Reading Text While Driving: Understanding Drivers’ Strategic and Tactical Adaptation to Distraction

por Liang, Yulan, Horrey, William J., Hoffman, Joshua D.
Publicado 2015

Neuromuscular Training Improves Self-Reported Function and Single-Leg Landing Hip Biomechanics in Athletes After Anterior Cruciate Ligament Reconstruction

por Nagelli, Christopher, Di Stasi, Stephanie, Tatarski, Rachel, Chen, Albert, Wordeman, Samuel, Hoffman, Joshua, Hewett, Timothy E.
Publicado 2020

The Application of Genetic Risk Scores in Age-Related Macular Degeneration: A Review

por Cooke Bailey, Jessica N., Hoffman, Joshua D., Sardell, Rebecca J., Scott, William K., Pericak-Vance, Margaret A., Haines, Jonathan L.
Publicado 2016

Factors Affecting Return to Play After Primary Achilles Tendon Tear: A Cohort of NFL Players

por Yang, JaeWon, Hodax, Jonathan D., Machan, Jason T., Krill, Michael K., Lemme, Nicholas J., Durand, Wesley M., Hoffman, Joshua T., Hewett, Timothy E., Owens, Brett D.
Publicado 2019

Genetic susceptibility to endomyocardial fibrosis

por Beaton, Andrea, Sable, Craig, Brown, Juliette, Hoffman, Joshua, Mungoma, Michael, Mondo, Charles, Cereb, Nezith, Brown, Colin, Summar, Marshall, Freers, Jurgen, Ferreira, Maria Beatriz, Yacoub, Magdi, Mocumbi, Ana Olga
Publicado 2014

Cis-eQTL-based trans-ethnic meta-analysis reveals novel genes associated with breast cancer risk

por Hoffman, Joshua D., Graff, Rebecca E., Emami, Nima C., Tai, Caroline G., Passarelli, Michael N., Hu, Donglei, Huntsman, Scott, Hadley, Dexter, Leong, Lancelote, Majumdar, Arunabha, Zaitlen, Noah, Ziv, Elad, Witte, John S.
Publicado 2017

Association of imputed prostate cancer transcriptome with disease risk reveals novel mechanisms

por Emami, Nima C., Kachuri, Linda, Meyers, Travis J., Das, Rajdeep, Hoffman, Joshua D., Hoffmann, Thomas J., Hu, Donglei, Shan, Jun, Feng, Felix Y., Ziv, Elad, Van Den Eeden, Stephen K., Witte, John S.
Publicado 2019

Author Correction: Association of imputed prostate cancer transcriptome with disease risk reveals novel mechanisms

por Emami, Nima C., Kachuri, Linda, Meyers, Travis J., Das, Rajdeep, Hoffman, Joshua D., Hoffmann, Thomas J., Hu, Donglei, Shan, Jun, Feng, Felix Y., Ziv, Elad, Van Den Eeden, Stephen K., Witte, John S.
Publicado 2019

Estimating cumulative pathway effects on risk for age-related macular degeneration using mixed linear models

por Hall, Jacob B., Cooke Bailey, Jessica N., Hoffman, Joshua D., Pericak-Vance, Margaret A., Scott, William K., Kovach, Jaclyn L., Schwartz, Stephen G., Agarwal, Anita, Brantley, Milam A., Haines, Jonathan L., Bush, William S.
Publicado 2015

Genetic Association Analysis of Drusen Progression

por Hoffman, Joshua D., van Grinsven, Mark J. J. P., Li, Chun, Brantley, Milam, McGrath, Josephine, Agarwal, Anita, Scott, William K., Schwartz, Stephen G., Kovach, Jaclyn, Pericak-Vance, Margaret, Sanchez, Clara I., Haines, Jonathan L.
Publicado 2016

Identification of novel common breast cancer risk variants at the 6q25 locus among Latinas

por Hoffman, Joshua, Fejerman, Laura, Hu, Donglei, Huntsman, Scott, Li, Min, John, Esther M., Torres-Mejia, Gabriela, Kushi, Larry, Ding, Yuan Chun, Weitzel, Jeffrey, Neuhausen, Susan L., Lott, Paul, Echeverry, Magdalena, Carvajal-Carmona, Luis, Burchard, Esteban, Eng, Celeste, Long, Jirong, Zheng, Wei, Olopade, Olufunmilayo, Huo, Dezheng, Haiman, Christopher, Ziv, Elad
Publicado 2019

