Resultados de procura - Denise Harold

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  1. 1
    Determining SNP Allele Frequencies in DNA Pools

    Determining SNP Allele Frequencies in DNA Pools por Gerome Breen, Denise Harold, Stuart H. Ralston, Duncan Shaw, David St Clair

    Publicado 2000
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  2. 2
    Evidence that PICALM affects age at onset of Alzheimer's dementia in Down syndrome

    Evidence that PICALM affects age at onset of Alzheimer's dementia in Down syndrome por Emma L. Jones, Kin Y. Mok, Marisa Hanney, Denise Harold, Rebecca Sims, Julie Williams, Clive Ballard

    Publicado 2013
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  3. 3
    Shared genetic contribution to ischemic stroke and Alzheimer's disease

    Shared genetic contribution to ischemic stroke and Alzheimer's disease por Matthew Traylor, Poneh Adib‐Samii, Denise Harold, Martin Dichgans, Julie Williams, Cathryn M. Lewis, Hugh S. Markus

    Publicado 2016
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  4. 4
    Polymorphisms in BACE2 may affect the age of onset Alzheimer's dementia in Down syndrome

    Polymorphisms in BACE2 may affect the age of onset Alzheimer's dementia in Down syndrome por Kin Y. Mok, Emma L. Jones, Marisa Hanney, Denise Harold, Rebecca Sims, Julie Williams, Clive Ballard, John Hardy

    Publicado 2014
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  5. 5
    Strong Evidence That KIAA0319 on Chromosome 6p Is a Susceptibility Gene for Developmental Dyslexia

    Strong Evidence That KIAA0319 on Chromosome 6p Is a Susceptibility Gene for Developmental Dyslexia por Natalie Cope, Denise Harold, Gary Hill, Valentina Moskvina, Jim Stevenson, Peter Holmans, Michael J. Owen, Michael O’Donovan, Julie Williams

    Publicado 2005
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  6. 6
    Estimation and partitioning of polygenic variation captured by common SNPs for Alzheimer's disease, multiple sclerosis and endometriosis

    Estimation and partitioning of polygenic variation captured by common SNPs for Alzheimer's disease, multiple sclerosis and endometriosis por Sang Lee, Denise Harold, Dale R. Nyholt, Michael E. Goddard, Krina T. Zondervan, Julie Williams, Grant W. Montgomery, Naomi R. Wray, Peter M. Visscher

    Publicado 2012
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  7. 7
    Suggestive synergy between genetic variants in TF and HFE as risk factors for Alzheimer's disease

    Suggestive synergy between genetic variants in TF and HFE as risk factors for Alzheimer's disease por John Kauwe, Sarah Bertelsen, Kevin H. Mayo, Carlos Cruchaga, Richard Abraham, Paul Hollingworth, Denise Harold, Michael J. Owen, Julie Williams, Simon Lovestone, Christopher M. Morris, Alison Goate

    Publicado 2009
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  8. 8
    DNA analysis of biological material on perforating bullets and crime scene reconstruction

    DNA analysis of biological material on perforating bullets and crime scene reconstruction por Samuel T.G. Ferreira, Aluisio Trindade-Filho, Karla A. Paula, Cláudia R.B.O. Mendes, Flávia A. Maia, H. Pak, Raul P. Neto, Denise Harold, Adriana V. Moraes

    Publicado 2009
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  9. 9
    A modifier of Huntington's disease onset at the MLH1 locus

    A modifier of Huntington's disease onset at the MLH1 locus por Jong‐Min Lee, Michael J. Chao, Denise Harold, Kawther Abu Elneel, Tammy Gillis, Peter Holmans, Lesley Jones, Michael Orth, Richard H. Myers, Seung Kwak, Vanessa C. Wheeler, Marcy E. MacDonald, James F. Gusella

    Publicado 2017
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  10. 10
    Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia

    Further evidence that the KIAA0319 gene confers susceptibility to developmental dyslexia por Denise Harold, Silvia Paracchini, Thomas Scerri, Megan Y. Dennis, Natalie Cope, Gary Hill, Valentina Moskvina, Janet G. Walter, A.J. Richardson, Mike Owen, John Stein, E D Green, Michael O’Donovan, Julie Williams, Anthony P. Monaco

    Publicado 2006
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  11. 11
    Cognitive analysis of schizophrenia risk genes that function as epigenetic regulators of gene expression

    Cognitive analysis of schizophrenia risk genes that function as epigenetic regulators of gene expression por Laura Whitton, Donna Cosgrove, Christopher Clarkson, Denise Harold, Kimberley Kendall, Alexander Richards, Kiran K. Mantripragada, Michael J. Owen, Michael O’Donovan, James Walters, Annette M. Hartmann, Betina Konte, Dan Rujescu, Michael Gill, Aiden Corvin, Stephen Rea, Gary Donohoe, Derek W. Morris

