Factors associated with emotional and behavioral outcomes in adolescents with multiple sclerosis by Till, C, Udler, E, Ghassemi, R, Narayanan, S, Arnold, DL, Banwell, BL

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Development of oil filters based on filter paper elements by Udler, . I., Shevchenko, N. N., Shilonosov, P. P.

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Laws governing the filtration of a polydisperse suspension through a porous filter medium by Udler, . I., Rybakov, K. V., Shostak, L. N.

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Variance-quantitative trait loci enable systematic discovery of gene-environment interactions for cardiometabolic serum biomarkers by Westerman, Kenneth E., Majarian, Timothy D., Giulianini, Franco, Jang, Dong-Keun, Miao, Jenkai, Florez, Jose C., Chen, Han, Chasman, Daniel I., Udler, Miriam S., Manning, Alisa K., Cole, Joanne B.

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High-throughput genetic clustering of type 2 diabetes loci reveals heterogeneous mechanistic pathways of metabolic disease by Kim, Hyunkyung, Westerman, Kenneth E., Smith, Kirk, Chiou, Joshua, Cole, Joanne B., Majarian, Timothy, von Grotthuss, Marcin, Kwak, Soo Heon, Kim, Jaegil, Mercader, Josep M., Florez, Jose C., Gaulton, Kyle, Manning, Alisa K., Udler, Miriam S.

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Effect of Genetic African Ancestry on eGFR and Kidney Disease by Udler, Miriam S, Nadkarni, Girish N, Belbin, Gillian, Lotay, Vaneet, Wyatt, Christina, Gottesman, Omri, Bottinger, Erwin P, Kenny, Eimear E, Peter, Inga

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Development and validation of a trans-ancestry polygenic risk score for type 2 diabetes in diverse populations by Ge, Tian, Irvin, Marguerite R, Patki, Amit, Srinivasasainagendra, Vinodh, Lin, Yen-Feng, Tiwari, Hemant K, Armstrong, Nicole D, Benoit, Barbara, Chen, Chia-Yen, Choi, Karmel W, Cimino, James J, Davis, Brittney H, Dikilitas, Ozan, Etheridge, Bethany, Feng, Yen-Chen Anne, Gainer, Vivian, Huang, Hailiang, Jarvik, Gail P, Kachulis, Christopher, Kenny, Eimear E, Khan, Atlas, Kiryluk, Krzysztof, Kottyan, Leah, Kullo, Iftikhar J, Lange, Christoph, Lennon, Niall, Leong, Aaron, Malolepsza, Edyta, Miles, Ayme D, Murphy, Shawn, Namjou, Bahram, Narayan, Renuka, O'Connor, Mark J, Pacheco, Jennifer A, Perez, Emma, Rasmussen-Torvik, Laura J, Rosenthal, Elisabeth A, Schaid, Daniel, Stamou, Maria, Udler, Miriam S, Wei, Wei-Qi, Weiss, Scott T, Ng, Maggie C Y, Smoller, Jordan W, Lebo, Matthew S, Meigs, James B, Limdi, Nita A, Karlson, Elizabeth W

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Genetic determinants of daytime napping and effects on cardiometabolic health by Dashti, Hassan S., Daghlas, Iyas, Lane, Jacqueline M., Huang, Yunru, Udler, Miriam S., Wang, Heming, Ollila, Hanna M., Jones, Samuel E., Kim, Jaegil, Wood, Andrew R., Weedon, Michael N., Aslibekyan, Stella, Garaulet, Marta, Saxena, Richa

