner, J.A and Bailey, A.J and Banaschewski, T and Barchas, J.D and Barnes, M.R and Barrett, T.B and Bass, N and Battaglia, A and Bauer, M and Bayes, M and Bellivier, F and Bergen, S.E and Berrettini, W and Betancur, C and Bettecken, T and Biederman, J and Binder, E.B and Black, D.W and Blackwood, D.H and Bloss, C.S and Boehnke, M and Boomsma, D.I and Breen, G and Breuer, R and Bruggeman, R and Cormican, P and Buccola, N.G and Buitelaar, J.K and Bunney, W.E and Buxbaum, J.D and Byerley, W.F and Byrne, E.M and Caesar, S and Cahn, W and Cantor, R.M and Casas, M and Chakravarti, A and Chambert, K and Choudhury, K and Cichon, S and Cloninger, C.R and Collier, D.A and Cook, E.H and Coon, H and Cormand, B and Corvin, A and Coryell, W.H and Craig, D.W and Craig, I.W and Crosbie, J and Cuccaro, M.L and Curtis, D and Czamara, D and Datta, S and Dawson, G and Day, R and Geus, E.J. de and Degenhardt, F and Djurovic, S and Donohoe, G.J and Doyle, A.E and Duan, J and Dudbridge, F and Duketis, E and Ebstein, R.P and Edenberg, H.J and Elia, J and Ennis, S and Etain, B and Fanous, A and Farmer, A.E and Ferrier, I.N and Flickinger, M and Fombonne, E and Foroud, T and Frank, J and Franke, B and et al and Cross-Disorder Grp Psychiat Genomi and Int Inflammatory Bowel Dis Genetic and Cross-Disorder Group of the Psychiatric Genomics Consortium
Nature Genetics, ISSN 1061-4036, 2013, Volume 45, Issue 9, pp. 984 - 994
Most psychiatric disorders are moderately to highly heritable. The degree to which genetic variation is unique to individual disorders or shared across... 
ATTENTION-DEFICIT/HYPERACTIVITY DISORDER | CROHNS-DISEASE | DEFICIT HYPERACTIVITY DISORDER | COMMON SNPS | GENETICS & HEREDITY | SCHIZOPHRENIA | RISK | AUTISM SPECTRUM DISORDERS | BIPOLAR DISORDER | ASSOCIATION | HERITABILITY | Usage | Genetic aspects | Research | Single nucleotide polymorphisms | Psychoses | Genomics | Life Sciences | Biochemistry, Molecular Biology
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4. Full Text Impact of Concurrent Indolent Lymphoma on the Clinical Outcome of Newly Diagnosed Diffuse Large B-Cell Lymphoma
by Wang, Yucai and Link, Brian K and Witzig, Thomas E and Maurer, Matthew J and Allmer, Cristine and King, Rebecca L and Feldman, Andrew L and Habermann, Thomas M and Ansell, Stephen M and Slager, Susan L and Cerhan, James R and Nowakowski, Grzegorz S
Blood, ISSN 0006-4971, 07/2019, Volume 134, Issue 16, pp. 1289 - 1297
Approximately 10-15% of patients with diffuse large B-cell lymphoma (DLBCL) present with a concurrent indolent lymphoma at initial diagnosis. Their outcomes in... 
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5. 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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6. Full Text Comparison of tumor staging systems for cutaneous squamous cell carcinoma in patients with chronic lymphocytic leukemia
by Inda, Jacob J and Kabat, Brian F and Larson, Melissa C and Slager, Susan L and Baum, Christian L
Journal of the American Academy of Dermatology, ISSN 0190-9622, 03/2019, Volume 80, Issue 3, pp. 639 - 645
Patients with chronic lymphocytic leukemia (CLL) are at increased risk for poor outcomes as a result of cutaneous squamous cell carcinoma (CSCC). To compare... 
