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1. Politicking online
: the transformation of election campaign communications
by Panagopoulos, Costas
2009, ISBN 9780813544892, viii, 302
Elections | Telecommunication | Internet in political campaigns | Political campaigns | Information technology | Effect of technological innovations on
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2. Full Text Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction
by Do, Ron and Stitziel, Nathan O and Won, Hong-Hee and Jørgensen, Anders Berg and Duga, Stefano and Angelica Merlini, Pier and Kiezun, Adam and Farrall, Martin and Goel, Anuj and Zuk, Or and Guella, Illaria and Asselta, Rosanna and Lange, Leslie A and Peloso, Gina M and Auer, Paul L and Girelli, Domenico and Martinelli, Nicola and Farlow, Deborah N and DePristo, Mark A and Roberts, Robert and Stewart, Alexander F. R and Saleheen, Danish and Danesh, John and Epstein, Stephen E and Sivapalaratnam, Suthesh and Hovingh, G. Kees and Kastelein, John J and Samani, Nilesh J and Schunkert, Heribert and Erdmann, Jeanette and Shah, Svati H and Kraus, William E and Davies, Robert and Nikpay, Majid and Johansen, Christopher T and Wang, Jian and Hegele, Robert A and Hechter, Eliana and Marz, Winfried and Kleber, Marcus E and Huang, Jie and Johnson, Anew D and Li, Mingyao and Burke, Greg L and Gross, Myron and Liu, Yongmei and Assimes, Themistocles L and Heiss, Gerardo and Lange, Ethan M and Folsom, Aaron R and NHLBI Exome Sequencing Project
Nature (London), ISSN 0028-0836, 2015, Volume 518, Issue 7537, pp. 102 - +
no | Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Genetics, Population | Myocardial Infarction - blood | Myocardial Infarction - genetics | Receptors, LDL - genetics | Apolipoprotein A-V | Genetic Predisposition to Disease - genetics | Apolipoproteins A - genetics | National Heart, Lung, and Blood Institute (U.S.) | Age Factors | United States | Humans | Middle Aged | Male | Mutation - genetics | Case-Control Studies | Exome - genetics | Age of Onset | Alleles | Coronary Artery Disease - genetics | Triglycerides - blood | Cholesterol, LDL - blood | Female | Heterozygote | Usage | Low density lipoproteins | Exome sequencing | Physiological aspects | Genetic aspects | Research | Diagnosis | Heart attack | Risk factors | Proteins | Studies | Algorithms | Heart attacks | Genes | Cardiovascular disease | Triglycerides | Mutation | Cholesterol | Index Medicus | Medicin och hälsovetenskap
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3. Full Text Whole-Exome Sequencing Identifies Rare and Low-Frequency Coding Variants Associated with LDL Cholesterol
by Lange, Leslie A and Hu, Youna and Zhang, He and Xue, Chenyi and Schmidt, Ellen M and Tang, Zheng-Zheng and Bizon, Chris and Lange, Ethan M and Smith, Joshua D and Turner, Emily H and Jun, Goo and Kang, Hyun Min and Peloso, Gina and Auer, Paul and Li, Kuo-ping and Flannick, Jason and Zhang, Ji and Fuchsberger, Christian and Gaulton, Kyle and Lindgren, Cecilia and Locke, Adam and Manning, Alisa and Sim, Xueling and Rivas, Manuel A and Holmen, Oddgeir L and Gottesman, Omri and Lu, Yingchang and Ruderfer, Douglas and Stahl, Eli A and Duan, Qing and Li, Yun and Durda, Peter and Jiao, Shuo and Isaacs, Aaron and Hofman, Albert and Bis, Joshua C and Correa, Adolfo and Griswold, Michael E and Jakobsdottir, Johanna and Smith, Albert V and Schreiner, Pamela J and Feitosa, Mary F and Zhang, Qunyuan and Huffman, Jennifer E and Crosby, Jacy and Wassel, Christina L and Do, Ron and Franceschini, Nora and Martin, Lisa W and Robinson, Jennifer G and Assimes, Themistocles L and Crosslin, David R and Rosenthal, Elisabeth A and Tsai, Michael and Rieder, Mark J and Farlow, Deborah N and Folsom, Aaron R and Lumley, Thomas and Fox, Ervin R and Carlson, Christopher S and Peters, Ulrike and Jackson, Rebecca D and van Duijn, Cornelia M and Uitterlinden, André G and Levy, Daniel and Rotter, Jerome I and Taylor, Herman A and Gudnason, Vilmundur and Siscovick, David S and Fornage, Myriam and Borecki, Ingrid B and Hayward, Caroline and