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1. Full Text Newly discovered breast cancer susceptibility loci on 3p24 and 17q23.2
by Yoo, Keun-Young and Nordestgaard, Børge G and Peto, Julian and Schmidt, Marjanka K and Bojesen, Stig and Seynaeve, Caroline and Humphreys, Manjeet K and Bogdanova, Natalia V and Meindl, Alfons and Berg, Christine D and Burwinkel, Barbara and van Asperen, Christi J and Hamann, Ute and van Hien, Richard R and Benitez, Javier and Brinton, Louise and Reed, Malcolm W R and Ghoussaini, Maya and English, Dallas R and Peplonska, Beata and Bermisheva, Marina and Hein, Rebecca and Severi, Gianluca and Fredericksen, Zachary and Prentice, Ross and Brauch, Hiltrud and Anton-Culver, Hoda and Lissowska, Jolanta and Luben, Robert and Smith, Letitia and Fedorova, Sardana and Liu, Jianjun and Fletcher, Olivia and Zalutsky, Iosif V and Hankinson, Susan E and Heikkinen, Tuomas and Mannermaa, Arto and Dörk, Thilo and Li, Yuqing and Chang-Claude, Jenny and Hall, Per and McCarty, Catherine A and Ziogas, Argyrios and Schmutzler, Rita K and Calle, Eugenia E and Milne, Roger L and Olson, Janet E and Sigurdson, Alice and Anderson, Garnet L and Doody, Michele and Kumle, Merethe and Rajkovic, Aleksandar and Karstens, Johann H and Elliott, Graeme and Chanock, Stephen J and Knight, Julia A and Flyger, Henrik and Thomas, Gilles and Goode, Ellen L and Oldenburg, Rogier A and van den Ouweland, Ans M W and Jacobs, Kevin and Vatten, Lars J and Ahmed, Shahana and Thun, Michael J and Beesley, Jonathan and Ziegler, Regina G and Morrison, Jonathan and Kang, Daehee and Pooley, Karen A and Brock, Ian and Kosma, Veli-Matti and Aittomäki, Kristiina and Platte, Radka and Kataja, Vesa and Bartram, Claus R and Cox, David G and Giles, Graham G and Diver, W Ryan and Southey, Melissa C and Maranian, Melanie and Rahman, Nazneen and Couch, Fergus and Chenevix-Trench, Georgia and Wang-Gohrke, Shan and Schutte, Mieke and Johnson, Nichola and Healey, Catherine S and Antonenkova, Natalia N and Garcia-Closas, Montserrat and Bhatti, Parveen and Broeks, Annegien and Chen, Shou-Tung and Hillemanns, Peter and Andrulis, Irene L and Ponder, Bruce A J and Feigelson, Heather Spencer and Ahn, Sei-Hyun and Devilee, Peter and Spurdle, Amanda B and ... and GENICA Consortium and KConFab and Australian Ovarian Cancer Study and SEARCH and Australian Ovarian Cancer Study Group and kConFab and The GENICA Consortium
Nature genetics, ISSN 1061-4036, 05/2009, Volume 41, Issue 5, pp. 585 - 590
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fundamental and applied biological sciences. Psychology | Classical genetics, quantitative genetics, hybrids | Gynecology. Andrology. Obstetrics | Mammary gland diseases | Biological and medical sciences | Genetics of eukaryotes. Biological and molecular evolution | Medical sciences | Methods, theories and miscellaneous | Tumors | Genetic Predisposition to Disease - genetics | Breast Neoplasms - genetics | Breast Neoplasms - pathology | Humans | Disease Susceptibility - metabolism | Female | Genotype | Chromosome Mapping | Genome, Human | Chromosomes, Human, Pair 17 - genetics | Chromosomes, Human, Pair 3 - genetics | Breast cancer | Genetic aspects | Disease susceptibility | Research | Single nucleotide polymorphisms | Risk factors | Medical research | Genetic markers | Gene loci | Hospitals | Regression analysis | chromosome 3 | Index Medicus | Medicin och hälsovetenskap