American Joint Committee on Cancer | chronic lymphocytic leukemia | system | Union for International Cancer Control | tumor | Brigham and Women's Hospital | staging | squamous cell carcinoma | BRIGHAM | 7TH | AMERICAN JOINT COMMITTEE | DERMATOLOGY | LYMPHOMA | EDITION | SKIN-CANCER | Medical colleges | Medical research | Care and treatment | Chronic lymphocytic leukemia | Squamous cell carcinoma | Tumor staging | Medicine, Experimental | Comparative analysis | Tumors
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7. Full Text The Role of Splenectomy in the Care and Treatment of the CLL Patient
by Conte, Michael J and Parikh, Sameer A and Bowen, Deborah A and Call, Timothy G and Kabat, Brian F and Chaffee, Kari G and Schwager, Susan M and Slager, Susan L and Ding, Wei and Kay, Neil E and Shanafelt, Tait D
Blood, ISSN 0006-4971, 12/2016, Volume 128, Issue 22, pp. 5575 - 5575
Abstract BACKGROUND: Infiltration of the spleen plays an important role in the disease progression of patients with chronic lymphocytic leukemia (CLL). Despite... 
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8. Full Text Abstract 3256: The prevalence of non-chronic lymphocytic leukemia (CLL) phenotype monoclonal B-cell lymphocytosis (MBL) in a population-based cohort of U.S. adults
by Parikh, Sameer A and Achenbach, Sara J and Chaffee, Kari G and Kay, Neil E and Lesnick, Connie E and Cerhan, James R and Hanson, Curtis A and Shanafelt, Tait D and Slager, Susan L
Cancer Research, ISSN 0008-5472, 07/2018, Volume 78, Issue 13 Supplement, pp. 3256 - 3256
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9. Full Text CORR® ORS Richard A. Brand Award: Disruption in Peroxisome Proliferator-Activated Receptor-γ (PPARG) Increases Osteonecrosis Risk Through Genetic Variance and Pharmacologic Modulation
by Wyles, Cody C and Paradise, Christopher R and Houdek, Matthew T and Slager, Susan L and Terzic, Andre and Behfar, Atta and van Wijnen, Andre J and Sierra, Rafael J
Clinical orthopaedics and related research, ISSN 0009-921X, 05/2019, Volume 477, Issue 8, pp. 1800 - 1812
The pathophysiology of osteonecrosis of the femoral head (ONFH) is poorly understood, and the diagnosis is idiopathic in as many as 40% of patients. Genetic... 
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10. Full Text Liver Biopsy in Patients with Chronic Lymphocytic Leukemia: Indications and Pathological Findings
by Hampel, Paul J and King, Rebecca L and Hanson, Curtis A and Simonetto, Douglas and Chaffee, Kari G and Call, Timothy G and Ding, Wei and Kenderian, Saad S and Slager, Susan L and Kay, Neil E and Shanafelt, Tait D and Parikh, Sameer A
Blood, ISSN 0006-4971, 12/2016, Volume 128, Issue 22, pp. 5592 - 5592
Abstract INTRODUCTION: Among patients (pts) with chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL), the indications for liver biopsy are not... 
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11. Full Text Role of Lncrnas in Early Stage Immunoglobulin Heavy Chain Variable Region (IGHV) Unmutated CLL Disease Progression
by Tschumper, Renee C and Slager, Susan L and Shanafelt, Tait D and Kay, Neil E and Jelinek, Diane F
Blood, ISSN 0006-4971, 12/2016, Volume 128, Issue 22, pp. 4364 - 4364
Abstract BACKGROUND: Chronic lymphocytic leukemia (CLL) remains a heterogeneous disease despite significant advances in disease classification based upon... 
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12. Full Text Clinical and Quality of Life Predictors of Failure to Achieve Event Free Survival at 24 Months in Patients Aged 70 Years and Older with Diffuse Large B-Cell Lymphoma
by Reagan, Patrick M and Baran, Andrea M and Maurer, Matthew J and Feldman, Andrew L and Habermann, Thomas M and Slager, Susan L and Thanarajasingam, Gita and Yost, Kathleen J and Link, Brian K and Cerhan, James R and Thompson, Carrie A
Blood, ISSN 0006-4971, 11/2018, Volume 132, Issue Supplement 1, pp. 3579 - 3579
Abstract Background Age has long been recognized as a poor prognostic factor in diffuse large B-cell lymphoma (DLBCL) and more recently, a lower baseline... 
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13. Full Text Atrial Fibrillation in Patients with Chronic Lymphocytic Leukemia (CLL)
by Shanafelt, Tait D and Chaffee, Kari G and Call, Timothy G and Parikh, Sameer A and Schwager, Susan M and Ding, Wei and Leis, Jose F and Chanan-Khan, Asher and Slager, Susan L and Kay, Neil E
Blood, ISSN 0006-4971, 12/2015, Volume 126, Issue 23, pp. 2950 - 2950
Abstract BACKGROUND: Consistent with the advanced age at diagnosis (median age ~70 years), most patients with CLL have co-existent health problems. These... 
