cMYB is involved in the regulation of fetal hemoglobin production in adults by Jiang, Jie, Best, Steve, Menzel, Stephan, Silver, Nicholas, Lai, Mei I., Surdulescu, Gabriela L., Spector, Tim D., Thein, Swee Lay

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The use of genome-wide eQTL associations in lymphoblastoid cell lines to identify novel genetic pathways involved in complex traits by Min, Josine L, Taylor, Jennifer M, Richards, J Brent, Watts, Tim, Pettersson, Fredrik H, Broxholme, John, Ahmadi, Kourosh R, Surdulescu, Gabriela L, Lowy, Ernesto, Gieger, Christian, Newton-Cheh, Chris, Perola, Markus, Soranzo, Nicole, Surakka, Ida, Lindgren, Cecilia M, Ragoussis, Jiannis, Morris, Andrew P, Cardon, Lon R, Spector, Tim D, Zondervan, Krina T

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Genome-wide association study with 1000 genomes imputation identifies signals for nine sex hormone-related phenotypes by Ruth, Katherine S, Campbell, Purdey J, Chew, Shelby, Lim, Ee Mun, Hadlow, Narelle, Stuckey, Bronwyn G A, Brown, Suzanne J, Feenstra, Bjarke, Joseph, John, Surdulescu, Gabriela L, Zheng, Hou Feng, Richards, J Brent, Murray, Anna, Spector, Tim D, Wilson, Scott G, Perry, John R B

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Higher serum vitamin D concentrations are associated with longer leukocyte telomere length in women by Richards, J. Brent, Valdes, Ana M, Gardner, Jeffrey P, Paximadas, Dimitri, Kimura, Masayuki, Nessa, Ayrun, Lu, Xiaobin, Surdulescu, Gabriela L, Swaminathan, Rami, Spector, Tim D, Aviv, Abraham

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Genome-wide association study using family-based cohorts identifies the WLS and CCDC170/ESR1 loci as associated with bone mineral density by Mullin, Benjamin H, Walsh, John P, Zheng, Hou-Feng, Brown, Suzanne J, Surdulescu, Gabriela L, Curtis, Charles, Breen, Gerome, Dudbridge, Frank, Richards, J Brent, Spector, Tim D, Wilson, Scott G

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Mapping Genetic Loci That Determine Leukocyte Telomere Length in a Large Sample of Unselected Female Sibling Pairs by Andrew, Toby, Aviv, Abraham, Falchi, Mario, Surdulescu, Gabriela L., Gardner, Jeffrey P., Lu, Xiaobin, Kimura, Masayuki, Kato, Bernet S., Valdes, Ana M., Spector, Tim D.

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A Locus on Chromosome 1p36 Is Associated with Thyrotropin and Thyroid Function as Identified by Genome-wide Association Study by Panicker, Vijay, Wilson, Scott G., Walsh, John P., Richards, J. Brent, Brown, Suzanne J., Beilby, John P., Bremner, Alexandra P., Surdulescu, Gabriela L., Qweitin, Emad, Gillham-Nasenya, Irina, Soranzo, Nicole, Lim, Ee M., Fletcher, Stephen J., Spector, Tim D.

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Copy number variation of the APC gene is associated with regulation of bone mineral density by Chew, Shelby, Dastani, Zari, Brown, Suzanne J, Lewis, Joshua R, Dudbridge, Frank, Soranzo, Nicole, Surdulescu, Gabriela L, Richards, J. Brent, Spector, Tim D, Wilson, Scott G