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Re-analysis of public genetic data reveals a rare X-chromosomal variant associated with type 2 diabetes by Bonàs-Guarch, Sílvia, Guindo-Martínez, Marta, Miguel-Escalada, Irene, Grarup, Niels, Sebastian, David, Rodriguez-Fos, Elias, Sánchez, Friman, Planas-Fèlix, Mercè, Cortes-Sánchez, Paula, González, Santi, Timshel, Pascal, Pers, Tune H., Morgan, Claire C., Moran, Ignasi, Atla, Goutham, González, Juan R., Puiggros, Montserrat, Martí, Jonathan, Andersson, Ehm A., Díaz, Carlos, Badia, Rosa M., Udler, Miriam, Leong, Aaron, Kaur, Varindepal, Flannick, Jason, Jørgensen, Torben, Linneberg, Allan, Jørgensen, Marit E., Witte, Daniel R., Christensen, Cramer, Brandslund, Ivan, Appel, Emil V., Scott, Robert A., Luan, Jian’an, Langenberg, Claudia, Wareham, Nicholas J., Pedersen, Oluf, Zorzano, Antonio, Florez, Jose C, Hansen, Torben, Ferrer, Jorge, Mercader, Josep Maria, Torrents, David

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Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum by Ganna, Andrea, Satterstrom, F. Kyle, Zekavat, Seyedeh M., Das, Indraniel, Kurki, Mitja I., Churchhouse, Claire, Alfoldi, Jessica, Martin, Alicia R., Havulinna, Aki S., Byrnes, Andrea, Thompson, Wesley K., Nielsen, Philip R., Karczewski, Konrad J., Saarentaus, Elmo, Rivas, Manuel A., Gupta, Namrata, Pietiläinen, Olli, Emdin, Connor A., Lescai, Francesco, Bybjerg-Grauholm, Jonas, Flannick, Jason, Mercader, Josep M., Udler, Miriam, Laakso, Markku, Salomaa, Veikko, Hultman, Christina, Ripatti, Samuli, Hämäläinen, Eija, Moilanen, Jukka S., Körkkö, Jarmo, Kuismin, Outi, Nordentoft, Merete, Hougaard, David M., Mors, Ole, Werge, Thomas, Mortensen, Preben Bo, MacArthur, Daniel, Daly, Mark J., Sullivan, Patrick F., Locke, Adam E., Palotie, Aarno, Børglum, Anders D., Kathiresan, Sekar, Neale, Benjamin M.

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Discovering cellular programs of intrinsic and extrinsic drivers of metabolic traits using LipocyteProfiler by Laber, Samantha, Strobel, Sophie, Mercader, Josep M., Dashti, Hesam, dos Santos, Felipe R.C., Kubitz, Phil, Jackson, Maya, Ainbinder, Alina, Honecker, Julius, Agrawal, Saaket, Garborcauskas, Garrett, Stirling, David R., Leong, Aaron, Figueroa, Katherine, Sinnott-Armstrong, Nasa, Kost-Alimova, Maria, Deodato, Giacomo, Harney, Alycen, Way, Gregory P., Saadat, Alham, Harken, Sierra, Reibe-Pal, Saskia, Ebert, Hannah, Zhang, Yixin, Calabuig-Navarro, Virtu, McGonagle, Elizabeth, Stefek, Adam, Dupuis, Josée, Cimini, Beth A., Hauner, Hans, Udler, Miriam S., Carpenter, Anne E., Florez, Jose C., Lindgren, Cecilia, Jacobs, Suzanne B.R., Claussnitzer, Melina

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Common germline polymorphisms in COMT, CYP19A1, ESR1, PGR, SULT1E1 and STS and survival after a diagnosis of breast cancer by Udler, Miriam S., Azzato, Elizabeth M., Healey, Catherine S., Ahmed, Shahana, Pooley, Karen A., Greenberg, David, Shah, Mitul, Teschendorff, Andrew E., Caldas, Carlos, Dunning, Alison M., Ostrander, Elaine A., Caporaso, Neil E., Easton, Douglas, Pharoah, Paul D.

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Genome-wide association analysis identifies ancestry-specific genetic variation associated with acute response to metformin and glipizide in SUGAR-MGH by Li, Josephine H., Brenner, Laura N., Kaur, Varinderpal, Figueroa, Katherine, Schroeder, Philip, Huerta-Chagoya, Alicia, Udler, Miriam S., Leong, Aaron, Mercader, Josep M., Florez, Jose C.

