Novel Genetic Loci Identified for the Pathophysiology of Childhood Obesity in the Hispanic Population by Comuzzie, Anthony G, Cole, Shelley A, Laston, Sandra L, Voruganti, V. Saroja, Haack, Karin, Gibbs, Richard A, Butte, Nancy F, Crawford, Dana C

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Incidence of Exposure of Patients in the United States to Multiple Drugs for Which Pharmacogenomic Guidelines Are Available by Samwald, Matthias, Xu, Hong, Blagec, Kathrin, Empey, Philip E, Malone, Daniel C, Ahmed, Seid Mussa, Ryan, Patrick, Hofer, Sebastian, Boyce, Richard D

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New rules for genomics-informed COVID-19 responses–Lessons learned from the first waves of the Omicron variant in Australia by Porter, Ashleigh F, Sherry, Norelle, Andersson, Patiyan, Johnson, Sandra A, Duchene, Sebastian, Howden, Benjamin P

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Cardiovascular disease risk factor burden and cognition: Implications of ethnic diversity within the Hispanic Community Health Study/Study of Latinos by Lamar, Melissa, Durazo-Arvizu, Ramon A, Sachdeva, Shruti, Pirzada, Amber, Perreira, Krista M, Rundek, Tatjana, Gallo, Linda C, Grober, Ellen, DeCarli, Charles, Lipton, Richard B, Tarraf, Wassim, González, Hector M, Daviglus, Martha L

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Whole genome variation in 27 Mexican indigenous populations, demographic and biomedical insights by Aguilar-Ordoñez, Israel, Pérez-Villatoro, Fernando, García-Ortiz, Humberto, Barajas-Olmos, Francisco, Ballesteros-Villascán, Judith, González-Buenfil, Ram, Fresno, Cristobal, Garcíarrubio, Alejandro, Fernández-López, Juan Carlos, Tovar, Hugo, Hernández-Lemus, Enrique, Orozco, Lorena, Soberón, Xavier, Morett, Enrique

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Oral microbiota reveals signs of acculturation in Mexican American women by Hoffman, Kristi L, Hutchinson, Diane S, Fowler, Jerry, Smith, Daniel P, Ajami, Nadim J, Zhao, Hua, Scheet, Paul, Chow, Wong-Ho, Petrosino, Joseph F, Daniel, Carrie R

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A genome-wide analysis of DNA methylation identifies a novel association signal for Lp(a) concentrations in the LPA promoter by Coassin, Stefan, Hermann-Kleiter, Natascha, Haun, Margot, Wahl, Simone, Wilson, Rory, Paulweber, Bernhard, Kunze, Sonja, Meitinger, Thomas, Strauch, Konstantin, Peters, Annette, Waldenberger, Melanie, Kronenberg, Florian, Lamina, Claudia

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Human genetic variation in GLS2 is associated with development of complicated Staphylococcus aureus bacteremia by Scott, William K, Medie, Felix Mba, Ruffin, Felicia, Sharma-Kuinkel, Batu K, Cyr, Derek D, Guo, Shengru, Dykxhoorn, Derek M, Skov, Robert L, Bruun, Niels E, Dahl, Anders, Lerche, Christian J, Petersen, Andreas, Larsen, Anders Rhod, Lauridsen, Trine Kiilerich, Johansen, Helle Krogh, Ullum, Henrik, Sørensen, Erik, Hassager, Christian, Bundgaard, Henning, Schønheyder, Henrik C, Torp-Pedersen, Christian, Østergaard, Louise Bruun, Arpi, Magnus, Rosenvinge, Flemming, Erikstrup, Lise T, Chehri, Mahtab, Søgaard, Peter, Andersen, Paal S, Fowler, Jr, Vance G

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Modulation of genetic associations with serum urate levels by body-mass-index in humans by Huffman, Jennifer E, Albrecht, Eva, Teumer, Alexander, Johnson, Toby, Kutalik, Zoltán, Pirastu, Nicola, Pistis, Giorgio, Lopez, Lorna M, Haller, Toomas, Salo, Perttu, Goel, Anuj, Tanaka, Toshiko, Dehghan, Abbas, Ruggiero, Daniela, Malerba, Giovanni, Smith, Albert V, Nolte, Ilja M, Phipps-Green, Amanda, Boteva, Lora, Navarro, Pau, Johansson, Asa, Polasek, Ozren, Esko, Tõnu, Peden, John F, Harris, Sarah E, Murgia, Federico, Wild, Sarah H, Tin, Adrienne, Mihailov, Evelin, Grotevendt, Anne, Gislason, Gauti K, Coresh, Josef, D'Adamo, Pio, Ulivi, Sheila, Vollenweider, Peter, Waeber, Gerard, Campbell, Susan, Viigimaa, Margus, Bombieri, Cristina, Sorice, Rossella, Döring, Angela, Reischl, Eva, Strauch, Konstantin, Hofman, Albert, Waldenberger, Melanie, Wichmann, H-Erich, Davies, Gail, Dalbeth, Nicola, Smit, Johannes H, Kirin, Mirna, Nagaraja, Ramaiah, Nauck, Matthias, Schurmann, Claudia, Budde, Kathrin, Farrington, Susan M, Theodoratou, Evropi, Jula, Antti, Salomaa, Veikko, Hengstenberg, Christian, Burnier, Michel, Mägi, Reedik, Klopp, Norman, Kloiber, Stefan, Schipf, Sabine, Ripatti, Samuli, Cabras, Stefano, Soranzo, Nicole, Homuth, Georg, Nutile, Teresa, Munroe, Patricia B, Hastie, Nicholas, Campbell, Harry, Rudan, Igor, Haley, Chris, Franco, Oscar H, Merriman, Tony R, Gudnason, Vilmundur, Pirastu, Mario, Snieder, Harold, Metspalu, Andres, Ciullo, Marina, van Duijn, Cornelia M, Ferrucci, Luigi, Deary, Ian J, Dunlop, Malcolm G, Wilson, James F, Gasparini, Paolo, Gyllensten, Ulf, Spector, Tim D, Wright, Alan F, Hayward, Caroline, Watkins, Hugh, Perola, Markus, Bochud, Murielle, Kao, W H Linda, Caulfield, Mark, Toniolo, Daniela, Völzke, Henry, Köttgen, Anna, Vitart, Veronique