Identification of new therapeutic targets for osteoarthritis through genome-wide analyses of UK Biobank

por Tachmazidou, Ioanna, Hatzikotoulas, Konstantinos, Southam, Lorraine, Esparza-Gordillo, Jorge, Haberland, Valeriia, Zheng, Jie, Johnson, Toby, Koprulu, Mine, Zengini, Eleni, Steinberg, Julia, Wilkinson, Jeremy M, Bhatnagar, Sahir, Hoffman, Joshua D, Buchan, Natalie, Süveges, Dániel, Yerges-Armstrong, Laura, Smith, George Davey, Gaunt, Tom R, Scott, Robert A, McCarthy, Linda C, Zeggini, Eleftheria
Publicado 2019

Up For A Challenge (U4C): Stimulating innovation in breast cancer genetic epidemiology

por Mechanic, Leah E., Lindström, Sara, Daily, Kenneth M., Sieberts, Solveig K., Amos, Christopher I., Chen, Huann-Sheng, Cox, Nancy J., Dathe, Marina, Feuer, Eric J., Guertin, Michael J., Hoffman, Joshua, Liu, Yunxian, Moore, Jason H., Myers, Chad L., Ritchie, Marylyn D., Schildkraut, Joellen, Schumacher, Fredrick, Witte, John S., Wang, Wen, Williams, Scott M., Gillanders, Elizabeth M.
Publicado 2017

Pan-cancer study detects genetic risk variants and shared genetic basis in two large cohorts

por Rashkin, Sara R., Graff, Rebecca E., Kachuri, Linda, Thai, Khanh K., Alexeeff, Stacey E., Blatchins, Maruta A., Cavazos, Taylor B., Corley, Douglas A., Emami, Nima C., Hoffman, Joshua D., Jorgenson, Eric, Kushi, Lawrence H., Meyers, Travis J., Van Den Eeden, Stephen K., Ziv, Elad, Habel, Laurel A., Hoffmann, Thomas J., Sakoda, Lori C., Witte, John S.
Publicado 2020

Cross-cancer evaluation of polygenic risk scores for 16 cancer types in two large cohorts

por Graff, Rebecca E., Cavazos, Taylor B., Thai, Khanh K., Kachuri, Linda, Rashkin, Sara R., Hoffman, Joshua D., Alexeeff, Stacey E., Blatchins, Maruta, Meyers, Travis J., Leong, Lancelote, Tai, Caroline G., Emami, Nima C., Corley, Douglas A., Kushi, Lawrence H., Ziv, Elad, Van Den Eeden, Stephen K., Jorgenson, Eric, Hoffmann, Thomas J., Habel, Laurel A., Witte, John S., Sakoda, Lori C.
Publicado 2021

Age-of-onset information helps identify 76 genetic variants associated with allergic disease

por Ferreira, Manuel A. R., Vonk, Judith M., Baurecht, Hansjörg, Marenholz, Ingo, Tian, Chao, Hoffman, Joshua D., Helmer, Quinta, Tillander, Annika, Ullemar, Vilhelmina, Lu, Yi, Grosche, Sarah, Rüschendorf, Franz, Granell, Raquel, Brumpton, Ben M., Fritsche, Lars G., Bhatta, Laxmi, Gabrielsen, Maiken E., Nielsen, Jonas B., Zhou, Wei, Hveem, Kristian, Langhammer, Arnulf, Holmen, Oddgeir L., Løset, Mari, Abecasis, Gonçalo R., Willer, Cristen J., Emami, Nima C., Cavazos, Taylor B., Witte, John S., Szwajda, Agnieszka, Hinds, David A., Hübner, Norbert, Weidinger, Stephan, Magnusson, Patrik KE, Jorgenson, Eric, Karlsson, Robert, Paternoster, Lavinia, Boomsma, Dorret I., Almqvist, Catarina, Lee, Young-Ae, Koppelman, Gerard H.
Publicado 2020

Exome sequencing and characterization of 49,960 individuals in the UK Biobank

por Van Hout, Cristopher V., Tachmazidou, Ioanna, Backman, Joshua D., Hoffman, Joshua D., Liu, Daren, Pandey, Ashutosh K., Gonzaga-Jauregui, Claudia, Khalid, Shareef, Ye, Bin, Banerjee, Nilanjana, Li, Alexander H., O’Dushlaine, Colm, Marcketta, Anthony, Staples, Jeffrey, Schurmann, Claudia, Hawes, Alicia, Maxwell, Evan, Barnard, Leland, Lopez, Alexander, Penn, John, Habegger, Lukas, Blumenfeld, Andrew L., Bai, Xiaodong, O’Keeffe, Sean, Yadav, Ashish, Praveen, Kavita, Jones, Marcus, Salerno, William J., Chung, Wendy K., Surakka, Ida, Willer, Cristen J., Hveem, Kristian, Leader, Joseph B., Carey, David J., Ledbetter, David H., Cardon, Lon, Yancopoulos, George D., Economides, Aris, Coppola, Giovanni, Shuldiner, Alan R., Balasubramanian, Suganthi, Cantor, Michael, Nelson, Matthew R., Whittaker, John, Reid, Jeffrey G., Marchini, Jonathan, Overton, John D., Scott, Robert A., Abecasis, Gonçalo R., Yerges-Armstrong, Laura, Baras, Aris
Publicado 2020

Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology

por Ferreira, Manuel A, Vonk, Judith M, Baurecht, Hansjörg, Marenholz, Ingo, Tian, Chao, Hoffman, Joshua D, Helmer, Quinta, Tillander, Annika, Ullemar, Vilhelmina, van Dongen, Jenny, Lu, Yi, Rüschendorf, Franz, Esparza-Gordillo, Jorge, Medway, Chris W, Mountjoy, Edward, Burrows, Kimberley, Hummel, Oliver, Grosche, Sarah, Brumpton, Ben M, Witte, John S, Hottenga, Jouke-Jan, Willemsen, Gonneke, Zheng, Jie, Rodríguez, Elke, Hotze, Melanie, Franke, Andre, Revez, Joana A, Beesley, Jonathan, Matheson, Melanie C, Dharmage, Shyamali C, Bain, Lisa M, Fritsche, Lars G, Gabrielsen, Maiken E, Balliu, Brunilda, Nielsen, Jonas B, Zhou, Wei, Hveem, Kristian, Langhammer, Arnulf, Holmen, Oddgeir L, Løset, Mari, Abecasis, Gonçalo R, Willer, Cristen J, Arnold, Andreas, Homuth, Georg, Schmidt, Carsten O, Thompson, Philip J, Martin, Nicholas G, Duffy, David L, Novak, Natalija, Schulz, Holger, Karrasch, Stefan, Gieger, Christian, Strauch, Konstantin, Melles, Ronald B, Hinds, David A, Hübner, Norbert, Weidinger, Stephan, Magnusson, Patrik KE, Jansen, Rick, Jorgenson, Eric, Lee, Young-Ae, Boomsma, Dorret I, Almqvist, Catarina, Karlsson, Robert, Koppelman, Gerard H, Paternoster, Lavinia
Publicado 2017

New genetic signals for lung function highlight pathways and chronic obstructive pulmonary disease associations across multiple ancestries.

por Shrine, Nick, Guyatt, Anna L, Erzurumluoglu, A Mesut, Jackson, Victoria E, Hobbs, Brian D, Melbourne, Carl A, Batini, Chiara, Fawcett, Katherine A, Song, Kijoung, Sakornsakolpat, Phuwanat, Li, Xingnan, Boxall, Ruth, Reeve, Nicola F, Obeidat, Ma’en, Zhao, Jing Hua, Wielscher, Matthias, Weiss, Stefan, Kentistou, Katherine A, Cook, James P, Sun, Benjamin B, Zhou, Jian, Hui, Jennie, Karrasch, Stefan, Imboden, Medea, Harris, Sarah E, Marten, Jonathan, Enroth, Stefan, Kerr, Shona M, Surakka, Ida, Vitart, Veronique, Lehtimäki, Terho, Allen, Richard J, Bakke, Per S, Beaty, Terri H, Bleecker, Eugene R, Bossé, Yohan, Brandsma, Corry-Anke, Chen, Zhengming, Crapo, James D, Danesh, John, DeMeo, Dawn L, Dudbridge, Frank, Ewert, Ralf, Gieger, Christian, Gulsvik, Amund, Hansell, Anna L, Hao, Ke, Hoffman, Joshua D, Hokanson, John E, Homuth, Georg, Joshi, Peter K, Joubert, Philippe, Langenberg, Claudia, Li, Xuan, Li, Liming, Lin, Kuang, Lind, Lars, Locantore, Nicholas, Luan, Jian’an, Mahajan, Anubha, Maranville, Joseph C, Murray, Alison, Nickle, David C, Packer, Richard, Parker, Margaret M, Paynton, Megan L, Porteous, David J, Prokopenko, Dmitry, Qiao, Dandi, Rawal, Rajesh, Runz, Heiko, Sayers, Ian, Sin, Don D, Smith, Blair H, Artigas, María Soler, Sparrow, David, Tal-Singer, Ruth, Timmers, Paul RHJ, Van den Berge, Maarten, Whittaker, John C, Woodruff, Prescott G, Yerges-Armstrong, Laura M, Troyanskaya, Olga G, Raitakari, Olli T, Kähönen, Mika, Polasek, Ozren, Gyllensten, Ulf, Rudan, Igor, Deary, Ian J, Probst-Hensch, Nicole M, Schulz, Holger, James, Alan L, Wilson, James F, Stubbe, Beate, Zeggini, Eleftheria, Jarvelin, Marjo-Riitta, Wareham, Nick, Silverman, Edwin K, Hayward, Caroline, Morris, Andrew P, Butterworth, Adam S, Scott, Robert A, Walters, Robin G, Meyers, Deborah A, Cho, Michael H, Strachan, David P, Hall, Ian P, Tobin, Martin D, Wain, Louise V
Publicado 2019

