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ArticlesPeer ReviewedFull Text
Genetic and epigenetic fine mapping of causal autoimmune disease variants
Author / Creator: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.
Publisher:London: Nature Publishing Group UK
Journal title:Nature (London), 2015-02, Vol.518 (7539), p.337-343
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Limited statistical evidence for shared genetic effects of eQTLs and autoimmune-disease-associated loci in three major immune-cell types
Author / Creator:Chun, Sung ; Casparino, Alexandra ; Patsopoulos, Nikolaos A ; Croteau-Chonka, Damien C ; Raby, Benjamin A ; De Jager, Philip L ; Sunyaev, Shamil R ; Cotsapas, Chris
Publisher:New York: Nature Publishing Group US
Journal title:Nature genetics, 2017-04, Vol.49 (4), p.600-605
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Fine-mapping the genetic association of the major histocompatibility complex in multiple sclerosis: HLA and non-HLA effects
Author / Creator: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
Publisher:United States: Public Library of Science
Journal title:PLoS genetics, 2013-11, Vol.9 (11), p.e1003926
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Heterogeneity in meta-analyses of genome-wide association investigations
Author / Creator:Ioannidis, John P A ; Patsopoulos, Nikolaos A ; Evangelou, Evangelos
Publisher:United States: Public Library of Science
Journal title:PloS one, 2007-09, Vol.2 (9), p.e841-e841
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Time-Dependent Changes in Microglia Transcriptional Networks Following Traumatic Brain Injury
Author / Creator: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
Publisher:Switzerland: Frontiers Research Foundation
Journal title:Frontiers in cellular neuroscience, 2019-08, Vol.13, p.307-307
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Dissection of multiple sclerosis genetics identifies B and CD4+ T cells as driver cell subsets
Author / Creator: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
Publisher:England: BioMed Central Ltd
Journal title:Genome Biology, 2022-06, Vol.23 (1), p.127-127, Article 127
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Ancestral risk modification for multiple sclerosis susceptibility detected across the Major Histocompatibility Complex in a multi-ethnic population
Author / Creator: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
Publisher:United States: Public Library of Science
Journal title:PloS one, 2022-12, Vol.17 (12), p.e0279132-e0279132
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Two genetic variants explain the association of European ancestry with multiple sclerosis risk in African-Americans
Author / Creator: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
Publisher:London: Nature Publishing Group UK
Journal title:Scientific reports, 2020-10, Vol.10 (1), p.16902-9, Article 16902
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ArticlesPeer ReviewedFull Text
Local Joint Testing Improves Power and Identifies Hidden Heritability in Association Studies
Author / Creator:Brown, Brielin C ; Price, Alkes L ; Patsopoulos, Nikolaos A ; Zaitlen, Noah
Publisher:United States: Genetics Society of America
Journal title:Genetics (Austin), 2016-07, Vol.203 (3), p.1105-1116
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ArticlesPeer ReviewedFull Text
Mother−child histocompatibility and risk of rheumatoid arthritis and systemic lupus erythematosus among mothers
Author / Creator: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.
Publisher:London: Nature Publishing Group UK
Journal title:Genes and immunity, 2020-01, Vol.21 (1), p.27-36
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ArticlesPeer ReviewedFull Text
International ranking systems for universities and institutions: a critical appraisal
Author / Creator:Ioannidis, John P A ; Patsopoulos, Nikolaos A ; Kavvoura, Fotini K ; Tatsioni, Athina ; Evangelou, Evangelos ; Kouri, Ioanna ; Contopoulos-Ioannidis, Despina G ; Liberopoulos, George
Publisher:England: BioMed Central Ltd
Journal title:BMC medicine, 2007-10, Vol.5 (1), p.30-30, Article 30
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ArticlesPeer ReviewedFull Text
Genetics and functional genomics of multiple sclerosis
Author / Creator:Kim, Woori ; Patsopoulos, Nikolaos A.
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Seminars in immunopathology, 2022-01, Vol.44 (1), p.63-79
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Susceptibility variants for rheumatoid arthritis in the TRAF1-C5 and 6q23 loci: a meta-analysis
Author / Creator:Patsopoulos, Nikolaos A ; Ioannidis, John P A
Publisher:London: BMJ Publishing Group Ltd and European League Against Rheumatism
Journal title:Annals of the rheumatic diseases, 2010-03, Vol.69 (3), p.561-566
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Polarization of the Effects of Autoimmune and Neurodegenerative Risk Alleles in Leukocytes
