نتائج البحث - Nicholas Walker
- يعرض 1 - 14 نتائج من 14
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Association of Neuregulin 1 with Schizophrenia Confirmed in a Scottish Population حسب 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
منشور في 2003Artigo -
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Oral administration of maternal vaginal microbes at birth to restore gut microbiome development in infants born by caesarean section: A pilot randomised placebo-controlled trial حسب Brooke C. Wilson, Éadaoin M. Butler, Celia P. Grigg, José G. B. Derraik, Valentina Chiavaroli, Nicholas Walker, Suma Mary Thampi, Christine Creagh, Abigail J. Reynolds, Tommi Vatanen, Justin M. O’Sullivan, Wayne S. Cutfield
منشور في 2021Artigo -
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A threonine to isoleucine missense mutation in the pericentriolar material 1 gene is strongly associated with schizophrenia حسب 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
منشور في 2008Artigo -
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Copy number variations of chromosome 16p13.1 region associated with schizophrenia حسب 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
منشور في 2009Artigo -
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Disruption of the neurexin 1 gene is associated with schizophrenia حسب 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
منشور في 2008Artigo -
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Expanding the range of ZNF804A variants conferring risk of psychosis حسب Stacy Steinberg, Ole Mors, Anders D. Børglum, Ómar Gústafsson, Thomas Werge, Preben Bo Mortensen, Ole A. Andreassen, Engilbert Sigurðsson, Thorgeir E. Thorgeirsson, Yvonne Böttcher, Pall I. Olason, Roel A. Ophoff, Sven Cichon, Iris H Gudjonsdottir, Olli Pietiläinen, Mette Nyegaard, Annamari Tuulio‐Henriksson, Andrés Ingason, Thomas Hansen, Lavinia Athanasiu, Jaana Suvisaari, Jouko Lönnqvist, Tiina Paunio, Annette M. Hartmann, Gesche Jürgens, Merete Nordentoft, David M. Hougaard, B Nørgaard‐Pedersen, René Breuer, HJ Möller, Ina Giegling, Birte Glenthøj, Henrik Berg Rasmussen, Manuel Mattheisen, István Bitter, János Réthelyi, Thordur Sigmundsson, Ragnheiður Fossdal, Unnur Þorsteinsdóttir, Mirella Ruggeri, Sarah Tosato, E Strengman, Lambertus A. Kiemeney, Ingrid Melle, Srdjan Djurovic, Л. И. Абрамова, В. Г. Каледа, Muriel Walshe, Elvira Bramon, Evangelos Vassos, Tao Li, G. T. Fraser, Nicholas Walker, T. Toulopoulou, Joeng Lim Yoon, Nelson B. Freimer, Rita M. Cantor, Robin Murray, Augustine Kong, В. Е. Голимбет, Erik G. Jönsson, Lars Terenius, Ingrid Agartz, Hannes Pétursson, Markus M. Nöthen, Marcella Rietschel, Leena Peltonen, Dan Rujescu, David Collier, Hreinn Stefánsson, David St Clair, Kāri Stefánsson
منشور في 2010Artigo -
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Large recurrent microdeletions associated with schizophrenia حسب 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
منشور في 2008Artigo -
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Common polygenic variation contributes to risk of schizophrenia and bipolar disorder حسب 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
منشور في 2009Artigo -
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Rare chromosomal deletions and duplications increase risk of schizophrenia حسب 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
منشور في 2008Artigo -
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Common variants at VRK2 and TCF4 conferring risk of schizophrenia حسب Stacy Steinberg, Simone de Jong, Ole A. Andreassen, Thomas Werge, Anders D. Børglum, Ole Mors, Preben Bo Mortensen, Ómar Gústafsson, Javier Costas, Olli Pietiläinen, Ditte Demontis, Sergi Papiol, Johanna Huttenlocher, Manuel Mattheisen, René Breuer, Evangelos Vassos, Ina Giegling, Gillian Fraser, Nicholas Walker, Annamari Tuulio‐Henriksson, Jaana Suvisaari, Jouko Lönnqvist, Tiina Paunio, Ingrid Agartz, Ingrid Melle, Srdjan Djurovic, Eric Strengman, Gesche Jürgens, Birte Glenthøj, Lars Terenius, David M. Hougaard, Torben Ørntoft, Carsten Wiuf, Michael Didriksen, Mads V. Hollegaard, Merete Nordentoft, Ruud van Winkel, Günter Kenis, Л. И. Абрамова, В. Г. Каледа, Manuel Arrojo, Julio Sanjuán, Celso Arango, Swetlana Sperling, Moritz J. Rossner, Michele Ribolsi, Valentina Magni, Alberto Siracusano, Claus Christiansen, Lambertus A. Kiemeney, Jan H. Veldink, Leonard van den Berg, Andrés Ingason, Pierandrea Muglia, Robin Murray, Markus M. Nöthen, Engilbert Sigurðsson, Hannes Pétursson, Unnur Þorsteinsdóttir, Augustine Kong, I. Alex Rubino, Marc D. Binder, János Réthelyi, István Bitter, Erik G. Jönsson, В. Е. Голимбет, Ãngel Carracedo, Hannelore Ehrenreich, Nick Craddock, Michael J. Owen, Michael O’Donovan, Mirella Ruggeri, Sarah Tosato, Leena Peltonen, Roel A. Ophoff, David Collier, David St Clair, Marcella Rietschel, Sven Cichon, Hreinn Stefánsson, Dan Rujescu, Kāri Stefánsson
