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 (...

av Pazoki, Raha, Nabipour, Iraj, Seyednezami, Nasrin, Imami, Seyed Reza
Publicerad 2007

Genetic Basis of Ventricular Arrhythmias

av Pazoki, Raha, Wilde, Arthur A. M., Bezzina, Connie R.
Publicerad 2010

The association of metabolic syndrome and Chlamydia pneumoniae, Helicobacter pylori, cytomegalovirus, and herpes simplex virus type 1: The Persian Gulf Healthy Heart Study

av Nabipour, Iraj, Vahdat, Katayon, Jafari, Seyed Mojtaba, Pazoki, Raha, Sanjdideh, Zahra
Publicerad 2006

Alcohol consumption in the general population is associated with structural changes in multiple organ systems

av Evangelou, Evangelos, Suzuki, Hideaki, Bai, Wenjia, Pazoki, Raha, Gao, He, Matthews, Paul M, Elliott, Paul
I publikationen eLife (2021)

Phenome-wide and genome-wide analyses of quality of life in schizophrenia

av Pazoki, Raha, Lin, Bochao Danae, van Eijk, Kristel R., Schijven, Dick, de Zwarte, Sonja, Guloksuz, Sinan, Luykx, Jurjen J.
I publikationen BJPsych Open (2020)

Phenome-wide and genome-wide analyses of quality of life in schizophrenia – ERRATUM

av Pazoki, Raha, Lin, Bochao Danae, van Eijk, Kristel R., Schijven, Dick, de Zwarte, Sonja, Guloksuz, Sinan, Luykx, Jurjen J.
I publikationen BJPsych Open (2021)

Oncogenic human papillomavirus genital infection in southern Iranian women: population-based study versus clinic-based data

av Eghbali, Seyed Sajjad, Amirinejad, Roya, Obeidi, Narges, Mosadeghzadeh, Shiva, Vahdat, Katayoun, Azizi, Fatemeh, Pazoki, Raha, Sanjdideh, Zahra, Amiri, Zahra, Nabipour, Iraj, Zandi, Keivan
Publicerad 2012

GWAS for urinary sodium and potassium excretion highlights pathways shared with cardiovascular traits

av Pazoki, Raha, Evangelou, Evangelos, Mosen-Ansorena, David, Pinto, Rui Climaco, Karaman, Ibrahim, Blakeley, Paul, Gill, Dipender, Zuber, Verena, Elliott, Paul, Tzoulaki, Ioanna, Dehghan, Abbas
I publikationen Nat Commun (2019)

SNPs Identified as Modulators of ECG Traits in the General Population Do Not Markedly Affect ECG Traits during Acute Myocardial Infarction nor Ventricular Fibrillation Risk in This...

av Pazoki, Raha, de Jong, Jonas S.S.G., Marsman, Roos F., Bruinsma, Nienke, Dekker, Lukas R. C., Wilde, Arthur A. M., Bezzina, Connie R., Tanck, Michael W. T.
Publicerad 2013

The global impact of non-communicable diseases on macro-economic productivity: a systematic review

av Chaker, Layal, Falla, Abby, van der Lee, Sven J., Muka, Taulant, Imo, David, Jaspers, Loes, Colpani, Veronica, Mendis, Shanthi, Chowdhury, Rajiv, Bramer, Wichor M., Pazoki, Raha, Franco, Oscar H.
I publikationen Eur J Epidemiol (2015)

No association between gluten sensitivity and amyotrophic lateral sclerosis

av Visser, Anne E., Pazoki, Raha, Pulit, Sara L., van Rheenen, Wouter, Raaphorst, Joost, van der Kooi, Anneke J., Ricaño-Ponce, Isis, Wijmenga, Cisca, Otten, Henny G., Veldink, Jan H., van den Berg, Leonard H.
I publikationen J Neurol (2017)

Determinants of accelerated metabolomic and epigenetic aging in a UK cohort

av Robinson, Oliver, Chadeau Hyam, Marc, Karaman, Ibrahim, Climaco Pinto, Rui, Ala-Korpela, Mika, Handakas, Evangelos, Fiorito, Giovanni, Gao, He, Heard, Andy, Jarvelin, Marjo‐Riitta, Lewis, Matthew, Pazoki, Raha, Polidoro, Silvia, Tzoulaki, Ioanna, Wielscher, Matthias, Elliott, Paul, Vineis, Paolo
I publikationen Aging Cell (2020)

