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

Por Keebler, Mary E., Sanders, Christopher L., Surti, Aarti, Guiducci, Candace, Burtt, Noel P, Kathiresan, Sekar
Publicado em 2009

IGF2R Missense Single-Nucleotide Polymorphisms and Breast Cancer Risk: The Multiethnic Cohort Study

Por Cheng, Iona, Stram, Daniel O., Burtt, Noël P., Gianniny, Lauren, Garcia, Rachel R., Pooler, Loreall, Henderson, Brian E., Marchand, Loïc Le, Haiman, Christopher A
Publicado em 2009

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...

Por 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
Publicado em 2007

Comparing strategies to fine map the association of common SNPs on chromosome 9p21 to Type 2 Diabetes and Myocardial Infarction

Por 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
Publicado em 2011

Genomewide Linkage Analysis of Stature in Multiple Populations Reveals Several Regions with Evidence of Linkage to Adult Height

Por 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.
Publicado em 2001

A genome-wide association study for blood lipid phenotypes in the Framingham Heart Study

Por 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
Publicado em 2007

High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency

Por 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
Publicado em 2010

Genetic Variants Near TNFAIP3 on 6q23 are Associated with Systemic Lupus Erythematosus (SLE)

Por 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.
Publicado em 2008

Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans

Por 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
Publicado em 2008

Assessing the phenotypic effects in the general population of rare variants in genes for a dominant mendelian form of diabetes

Por 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
Publicado em 2013

A common variant of HMGA2 is associated with adult and childhood height in the general population

Por 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
Publicado em 2007

Two independent alleles at 6q23 associated with risk of rheumatoid arthritis

Por 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
Publicado em 2007

Genetic Variation in the HSD17B1 Gene and Risk of Prostate Cancer

Por 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
Publicado em 2005

Common variants at CD40 and other loci confer risk of rheumatoid arthritis

Por 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
Publicado em 2008

The Metabochip, a Custom Genotyping Array for Genetic Studies of Metabolic, Cardiovascular, and Anthropometric Traits

Por 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
Publicado em 2012

Correction: The Metabochip, a Custom Genotyping Array for Genetic Studies of Metabolic, Cardiovascular, and Anthropometric Traits

Por 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
Publicado em 2013

Genetic Variants Associated With Quantitative Glucose Homeostasis Traits Translate to Type 2 Diabetes in Mexican Americans: The GUARDIAN (Genetics Underlying Diabetes in Hispanics)...

Por 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.
Publicado no Diabetes (2015)

Transancestral fine-mapping of four type 2 diabetes susceptibility loci highlights potential causal regulatory mechanisms

Por 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.
Publicado no Hum Mol Genet (2016)

Genome-wide association studies in the Japanese population identify seven novel loci for type 2 diabetes

Por Imamura, Minako, Takahashi, Atsushi, Yamauchi, Toshimasa, Hara, Kazuo, Yasuda, Kazuki, Grarup, Niels, Zhao, Wei, Wang, Xu, Huerta-Chagoya, Alicia, Hu, Cheng, Moon, Sanghoon, Long, Jirong, Kwak, Soo Heon, Rasheed, Asif, Saxena, Richa, Ma, Ronald C. W., Okada, Yukinori, Iwata, Minoru, Hosoe, Jun, Shojima, Nobuhiro, Iwasaki, Minaka, Fujita, Hayato, Suzuki, Ken, Danesh, John, Jørgensen, Torben, Jørgensen, Marit E., Witte, Daniel R., Brandslund, Ivan, Christensen, Cramer, Hansen, Torben, Mercader, Josep M., Flannick, Jason, Moreno-Macías, Hortensia, Burtt, Noël P., Zhang, Rong, Kim, Young Jin, Zheng, Wei, Singh, Jai Rup, Tam, Claudia H. T., Hirose, Hiroshi, Maegawa, Hiroshi, Ito, Chikako, Kaku, Kohei, Watada, Hirotaka, Tanaka, Yasushi, Tobe, Kazuyuki, Kawamori, Ryuzo, Kubo, Michiaki, Cho, Yoon Shin, Chan, Juliana C. N., Sanghera, Dharambir, Frossard, Philippe, Park, Kyong Soo, Shu, Xiao-Ou, Kim, Bong-Jo, Florez, Jose C., Tusié-Luna, Teresa, Jia, Weiping, Tai, E Shyong, Pedersen, Oluf, Saleheen, Danish, Maeda, Shiro, Kadowaki, Takashi
Publicado no Nat Commun (2016)

Genetic variants at CD28, PRDM1, and CD2/CD58 are associated with rheumatoid arthritis risk

Por Raychaudhuri, Soumya, Thomson, Brian P., Remmers, Elaine F., Eyre, Stephen, Hinks, Anne, Guiducci, Candace, Catanese, Joseph J., Xie, Gang, Stahl, Eli A., Chen, Robert, Alfredsson, Lars, Amos, Christopher I., Ardlie, Kristin G., Barton, Anne, Bowes, John, Burtt, Noel P., Chang, Monica, Coblyn, Jonathan, Costenbader, Karen H., Criswell, Lindsey A., Crusius, J. Bart A., Cui, Jing, De Jager, Phillip L., Ding, Bo, Emery, Paul, Flynn, Edward, Harrison, Pille, Hocking, Lynne J., Huizinga, Tom W. J., Kastner, Daniel L., Ke, Xiayi, Kurreeman, Fina A. S., Lee, Annette T., Liu, Xiangdong, Li, Yonghong, Martin, Paul, Morgan, Ann W., Padyukov, Leonid, Reid, David M., Seielstad, Mark, Seldin, Michael F., Shadick, Nancy A., Steer, Sophia, Tak, Paul P., Thomson, Wendy, van der Helm-van Mil, Annette H. M., van der Horst-Bruinsma, Irene E., Weinblatt, Michael E., Wilson, Anthony G., Wolbink, Gert Jan, Wordsworth, Paul, Altshuler, David, Karlson, Elizabeth W., Toes, Rene E. M., de Vries, Niek, Begovich, Ann B., Siminovitch, Katherine A., Worthington, Jane, Klareskog, Lars, Gregersen, Peter K., Daly, Mark J., Plenge, Robert M.
Publicado em 2009