Pesquisa | Biblioteca Virtual em Saúde

1.

Sequencing chromosomal abnormalities reveals neurodevelopmental loci that confer risk across diagnostic boundaries.

Talkowski, Michael E; Rosenfeld, Jill A; Blumenthal, Ian; Pillalamarri, Vamsee; Chiang, Colby; Heilbut, Adrian; Ernst, Carl; Hanscom, Carrie; Rossin, Elizabeth; Lindgren, Amelia M; Pereira, Shahrin; Ruderfer, Douglas; Kirby, Andrew; Ripke, Stephan; Harris, David J; Lee, Ji-Hyun; Ha, Kyungsoo; Kim, Hyung-Goo; Solomon, Benjamin D; Gropman, Andrea L; Lucente, Diane; Sims, Katherine; Ohsumi, Toshiro K; Borowsky, Mark L; Loranger, Stephanie; Quade, Bradley; Lage, Kasper; Miles, Judith; Wu, Bai-Lin; Shen, Yiping; Neale, Benjamin; Shaffer, Lisa G; Daly, Mark J; Morton, Cynthia C; Gusella, James F.

Cell; 149(3): 525-37, 2012 Apr 27.

Artigo em Inglês | MEDLINE | ID: mdl-22521361

2.

RICOPILI: Rapid Imputation for COnsortias PIpeLIne.

Lam, Max; Awasthi, Swapnil; Watson, Hunna J; Goldstein, Jackie; Panagiotaropoulou, Georgia; Trubetskoy, Vassily; Karlsson, Robert; Frei, Oleksander; Fan, Chun-Chieh; De Witte, Ward; Mota, Nina R; Mullins, Niamh; Brügger, Kim; Lee, Hong; Wray, Naomi; Skarabis, Nora; Huang, Hailiang; Neale, Benjamin; Daly, Mark; Mattheissen, Manuel; Walters, Raymond; Ripke, Stephan.

Bioinformatics; 2019 Aug 08.

Artigo em Inglês | MEDLINE | ID: mdl-31393554

3.

A Method to Exploit the Structure of Genetic Ancestry Space to Enhance Case-Control Studies.

Bodea, Corneliu A; Neale, Benjamin M; Ripke, Stephan; Daly, Mark J; Devlin, Bernie; Roeder, Kathryn.

Am J Hum Genet; 98(5): 857-868, 2016 05 05.

Artigo em Inglês | MEDLINE | ID: mdl-27087321

4.

Genome-wide analysis of insomnia disorder.

Stein, Murray B; McCarthy, Michael J; Chen, Chia-Yen; Jain, Sonia; Gelernter, Joel; He, Feng; Heeringa, Steven G; Kessler, Ronald C; Nock, Matthew K; Ripke, Stephan; Sun, Xiaoying; Wynn, Gary H; Smoller, Jordan W; Ursano, Robert J.

Mol Psychiatry; 23(11): 2238-2250, 2018 Nov.

Artigo em Inglês | MEDLINE | ID: mdl-29520036

5.

Genome-wide analyses of psychological resilience in U.S. Army soldiers.

Stein, Murray B; Choi, Karmel W; Jain, Sonia; Campbell-Sills, Laura; Chen, Chia-Yen; Gelernter, Joel; He, Feng; Heeringa, Steven G; Maihofer, Adam X; Nievergelt, Caroline; Nock, Matthew K; Ripke, Stephan; Sun, Xiaoying; Kessler, Ronald C; Smoller, Jordan W; Ursano, Robert J.

Am J Med Genet B Neuropsychiatr Genet; 180(5): 310-319, 2019 Jul.

Artigo em Inglês | MEDLINE | ID: mdl-31081985

6.

Quantifying between-cohort and between-sex genetic heterogeneity in major depressive disorder.

Trzaskowski, Maciej; Mehta, Divya; Peyrot, Wouter J; Hawkes, David; Davies, Daniel; Howard, David M; Kemper, Kathryn E; Sidorenko, Julia; Maier, Robert; Ripke, Stephan; Mattheisen, Manuel; Baune, Bernhard T; Grabe, Hans J; Heath, Andrew C; Jones, Lisa; Jones, Ian; Madden, Pamela A F; McIntosh, Andrew M; Breen, Gerome; Lewis, Cathryn M; Børglum, Anders D; Sullivan, Patrick F; Martin, Nicholas G; Kendler, Kenneth S; Levinson, Douglas F; Wray, Naomi R.

