Search Results - Burtt, Noël P.

The Musculoskeletal Knowledge Portal: improving access to multi-omics data by Westendorf, Jennifer J., Bonewald, Lynda F., Kiel, Douglas P., Burtt, Noël P.

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Association of Blood Lipids with Common DNA Sequence Variants at Nineteen Genetic Loci in the Multiethnic United States National Health and Nutrition Examination Survey III by Keebler, Mary E., Sanders, Christopher L., Surti, Aarti, Guiducci, Candace, Burtt, Noel P, Kathiresan, Sekar

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IGF2R Missense Single-Nucleotide Polymorphisms and Breast Cancer Risk: The Multiethnic Cohort Study by Cheng, Iona, Stram, Daniel O., Burtt, Noël P., Gianniny, Lauren, Garcia, Rachel R., Pooler, Loreall, Henderson, Brian E., Marchand, Loïc Le, Haiman, Christopher A

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A comprehensive analysis of common genetic variation in prolactin (PRL) and PRL receptor (PRLR) genes in relation to plasma prolactin levels and breast cancer risk: the Multiethnic... by Lee, Sulggi A, Haiman, Christopher A, Burtt, Noel P, Pooler, Loreall C, Cheng, Iona, Kolonel, Laurence N, Pike, Malcolm C, Altshuler, David, Hirschhorn, Joel N, Henderson, Brian E, Stram, Daniel O

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Comparing strategies to fine map the association of common SNPs on chromosome 9p21 to Type 2 Diabetes and Myocardial Infarction by Shea, Jessica, Agarwala, Vineeta, Philippakis, Anthony A., Maguire, Jared, Banks, Eric, DePristo, Mark, Thomson, Brian, Guiducci, Candace, Kathiresan, Sekar, Gabriel, Stacey, Burtt, Noël P, Daly, Mark J., Groop, Leif, Altshuler, David

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Genomewide Linkage Analysis of Stature in Multiple Populations Reveals Several Regions with Evidence of Linkage to Adult Height by Hirschhorn, Joel N., Lindgren, Cecilia M., Daly, Mark J., Kirby, Andrew, Schaffner, Stephen F., Burtt, Noel P., Altshuler, David, Parker, Alex, Rioux, John D., Platko, Jill, Gaudet, Daniel, Hudson, Thomas J., Groop, Leif C., Lander, Eric S.

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A genome-wide association study for blood lipid phenotypes in the Framingham Heart Study by Kathiresan, Sekar, Manning, Alisa K, Demissie, Serkalem, D'Agostino, Ralph B, Surti, Aarti, Guiducci, Candace, Gianniny, Lauren, Burtt, Nöel P, Melander, Olle, Orho-Melander, Marju, Arnett, Donna K, Peloso, Gina M, Ordovas, Jose M, Cupples, L Adrienne

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The Lipid Droplet Knowledge Portal: A resource for systematic analyses of lipid droplet biology by Mejhert, Niklas, Gabriel, Katlyn R., Frendo-Cumbo, Scott, Krahmer, Natalie, Song, Jiunn, Kuruvilla, Leena, Chitraju, Chandramohan, Boland, Sebastian, Jang, Dong-Keun, von Grotthuss, Marcin, Costanzo, Maria C., Rydén, Mikael, Olzmann, James A., Flannick, Jason, Burtt, Noël P., Farese, Robert V., Walther, Tobias C.

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High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency by Calvo, Sarah E, Tucker, Elena J, Compton, Alison G, Kirby, Denise M, Crawford, Gabriel, Burtt, Noel P, Rivas, Manuel A, Guiducci, Candace, Bruno, Damien L, Goldberger, Olga A, Redman, Michelle C, Wiltshire, Esko, Wilson, Callum J, Altshuler, David, Gabriel, Stacey B, Daly, Mark J, Thorburn, David R, Mootha, Vamsi K

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Genetic Variants Near TNFAIP3 on 6q23 are Associated with Systemic Lupus Erythematosus (SLE) by Graham, Robert R., Cotsapas, Chris, Davies, Leela, Hackett, Rachel, Lessard, Christopher J., Leon, Joanlise M., Burtt, Noel P., Guiducci, Candace, Parkin, Melissa, Gates, Casey, Plenge, Robert M., Behrens, Timothy W., Wither, Joan E., Rioux, John D., Fortin, Paul R., Graham, Deborah Cunninghame, Wong, Andrew K., Vyse, Timothy J., Daly, Mark J., Altshuler, David, Moser, Kathy L., Gaffney, Patrick M.

