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1. Full Text LA-MB-FTMW spectroscopy of AlCCH and AgCCH with a discharge source
by Cabezas, Carlos and Mata, Santiago and Daly, Adam M and Martín, Agustín and Alonso, José L and Cernicharo, José
Journal of Molecular Spectroscopy, ISSN 0022-2852, 08/2012, Volume 278, Issue 1, pp. 31 - 34
► Microwave spectra of AlCCH and AgCCH have been recorded using FTMW spectroscopy. ► Metallic acetylides produced by ablation of the pure metal and reaction... 
Silver acetylide | Laser ablation | Aluminum acetylide | Microwave spectroscopy | WAVE SPECTRUM | PHYSICS, ATOMIC, MOLECULAR & CHEMICAL | ROTATIONAL SPECTRUM | LABORATORY DETECTION | INFRARED-SPECTRA | SPECTROSCOPY | GAS-PHASE | LICCH | NACCH | Spectrum analysis | Explosives
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2. Full Text Segmental phylogenetic relationships of inbred mouse strains revealed by fine-scale analysis of sequence variation across 4.6 Mb of mouse genome
by Frazer, Kelly A and Wade, Claire M and Hinds, David A and Patil, Nila and Cox, David R and Daly, Mark J
Genome Research, ISSN 1088-9051, 08/2004, Volume 14, Issue 8, pp. 1493 - 1500
High-density SNP screening of panels of inbred mouse strains has been proposed as a method to accelerate the identification of genes associated with complex... 
BIOTECHNOLOGY & APPLIED MICROBIOLOGY | BIOCHEMISTRY & MOLECULAR BIOLOGY | SINGLE-NUCLEOTIDE POLYMORPHISMS | GENETICS & HEREDITY | Haplotypes | Mice - genetics | Mice, Inbred Strains - genetics | Oligonucleotide Array Sequence Analysis - methods | Physical Chromosome Mapping | Mice, Inbred C57BL | Molecular Sequence Data | Phylogeny | Mice, Inbred C3H | Genetic Variation | Animals | Base Sequence | Mice, Inbred BALB C | Polymorphism, Single Nucleotide | Genome | Genetic research | Genomes | Genetic aspects | DNA microarrays | Research | Mice as laboratory animals | Letters
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3. Full Text Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
by Sawcer, Stephen and Hellenthal, Garrett and Pirinen, Matti and Spencer, Chris C.A and Patsopoulos, Nikolaos A and Moutsianas, Loukas and Dilthey, Alexander and Su, Zhan and Freeman, Colin and Hunt, Sarah E and Edkins, Sarah and Gray, Emma and Booth, David R and Potter, Simon C and Goris, An and Band, Gavin and Oturai, Annette Bang and Strange, Amy and Saarela, Janna and Bellenguez, Céline and Fontaine, Bertrand and Gillman, Matthew and Hemmer, Bernhard and Gwilliam, Rhian and Zipp, Frauke and Jayakumar, Alagurevathi and Martin, Roland and Leslie, Stephen and Hawkins, Stanley and Giannoulatou, Eleni and D'Alfonso, Sandra and Blackburn, Hannah and Boneschi, Filippo Martinelli and Liddle, Jennifer and Harbo, Hanne F and Perez, Marc L and Spurkland, Anne and Waller, Matthew J and Mycko, Marcin P and Ricketts, Michelle and Comabella, Manuel and Hammond, Naomi and Kockum, Ingrid and McCann, Owen T and Ban, Maria and Whittaker, Pamela and Kemppinen, Anu and Weston, Paul and Hawkins, Clive and Widaa, Sara and Zajicek, John and Dronov, Serge and Robertson, Neil and Bumpstead, Suzannah J and Barcellos, Lisa F and Ravindrarajah, Rathi and Abraham, Roby and Alfredsson, Lars and Ardlie, Kristin and Aubin, Cristin and Baker, Amie and Baker, Katharine and Baranzini, Sergio E and Bergamaschi, Laura and Bergamaschi, Roberto and Bernstein, Allan and Berthele, Achim and Boggild, Mike and Bradfield, Jonathan P and Brassat, David and Broadley, Simon A and Buck, Dorothea and Butzkueven, Helmut and Capra, Ruggero and Carroll, William M and Cavalla, Paola and Celius, Elisabeth G and Cepok, Sabine and Chiavacci, Rosetta and Clerget-Darpoux, Françoise and Clysters, Katleen and Comi, Giancarlo and Cossburn, Mark and Cournu-Rebeix, Isabelle and Cox, Mathew B and Cozen, Wendy and Cree, Bruce A.C and Cross, Anne H and Cusi, Daniele and Daly, Mark J and Davis, Emma and De Bakker, Paul I.W and Debouverie, Marc and D'Hooghe, Marie Beatrice and Dixon, Katherine and Dobosi, Rita and Dubois, Bénédicte and Ellinghaus, David and Elovaara, Irina and Esposito, Federica and ... and Wellcome Trust Case Control Consor and Int Multiple Sclerosis Genetics Co and Wellcome Trust Case Control Consortium 2 and International Multiple Sclerosis Genetics Consortium and The International Multiple Sclerosis Genetics Consortium & The Wellcome Trust Case Control Consortium 2 and Medicinska fakulteten and Science for Life Laboratory, SciLifeLab and Medicinska och farmaceutiska vetenskapsområdet and Molekylär medicin and Uppsala universitet and Institutionen för medicinska vetenskaper
Nature, ISSN 0028-0836, 08/2011, Volume 476, Issue 7359, pp. 214 - 219
Multiple sclerosis is a common disease of the central nervous system in which the interplay between inflammatory and neurodegenerative processes typically... 