Rudan, Igor and Chen, Y. Eugene and Bottinger, Erwin P and Loos, Ruth J.F and Sætrom, Pål and Hveem, Kristian and Boehnke, Michael and Groop, Leif and McCarthy, Mark and Meitinger, Thomas and Ballantyne, Christie M and Gabriel, Stacey B and O’Donnell, Christopher J and Post, Wendy S and North, Kari E and Reiner, Alexander P and Boerwinkle, Eric and Psaty, Bruce M and Altshuler, David and Kathiresan, Sekar and Lin, Dan-Yu and Jarvik, Gail P and Cupples, L. Adrienne and Kooperberg, Charles and Wilson, James G and Nickerson, Deborah A and Abecasis, Goncalo R and Rich, Stephen S and ... and the NHLBI Grand Opportunity Exome Sequencing Project and NHLBI Grand Opportunity Exome Sequ and NHLBI Grand Opportunity Exome Sequencing Project
American journal of human genetics, ISSN 0002-9297, 02/2014, Volume 94, Issue 2, pp. 233 - 245
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Dyslipidemias - genetics | Genetic Code | Follow-Up Studies | Humans | Middle Aged | Male | Proprotein Convertases - genetics | Exome | Dyslipidemias - blood | Serine Endopeptidases - genetics | Adult | Female | Receptors, LDL - genetics | Genome-Wide Association Study | Gene Frequency | Genotype | Sequence Analysis, DNA | Cholesterol, LDL - genetics | Phenotype | Apolipoproteins E - blood | Apolipoproteins E - genetics | Aged | Polymorphism, Single Nucleotide | Cohort Studies | Lipase - genetics | Proprotein Convertase 9 | Genetic code | Genetic variation | Physiological aspects | Genetic research | Cholesterol, LDL | Genetic aspects | Research | Nucleotide sequencing | DNA sequencing | Genotype & phenotype | Low density lipoprotein | Genes | Cholesterol | Risk factors | Index Medicus | Medicinsk genetik | Basic Medicine | Medical Genetics | Medical and Health Sciences | Medicin och hälsovetenskap | Medicinska och farmaceutiska grundvetenskaper
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4. Full Text Discovery of common and rare genetic risk variants for colorectal cancer
by Huyghe, Jeroen R and Bien, Stephanie A and Harrison, Tabitha A and Kang, Hyun Min and Chen, Sai and Schmit, Stephanie L and Conti, David V and Qu, Conghui and Jeon, Jihyoun and Edlund, Christopher K and Greenside, Peyton and Wainberg, Michael and Schumacher, Freick R and Smith, Joshua D and Levine, David M and Nelson, Sarah C and Sinnott-Armstrong, Nasa A and Albanes, Demetrius and Alonso, M. Henar and Anderson, Kristin and Arnau-Collell, Coral and Arndt, Volker and Bamia, Christina and Banbury, Barbara L and Baron, John A and Berndt, Sonja I and Bézieau, Stéphane and Bishop, D. Timothy and Boehm, Juergen and Boeing, Heiner and Brenner, Hermann and Brezina, Stefanie and Buch, Stephan and Buchanan, Daniel D and Burnett-Hartman, Anea and Butterbach, Katja and Caan, Bette J and Campbell, Peter T and Carlson, Christopher S and Castellví-Bel, Sergi and Chan, Anew T and Chang-Claude, Jenny and Chanock, Stephen J and Chirlaque, Maria Dolores and Cho, Sang Hee and Connolly, Charles M and Cross, Amanda J and Cuk, Katarina and Curtis, Keith R and de la Chapelle, Albert and Doheny, Kimberly F and Duggan, David and Easton, Douglas F and Elias, Sjoerd G and Elliott, Faye and English, Dallas R and Feskens, Edith J.M and Figueiredo, Jane C and Fischer, Rocky and FitzGerald, Liesel M and Forman, David and Gala, Manish and Gallinger, Steven and Gauderman, W. James and Giles, Graham G and Gillanders, Elizabeth and Gong, Jian and Goodman, Phyllis J and Grady, William M and Grove, John S and Gsur, Anea and Gunter, Marc J and Haile, Robert W and Hampe, Jochen and Hampel, Heather and Harlid, Sophia and Hayes, Richard B and Hofer, Philipp and Hoffmeister, Michael and Hopper, John L and Hsu, Wan Ling and Huang, Wen Yi and Hudson, Thomas J and Hunter, David J and Ibañez-Sanz, Gemma and Idos, Gregory E and Ingersoll, Roxann and Jackson, Rebecca D and Jacobs, Eric J and Jenkins, Mark A and Joshi, Amit D and Joshu, Corinne E and Keku, Temitope O and Key, Timothy J and Kim, Hyeong Rok and Kobayashi, Emiko and Kolonel, Laurence N and Kooperberg, Charles and Kühn, Tilman and Küry, Sébastien and ...