Genome-wide association study identifies a susceptibility locus at 21q21 for ventricular fibrillation in acute myocardial infarction

av Bezzina, Connie R, Pazoki, Raha, Bardai, Abdennasser, Marsman, Roos F, de Jong, Jonas S S G, Blom, Marieke T, Scicluna, Brendon P, Jukema, J Wouter, Bindraban, Navin R, Lichtner, Peter, Pfeufer, Arne, Bishopric, Nanette H, Roden, Dan M, Meitinger, Thomas, Chugh, Sumeet S, Myerburg, Robert J, Jouven, Xavier, Kääb, Stefan, Dekker, Lukas R C, Tan, Hanno L, Tanck, Michael W T, Wilde, Arthur A M
Publicerad 2010

Genetic analysis in European ancestry individuals identifies 517 loci associated with liver enzymes

av Pazoki, Raha, Vujkovic, Marijana, Elliott, Joshua, Evangelou, Evangelos, Gill, Dipender, Ghanbari, Mohsen, van der Most, Peter J., Pinto, Rui Climaco, Wielscher, Matthias, Farlik, Matthias, Zuber, Verena, de Knegt, Robert J., Snieder, Harold, Uitterlinden, André G., Lynch, Julie A., Jiang, Xiyun, Said, Saredo, Kaplan, David E., Lee, Kyung Min, Serper, Marina, Carr, Rotonya M., Tsao, Philip S., Atkinson, Stephen R., Dehghan, Abbas, Tzoulaki, Ioanna, Ikram, M. Arfan, Herzig, Karl-Heinz, Järvelin, Marjo-Riitta, Alizadeh, Behrooz Z., O’Donnell, Christopher J., Saleheen, Danish, Voight, Benjamin F., Chang, Kyong-Mi, Thursz, Mark R., Elliott, Paul
I publikationen Nat Commun (2021)

Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis

av Polfus, Linda M., Khajuria, Rajiv K., Schick, Ursula M., Pankratz, Nathan, Pazoki, Raha, Brody, Jennifer A., Chen, Ming-Huei, Auer, Paul L., Floyd, James S., Huang, Jie, Lange, Leslie, van Rooij, Frank J.A., Gibbs, Richard A., Metcalf, Ginger, Muzny, Donna, Veeraraghavan, Narayanan, Walter, Klaudia, Chen, Lu, Yanek, Lisa, Becker, Lewis C., Peloso, Gina M., Wakabayashi, Aoi, Kals, Mart, Metspalu, Andres, Esko, Tõnu, Fox, Keolu, Wallace, Robert, Franceshini, Nora, Matijevic, Nena, Rice, Kenneth M., Bartz, Traci M., Lyytikäinen, Leo-Pekka, Kähönen, Mika, Lehtimäki, Terho, Raitakari, Olli T., Li-Gao, Ruifang, Mook-Kanamori, Dennis O., Lettre, Guillaume, van Duijn, Cornelia M., Franco, Oscar H., Rich, Stephen S., Rivadeneira, Fernando, Hofman, Albert, Uitterlinden, André G., Wilson, James G., Psaty, Bruce M., Soranzo, Nicole, Dehghan, Abbas, Boerwinkle, Eric, Zhang, Xiaoling, Johnson, Andrew D., O’Donnell, Christopher J., Johnsen, Jill M., Reiner, Alexander P., Ganesh, Santhi K., Sankaran, Vijay G.
I publikationen Am J Hum Genet (2016)

Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human Hematopoiesis

av Polfus, Linda M., Khajuria, Rajiv K., Schick, Ursula M., Pankratz, Nathan, Pazoki, Raha, Brody, Jennifer A., Chen, Ming-Huei, Auer, Paul L., Floyd, James S., Huang, Jie, Lange, Leslie, van Rooij, Frank J.A., Gibbs, Richard A., Metcalf, Ginger, Muzny, Donna, Veeraraghavan, Narayanan, Walter, Klaudia, Chen, Lu, Yanek, Lisa, Becker, Lewis C., Peloso, Gina M., Wakabayashi, Aoi, Kals, Mart, Metspalu, Andres, Esko, Tõnu, Fox, Keolu, Wallace, Robert, Franceschini, Nora, Matijevic, Nena, Rice, Kenneth M., Bartz, Traci M., Lyytikäinen, Leo-Pekka, Kähönen, Mika, Lehtimäki, Terho, Raitakari, Olli T., Li-Gao, Ruifang, Mook-Kanamori, Dennis O., Lettre, Guillaume, van Duijn, Cornelia M., Franco, Oscar H., Rich, Stephen S., Rivadeneira, Fernando, Hofman, Albert, Uitterlinden, André G., Wilson, James G., Psaty, Bruce M., Soranzo, Nicole, Dehghan, Abbas, Boerwinkle, Eric, Zhang, Xiaoling, Johnson, Andrew D., O’Donnell, Christopher J., Johnsen, Jill M., Reiner, Alexander P., Ganesh, Santhi K., Sankaran, Vijay G.
I publikationen Am J Hum Genet (2016)