HETEROGENEITY | ALLELES | VARIANTS | MULTIDISCIPLINARY SCIENCES | SUSCEPTIBILITY LOCI | HAPLOTYPES | GENOME-WIDE ASSOCIATION | Genetic Predisposition to Disease - genetics | Genome-Wide Association Study | Immunity, Cellular - genetics | Major Histocompatibility Complex - genetics | Humans | Multiple Sclerosis - genetics | Europe - ethnology | Genome, Human - genetics | HLA-DR Antigens - genetics | Cell Differentiation - immunology | Immunity, Cellular - immunology | Sample Size | T-Lymphocytes, Helper-Inducer - immunology | HLA-DRB1 Chains | Alleles | HLA-A Antigens - genetics | T-Lymphocytes, Helper-Inducer - cytology | Multiple Sclerosis - immunology | Polymorphism, Single Nucleotide - genetics | Physiological aspects | Multiple sclerosis | Genetic aspects | Immune response | Research | Epidemiology | Genealogy | Disease | Quality control | Genetics | Genomes | Statistical methods | Mutation | Regression analysis | Autoimmune diseases | Meta-analysis | Medical and Health Sciences | MEDICINE | Medicin och hälsovetenskap | MEDICIN
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4. 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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5. Full Text Dietary isoflavone intake and all‐cause mortality in breast cancer survivors: The Breast Cancer Family Registry
by Zhang, Fang Fang and Haslam, Danielle E and Terry, Mary Beth and Knight, Julia A and Andrulis, Irene L and Daly, Mary B and Buys, Saundra S and John, Esther M
Cancer, ISSN 0008-543X, 06/2017, Volume 123, Issue 11, pp. 2070 - 2079
BACKGROUND Soy foods possess both antiestrogenic and estrogen‐like properties. It remains controversial whether women diagnosed with breast cancer should be... 
mortality | breast cancer | isoflavone | soy | breast cancer survivors | survival | DIAGNOSIS | MULTIETHNIC COHORT | RISK | SOY FOOD-INTAKE | WOMEN | ONCOLOGY | RECURRENCE | CONSUMPTION | Receptors, Estrogen - metabolism | Diet - statistics & numerical data | Humans | Middle Aged | Mortality | Proportional Hazards Models | Survivors | Cause of Death | Breast Neoplasms - metabolism | Receptors, Progesterone - metabolism | Adult | Breast Neoplasms - mortality | Female | Registries | Cohort Studies | Isoflavones | Women | Breast cancer | Diagnosis | Health aspects | Therapy | Soybeans | Estrogens | Endocrine therapy | Dietary intake | Cancer therapies | Confidence intervals | Receptors | Diet | Soy products | Breast | Progesterone | Health risk assessment | Tumors | Food | Cancer | Soy
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6. Full Text Shared heritability and functional enrichment across six solid cancers
by Jiang, Xia and Finucane, H.K and Schumacher, F and Schmit, Stephanie L and Tyrer, J.P and Han, Y and Kiemeney, B and Kraft, P and Lindstrom, Sara and Medicinska fakulteten and Klinisk kemi and Institutionen för medicinsk biovetenskap and Institutionen för strålningsvetenskaper and Umeå universitet
Nature Communications, ISSN 2041-1723, 2019, Volume 10, Issue 1, pp. 431 - 23
Quantifying the genetic correlation between cancers can provide important insights into the mechanisms driving cancer etiology. Using genome-wide association... 
