Using Machine Learning to Evaluate the Value of Genetic Liabilities in the Classification of Hypertension within the UK Biobank.

Autor: MacCarthy, Gideon¹ (AUTHOR), Pazoki, Raha^1,2 (AUTHOR) raha.pazoki@brunel.ac.uk

Publikováno v: Journal of Clinical Medicine. May2024, Vol. 13 Issue 10, p2955. 20p.

Effects of a community-based healthy heart program on increasing healthy women's physical activity: a randomized controlled trial guided by Community-based Participatory Research (CBPR)

Autor: Seyednezami Nasrin, Nabipour Iraj, Pazoki Raha, Imami Seyed

Publikováno v: BMC Public Health, Vol 7, Iss 1, p 216 (2007)

Abstract Background Cardiovascular disease remains the leading killer of women in most developed areas of the world. Rates of physical inactivity and poor nutrition, which are two of the most important modifiable risk factors for cardiovascular disea

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PCSK9 genetic variants and risk of type 2 diabetes: a mendelian randomisation study

Autor: Schmidt, Amand F, Swerdlow, Daniel I, Holmes, Michael V, Patel, Riyaz S, Fairhurst-Hunter, Zammy, Lyall, Donald M, Hartwig, Fernando Pires, Horta, Bernardo Lessa, Hyppönen, Elina, Power, Christine, Moldovan, Max, van Iperen, Erik, Hovingh, G Kees, Demuth, Ilja, Norman, Kristina, Steinhagen-Thiessen, Elisabeth, Demuth, Juri, Bertram, Lars, Liu, Tian, Coassin, Stefan, Willeit, Johann, Kiechl, Stefan, Willeit, Karin, Mason, Dan, Wright, John, Morris, Richard, Wanamethee, Goya, Whincup, Peter, Ben-Shlomo, Yoav, McLachlan, Stela, Price, Jackie F, Kivimaki, Mika, Welch, Catherine, Sanchez-Galvez, Adelaida, Marques-Vidal, Pedro, Nicolaides, Andrew, Panayiotou, Andrie G, Onland-Moret, N Charlotte, van der Schouw, Yvonne T, Matullo, Giuseppe, Fiorito, Giovanni, Guarrera, Simonetta, Sacerdote, Carlotta, Wareham, Nicholas J, Langenberg, Claudia, Scott, Robert, Luan, Jian'an, Bobak, Martin, Malyutina, Sofia, Pająk, Andrzej, Kubinova, Ruzena, Tamosiunas, Abdonas, Pikhart, Hynek, Husemoen, Lise Lotte Nystrup, Grarup, Niels, Pedersen, Oluf, Hansen, Torben, Linneberg, Allan, Simonsen, Kenneth Starup, Cooper, Jackie, Humphries, Steve E, Brilliant, Murray, Kitchner, Terrie, Hakonarson, Hakon, Carrell, David S, McCarty, Catherine A, Kirchner, H Lester, Larson, Eric B, Crosslin, David R, de Andrade, Mariza, Roden, Dan M, Denny, Joshua C, Carty, Cara, Hancock, Stephen, Attia, John, Holliday, Elizabeth, O'Donnell, Martin, Yusuf, Salim, Chong, Michael, Pare, Guillaume, van der Harst, Pim, Said, M Abdullah, Eppinga, Ruben N, Verweij, Niek, Snieder, Harold, Christen, Tim, Mook-Kanamori, Dennis O, Gustafsson, Stefan, Lind, Lars, Ingelsson, Erik, Pazoki, Raha, Franco, Oscar, Hofman, Albert, Uitterlinden, Andre, Dehghan, Abbas, Teumer, Alexander, Baumeister, Sebastian, Dörr, Marcus, Lerch, Markus M, Völker, Uwe, Völzke, Henry, Ward, Joey, Pell, Jill P, Smith, Daniel J, Meade, Tom, Maitland-van der Zee, Anke H, Baranova, Ekaterina V, Young, Robin, Ford, Ian, Campbell, Archie, Padmanabhan, Sandosh, Bots, Michiel L, Grobbee, Diederick E, Froguel, Philippe, Thuillier, Dorothée, Balkau, Beverley, Bonnefond, Amélie, Cariou, Bertrand, Smart, Melissa, Bao, Yanchun, Kumari, Meena, Mahajan, Anubha, Ridker, Paul M, Chasman, Daniel I, Reiner, Alex P, Lange, Leslie A, Ritchie, Marylyn D, Asselbergs, Folkert W, Casas, Juan-Pablo, Keating, Brendan J, Preiss, David, Hingorani, Aroon D, Sattar, Naveed

