A pragmatic view on pragmatic trials

por Patsopoulos, Nikolaos A.
Publicado 2011

The use of older studies in meta-analyses of medical interventions: a survey

por Patsopoulos, Nikolaos A, Ioannidis, John PA
Publicado 2009

Heterogeneity in Meta-Analyses of Genome-Wide Association Investigations

por Ioannidis, John P.A., Patsopoulos, Nikolaos A., Evangelou, Evangelos
Publicado 2007

Selection and Presentation of Imaging Figures in the Medical Literature

por Siontis, George C. M., Patsopoulos, Nikolaos A., Vlahos, Antonios P., Ioannidis, John P. A.
Publicado 2010

International ranking systems for universities and institutions: a critical appraisal

por Ioannidis, John PA, Patsopoulos, Nikolaos A, Kavvoura, Fotini K, Tatsioni, Athina, Evangelou, Evangelos, Kouri, Ioanna, Contopoulos-Ioannidis, Despina G, Liberopoulos, George
Publicado 2007

Limited statistical evidence for shared genetic effects of eQTLs and autoimmune disease-associated loci in three major immune cell types

por Chun, Sung, Casparino, Alexandra, Patsopoulos, Nikolaos A, Croteau-Chonka, Damien C, Raby, Benjamin A, De Jager, Philip L, Sunyaev, Shamil R, Cotsapas, Chris
Publicado 2017

Reporting of Human Genome Epidemiology (HuGE) association studies: An empirical assessment

por Yesupriya, Ajay, Evangelou, Evangelos, Kavvoura, Fotini K, Patsopoulos, Nikolaos A, Clyne, Melinda, Walsh, Matthew C, Lin, Bruce K, Yu, Wei, Gwinn, Marta, Ioannidis, John PA, Khoury, Muin J
Publicado 2008

Two genetic variants explain the association of European ancestry with multiple sclerosis risk in African-Americans

por Nakatsuka, Nathan, Patterson, Nick, Patsopoulos, Nikolaos A., Altemose, Nicolas, Tandon, Arti, Beecham, Ashley H., McCauley, Jacob L., Isobe, Noriko, Hauser, Stephen, De Jager, Philip L., Hafler, David A., Oksenberg, Jorge R., Reich, David
Publicado 2020

Time-Dependent Changes in Microglia Transcriptional Networks Following Traumatic Brain Injury

por Izzy, Saef, Liu, Qiong, Fang, Zhou, Lule, Sevda, Wu, Limin, Chung, Joon Yong, Sarro-Schwartz, Aliyah, Brown-Whalen, Alexander, Perner, Caroline, Hickman, Suzanne E., Kaplan, David L., Patsopoulos, Nikolaos A., El Khoury, Joseph, Whalen, Michael J.
Publicado 2019

Dissection of multiple sclerosis genetics identifies B and CD4+ T cells as driver cell subsets

por Guo, Michael H., Sama, Prashanth, LaBarre, Brenna A., Lokhande, Hrishikesh, Balibalos, John, Chu, Ci, Du, Xiaomi, Kheradpour, Pouya, Kim, Charles C., Oniskey, Taylor, Snyder, Thomas, Soghoian, Damien Z., Weiner, Howard L., Chitnis, Tanuja, Patsopoulos, Nikolaos A.
Publicado 2022

Mother−child histocompatibility and risk of rheumatoid arthritis and systemic lupus erythematosus among mothers

por Cruz, Giovanna I., Shao, Xiaorong, Quach, Hong, Quach, Diana, Ho, Kimberly A., Sterba, Kirsten, Noble, Janelle A., Patsopoulos, Nikolaos A., Busch, Michael P., Triulzi, Darrell J., Ladas, Nektarios, Blasczyk, Rainer, Wong, Wendy S. W., Solomon, Benjamin D., Niederhuber, John E., Criswell, Lindsey A., Barcellos, Lisa F.
Publicado 2019

