Search Results - Janet L. Sobell

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  1. 1
    Comorbidity of Severe Psychotic Disorders With Measures of Substance Use

    Comorbidity of Severe Psychotic Disorders With Measures of Substance Use by Sarah M. Hartz, Carlos N. Pato, Helena Medeiros, Patricia Cavazos‐Rehg, Janet L. Sobell, James A. Knowles, Laura J. Bierut, Michele T. Pato

    Published 2014
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  2. 2
    The genomic psychiatry cohort: Partners in discovery

    The genomic psychiatry cohort: Partners in discovery by Michele T. Pato, Janet L. Sobell, Helena Medeiros, Colony Abbott, Brooke M. Sklar, P.F. Buckley, Evelyn J. Bromet, Michael Escamilla, Ayman H. Fanous, Douglas S. Lehrer, Fabìo Macciardi, Dolores Malaspina, Steve McCarroll, Stephen R. Marder, Jennifer L. Moran, Christopher P. Morley, Humberto Nicolini, Diana O. Perkins, Shaun M. Purcell, Mark Hyman Rapaport, Pamela Sklar, Jordan W. Smoller, James A. Knowles, Carlos N. Pato

    Published 2013
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  3. 3
    Extremely rare variants reveal patterns of germline mutation rate heterogeneity in humans

    Extremely rare variants reveal patterns of germline mutation rate heterogeneity in humans by Jedidiah Carlson, Adam E. Locke, Matthew Flickinger, Matthew Zawistowski, Shawn Levy, R Myers, Michael Boehnke, Hyun Min Kang, Laura J. Scott, Jun Z. Li, Sebastian Zöllner, Devin Absher, Huda Akil, Gerome Breen, Margit Burmeister, Sarah Cohen‐Woods, William G. Iacono, James A. Knowles, Lisa N. Legrand, Qing Lu, Matthew McGue, Melvin G. McInnis, Carlos N. Pato, Michele T. Pato, Margarita Rivera, Janet L. Sobell, John B. Vincent, Stanley J. Watson

    Published 2018
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  4. 4
    Association of DNA Methylation Differences With Schizophrenia in an Epigenome-Wide Association Study

    Association of DNA Methylation Differences With Schizophrenia in an Epigenome-Wide Association Study by Carolina Montaño, Margaret A. Taub, Andrew E. Jaffe, Eiríkur Briem, Jason I. Feinberg, Rakel Trygvadottir, Adrian Idrizi, Árni Rafn Rúnarsson, Birna Berndsen, Ruben C. Gur, Tyler M. Moore, Rodney T. Perry, Doug Fugman, Sarven Sabunciyan, Robert H. Yolken, Thomas M. Hyde, Joel E. Kleinman, Janet L. Sobell, Carlos N. Pato, Michele T. Pato, Rodney C.P. Go, Vishwajit L. Nimgaonkar, Daniel R. Weinberger, David Braff, Raquel E. Gur, Margaret Daniele Fallin, Andrew P. Feinberg

    Published 2016
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  5. 5
    Evaluation of a Susceptibility Gene for Schizophrenia: Genotype Based Meta-Analysis of RGS4 Polymorphisms from Thirteen Independent Samples

    Evaluation of a Susceptibility Gene for Schizophrenia: Genotype Based Meta-Analysis of RGS4 Polymorphisms from Thirteen Independent Samples by Michael E. Talkowski, Howard Seltman, Anne S. Bassett, Linda M. Brzustowicz, Xiangning Chen, Kodavali V. Chowdari, David Collier, Quirino Cordeiro, Aiden Corvin, Smita N. Deshpande, Michael Egan, Michael Gill, Kenneth S. Kendler, George Kirov, Leonard L. Heston, Pat Levitt, David A. Lewis, Tao Li, Károly Mirnics, Derek W. Morris, Nadine Norton, Michael O’Donovan, Michael J. Owen, Christian Richard, Prachi Semwal, Janet L. Sobell, David St Clair, Richard E. Straub, B.K. Thelma, Homero Vallada, Daniel R. Weinberger, Nigel Williams, Joel Wood, Feng Zhang, Bernie Devlin, Vishwajit L. Nimgaonkar