Author / Creator:Raj, Towfique ; Rothamel, Katie ; Mostafavi, Sara ; Ye, Chun ; Lee, Mark N. ; Replogle, Joseph M. ; Feng, Ting ; Lee, Michelle ; Asinovski, Natasha ; Frohlich, Irene ; Imboywa, Selina ; Von Korff, Alina ; Okada, Yukinori ; Patsopoulos, Nikolaos A. ; Davis, Scott ; McCabe, Cristin ; Paik, Hyun-il ; Srivastava, Gyan P. ; Raychaudhuri, Soumya ; Hafler, David A. ; Koller, Daphne ; Regev, Aviv ; Hacohen, Nir ; Mathis, Diane ; Benoist, Christophe ; Stranger, Barbara E. ; De Jager, Philip L.
Publisher:United States: American Association for the Advancement of Science
Journal title:Science (American Association for the Advancement of Science), 2014-05, Vol.344 (6183), p.519-523
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Reporting of human genome epidemiology (HuGE) association studies: an empirical assessment
Author / Creator:Yesupriya, Ajay ; Evangelou, Evangelos ; Kavvoura, Fotini K ; Patsopoulos, Nikolaos A ; Clyne, Melinda ; Walsh, Matthew C ; Lin, Bruce K ; Yu, Wei ; Gwinn, Marta ; Ioannidis, John P A ; Khoury, Muin J
Publisher:England: BioMed Central Ltd
Journal title:BMC medical research methodology, 2008-05, Vol.8 (1), p.31-31, Article 31
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Selection and presentation of imaging figures in the medical literature
Author / Creator:Siontis, George C M ; Patsopoulos, Nikolaos A ; Vlahos, Antonios P ; Ioannidis, John P A
Publisher:United States: Public Library of Science
Journal title:PloS one, 2010-05, Vol.5 (5), p.e10888-e10888
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Burden of risk variants correlates with phenotype of multiple sclerosis
Author / Creator:Hilven, Kelly ; Patsopoulos, Nikolaos A ; Dubois, Bénédicte ; Goris, An
Publisher:London, England: SAGE Publications
Journal title:Multiple sclerosis, 2015-11, Vol.21 (13), p.1670-1680
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A multi-step genomic approach prioritized TBKBP1 gene as relevant for multiple sclerosis susceptibility
Author / Creator: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
Publisher:Berlin/Heidelberg: Springer Berlin Heidelberg
Journal title:Journal of neurology, 2022-08, Vol.269 (8), p.4510-4522
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ArticlesPeer ReviewedFull Text
Unexpected similarities between C9ORF72 and sporadic forms of ALS/FTD suggest a common disease mechanism
Author / Creator:Conlon, Erin G ; Fagegaltier, Delphine ; Agius, Phaedra ; Davis-Porada, Julia ; Gregory, James ; Hubbard, Isabel ; Kang, Kristy ; Kim, Duyang ; Phatnani, Hemali ; Shneider, Neil A ; Manley, James L
Publisher:England: eLife Science Publications, Ltd
Journal title:eLife, 2018-07, Vol.7
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Replication of past candidate loci for common diseases and phenotypes in 100 genome-wide association studies
Author / Creator:Siontis, Konstantinos C M ; Patsopoulos, Nikolaos A ; Ioannidis, John P A
Publisher:Cham: Springer International Publishing
Journal title:European journal of human genetics : EJHG, 2010-07, Vol.18 (7), p.832-837
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Showing 1 to 20 of 47 results

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Genetic and epigenetic fine mapping of causal autoimmune disease variants

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

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Fine-mapping the genetic association of the major histocompatibility complex in multiple sclerosis: HLA and non-HLA effects

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Heterogeneity in meta-analyses of genome-wide association investigations

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

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

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

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

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

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

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International ranking systems for universities and institutions: a critical appraisal

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Genetics and functional genomics of multiple sclerosis

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Susceptibility variants for rheumatoid arthritis in the TRAF1-C5 and 6q23 loci: a meta-analysis

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Polarization of the Effects of Autoimmune and Neurodegenerative Risk Alleles in Leukocytes

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Reporting of human genome epidemiology (HuGE) association studies: an empirical assessment

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Selection and presentation of imaging figures in the medical literature

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Burden of risk variants correlates with phenotype of multiple sclerosis

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

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Unexpected similarities between C9ORF72 and sporadic forms of ALS/FTD suggest a common disease mechanism

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

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