Bilaketaren emaitzak - Christopher P. Morley
- Erakusten 1 - 14 emaitzak -- 14
-
1
-
2
-
3
A Practice Facilitation and Academic Detailing Intervention Can Improve Cancer Screening Rates in Primary Care Safety Net Clinics nork Emily M. Mader, Chester H. Fox, John W. Epling, Gary J. Noronha, Carlos Swanger, Angela M. Wisniewski, Karen Vitale, Amanda Norton, Christopher P. Morley
Argitaratua 2016Artigo -
4
Gene expression analysis of peripheral blood leukocytes from discordant sib-pairs with schizophrenia and bipolar disorder reveals points of convergence between genetic and function... nork Frank A. Middleton, Carlos N. Pato, Karen Gentile, L McGann, Andrea M. Brown, Marco Trauzzi, Heba I. Diab, Christopher P. Morley, Helena Medeiros, A. Macedo, Maria Helena Pinto de Azevedo, Michele T. Pato
Argitaratua 2005Artigo -
5
Support for involvement of neuregulin 1 in schizophrenia pathophysiology nork Tracey L. Petryshen, Frank A. Middleton, Andrew Kirby, Kimberly A. Aldinger, Shaun Purcell, A R Tahl, Christopher P. Morley, L McGann, Karen Gentile, Graham N. Rockwell, Helena Medeiros, Célia Barreto Carvalho, A. Macedo, A. Dourado, J. Valente, Carlos Paz Ferreira, Nick J. Patterson, Maria Helena Pinto de Azevedo, Mark Daly, Carlos N. Pato, Michele T. Pato, Pamela Sklar
Argitaratua 2004Artigo -
6
The genomic psychiatry cohort: Partners in discovery nork 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
Argitaratua 2013Artigo -
7
Genomewide Linkage Analysis of Bipolar Disorder by Use of a High-Density Single-Nucleotide–Polymorphism (SNP) Genotyping Assay: A Comparison with Microsatellite Marker Assays and F... nork Frank A. Middleton, Michele T. Pato, Karen Gentile, Christopher P. Morley, Xinzhi Zhao, Amy F. Eisener, Andrea M. Brown, Tracey L. Petryshen, Andrew Kirby, Helena Medeiros, Célia Barreto Carvalho, A. Macedo, A. Dourado, I. Coelho, J. Valente, M.J. Soares, Carlos Paz Ferreira, M. Lei, Maria Helena Pinto de Azevedo, James L. Kennedy, Mark J. Daly, Pamela Sklar, Carlos N. Pato
Argitaratua 2004Artigo -
8
Evidence for genetic heterogeneity between clinical subtypes of bipolar disorder nork 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
Argitaratua 2017Artigo -
9
Contribution of Rare Copy Number Variants to Bipolar Disorder Risk Is Limited to Schizoaffective Cases nork 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
Argitaratua 2018Artigo -
10
A Rare Functional Noncoding Variant at the GWAS-Implicated MIR137/MIR2682 Locus Might Confer Risk to Schizophrenia and Bipolar Disorder nork 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
Argitaratua 2014Artigo -
11
Common polygenic variation contributes to risk of schizophrenia and bipolar disorder nork Shaun Purcell, Naomi R. Wray, Jennifer Stone, Peter M. Visscher, Michael O’Donovan, Patrick F. Sullivan, Pamela Sklar, Douglas M. Ruderfer, Andrew McQuillin, Derek W. Morris, Colm O’Dushlaine, Aiden Corvin, Peter Holmans, Stuart MacGregor, Hugh Gurling, Douglas Blackwood, Nick Craddock, Michael Gill, Christina M. Hultman, George Kirov, Paul Lichtenstein, Walter Muir, Michael J. Owen, Carlos N. Pato, Edward M. Scolnick, David St Clair, Nigel Williams, Lyudmila Georgieva, Ivan Nikolov, Nadine Norton, Hywel Williams, Драга Тончева, Mariofanna Milanova, Emma Flordal Thelander, Patrick Sullivan, Elaine Kenny, Emma M. Quinn, Khalid Choudhury, Susmita Datta, Jonathan Pimm, Srinivasa Thirumalai, Vinay Puri, Robert Krasucki, Jacob Lawrence, Digby Quested, Nicholas Bass, Caroline Crombie, Gillian Fraser, Soh Leh Kuan, Nicholas Walker, Kevin A. McGhee, Ben Pickard, P. Malloy, Alan Maclean, M. Van Beck, Michele T. Pato, Helena Medeiros, Frank A. Middleton, Célia Barreto Carvalho, Christopher P. Morley, Ayman H. Fanous, David V. Conti, James A. Knowles, Carlos Paz Ferreira, A. Macedo, M.H. Azevedo, Andrew Kirby, Manuel A. R. Ferreira, Mark Daly, Kimberly Chambert, Finny G. Kuruvilla, Stacey B. Gabriel, Kristin Ardlie, Jennifer L. Moran
Argitaratua 2009Artigo -
12
Rare chromosomal deletions and duplications increase risk of schizophrenia nork Jennifer Stone, Michael O’Donovan, Hugh Gurling, George Kirov, Douglas H. R. Blackwood, Aiden Corvin, Nick Craddock, Michael Gill, Christina M. Hultman, Paul Lichtenstein, Andrew McQuillin, Carlos N. Pato, Douglas M. Ruderfer, Michael J. Owen, David St Clair, Patrick F. Sullivan, Pamela Sklar, Shaun Purcell, Joshua M. Korn, Stuart MacGregor, Derek W. Morris, Colm Ó'Dúshláine, Mark Daly, Peter M. Visscher, Peter Holmans, Edward M. Scolnick, Nigel Williams, L. Georgieva, Ivan Nikolov, Nadine Norton, Hywel Williams, Драга Тончева, Vihra Milanova, Emma Flordal Thelander, Patrick Sullivan, Elaine Kenny, John L. Waddington, Khalid Choudhury, Susmita Datta, Jonathan Pimm, Srinivasa Thirumalai, Vinay Puri, Robert Krasucki, Jacob Lawrence, Digby Quested, Nicholas Bass, David Curtis, Caroline Crombie, Gillian Fraser, Soh Leh Kwan, Nicholas Walker, Walter J. Muir, Kevin A. McGhee, Ben Pickard, P. Malloy, Alan Maclean, M. Van Beck, Michele T. Pato, Helena Medeiros, Frank A. Middleton, Célia Barreto Carvalho, Christopher P. Morley, Ayman H. Fanous, David V. Conti, James A. Knowles, Carlos Paz Ferreira, A. Macedo, Maria Helena Pinto de Azevedo, Steve McCarroll, Mark Daly, Kimberly Chambert, Casey Gates, Stacey B. Gabriel, Scott Mahon, Kristen Ardlie
Argitaratua 2008Artigo -
13
Contributions of common genetic variants to risk of schizophrenia among individuals of African and Latino ancestry nork 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
Argitaratua 2019Artigo -
14
Rare coding variants in ten genes confer substantial risk for schizophrenia nork 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
Argitaratua 2022Artigo
Bilaketa egiteko lanabesak:
Antzeko gaiak
Medicine
Biology
Psychiatry
Gene
Genetics
Schizophrenia (object-oriented programming)
Genotype
Single-nucleotide polymorphism
Psychology
Bipolar disorder
Computational biology
Genome-wide association study
Allele
Genetic association
Internal medicine
Neuroscience
Pathology
Psychosis
SNP
Cognition
Computer science
Copy-number variation
Economics
Environmental health
Genetic variation
Genome
Heritability
Mood
Population
Psychological intervention