The association between galactosylation of immunoglobulin G and body mass index von Nikolac Perkovic, Matea, Pucic Bakovic, Maja, Kristic, Jasminka, Novokmet, Mislav, Huffman, Jennifer E., Vitart, Veronique, Hayward, Caroline, Rudan, Igor, Wilson, James F., Campbell, Harry, Polasek, Ozren, Lauc, Gordan, Pivac, Nela

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A general approach for haplotype phasing across the full spectrum of relatedness von O'Connell, Jared, Gurdasani, Deepti, Delaneau, Olivier, Pirastu, Nicola, Ulivi, Sheila, Cocca, Massimiliano, Traglia, Michela, Huang, Jie, Huffman, Jennifer E, Rudan, Igor, McQuillan, Ruth, Fraser, Ross M, Campbell, Harry, Polasek, Ozren, Asiki, Gershim, Ekoru, Kenneth, Hayward, Caroline, Wright, Alan F, Vitart, Veronique, Navarro, Pau, Zagury, Jean-Francois, Wilson, James F, Toniolo, Daniela, Gasparini, Paolo, Soranzo, Nicole, Sandhu, Manjinder S, Marchini, Jonathan

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Multi-ancestry fine mapping implicates OAS1 splicing in risk of severe COVID-19 von Huffman, Jennifer E., Butler-Laporte, Guillaume, Khan, Atlas, Pairo-Castineira, Erola, Drivas, Theodore G., Peloso, Gina M., Nakanishi, Tomoko, Ganna, Andrea, Verma, Anurag, Baillie, J. Kenneth, Kiryluk, Krzysztof, Richards, J. Brent, Zeberg, Hugo

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Genome-wide and phenome-wide analysis of ideal cardiovascular health in the VA Million Veteran Program von Huang, Rose D L, Nguyen, Xuan-Mai T, Peloso, Gina M, Trinder, Mark, Posner, Daniel C, Aragam, Krishna G, Ho, Yuk-Lam, Lynch, Julie A, Damrauer, Scott M, Chang, Kyong-Mi, Tsao, Philip S, Natarajan, Pradeep, Assimes, Themistocles, Gaziano, J Michael, Djousse, Luc, Cho, Kelly, Wilson, Peter W F, Huffman, Jennifer E, O'Donnell, Christopher J

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Genomic and transcriptomic association studies identify 16 novel susceptibility loci for venous thromboembolism von Lindström, Sara, Wang, Lu, Smith, Erin N., Gordon, William, van Hylckama Vlieg, Astrid, de Andrade, Mariza, Brody, Jennifer A., Pattee, Jack W., Haessler, Jeffrey, Brumpton, Ben M., Chasman, Daniel I., Suchon, Pierre, Chen, Ming-Huei, Turman, Constance, Germain, Marine, Wiggins, Kerri L., MacDonald, James, Braekkan, Sigrid K., Armasu, Sebastian M., Pankratz, Nathan, Jackson, Rebecca D., Nielsen, Jonas B., Giulianini, Franco, Puurunen, Marja K., Ibrahim, Manal, Heckbert, Susan R., Damrauer, Scott M., Natarajan, Pradeep, Klarin, Derek, de Vries, Paul S., Sabater-Lleal, Maria, Huffman, Jennifer E., Bammler, Theo K., Frazer, Kelly A., McCauley, Bryan M., Taylor, Kent, Pankow, James S., Reiner, Alexander P., Gabrielsen, Maiken E., Deleuze, Jean-François, O'Donnell, Chris J., Kim, Jihye, McKnight, Barbara, Kraft, Peter, Hansen, John-Bjarne, Rosendaal, Frits R., Heit, John A., Psaty, Bruce M., Tang, Weihong, Kooperberg, Charles, Hveem, Kristian, Ridker, Paul M., Morange, Pierre-Emmanuel, Johnson, Andrew D., Kabrhel, Christopher, Trégouët, David-Alexandre, Smith, Nicholas L.

