A Validated Phenotyping Algorithm for Genetic Association Studies in Age-related Macular Degeneration

por Simonett, Joseph M., Sohrab, Mahsa A., Pacheco, Jennifer, Armstrong, Loren L., Rzhetskaya, Margarita, Smith, Maureen, Geoffrey Hayes, M., Fawzi, Amani A.
Publicado 2015

Coordinated Regulatory Variation Associated with Gestational Hyperglycemia Regulates Expression of the Novel Hexokinase HKDC1

por Guo, Cong, Ludvik, Anton E., Arlotto, Michelle E., Hayes, M. Geoffrey, Armstrong, Loren L., Scholtens, Denise M., Brown, Christopher D., Newgard, Christopher B., Becker, Thomas C., Layden, Brian T., Lowe, William L., Reddy, Timothy E.
Publicado 2015

Admixture Mapping and Subsequent Fine-Mapping Suggests a Biologically Relevant and Novel Association on Chromosome 11 for Type 2 Diabetes in African Americans

por Jeff, Janina M., Armstrong, Loren L., Ritchie, Marylyn D., Denny, Joshua C., Kho, Abel N., Basford, Melissa A., Wolf, Wendy A., Pacheco, Jennifer A., Li, Rongling, Chisholm, Rex L., Roden, Dan M., Hayes, M. Geoffrey, Crawford, Dana C.
Publicado 2014

A candidate gene study reveals association between a variant of the Peroxisome Proliferator-Activated Receptor Gamma (PPAR-γ) gene and systemic sclerosis

por Marangoni, Roberta Goncalves, Korman, Benjamin D, Allanore, Yannick, Dieude, Philippe, Armstrong, Loren L, Rzhetskaya, Margarita, Hinchcliff, Monique, Carns, Mary, Podlusky, Sofia, Shah, Sanjiv J, Ruiz, Barbara, Hachulla, Eric, Tiev, Kiet, Cracowski, Jean-Luc, Varga, John, Hayes, M Geoffrey
Publicado 2015

Genome-wide association of polycystic ovary syndrome implicates alterations in gonadotropin secretion in European ancestry populations

por Hayes, M. Geoffrey, Urbanek, Margrit, Ehrmann, David A., Armstrong, Loren L., Lee, Ji Young, Sisk, Ryan, Karaderi, Tugce, Barber, Thomas M., McCarthy, Mark I., Franks, Stephen, Lindgren, Cecilia M., Welt, Corrine K., Diamanti-Kandarakis, Evanthia, Panidis, Dimitrios, Goodarzi, Mark O., Azziz, Ricardo, Zhang, Yi, James, Roland G., Olivier, Michael, Kissebah, Ahmed H., Stener-Victorin, Elisabet, Legro, Richard S., Dunaif, Andrea
Publicado 2015

Corrigendum: Genome-wide association of polycystic ovary syndrome implicates alterations in gonadotropin secretion in European ancestry populations

por Hayes, M. Geoffrey, Urbanek, Margrit, Ehrmann, David A., Armstrong, Loren L., Lee, Ji Young, Sisk, Ryan, Karaderi, Tugce, Barber, Thomas M., McCarthy, Mark I., Franks, Stephen, Lindgren, Cecilia M., Welt, Corrine K., Diamanti-Kandarakis, Evanthia, Panidis, Dimitrios, Goodarzi, Mark O., Azziz, Ricardo, Zhang, Yi, James, Roland G., Olivier, Michael, Kissebah, Ahmed H., Stener-Victorin, Elisabet, Legro, Richard S., Dunaif, Andrea
Publicado 2016

Publisher Correction: Genome-wide association of polycystic ovary syndrome implicates alterations in gonadotropin secretion in European ancestry populations

por Hayes, M. Geoffrey, Urbanek, Margrit, Ehrmann, David A., Armstrong, Loren L., Lee, Ji Young, Sisk, Ryan, Karaderi, Tugce, Barber, Thomas M., McCarthy, Mark I., Franks, Stephen, Lindgren, Cecilia M., Welt, Corrine K., Diamanti-Kandarakis, Evanthia, Panidis, Dimitrios, Goodarzi, Mark O., Azziz, Ricardo, Zhang, Yi, James, Roland G., Olivier, Michael, Kissebah, Ahmed H., Stener-Victorin, Elisabet, Legro, Richard S., Dunaif, Andrea
Publicado 2020

Identification of HKDC1 and BACE2 as Genes Influencing Glycemic Traits During Pregnancy Through Genome-Wide Association Studies

por Hayes, M. Geoffrey, Urbanek, Margrit, Hivert, Marie-France, Armstrong, Loren L., Morrison, Jean, Guo, Cong, Lowe, Lynn P., Scheftner, Douglas A., Pluzhnikov, Anna, Levine, David M., McHugh, Caitlin P., Ackerman, Christine M., Bouchard, Luigi, Brisson, Diane, Layden, Brian T., Mirel, Daniel, Doheny, Kimberly F., Leya, Marysa V., Lown-Hecht, Rachel N., Dyer, Alan R., Metzger, Boyd E., Reddy, Timothy E., Cox, Nancy J., Lowe, William L.
Publicado 2013

