Parsing psychosis subtypes through investigations of rare genetic variants

Por Bergen, Sarah E.
Publicado no EBioMedicine (2016)

Genome-wide association studies (GWAS) of schizophrenia: does bigger lead to better results?

Por Bergen, Sarah E., Petryshen, Tracey L.
Publicado em 2012

Detection of susceptibility genes as modifiers due to subgroup differences in complex disease

Por Bergen, Sarah E, Maher, Brion S, Fanous, Ayman H, Kendler, Kenneth S
Publicado em 2010

Socioeconomic Status and Social Support Following Illicit Drug Use: Causal Pathways or Common Liability?

Por Bergen, Sarah E., Gardner, Charles O., Aggen, Steven H., Kendler, Kenneth S.
Publicado em 2008

Polymorphisms in SLC6A4, PAH, GABRB3, and MAOB and Modification of Psychotic Disorder Features

Por Bergen, Sarah E., Fanous, Ayman H., Walsh, Dermot, O’Neill, Francis Anthony, Kendler, Kenneth S.
Publicado em 2009

No Association of Dysbindin With Symptom Factors of Schizophrenia in an Irish Case–Control Sample

Por Bergen, Sarah E., Fanous, Ayman H., Kuo, Po-Hsiu, Wormley, Brandon K., O’Neill, F. Anthony, Walsh, Dermot, Riley, Brien P., Kendler, Kenneth S.
Publicado em 2010

Genetic modifiers and subtypes in schizophrenia: Investigations of age at onset, severity, sex and family history

Por Bergen, Sarah E., O’Dushlaine, Colm T., Lee, Phil H., Fanous, Ayman H., Ruderfer, Douglas M., Ripke, Stephan, Sullivan, Patrick F., Smoller, Jordan W., Purcell, Shaun M., Corvin, Aiden
Publicado no Schizophr Res (2014)

Genetic variation in 117 myelination-related genes in schizophrenia: Replication of association to lipid biosynthesis genes

Por Stokowy, Tomasz, Polushina, Tatiana, Sønderby, Ida E., Karlsson, Robert, Giddaluru, Sudheer, Le Hellard, Stephanie, Bergen, Sarah E., Sullivan, Patrick F., Andreassen, Ole A., Djurovic, Srdjan, Hultman, Christina M., Steen, Vidar M.
Publicado no Sci Rep (2018)

Cis-Acting Regulation of Brain-Specific ANK3 Gene Expression by a Genetic Variant Associated with Bipolar Disorder

Por Rueckert, Erroll H., Barker, Douglas, Ruderfer, Douglas, Bergen, Sarah E., O’Dushlaine, Colm, Luce, Catherine J., Sheridan, Steven D., Theriault, Kraig M., Chambert, Kimberly, Moran, Jennifer, Purcell, Shaun, Madison, Jon M., Haggarty, Stephen J., Sklar, Pamela
Publicado em 2012

Discovery and Statistical Genotyping of Copy-Number Variation from Whole-Exome Sequencing Depth

Por Fromer, Menachem, Moran, Jennifer L., Chambert, Kimberly, Banks, Eric, Bergen, Sarah E., Ruderfer, Douglas M., Handsaker, Robert E., McCarroll, Steven A., O’Donovan, Michael C., Owen, Michael J., Kirov, George, Sullivan, Patrick F., Hultman, Christina M., Sklar, Pamela, Purcell, Shaun M.
Publicado em 2012

Association Study of 167 Candidate Genes for Schizophrenia Selected by a Multi-Domain Evidence-Based Prioritization Algorithm and Neurodevelopmental Hypothesis

Por Zhao, Zhongming, Webb, Bradley T., Jia, Peilin, Bigdeli, T. Bernard, Maher, Brion S., van den Oord, Edwin, Bergen, Sarah E., Amdur, Richard L., O'Neill, Francis A., Walsh, Dermot, Thiselton, Dawn L., Chen, Xiangning, Pato, Carlos N., Riley, Brien P., Kendler, Kenneth S., Fanous, Ayman H.
Publicado em 2013

High density methylation QTL analysis in human blood via next-generation sequencing of the methylated genomic DNA fraction

Por McClay, Joseph L., Shabalin, Andrey A., Dozmorov, Mikhail G., Adkins, Daniel E., Kumar, Gaurav, Nerella, Srilaxmi, Clark, Shaunna L., Bergen, Sarah E., Hultman, Christina M., Magnusson, Patrik K. E., Sullivan, Patrick F., Aberg, Karolina A., van den Oord, Edwin J. C. G.
Publicado no Genome Biol (2015)

Combined whole methylome and genome-wide association study implicates CNTN4 in alcohol use

Por Clark, Shaunna L., Aberg, Karolina A., Nerella, Srilaxmi, Kumar, Gaurav, McClay, Joseph L., Chen, Wenan, Xie, Linying Y., Harada, Aki, Shabalin, Andrey A., Gao, Guimin, Bergen, Sarah E., Hultman, Christina M., Magnusson, Patrik K.E., Sullivan, Patrick F, van den Oord, Edwin JCG
Publicado no Alcohol Clin Exp Res (2015)

