Search Results - Morgan, Kevin

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  1. 1
    A candidate regulatory variant at the TREM gene cluster associates with decreased Alzheimer's disease risk and increased TREML1 and TREM2 brain gene expression

    A candidate regulatory variant at the TREM gene cluster associates with decreased Alzheimer's disease risk and increased TREML1 and TREM2 brain gene expression by Carrasquillo, Minerva, Allen, Mariet, Burgess, Jeremy D., Medway, Christopher, Morgan, Kevin

    Published 2017
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  2. 2
    Blood type gene locus has no influence on ACE association with Alzheimer's disease

    Blood type gene locus has no influence on ACE association with Alzheimer's disease by Braae, Anne, Medway, Christopher, Carrasquillo, Minerva, Younkin, Steven, Kehoe, Patrick G., Morgan, Kevin

    Published 2015
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  3. 3
    Complement receptor 1 gene (CR1) intragenic duplication and risk of Alzheimer’s disease

    Complement receptor 1 gene (CR1) intragenic duplication and risk of Alzheimer’s disease by Kucukkilic, Ezgi, Brookes, Keeley, Barber, Imelda, Guetta-Baranes, Tamar, Morgan, Kevin, Hollox, Edward

    Published 2018
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  4. 4
    Rationalising the role of Keratin 9 as a biomarker for Alzheimer’s disease

    Rationalising the role of Keratin 9 as a biomarker for Alzheimer’s disease by Richens, Joanna L., Spencer, Hannah L., Butler, Molly, Cantlay, Fiona, Vere, Kelly-Ann, Bajaj, Nin, Morgan, Kevin, O'Shea, Paul

    Published 2016
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  5. 5
    Next generation sequencing of CLU, PICALM and CR1: pitfalls and potential solutions

    Next generation sequencing of CLU, PICALM and CR1: pitfalls and potential solutions by Lord, Jenny, Turton, James, Medway, Christopher, Shi, Hui, Brown, Kristelle, Lowe, James, Mann, David, Pickering-Brown, Stuart, Kalsheker, Noor, Passmore, Peter, Morgan, Kevin

    Published 2012
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  6. 6
    Allele-specific RNA interference rescues the long-QT syndrome phenotype in human-induced pluripotency stem cell cardiomyocytes

    Allele-specific RNA interference rescues the long-QT syndrome phenotype in human-induced pluripotency stem cell cardiomyocytes by Matsa, Elena, Dixon, James E., Medway, Christopher, Georgiou, Orestis, Patel, Minal J., Morgan, Kevin, Kemp, Paul J., Staniforth, Andrew, Mellor, Ian, Denning, Chris

    Published 2013
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  7. 7
    Genotyping of the Alzheimer’s disease Genome-Wide Association Study index single nucleotide polymorphisms in the Brains for Dementia research cohort

    Genotyping of the Alzheimer’s disease Genome-Wide Association Study index single nucleotide polymorphisms in the Brains for Dementia research cohort by Brookes, Keeley J., McConnell, G., Williams, K., Chaudhury, Sultan R, Madhan, G., Patel, T., Turley, C., Guetta-Baranes, Tamar, Francis, Paul T., Morgan, Kevin

    Published 2018
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  8. 8
    Whole-exome sequencing of the BDR cohort: evidence to support the role of the PILRA gene in Alzheimer’s disease

    Whole-exome sequencing of the BDR cohort: evidence to support the role of the PILRA gene in Alzheimer’s disease by Patel, Tulsi, Brookes, Keeley J., Turton, James, Chaudhury, Sultan, Guetta-Baranes, Tamar, Guerreiro, Rita, Bras, Jose, Hernandez, Dena, Singleton, Andrew, Francis, Paul T., Hardy, John, Morgan, Kevin

    Published 2017
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  9. 9
    Practical detection of a definitive biomarker panel for Alzheimer's disease: comparisons between matched plasma and cerebrospinal fluid

    Practical detection of a definitive biomarker panel for Alzheimer's disease: comparisons between matched plasma and cerebrospinal fluid by Richens, Joanna L., Vere, Kelly-Ann, Light, Roger A., Soria, Daniele, Garibaldi, Jonathan, Smith, A. David, Warden, Donald, Wilcock, Gordon, Bajaj, Nin, Morgan, Kevin, O’Shea, Paul

    Published 2014
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  10. 10
    Methylation profiling RIN3 and MEF2C identifies epigenetic marks associated with sporadic early onset Alzheimer’s disease