    Publicado 2016
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  12. 12
    Genome-wide association interaction analysis for Alzheimer's disease

    Genome-wide association interaction analysis for Alzheimer's disease por Elena S. Gusareva, Minerva M. Carrasquillo, Céline Bellenguez, Elise Cuyvers, Samuel Colon, Neill R. Graff‐Radford, Ronald C. Petersen, Dennis W. Dickson, Jestinah Mahachie John, Kyrylo Bessonov, Christine Van Broeckhoven, Denise Harold, Julie Williams, Philippe Amouyel, Kristel Sleegers, Nilüfer Ertekin‐Taner, Jean‐Charles Lambert, Kristel Van Steen

    Publicado 2014
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  13. 13
    SNPs Associated with Cerebrospinal Fluid Phospho-Tau Levels Influence Rate of Decline in Alzheimer's Disease

    SNPs Associated with Cerebrospinal Fluid Phospho-Tau Levels Influence Rate of Decline in Alzheimer's Disease por Carlos Cruchaga, John Kauwe, Kevin H. Mayo, Noah Spiegel, Sarah Bertelsen, Petra Nowotny, Aarti R. Shah, Richard Abraham, Paul Hollingworth, Denise Harold, Michael M. Owen, Julie Williams, Simon Lovestone, Elaine R. Peskind, Ge Li, James B. Leverenz, Douglas Galasko, Christopher M. Morris, Anne M. Fagan, David M. Holtzman, Alison Goate

    Publicado 2010
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  14. 14
    Common polygenic variation enhances risk prediction for Alzheimer’s disease

    Common polygenic variation enhances risk prediction for Alzheimer’s disease por Valentina Escott‐Price, Rebecca Sims, Christian Bannister, Denise Harold, Maria Vronskaya, Elisa Majounie, Nandini Badarinarayan, Kevin Morgan, Peter Passmore, Clive Holmes, John Powell, Carol Brayne, Michael Gill, Simon Mead, Alison Goate, Carlos Cruchaga, Jean‐Charles Lambert, Cornelia M. van Duijn, Wolfgang Maier, Alfredo Ramı́rez, Peter Holmans, Lesley Jones, John Hardy, Sudha Seshadri, Gerard D. Schellenberg, Philippe Amouyel, Julie Williams

    Publicado 2015
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  15. 15
    Characterization of a Family with Rare Deletions in CNTNAP5 and DOCK4 Suggests Novel Risk Loci for Autism and Dyslexia

    Characterization of a Family with Rare Deletions in CNTNAP5 and DOCK4 Suggests Novel Risk Loci for Autism and Dyslexia por Alistair T. Pagnamenta, Elena Bacchelli, Maretha Jonge, Ghazala Mirza, Thomas Scerri, Fiorella Minopoli, Andreas G. Chiocchetti, Kerstin U. Ludwig, Per Hoffmann, Silvia Paracchini, Ernesto Lowy, Denise Harold, Jade Chapman, Sabine M. Klauck, Fritz Poustka, Renske H. Houben, Wouter Staal, Roel A. Ophoff, Michael O’Donovan, Julie Williams, Markus M. Nöthen, Gerd Schulte‐Körne, Panos Deloukas, Jiannis Ragoussis, Anthony Bailey, Elena Maestrini, Anthony P. Monaco

    Publicado 2010
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  16. 16
    Identification of Genetic Factors that Modify Clinical Onset of Huntington’s Disease

    Identification of Genetic Factors that Modify Clinical Onset of Huntington’s Disease por Jong‐Min Lee, Vanessa C. Wheeler, Michael J. Chao, Jean Paul Vonsattel, Ricardo Mouro Pinto, Diane Lucente, Kawther Abu-Elneel, Eliana Marisa Ramos, Jayalakshmi Srinidhi Mysore, Tammy Gillis, Marcy E. MacDonald, James F. Gusella, Denise Harold, Timothy Stone, Valentina Escott‐Price, Jun Han, Alexey Vedernikov, Peter Holmans, Lesley Jones, Seung Kwak, Mithra Mahmoudi, Michael Orth, G. Bernhard Landwehrmeyer, Jane S. Paulsen, E. Ray Dorsey, Ira Shoulson, Richard H. Myers

    Publicado 2015
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  17. 17
    Analysis of Genome-Wide Association Studies of Alzheimer Disease and of Parkinson Disease to Determine If These 2 Diseases Share a Common Genetic Risk

    Analysis of Genome-Wide Association Studies of Alzheimer Disease and of Parkinson Disease to Determine If These 2 Diseases Share a Common Genetic Risk por Valentina Moskvina, Denise Harold, Gian Carlo Russo, Alexey Vedernikov, Manu Sharma, Mohamad Saad, Peter Holmans, José Brás, Francesco Bettella, Margaux F. Keller, Nayia Nicolaou, Javier Simón‐Sánchez, J. Raphael Gibbs, Claudia Schulte, Alexandra Dürr, Rita Guerreiro, Dena Hernandez, Alexis Brice, Hreinn Stefánsson, Kari Majamaa, Thomas Gasser, Peter Heutink, Nicholas Wood, María Martínez, Andrew B. Singleton, Michael A. Nalls, John Hardy, Michael J. Owen, Michael O’Donovan, Julie Williams, Huw R. Morris, Nigel Williams