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Erratum: Whole-genome sequence-based analysis of thyroid function by Taylor, Peter N, Porcu, Eleonora, Chew, Shelby, Campbell, Purdey J, Traglia, Michela, Brown, Suzanne J, Mullin, Benjamin H, Shihab, Hashem A, Min, Josine, Walter, Klaudia, Memari, Yasin, Huang, Jie, Barnes, Michael R, Beilby, John P, Charoen, Pimphen, Danecek, Petr, Dudbridge, Frank, Forgetta, Vincenzo, Greenwood, Celia, Grundberg, Elin, Johnson, Andrew D, Hui, Jennie, Lim, Ee M, McCarthy, Shane, Muddyman, Dawn, Panicker, Vijay, Perry, John R B, Bell, Jordana T, Yuan, Wei, Relton, Caroline, Gaunt, Tom, Schlessinger, David, Abecasis, Goncalo, Cucca, Francesco, Surdulescu, Gabriela L, Woltersdorf, Wolfram, Zeggini, Eleftheria, Zheng, Hou-Feng, Toniolo, Daniela, Dayan, Colin M, Naitza, Silvia, Walsh, John P, Spector, Tim, Smith, George Davey, Durbin, Richard, Richards, J Brent, Sanna, Serena, Soranzo, Nicole, Timpson, Nicholas J, Wilson, Scott G

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Genetic Loci Linked to Pituitary-Thyroid Axis Set Points: A Genome-Wide Scan of a Large Twin Cohort by Panicker, Vijay, Wilson, Scott G, Spector, Tim D, Brown, Suzanne J, Kato, Bernet S, Reed, Peter W, Falchi, Mario, Richards, J. Brent, Surdulescu, Gabriela L, Lim, Ee M, Fletcher, Steven J, Walsh, John P

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Common Sequence Variation in FLNB Regulates Bone Structure in Women in the General Population and FLNB mRNA Expression in Osteoblasts In Vitro by Wilson, Scott G, Jones, Michelle R, Mullin, Ben H, Dick, Ian M, Richards, J Brent, Pastinen, Tomi M, Grundberg, Elin, Ljunggren, Östen, Surdulescu, Gabriela L, Dudbridge, Frank, Elliott, Katherine S, Cervino, Alessandra CL, Spector, Timothy D, Prince, Richard L

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The genetic architecture of type 2 diabetes by Teslovich, Tanya M, Mahajan, Anubha, Fontanillas, Pierre, Moutsianas, Loukas, Rivas, Manuel A, Rayner, N William, Cingolani, Pablo, Lindgren, Cecilia M, Chen, Yuhui, Huang, Jinyan, Varga, Tibor V, Green, Todd, Fingerlin, Tasha, Horikoshi, Momoko, Huh, Iksoo, Lee, Juyoung, Lee, Selyeong, Maxwell, Taylor J, Yoon, Joon, Barzilai, Nir, Han, Bok-Ghee, Kuulasmaa, Teemu, Balkau, Beverley, Giedraitis, Vilmantas, Purcell, Shaun, Kwak, Soo-Heon, Afzal, Uzma, Aguilar, David, Cheng, Ching-Yu, Palli, Domenico, Fowler, Sharon P, Freedman, Barry I, Hicks, Pamela J, Musani, Solomon K, Puppala, Sobha, Wilson, Sr, Gregory, Surdulescu, Gabriela L, Herder, Christian, Doney, Alex S F, Kinnunen, Leena, Hakaste, Liisa, Jørgensen, Marit E, Justesen, Johanne Marie, Käräjämäki, Annemari, Lannfelt, Lars, Narisu, Narisu, Melander, Olle, Milani, Lili, Neville, Matt, Qi, Qibin, Rolandsson, Olov, Stirrups, Kathleen, Blancher, Christine, Maguire, Jared, Shakir, Khalid, DePristo, Mark, de Angelis, Martin Hrabé, Jun, Goo, Murphy, Jacquelyn, Onofrio, Robert, Thorand, Barbara, Meisinger, Christa, Isomaa, Bo, Rauramaa, Rainer, Watanabe, Richard M, Bergman, Richard N, Bottinger, Erwin P, Chan, Juliana C N, Langenberg, Claudia, Jablonski, Kathleen A, Lehman, Donna M, Froguel, Philippe, Small, Kerrin S, Grallert, Harald, Glaser, Benjamin, Banks, Eric, Gieger, Christian, Illig, Thomas, Buck, Gemma, Trakalo, Joseph, Mägi, Reedik, Farjoun, Yossi, Owen, Katharine R, Gloyn, Anna L, Tuomi, Tiinamaija, Kooner, Jaspal Singh, Donnelly, Peter, Morris, Andrew D, Hattersley, Andrew T, Bowden, Donald W, Laakso, Markku, Bell, Graeme I, Duggirala, Ravindranath, McVean, Gilean, Meigs, James B, Cox, Nancy J, Mohlke, Karen L, Florez, Jose C, Morris, Andrew P, Kang, Hyun Min