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2. 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 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 and Lophatananon, Artitaya and Muir, K and Beckmann, Matthias 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
Nature genetics, ISSN 1061-4036, 03/2016, Volume 48, Issue 4, pp. 374 - 386
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | 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 | Index Medicus | Clinical Medicine | Medical and Health Sciences | Klinisk medicin | Cancer and Oncology | Medicin och hälsovetenskap | Cancer och onkologi
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3. Full Text Irbesartan in Marfan syndrome (AIMS): a double-blind, placebo-controlled randomised trial
by Mullen, Michael and Jin, Xu Yu and Child, Anne and Stuart, A Graham and Dodd, Matthew and Aragon-Martin, José Antonio and Gaze, David and Kiotsekoglou, Anatoli and Yuan, Li and Hu, Jiangting and Foley, Claire and Van Dyck, Laura and Knight, Rosemary and Clayton, Tim and Swan, Lorna and Thomson, John D R and Erdem, Guliz and Crossman, David and Flather, Marcus and Dean, John and Was, Bartosz and Gow, Heather and Murray, Jane and D'Allessandro, Mariella and Christie, Michael and Cooper, Patricia and Booth, Philip and Burns, Sharon and Paterson, Yvonne and Chikermane, Ashish and Assing, Anthony and Cotter, Catherine and Atkins, Gillian and Williamson, Helen and Barclay, Justin and Jennison, Alan and Henderson, Alex and McSkeane, Anna and Fairlamb, Helen and Kelly, Julie and Kelsall, Nicola and Prentice, Scott and O'Sullivan, John and Head-Baister, Alison and Phillipson, Angela and Johnson, Anna and Crossland, D and Oliver, Jack and Davison, Jade and Wake, Jill and Quinn, Louise and Foreman, Maureen and Wealleans, Vera and Walker, Niki and Duncan, Alexis and Tibbs, Evelyn and Kelly, Ruth and Khambadkone, Sachin and Zotti, Bridget and Brady, Cassie and Cervi, Elena and Field, Ella and Szepezvary, Eszter and Mantey, Florence and Riley, Gillian and Titmus, Heather and Bo, Ilaria and Kaski, Juan Pablo and Green, Loren and Jones, Nigel and Banks, Rebecca and Kiesewetter, Christopher and Mathur, Sujeev and Frigiola, Alessandra and Savis, Alex and Belfield, Holly and Guzman, Josephine and Harris, Julia and Wilson, Karen and Peacock, Kelly and Gibson, Kirsty and Wellman, Paul and Simpson, John and Kabir, Saleha and Mushemi, Sitali and Stewart, Michael and Atkinson, Bev and Richardson, Cath and Leng, Elaine and Brennan, Paul and Nixon, Annabel and Spencer, Collette and Oliver, James and Forster, Jan and Turner, Louise and Bainbridge, Samantha and Choy, Anna Maria and Dawson, Adelle and Kiddie, Gwen and Kerr, Heather and ... and AIMS Investigators
The Lancet (British edition), ISSN 0140-6736, 12/2019, Volume 394, Issue 10216, pp. 2263 - 2270
Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Echocardiography | Aorta - diagnostic imaging | Double-Blind Method | Drug Administration Schedule | Aorta - drug effects | Humans | Male | Treatment Outcome | United Kingdom | Angiotensin II Type 1 Receptor Blockers - pharmacology | Young Adult | Marfan Syndrome - drug therapy | Adolescent | Adult | Female | Marfan Syndrome - diagnostic imaging | Irbesartan - administration & dosage | Child | Angiotensin II Type 1 Receptor Blockers - administration & dosage | Irbesartan - pharmacology | Irbesartan | Clinical trials | Marfan syndrome | Marfan's syndrome | Young adults | Sensitivity analysis | Laboratories | Complications | Research | Diameters | Randomization | Consent | Angiotensin | Aorta | Blood pressure | Adults | Mutation | Children | Mercury | Stretching | Index Medicus | Abridged Index Medicus