    Published 2006
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  6. 6
    Evidence for genetic heterogeneity between clinical subtypes of bipolar disorder

    Evidence for genetic heterogeneity between clinical subtypes of bipolar disorder by Alexander W. Charney, Douglas M. Ruderfer, Eli A. Stahl, Jennifer L. Moran, Kimberly Chambert, Rich Belliveau, Liz Forty, Katherine Gordon‐Smith, Arianna Di Florio, P H Lee, Evelyn J. Bromet, P.F. Buckley, Michael Escamilla, Ayman H. Fanous, Laura J. Fochtmann, Douglas S. Lehrer, Dolores Malaspina, Stephen R. Marder, Christopher P. Morley, Humberto Nicolini, Diana O. Perkins, Jeffrey J. Rakofsky, Mark Hyman Rapaport, Helena Medeiros, Janet L. Sobell, E K Green, Lena Backlund, Sarah E. Bergen, Anders Juréus, Martin Schalling, Paul Lichtenstein, Panos Roussos, James A. Knowles, Ian Jones, Lisa Jones, Christina M. Hultman, Roy H. Perlis, Shaun Purcell, Steven A. McCarroll, Carlos N. Pato, Michele T. Pato, Nick Craddock, Mikael Landén, Jordan W. Smoller, Pamela Sklar

    Published 2017
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  7. 7
    Contribution of Rare Copy Number Variants to Bipolar Disorder Risk Is Limited to Schizoaffective Cases

    Contribution of Rare Copy Number Variants to Bipolar Disorder Risk Is Limited to Schizoaffective Cases by Alexander W. Charney, Eli A. Stahl, Elaine Green, Chia‐Yen Chen, Jennifer L. Moran, Kimberly Chambert, Richard A. Belliveau, Liz Forty, Katherine Gordon‐Smith, Sang Hyuck Lee, Evelyn J. Bromet, P.F. Buckley, Michael Escamilla, Ayman H. Fanous, Laura J. Fochtmann, Douglas S. Lehrer, Dolores Malaspina, Stephen R. Marder, Christopher P. Morley, Humberto Nicolini, Diana O. Perkins, Jeffrey J. Rakofsky, Mark Hyman Rapaport, Helena Medeiros, Janet L. Sobell, Lena Backlund, Sarah E. Bergen, Anders Juréus, Martin Schalling, Paul Lichtenstein, James A. Knowles, Katherine E. Burdick, Ian Jones, Lisa Jones, Christina M. Hultman, Roy H. Perlis, Shaun Purcell, Steven A. McCarroll, Carlos N. Pato, Michele T. Pato, Ariana Di Florio, Nick Craddock, Mikael Landén, Jordan W. Smoller, Douglas M. Ruderfer, Pamela Sklar

    Published 2018
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  8. 8
    A Rare Functional Noncoding Variant at the GWAS-Implicated MIR137/MIR2682 Locus Might Confer Risk to Schizophrenia and Bipolar Disorder

    A Rare Functional Noncoding Variant at the GWAS-Implicated MIR137/MIR2682 Locus Might Confer Risk to Schizophrenia and Bipolar Disorder by Jubao Duan, Jianxin Shi, Alessia Fiorentino, Catherine Leites, Xiangning Chen, Winton Moy, Jingchun Chen, Boian S. Alexandrov, Anny Usheva, Deli He, Jessica Freda, Niamh L. O’Brien, Andrew McQuillin, Alan R. Sanders, Elliot S. Gershon, Lynn E. DeLisi, A. R. Bishop, Hugh Gurling, Michele T. Pato, Douglas F. Levinson, Kenneth S. Kendler, Carlos N. Pato, Pablo V. Gejman, Pablo V. Gejman, Alan R. Sanders, Jubao Duan, Douglas F. Levinson, Jianxin Shi, Nancy G. Buccola, Bryan Mowry, Robert Freedman, Ann Olincy, Farooq Amin, Donald W. Black, Jeremy M. Silverman, William Byerley, Dragan M. Švrakić, C. Robert Cloninger, Michele T. Pato, Janet L. Sobell, Helena Medeiros, Colony Abbott, Brooke Skar, P.F. Buckley, Evelyn J. Bromet, Michael Escamilla, Ayman H. Fanous, Douglas S. Lehrer, Fabìo Macciardi, Dolores Malaspina, Steve McCarroll, Stephen R. Marder, Jennifer L. Moran, Christopher P. Morley, Humberto Nicolini, Diana O. Perkins, Shaun Purcell, Mark Hyman Rapaport, Pamela Sklar, Jordan W. Smoller, James A. Knowles, Carlos N. Pato