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The choline transporter Slc44a2 controls platelet activation and thrombosis by regulating mitochondrial function von Bennett, J. Allen, Mastrangelo, Michael A., Ture, Sara K., Smith, Charles O., Loelius, Shannon G., Berg, Rachel A., Shi, Xu, Burke, Ryan M., Spinelli, Sherry L., Cameron, Scott J., Carey, Thomas E., Brookes, Paul S., Gerszten, Robert E., Sabater-Lleal, Maria, de Vries, Paul S., Huffman, Jennifer E., Smith, Nicholas L., Morrell, Craig N., Lowenstein, Charles J.

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Loci associated with N-glycosylation of human immunoglobulin G show pleiotropy with autoimmune diseases and haematological cancers von Lauc, Gordan, Huffman, Jennifer E, Pučić, Maja, Zgaga, Lina, Adamczyk, Barbara, Mužinić, Ana, Novokmet, Mislav, Polašek, Ozren, Gornik, Olga, Krištić, Jasminka, Keser, Toma, Vitart, Veronique, Scheijen, Blanca, Uh, Hae-Won, Molokhia, Mariam, Patrick, Alan Leslie, McKeigue, Paul, Kolčić, Ivana, Lukić, Ivan Krešimir, Swann, Olivia, van Leeuwen, Frank N, Ruhaak, L Renee, Houwing-Duistermaat, Jeanine J, Slagboom, P Eline, Beekman, Marian, de Craen, Anton J M, Deelder, André M, Zeng, Qiang, Wang, Wei, Hastie, Nicholas D, Gyllensten, Ulf, Wilson, James F, Wuhrer, Manfred, Wright, Alan F, Rudd, Pauline M, Hayward, Caroline, Aulchenko, Yurii, Campbell, Harry, Rudan, Igor

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Rare coding variants pinpoint genes that control human hematological traits von Mousas, Abdou, Ntritsos, Georgios, Chen, Ming-Huei, Song, Ci, Huffman, Jennifer E, Tzoulaki, Ioanna, Elliott, Paul, Psaty, Bruce M, Auer, Paul L, Johnson, Andrew D, Evangelou, Evangelos, Lettre, Guillaume, Reiner, Alexander P

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A genome-wide association study of suicide attempts in the million veterans program identifies evidence of pan-ancestry and ancestry-specific risk loci von Kimbrel, Nathan A., Ashley-Koch, Allison E., Qin, Xue J., Lindquist, Jennifer H., Garrett, Melanie E., Dennis, Michelle F., Hair, Lauren P., Huffman, Jennifer E., Jacobson, Daniel A., Madduri, Ravi K., Trafton, Jodie A., Coon, Hilary, Docherty, Anna R., Kang, Jooeun, Mullins, Niamh, Ruderfer, Douglas M., Harvey, Philip D., McMahon, Benjamin H., Oslin, David W., Hauser, Elizabeth R., Hauser, Michael A., Beckham, Jean C.

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Phenome-wide association of 1809 phenotypes and COVID-19 disease progression in the Veterans Health Administration Million Veteran Program von Song, Rebecca J, Ho, Yuk-Lam, Schubert, Petra, Park, Yojin, Posner, Daniel, Lord, Emily M, Costa, Lauren, Gerlovin, Hanna, Kurgansky, Katherine E, Anglin-Foote, Tori, DuVall, Scott, Huffman, Jennifer E, Pyarajan, Saiju, Beckham, Jean C, Chang, Kyong-Mi, Liao, Katherine P, Djousse, Luc, Gagnon, David R, Whitbourne, Stacey B, Ramoni, Rachel, Muralidhar, Sumitra, Tsao, Philip S, O'Donnell, Christopher J, Gaziano, John Michael, Casas, Juan P, Cho, Kelly

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Genetic architecture of heart failure with preserved versus reduced ejection fraction von Joseph, Jacob, Liu, Chang, Hui, Qin, Aragam, Krishna, Wang, Zeyuan, Charest, Brian, Huffman, Jennifer E., Keaton, Jacob M., Edwards, Todd L., Demissie, Serkalem, Djousse, Luc, Casas, Juan P., Gaziano, J. Michael, Cho, Kelly, Wilson, Peter W. F., Phillips, Lawrence S., O’Donnell, Christopher J., Sun, Yan V.

