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2003, Methods in molecular biology, ISBN 9780896039681, Volume 212., xi, 269
Single nucleotide polymorphisms (SNPs) have become the markers of choice in elucidating the relationship between DNA sequence variation and susceptibility to... 
Chromosome polymorphism | Genetic markers | Variation | Human genetics | Laboratory manuals | Human Genetics | Biomedicine
Book
Bioinformatics, ISSN 1367-4803, 05/2015, Volume 31, Issue 22, pp. 3673 - 3675
A Summary: Mutational signatures are patterns in the occurrence of somatic single-nucleotide variants that can reflect underlying mutational processes. The... 
BIOTECHNOLOGY & APPLIED MICROBIOLOGY | HUMAN CANCER | BIOCHEMICAL RESEARCH METHODS | MATHEMATICAL & COMPUTATIONAL BIOLOGY | BIOCONDUCTOR | Polymorphism, Single Nucleotide - genetics | Software | Neoplasms - genetics | Genome, Human | Mutation - genetics | Humans | Applications Notes
Journal Article
Plant Biotechnology Journal, ISSN 1467-7644, 08/2014, Volume 12, Issue 6, pp. 787 - 796
Journal Article
Lancet, The, ISSN 0140-6736, 2010, Volume 376, Issue 9749, pp. 1320 - 1328
Summary Background In the PLATO trial of ticagrelor versus clopidogrel for treatment of acute coronary syndromes, ticagrelor reduced the composite outcome of... 
Internal Medicine | ALLELE | MEDICINE, GENERAL & INTERNAL | INHIBITION | ANTAGONIST | PLATELET-AGGREGATION | STENT THROMBOSIS | OF-FUNCTION POLYMORPHISM | P-GLYCOPROTEIN EXPRESSION | PRASUGREL | PHARMACOGENETICS | TREATED PATIENTS | Ticlopidine - therapeutic use | Cardiovascular Diseases - prevention & control | Humans | Aryl Hydrocarbon Hydroxylases - genetics | Male | Adenosine - adverse effects | Adenosine - therapeutic use | Ticlopidine - adverse effects | Female | Platelet Aggregation Inhibitors - therapeutic use | Platelet Aggregation Inhibitors - adverse effects | Cardiovascular Diseases - etiology | Pharmacogenetics | Genotype | Ticlopidine - analogs & derivatives | Randomized Controlled Trials as Topic | Acute Coronary Syndrome - drug therapy | Phenotype | ATP-Binding Cassette, Sub-Family B, Member 1 - genetics | Cytochrome P-450 CYP2C19 | Adenosine - analogs & derivatives | ATP Binding Cassette Transporter, Sub-Family B | Aged | Polymorphism, Single Nucleotide | Acute Coronary Syndrome - genetics | Care and treatment | Patient outcomes | Physiological aspects | Clopidogrel | Dosage and administration | Single nucleotide polymorphisms | Health aspects | Coronary heart disease | Studies | Heart attacks | Statistical analysis | Metabolites | Genetics | Drug therapy | Gene expression | Acute coronary syndromes | Myocardial infarction | Stroke | Single-nucleotide polymorphism | Arteries | Bleeding | Medical and Health Sciences | MEDICINE | Medicin och hälsovetenskap | MEDICIN
Journal Article
Cell, ISSN 0092-8674, 03/2012, Volume 148, Issue 5, pp. 886 - 895
Journal Article
Nature Reviews Genetics, ISSN 1471-0056, 12/2001, Volume 2, Issue 12, pp. 930 - 942
Journal Article
by Kathiresan, Sekar and Voight, Benjamin F and Purcell, Shaun and Musunuru, Kiran and Ardissino, Diego and Mannucci, Pier M and Anand, Sonia and Engert, James C and Samani, Nilesh J and Schunkert, Heribert and Erdmann, Jeanette and Reilly, Muredach P and Rader, Daniel J and Morgan, Thomas and Spertus, John A and Stoll, Monika and Girelli, Domenico and McKeown, Pascal P and Patterson, Chris C and Siscovick, David S and O'Donnell, Christopher J and Elosua, Roberto and Peltonen, Leena and Salomaa, Veikko and Schwartz, Stephen M and Melander, Olle and Altshuler, David and Merlini, Pier Angelica and Berzuini, Carlo and Bernardinelli, Luisa and Peyvandi, Flora and Tubaro, Marco and Celli, Patrizia and Ferrario, Maurizio and Fetiveau, Raffaela and Marziliano, Nicola and Casari, Giorgio and Galli, Michele and Ribichini, Flavio and Rossi, Marco and Bernardi, Francesco and Zonzin, Pietro and Piazza, Alberto and Yee, Jean and Friedlander, Yechiel and Marrugat, Jaume and Lucas, Gavin and Subirana, Isaac and Sala, Joan and Ramos, Rafael and Meigs, James B and Williams, Gordon and Nathan, David M and MacRae, Calum A and Havulinna, Aki S and Berglund, Goran and Hirschhorn, Joel N and Asselta, Rosanna and Duga, Stefano and Spreafico, Marta and Daly, Mark J and Nemesh, James and Korn, Joshua M and McCarroll, Steven A and Surti, Aarti and Guiducci, Candace and Gianniny, Lauren and Mirel, Daniel and Parkin, Melissa and Burtt, Noel and Gabriel, Stacey B and Thompson, John R and Braund, Peter S and Wright, Benjamin J and Balmforth, Anthony J and Ball, Stephen G and Hall, Alistair S and Linsel-Nitschke, Patrick and Lieb, Wolfgang and Ziegler, Andreas and König, Inke R and Hengstenberg, Christian and Fischer, Marcus and Stark, Klaus and Grosshennig, Anika and Preuss, Michael and Wichmann, H.-Erich and Schreiber, Stefan and Ouwehand, Willem and Deloukas, Panos and Scholz, Michael and Cambien, Francois and Cardiogenics, Cardiogenics and Li, Mingyao and Chen, Zhen and Wilensky, Robert and Matthai, William and Qasim, Atif and Hakonarson, Hakon H and Devaney, Joe and ... and Myocardial Infarction Genetics Consortium and Wellcome Trust Case Control Consortium
Nature Genetics, ISSN 1061-4036, 2009, Volume 41, Issue 3, pp. 334 - 341
Journal Article