Meta-Analysis of Genome-Wide Association Studies in African Americans Provides Insights into the Genetic Architecture of Type 2 Diabetes

por Ng, Maggie C. Y., Shriner, Daniel, Chen, Brian H., Li, Jiang, Chen, Wei-Min, Guo, Xiuqing, Liu, Jiankang, Bielinski, Suzette J., Yanek, Lisa R., Nalls, Michael A., Comeau, Mary E., Rasmussen-Torvik, Laura J., Jensen, Richard A., Evans, Daniel S., Sun, Yan V., An, Ping, Patel, Sanjay R., Lu, Yingchang, Long, Jirong, Armstrong, Loren L., Wagenknecht, Lynne, Yang, Lingyao, Snively, Beverly M., Palmer, Nicholette D., Mudgal, Poorva, Langefeld, Carl D., Keene, Keith L., Freedman, Barry I., Mychaleckyj, Josyf C., Nayak, Uma, Raffel, Leslie J., Goodarzi, Mark O., Chen, Y-D Ida, Taylor, Herman A., Correa, Adolfo, Sims, Mario, Couper, David, Pankow, James S., Boerwinkle, Eric, Adeyemo, Adebowale, Doumatey, Ayo, Chen, Guanjie, Mathias, Rasika A., Vaidya, Dhananjay, Singleton, Andrew B., Zonderman, Alan B., Igo, Robert P., Sedor, John R., Kabagambe, Edmond K., Siscovick, David S., McKnight, Barbara, Rice, Kenneth, Liu, Yongmei, Hsueh, Wen-Chi, Zhao, Wei, Bielak, Lawrence F., Kraja, Aldi, Province, Michael A., Bottinger, Erwin P., Gottesman, Omri, Cai, Qiuyin, Zheng, Wei, Blot, William J., Lowe, William L., Pacheco, Jennifer A., Crawford, Dana C., Grundberg, Elin, Rich, Stephen S., Hayes, M. Geoffrey, Shu, Xiao-Ou, Loos, Ruth J. F., Borecki, Ingrid B., Peyser, Patricia A., Cummings, Steven R., Psaty, Bruce M., Fornage, Myriam, Iyengar, Sudha K., Evans, Michele K., Becker, Diane M., Kao, W. H. Linda, Wilson, James G., Rotter, Jerome I., Sale, Michèle M., Liu, Simin, Rotimi, Charles N., Bowden, Donald W.
Publicado 2014

A novel common variant in DCST2 is associated with length in early life and height in adulthood

por van der Valk, Ralf J.P., Kreiner-Møller, Eskil, Kooijman, Marjolein N., Guxens, Mònica, Stergiakouli, Evangelia, Sääf, Annika, Bradfield, Jonathan P., Geller, Frank, Hayes, M. Geoffrey, Cousminer, Diana L., Körner, Antje, Thiering, Elisabeth, Curtin, John A., Myhre, Ronny, Huikari, Ville, Joro, Raimo, Kerkhof, Marjan, Warrington, Nicole M., Pitkänen, Niina, Ntalla, Ioanna, Horikoshi, Momoko, Veijola, Riitta, Freathy, Rachel M., Teo, Yik-Ying, Barton, Sheila J., Evans, David M., Kemp, John P., St Pourcain, Beate, Ring, Susan M., Davey Smith, George, Bergström, Anna, Kull, Inger, Hakonarson, Hakon, Mentch, Frank D., Bisgaard, Hans, Chawes, Bo, Stokholm, Jakob, Waage, Johannes, Eriksen, Patrick, Sevelsted, Astrid, Melbye, Mads, van Duijn, Cornelia M., Medina-Gomez, Carolina, Hofman, Albert, de Jongste, Johan C., Taal, H. Rob, Uitterlinden, André G., Armstrong, Loren L., Eriksson, Johan, Palotie, Aarno, Bustamante, Mariona, Estivill, Xavier, Gonzalez, Juan R., Llop, Sabrina, Kiess, Wieland, Mahajan, Anubha, Flexeder, Claudia, Tiesler, Carla M.T., Murray, Clare S., Simpson, Angela, Magnus, Per, Sengpiel, Verena, Hartikainen, Anna-Liisa, Keinanen-Kiukaanniemi, Sirkka, Lewin, Alexandra, Da Silva Couto Alves, Alexessander, Blakemore, Alexandra I., Buxton, Jessica L., Kaakinen, Marika, Rodriguez, Alina, Sebert, Sylvain, Vaarasmaki, Marja, Lakka, Timo, Lindi, Virpi, Gehring, Ulrike, Postma, Dirkje S., Ang, Wei, Newnham, John P., Lyytikäinen, Leo-Pekka, Pahkala, Katja, Raitakari, Olli T., Panoutsopoulou, Kalliope, Zeggini, Eleftheria, Boomsma, Dorret I., Groen-Blokhuis, Maria, Ilonen, Jorma, Franke, Lude, Hirschhorn, Joel N., Pers, Tune H., Liang, Liming, Huang, Jinyan, Hocher, Berthold, Knip, Mikael, Saw, Seang-Mei, Holloway, John W., Melén, Erik, Grant, Struan F.A., Feenstra, Bjarke, Lowe, William L., Widén, Elisabeth, Sergeyev, Elena, Grallert, Harald, Custovic, Adnan, Jacobsson, Bo, Jarvelin, Marjo-Riitta, Atalay, Mustafa, Koppelman, Gerard H., Pennell, Craig E., Niinikoski, Harri, Dedoussis, George V., Mccarthy, Mark I., Frayling, Timothy M., Sunyer, Jordi, Timpson, Nicholas J., Rivadeneira, Fernando, Bønnelykke, Klaus, Jaddoe, Vincent W.V.
Publicado 2015