Resultados da busca - Caroline Crombie
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Association of Neuregulin 1 with Schizophrenia Confirmed in a Scottish Population por Hreinn Stefánsson, Jane Sarginson, Augustine Kong, Phil Yates, Valgerður Steinthórsdóttir, Einar Gudfinnsson, Steinunn Gunnarsdottir, Nicholas Walker, Hannes Pétursson, Caroline Crombie, Andrés Ingason, Jeffrey R. Gulcher, Kāri Stefánsson, David St Clair
Publicado em 2003Artigo -
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A threonine to isoleucine missense mutation in the pericentriolar material 1 gene is strongly associated with schizophrenia por Susmita Datta, Andrew McQuillin, Mie Rizig, Ekaterini Blaveri, Srinivasa Thirumalai, Gursharan Kalsi, Jacob Lawrence, Nicholas Bass, Vinita Puri, Khalid Choudhury, J Pimm, Caroline Crombie, G. T. Fraser, Nicholas Walker, David Curtis, Marketa Zvelebil, A C Pereira, Radhika Kandaswamy, David St Clair, Hugh Gurling
Publicado em 2008Artigo -
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A Genome-Wide Investigation of SNPs and CNVs in Schizophrenia por Anna C. Need, Dongliang Ge, Michael E. Weale, Jessica M. Maia, Sheng Feng, Erin L. Heinzen, Kevin V. Shianna, Woohyun Yoon, Dalia Kasperavičiūtė, Massimo Gennarelli, Warren J. Strittmatter, Cristian Bonvicini, Giuseppe Rossi, Karu Jayathilake, Philip A. Cola, Joseph P. McEvoy, Richard S.E. Keefe, Elizabeth Fisher, Pamela L. St. Jean, Ina Giegling, Annette M. Hartmann, Hans‐Jürgen Möller, Andreas Ruppert, Gillian Fraser, Caroline Crombie, Lefkos Middleton, David St Clair, Allen D. Roses, Pierandrea Muglia, Clyde Francks, Dan Rujescu, Herbert Y. Meltzer, David B. Goldstein
Publicado em 2009Artigo -
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Copy number variations of chromosome 16p13.1 region associated with schizophrenia por Andrés Ingason, Dan Rujescu, Sven Cichon, Engilbert Sigurðsson, Thordur Sigmundsson, Olli Pietiläinen, Jacobine E. Buizer‐Voskamp, E Strengman, Clyde Francks, Pierandrea Muglia, Arnaldur Gylfason, Ómar Gústafsson, Pall I. Olason, Stacy Steinberg, Thomas Hansen, Klaus D. Jakobsen, Henrik B. Rasmussen, Ina Giegling, HJ Möller, A. Hartmann, Caroline Crombie, G. T. Fraser, Nicholas Walker, Jouko Lönnqvist, Jaana Suvisaari, Annamari Tuulio‐Henriksson, Elvira Bramon, Lambertus A. Kiemeney, Barbara Franke, Robin Murray, Evangelos Vassos, Timothea Toulopoulou, Thomas W. Mühleisen, Sarah Tosato, Mirella Ruggeri, Srdjan Djurovic, Ole A. Andreassen, Z Zhang, Thomas Werge, Roel A. Ophoff, Marcella Rietschel, Markus M. Nöthen, Hannes Pétursson, Hreinn Stefánsson, L. Peltonen, David Collier, Hreinn Stefánsson, David M. St. Clair
Publicado em 2009Artigo -