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Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans by Kathiresan, Sekar, Melander, Olle, Guiducci, Candace, Surti, Aarti, Burtt, Noël P, Rieder, Mark J, Cooper, Gregory M, Roos, Charlotta, Voight, Benjamin F, Havulinna, Aki S, Wahlstrand, Björn, Hedner, Thomas, Corella, Dolores, Tai, E Shyong, Ordovas, Jose M, Berglund, Göran, Vartiainen, Erkki, Jousilahti, Pekka, Hedblad, Bo, Taskinen, Marja-Riitta, Newton-Cheh, Christopher, Salomaa, Veikko, Peltonen, Leena, Groop, Leif, Altshuler, David M, Orho-Melander, Marju

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Assessing the phenotypic effects in the general population of rare variants in genes for a dominant mendelian form of diabetes by Flannick, Jason, Beer, Nicola L, Bick, Alexander G, Agarwala, Vineeta, Molnes, Janne, Gupta, Namrata, Burtt, Noel P, Florez, Jose C, Meigs, James B, Taylor, Herman, Lyssenko, Valeriya, Irgens, Henrik, Fox, Ervin, Burslem, Frank, Johansson, Stefan, Brosnan, M Julia, Trimmer, Jeff K, Newton-Cheh, Christopher, Tuomi, Tiinamaija, Molven, Anders, Wilson, James G, O'Donnell, Christopher J, Kathiresan, Sekar, Hirschhorn, Joel N, Njølstad, Pål R, Rolph, Tim, Seidman, J.G., Gabriel, Stacey, Cox, David R, Seidman, Christine, Groop, Leif, Altshuler, David

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A common variant of HMGA2 is associated with adult and childhood height in the general population by Weedon, Michael N, Lettre, Guillaume, Freathy, Rachel M, Lindgren, Cecilia M, Voight, Benjamin F, Perry, John R B, Elliott, Katherine S, Hackett, Rachel, Guiducci, Candace, Shields, Beverley, Zeggini, Eleftheria, Lango, Hana, Lyssenko, Valeriya, Timpson, Nicholas J, Burtt, Noel P, Rayner, Nigel W, Saxena, Richa, Ardlie, Kristin, Tobias, Jonathan H, Ness, Andrew R, Ring, Susan M, Palmer, Colin N A, Morris, Andrew D, Peltonen, Leena, Salomaa, Veikko, Smith, George Davey, Groop, Leif C, Hattersley, Andrew T, McCarthy, Mark I, Hirschhorn, Joel N, Frayling, Timothy M

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Two independent alleles at 6q23 associated with risk of rheumatoid arthritis by Plenge, Robert M, Cotsapas, Chris, Davies, Leela, Price, Alkes L, de Bakker, Paul I W, Maller, Julian, Pe'er, Itsik, Burtt, Noel P, Blumenstiel, Brendan, DeFelice, Matt, Parkin, Melissa, Barry, Rachel, Winslow, Wendy, Healy, Claire, Graham, Robert R, Neale, Benjamin M, Izmailova, Elena, Roubenoff, Ronenn, Parker, Alexander N, Glass, Roberta, Karlson, Elizabeth W, Maher, Nancy, Hafler, David A, Lee, David M, Seldin, Michael F, Remmers, Elaine F, Lee, Annette T, Padyukov, Leonid, Alfredsson, Lars, Coblyn, Jonathan, Weinblatt, Michael E, Gabriel, Stacey B, Purcell, Shaun, Klareskog, Lars, Gregersen, Peter K, Shadick, Nancy A, Daly, Mark J, Altshuler, David