    Published 2014
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  9. 9
    Contributions of common genetic variants to risk of schizophrenia among individuals of African and Latino ancestry

    Contributions of common genetic variants to risk of schizophrenia among individuals of African and Latino ancestry by Tim B. Bigdeli, Giulio Genovese, Penelope Georgakopoulos, Jacquelyn L. Meyers, Roseann E. Peterson, Conrad Iyegbe, Helena Medeiros, Jorge Valderrama, Eric D. Achtyes, Roman Kotov, Eli A. Stahl, Colony Abbott, Maria Helena Pinto de Azevedo, Richard A. Belliveau, Elizabeth Bevilacqua, Evelyn J. Bromet, William Byerley, Célia Barreto Carvalho, Sinéad B. Chapman, Lynn E. DeLisi, Ashley Dumont, Colm O’Dushlaine, Oleg V. Evgrafov, Laura J. Fochtmann, Diane Gage, James L. Kennedy, Becky Kinkead, A. Macedo, Jennifer L. Moran, Christopher P. Morley, Mantosh Dewan, James Nemesh, Diana O. Perkins, Shaun Purcell, Jeffrey J. Rakofsky, Edward M. Scolnick, Brooke M. Sklar, Pamela Sklar, Jordan W. Smoller, Patrick F. Sullivan, Fabìo Macciardi, Stephen R. Marder, Ruben C. Gur, Raquel E. Gur, David Braff, Monica E. Calkins, Robert Freedman, Michael F. Green, Tiffany A. Greenwood, Laura C. Lazzeroni, Gregory A. Light, Keith H. Nuechterlein, Allen D. Radant, Larry J. Seidman, Larry J. Siever, Jeremy M. Silverman, William S. Stone, Catherine A. Sugar, Neal R. Swerdlow, Debby W. Tsuang, Ming T. Tsuang, Bruce I. Turetsky, Humberto Nicolini, Michael Escamilla, Marquis P. Vawter, Janet L. Sobell, Dolores Malaspina, Douglas S. Lehrer, P.F. Buckley, Mark Hyman Rapaport, James A. Knowles, Ayman H. Fanous, Michele T. Pato, Steven A. McCarroll, Carlos N. Pato

    Published 2019
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  10. 10
    Genome-wide association study identifies new locus associated with OCD