Identification of a Sudden Cardiac Death Susceptibility Locus at 2q24.2 through Genome-Wide Association in European Ancestry Individuals

av Arking, Dan E., Junttila, M. Juhani, Goyette, Philippe, Huertas-Vazquez, Adriana, Eijgelsheim, Mark, Blom, Marieke T., Newton-Cheh, Christopher, Reinier, Kyndaron, Teodorescu, Carmen, Uy-Evanado, Audrey, Carter-Monroe, Naima, Kaikkonen, Kari S., Kortelainen, Marja-Leena, Boucher, Gabrielle, Lagacé, Caroline, Moes, Anna, Zhao, XiaoQing, Kolodgie, Frank, Rivadeneira, Fernando, Hofman, Albert, Witteman, Jacqueline C. M., Uitterlinden, André G., Marsman, Roos F., Pazoki, Raha, Bardai, Abdennasser, Koster, Rudolph W., Dehghan, Abbas, Hwang, Shih-Jen, Bhatnagar, Pallav, Post, Wendy, Hilton, Gina, Prineas, Ronald J., Li, Man, Köttgen, Anna, Ehret, Georg, Boerwinkle, Eric, Coresh, Josef, Kao, W. H. Linda, Psaty, Bruce M., Tomaselli, Gordon F., Sotoodehnia, Nona, Siscovick, David S., Burke, Greg L., Marbán, Eduardo, Spooner, Peter M., Cupples, L. Adrienne, Jui, Jonathan, Gunson, Karen, Kesäniemi, Y. Antero, Wilde, Arthur A. M., Tardif, Jean-Claude, O'Donnell, Christopher J., Bezzina, Connie R., Virmani, Renu, Stricker, Bruno H. C. h., Tan, Hanno L., Albert, Christine M., Chakravarti, Aravinda, Rioux, John D., Huikuri, Heikki V., Chugh, Sumeet S.
Publicerad 2011

Discovery and refinement of genetic loci associated with cardiometabolic risk using dense imputation maps

av Iotchkova, Valentina, Huang, Jie, Morris, John A., Jain, Deepti, Barbieri, Caterina, Walter, Klaudia, Min, Josine L., Chen, Lu, Astle, William, Cocca, Massimilian, Deelen, Patrick, Elding, Heather, Farmaki, Aliki-Eleni, Franklin, Christopher S., Franberg, Mattias, Gaunt, Tom R., Hofman, Albert, Jiang, Tao, Kleber, Marcus E., Lachance, Genevieve, Luan, Jian'an, Malerba, Giovanni, Matchan, Angela, Mead, Daniel, Memari, Yasin, Ntalla, Ioanna, Panoutsopoulou, Kalliope, Pazoki, Raha, Perry, John R.B., Rivadeneira, Fernando, Sabater-Lleal, Maria, Sennblad, Bengt, Shin, So-Youn, Southam, Lorraine, Traglia, Michela, van Dijk, Freerk, van Leeuwen, Elisabeth M., Zaza, Gianluigi, Zhang, Weihua, Amin, Najaf, Butterworth, Adam, Chambers, John C., Dedoussis, George, Dehghan, Abbas, Franco, Oscar H., Franke, Lude, Frontini, Mattia, Gambaro, Giovanni, Gasparini, Paolo, Hamsten, Anders, Issacs, Aaron, Kooner, Jaspal S., Kooperberg, Charles, Langenberg, Claudia, Marz, Winfried, Scott, Robert A., Swertz, Morris A., Toniolo, Daniela, Uitterlinden, Andre G., van Duijn, Cornelia M., Watkins, Hugh, Zeggini, Eleftheria, Maurano, Mathew T., Timpson, Nicholas J., Reiner, Alexander P., Auer, Paul L., Soranzo, Nicole
I publikationen Nat Genet (2016)