Nature genetics, ISSN 1061-4036, 01/2019, Volume 51, Issue 1, pp. 76 - 87
Genetics | Journal Article | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Genetic aspects | Research | Genetic variation | Risk factors | Colorectal cancer | Haplotypes | Immune response | Nucleotide sequence | Colorectal carcinoma | Health risks | Risk | Systematic review | Genomes | Drug development | Gene expression | Epidemiology | Gene sequencing | Meta-analysis | Consortia | Yes-associated protein | Studies | Signaling | Hedgehog protein | Gastroenterology | Heritability | Mutation | Cancer | Index Medicus | Life Sciences | Santé publique et épidémiologie | Medicin och hälsovetenskap
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5. Full Text A map of human genome variation from population-scale sequencing
by Altshuler, David L and Durbin, Richard M and Abecasis, Gonçalo R and Bentley, David R and Chakravarti, Aravinda and Clark, Andrew G and Collins, Francis S and De La Vega, Francisco M and Donnelly, Peter and Egholm, Michael and Flicek, Paul and Gabriel, Stacey B and Gibbs, Richard A and Knoppers, Bartha M and Lander, Eric S and Lehrach, Hans and Mardis, Elaine R and McVean, Gil A and Nickerson, Debbie A and Peltonen, Leena and Schafer, Alan J and Sherry, Stephen T and Wang, Jun and Wilson, Richard K and Deiros, David and Metzker, Mike and Muzny, Donna and Reid, Jeff and Wheeler, David and Wang, Shenzhen Jun and Li, Jingxiang and Jian, Min and Li, Guoqing and Li, Ruiqiang and Liang, Huiqing and Tian, Geng and Wang, Bo and Wang, Jian and Wang, Wei and Yang, Huanming and Zhang, Xiuqing and Zheng, Huisong and Ambrogio, Lauren and Bloom, Toby and Cibulskis, Kristian and Fennell, Tim J and Jaffe, David B and Shefler, Erica and Sougnez, Carrie L and Bentley, Illumina David R and Gormley, Niall and Humphray, Sean and Kingsbury, Zoya and Koko-Gonzales, Paula and Stone, Jennifer and Mc Kernan, Kevin J and Costa, Gina L and Ichikawa, Jeffry K and Lee, Clarence C and Sudbrak, Ralf and Borodina, Tatiana A and Dahl, Andreas and Davydov, Alexey N and Marquardt, Peter and Mertes, Florian and Nietfeld, Wilfiried and Rosenstiel, Philip and Schreiber, Stefan and Soldatov, Aleksey V and Timmermann, Bernd and Tolzmann, Marius and Affourtit, Jason and Ashworth, Dana and Attiya, Said and Bachorski, Melissa and Buglione, Eli and Burke, Adam and Caprio, Amanda and Celone, Christopher and Clark, Shauna and Conners, David and Desany, Brian and Gu, Lisa and Guccione, Lorri and Kao, Kalvin and Kebbel, Andrew and Knowlton, Jennifer and Labrecque, Matthew and McDade, Louise and Mealmaker, Craig and Minderman, Melissa and Nawrocki, Anne and Niazi, Faheem and Pareja, Kristen and Ramenani, Ravi and Riches, David and Song, Wanmin and Turcotte, Cynthia and Wang, Shally and Dooling, David and ... and 1000 Genomes Project Consortium and The 1000 Genomes Project Consortium
Nature (London), ISSN 0028-0836, 10/2010, Volume 467, Issue 7319, pp. 1061 - 1073
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Fundamental and applied biological sciences. Psychology | Human | Biological and medical sciences | Genetics of eukaryotes. Biological and molecular evolution | Population genetics, reproduction patterns | Humans | Male | Selection, Genetic - genetics | Haplotypes - genetics | DNA, Mitochondrial - genetics | DNA Mutational Analysis | Recombination, Genetic - genetics | Female | Genomics - methods | Genome-Wide Association Study | Genetic Association Studies | Computational Biology | Genotype | Calibration | Mutation - genetics | Genome, Human - genetics | Chromosomes, Human, Y - genetics | Pilot Projects | Sample Size | Sequence Alignment | Genetics, Population - methods | Polymorphism, Single Nucleotide - genetics | Genetic Variation - genetics | Sequence Analysis, DNA - methods | Evolution, Molecular | Research | Nucleotide sequencing | Human genome | Human population genetics | Identification and classification | Methods | Studies | Design | Pilot projects | Genomics | Genetics | Mutation | Deoxyribonucleic acid--DNA | Index Medicus | Life Sciences
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