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Fine scale mapping of the breast cancer 16q12 locus by Udler, Miriam S., Ahmed, Shahana, Healey, Catherine S., Meyer, Kerstin, Struewing, Jeffrey, Maranian, Melanie, Kwon, Erika M., Zhang, Jinghui, Tyrer, Jonathan, Karlins, Eric, Platte, Radka, Kalmyrzaev, Bolot, Dicks, Ed, Field, Helen, Maia, Ana-Teresa, Prathalingam, Radhika, Teschendorff, Andrew, McArthur, Stewart, Doody, David R., Luben, Robert, Caldas, Carlos, Bernstein, Leslie, Kolonel, Laurence K., Henderson, Brian E., Wu, Anna H., Le Marchand, Loic, Ursin, Giske, Press, Michael F., Lindblom, Annika, Margolin, Sara, Shen, Chen-Yang, Yang, Show-Lin, Hsiung, Chia-Ni, Kang, Daehee, Yoo, Keun-Young, Noh, Dong-Young, Ahn, Sei-Hyun, Malone, Kathleen E., Haiman, Christopher A., Pharoah, Paul D., Ponder, Bruce A.J., Ostrander, Elaine A., Easton, Douglas F., Dunning, Alison M.

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Identification of atypical pediatric diabetes mellitus cases using electronic medical records by Astudillo, Marcela F, Winter, William E, Billings, Liana K, Kreienkamp, Raymond, Balasubramanyam, Ashok, Redondo, Maria J, Tosur, Mustafa

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Publisher Correction: Re-analysis of public genetic data reveals a rare X-chromosomal variant associated with type 2 diabetes by Bonàs-Guarch, Sílvia, Guindo-Martínez, Marta, Miguel-Escalada, Irene, Grarup, Niels, Sebastian, David, Rodriguez-Fos, Elias, Sánchez, Friman, Planas-Fèlix, Mercè, Cortes-Sánchez, Paula, González, Santi, Timshel, Pascal, Pers, Tune H., Morgan, Claire C., Moran, Ignasi, Atla, Goutham, González, Juan R., Puiggros, Montserrat, Martí, Jonathan, Andersson, Ehm A., Díaz, Carlos, Badia, Rosa M., Udler, Miriam, Leong, Aaron, Kaur, Varindepal, Flannick, Jason, Jørgensen, Torben, Linneberg, Allan, Jørgensen, Marit E., Witte, Daniel R., Christensen, Cramer, Brandslund, Ivan, Appel, Emil V., Scott, Robert A., Luan, Jian’an, Langenberg, Claudia, Wareham, Nicholas J., Pedersen, Oluf, Zorzano, Antonio, Florez, Jose C, Hansen, Torben, Ferrer, Jorge, Mercader, Josep Maria, Torrents, David

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Re-analysis of public genetic data reveals a rare X-chromosomal variant associated with type 2 diabetes by Bonàs Guarch, Sílvia, Guindo-Martínez, Marta, Miguel-Escalada, Irene, Grarup, Niels, Sebastián Muñoz, David, Rodriguez-Fos, Elias, Sánchez, Friman, Planas-Fèlix, Mercè, Cortes-Sánchez, Paula, González, Santi, Timshel, Pascal, Pers, Tune H, Morgan, Claire C, Moran, Ignasi, Atla, Goutham, González, Juan Ramón, Puiggros, Montserrat, Martí, Jonathan, Andersson, Ehm A, Díaz, Carlos, Badia, Rosa M, Udler, Miriam, Leong, Aaron, Kaur, Varindepal, Flannick, Jason, Jørgensen, Torben, Linneberg, Allan, Jørgensen, Marit E, Witte, Daniel R, Christensen, Cramer, Brandslund, Ivan, Appel, Emil V, Scott, Robert A, Luan, Jian'an, Langenberg, Claudia, Wareham, Nicholas J, Pedersen, Oluf, Zorzano Olarte, Antonio, Florez, Jose C, Hansen, Torben

