A pragmatic view on pragmatic trials

von Patsopoulos, Nikolaos A.
Veröffentlicht 2011

Genetics of Multiple Sclerosis: An Overview and New Directions

von Patsopoulos, Nikolaos A.
Veröffentlicht in Cold Spring Harb Perspect Med (2018)

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

von Patsopoulos, Nikolaos A, Ioannidis, John PA
Veröffentlicht 2009

Genomewide meta-analysis identifies novel multiple sclerosis susceptibility loci

von Patsopoulos, Nikolaos A., de Bakker, Paul I.W.
Veröffentlicht 2011

Heterogeneous views on heterogeneity

von Patsopoulos, Nikolaos A, Evangelou, Evangelos, Ioannidis, John PA
Veröffentlicht in Int J Epidemiol (2009)

Sensitivity of between-study heterogeneity in meta-analysis: proposed metrics and empirical evaluation

von Patsopoulos, Nikolaos A, Evangelou, Evangelos, Ioannidis, John PA
Veröffentlicht in Int J Epidemiol (2008)

Heterogeneity in Meta-Analyses of Genome-Wide Association Investigations

von Ioannidis, John P.A., Patsopoulos, Nikolaos A., Evangelou, Evangelos
Veröffentlicht 2007

Uncertainty in heterogeneity estimates in meta-analyses

von Ioannidis, John P A, Patsopoulos, Nikolaos A, Evangelou, Evangelos
Veröffentlicht 2007

Origin and funding of the most frequently cited papers in medicine: database analysis

von Patsopoulos, Nikolaos A, Ioannidis, John P A, Analatos, Apostolos A
Veröffentlicht 2006

Reasons or excuses for avoiding meta-analysis in forest plots

von Ioannidis, John P A, Patsopoulos, Nikolaos A, Rothstein, Hannah R
Veröffentlicht 2008

Replication of past candidate loci for common diseases and phenotypes in 100 genome-wide association studies

von Siontis, Konstantinos C M, Patsopoulos, Nikolaos A, Ioannidis, John P A
Veröffentlicht 2010

Local Joint Testing Improves Power and Identifies Hidden Heritability in Association Studies

von Brown, Brielin C., Price, Alkes L., Patsopoulos, Nikolaos A., Zaitlen, Noah
Veröffentlicht in Genetics (2016)

Discovery Properties of Genome-wide Association Signals From Cumulatively Combined Data Sets

von Pereira, Tiago V., Patsopoulos, Nikolaos A., Salanti, Georgia, Ioannidis, John P. A.
Veröffentlicht 2009

Selection and Presentation of Imaging Figures in the Medical Literature

von Siontis, George C. M., Patsopoulos, Nikolaos A., Vlahos, Antonios P., Ioannidis, John P. A.
Veröffentlicht 2010

Polygenic analysis of inflammatory disease variants and effects on microglia in the aging brain

von Felsky, Daniel, Patrick, Ellis, Schneider, Julie A., Mostafavi, Sara, Gaiteri, Chris, Patsopoulos, Nikolaos, Bennett, David A., De Jager, Philip L.
Veröffentlicht in Mol Neurodegener (2018)

Non-parametric Polygenic Risk Prediction via Partitioned GWAS Summary Statistics

von Chun, Sung, Imakaev, Maxim, Hui, Daniel, Patsopoulos, Nikolaos A., Neale, Benjamin M., Kathiresan, Sekar, Stitziel, Nathan O., Sunyaev, Shamil R.
Veröffentlicht in Am J Hum Genet (2020)

International ranking systems for universities and institutions: a critical appraisal

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

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

von Chun, Sung, Casparino, Alexandra, Patsopoulos, Nikolaos A, Croteau-Chonka, Damien C, Raby, Benjamin A, De Jager, Philip L, Sunyaev, Shamil R, Cotsapas, Chris
Veröffentlicht in Nat Genet (2017)

Effect of Genetic Variants, Especially CYP2C9 and VKORC1, on the Pharmacology of Warfarin

von Fung, Erik, Patsopoulos, Nikolaos A., Belknap, Steven M., O’Rourke, Daniel J., Robb, John F., Anderson, Jeffrey L., Shworak, Nicholas W., Moore, Jason H.
Veröffentlicht 2012

A non-synonymous single-nucleotide polymorphism associated with multiple sclerosis risk affects the EVI5 interactome

von Didonna, Alessandro, Isobe, Noriko, Caillier, Stacy J., Li, Kathy H., Burlingame, Alma L., Hauser, Stephen L., Baranzini, Sergio E., Patsopoulos, Nikolaos A., Oksenberg, Jorge R.
Veröffentlicht in Hum Mol Genet (2015)