    Genome-wide association study identifies new locus associated with OCD by Nora I. Strom, Dongmei Yu, Zachary F. Gerring, Matthew Halvorsen, Abdel Abdellaoui, Cristina Rodríguez-Fontenla, Julia Sealock, Tim B. Bigdeli, Jonathan R. I. Coleman, Behrang Mahjani, Jackson G. Thorp, Katharina Bey, Christie L. Burton, Jurjen J. Luykx, Gwyneth Zai, Kathleen D. Askland, Cristina Barlassina, Judith Becker Nissen, Laura Bellodi, O. Joseph Bienvenu, Donald W. Black, Michael H. Bloch, Julia Boberg, Rosa Bosch, Michael S. Breen, Brian P. Brennan, Helena Brentani, Joseph D. Buxbaum, Jonas Bybjerg‐Grauholm, Enda M. Byrne, Beatríz Camarena, Adrian Camarena, Carolina Cappi, Ángel Carracedo, Miguel Casas, Maria Cristina Cavallini, Valentina Ciullo, Edwin H. Cook, Vladimir Coric, Bernadette Cullen, Elles de Schipper, Bernie Devlin, Srdjan Djurovic, Jason A. Elias, Lauren Erdman, Xavier Estivil, Martha J. Falkenstein, Bengt T. Fundín, Maiken E. Gabrielsen, Fernando S. Goes, Marco A. Grados, Jakob Grove, Wei Guo, Jan Haavik, Kristen Hagen, Alexandra Havdahl, Ana Gabriela Hounie, Donald Hucks, Christina M. Hultman, Magdalena Janecka, Michael A. Jenike, Elinor K. Karlsson, Julia Klawohn, Lambertus Klei, Janice Krasnow, Kristi Krebs, Jason W. Krompinger, Nuria Lanzagorta, Fabìo Macciardi, Brion S. Maher, Evonne McArthur, Nathaniel W. McGregor, Nicole McLaughlin, Sandra Meier, Eurípedes C. Miguel, Maureen Mulhern, Paul S. Nestadt, Erika L. Nurmi, Kevin S. O’Connell, Lisa Osiecki, Teemu Palviainen, Fabrizio Piras, Federica Piras, Ann E. Pulver, Raquel Rabionet, Alfredo Ramı́rez, Scott L. Rauch, Abraham Reichenberg, Jennifer Reichert, Mark A. Riddle, Stephan Ripke, Aline S. Sampaio, Miriam A. Schiele, Laura Sloofman, Jan Smit, Janet L. Sobell, María Soler Artigas, Laurent F. Thomas, Homero Vallada, Jeremy Veenstra‐VanderWeele

    Published 2021
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  11. 11
    Rare coding variants in ten genes confer substantial risk for schizophrenia

    Rare coding variants in ten genes confer substantial risk for schizophrenia by Tarjinder Singh, Timothy Poterba, David Curtis, Huda Akil, Mariam Al Eissa, Jack D. Barchas, Nicholas Bass, Tim B. Bigdeli, Gerome Breen, Evelyn J. Bromet, P.F. Buckley, William E. Bunney, Jonas Bybjerg‐Grauholm, William Byerley, Sinéad B. Chapman, Wei J. Chen, Claire Churchhouse, Nicholas Craddock, Caroline Cusick, Lynn E. DeLisi, Sheila Dodge, Michael Escamilla, Saana Eskelinen, Ayman H. Fanous, Stephen V. Faraone, Alessia Fiorentino, Laurent C. Francioli, Stacey Gabriel, Diane Gage, Sarah A. Gagliano Taliun, Andrea Ganna, Giulio Genovese, David C. Glahn, Jakob Grove, Mei‐Hua Hall, Eija Hämäläinen, Henrike Heyne, Matti Holi, David M. Hougaard, Daniel P. Howrigan, Hailiang Huang, Hai‐Gwo Hwu, René S. Kahn, Hyun Min Kang, Konrad J. Karczewski, George Kirov, James A. Knowles, Francis S. Lee, Douglas S. Lehrer, Francesco Lescai, Dolores Malaspina, Stephen R. Marder, Steven A. McCarroll, Andrew M. McIntosh, Helena Medeiros, Lili Milani, Christopher P. Morley, Derek W. Morris, Preben Bo Mortensen, R Myers, Merete Nordentoft, Niamh L. O’Brien, Ana Maria Olivares, Döst Öngür, Willem H. Ouwehand, Duncan S. Palmer, Tiina Paunio, Digby Quested, Mark Hyman Rapaport, Elliott Rees, Brandi Rollins, F. Kyle Satterstrom, Alan F. Schatzberg, Edward M. Scolnick, Laura J. Scott, Sally I. Sharp, Pamela Sklar, Jordan W. Smoller, Janet L. Sobell, Matthew Solomonson, Eli A. Stahl, Christine Stevens, Jaana Suvisaari, Grace Tiao, Stanley J. Watson, Nicholas A. Watts, Douglas Blackwood, Anders D. Børglum, Bruce M. Cohen, Aiden Corvin, Tõnu Esko, Nelson B. Freimer, Stephen J. Glatt, Christina M. Hultman, Andrew McQuillin, Aarno Palotie, Carlos N. Pato, Michele T. Pato, Ann E. Pulver, David St Clair

    Published 2022
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