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4. Full Text Contrasting patterns of leaf trait variation among and within species during tropical dry forest succession in Costa Rica
by Derroire, Géraldine and Powers, Jennifer S and Hulshof, Catherine M and Cárdenas Varela, Luis E and Healey, John R
Scientific reports, ISSN 2045-2322, 12/2018, Volume 8, Issue 1, pp. 285 - 285
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Forests | Phenotype | Quantitative Trait, Heritable | Tropical Climate | Plant Leaves | Biological Variation, Population | Plants | Biodiversity | Costa Rica | Economics | Leaves | Succession | Drought resistance | Ordination | Environmental changes | Ontogeny | Leaf area | Variation | Species | Index Medicus
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5. Dracula
by Cazacu, Matei, author and Nizet, Marie, 1859-1922 and Reinert, Stephen W., editor,author of introduction, etc.,translator and Mordarski, Nicole, translator and Brinton, Alice, translator and Healey, Catherine, translator
2017, East Central and Eastern Europe in the Middle Ages, 450-1450, ISBN 9004347259, Volume 46, xxxiii, 457 pages
Dracula, Count (Fictitious character) | Romania | Dracula (Stoker, Bram) | Stoker, Bram, 1847-1912. Dracula | Vampires | Dracula films | Kings and rulers | History and criticism | Wallachia Kings and rulers | Vlad III, Prince of Wallachia, 1430 or 1431-1476 or 1477
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6. Full Text Prenatal exome sequencing analysis in fetal structural anomalies detected by ultrasonography (PAGE): a cohort study
by Lord, Jenny and McMullan, Dominic J and Eberhardt, Ruth Y and Rinck, Gabriele and Hamilton, Susan J and Quinlan-Jones, Elizabeth and Prigmore, Elena and Keelagher, Rebecca and Best, Sunayna K and Carey, Georgina K and Mellis, Rhiannon and Robart, Sarah and Berry, Ian R and Chandler, Kate E and Cilliers, Deirdre and Cresswell, Lara and Edwards, Sandra L and Gardiner, Carol and Henderson, Alex and Holden, Simon T and Homfray, Tessa and Lester, Tracy and Lewis, Rebecca A and Newbury-Ecob, Ruth and Prescott, Katrina and Quarrell, Oliver W and Ramsden, Simon C and Roberts, Eileen and Tapon, Dagmar and Tooley, Madeleine J and Vasudevan, Pradeep C and Weber, Astrid P and Wellesley, Diana G and Westwood, Paul and White, Helen and Parker, Michael and Williams, Denise and Jenkins, Lucy and Scott, Richard H and Kilby, Mark D and Chitty, Lyn S and Hurles, Matthew E and Maher, Eamonn R and Bateman, Mark and Berry, Ian R and Best, Sunayna K and Campbell, Carolyn and Campbell, Jenni and Carey, Georgina and Chandler, Kate E and Chitty, Lyn S and Cilliers, Deirdre and Cohen, Kelly and Collingwood, Emma and Constantinou, Panayiotis and Cresswell, Lara and Delmege, Catherine and Eberhardt, Ruth Y and Edwards, Sandra L and Ellis, Richard and Evans, Jerry and Everett, Thomas and Pinto, Clare F and Forrester, Natalie and Fowler, Emma and Gardiner, Carol and Hamilton, Susan and Healey, Karen and Henderson, Alex and Holden, Simon T and Homfray, Tessa and Hudson, Rebecca and Hurles, Matthew E and Jenkins, Lucy and Keelagher, Rebecca and Kilby, Mark D and Lester, Tracey and Lewis, Rebecca and Lord, Jenny and Maher, Eamonn R and Marton, Tamas and McMullan, Dominic J and Mehta, Sarju and Mellis, Rhiannon and Newbury-Ecob, Ruth and Park, Soo-Mi and Parker, Michael and Prescott, Katrina and Prigmore, Elena and Quarrell, Oliver W and Quinlan-Jones, Elizabeth and Ramsden, Simon C and Rinck, Gabriele and Robart, Sarah and Roberts, Eileen and Rowland, Jayne and Scott, Richard H and Steer, James and Tapon, Dagmar and Taylor, Emma J and ... and Prenatal Assessment of Genomes and Exomes Consortium and Prenatal Assessment Genomes Exomes