A comprehensive evaluation of the genetic architecture of sudden cardiac arrest

av Ashar, Foram N, Mitchell, Rebecca N, Albert, Christine M, Newton-Cheh, Christopher, Brody, Jennifer A, Müller-Nurasyid, Martina, Moes, Anna, Meitinger, Thomas, Mak, Angel, Huikuri, Heikki, Junttila, M Juhani, Goyette, Philippe, Pulit, Sara L, Pazoki, Raha, Tanck, Michael W, Blom, Marieke T, Zhao, XiaoQing, Havulinna, Aki S, Jabbari, Reza, Glinge, Charlotte, Tragante, Vinicius, Escher, Stefan A, Chakravarti, Aravinda, Ehret, Georg, Coresh, Josef, Li, Man, Prineas, Ronald J, Franco, Oscar H, Kwok, Pui-Yan, Lumley, Thomas, Dumas, Florence, McKnight, Barbara, Rotter, Jerome I, Lemaitre, Rozenn N, Heckbert, Susan R, O’Donnell, Christopher J, Hwang, Shih-Jen, Tardif, Jean-Claude, VanDenburgh, Martin, Uitterlinden, André G, Hofman, Albert, Stricker, Bruno H C, de Bakker, Paul I W, Franks, Paul W, Jansson, Jan-Hakan, Asselbergs, Folkert W, Halushka, Marc K, Maleszewski, Joseph J, Tfelt-Hansen, Jacob, Engstrøm, Thomas, Salomaa, Veikko, Virmani, Renu, Kolodgie, Frank, Wilde, Arthur A M, Tan, Hanno L, Bezzina, Connie R, Eijgelsheim, Mark, Rioux, John D, Jouven, Xavier, Kääb, Stefan, Psaty, Bruce M, Siscovick, David S, Arking, Dan E, Sotoodehnia, Nona
I publikationen Eur Heart J (2018)

Meta-analysis of rare and common exome chip variants identifies S1PR4 and other loci influencing blood cell traits

av Pankratz, Nathan, Schick, Ursula M, Zhou, Yi, Zhou, Wei, Ahluwalia, Tarunveer Singh, Allende, Maria Laura, Auer, Paul L, Bork-Jensen, Jette, Brody, Jennifer A, Chen, Ming-Huei, Clavo, Vinna, Eicher, John D, Grarup, Niels, Hagedorn, Elliott J, Hu, Bella, Hunker, Kristina, Johnson, Andrew D, Leusink, Maarten, Lu, Yingchang, Lyytikäinen, Leo-Pekka, Manichaikul, Ani, Marioni, Riccardo E, Nalls, Mike A, Pazoki, Raha, Smith, Albert Vernon, van Rooij, Frank J A, Yang, Min-Lee, Zhang, Xiaoling, Zhang, Yan, Asselbergs, Folkert W, Boerwinkle, Eric, Borecki, Ingrid B, Bottinger, Erwin P, Cushman, Mary, de Bakker, Paul I W, Deary, Ian J, Dong, Liguang, Feitosa, Mary F, Floyd, James S, Franceschini, Nora, Franco, Oscar H, Garcia, Melissa E, Grove, Megan L, Gudnason, Vilmundur, Hansen, Torben, Harris, Tamara B, Hofman, Albert, Jackson, Rebecca D, Jia, Jia, Kähönen, Mika, Launer, Lenore J, Lehtimäki, Terho, Liewald, David C, Linneberg, Allan, Liu, Yongmei, Loos, Ruth J F, Nguyen, Vy M, Numans, Mattijs E, Pedersen, Oluf, Psaty, Bruce M, Raitakari, Olli T, Rich, Stephen S, Rivadeneira, Fernando, Di Sant, Amanda M Rosa, Rotter, Jerome I, Starr, John M, Taylor, Kent D, Thuesen, Betina Heinsbæk, Tracy, Russell P, Uitterlinden, Andre G, Wang, Jiansong, Wang, Judy, Dehghan, Abbas, Huo, Yong, Cupples, L Adrienne, Wilson, James G, Proia, Richard L, Zon, Leonard I, O’Donnell, Christopher J, Reiner, Alex P, Ganesh, Santhi K
I publikationen Nat Genet (2016)