منشور في 2011Revisão -
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Common variants conferring risk of schizophrenia حسب Hreinn Stefánsson, Roel A. Ophoff, Stacy Steinberg, Ole A. Andreassen, Sven Cichon, Dan Rujescu, Thomas Werge, Olli Pietiläinen, Ole Mors, Preben Bo Mortensen, Engilbert Sigurðsson, Ómar Gústafsson, Mette Nyegaard, Annamari Tuulio‐Henriksson, Andrés Ingason, Thomas Hansen, Jaana Suvisaari, Jouko Lönnqvist, Tiina Paunio, Anders D. Børglum, Annette M. Hartmann, Anders Fink‐Jensen, Merete Nordentoft, David M. Hougaard, Bent Nørgaard‐Pedersen, Yvonne Böttcher, Jes Olesen, René Breuer, Hans‐Jürgen Möller, Ina Giegling, Henrik B. Rasmussen, Sally Timm, Manuel Mattheisen, István Bitter, János Réthelyi, Brynja B. Magnúsdóttir, Thordur Sigmundsson, Pall I. Olason, Gísli Másson, Jeffrey R. Gulcher, Magnús Haraldsson, Ragnheiður Fossdal, Thorgeir E. Thorgeirsson, Unnur Þorsteinsdóttir, Mirella Ruggeri, Sarah Tosato, Barbara Franke, Eric Strengman, Lambertus A. Kiemeney, Ingrid Melle, Srdjan Djurovic, Л. И. Абрамова, В. Г. Каледа, Julio Sanjuán, Rosa de Llanos, Elvira Bramon, Evangelos Vassos, Gillian Fraser, Ulrich Ettinger, Marco Picchioni, Nicholas Walker, Timi Toulopoulou, Anna C. Need, Dongliang Ge, Joeng Lim Yoon, Kevin V. Shianna, Nelson B. Freimer, Rita M. Cantor, Robin Murray, Augustine Kong, В. Е. Голимбет, Ãngel Carracedo, Celso Arango, Javier Costas, Erik G. Jönsson, Lars Terenius, Ingrid Agartz, Hannes Pétursson, Markus M. Nöthen, Marcella Rietschel, Paul M. Matthews, Pierandrea Muglia, Leena Peltonen, David St Clair, David B. Goldstein, Kāri Stefánsson, David Collier
منشور في 2009Artigo -
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Common variant at 16p11.2 conferring risk of psychosis حسب Stacy Steinberg, Simone de Jong, Manuel Mattheisen, Javier Costas, Ditte Demontis, Stéphane Jamain, Olli Pietiläinen, Kuang Lin, Sergi Papiol, Johanna Huttenlocher, Engilbert Sigurðsson, Evangelos Vassos, Ina Giegling, René Breuer, G. T. Fraser, Nicholas Walker, Ingrid Melle, Srdjan Djurovic, Ingrid Agartz, Annamari Tuulio‐Henriksson, Jaana Suvisaari, Jouko Lönnqvist, Tiina Paunio, Line Olsen, Thomas Hansen, Andrés Ingason, Matti Pirinen, E Strengman, David M. Hougaard, Torben Ørntoft, Michael Didriksen, Mads V. Hollegaard, Merete Nordentoft, Л. И. Абрамова, В. Г. Каледа, Manuel Arrojo, Julio Sanjuán, Celso Arango, Bruno Étain, Frank Bellivier, A. Méary, Franck Schürhoff, Andreı̈ Szöke, Michele Ribolsi, Valentina Magni, Alberto Siracusano, Swetlana Sperling, Moritz J. Rossner, Claus Christiansen, Lambertus A. Kiemeney, Barbara Franke, Leonard H. van den Berg, Jan H. Veldink, Sarah Curran, Patrick Bolton, Martin Poot, Wouter Staal, Karola Rehnström, Helena Kilpinen, Christine M. Freitag, Jobst Meyer, Patrik K. E. Magnusson, Evald Sæmundsen, Igor Martsenkovsky, I Bikshaieva, I.I. Martsenkovska, O.S. Vashchenko, Marija Raleva, K Paketchieva, Branislav Stefanovski, Naser Durmishi, Milica Pejović-Milovančević, Dušica Lečić Toševski, Teimuraz Silagadze, N Naneishvili, Nina Mikeladze, Simon Surguladze, John B. Vincent, Anne Farmer, Philip B. Mitchell, A. Jordan Wright, Peter R. Schofield, Janice M. Fullerton, Grant W. Montgomery, Nicholas G. Martin, I. Alex Rubino, Ruud van Winkel, Günter Kenis, Marc D. Binder, János Réthelyi, István Bitter, Lars Terenius, Erik G. Jönsson, S C Bakker, Jim van Os, Assen Jablensky, Marion Leboyer, Elvira Bramon, John Powell, Robin Murray
منشور في 2012Artigo
أدوات البحث:
موضوعات ذات صلة
Biology
Genetics
Psychiatry
Schizophrenia (object-oriented programming)
Gene
Medicine
Psychology
Genotype
Single-nucleotide polymorphism
Allele
Copy-number variation
Genome
Psychosis
Environmental health
Haplotype
Population
Autism
Bipolar disorder
Chromosome
Cognition
Computational biology
Exon
Genetic association
Genome-wide association study
Internal medicine
Linkage disequilibrium
Mutation
Physics
Adverse effect
Alternative medicine