खोज परिणाम - Célia Barreto Carvalho
- प्रदर्शित 1 - 6 परिणाम 6
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1
Evidence for linkage disequilibrium between the alpha 7‐nicotinic receptor gene (CHRNA7) locus and schizophrenia in Azorean families* द्वारा Junzhe Xu, Michele T. Pato, Camille Dalla Torre, Helena Medeiros, Célia Barreto Carvalho, Vincenzo S. Basile, Amy L. Bauer, Ana Dourado, J. Valente, M.J. Soares, A. Macedo, Isabel Coelho, Carlos Paz Ferreira, M.H. Azevedo, Fabìo Macciardi, James L. Kennedy, Carlos N. Pato
प्रकाशित 2001Artigo -
2
Support for involvement of neuregulin 1 in schizophrenia pathophysiology द्वारा 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
प्रकाशित 2004Artigo -
3
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... द्वारा 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
प्रकाशित 2004Artigo -
4
Common polygenic variation contributes to risk of schizophrenia and bipolar disorder द्वारा 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
प्रकाशित 2009Artigo -
5
Rare chromosomal deletions and duplications increase risk of schizophrenia द्वारा 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
प्रकाशित 2008Artigo -
6
Contributions of common genetic variants to risk of schizophrenia among individuals of African and Latino ancestry द्वारा 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
प्रकाशित 2019Artigo
खोज साधन:
संबंधित विषय
Biology
Gene
Genetics
Genotype
Single-nucleotide polymorphism
Psychiatry
Schizophrenia (object-oriented programming)
Allele
Medicine
Genetic association
Genome-wide association study
Haplotype
Linkage disequilibrium
Psychology
1000 Genomes Project
Astrophysics
Bipolar disorder
Candidate gene
Chromosome
Cognition
Computational biology
Copy-number variation
Demography
Environmental health
Exon
Genetic linkage
Genetic variation
Genome
Genotyping
Heritability