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PCSK9 loss of function is protective against extra-coronary atherosclerotic cardiovascular disease in a large multi-ethnic cohort von Small, Aeron M, Huffman, Jennifer E, Klarin, Derek, Lynch, Julie A, Assimes, Themistocles, DuVall, Scott, Sun, Yan V, Shere, Labiba, Natarajan, Pradeep, Gaziano, Michael, Rader, Daniel J, Wilson, Peter W F, Tsao, Philip S, Chang, Kyong-Mi, Cho, Kelly, O'Donnell, Christopher J, Casas, Juan P, Damrauer, Scott M

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Lipid levels and risk of acute pancreatitis using bidirectional Mendelian randomization von Wang, Biqi, Dron, Jacqueline S., Wang, Yuxuan, Choi, Seung Hoan, Huffman, Jennifer E., Cho, Kelly, Wilson, Peter W. F., Natarajan, Pradeep, Peloso, Gina M.

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Comparative Performance of Four Methods for High-throughput Glycosylation Analysis of Immunoglobulin G in Genetic and Epidemiological Research von Huffman, Jennifer E., Pučić-Baković, Maja, Klarić, Lucija, Hennig, René, Selman, Maurice H.J., Vučković, Frano, Novokmet, Mislav, Krištić, Jasminka, Borowiak, Matthias, Muth, Thilo, Polašek, Ozren, Razdorov, Genadij, Gornik, Olga, Plomp, Rosina, Theodoratou, Evropi, Wright, Alan F., Rudan, Igor, Hayward, Caroline, Campbell, Harry, Deelder, André M., Reichl, Udo, Aulchenko, Yurii S., Rapp, Erdmann, Wuhrer, Manfred, Lauc, Gordan

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High-throughput multimodal automated phenotyping (MAP) with application to PheWAS von Liao, Katherine P, Sun, Jiehuan, Cai, Tianrun A, Link, Nicholas, Hong, Chuan, Huang, Jie, Huffman, Jennifer E, Gronsbell, Jessica, Zhang, Yichi, Ho, Yuk-Lam, Castro, Victor, Gainer, Vivian, Murphy, Shawn N, O’Donnell, Christopher J, Gaziano, J Michael, Cho, Kelly, Szolovits, Peter, Kohane, Isaac S, Yu, Sheng, Cai, Tianxi

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Efficient Variant Set Mixed Model Association Tests for Continuous and Binary Traits in Large-Scale Whole-Genome Sequencing Studies von Chen, Han, Huffman, Jennifer E., Brody, Jennifer A., Wang, Chaolong, Lee, Seunggeun, Li, Zilin, Gogarten, Stephanie M., Sofer, Tamar, Bielak, Lawrence F., Bis, Joshua C., Blangero, John, Bowler, Russell P., Cade, Brian E., Cho, Michael H., Correa, Adolfo, Curran, Joanne E., de Vries, Paul S., Glahn, David C., Guo, Xiuqing, Johnson, Andrew D., Kardia, Sharon, Kooperberg, Charles, Lewis, Joshua P., Liu, Xiaoming, Mathias, Rasika A., Mitchell, Braxton D., O’Connell, Jeffrey R., Peyser, Patricia A., Post, Wendy S., Reiner, Alex P., Rich, Stephen S., Rotter, Jerome I., Silverman, Edwin K., Smith, Jennifer A., Vasan, Ramachandran S., Wilson, James G., Yanek, Lisa R., Redline, Susan, Smith, Nicholas L., Boerwinkle, Eric, Borecki, Ingrid B., Cupples, L. Adrienne, Laurie, Cathy C., Morrison, Alanna C., Rice, Kenneth M., Lin, Xihong