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14. Full Text Racial Variations in Disease Characteristics, Presentations, Treatments, and Outcomes in Chronic Lymphocytic Leukemia (CLL)
by Nabhan, Chadi and Rabe, Kari G and Slager, Susan L and Achenbach, Sara J and Schwager, Susan and Kay, Neil E and Shanafelt, Tait D
Blood, ISSN 0006-4971, 12/2014, Volume 124, Issue 21, pp. 1989 - 1989
Abstract Introduction: Our current understanding of CLL biology and optimal therapies is based on clinical trials that have largely enrolled White patient... 
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15. Full Text A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor-negative breast cancer
by Haiman, CA and Chen, GK and Vachon, CM and Canzian, F and Dunning, A and Millikan, RC and Wang, XS and Ademuyiwa, F and Ahmed, S and Ambrosone, CB and Baglietto, L and Balleine, R and Bandera, EV and Beckmann, MW and Berg, CD and Bernstein, L and Blomqvist, C and Blot, WJ and Brauch, H and Buring, JE and Carey, LA and Carpenter, JE and Chang-Claude, J and Chanock, SJ and Chasman, DI and Clarke, CL and Cox, A and Cross, SS and Deming, SL and Diasio, RB and Dimopoulos, AM and Driver, WR and Dunnebier, T and Durcan, L and Eccles, D and Edlund, CK and Ekici, AB and Fasching, PA and Feigelson, HS and Flesch-Janys, D and Fostira, F and Forsti, A and Fountzilas, G and Gerty, SM and Giles, GG and Godwin, AK and Goodfellow, P and Graham, N and Greco, D and Hamann, U and Hankinson, SE and Hartmann, A and Hein, R and Heinz, J and Holbrook, A and Hoover, RN and Hu, JJ and Hunter, DJ and Ingles, SA and Irwanto, A and Ivanovich, J and John, EM and Johnson, N and Jukkola-Vuorinen, A and Kaaks, R and Ko, YD and Kolonel, LN and Konstantopoulou, I and Kosma, VM and Kulkarni, S and Lambrechts, D and Lee, AM and Le Marchand, L and Lesnick, T and Liu, JJ and Lindstrom, S and Mannermaa, A and Margolin, S and Martin, NG and Miron, P and Montgomery, GW and Nevanlinna, H and Nickels, S and Nyante, S and Olswold, C and Palmer, J and Pathak, H and Pectasides, D and Perou, CM and Peto, J and Pharoah, PDP and Pooler, LC and Press, MF and Pylkas, K and Rebbeck, TR and Rodriguez-Gil, JL and Rosenberg, L and Ross, E and Rudiger, T and Silva, ID and ... and Gene Environm Interaction Breast C and Gene Environment Interaction and Breast Cancer in Germany (GENICA) Consortium and The Gene Environment Interaction and Breast Cancer in Germany (GENICA) Consortium
NATURE GENETICS, ISSN 1061-4036, 12/2011, Volume 43, Issue 12, pp. 1210 - U61
Estrogen receptor (ER)-negative breast cancer shows a higher incidence in women of African ancestry compared to women of European ancestry. In search of common... 
IDENTIFIES 5 | SUSCEPTIBILITY LOCI | RISK | PROSTATE-CANCER | GENETICS & HEREDITY | GENOME-WIDE ASSOCIATION | Genetic Predisposition to Disease | Genome-Wide Association Study | Receptors, Estrogen - metabolism | Receptors, Estrogen - genetics | Membrane Proteins - genetics | Humans | Middle Aged | African Americans | European Continental Ancestry Group | Genotype | Genetic Loci | Case-Control Studies | Breast Neoplasms - metabolism | Breast Neoplasms - genetics | Telomerase - genetics | Female | Aged | Polymorphism, Single Nucleotide | Neoplasm Proteins - genetics | Breast Neoplasms - ethnology | Receptors | Estrogen | Physiological aspects | Breast cancer | Genetic aspects | Research | Single nucleotide polymorphisms | Risk factors | Confidence intervals | Medical research | Genealogy | Womens health | Genetics | Genomes
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