Editorial: Recent advances in nutrigenomics: Making strides towards precision nutrition

por Cole, Joanne B., Gabbianelli, Rosita
Publicado 2022

Comprehensive genomic analysis of dietary habits in UK Biobank identifies hundreds of genetic associations

por Cole, Joanne B., Florez, Jose C., Hirschhorn, Joel N.
Publicado 2020

Corrigendum: Genetic heritability as a tool to evaluate the precision of 24-hour recall dietary questionnaire variables in UK Biobank

por Cole, Joanne B., Westerman, Kenneth E., Manning, Alisa K., Florez, Jose C., Hirschhorn, Joel N.
Publicado 2023

Genetic heritability as a tool to evaluate the precision of 24-hour recall dietary questionnaire variables in UK Biobank

por Cole, Joanne B., Westerman, Kenneth E., Manning, Alisa K., Florez, Jose C., Hirschhorn, Joel N.
Publicado 2023

Cardiometabolic risk factors for COVID-19 susceptibility and severity: A Mendelian randomization analysis

por Leong, Aaron, Cole, Joanne B., Brenner, Laura N., Meigs, James B., Florez, Jose C., Mercader, Josep M.
Publicado 2021

Genome-wide analysis of copy number variants and normal facial variation in a large cohort of Bantu Africans

por Null, Megan, Yilmaz, Feyza, Astling, David, Yu, Hung-Chun, Cole, Joanne B., Hallgrímsson, Benedikt, Santorico, Stephanie A., Spritz, Richard A., Shaikh, Tamim H., Hendricks, Audrey E.
Publicado 2021

Variance-quantitative trait loci enable systematic discovery of gene-environment interactions for cardiometabolic serum biomarkers

por 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.
Publicado 2022

The comparative effect of exposure to various risk factors on the risk of hyperuricaemia: diet has a weak causal effect

por Topless, Ruth K. G., Major, Tanya J., Florez, Jose C., Hirschhorn, Joel N., Cadzow, Murray, Dalbeth, Nicola, Stamp, Lisa K., Wilcox, Philip L., Reynolds, Richard J., Cole, Joanne B., Merriman, Tony R.
Publicado 2021

Integrating untargeted metabolomics, genetically informed causal inference, and pathway enrichment to define the obesity metabolome

por Hsu, Yu-Han H., Astley, Christina M., Cole, Joanne B., Vedantam, Sailaja, Mercader, Josep M., Metspalu, Andres, Fischer, Krista, Fortney, Kristen, Morgen, Eric K., Gonzalez, Clicerio, Gonzalez, Maria E., Esko, Tonu, Hirschhorn, Joel N.
Publicado 2020

Type 2 diabetes genetic loci informed by multi-trait associations point to disease mechanisms and subtypes: A soft clustering analysis

por Udler, Miriam S., Kim, Jaegil, von Grotthuss, Marcin, Bonàs-Guarch, Sílvia, Cole, Joanne B., Chiou, Joshua, Boehnke, Michael, Laakso, Markku, Atzmon, Gil, Glaser, Benjamin, Mercader, Josep M., Gaulton, Kyle, Flannick, Jason, Getz, Gad, Florez, Jose C.
Publicado 2018

Post-translational control of beige fat biogenesis by PRDM16 stabilization

por Wang, Qiang, Li, Huixia, Tajima, Kazuki, Verkerke, Anthony R. P., Taxin, Zachary H., Hou, Zhishuai, Cole, Joanne B., Li, Fei, Wong, Jake, Abe, Ichitaro, Pradhan, Rachana N., Yamamuro, Tadashi, Yoneshiro, Takeshi, Hirschhorn, Joel N., Kajimura, Shingo
Publicado 2022

Rare variant association analysis in 51,256 type 2 diabetes cases and 370,487 controls informs the spectrum of pathogenicity of monogenic diabetes genes

por Schroeder, Philip, Mandla, Ravi, Huerta-Chagoya, Alicia, Alkanak, Ahmed, Nagy, Dorka, Szczerbinski, Lukasz, Madsen, Jesper G.S., Cole, Joanne B., Porneala, Bianca, Westerman, Kenneth, Li, Josephine H., Pollin, Toni I., Florez, Jose C., Gloyn, Anna L., Cebola, Inês, Manning, Alisa, Leong, Aaron, Udler, Miriam, Mercader, Josep M.
Publicado 2023

