Zobrazeno 1 - 10
of 185
pro vyhledávání: '"Brien P Riley"'
Publikováno v:
PLoS ONE, Vol 14, Iss 4, p e0202063 (2019)
Genome-wide association studies on alcohol dependence, by themselves, have yet to account for the estimated heritability of the disorder and provide incomplete mechanistic understanding of this complex trait. Integrating brain ethanol-responsive gene
Externí odkaz:
https://doaj.org/article/0ea67ab44f044813ac8eab92e14b6e8f
Autor:
Mohammed Mamdani, Vernell Williamson, Gowon O McMichael, Tana Blevins, Fazil Aliev, Amy Adkins, Laura Hack, Tim Bigdeli, Andrew D van der Vaart, Bradley Todd Web, Silviu-Alin Bacanu, Gursharan Kalsi, COGA Consortium, Kenneth S Kendler, Michael F Miles, Danielle Dick, Brien P Riley, Catherine Dumur, Vladimir I Vladimirov
Publikováno v:
PLoS ONE, Vol 10, Iss 9, p e0137671 (2015)
Alcohol consumption is known to lead to gene expression changes in the brain. After performing weighted gene co-expression network analyses (WGCNA) on genome-wide mRNA and microRNA (miRNA) expression in Nucleus Accumbens (NAc) of subjects with alcoho
Externí odkaz:
https://doaj.org/article/7889488b240948f9b2952c8dfa49b6f0
Autor:
Zhongming Zhao, Bradley T Webb, Peilin Jia, T Bernard Bigdeli, Brion S Maher, Edwin van den Oord, Sarah E Bergen, Richard L Amdur, Francis A O'Neill, Dermot Walsh, Dawn L Thiselton, Xiangning Chen, Carlos N Pato, International Schizophrenia Consortium, Brien P Riley, Kenneth S Kendler, Ayman H Fanous
Publikováno v:
PLoS ONE, Vol 8, Iss 7, p e67776 (2013)
Integrating evidence from multiple domains is useful in prioritizing disease candidate genes for subsequent testing. We ranked all known human genes (n=3819) under linkage peaks in the Irish Study of High-Density Schizophrenia Families using three di
Externí odkaz:
https://doaj.org/article/e23b3ee76ed54800bdaa5b1763265c63
Autor:
T Bernard Bigdeli, Brion S Maher, Zhongming Zhao, Edwin J C G van den Oord, Dawn L Thiselton, Jingchun Sun, Bradley T Webb, Richard L Amdur, Brandon Wormley, Francis A O'Neill, Dermot Walsh, Brien P Riley, Kenneth S Kendler, Ayman H Fanous
Publikováno v:
PLoS ONE, Vol 6, Iss 12, p e21440 (2011)
Prior genomewide scans of schizophrenia support evidence of linkage to regions of chromosome 20. However, association analyses have yet to provide support for any etiologically relevant variants.We analyzed 2988 LD-tagging single nucleotide polymorph
Externí odkaz:
https://doaj.org/article/2d2d05f6ed854f6da9f843265cf68463
Autor:
Jingchun Sun, Peilin Jia, Ayman H Fanous, Edwin van den Oord, Xiangning Chen, Brien P Riley, Richard L Amdur, Kenneth S Kendler, Zhongming Zhao
Publikováno v:
PLoS ONE, Vol 5, Iss 6, p e11351 (2010)
Schizophrenia (SZ) is a heritable, complex mental disorder. We have seen limited success in finding causal genes for schizophrenia from numerous conventional studies. Protein interaction network and pathway-based analysis may provide us an alternativ
Externí odkaz:
https://doaj.org/article/899b0c7b8b464c16b4c6fff5414bc732
Autor:
Mohammad Ahangari, Elif Everest, Tan-Hoang Nguyen, Brian C. Verrelli, Bradley T. Webb, Silviu-Alin Bacanu, Eda Tahir Turanli, Brien P. Riley
Publikováno v:
Brain, Behavior, and Immunity. 104:183-190
Common genetic variants identified in genome-wide association studies (GWAS) show varying degrees of genetic pleiotropy across complex human disorders. Clinical studies of schizophrenia (SCZ) suggest that in addition to neuropsychiatric symptoms, pat
Autor:
Yu-Han H. Hsu, Greta Pintacuda, Ruize Liu, Eugeniu Nacu, April Kim, Kalliopi Tsafou, Natalie Petrossian, William Crotty, Jung Min Suh, Jackson Riseman, Jacqueline M. Martin, Julia C. Biagini, Daya Mena, Joshua K.T. Ching, Edyta Malolepsza, Taibo Li, Tarjinder Singh, Tian Ge, Shawn B. Egri, Benjamin Tanenbaum, Caroline R. Stanclift, Annie M. Apffel, Steven A. Carr, Monica Schenone, Jake Jaffe, Nadine Fornelos, Hailiang Huang, Kevin C. Eggan, Kasper Lage, Stephan Ripke, Benjamin M. Neale, Aiden Corvin, James T.R. Walters, Kai-How Farh, Peter A. Holmans, Phil Lee, Brendan Bulik-Sullivan, David A. Collier, Tune H. Pers, Ingrid Agartz, Esben Agerbo, Margot Albus, Madeline Alexander, Farooq Amin, Silviu A. Bacanu, Martin Begemann, Richard A. Belliveau, Judit Bene, Sarah E. Bergen, Elizabeth Bevilacqua, Tim B. Bigdeli, Donald W. Black, Richard Bruggeman, Nancy G. Buccola, Randy L. Buckner, William Byerley, Wiepke Cahn, Guiqing Cai, Dominique Campion, Rita M. Cantor, Vaughan J. Carr, Noa Carrera, Stanley V. Catts, Kimberley D. Chambert, Raymond C.K. Chan, Ronald Y.L. Chan, Eric Y.H. Chen, Wei Cheng, Eric FC. Cheung, Siow Ann Chong, C. Robert Cloninger, David Cohen, Nadine Cohen, Paul Cormican, Nick Craddock, James J. Crowley, David Curtis, Michael Davidson, Kenneth L. Davis, Franziska Degenhardt, Jurgen Del Favero, Ditte Demontis, Dimitris Dikeos, Timothy Dinan, Srdjan Djurovic, Gary Donohoe, Elodie Drapeau, Jubao Duan, Frank Dudbridge, Naser Durmishi, Peter Eichhammer, Johan Eriksson, Valentina Escott-Price, Laurent Essioux, Ayman H. Fanous, Martilias S. Farrell, Josef Frank, Lude Franke, Robert Freedman, Nelson B. Freimer, Marion Friedl, Joseph I. Friedman, Menachem Fromer, Giulio Genovese, Lyudmila Georgieva, Ina Giegling, Paola Giusti-Rodríguez, Stephanie Godard, Jacqueline I. Goldstein, Vera Golimbet, Srihari Gopal, Jacob Gratten, Lieuwe de Haan, Christian Hammer, Marian L. Hamshere, Mark Hansen, Thomas Hansen, Vahram Haroutunian, Annette M. Hartmann, Frans A. Henskens, Stefan Herms, Joel N. Hirschhorn, Per Hoffmann, Andrea Hofman, Mads V. Hollegaard, David M. Hougaard, Masashi Ikeda, Inge Joa, Antonio Julià, René S. Kahn, Luba Kalaydjieva, Sena Karachanak-Yankova, Juha Karjalainen, David Kavanagh, Matthew C. Keller, James L. Kennedy, Andrey Khrunin, Yunjung Kim, Janis Klovins, James A. Knowles, Bettina Konte, Vaidutis Kucinskas, Zita Ausrele Kucinskiene, Hana Kuzelova-Ptackova, Anna K. Kähler, Claudine Laurent, Jimmy Lee, S. Hong Lee, Sophie E. Legge, Bernard Lerer, Miaoxin Li, Tao Li, Kung-Yee Liang, Jeffrey Lieberman, Svetlana Limborska, Carmel M. Loughland, Jan Lubinski, Jouko Lönnqvist, Milan Macek, Patrik K.E. Magnusson, Brion S. Maher, Wolfgang Maier, Jacques Mallet, Sara Marsal, Manuel Mattheisen, Morten Mattingsdal, Robert W. McCarley, Colm McDonald, Andrew M. McIntosh, Sandra Meier, Carin J. Meijer, Bela Melegh, Ingrid Melle, Raquelle