Genome-Wide Association Study of Clinical Dimensions of Schizophrenia: Polygenic Effect on Disorganized Symptoms

Por Fanous, Ayman H., Zhou, Baiyu, Aggen, Steven H., Bergen, Sarah E., Amdur, Richard L., Duan, Jubao, Sanders, Alan R., Shi, Jianxin, Mowry, Bryan J., Olincy, Ann, Amin, Farooq, Cloninger, C. Robert, Silverman, Jeremy M., Buccola, Nancy G., Byerley, William F., Black, Donald W., Freedman, Robert, Dudbridge, Frank, Holmans, Peter A., Ripke, Stephan, Gejman, Pablo V., Kendler, Kenneth S., Levinson, Douglas F.
Publicado em 2012

Copy Number Variants in Schizophrenia: Confirmation of Five Previous Findings and New Evidence for 3q29 Microdeletions and VIPR2 Duplications

Por Levinson, Douglas F., Duan, Jubao, Oh, Sang, Wang, Kai, Sanders, Alan R., Shi, Jianxin, Zhang, Nancy, Mowry, Bryan J., Olincy, Ann, Amin, Farooq, Cloninger, C. Robert, Silverman, Jeremy M., Buccola, Nancy G., Byerley, William F., Black, Donald W., Kendler, Kenneth S., Freedman, Robert, Dudbridge, Frank, Pe’er, Itsik, Hakonarson, Hakon, Bergen, Sarah E., Fanous, Ayman H., Holmans, Peter A., Gejman, Pablo V.
Publicado no Am J Psychiatry (2011)

Copy Number Variation in Schizophrenia in Sweden

Por Szatkiewicz, Jin P., O’Dushlaine, Colm, Chen, Guanhua, Chambert, Kimberly, Moran, Jennifer L., Neale, Benjamin M, Fromer, Menachem, Ruderfer, Douglas, Akterin, Susanne, Bergen, Sarah E, Kähler, Anna, Magnusson, Patrik KE, Kim, Yunjung, Crowley, James J, Rees, Elliott, Kirov, George, O’Donovan, Michael C., Owen, Michael J., Walters, James, Scolnick, Edward, Sklar, Pamela, Purcell, Shaun, Hultman, Christina M., McCarroll, Steven A., Sullivan, Patrick F.
Publicado no Mol Psychiatry (2014)

A polygenic burden of rare disruptive mutations in schizophrenia

Por Purcell, Shaun M., Moran, Jennifer L., Fromer, Menachem, Ruderfer, Douglas, Solovieff, Nadia, Roussos, Panos, O’Dushlaine, Colm, Chambert, Kimberly, Bergen, Sarah E., Kähler, Anna, Duncan, Laramie, Stahl, Eli, Genovese, Giulio, Fernández, Esperanza, Collins, Mark O, Komiyama, Noboru H., Choudhary, Jyoti S., Magnusson, Patrik K. E., Banks, Eric, Shakir, Khalid, Garimella, Kiran, Fennell, Tim, de Pristo, Mark, Grant, Seth G.N., Haggarty, Stephen, Gabriel, Stacey, Scolnick, Edward M., Lander, Eric S., Hultman, Christina, Sullivan, Patrick F., McCarroll, Steven A., Sklar, Pamela
Publicado em 2014

Impact of a cis-associated gene expression SNP in 20q11.22 on bipolar disorder susceptibility, hippocampal structure and cognitive performance

Por Li, Ming, Luo, Xiong-jian, Landén, Mikael, Bergen, Sarah E., Hultman, Christina M., Li, Xiao, Zhang, Wen, Yao, Yong-Gang, Zhang, Chen, Liu, Jiewei, Mattheisen, Manuel, Cichon, Sven, Mühleisen, Thomas W., Degenhardt, Franziska A., Nöthen, Markus M., Schulze, Thomas G., Grigoroiu-Serbanescu, Maria, Li, Hao, Fuller, Chris K., Chen, Chunhui, Dong, Qi, Chen, Chuansheng, Jamain, Stéphane, Leboyer, Marion, Bellivier, Frank, Etain, Bruno, Kahn, Jean-Pierre, Henry, Chantal, Preisig, Martin, Kutalik, Zoltán, Castelao, Enrique, Wright, Adam, Mitchell, Philip B., Fullerton, Janice M., Schofield, Peter R., Montgomery, Grant W., Medland, Sarah E., Gordon, Scott D., Martin, Nicholas G., Rietschel, Marcella, Liu, Chunyu, Kleinman, Joel E., Hyde, Thomas M., Weinberger, Daniel R., Su, Bing
Publicado no Br J Psychiatry (2015)