Publikováno v: In The Lancet Diabetes & Endocrinology February 2017 5(2):97-105

Exome Genotyping Identifies Pleiotropic Variants Associated with Red Blood Cell Traits

Autor: Chami, Nathalie, Chen, Ming-Huei, Slater, Andrew J., Eicher, John D., Evangelou, Evangelos, Tajuddin, Salman M., Love-Gregory, Latisha, Kacprowski, Tim, Schick, Ursula M., Nomura, Akihiro, Giri, Ayush, Lessard, Samuel, Brody, Jennifer A., Schurmann, Claudia, Pankratz, Nathan, Yanek, Lisa R., Manichaikul, Ani, Pazoki, Raha, Mihailov, Evelin, Hill, W. David, Raffield, Laura M., Burt, Amber, Bartz, Traci M., Becker, Diane M., Becker, Lewis C., Boerwinkle, Eric, Bork-Jensen, Jette, Bottinger, Erwin P., O’Donoghue, Michelle L., Crosslin, David R., de Denus, Simon, Dubé, Marie-Pierre, Elliott, Paul, Engström, Gunnar, Evans, Michele K., Floyd, James S., Fornage, Myriam, Gao, He, Greinacher, Andreas, Gudnason, Vilmundur, Hansen, Torben, Harris, Tamara B., Hayward, Caroline, Hernesniemi, Jussi, Highland, Heather M., Hirschhorn, Joel N., Hofman, Albert, Irvin, Marguerite R., Kähönen, Mika, Lange, Ethan, Launer, Lenore J., Lehtimäki, Terho, Li, Jin, Liewald, David C.M., Linneberg, Allan, Liu, Yongmei, Lu, Yingchang, Lyytikäinen, Leo-Pekka, Mägi, Reedik, Mathias, Rasika A., Melander, Olle, Metspalu, Andres, Mononen, Nina, Nalls, Mike A., Nickerson, Deborah A., Nikus, Kjell, O’Donnell, Chris J., Orho-Melander, Marju, Pedersen, Oluf, Petersmann, Astrid, Polfus, Linda, Psaty, Bruce M., Raitakari, Olli T., Raitoharju, Emma, Richard, Melissa, Rice, Kenneth M., Rivadeneira, Fernando, Rotter, Jerome I., Schmidt, Frank, Smith, Albert Vernon, Starr, John M., Taylor, Kent D., Teumer, Alexander, Thuesen, Betina H., Torstenson, Eric S., Tracy, Russell P., Tzoulaki, Ioanna, Zakai, Neil A., Vacchi-Suzzi, Caterina, van Duijn, Cornelia M., van Rooij, Frank J.A., Cushman, Mary, Deary, Ian J., Velez Edwards, Digna R., Vergnaud, Anne-Claire, Wallentin, Lars, Waterworth, Dawn M., White, Harvey D., Wilson, James G., Zonderman, Alan B., Kathiresan, Sekar, Grarup, Niels, Esko, Tõnu, Loos, Ruth J.F., Lange, Leslie A., Faraday, Nauder, Abumrad, Nada A., Edwards, Todd L., Ganesh, Santhi K., Auer, Paul L., Johnson, Andrew D., Reiner, Alexander P., Lettre, Guillaume

Publikováno v: In The American Journal of Human Genetics 7 July 2016 99(1):8-21