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Identification of QTLs for serum lipid levels in a female sib-pair cohort: a novel application to improve the power of two-locus linkage analysis by Falchi, Mario, Andrew, Toby, Snieder, Harold, Swaminathan, Ramasamyiyer, Surdulescu, Gabriela L., Spector, Tim D.

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Reproducible genetic associations between candidate genes and clinical knee osteoarthritis in men and women by Valdes, Ana M., Van Oene, Mark, Hart, Deborah J., Surdulescu, Gabriela L., Loughlin, John, Doherty, Michael, Spector, Tim D.

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Identification of novel genetic Loci associated with thyroid peroxidase antibodies and clinical thyroid disease by Medici, Marco, Porcu, Eleonora, Teumer, Alexander, Brown, Suzanne J, Rawal, Rajesh, Roef, Greet L, Plantinga, Theo S, Vermeulen, Sita H, Lahti, Jari, Simmonds, Matthew J, Husemoen, Lise Lotte N, Freathy, Rachel M, Shields, Beverley M, Pietzner, Diana, Nagy, Rebecca, Broer, Linda, Chaker, Layal, Korevaar, Tim I M, Plia, Maria Grazia, Sala, Cinzia, Völker, Uwe, Richards, J Brent, Sweep, Fred C, Gieger, Christian, Corre, Tanguy, Kajantie, Eero, Thuesen, Betina, Taes, Youri E, Visser, W Edward, Hattersley, Andrew T, Kratzsch, Jürgen, Hamilton, Alexander, Li, Wei, Homuth, Georg, Mariotti, Stefano, Soranzo, Nicole, Ross, Alec, Arnold, Alice, van de Bunt, Martijn, Liyanarachchi, Sandya, Heier, Margit, Grabe, Hans Jörgen, Masciullo, Corrado, Galesloot, Tessel E, Lim, Ee M, Reischl, Eva, Leedman, Peter J, Lai, Sandra, Delitala, Alessandro, Bremner, Alexandra P, Philips, David I W, Beilby, John P, Mulas, Antonella, Vocale, Matteo, Abecasis, Goncalo, Forsen, Tom, James, Alan, Widen, Elisabeth, Hui, Jennie, Prokisch, Holger, Rietzschel, Ernst E, Palotie, Aarno, Feddema, Peter, Rotter, Jerome I, Kluttig, Alexander, Radke, Dörte, Traglia, Michela, Surdulescu, Gabriela L, He, Huiling, Franklyn, Jayne A, Vaidya, Bijay, de Meyer, Tim, Jørgensen, Torben, Eriksson, Johan G, O'Leary, Peter C, Hermus, Ad R, Psaty, Bruce M, Ittermann, Till, Hofman, Albert, Schlessinger, David, Pirastu, Nicola, Aulchenko, Yurii S, de la Chapelle, Albert, Gough, Stephen C L, Meyer Zu Schwabedissen, Henriette, Frayling, Timothy M, Kaufman, Jean-Marc, Räikkönen, Katri, Smit, Johannes W A, Rivadeneira, Fernando, Uitterlinden, André G, Walsh, John P, Meisinger, Christa, den Heijer, Martin, Visser, Theo J, Wilson, Scott G, Völzke, Henry, Toniolo, Daniela, Sanna, Serena, Naitza, Silvia