Characterization of CD41(+) cells in the lymph node

por Dai, Li, Uehara, Mayuko, Li, Xiaofei, LaBarre, Brenna A., Banouni, Naima, Ichimura, Takaharu, Lee-Sundlov, Melissa M., Kasinath, Vivek, Sullivan, Jade A., Ni, Heyu, Barone, Francesca, Giannini, Silvia, Bahmani, Baharak, Sage, Peter T., Patsopoulos, Nikolaos A., Tsokos, George C., Bromberg, Jonathan S., Hoffmeister, Karin, Jiang, Liwei, Abdi, Reza
Publicado 2022

Fine-Mapping the Genetic Association of the Major Histocompatibility Complex in Multiple Sclerosis: HLA and Non-HLA Effects

por Patsopoulos, Nikolaos A., Barcellos, Lisa F., Hintzen, Rogier Q., Schaefer, Catherine, van Duijn, Cornelia M., Noble, Janelle A., Raj, Towfique, Gourraud, Pierre-Antoine, Stranger, Barbara E., Oksenberg, Jorge, Olsson, Tomas, Taylor, Bruce V., Sawcer, Stephen, Hafler, David A., Carrington, Mary, De Jager, Philip L., de Bakker, Paul I. W.
Publicado 2013

Ancestral risk modification for multiple sclerosis susceptibility detected across the Major Histocompatibility Complex in a multi-ethnic population

por Beecham, Ashley H., Amezcua, Lilyana, Chinea, Angel, Manrique, Clara P., Gomez, Lissette, Martinez, Andrea, Beecham, Gary W., Patsopoulos, Nikolaos A., Chitnis, Tanuja, Weiner, Howard L., De Jager, Philip L., Burchard, Esteban G., Lund, Brett T., Fitzgerald, Kathryn C., Calabresi, Peter A., Delgado, Silvia R., Oksenberg, Jorge R., McCauley, Jacob L.
Publicado 2022

Genetic and Epigenetic Fine-Mapping of Causal Autoimmune Disease Variants

por Farh, Kyle Kai-How, Marson, Alexander, Zhu, Jiang, Kleinewietfeld, Markus, Housley, William J., Beik, Samantha, Shoresh, Noam, Whitton, Holly, Ryan, Russell J.H., Shishkin, Alexander A., Hatan, Meital, Carrasco-Alfonso, Marlene J., Mayer, Dita, Luckey, C. John, Patsopoulos, Nikolaos A., De Jager, Philip L., Kuchroo, Vijay K., Epstein, Charles B, Daly, Mark J., Hafler, David A., Bernstein, Bradley E.
Publicado 2014

Correction to: A multi-step genomic approach prioritized TBKBP1 gene as relevant for multiple sclerosis susceptibility

por Sorosina, Melissa, Barizzone, Nadia, Clarelli, Ferdinando, Anand, Santosh, Lupoli, Sara, Salvi, Erika, Mangano, Eleonora, Bordoni, Roberta, Roostaei, Tina, Mascia, Elisabetta, Zuccalà, Miriam, Vecchio, Domizia, Cavalla, Paola, Santoro, Silvia, Ferrè, Laura, Zollo, Alen, Barlassina, Cristina, Cusi, Daniele, Martinelli, Vittorio, Comi, Giancarlo, Leone, Maurizio, Filippi, Massimo, Patsopoulos, Nikolaos A., De Jager, Philip L., De Bellis, Gianluca, Esposito, Federica, D’Alfonso, Sandra, Martinelli Boneschi, Filippo
Publicado 2022

A multi-step genomic approach prioritized TBKBP1 gene as relevant for multiple sclerosis susceptibility

por Sorosina, Melissa, Barizzone, Nadia, Clarelli, Ferdinando, Anand, Santosh, Lupoli, Sara, Salvi, Erika, Mangano, Eleonora, Bordoni, Roberta, Roostaei, Tina, Mascia, Elisabetta, Zuccalà, Miriam, Vecchio, Domizia, Cavalla, Paola, Santoro, Silvia, Ferrè, Laura, Zollo, Alen, Barlassina, Cristina, Cusi, Daniele, Martinelli, Vittorio, Comi, Giancarlo, Leone, Maurizio, Filippi, Massimo, Patsopoulos, Nikolaos A., De Jager, Philip L., De Bellis, Gianluca, Esposito, Federica, D’Alfonso, Sandra, Martinelli Boneschi, Filippo
Publicado 2022

