Search Results - "SLATER, Andrew J"

Performance of genotype imputation for rare variants identified in exons and flanking regions of genes by Li, Li, Li, Yun, Browning, Sharon R, Browning, Brian L, Slater, Andrew J, Kong, Xiangyang, Aponte, Jennifer L, Mooser, Vincent E, Chissoe, Stephanie L, Whittaker, John C, Nelson, Matthew R, Ehm, Margaret Gelder

“…Genotype imputation has the potential to assess human genetic variation at a lower cost than assaying the variants using laboratory techniques. The performance…”
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A comparison of internal validation techniques for multifactor dimensionality reduction by Winham, Stacey J, Slater, Andrew J, Motsinger-Reif, Alison A

“…It is hypothesized that common, complex diseases may be due to complex interactions between genetic and environmental factors, which are difficult to detect in…”
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Candidate single-nucleotide polymorphisms from a genomewide association study of Alzheimer disease by Li, Hao, Wetten, Sally, Li, Li, St Jean, Pamela L, Upmanyu, Ruchi, Surh, Linda, Hosford, David, Barnes, Michael R, Briley, James David, Borrie, Michael, Coletta, Natalie, Delisle, Richard, Dhalla, Daniella, Ehm, Margaret G, Feldman, Howard H, Fornazzari, Luis, Gauthier, Serge, Goodgame, Neil, Guzman, Danilo, Hammond, Sandra, Hollingworth, Paul, Hsiung, Ging-Yuek, Johnson, Joan, Kelly, Devon D, Keren, Ron, Kertesz, Andrew, King, Karen S, Lovestone, Simon, Loy-English, Inge, Matthews, Paul M, Owen, Michael J, Plumpton, Mary, Pryse-Phillips, William, Prinjha, Rab K, Richardson, Jill C, Saunders, Ann, Slater, Andrew J, St George-Hyslop, Peter H, Stinnett, Sandra W, Swartz, Jina E, Taylor, Rachel L, Wherrett, John, Williams, Julie, Yarnall, David P, Gibson, Rachel A, Irizarry, Michael C, Middleton, Lefkos T, Roses, Allen D

“…To identify single-nucleotide polymorphisms (SNPs) associated with risk and age at onset of Alzheimer disease (AD) in a genomewide association study of 469 438…”
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STOPGAP: a database for systematic target opportunity assessment by genetic association predictions by Shen, Judong, Song, Kijoung, Slater, Andrew J, Ferrero, Enrico, Nelson, Matthew R

“…We developed the STOPGAP (Systematic Target OPportunity assessment by Genetic Association Predictions) database, an extensive catalog of human genetic…”
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Deep Resequencing Unveils Genetic Architecture of ADIPOQ and Identifies a Novel Low-Frequency Variant Strongly Associated With Adiponectin Variation by WARREN, Liling L, LI LI, HALL, Matt D, TOPP, Simon D, XIN YUAN, CARDON, Lon R, CHISSOE, Stephanie L, MOOSER, Vincent, MORRIS, Andrew D, PALMER, Colin N. A, PERRY, John R, FRAYLING, Timothy M, NELSON, Matthew R, WHITTAKER, John C, WATERWORTH, Dawn M, EHM, Margaret G, JUDONG SHEN, FRASER, Dana J, APONTE, Jennifer L, NANGLE, Keith L, SLATER, Andrew J, WOOLLARD, Peter M