Am J Med Genet B Neuropsychiatr Genet; 180(6): 439-447, 2019 Sep.

Artigo em Inglês | MEDLINE | ID: mdl-30708398

7.

Comprehensive analysis of schizophrenia-associated loci highlights ion channel pathways and biologically plausible candidate causal genes.

Pers, Tune H; Timshel, Pascal; Ripke, Stephan; Lent, Samantha; Sullivan, Patrick F; O'Donovan, Michael C; Franke, Lude; Hirschhorn, Joel N.

Hum Mol Genet; 25(6): 1247-54, 2016 Mar 15.

Artigo em Inglês | MEDLINE | ID: mdl-26755824

8.

Joint analysis of psychiatric disorders increases accuracy of risk prediction for schizophrenia, bipolar disorder, and major depressive disorder.

Maier, Robert; Moser, Gerhard; Chen, Guo-Bo; Ripke, Stephan; Coryell, William; Potash, James B; Scheftner, William A; Shi, Jianxin; Weissman, Myrna M; Hultman, Christina M; Landén, Mikael; Levinson, Douglas F; Kendler, Kenneth S; Smoller, Jordan W; Wray, Naomi R; Lee, S Hong.

Am J Hum Genet; 96(2): 283-94, 2015 Feb 05.

Artigo em Inglês | MEDLINE | ID: mdl-25640677

9.

Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores.

Vilhjálmsson, Bjarni J; Yang, Jian; Finucane, Hilary K; Gusev, Alexander; Lindström, Sara; Ripke, Stephan; Genovese, Giulio; Loh, Po-Ru; Bhatia, Gaurav; Do, Ron; Hayeck, Tristan; Won, Hong-Hee; Kathiresan, Sekar; Pato, Michele; Pato, Carlos; Tamimi, Rulla; Stahl, Eli; Zaitlen, Noah; Pasaniuc, Bogdan; Belbin, Gillian; Kenny, Eimear E; Schierup, Mikkel H; De Jager, Philip; Patsopoulos, Nikolaos A; McCarroll, Steve; Daly, Mark; Purcell, Shaun; Chasman, Daniel; Neale, Benjamin; Goddard, Michael; Visscher, Peter M; Kraft, Peter; Patterson, Nick; Price, Alkes L.

Am J Hum Genet; 97(4): 576-92, 2015 Oct 01.

Artigo em Inglês | MEDLINE | ID: mdl-26430803

10.

Host-microbe interactions have shaped the genetic architecture of inflammatory bowel disease.

Jostins, Luke; Ripke, Stephan; Weersma, Rinse K; Duerr, Richard H; McGovern, Dermot P; Hui, Ken Y; Lee, James C; Schumm, L Philip; Sharma, Yashoda; Anderson, Carl A; Essers, Jonah; Mitrovic, Mitja; Ning, Kaida; Cleynen, Isabelle; Theatre, Emilie; Spain, Sarah L; Raychaudhuri, Soumya; Goyette, Philippe; Wei, Zhi; Abraham, Clara; Achkar, Jean-Paul; Ahmad, Tariq; Amininejad, Leila; Ananthakrishnan, Ashwin N; Andersen, Vibeke; Andrews, Jane M; Baidoo, Leonard; Balschun, Tobias; Bampton, Peter A; Bitton, Alain; Boucher, Gabrielle; Brand, Stephan; Büning, Carsten; Cohain, Ariella; Cichon, Sven; D'Amato, Mauro; De Jong, Dirk; Devaney, Kathy L; Dubinsky, Marla; Edwards, Cathryn; Ellinghaus, David; Ferguson, Lynnette R; Franchimont, Denis; Fransen, Karin; Gearry, Richard; Georges, Michel; Gieger, Christian; Glas, Jürgen; Haritunians, Talin; Hart, Ailsa.

Nature; 491(7422): 119-24, 2012 Nov 01.