A large genome-wide association study of age-related macular degeneration highlights contributions of rare and common variants

por Fritsche, Lars G., Igl, Wilmar, Cooke Bailey, Jessica N., Grassmann, Felix, Sengupta, Sebanti, Bragg-Gresham, Jennifer L., Burdon, Kathryn P., Hebbring, Scott J., Wen, Cindy, Gorski, Mathias, Kim, Ivana K., Cho, David, Zack, Donald, Souied, Eric, Scholl, Hendrik P. N., Bala, Elisa, Lee, Kristine E., Hunter, David J., Sardell, Rebecca J., Mitchell, Paul, Merriam, Joanna E., Cipriani, Valentina, Hoffman, Joshua D., Schick, Tina, Lechanteur, Yara T. E., Guymer, Robyn H., Johnson, Matthew P., Jiang, Yingda, Stanton, Chloe M., Buitendijk, Gabriëlle H. S., Zhan, Xiaowei, Kwong, Alan M., Boleda, Alexis, Brooks, Matthew, Gieser, Linn, Ratnapriya, Rinki, Branham, Kari E., Foerster, Johanna R., Heckenlively, John R., Othman, Mohammad I., Vote, Brendan J., Liang, Helena Hai, Souzeau, Emmanuelle, McAllister, Ian L., Isaacs, Timothy, Hall, Janette, Lake, Stewart, Mackey, David A., Constable, Ian J., Craig, Jamie E., Kitchner, Terrie E., Yang, Zhenglin, Su, Zhiguang, Luo, Hongrong, Chen, Daniel, Ouyang, Hong, Flagg, Ken, Lin, Danni, Mao, Guanping, Ferreyra, Henry, Stark, Klaus, von Strachwitz, Claudia N., Wolf, Armin, Brandl, Caroline, Rudolph, Guenther, Olden, Matthias, Morrison, Margaux A., Morgan, Denise J., Schu, Matthew, Ahn, Jeeyun, Silvestri, Giuliana, Tsironi, Evangelia E., Park, Kyu Hyung, Farrer, Lindsay A., Orlin, Anton, Brucker, Alexander, Li, Mingyao, Curcio, Christine, Mohand-Saïd, Saddek, Sahel, José-Alain, Audo, Isabelle, Benchaboune, Mustapha, Cree, Angela J., Rennie, Christina A., Goverdhan, Srinivas V., Grunin, Michelle, Hagbi-Levi, Shira, Campochiaro, Peter, Katsanis, Nicholas, Holz, Frank G., Blond, Frédéric, Blanché, Hélène, Deleuze, Jean-François, Igo, Robert P., Truitt, Barbara, Peachey, Neal S., Meuer, Stacy M., Myers, Chelsea E., Moore, Emily L., Klein, Ronald, Hauser, Michael A., Postel, Eric A., Courtenay, Monique D., Schwartz, Stephen G., Kovach, Jaclyn L., Scott, William K., Liew, Gerald, Tƒan, Ava G., Gopinath, Bamini, Merriam, John C., Smith, R. Theodore, Khan, Jane C., Shahid, Humma, Moore, Anthony T., McGrath, J. Allie, Laux, Reneé, Brantley, Milam A., Agarwal, Anita, Ersoy, Lebriz, Caramoy, Albert, Langmann, Thomas, Saksens, Nicole T. M., de Jong, Eiko K., Hoyng, Carel B., Cain, Melinda S., Richardson, Andrea J., Martin, Tammy M., Blangero, John, Weeks, Daniel E., Dhillon, Bal, van Duijn, Cornelia M., Doheny, Kimberly F., Romm, Jane, Klaver, Caroline C. W., Hayward, Caroline, Gorin, Michael B., Klein, Michael L., Baird, Paul N., den Hollander, Anneke I., Fauser, Sascha, Yates, John R. W., Allikmets, Rando, Wang, Jie Jin, Schaumberg, Debra A., Klein, Barbara E. K., Hagstrom, Stephanie A., Chowers, Itay, Lotery, Andrew J., Léveillard, Thierry, Zhang, Kang, Brilliant, Murray H., Hewitt, Alex W., Swaroop, Anand, Chew, Emily Y., Pericak-Vance, Margaret A., DeAngelis, Margaret, Stambolian, Dwight, Haines, Jonathan L., Iyengar, Sudha K., Weber, Bernhard H. F., Abecasis, Gonçalo R., Heid, Iris M.
Publicado 2015