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Genetic Variation in the HSD17B1 Gene and Risk of Prostate Cancer by Kraft, Peter, Pharoah, Paul, Chanock, Stephen J, Albanes, Demetrius, Kolonel, Laurence N, Hayes, Richard B, Altshuler, David, Andriole, Gerald, Berg, Christine, Boeing, Heiner, Burtt, Noel P, Bueno-de-Mesquita, Bas, Calle, Eugenia E, Cann, Howard, Canzian, Federico, Chen, Yen-Ching, Crawford, David E, Dunning, Alison M, Feigelson, Heather S, Freedman, Matthew L, Gaziano, John M, Giovannucci, Ed, Gonzalez, Carlos Alberto, Haiman, Christopher A, Hallmans, Goran, Henderson, Brian E, Hirschhorn, Joel N, Hunter, David J, Kaaks, Rudolf, Key, Timothy, Marchand, Loic Le, Ma, Jing, Overvad, Kim, Palli, Domenico, Pike, Malcolm C, Riboli, Elio, Rodriguez, Carmen, Setiawan, Wendy V, Stampfer, Meir J, Stram, Daniel O, Thomas, Gilles, Thun, Michael J, Travis, Ruth, Trichopoulou, Antonia, Virtamo, Jarmo, Wacholder, Sholom

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Common variants at CD40 and other loci confer risk of rheumatoid arthritis by Raychaudhuri, Soumya, Remmers, Elaine F, Lee, Annette T, Hackett, Rachel, Guiducci, Candace, Burtt, Noël P, Gianniny, Lauren, Korman, Benjamin D, Padyukov, Leonid, Kurreeman, Fina A S, Chang, Monica, Catanese, Joseph J, Ding, Bo, Wong, Sandra, van der Helm-van Mil, Annette H M, Neale, Benjamin M, Coblyn, Jonathan, Cui, Jing, Tak, Paul P, Wolbink, Gert Jan, Crusius, J Bart A, van der Horst-Bruinsma, Irene E, Criswell, Lindsey A, Amos, Christopher I, Seldin, Michael F, Kastner, Daniel L, Ardlie, Kristin G, Alfredsson, Lars, Costenbader, Karen H, Altshuler, David, Huizinga, Tom W J, Shadick, Nancy A, Weinblatt, Michael E, de Vries, Niek, Worthington, Jane, Seielstad, Mark, Toes, Rene E M, Karlson, Elizabeth W, Begovich, Ann B, Klareskog, Lars, Gregersen, Peter K, Daly, Mark J, Plenge, Robert M

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The Metabochip, a Custom Genotyping Array for Genetic Studies of Metabolic, Cardiovascular, and Anthropometric Traits by Voight, Benjamin F., Kang, Hyun Min, Ding, Jun, Palmer, Cameron D., Sidore, Carlo, Chines, Peter S., Burtt, Noël P., Fuchsberger, Christian, Li, Yanming, Erdmann, Jeanette, Frayling, Timothy M., Heid, Iris M., Jackson, Anne U., Johnson, Toby, Kilpeläinen, Tuomas O., Lindgren, Cecilia M., Morris, Andrew P., Prokopenko, Inga, Randall, Joshua C., Saxena, Richa, Soranzo, Nicole, Speliotes, Elizabeth K., Teslovich, Tanya M., Wheeler, Eleanor, Maguire, Jared, Parkin, Melissa, Potter, Simon, Rayner, N. William, Robertson, Neil, Stirrups, Kathleen, Winckler, Wendy, Sanna, Serena, Mulas, Antonella, Nagaraja, Ramaiah, Cucca, Francesco, Barroso, Inês, Deloukas, Panos, Loos, Ruth J. F., Kathiresan, Sekar, Munroe, Patricia B., Newton-Cheh, Christopher, Pfeufer, Arne, Samani, Nilesh J., Schunkert, Heribert, Hirschhorn, Joel N., Altshuler, David, McCarthy, Mark I., Abecasis, Gonçalo R., Boehnke, Michael

