检索结果 - David Curtis

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  1. 1
    A rapid method for combined analysis of common and rare variants at the level of a region, gene, or pathway

    A rapid method for combined analysis of common and rare variants at the level of a region, gene, or pathway 由 David Curtis

    出版 2012
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  2. 2
    Pathway analysis of whole exome sequence data provides further support for the involvement of histone modification in the aetiology of schizophrenia

    Pathway analysis of whole exome sequence data provides further support for the involvement of histone modification in the aetiology of schizophrenia 由 David Curtis

    出版 2016
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  3. 3
    Polygenic risk score for schizophrenia is more strongly associated with ancestry than with schizophrenia

    Polygenic risk score for schizophrenia is more strongly associated with ancestry than with schizophrenia 由 David Curtis

    出版 2018
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  4. 4
    Analysis of Rare Coding Variants in 470,000 UK Biobank Participants Reveals Genetic Associations With Childhood Asthma Predisposition

    Analysis of Rare Coding Variants in 470,000 UK Biobank Participants Reveals Genetic Associations With Childhood Asthma Predisposition 由 Zhenzhen Liu, David Curtis

    出版 2025
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  5. 5
    Study of Regions of Extended Homozygosity Provides a Powerful Method to Explore Haplotype Structure of Human Populations

    Study of Regions of Extended Homozygosity Provides a Powerful Method to Explore Haplotype Structure of Human Populations 由 David Curtis, Anna E. Vine, Jo Knight

    出版 2008
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  6. 6
    Case–control studies show that a non-conservative amino-acid change from a glutamine to arginine in the P2RX7 purinergic receptor protein is associated with both bipolar- and unipolar-affective disorders

    Case–control studies show that a non-conservative amino-acid change from a glutamine to arginine in the P2RX7 purinergic receptor protein is associated with both bipolar- and unipo... 由 Andrew McQuillin, Nicholas Bass, Khalid Choudhury, Vinita Puri, Michael Kosmin, Jacob Lawrence, David Curtis, Hugh Gurling

    出版 2008
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  7. 7
    National consensus statement on opioid agonist treatment in custodial settings

    National consensus statement on opioid agonist treatment in custodial settings 由 Jocelyn Chan, Jon Cook, M. David Curtis, Adrian Dunlop, Ele Morrison, Suzanne Nielsen, Rebecca Winter, Thileepan Naren

    出版 2025
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  8. 8
    Allelic variation in the vitamin D receptor influences susceptibility to IDDM in Indian Asians

    Allelic variation in the vitamin D receptor influences susceptibility to IDDM in Indian Asians 由 Michael McDermott, Anupama Ramachandran, B Ogunkolade, E Aganna, David Curtis, Barbara J. Boucher, Chamukuttan Snehalatha, G. A. Hitman

    出版 1997
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  9. 9
    Genetic association of the tachykinin receptor 1 <i>TACR1</i> gene in bipolar disorder, attention deficit hyperactivity disorder, and the alcohol dependence syndrome

    Genetic association of the tachykinin receptor 1 <i>TACR1</i> gene in bipolar disorder, attention deficit hyperactivity disorder, and the alcohol dependence syndrome 由 Sally I. Sharp, Andrew McQuillin, Michael Marks, Stephen P. Hunt, S. Clare Stanford, G. Lydall, Marsha Y. Morgan, Philip Asherson, David Curtis, Hugh Gurling

    出版 2014
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  10. 10
    Analysis of <i>ANK3</i> and <i>CACNA1C</i> variants identified in bipolar disorder whole genome sequence data

    Analysis of <i>ANK3</i> and <i>CACNA1C</i> variants identified in bipolar disorder whole genome sequence data 由 Alessia Fiorentino, Niamh L. O’Brien, Devin P. Locke, Andrew McQuillin, A Jarram, Adebayo Anjorin, Radhika Kandaswamy, David Curtis, Robert Blizard, Hugh Gurling

    出版 2014
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  11. 11
    The Prison and Transition Health (PATH) Cohort Study: Study Protocol and Baseline Characteristics of a Cohort of Men with a History of Injecting Drug Use Leaving Prison in Australia

    The Prison and Transition Health (PATH) Cohort Study: Study Protocol and Baseline Characteristics of a Cohort of Men with a History of Injecting Drug Use Leaving Prison in Australi... 由 Amy Kirwan, M. David Curtis, Paul Dietze, Campbell Aitken, Emma Woods, Shelley Walker, Stuart A. Kinner, James R. P. Ogloff, Tony Butler, Mark Stoové

    出版 2019
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  12. 12
    Concerns, Healthcare Use, and Treatment Interruptions in Patients With Common Autoimmune Rheumatic Diseases During the COVID-19 Pandemic

    Concerns, Healthcare Use, and Treatment Interruptions in Patients With Common Autoimmune Rheumatic Diseases During the COVID-19 Pandemic 由 Michael George, Shilpa Venkatachalam, Shubhasree Banerjee, Joshua F. Baker, Peter A. Merkel, Kelly Gavigan, David Curtis, Maria I. Danila, Jeffrey R. Curtis, W. Benjamin Nowell