“…Increased adiponectin levels have been shown to be associated with a lower risk of type 2 diabetes. To understand the relations between genetic variation at…”
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Platelet-Related Variants Identified by Exomechip Meta-analysis in 157,293 Individuals by Eicher, John D., Kacprowski, Tim, Nomura, Akihiro, Chen, Ming-Huei, Yanek, Lisa R., Tajuddin, Salman M., Slater, Andrew J., Polfus, Linda, Schurmann, Claudia, Brody, Jennifer A., Manichaikul, Ani, Hill, W. David, Pazoki, Raha, Elliot, Paul, Evangelou, Evangelos, Tzoulaki, Ioanna, Gao, He, Vergnaud, Anne-Claire, Mathias, Rasika A., Becker, Diane M., Becker, Lewis C., Burt, Amber, Crosslin, David R., Lyytikäinen, Leo-Pekka, Nikus, Kjell, Hernesniemi, Jussi, Kähönen, Mika, Raitoharju, Emma, Mononen, Nina, Raitakari, Olli T., Lehtimäki, Terho, Cushman, Mary, Zakai, Neil A., Nickerson, Deborah A., Raffield, Laura M., Quarells, Rakale, Willer, Cristen J., Peloso, Gina M., Abecasis, Goncalo R., Liu, Dajiang J., Deloukas, Panos, Samani, Nilesh J., Schunkert, Heribert, Erdmann, Jeanette, Fornage, Myriam, Richard, Melissa, Tardif, Jean-Claude, Rioux, John D., Dube, Marie-Pierre, de Denus, Simon, Bottinger, Erwin P., Loos, Ruth J.F., Smith, Albert Vernon, Harris, Tamara B., Launer, Lenore J., Gudnason, Vilmundur, Velez Edwards, Digna R., Torstenson, Eric S., Liu, Yongmei, Tracy, Russell P., Rotter, Jerome I., Rich, Stephen S., Highland, Heather M., Li, Jin, Lange, Ethan, Wilson, James G., Mihailov, Evelin, Hirschhorn, Joel, Metspalu, Andres, Esko, Tõnu, Vacchi-Suzzi, Caterina, Zonderman, Alan B., Evans, Michele K., Engström, Gunnar, Orho-Melander, Marju, Melander, Olle, O’Donoghue, Michelle L., Waterworth, Dawn M., Floyd, James S., Rice, Kenneth M., Psaty, Bruce M., Starr, J.M., Liewald, David C.M., Hayward, Caroline, Deary, Ian J., Greinacher, Andreas, Völker, Uwe, Thiele, Thomas, Völzke, Henry, van Rooij, Frank J.A., Uitterlinden, André G., Franco, Oscar H., Dehghan, Abbas, Edwards, Todd L., Ganesh, Santhi K., Kathiresan, Sekar, Faraday, Nauder, Reiner, Alex P., Lettre, Guillaume, Johnson, Andrew D.

“…Platelet production, maintenance, and clearance are tightly controlled processes indicative of platelets’ important roles in hemostasis and thrombosis…”
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Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits by Chami, Nathalie, Chen, Ming-Huei, Slater, Andrew J., Eicher, John D., Evangelou, Evangelos, Tajuddin, Salman M., Love-Gregory, Latisha, Schick, Ursula M., Nomura, Akihiro, Giri, Ayush, Lessard, Samuel, Brody, Jennifer A., Schurmann, Claudia, Pankratz, Nathan, Yanek, Lisa R., Manichaikul, Ani, Mihailov, Evelin, Hill, W. David, Raffield, Laura M., Burt, Amber, Bartz, Traci M., Becker, Diane M., Becker, Lewis C., Boerwinkle, Eric, Bork-Jensen, Jette, Bottinger, Erwin P., O’Donoghue, Michelle L., Crosslin, David R., de Denus, Simon, Dubé, Marie-Pierre, Engström, Gunnar, Evans, Michele K., Floyd, James S., Gao, He, Greinacher, Andreas, Gudnason, Vilmundur, Hansen, Torben, Hayward, Caroline, Hernesniemi, Jussi, Highland, Heather M., Hirschhorn, Joel N., Hofman, Albert, Irvin, Marguerite R., Kähönen, Mika, Lange, Ethan, Launer, Lenore J., Lehtimäki, Terho, Li, Jin, Liewald, David C.M., Liu, Yongmei, Lu, Yingchang, Lyytikäinen, Leo-Pekka, Mägi, Reedik, Mathias, Rasika A., Melander, Olle, Mononen, Nina, Nalls, Mike A., Nickerson, Deborah A., Nikus, Kjell, O’Donnell, Chris J., Orho-Melander, Marju, Polfus, Linda, Psaty, Bruce M., Raitoharju, Emma, Richard, Melissa, Rice, Kenneth M., Rivadeneira, Fernando, Rotter, Jerome I., Schmidt, Frank, Smith, Albert Vernon, Starr, John M., Taylor, Kent D., Teumer, Alexander, Thuesen, Betina H., Torstenson, Eric S., Tzoulaki, Ioanna, Zakai, Neil A., Vacchi-Suzzi, Caterina, van Duijn, Cornelia M., van Rooij, Frank J.A., Cushman, Mary, Deary, Ian J., Velez Edwards, Digna R., Vergnaud, Anne-Claire, Wallentin, Lars, Waterworth, Dawn M., White, Harvey D., Wilson, James G., Zonderman, Alan B., Kathiresan, Sekar, Grarup, Niels, Esko, Tõnu, Loos, Ruth J.F., Lange, Leslie A., Faraday, Nauder, Abumrad, Nada A., Edwards, Todd L., Ganesh, Santhi K., Johnson, Andrew D., Reiner, Alexander P.