Artigo em Inglês | MEDLINE | ID: mdl-23128233

11.

Genome-wide gene-environment interaction in depression: A systematic evaluation of candidate genes: The childhood trauma working-group of PGC-MDD.

Van der Auwera, Sandra; Peyrot, Wouter J; Milaneschi, Yuri; Hertel, Johannes; Baune, Bernhard; Breen, Gerome; Byrne, Enda; Dunn, Erin C; Fisher, Helen; Homuth, Georg; Levinson, Douglas; Lewis, Cathryn; Mills, Natalie; Mullins, Niamh; Nauck, Matthias; Pistis, Giorgio; Preisig, Martin; Rietschel, Marcella; Ripke, Stephan; Sullivan, Patrick; Teumer, Alexander; Völzke, Henry; Boomsma, Dorret I; Wray, Naomi R; Penninx, Brenda; Grabe, Hans.

Am J Med Genet B Neuropsychiatr Genet; 177(1): 40-49, 2018 Jan.

Artigo em Inglês | MEDLINE | ID: mdl-29159863

12.

An excess of risk-increasing low-frequency variants can be a signal of polygenic inheritance in complex diseases.

Chan, Yingleong; Lim, Elaine T; Sandholm, Niina; Wang, Sophie R; McKnight, Amy Jayne; Ripke, Stephan; Daly, Mark J; Neale, Benjamin M; Salem, Rany M; Hirschhorn, Joel N.

Am J Hum Genet; 94(3): 437-52, 2014 Mar 06.

Artigo em Inglês | MEDLINE | ID: mdl-24607388

13.

Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases.

Gusev, Alexander; Lee, S Hong; Trynka, Gosia; Finucane, Hilary; Vilhjálmsson, Bjarni J; Xu, Han; Zang, Chongzhi; Ripke, Stephan; Bulik-Sullivan, Brendan; Stahl, Eli; Kähler, Anna K; Hultman, Christina M; Purcell, Shaun M; McCarroll, Steven A; Daly, Mark; Pasaniuc, Bogdan; Sullivan, Patrick F; Neale, Benjamin M; Wray, Naomi R; Raychaudhuri, Soumya; Price, Alkes L.

Am J Hum Genet; 95(5): 535-52, 2014 Nov 06.

Artigo em Inglês | MEDLINE | ID: mdl-25439723

14.

Integrated pathway-based approach identifies association between genomic regions at CTCF and CACNB2 and schizophrenia.

Juraeva, Dilafruz; Haenisch, Britta; Zapatka, Marc; Frank, Josef; Witt, Stephanie H; Mühleisen, Thomas W; Treutlein, Jens; Strohmaier, Jana; Meier, Sandra; Degenhardt, Franziska; Giegling, Ina; Ripke, Stephan; Leber, Markus; Lange, Christoph; Schulze, Thomas G; Mössner, Rainald; Nenadic, Igor; Sauer, Heinrich; Rujescu, Dan; Maier, Wolfgang; Børglum, Anders; Ophoff, Roel; Cichon, Sven; Nöthen, Markus M; Rietschel, Marcella; Mattheisen, Manuel; Brors, Benedikt.

PLoS Genet; 10(6): e1004345, 2014 Jun.

Artigo em Inglês | MEDLINE | ID: mdl-24901509

15.

Genetic risk variants for social anxiety.

Stein, Murray B; Chen, Chia-Yen; Jain, Sonia; Jensen, Kevin P; He, Feng; Heeringa, Steven G; Kessler, Ronald C; Maihofer, Adam; Nock, Matthew K; Ripke, Stephan; Sun, Xiaoying; Thomas, Michael L; Ursano, Robert J; Smoller, Jordan W; Gelernter, Joel.

Am J Med Genet B Neuropsychiatr Genet; 174(2): 120-131, 2017 03.

Artigo em Inglês | MEDLINE | ID: mdl-28224735

16.

Genomewide association studies of suicide attempts in US soldiers.

Stein, Murray B; Ware, Erin B; Mitchell, Colter; Chen, Chia-Yen; Borja, Susan; Cai, Tianxi; Dempsey, Catherine L; Fullerton, Carol S; Gelernter, Joel; Heeringa, Steven G; Jain, Sonia; Kessler, Ronald C; Naifeh, James A; Nock, Matthew K; Ripke, Stephan; Sun, Xiaoying; Beckham, Jean C; Kimbrel, Nathan A; Ursano, Robert J; Smoller, Jordan W.