A genome-wide association study identifies only two ancestry specific variants associated with spontaneous preterm birth

por Rappoport, Nadav, Toung, Jonathan, Hadley, Dexter, Wong, Ronald J., Fujioka, Kazumichi, Reuter, Jason, Abbott, Charles W., Oh, Sam, Hu, Donglei, Eng, Celeste, Huntsman, Scott, Bodian, Dale L., Niederhuber, John E., Hong, Xiumei, Zhang, Ge, Sikora-Wohfeld, Weronika, Gignoux, Christopher R., Wang, Hui, Oehlert, John, Jelliffe-Pawlowski, Laura L., Gould, Jeffrey B., Darmstadt, Gary L., Wang, Xiaobin, Bustamante, Carlos D., Snyder, Michael P., Ziv, Elad, Patsopoulos, Nikolaos A., Muglia, Louis J., Burchard, Esteban, Shaw, Gary M., O’Brodovich, Hugh M., Stevenson, David K., Butte, Atul J., Sirota, Marina
Publicado 2018

Multiple sclerosis risk loci and disease severity in 7,125 individuals from 10 studies

por George, Michaela F., Briggs, Farren B.S., Shao, Xiaorong, Gianfrancesco, Milena A., Kockum, Ingrid, Harbo, Hanne F., Celius, Elisabeth G., Bos, Steffan D., Hedström, Anna, Shen, Ling, Bernstein, Allan, Alfredsson, Lars, Hillert, Jan, Olsson, Tomas, Patsopoulos, Nikolaos A., De Jager, Philip L., Oturai, Annette B., Søndergaard, Helle B., Sellebjerg, Finn, Sorensen, Per S., Gomez, Refujia, Caillier, Stacy J., Cree, Bruce A.C., Oksenberg, Jorge R., Hauser, Stephen L., D'Alfonso, Sandra, Leone, Maurizio A., Boneschi, Filippo Martinelli, Sorosina, Melissa, van der Mei, Ingrid, Taylor, Bruce V., Zhou, Yuan, Schaefer, Catherine, Barcellos, Lisa F.
Publicado 2016

An integrated clinical program and crowdsourcing strategy for genomic sequencing and Mendelian disease gene discovery

por Haghighi, Alireza, Krier, Joel B., Toth-Petroczy, Agnes, Cassa, Christopher A., Frank, Natasha Y., Carmichael, Nikkola, Fieg, Elizabeth, Bjonnes, Andrew, Mohanty, Anwoy, Briere, Lauren C., Lincoln, Sharyn, Lucia, Stephanie, Gupta, Vandana A., Söylemez, Onuralp, Sutti, Sheila, Kooshesh, Kameron, Qiu, Haiyan, Fay, Christopher J., Perroni, Victoria, Valerius, Jamie, Hanna, Meredith, Frank, Alexander, Ouahed, Jodie, Snapper, Scott B., Pantazi, Angeliki, Chopra, Sameer S., Leshchiner, Ignaty, Stitziel, Nathan O., Feldweg, Anna, Mannstadt, Michael, Loscalzo, Joseph, Sweetser, David A., Liao, Eric, Stoler, Joan M., Nowak, Catherine B., Sanchez-Lara, Pedro A., Klein, Ophir D., Perry, Hazel, Patsopoulos, Nikolaos A., Raychaudhuri, Soumya, Goessling, Wolfram, Green, Robert C., Seidman, Christine E., MacRae, Calum A., Sunyaev, Shamil R., Maas, Richard L., Vuzman, Dana
Publicado 2018