    Publicado 2013
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  18. 18
    Genome-wide association study of Alzheimer's disease with psychotic symptoms

    Genome-wide association study of Alzheimer's disease with psychotic symptoms por Paul Hollingworth, Robert A. Sweet, Rebecca Sims, Denise Harold, Giancarlo Russo, R Abraham, Antony O.W. Stretton, Nicola Jones, Amy Gerrish, Jade Chapman, Dobril Ivanov, Valentina Moskvina, Simon Lovestone, P Priotsi, M Lupton, Carol Brayne, Michael Gill, Brian Lawlor, Aoibhinn Lynch, D Craig, Bernadette McGuinness, J Johnston, C Holmes, Gill Livingston, N J Bass, H. Gurling, Andrew McQuillin, Peter Holmans, Lesley Jones, B. Devlin, Lambertus Klei, M M Barmada, F Y Demirci, Steven T. DeKosky, O L Lopez, Peter Passmore, Michael J. Owen, Michael O’Donovan, R Mayeux, M I Kamboh, Julie Williams

    Publicado 2011
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  19. 19
    GWAS of Cerebrospinal Fluid Tau Levels Identifies Risk Variants for Alzheimer’s Disease

    GWAS of Cerebrospinal Fluid Tau Levels Identifies Risk Variants for Alzheimer’s Disease por Carlos Cruchaga, John S. K. Kauwe, Oscar Harari, Sheng Chih Jin, Yefei Cai, Celeste M. Karch, Bruno A. Benítez, Amanda T. Jeng, Tara Skorupa, David Carrell, Sarah Bertelsen, Matthew H. Bailey, David McKean, Joshua Shulman, Philip L. De Jager, Lori B. Chibnik, David Bennett, S. E. Arnold, Denise Harold, Rebecca Sims, Amy Gerrish, Julie Williams, Vivianna M. Van Deerlin, Virginia M.‐Y. Lee, Leslie M. Shaw, John Q. Trojanowski, Jonathan L. Haines, Richard Mayeux, Margaret A. Pericak‐Vance, Lindsay A. Farrer, Gerard D. Schellenberg, Elaine R. Peskind, Douglas Galasko, Anne M. Fagan, David M. Holtzman, John C. Morris, Alison Goate

    Publicado 2013
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  20. 20
    No consistent evidence for association between mtDNA variants and Alzheimer disease

    No consistent evidence for association between mtDNA variants and Alzheimer disease por Gavin Hudson, Rebecca Sims, Denise Harold, Jade Chapman, Paul Hollingworth, Amy Gerrish, Gian Carlo Russo, Marian L. Hamshere, V. Moskvina, Nicola Jones, Charlene Thomas, Alexandra Stretton, Peter Holmans, Michael O’Donovan, M J Owen, Julie Williams, Patrick F. Chinnery, Denise Harold, Richard Abraham, Paul Hollingworth, Rebecca Sims, Amy Gerrish, Jade Chapman, Giancarlo Russo, Marian Hamshere, Jaspreet Singh Pahwa, Valentina Moskvina, Kimberley Dowzell, Amy L. Williams, Nicola Jones, Charlene Thomas, Alexandra Stretton, Angharad R. Morgan, Simon Lovestone, John Powell, Petroula Proitsi, Michelle K. Lupton, Carol Brayne, David C. Rubinsztein, Michael Gill, Brian Lawlor, Aoibhinn Lynch, Kevin Morgan, Kristelle Brown, Peter Passmore, David Craig, Bernadette McGuinness, Stephen Todd, Janet Johnston, Clive Holmes, David Mann, A. David Smith, Seth Love, Patrick G. Kehoe, John Hardy, Simon Mead, Nick C. Fox, Martin N. Rossor, John Collinge, Wolfgang Maier, Frank Jessen, Reiner Heun, Heike Kölsch, Britta Schürmann, Hendrik van den Bussche, Isabella Heuser, Johannes Kornhuber, Jens Wiltfang, Martin Dichgans, Lutz Frölich, Harald Hampel, Michael Hüll, Dan Rujescu, Alison Goate, John S.K. Kauwe, Carlos Cruchaga, Petra Nowotny, John C. Morris, Kevin H. Mayo, Gill Livingston, Nicholas Bass, Hugh Gurling, Andrew McQuillin, Rhian Gwilliam, Panos Deloukas, Peter Holmans, Michael O’Donovan, Michael J. Owen, Julie Williams

    Publicado 2012
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