A rare deletion at distal 16p11.2 is implicated in schizophrenia

Por Guha, Saurav, Rees, Elliott, Darvasi, Ariel, Ivanov, Dobril, Ikeda, Masashi, Bergen, Sarah E., Magnusson, Patrik K, Cormican, Paul, Morris, Derek, Gill, Michael, Cichon, Sven, Rosenfeld, Jeffrey A., Lee, Annette, Gregersen, Peter K., Kane, John M., Malhotra, Anil K., Rietschel, Marcella, Nöthen, Markus M., Degenhardt, Franziska, Priebe, Lutz, Breuer, René, Strohmaier, Jana, Ruderfer, Douglas M, Moran, Jennifer L, Chambert, Kimberly D, Sanders, Alan R., Shi, Jianxin, Kendler, Kenneth, Riley, Brien, O’Neill, Tony, Walsh, Dermot, Malhotra, Dheeraj, Corvin, Aiden, Purcell, Shaun, Sklar, Pamela, Iwata, Nakao, Hultman, Christina M, Sullivan, Patrick F., Sebat, Jonathan, McCarthy, Shane, Gejman, Pablo V., Levinson, Douglas F., Owen, Michael J, O’Donovan, Michael C, Lencz, Todd, Kirov, George
Publicado em 2013

Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder

Por Hou, Liping, Bergen, Sarah E., Akula, Nirmala, Song, Jie, Hultman, Christina M., Landén, Mikael, Adli, Mazda, Alda, Martin, Ardau, Raffaella, Arias, Bárbara, Aubry, Jean-Michel, Backlund, Lena, Badner, Judith A., Barrett, Thomas B., Bauer, Michael, Baune, Bernhard T., Bellivier, Frank, Benabarre, Antonio, Bengesser, Susanne, Berrettini, Wade H., Bhattacharjee, Abesh Kumar, Biernacka, Joanna M., Birner, Armin, Bloss, Cinnamon S., Brichant-Petitjean, Clara, Bui, Elise T., Byerley, William, Cervantes, Pablo, Chillotti, Caterina, Cichon, Sven, Colom, Francesc, Coryell, William, Craig, David W., Cruceanu, Cristiana, Czerski, Piotr M., Davis, Tony, Dayer, Alexandre, Degenhardt, Franziska, Del Zompo, Maria, DePaulo, J. Raymond, Edenberg, Howard J., Étain, Bruno, Falkai, Peter, Foroud, Tatiana, Forstner, Andreas J., Frisén, Louise, Frye, Mark A., Fullerton, Janice M., Gard, Sébastien, Garnham, Julie S., Gershon, Elliot S., Goes, Fernando S., Greenwood, Tiffany A., Grigoroiu-Serbanescu, Maria, Hauser, Joanna, Heilbronner, Urs, Heilmann-Heimbach, Stefanie, Herms, Stefan, Hipolito, Maria, Hitturlingappa, Shashi, Hoffmann, Per, Hofmann, Andrea, Jamain, Stephane, Jiménez, Esther, Kahn, Jean-Pierre, Kassem, Layla, Kelsoe, John R., Kittel-Schneider, Sarah, Kliwicki, Sebastian, Koller, Daniel L., König, Barbara, Lackner, Nina, Laje, Gonzalo, Lang, Maren, Lavebratt, Catharina, Lawson, William B., Leboyer, Marion, Leckband, Susan G., Liu, Chunyu, Maaser, Anna, Mahon, Pamela B., Maier, Wolfgang, Maj, Mario, Manchia, Mirko, Martinsson, Lina, McCarthy, Michael J., McElroy, Susan L., McInnis, Melvin G., McKinney, Rebecca, Mitchell, Philip B., Mitjans, Marina, Mondimore, Francis M., Monteleone, Palmiero, Mühleisen, Thomas W., Nievergelt, Caroline M., Nöthen, Markus M., Novák, Tomas, Nurnberger, John I., Nwulia, Evaristus A., Ösby, Urban, Pfennig, Andrea, Potash, James B., Propping, Peter, Reif, Andreas, Reininghaus, Eva, Rice, John, Rietschel, Marcella, Rouleau, Guy A., Rybakowski, Janusz K., Schalling, Martin, Scheftner, William A., Schofield, Peter R., Schork, Nicholas J., Schulze, Thomas G., Schumacher, Johannes, Schweizer, Barbara W., Severino, Giovanni, Shekhtman, Tatyana, Shilling, Paul D., Simhandl, Christian, Slaney, Claire M., Smith, Erin N., Squassina, Alessio, Stamm, Thomas, Stopkova, Pavla, Streit, Fabian, Strohmaier, Jana, Szelinger, Szabolcs, Tighe, Sarah K., Tortorella, Alfonso, Turecki, Gustavo, Vieta, Eduard, Volkert, Julia, Witt, Stephanie H., Wright, Adam, Zandi, Peter P., Zhang, Peng, Zollner, Sebastian, McMahon, Francis J.
Publicado no Hum Mol Genet (2016)