I. Mesholam-Gately, Andres Metspalu, Patricia T. Michie, Lili Milani, Vihra Milanova, Younes Mokrab, Derek W. Morris, Ole Mors, Kieran C. Murphy, Robin M. Murray, Inez Myin-Germeys, Bertram Müller-Myhsok, Mari Nelis, Igor Nenadic, Deborah A. Nertney, Gerald Nestadt, Kristin K. Nicodemus, Liene Nikitina-Zake, Laura Nisenbaum, Annelie Nordin, Eadbhard O'Callaghan, Colm O'Dushlaine, F. Anthony O'Neill, Sang-Yun Oh, Ann Olincy, Line Olsen, Jim Van Os, Christos Pantelis, George N. Papadimitriou, Sergi Papiol, Elena Parkhomenko, Michele T. Pato, Tiina Paunio, Milica Pejovic-Milovancevic, Diana O. Perkins, Olli Pietiläinen, Jonathan Pimm, Andrew J. Pocklington, John Powell, Alkes Price, Ann E. Pulver, Shaun M. Purcell, Digby Quested, Henrik B. Rasmussen, Abraham Reichenberg, Mark A. Reimers, Alexander L. Richards, Joshua L. Roffman, Panos Roussos, Douglas M. Ruderfer, Veikko Salomaa, Alan R. Sanders, Ulrich Schall, Christian R. Schubert, Thomas G. Schulze, Sibylle G. Schwab, Edward M. Scolnick, Rodney J. Scott, Larry J. Seidman, Jianxin Shi, Engilbert Sigurdsson, Teimuraz Silagadze, Jeremy M. Silverman, Kang Sim, Petr Slominsky, Jordan W. Smoller, Hon-Cheong So, Chris C.A. Spencer, Eli A. Stahl, Hreinn Stefansson, Stacy Steinberg, Elisabeth Stogmann, Richard E. Straub, Eric Strengman, Jana Strohmaier, T Scott Stroup, Mythily Subramaniam, Jaana Suvisaari, Dragan M. Svrakic, Jin P. Szatkiewicz, Erik Söderman, Srinivas Thirumalai, Draga Toncheva, Sarah Tosato, Juha Veijola, John Waddington, Dermot Walsh, Dai Wang, Qiang Wang, Bradley T. Webb, Mark Weiser, Dieter B. Wildenauer, Nigel M. Williams, Stephanie Williams, Stephanie H. Witt, Aaron R. Wolen, Emily H.M. Wong, Brandon K. Wormley, Hualin Simon Xi, Clement C. Zai, Xuebin Zheng, Fritz Zimprich, Naomi R. Wray, Kari Stefansson, Peter M. Visscher, Rolf Adolfsson, Ole A. Andreassen, Douglas H.R. Blackwood, Elvira Bramon, Joseph D. Buxbaum, Anders D. Børglum, Sven Cichon, Ariel Darvasi, Enrico Domenici, Hannelore Ehrenreich, Tõnu Esko, Pablo V. Gejman, Michael Gill, Hugh Gurling, Christina M. Hultman, Nakao Iwata, Assen V. Jablensky, Erik G. Jönsson, Kenneth S. Kendler, George Kirov, Jo Knight, Todd Lencz, Douglas F. Levinson, Qingqin S. Li, Jianjun Liu, Anil K. Malhotra, Steven A. McCarroll, Andrew McQuillin, Jennifer L. Moran, Preben B. Mortensen, Bryan J. Mowry, Markus M. Nöthen, Roel A. Ophoff, Michael J. Owen, Aarno Palotie, Carlos N. Pato, Tracey L. Petryshen, Danielle Posthuma, Marcella Rietschel, Brien P. Riley, Dan Rujescu, Pak C. Sham, Pamela Sklar, David St Clair, Daniel R. Weinberger, Jens R. Wendland, Thomas Werge, Mark J. Daly, Patrick F. Sullivan, Michael C. O'Donovan, Shengying Qin, Akira Sawa, Rene Kahn, Kyung Sue Hong, Wenzhao Shi, Ming Tsuang, Masanari Itokawa, Gang Feng, Stephen J. Glatt, Xiancang Ma, Jinsong Tang, Yunfeng Ruan, Feng Zhu, Yasue Horiuchi, Byung Dae Lee, Eun-Jeong Joo, Woojae Myung, Kyooseob Ha, Hong-Hee Won, Ji Hyung Baek, Young Chul Chung, Sung-Wan Kim, Agung Kusumawardhani, Wei J. Chen, Hai-Gwo Hwu, Akitoyo Hishimoto, Ikuo Otsuka, Ichiro Sora, Tomoko Toyota, Takeo Yoshikawa, Hiroshi Kunugi, Kotaro Hattori, Sayuri Ishiwata, Shusuke Numata, Tetsuro Ohmori, Makoto Arai, Yuji Ozeki, Kumiko Fujii, Se Joo Kim, Heon-Jeong Lee, Yong Min Ahn, Se Hyun Kim, Kazufumi Akiyama, Kazutaka Shimoda, Makoto Kinoshita