Am J Med Genet B Neuropsychiatr Genet; 174(8): 786-797, 2017 Dec.

Artigo em Inglês | MEDLINE | ID: mdl-28902444

17.

No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosis.

Goris, An; van Setten, Jessica; Diekstra, Frank; Ripke, Stephan; Patsopoulos, Nikolaos A; Sawcer, Stephen J; van Es, Michael; Andersen, Peter M; Melki, Judith; Meininger, Vincent; Hardiman, Orla; Landers, John E; Brown, Robert H; Shatunov, Aleksey; Leigh, Nigel; Al-Chalabi, Ammar; Shaw, Christopher E; Traynor, Bryan J; Chiò, Adriano; Restagno, Gabriella; Mora, Gabriele; Ophoff, Roel A; Oksenberg, Jorge R; Van Damme, Philip; Compston, Alastair; Robberecht, Wim; Dubois, Bénédicte; van den Berg, Leonard H; De Jager, Philip L; Veldink, Jan H; de Bakker, Paul I W.

Hum Mol Genet; 23(7): 1916-22, 2014 Apr 01.

Artigo em Inglês | MEDLINE | ID: mdl-24234648

18.

A genome-wide association study identifies a functional ERAP2 haplotype associated with birdshot chorioretinopathy.

Kuiper, Jonas J W; Van Setten, Jessica; Ripke, Stephan; Van 'T Slot, Ruben; Mulder, Flip; Missotten, Tom; Baarsma, G Seerp; Francioli, Laurent C; Pulit, Sara L; De Kovel, Carolien G F; Ten Dam-Van Loon, Ninette; Den Hollander, Anneke I; Huis in het Veld, Paulien; Hoyng, Carel B; Cordero-Coma, Miguel; Martín, Javier; Llorenç, Victor; Arya, Bharti; Thomas, Dhanes; Bakker, Steven C; Ophoff, Roel A; Rothova, Aniki; De Bakker, Paul I W; Mutis, Tuna; Koeleman, Bobby P C.

Hum Mol Genet; 23(22): 6081-7, 2014 Nov 15.

Artigo em Inglês | MEDLINE | ID: mdl-24957906

19.

Rare, low-frequency, and common variants in the protein-coding sequence of biological candidate genes from GWASs contribute to risk of rheumatoid arthritis.

Diogo, Dorothée; Kurreeman, Fina; Stahl, Eli A; Liao, Katherine P; Gupta, Namrata; Greenberg, Jeffrey D; Rivas, Manuel A; Hickey, Brendan; Flannick, Jason; Thomson, Brian; Guiducci, Candace; Ripke, Stephan; Adzhubey, Ivan; Barton, Anne; Kremer, Joel M; Alfredsson, Lars; Sunyaev, Shamil; Martin, Javier; Zhernakova, Alexandra; Bowes, John; Eyre, Steve; Siminovitch, Katherine A; Gregersen, Peter K; Worthington, Jane; Klareskog, Lars; Padyukov, Leonid; Raychaudhuri, Soumya; Plenge, Robert M.

Am J Hum Genet; 92(1): 15-27, 2013 Jan 10.

Artigo em Inglês | MEDLINE | ID: mdl-23261300

20.

Improved detection of common variants associated with schizophrenia and bipolar disorder using pleiotropy-informed conditional false discovery rate.

Andreassen, Ole A; Thompson, Wesley K; Schork, Andrew J; Ripke, Stephan; Mattingsdal, Morten; Kelsoe, John R; Kendler, Kenneth S; O'Donovan, Michael C; Rujescu, Dan; Werge, Thomas; Sklar, Pamela; Roddey, J Cooper; Chen, Chi-Hua; McEvoy, Linda; Desikan, Rahul S; Djurovic, Srdjan; Dale, Anders M.

PLoS Genet; 9(4): e1003455, 2013 Apr.

Artigo em Inglês | MEDLINE | ID: mdl-23637625

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