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Correction: The Metabochip, a Custom Genotyping Array for Genetic Studies of Metabolic, Cardiovascular, and Anthropometric Traits by Voight, Benjamin F., Kang, Hyun Min, Ding, Jun, Palmer, Cameron D., Sidore, Carlo, Chines, Peter S., Burtt, Noël P., Fuchsberger, Christian, Li, Yanming, Erdmann, Jeanette, Frayling, Timothy M., Heid, Iris M., Jackson, Anne U., Johnson, Toby, Kilpeläinen, Tuomas O., Lindgren, Cecilia M., Morris, Andrew P., Prokopenko, Inga, Randall, Joshua C., Saxena, Richa, Soranzo, Nicole, Speliotes, Elizabeth K., Teslovich, Tanya M., Wheeler, Eleanor, Maguire, Jared, Parkin, Melissa, Potter, Simon, Rayner, N. William, Robertson, Neil, Stirrups, Kathleen, Winckler, Wendy, Sanna, Serena, Mulas, Antonella, Nagaraja, Ramaiah, Cucca, Francesco, Barroso, Inês, Deloukas, Panos, Loos, Ruth J. F., Kathiresan, Sekar, Munroe, Patricia B., Newton-Cheh, Christopher, Pfeufer, Arne, Samani, Nilesh J., Schunkert, Heribert, Hirschhorn, Joel N., Altshuler, David, McCarthy, Mark I., Abecasis, Gonçalo R., Boehnke, Michael

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Genetic Variants Associated With Quantitative Glucose Homeostasis Traits Translate to Type 2 Diabetes in Mexican Americans: The GUARDIAN (Genetics Underlying Diabetes in Hispanics)... by Palmer, Nicholette D., Goodarzi, Mark O., Langefeld, Carl D., Wang, Nan, Guo, Xiuqing, Taylor, Kent D., Fingerlin, Tasha E., Norris, Jill M., Buchanan, Thomas A., Xiang, Anny H., Haritunians, Talin, Ziegler, Julie T., Williams, Adrienne H., Stefanovski, Darko, Cui, Jinrui, Mackay, Adrienne W., Henkin, Leora F., Bergman, Richard N., Gao, Xiaoyi, Gauderman, James, Varma, Rohit, Hanis, Craig L., Cox, Nancy J., Highland, Heather M., Below, Jennifer E., Williams, Amy L., Burtt, Noel P., Aguilar-Salinas, Carlos A., Huerta-Chagoya, Alicia, Gonzalez-Villalpando, Clicerio, Orozco, Lorena, Haiman, Christopher A., Tsai, Michael Y., Johnson, W. Craig, Yao, Jie, Rasmussen-Torvik, Laura, Pankow, James, Snively, Beverly, Jackson, Rebecca D., Liu, Simin, Nadler, Jerry L., Kandeel, Fouad, Chen, Yii-Der I., Bowden, Donald W., Rich, Stephen S., Raffel, Leslie J., Rotter, Jerome I., Watanabe, Richard M., Wagenknecht, Lynne E.

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Transancestral fine-mapping of four type 2 diabetes susceptibility loci highlights potential causal regulatory mechanisms by Horikoshi, Momoko, Pasquali, Lorenzo, Wiltshire, Steven, Huyghe, Jeroen R., Mahajan, Anubha, Asimit, Jennifer L., Ferreira, Teresa, Locke, Adam E., Robertson, Neil R., Wang, Xu, Sim, Xueling, Fujita, Hayato, Hara, Kazuo, Young, Robin, Zhang, Weihua, Choi, Sungkyoung, Chen, Han, Kaur, Ismeet, Takeuchi, Fumihiko, Fontanillas, Pierre, Thuillier, Dorothée, Yengo, Loic, Below, Jennifer E., Tam, Claudia H.T., Wu, Ying, Abecasis, Gonçalo, Altshuler, David, Bell, Graeme I., Blangero, John, Burtt, Noél P., Duggirala, Ravindranath, Florez, Jose C., Hanis, Craig L., Seielstad, Mark, Atzmon, Gil, Chan, Juliana C.N., Ma, Ronald C.W., Froguel, Philippe, Wilson, James G., Bharadwaj, Dwaipayan, Dupuis, Josee, Meigs, James B., Cho, Yoon Shin, Park, Taesung, Kooner, Jaspal S., Chambers, John C., Saleheen, Danish, Kadowaki, Takashi, Tai, E. Shyong, Mohlke, Karen L., Cox, Nancy J., Ferrer, Jorge, Zeggini, Eleftheria, Kato, Norihiro, Teo, Yik Ying, Boehnke, Michael, McCarthy, Mark I., Morris, Andrew P.

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