Publikováno v:
Wellcome Trust Case-Control Consortium, Schizophrenia Working Group of the Psychiatric Genomics Consortium, Psychosis Endophenotypes International Consortium & Stanley Global Asia Initiatives 2023, ' Using brain cell-type-specific protein interactomes to interpret neurodevelopmental genetic signals in schizophrenia ', iScience, vol. 26, no. 5, 106701 . https://doi.org/10.1016/j.isci.2023.106701
iScience, 26(5):106701. Elsevier Inc.
iScience, 26(5):106701. Elsevier Inc.
Genetics have nominated many schizophrenia risk genes and identified convergent signals between schizophrenia and neurodevelopmental disorders. However, functional interpretation of the nominated genes in the relevant brain cell types is often lackin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::899b91d0037451c5ae8ba33bd85556af
https://research.vumc.nl/en/publications/09e21c68-1cb0-4953-99f3-d4555dd05c4e
https://research.vumc.nl/en/publications/09e21c68-1cb0-4953-99f3-d4555dd05c4e
Autor:
Huseyin Gedik, Roseann E. Peterson, Brien P. Riley, Vladimir I Vladimirov, Silviu-Alin Bacanu, Alexander Josephs
Publikováno v:
Complex Psychiatry.
Background The genome-wide association study (GWAS) is a common tool to identify genetic variants associated with complex traits, including psychiatric disorders (PDs). However, post-GWAS analyses are needed to extend the statistical inference to bio
Autor:
Huseyin Gedik, Tan Hoang Nguyen, Roseann E. Peterson, Christos Chatzinakos, Brien P. Riley, Vladimir I. Vladimirov, Silviu-Alin Bacanu
Neuropsychiatric and substance use disorders (NPSUD) have a complex etiology that includes environmental and polygenic risk factors with significant cross-trait rG. Genome Wide Association Studies (GWAS) of NPSUD yield numerous association signals. H
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f67821d8cb52fcd9a0e878e27d260f80
https://doi.org/10.1101/2023.03.15.23287330
https://doi.org/10.1101/2023.03.15.23287330
Autor:
Silviu-Alin Bacanu, Tan-Hoang Nguyen, Bradley T. Webb, Brien P. Riley, Kenneth S. Kendler, Amanda Elswick Gentry, Robert M. Kirkpatrick, Brian C. Verrelli, Mohammad Ahangari
Publikováno v:
Ahangari, M, Gentry, A E, Nguyen, T-H, Kirkpatrick, R, Verrelli, B C, Bacanu, S-A, Kendler, K S, Webb, B T, Riley, B P & Irish Schizophrenia Genomics Consortium 2022, ' Evaluating the role of common risk variation in the recurrence risk of schizophrenia in multiplex schizophrenia families ', Translational Psychiatry, vol. 12, 291 . https://doi.org/10.1038/s41398-022-02060-3
Importance Multiplex schizophrenia families have higher recurrence risk of schizophrenia compared to the families of singleton cases in the population, but the source of increased familial recurrence risk is unknown. Determining the source of this ob
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30cbb7de3772d26cebc24dda21347b85
https://pure.qub.ac.uk/en/publications/15adc2c2-bbca-4fc7-8ee9-998b1468310a
https://pure.qub.ac.uk/en/publications/15adc2c2-bbca-4fc7-8ee9-998b1468310a