BREAST-CANCER | LUNG-CANCER | RISK-FACTORS | PARTITIONING HERITABILITY | MULTIDISCIPLINARY SCIENCES | SUSCEPTIBILITY LOCI | GENETIC ARCHITECTURE | ANALYSES IDENTIFY | MENDELIAN RANDOMIZATION | CELL-TYPES | GENOME-WIDE ASSOCIATION | Lung Neoplasms - ethnology | Colorectal Neoplasms - genetics | Humans | Ovarian Neoplasms - pathology | Lung Neoplasms - pathology | Male | Prostatic Neoplasms - diagnosis | Case-Control Studies | Colorectal Neoplasms - diagnosis | Ovarian Neoplasms - ethnology | Inheritance Patterns | Ovarian Neoplasms - genetics | Mental Disorders - genetics | Prostatic Neoplasms - genetics | Smoking - physiopathology | Head and Neck Neoplasms - ethnology | Female | Neoplasm Proteins - genetics | Breast Neoplasms - ethnology | Lung Neoplasms - genetics | Prostatic Neoplasms - pathology | Genetic Predisposition to Disease | Genome-Wide Association Study | Colorectal Neoplasms - ethnology | Ovarian Neoplasms - diagnosis | European Continental Ancestry Group | Smoking - genetics | Prostatic Neoplasms - ethnology | Head and Neck Neoplasms - pathology | Mental Disorders - physiopathology | Smoking - ethnology | Phenotype | Breast Neoplasms - genetics | Breast Neoplasms - pathology | Head and Neck Neoplasms - diagnosis | Head and Neck Neoplasms - genetics | Breast Neoplasms - diagnosis | Mental Disorders - ethnology | Polymorphism, Single Nucleotide | Colorectal Neoplasms - pathology | Lung Neoplasms - diagnosis | Enrichment | Correlation | Statistical analysis | Ovarian carcinoma | Mental disorders | Lung cancer | Colorectal carcinoma | Genomes | Breast cancer | Regulatory sequences | Ovarian cancer | Etiology | Breast | Heritability | Neck | Solid tumors | Prostate cancer | Prostate | Cancer | Smoking | Basic Medicine | Medical Genetics | Medicinsk genetik | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper
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7. Full Text Tamoxifen and Risk of Contralateral Breast Cancer for BRCA1 and BRCA2 Mutation Carriers
by Kelly-Anne Phillips and Roger L. Milne and Matti A. Rookus and Mary B. Daly and Antonis C. Antoniou and Susan Peock and Debra Frost and Douglas F. Easton and Steve Ellis and Michael L. Friedlander and Saundra S. Buys and Nadine Andrieu and Catherine Noguès and Dominique Stoppa-Lyonnet and Valérie Bonadona and Pascal Pujol and Sue Anne McLachlan and Esther M. John and Maartje J. Hooning and Caroline Seynaeve and Rob A.E.M. Tollenaar and David E. Goldgar and Mary Beth Terry and Trinidad Caldes and Prue C. Weideman and Irene L. Andrulis and Christian F. Singer and Kate Birch and Jacques Simard and Melissa C. Southey and Håkan L. Olsson and Anna Jakubowska and Edith Olah and Anne-Marie Gerdes and Lenka Foretova and John L. Hopper and Onkologi och Patologi, MV and EpiHealth: Epidemiology for Health and Lund University and BioCARE: Biomarkers in Cancer Medicine improving Health Care, Education and Innovation and Oncology and Pathology, MV and Lunds universitet
Journal of Clinical Oncology, ISSN 0732-183X, 09/2013, Volume 31, Issue 25, pp. 3091 - 3099
textabstractPurpose To determine whether adjuvant tamoxifen treatment for breast cancer (BC) is associated with reduced contralateral breast cancer (CBC) risk... 
ESTROGEN-RECEPTOR-BETA | WOMEN | SURGICAL ADJUVANT BREAST | ONCOLOGY | SALPINGO-OOPHORECTOMY | SURVEILLANCE | FOLLOW-UP | OVARIAN-CANCER | REDUCING SURGERY | PREVENTION TRIAL | ENDOMETRIAL CANCER | Humans | Middle Aged | Risk Factors | Proportional Hazards Models | Breast Neoplasms - prevention & control | Breast Neoplasms - genetics | Estrogen Antagonists - therapeutic use | Tamoxifen - therapeutic use | Genes, BRCA2 | Adult | Female | Heterozygote | Aged | Genes, BRCA1 | Mutation | ORIGINAL REPORTS | Bc7 | Clinical Medicine | Medical and Health Sciences | Klinisk medicin | Cancer and Oncology | Medicin och hälsovetenskap | Cancer och onkologi
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8. Full Text Abstract P6-09-04: Benign breast disease and breast cancer risk across the spectrum of familial risk using a prospective family study cohort (ProF-SC)
by Zeinomar, N and Phillips, KA and Liao, Y and MacInnis, RJ and Dite, GS and Daly, MB and John, EM and Andrulis, IL and Buys, SS and Hopper, JL and Terry, MB
Cancer Research, ISSN 0008-5472, 02/2018, Volume 78, Issue 4 Supplement, pp. P6 - P6-09-04
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9. 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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