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A genome-wide association study of energy intake and expenditure by Jiang, Lai, Penney, Kathryn L, Giovannucci, Edward, Kraft, Peter, Wilson, Kathryn M

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A dietary-wide association study (DWAS) of environmental metal exposure in US children and adults by Davis, Matthew A, Gilbert-Diamond, Diane, Karagas, Margaret R, Li, Zhigang, Moore, Jason H, Williams, Scott M, Frost, H Robert

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Genetic Variation in the Platelet Endothelial Aggregation Receptor 1 Gene Results in Endothelial Dysfunction by Fisch, Adam S, Yerges-Armstrong, Laura M, Backman, Joshua D, Wang, Hong, Donnelly, Patrick, Ryan, Kathleen A, Parihar, Ankita, Pavlovich, Mary A, Mitchell, Braxton D, O'Connell, Jeffrey R, Herzog, William, Harman, Christopher R, Wren, Jonathan D, Lewis, Joshua P

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KCNJ11 variants and their effect on the association between serum potassium and diabetes risk in the Atherosclerosis Risk in Communities (ARIC) Study and Jackson Heart Study (JHS)... by Chatterjee, Ranee, Davenport, Clemontina A, Raffield, Laura M, Maruthur, Nisa, Lange, Leslie, Selvin, Elizabeth, Butler, Kenneth, Yeh, Hsin-Chieh, Wilson, James G, Correa, Adolfo, Edelman, David, Hauser, Elizabeth

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Effects of APOA5 -1131T>C (rs662799) on fasting plasma lipids and risk of metabolic syndrome: evidence from a case-control study in China and a meta-analysis by Xu, Chunxiao, Bai, Rongpan, Zhang, Dandan, Li, Zhenli, Zhu, Honghong, Lai, Maode, Zhu, Yimin

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Genetic Determinants of Pelvic Organ Prolapse among African American and Hispanic Women in the Women's Health Initiative by Giri, Ayush, Wu, Jennifer M, Ward, Renee M, Hartmann, Katherine E, Park, Amy J, North, Kari E, Graff, Mariaelisa, Wallace, Robert B, Bareh, Gihan, Qi, Lihong, O'Sullivan, Mary J, Reiner, Alexander P, Edwards, Todd L, Velez Edwards, Digna R

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Common Genetic Variants in FOXP2 Are Not Associated with Individual Differences in Language Development by Mueller, Kathryn L, Murray, Jeffrey C, Michaelson, Jacob J, Christiansen, Morten H, Reilly, Sheena, Tomblin, J Bruce

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Targeted deep resequencing identifies coding variants in the PEAR1 gene that play a role in platelet aggregation by Kim, Yoonhee, Suktitipat, Bhoom, Yanek, Lisa R, Faraday, Nauder, Wilson, Alexander F, Becker, Diane M, Becker, Lewis C, Mathias, Rasika A

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APOL1 risk alleles among individuals with CKD in Northern Tanzania: A pilot study by Stanifer, John W, Karia, Francis, Maro, Venance, Kilonzo, Kajiru, Qin, Xuejun, Patel, Uptal D, Hauser, Elizabeth R

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The Integration of Epistasis Network and Functional Interactions in a GWAS Implicates RXR Pathway Genes in the Immune Response to Smallpox Vaccine by McKinney, Brett A, Lareau, Caleb, Oberg, Ann L, Kennedy, Richard B, Ovsyannikova, Inna G, Poland, Gregory A

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Genetic variation in SULF2 is associated with postprandial clearance of triglyceride-rich remnant particles and triglyceride levels in healthy subjects by Matikainen, Niina, Burza, Maria Antonella, Romeo, Stefano, Hakkarainen, Antti, Adiels, Martin, Folkersen, Lasse, Eriksson, Per, Lundbom, Nina, Ehrenborg, Ewa, Orho-Melander, Marju, Taskinen, Marja-Riitta, Borén, Jan

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