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Disruption of the neurexin 1 gene is associated with schizophrenia por Dan Rujescu, Andrés Ingason, Sven Cichon, Olli Pietiläinen, Michael R. Barnes, Timothea Toulopoulou, Marco Picchioni, Evangelos Vassos, Ulrich Ettinger, Elvira Bramon, Robin Murray, Mirella Ruggeri, Sarah Tosato, Chiara Bonetto, Stacy Steinberg, Engilbert Sigurðsson, Thordur Sigmundsson, Hannes Pétursson, Arnaldur Gylfason, Pall I. Olason, Gudmundur Hardarsson, Guðrún A. Jónsdóttir, Ómar Gústafsson, Ragnheiður Fossdal, Ina Giegling, Hans‐Jürgen Möller, Annette M. Hartmann, Per Hoffmann, Caroline Crombie, Gillian Fraser, Nicholas Walker, Jouko Lönnqvist, Jaana Suvisaari, Annamari Tuulio‐Henriksson, Srdjan Djurovic, Ingrid Melle, Ole A. Andreassen, Thomas Hansen, Thomas Werge, Lambertus A. Kiemeney, Barbara Franke, Joris A. Veltman, Jacobine E. Buizer‐Voskamp, Chiara Sabatti, Roel A. Ophoff, Marcella Rietschel, Markus M. Nöthen, Kāri Stefánsson, Leena Peltonen, David St Clair, Hreinn Stefánsson, David Collier
Publicado em 2008Artigo -
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Large recurrent microdeletions associated with schizophrenia por Hreinn Stefánsson, Dan Rujescu, Sven Cichon, Olli Pietiläinen, Andrés Ingason, Stacy Steinberg, Ragnheiður Fossdal, Engilbert Sigurðsson, Thordur Sigmundsson, Jacobine E. Buizer‐Voskamp, Thomas Hansen, Klaus D. Jakobsen, Pierandrea Muglia, Clyde Francks, Paul M. Matthews, Arnaldur Gylfason, Bjarni V. Halldórsson, Daníel F. Guðbjartsson, Thorgeir E. Thorgeirsson, Ásgeir Sigurðsson, Aðalbjörg Jónasdóttir, Áslaug Jónasdóttir, Ásgeir Björnsson, Sigurborg Mattiasdottir, Thórarinn Blöndal, Magnús Haraldsson, Brynja B. Magnúsdóttir, Ina Giegling, Hans‐Jürgen Möller, Annette M. Hartmann, Kevin V. Shianna, Dongliang Ge, Anna C. Need, Caroline Crombie, Gillian Fraser, Nicholas Walker, Jouko Lönnqvist, Jaana Suvisaari, Annamarie Tuulio-Henriksson, Tiina Paunio, Timi Toulopoulou, Elvira Bramon, Marta Di Forti, Robin Murray, Mirella Ruggeri, Evangelos Vassos, Sarah Tosato, Muriel Walshe, Tao Li, Catalina Vasilescu, Thomas W. Mühleisen, August G. Wang, Henrik Ullum, Srdjan Djurovic, Ingrid Melle, Jes Olesen, Lambertus A. Kiemeney, Barbara Franke, Chiara Sabatti, Nelson B. Freimer, Jeffrey R. Gulcher, Unnur Þorsteinsdóttir, Augustine Kong, Ole A. Andreassen, Roel A. Ophoff, Alexander Georgi, Marcella Rietschel, Thomas Werge, Hannes Pétursson, David B. Goldstein, Markus M. Nöthen, Leena Peltonen, David Collier, David St Clair, Kāri Stefánsson
Publicado em 2008Artigo -
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Common polygenic variation contributes to risk of schizophrenia and bipolar disorder por 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
Publicado em 2009Artigo -
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Rare chromosomal deletions and duplications increase risk of schizophrenia por 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
Publicado em 2008Artigo
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Assuntos relacionados
Biology
Gene
Genetics
Psychiatry
Schizophrenia (object-oriented programming)
Genotype
Medicine
Single-nucleotide polymorphism
Copy-number variation
Genome
Allele
Psychology
Environmental health
Genome-wide association study
Haplotype
Population
Autism
Bipolar disorder
Chromosome
Cognition
Exon
Genetic association
Linkage disequilibrium
Mutation
Psychosis
Astrophysics
Candidate gene
Chemistry
Chromatography
Clinical psychology