Genomewide Association Study of African Children Identifies Association of SCHIP1 and PDE8A with Facial Size and Shape

por Cole, Joanne B., Manyama, Mange, Kimwaga, Emmanuel, Mathayo, Joshua, Larson, Jacinda R., Liberton, Denise K., Lukowiak, Ken, Ferrara, Tracey M., Riccardi, Sheri L., Li, Mao, Mio, Washington, Prochazkova, Michaela, Williams, Trevor, Li, Hong, Jones, Kenneth L., Klein, Ophir D., Santorico, Stephanie A., Hallgrimsson, Benedikt, Spritz, Richard A.
Publicado 2016

The impact of non-additive genetic associations on age-related complex diseases

por Guindo-Martínez, Marta, Amela, Ramon, Bonàs-Guarch, Silvia, Puiggròs, Montserrat, Salvoro, Cecilia, Miguel-Escalada, Irene, Carey, Caitlin E., Cole, Joanne B., Rüeger, Sina, Atkinson, Elizabeth, Leong, Aaron, Sanchez, Friman, Ramon-Cortes, Cristian, Ejarque, Jorge, Palmer, Duncan S., Kurki, Mitja, Aragam, Krishna, Florez, Jose C., Badia, Rosa M., Mercader, Josep M., Torrents, David
Publicado 2021

Epigenome-wide meta-analysis identifies DNA methylation biomarkers associated with diabetic kidney disease

por Smyth, Laura J., Dahlström, Emma H., Syreeni, Anna, Kerr, Katie, Kilner, Jill, Doyle, Ross, Brennan, Eoin, Nair, Viji, Fermin, Damian, Nelson, Robert G., Looker, Helen C., Wooster, Christopher, Andrews, Darrell, Anderson, Kerry, McKay, Gareth J., Cole, Joanne B., Salem, Rany M., Conlon, Peter J., Kretzler, Matthias, Hirschhorn, Joel N., Sadlier, Denise, Godson, Catherine, Florez, Jose C., Forsblom, Carol, Maxwell, Alexander P., Groop, Per-Henrik, Sandholm, Niina, McKnight, Amy Jayne
Publicado 2022

Genome-wide association analyses identify 13 new susceptibility loci for generalized vitiligo

por Jin, Ying, Birlea, Stanca A, Fain, Pamela R, Ferrara, Tracey M, Ben, Songtao, Riccardi, Sheri L, Cole, Joanne B, Gowan, Katherine, Holland, Paulene J, Bennett, Dorothy C, Luiten, Rosalie M, Wolkerstorfer, Albert, van der Veen, JP Wietze, Hartmann, Anke, Eichner, Saskia, Schuler, Gerold, van Geel, Nanja, Lambert, Jo, Kemp, E Helen, Gawkrodger, David J, Weetman, Anthony P, Taïeb, Alain, Jouary, Thomas, Ezzedine, Khaled, Wallace, Margaret R, McCormack, Wayne T, Picardo, Mauro, Leone, Giovanni, Overbeck, Andreas, Silverberg, Nanette B, Spritz, Richard A
Publicado 2012

Genome-wide meta-analysis and omics integration identifies novel genes associated with diabetic kidney disease

por Sandholm, Niina, Cole, Joanne B., Nair, Viji, Sheng, Xin, Liu, Hongbo, Ahlqvist, Emma, van Zuydam, Natalie, Dahlström, Emma H., Fermin, Damian, Smyth, Laura J., Salem, Rany M., Forsblom, Carol, Valo, Erkka, Harjutsalo, Valma, Brennan, Eoin P., McKay, Gareth J., Andrews, Darrell, Doyle, Ross, Looker, Helen C., Nelson, Robert G., Palmer, Colin, McKnight, Amy Jayne, Godson, Catherine, Maxwell, Alexander P., Groop, Leif, McCarthy, Mark I., Kretzler, Matthias, Susztak, Katalin, Hirschhorn, Joel N., Florez, Jose C., Groop, Per-Henrik
Publicado 2022