    出版 2020
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  13. 13
    Mutations in the medium chain acyl-CoA dehydrogenase (MCAD) gene

    Mutations in the medium chain acyl-CoA dehydrogenase (MCAD) gene 由 Kay Tanaka, Ichiro Yokota, Paul M. Coates, Arnold W. Strauss, Daniel P. Kelly, Z. Zhang, N. Gregersen, Brage Storstein Andresen, Yoichi Matsubara, David Curtis, Y.-T. Chen

    出版 1992
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  14. 14
    Genomewide Genetic Linkage Analysis Confirms the Presence of Susceptibility Loci for Schizophrenia, on Chromosomes 1q32.2, 5q33.2, and 8p21-22 and Provides Support for Linkage to Schizophrenia, on Chromosomes 11q23.3-24 and 20q12.1-11.23

    Genomewide Genetic Linkage Analysis Confirms the Presence of Susceptibility Loci for Schizophrenia, on Chromosomes 1q32.2, 5q33.2, and 8p21-22 and Provides Support for Linkage to S... 由 Hugh Gurling, Gursharan Kalsi, Jon Brynjolfson, Thordur Sigmundsson, Robin Sherrington, Baljinder S. Mankoo, Timothy D. Read, P. L. Murphy, Ekaterina Blaveri, Andrew McQuillin, Hannes Pétursson, David Curtis

    出版 2001
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  15. 15
    Confirmation of prior evidence of genetic susceptibility to alcoholism in a genome-wide association study of comorbid alcoholism and bipolar disorder

    Confirmation of prior evidence of genetic susceptibility to alcoholism in a genome-wide association study of comorbid alcoholism and bipolar disorder 由 Gregory Lydall, Nicholas Bass, Andrew McQuillin, Jacob Lawrence, Adebayo Anjorin, Radhika Kandaswamy, A C Pereira, Irene Guerrini, David Curtis, Anna E. Vine, Pamela Sklar, Shaun Purcell, Hugh Gurling

    出版 2011
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  16. 16
    Haplotype Combinations of Calpain 10 Gene Polymorphisms Associate With Increased Risk of Impaired Glucose Tolerance and Type 2 Diabetes in South Indians

    Haplotype Combinations of Calpain 10 Gene Polymorphisms Associate With Increased Risk of Impaired Glucose Tolerance and Type 2 Diabetes in South Indians 由 Paul G. Cassell, Alan E. Jackson, Bernard V. North, Julie Evans, Denise Syndercombe‐Court, Christopher Phillips, Ambady Ramachandran, Chamukuttan Snehalatha, Susan Gelding, Shanti Vijayaravaghan, David Curtis, G. A. Hitman

    出版 2002
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  17. 17
    Case–case genome-wide association analysis shows markers differentially associated with schizophrenia and bipolar disorder and implicates calcium channel genes

    Case–case genome-wide association analysis shows markers differentially associated with schizophrenia and bipolar disorder and implicates calcium channel genes 由 David Curtis, Anna E. Vine, Andrew McQuillin, Nicholas Bass, A C Pereira, Radhika Kandaswamy, Jacob Lawrence, Adebayo Anjorin, Khalid Choudhury, Susmita Datta, Vinay Puri, Robert Krasucki, Jonathan Pimm, Srinivasa Thirumalai, Digby Quested, Hugh Gurling

    出版 2010
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  18. 18
    Genetic mapping of a major susceptibility locus for juvenile myoclonic epilepsy on chromosome 15q

    Genetic mapping of a major susceptibility locus for juvenile myoclonic epilepsy on chromosome 15q 由 Frances Elmslie, Michelle Rees, Magali Williamson, Michael Kerr, Marianne Juel Kjeldsen, Kiang An Pang, Anders Sundqvist, M. L. Friis, David Chadwick, A. Richens, Athanasios Covanis, Mauro Santos, Alexis Arzimanoglou, C. P. Panayiotopoulos, David Curtis, William Whitehouse, R M Gardiner

    出版 1997
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  19. 19
    A threonine to isoleucine missense mutation in the pericentriolar material 1 gene is strongly associated with schizophrenia

    A threonine to isoleucine missense mutation in the pericentriolar material 1 gene is strongly associated with schizophrenia 由 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

    出版 2008
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  20. 20
    SPINK1 Is a Susceptibility Gene for Fibrocalculous Pancreatic Diabetes in Subjects from the Indian Subcontinent

    SPINK1 Is a Susceptibility Gene for Fibrocalculous Pancreatic Diabetes in Subjects from the Indian Subcontinent 由 Zahid Hassan, Viswanathan Mohan, Liaquat Ali, Rebecca Allotey, Khalid Barakat, M.O. Faruque, R Deepa, Michael McDermott, Alan E. Jackson, Paul G. Cassell, David Curtis, Susan Gelding, Shanti Vijayaravaghan, Niklaus Gyr, David C. Whitcomb, A. K. Azad Khan, G. A. Hitman

    出版 2002
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