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Re-analysis of public genetic data reveals a rare X-chromosomal variant associated with type 2 diabetes by Bonàs Guarch, Sílvia, Guindo-Martínez, Marta, Miguel-Escalada, Irene, Grarup, Niels, Sebastián Muñoz, David, Rodriguez-Fos, Elias, Sánchez, Friman, Planas-Fèlix, Mercè, Cortes-Sánchez, Paula, González, Santi, Timshel, Pascal, Pers, Tune H, Morgan, Claire C, Moran, Ignasi, Atla, Goutham, González, Juan Ramón, Puiggros, Montserrat, Martí, Jonathan, Andersson, Ehm A, Díaz, Carlos, Badia, Rosa M, Udler, Miriam, Leong, Aaron, Kaur, Varindepal, Flannick, Jason, Jørgensen, Torben, Linneberg, Allan, Jørgensen, Marit E, Witte, Daniel R, Christensen, Cramer, Brandslund, Ivan, Appel, Emil V, Scott, Robert A, Luan, Jian'an, Langenberg, Claudia, Wareham, Nicholas J, Pedersen, Oluf, Zorzano Olarte, Antonio, Florez, Jose C, Hansen, Torben

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Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls by Mercader, Josep M., Udler, Miriam S., Mahajan, Anubha, Caulkins, Lizz, Barajas-Olmos, Francisco, Blackwell, Thomas W., Boerwinkle, Eric, Brody, Jennifer A., Chen, Siying, Contreras-Cubas, Cecilia, Córdova, Emilio, Correa, Adolfo, Cortes, Maria, Dolan, Lawrence, Drews, Kimberly L., Gabriel, Stacey, Garay-Sevilla, Maria Eugenia, García-Ortiz, Humberto, Gross, Myron, Heard-Costa, Nancy L., Jackson, Anne U., Jørgensen, Marit E., Kang, Hyun Min, Kim, Bong-Jo, Lyssenko, Valeriya, Manning, Alisa K., Marcketta, Anthony, Martínez-Hernández, Angélica, Matsuo, Karen, Mayer-Davis, Elizabeth, Mohlke, Karen L., Morrison, Alanna C., Ndungu, Anne, Ng, Maggie C. Y., O’Dushlaine, Colm, Payne, Anthony J., Pihoker, Catherine, Preuss, Michael, Psaty, Bruce M., Reiner, Alexander P., Robertson, Neil R., Santoro, Nicola, Schurmann, Claudia, So, Wing Yee, Soberón, Xavier, Thameem, Farook, Tomlinson, Brian, van Dam, Rob M., Vujkovic, Marijana, Witte, Daniel R., Barzilai, Nir, Bonnycastle, Lori L., Bowden, Donald W., Chambers, John C., Cheng, Ching-Yu, de Vries, Paul S., Glaser, Benjamin, Groop, Leif, Kooner, Jaspal Singh, Kwak, Soo Heon, Lehman, Donna M., Spector, Timothy D., Tai, E. Shyong, Tuomilehto, Jaakko, Wilson, James G., Burke, Brian, Carey, David J., Chan, Juliana C. N., Dupuis, Josée, Frossard, Philippe, Heckbert, Susan R., Hwang, Mi Yeong, Kim, Young Jin, Kirchner, H. Lester, Lee, Jong-Young, Lee, Juyoung, Loos, Ruth J. F., Ma, Ronald C. W., O’Donnell, Christopher J., Park, Kyong Soo, Rasheed, Asif, Saleheen, Danish, Sim, Xueling, Hanis, Craig L., Orozco, Lorena, Dewey, Frederick E., Baras, Aris, Gieger, Christian, Meitinger, Thomas, Strauch, Konstantin, Lange, Leslie, Hansen, Torben, Pedersen, Oluf, Dabelea, Dana, Bell, Graeme I., Sladek, Rob, Rich, Steve S., Rotter, Jerome I., Altshuler, David, Boehnke, Michael

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Comparison of Risk Estimates for Selected Diseases and Causes of Death by Merrill, Ray M, Kessler, Larry G, Udler, Joshua M, Rasband, Gloria C, Feuer, Eric J

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