The effect of LRRK2 loss-of-function variants in humans

por Whiffin, Nicola, Armean, Irina M., Kleinman, Aaron, Marshall, Jamie L., Minikel, Eric V., Goodrich, Julia K., Quaife, Nicholas M., Cole, Joanne B., Wang, Qingbo, Karczewski, Konrad J., Cummings, Beryl B., Francioli, Laurent, Laricchia, Kristen, Guan, Anna, Alipanahi, Babak, Morrison, Peter, Baptista, Marco A. S., Merchant, Kalpana M., Ware, James S., Havulinna, Aki S., Iliadou, Bozenna, Lee, Jung-Jin, Nadkarni, Girish N., Whiteman, Cole, Daly, Mark, Esko, Tõnu, Hultman, Christina, Loos, Ruth J. F., Milani, Lili, Palotie, Aarno, Pato, Carlos, Pato, Michele, Saleheen, Danish, Sullivan, Patrick F., Alföldi, Jessica, Cannon, Paul, MacArthur, Daniel G.
Publicado 2020

Type 2 Diabetes Partitioned Polygenic Scores Associate With Disease Outcomes in 454,193 Individuals Across 13 Cohorts

por DiCorpo, Daniel, LeClair, Jessica, Cole, Joanne B., Sarnowski, Chloé, Ahmadizar, Fariba, Bielak, Lawrence F., Blokstra, Anneke, Bottinger, Erwin P., Chaker, Layal, Chen, Yii-Der I., Chen, Ye, de Vries, Paul S., Faquih, Tariq, Ghanbari, Mohsen, Gudmundsdottir, Valborg, Guo, Xiuqing, Hasbani, Natalie R., Ibi, Dorina, Ikram, M. Arfan, Kavousi, Maryam, Leonard, Hampton L., Leong, Aaron, Mercader, Josep M., Morrison, Alanna C., Nadkarni, Girish N., Nalls, Mike A., Noordam, Raymond, Preuss, Michael, Smith, Jennifer A., Trompet, Stella, Vissink, Petra, Yao, Jie, Zhao, Wei, Boerwinkle, Eric, Goodarzi, Mark O., Gudnason, Vilmundur, Jukema, J. Wouter, Kardia, Sharon L.R., Loos, Ruth J.F., Liu, Ching-Ti, Manning, Alisa K., Mook-Kanamori, Dennis, Pankow, James S., Picavet, H. Susan J., Sattar, Naveed, Simonsick, Eleanor M., Verschuren, W.M. Monique, Willems van Dijk, Ko, Florez, Jose C., Rotter, Jerome I., Meigs, James B., Dupuis, Josée, Udler, Miriam S.
Publicado 2022

The power of TOPMed imputation for the discovery of Latino-enriched rare variants associated with type 2 diabetes

por Huerta-Chagoya, Alicia, Schroeder, Philip, Mandla, Ravi, Deutsch, Aaron J., Zhu, Wanying, Petty, Lauren, Yi, Xiaoyan, Cole, Joanne B., Udler, Miriam S., Dornbos, Peter, Porneala, Bianca, DiCorpo, Daniel, Liu, Ching-Ti, Li, Josephine H., Szczerbiński, Lukasz, Kaur, Varinderpal, Kim, Joohyun, Lu, Yingchang, Martin, Alicia, Eizirik, Decio L., Marchetti, Piero, Marselli, Lorella, Chen, Ling, Srinivasan, Shylaja, Todd, Jennifer, Flannick, Jason, Gubitosi-Klug, Rose, Levitsky, Lynne, Shah, Rachana, Kelsey, Megan, Burke, Brian, Dabelea, Dana M., Divers, Jasmin, Marcovina, Santica, Stalbow, Lauren, Loos, Ruth J. F., Darst, Burcu F., Kooperberg, Charles, Raffield, Laura M., Haiman, Christopher, Sun, Quan, McCormick, Joseph B., Fisher-Hoch, Susan P., Ordoñez, Maria L., Meigs, James, Baier, Leslie J., González-Villalpando, Clicerio, González-Villalpando, Maria Elena, Orozco, Lorena, García-García, Lourdes, Moreno-Estrada, Andrés, Aguilar-Salinas, Carlos A., Tusié, Teresa, Dupuis, Josée, Ng, Maggie C. Y., Manning, Alisa, Highland, Heather M., Cnop, Miriam, Hanson, Robert, Below, Jennifer, Florez, Jose C., Leong, Aaron, Mercader, Josep M.
Publicado 2023