The Lancet (British edition), ISSN 0140-6736, 02/2019, Volume 393, Issue 10173, pp. 747 - 757
Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Fetus - abnormalities | Congenital Abnormalities - epidemiology | Fetus - diagnostic imaging | Prospective Studies | Humans | Parents | Perinatal Death - etiology | Male | DNA Copy Number Variations - genetics | Whole Exome Sequencing - methods | Abnormal Karyotype - embryology | Congenital Abnormalities - diagnosis | Pregnancy | Abortion, Spontaneous - epidemiology | Congenital Abnormalities - genetics | Nuchal Translucency Measurement | Stillbirth - epidemiology | Abnormal Karyotype - statistics & numerical data | Female | Live Birth - epidemiology | Fetal Development - genetics | Abortion, Eugenic - statistics & numerical data | Infant, Newborn | Whole Exome Sequencing - statistics & numerical data | Ultrasound imaging | Pregnant women | Heart | Intellectual disabilities | Copy number | Genes | Disorders | Prenatal development | Aneuploidy | Genomes | Gestation | Microcephaly | Genetic screening | Gene sequencing | Disability | Proteins | Parents & parenting | Ultrasonic imaging | Next-generation sequencing | Scoliosis | Heart diseases | Ultrasound | Deoxyribonucleic acid--DNA | Phenotypes | Congenital diseases | Research & development--R&D | Fetuses | Abnormalities | Birth defects | Heredity | Hearing impairment | Coronary artery disease | Genetic variance | DNA microarrays | Gene frequency | Diagnostic systems | Cardiovascular diseases | Anomalies | Index Medicus | Abridged Index Medicus
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7. Full Text Genome-wide association study identifies five new breast cancer susceptibility loci
by Turnbull, Clare and Ahmed, Shahana and Morrison, Jonathan and Pernet, David and Renwick, Anthony and Maranian, Mel and Seal, Sheila and Ghoussaini, Maya and Hines, Sarah and Healey, Catherine S and Hughes, Deborah and Warren-Perry, Margaret and Tapper, William and Eccles, Diana and Evans, D Gareth and Hooning, Maartje and Schutte, Mieke and Van Den Ouweland, Ans and Houlston, Richard and Ross, Gillian and Langford, Cordelia and Pharoah, Paul D.P and Stratton, Michael R and Dunning, Alison M and Rahman, Nazneen and Easton, Douglas F and Breast Canc Susceptibility and Breast Cancer Susceptibility Collaboration (UK) and The Breast Cancer Susceptibility Collaboration (UK)
Nature genetics, ISSN 1061-4036, 06/2010, Volume 42, Issue 6, pp. 504 - 507
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Fundamental and applied biological sciences. Psychology | Gynecology. Andrology. Obstetrics | Mammary gland diseases | Biological and medical sciences | Genetics of eukaryotes. Biological and molecular evolution | Medical sciences | Tumors | Genetic Predisposition to Disease | Genome-Wide Association Study | Breast Neoplasms - genetics | Humans | Female | Genotype | Chromosomes, Human, Pair 11 | Chromosomes, Human, Pair 8 | Polymorphism, Single Nucleotide | Chromosomes, Human, Pair 9 | Chromosomes, Human, Pair 6 | Chromosomes, Human, Pair 10 | Gene mutations | Breast cancer | Genetic aspects | Disease susceptibility | Diagnosis | Research | Single nucleotide polymorphisms | Health aspects | Risk factors | Studies | Medical research | Genetics | Family medical history | Index Medicus
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