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FTO genotype is associated with phenotypic variability of body mass index von Loos, Ruth J. F., Medland, Sarah E., Rose, Lynda M., Steinthorsdottir, Valgerdur, Mägi, Reedik, Waite, Lindsay, Monda, Keri L., Hadley, David, Mahajan, Anubha, Kapur, Karen, Vitart, Veronique, Palmer, Cameron, Esko, Tõnu, Fischer, Krista, Hua Zhao, Jing, Demirkan, Ayşe, Isaacs, Aaron, Feitosa, Mary F., Jackson, Anne U., Preuss, Michael, Ziegler, Andreas, Eriksson, Joel, Van Vliet-Ostaptchouk, Jana V., Jacobs, Kevin B., Goel, Anuj, Medina-Gomez, Carolina, Estrada, Karol, Lynn Bragg-Gresham, Jennifer, Sanna, Serena, Tyrer, Jonathan, Teumer, Alexander, Lindgren, Cecilia M., Assimes, Themistocles L., McArdle, Wendy L., Haritunians, Talin, Zgaga, Lina, Juhani Junttila, M., Schreiber, Stefan, Peters, Annette, Hicks, Andrew A., Stephens, Jonathan, Laitinen, Jaana, Kaakinen, Marika, Willemsen, Gonneke, Navis, Gerjan, John, Ulrich, Harris, Tamara, Gudnason, Vilmundur, Boerwinkle, Eric, James, Alan L., Ingelsson, Erik, Psaty, Bruce M., Beckmann, Jacques S., Waeber, Gerard, Wright, Alan F., Rudan, Igor, van Duijn, Cornelia M., Borecki, Ingrid B., Province, Michael A., Tardif, Jean-Claude, Atwood, Larry D., Fox, Caroline S., Boehnke, Michael, Collins, Francis S., Mohlke, Karen L., Erdmann, Jeanette, Schunkert, Heribert, Stark, Klaus, Lorentzon, Mattias, Ohlsson, Claes, Staessen, Jan A., Kathiresan, Sekar, Jolley, Jennifer D., Ripatti, Samuli, Penninx, Brenda, Wilson, James F., Campbell, Harry, van der Harst, Pim, Watkins, Hugh, Hofman, Albert, Witteman, Jacqueline C., Zillikens, M. Carola, Carola Zillikens, M., Kiemeney, Lambertus A., Abecasis, Goncalo R., Schipf, Sabine, Stumvoll, Michael, Lettre, Guillaume, Berndt, Sonja I., Heath, Andrew C., Madden, Pamela A. F., Martin, Nicholas G., McKnight, Barbara, Strachan, David P., Hill, William G., Snieder, Harold, Ridker, Paul M., Thorsteinsdottir, Unnur, Frayling, Timothy M., Hirschhorn, Joel N.

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Genomics meets glycomics-the first GWAS study of human N-Glycome identifies HNF1α as a master regulator of plasma protein fucosylation von Lauc, Gordan, Essafi, Abdelkader, Huffman, Jennifer E, Hayward, Caroline, Knežević, Ana, Kattla, Jayesh J, Polašek, Ozren, Gornik, Olga, Vitart, Veronique, Abrahams, Jodie L, Pučić, Maja, Novokmet, Mislav, Redžić, Irma, Campbell, Susan, Wild, Sarah H, Borovečki, Fran, Wang, Wei, Kolčić, Ivana, Zgaga, Lina, Gyllensten, Ulf, Wilson, James F, Wright, Alan F, Hastie, Nicholas D, Campbell, Harry, Rudd, Pauline M, Rudan, Igor

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Exploration of haplotype research consortium imputation for genome-wide association studies in 20,032 Generation Scotland participants von Nagy, Reka, Boutin, Thibaud S, Marten, Jonathan, Huffman, Jennifer E, Kerr, Shona M, Campbell, Archie, Evenden, Louise, Gibson, Jude, Amador, Carmen, Howard, David M, Navarro, Pau, Morris, Andrew, Deary, Ian J, Hocking, Lynne J, Padmanabhan, Sandosh, Smith, Blair H, Joshi, Peter, Wilson, James F, Hastie, Nicholas D, Wright, Alan F, McIntosh, Andrew M, Porteous, David J, Haley, Chris S, Vitart, Veronique, Hayward, Caroline

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Transcriptome-wide association study in UK Biobank Europeans identifies associations with blood cell traits von Rowland, Bryce, Venkatesh, Sanan, Tardaguila, Manuel, Wen, Jia, Rosen, Jonathan D, Tapia, Amanda L, Sun, Quan, Graff, Mariaelisa, Vuckovic, Dragana, Lettre, Guillaume, Sankaran, Vijay G, Voloudakis, Georgios, Roussos, Panos, Huffman, Jennifer E, Reiner, Alexander P, Soranzo, Nicole, Raffield, Laura M, Li, Yun

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