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Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population by Rivas, Manuel A, Avila, Brandon E, Koskela, Jukka, Huang, Hailiang, Stevens, Christine, Pirinen, Matti, Haritunians, Talin, Neale, Benjamin M, Kurki, Mitja, Ganna, Andrea, Graham, Daniel, Glaser, Benjamin, Peter, Inga, Atzmon, Gil, Barzilai, Nir, Levine, Adam P, Schiff, Elena, Pontikos, Nikolas, Weisburd, Ben, Lek, Monkol, Karczewski, Konrad J, Bloom, Jonathan, Minikel, Eric V, Petersen, Britt-Sabina, Beaugerie, Laurent, Seksik, Philippe, Cosnes, Jacques, Schreiber, Stefan, Bokemeyer, Bernd, Bethge, Johannes, Heap, Graham, Ahmad, Tariq, Plagnol, Vincent, Segal, Anthony W, Targan, Stephan, Turner, Dan, Saavalainen, Paivi, Farkkila, Martti, Kontula, Kimmo, Palotie, Aarno, Brant, Steven R, Duerr, Richard H, Silverberg, Mark S, Rioux, John D, Weersma, Rinse K, Franke, Andre, Jostins, Luke, Anderson, Carl A, Barrett, Jeffrey C, MacArthur, Daniel G, Jalas, Chaim, Sokol, Harry, Xavier, Ramnik J, Pulver, Ann, Cho, Judy H, McGovern, Dermot P B, Daly, Mark J

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Whole-genome sequence-based analysis of thyroid function by Taylor, Peter N, Porcu, Eleonora, Chew, Shelby, Campbell, Purdey J, Traglia, Michela, Brown, Suzanne J, Mullin, Benjamin H, Shihab, Hashem A, Min, Josine, Walter, Klaudia, Memari, Yasin, Huang, Jie, Barnes, Michael R, Beilby, John P, Charoen, Pimphen, Danecek, Petr, Dudbridge, Frank, Forgetta, Vincenzo, Greenwood, Celia, Grundberg, Elin, Johnson, Andrew D, Hui, Jennie, Lim, Ee M, McCarthy, Shane, Muddyman, Dawn, Panicker, Vijay, Perry, John R B, Bell, Jordana T, Yuan, Wei, Relton, Caroline, Gaunt, Tom, Schlessinger, David, Abecasis, Goncalo, Cucca, Francesco, Surdulescu, Gabriela L, Woltersdorf, Wolfram, Zeggini, Eleftheria, Zheng, Hou-Feng, Toniolo, Daniela, Dayan, Colin M, Naitza, Silvia, Walsh, John P, Spector, Tim, Davey Smith, George, Durbin, Richard, Richards, J Brent, Sanna, Serena, Soranzo, Nicole, Timpson, Nicholas J, Wilson, Scott G

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Sex and ethnic differences in the association of ASPN, CALM1, COL2A1, COMP, and FRZB with genetic susceptibility to osteoarthritis of the knee by Valdes, Ana M., Loughlin, John, Oene, Mark Van, Chapman, Kay, Surdulescu, Gabriela L., Doherty, Michael, Spector, Tim D.