“…Red blood cell (RBC) traits are important heritable clinical biomarkers and modifiers of disease severity. To identify coding genetic variants associated with…”
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Large-Scale Exome-wide Association Analysis Identifies Loci for White Blood Cell Traits and Pleiotropy with Immune-Mediated Diseases by Tajuddin, Salman M., Schick, Ursula M., Eicher, John D., Chami, Nathalie, Giri, Ayush, Brody, Jennifer A., Hill, W. David, Kacprowski, Tim, Li, Jin, Lyytikäinen, Leo-Pekka, Manichaikul, Ani, Mihailov, Evelin, O’Donoghue, Michelle L., Pankratz, Nathan, Pazoki, Raha, Polfus, Linda M., Smith, Albert Vernon, Schurmann, Claudia, Vacchi-Suzzi, Caterina, Waterworth, Dawn M., Evangelou, Evangelos, Yanek, Lisa R., Burt, Amber, Chen, Ming-Huei, van Rooij, Frank J.A., Floyd, James S., Greinacher, Andreas, Harris, Tamara B., Highland, Heather M., Lange, Leslie A., Liu, Yongmei, Mägi, Reedik, Nalls, Mike A., Mathias, Rasika A., Nickerson, Deborah A., Nikus, Kjell, Starr, John M., Tardif, Jean-Claude, Tzoulaki, Ioanna, Velez Edwards, Digna R., Wallentin, Lars, Bartz, Traci M., Becker, Lewis C., Denny, Joshua C., Raffield, Laura M., Rioux, John D., Friedrich, Nele, Fornage, Myriam, Gao, He, Hirschhorn, Joel N., Liewald, David C.M., Rich, Stephen S., Uitterlinden, Andre, Bastarache, Lisa, Becker, Diane M., Boerwinkle, Eric, de Denus, Simon, Bottinger, Erwin P., Hayward, Caroline, Hofman, Albert, Homuth, Georg, Lange, Ethan, Launer, Lenore J., Lehtimäki, Terho, Lu, Yingchang, Metspalu, Andres, O’Donnell, Chris J., Quarells, Rakale C., Richard, Melissa, Torstenson, Eric S., Taylor, Kent D., Vergnaud, Anne-Claire, Zonderman, Alan B., Crosslin, David R., Deary, Ian J., Dörr, Marcus, Elliott, Paul, Evans, Michele K., Gudnason, Vilmundur, Kähönen, Mika, Psaty, Bruce M., Rotter, Jerome I., Slater, Andrew J., Dehghan, Abbas, White, Harvey D., Ganesh, Santhi K., Loos, Ruth J.F., Esko, Tõnu, Faraday, Nauder, Wilson, James G., Cushman, Mary, Johnson, Andrew D., Edwards, Todd L., Zakai, Neil A., Lettre, Guillaume, Reiner, Alex P., Auer, Paul L.

“…White blood cells play diverse roles in innate and adaptive immunity. Genetic association analyses of phenotypic variation in circulating white blood cell…”
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