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Data Descriptor: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls by Mahajan, Anubha, Agarwala, Vineeta, Koesterer, Ryan, Blackwell, Thomas W., Robertson, Neil R., Rayner, N. William, Pearson, Richard D., Stringham, Heather M., Gamazon, Eric R., Lee, Jaehoon, Go, Min Jin, Stitzel, Michael L., Varga, Tibor V., Ferreira, Teresa, Huh, Iksoo, Lee, Selyeong, Lin, Keng-Han, Maxwell, Taylor J., Welch, Ryan P., Zhang, Weihua, Barzilai, Nir, Han, Bok-Ghee, Manning, Alisa, Balkau, Beverley, Abboud, Hanna E., Giedraitis, Vilmantas, Kwan, Phoenix, Neale, Benjamin M., Butterworth, Adam S., Lam, Vincent K. L., Arya, Rector, Chan, Edmund, Navarro, Carmen, Palli, Domenico, Rybin, Dennis, Fowler, Sharon P., Griswold, Michael, Kumar, Satish, Thuillier, Dorothee, Liu, Jianjun, Puppala, Sobha, Yengo, Loic, Tan, Sian-Tsung, Njolstad, Pal Rasmus, Mangino, Massimo, Fadista, Joao, Herder, Christian, Groves, Christopher J., Wieland, Thomas, Christensen, Cramer, Koistinen, Heikki A., Doney, Alex S. F., Farmer, Andrew J., Kravic, Jasmina, Justesen, Johanne Marie, Lauritzen, Torsten, Milani, Lili, Neville, Matt, Qi, Lu, Rolandsson, Olov, Swift, Amy, Wood, Andrew R., Mihailov, Evelin, Fennell, Timothy, Huth, Cornelia, Palmer, Colin N. A., Watanabe, Richard M., Syvänen, Ann-Christine, Cho, Yoon Shin, Chandak, Giriraj R., Jablonski, Kathleen A., Jia, Weiping, Ma, Ronald Cw, Froguel, Philippe, Teo, Yik Ying, Grallert, Harald, Glaser, Benjamin, Metspalu, Andres, Walker, Mark, Banks, Eric, Ingelsson, Erik, Im, Hae Kyung, Illig, Thomas, Trakalo, Joseph, Buck, David, Magi, Reedik, Farjoun, Yossi, Gloyn, Anna L., Strauch, Konstantin, Tuomi, Tiinamaija, Donnelly, Peter, Bowden, Donald W., Strom, Tim M., Blangero, John, Frayling, Timothy M., Gabriel, Stacey, Mohlke, Karen L., Abecasis, Goncalo, Morris, Andrew P., Kang, Hyun Min

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Identification and Functional Characterization of G6PC2 Coding Variants Influencing Glycemic Traits Define an Effector Transcript at the G6PC2-ABCB11 Locus: e1004876 by Mahajan, Anubha, Sim, Xueling, Ng, Hui Jin, Manning, Alisa, Rivas, Manuel A, Highland, Heather M, Locke, Adam E, Grarup, Niels, Im, Hae Kyung, Cingolani, Pablo, Flannick, Jason, Fontanillas, Pierre, Fuchsberger, Christian, Gaulton, Kyle J, Teslovich, Tanya M, Rayner, N William, Robertson, Neil R, Beer, Nicola L, Rundle, Jana K, Bork-Jensen, Jette, Ladenvall, Claes, Blancher, Christine, Buck, David, Buck, Gemma, Burtt, Noël P, Gabriel, Stacey, Gjesing, Anette P, Groves, Christopher J, Hollensted, Mette, Huyghe, Jeroen R, Jackson, Anne U, Jun, Goo, Justesen, Johanne Marie, Mangino, Massimo, Murphy, Jacquelyn, Neville, Matt, Onofrio, Robert, Small, Kerrin S, Stringham, Heather M, Syvänen, Ann-Christine, Trakalo, Joseph, Abecasis, Goncalo, Bell, Graeme I, Blangero, John, Cox, Nancy J, Duggirala, Ravindranath, Hanis, Craig L, Seielstad, Mark, Wilson, James G, Christensen, Cramer, Brandslund, Ivan, Rauramaa, Rainer, Surdulescu, Gabriela L, Doney, Alex SF, Lannfelt, Lars, Linneberg, Allan, Isomaa, Bo, Tuomi, Tiinamaija, Jørgensen, Marit E, Jørgensen, Torben, Kuusisto, Johanna, Uusitupa, Matti, Salomaa, Veikko, Spector, Timothy D, Morris, Andrew D, Palmer, Colin NA, Collins, Francis S, Mohlke, Karen L, Bergman, Richard N, Ingelsson, Erik, Lind, Lars, Tuomilehto, Jaakko, Hansen, Torben, Watanabe, Richard M, Prokopenko, Inga, Dupuis, Josee, Karpe, Fredrik, Groop, Leif, Laakso, Markku, Pedersen, Oluf, Florez, Jose C, Morris, Andrew P, Altshuler, David, Meigs, James B, Boehnke, Michael, McCarthy, Mark I, Lindgren, Cecilia M, Gloyn, Anna L, consortium, of theT2D-GENES, consortium, GoT2D

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