    Methylation profiling RIN3 and MEF2C identifies epigenetic marks associated with sporadic early onset Alzheimer’s disease by Boden, Kirsty A., Barber, Imelda S., Clement, Naomi, Patel, Tulsi, Guetta-Baranes, Tamar, Brookes, Keeley, Chappell, Sally, Craigon, Jim, Chapman, Natalie H., Morgan, Kevin, Seymour, Graham B., Bottley, Andrew

    Published 2017
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  11. 11
    Polygenic risk score in postmortem diagnosed sporadic early-onset Alzheimer’s disease

    Polygenic risk score in postmortem diagnosed sporadic early-onset Alzheimer’s disease by Chaudhary, Sultan, Patel, Tulsi, Barber, Imelda S., Guetta-Baranes, Tamar, Brookes, Keeley, Chappell, Sally, Turton, James, Guerreiro, Rita, Bras, Jose, Hernandez, Dena, Singleton, Andrew, Hardy, John, Mann, David, Morgan, Kevin

    Published 2018
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  12. 12
    Mutation analysis of sporadic early-onset Alzheimer's disease using the NeuroX array

    Mutation analysis of sporadic early-onset Alzheimer's disease using the NeuroX array by Barber, Imelda S., Braae, Anne, Clement, Naomi, Patel, Tulsi, Guetta-Baranes, Tamar, Brookes, Keeley, Medway, Christopher, Chappell, Sally, Guerreiro, Rita, Bras, Jose, Hernandez, Dena, Singleton, Andrew, Hardy, John, Mann, David M., Morgan, Kevin

    Published 2017
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  13. 13
    Investigating splicing variants uncovered by next-generation sequencing the Alzheimer’s disease candidate genes, CLU, PICALM, CR1, ABCA7, BIN1, the MS4A locus, CD2AP, EPHA1 and CD33

    Investigating splicing variants uncovered by next-generation sequencing the Alzheimer’s disease candidate genes, CLU, PICALM, CR1, ABCA7, BIN1, the MS4A locus, CD2AP, EPHA1 and CD3... by Clement, Naomi, Braae, Anne, Turton, James, Lord, Jenny, Guetta-Baranes, Tamar, Medway, Christopher, Brookes, Keeley, Barber, Imelda S., Patel, Tulsi, Milla, Lucy, Azzopardi, Maria, Lowe, James, Mann, David, Pickering-Brown, Stuart, Kalsheker, Noor, Passmore, Peter, Chappell, Sally, Morgan, Kevin

    Published 2016
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  14. 14
    A comprehensive assessment of benign genetic variability for neurodegenerative disorders

    A comprehensive assessment of benign genetic variability for neurodegenerative disorders by Guerreiro, Rita, Sassi, Celeste, Gibbs, Jesse, Edsall, Connor, Hernandez, Dena, Brown, Kristelle, Lupton, Michelle, Parkinnen, Laura, Ansorge, Olaf, Hodges, Angela, Ryten, Mina, Tienari, Pentti, Van Deerlin, Vivanna, Trojanowski, John, Morgan, Kevin, Powell, John, Singleton, Andrew, Hardy, John, Bras, Jose

    Published 2018
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  15. 15
    Screening exon 16 and 17 of the amyloid precursor protein gene in sporadic early-onset Alzheimer's disease

    Screening exon 16 and 17 of the amyloid precursor protein gene in sporadic early-onset Alzheimer's disease by Barber, Imelda S., García-Cárdenas, Jennyfer M., Sakdapanichkul, Chidchanok, Deacon, Christopher, Zapata Erazo, Gabriela, Guerreiro, Rita, Bras, Jose, Hernandez, Dena, Singleton, Andrew, Guetta-Baranes, Tamar, Braae, Anne, Clement, Naomi, Patel, Tulsi, Brookes, Keeley, Medway, Christopher, Chappell, Sally, Mann, David M., Morgan, Kevin

    Published 2016
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  16. 16
    A novel Alzheimer disease locus located near the gene encoding tau protein

    A novel Alzheimer disease locus located near the gene encoding tau protein by Jun, Gyungah, Ibrahim-Verbaas, Carla A., Vronskaya, Maria, Lambert, Jean-Charles, Chung, Jaeyoon, Naj, Adam C., Kunkle, Brian W., Wang, Li-San, Bis, Joshua C., Bellenguez, Céline, Harold, Denise, Lunetta, Kathryn L., Destefano, Anita L., Grenier-Boley, Benjamin, Sims, Rebecca, Morgan, Kevin

    Published 2015
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  17. 17
    Genome-wide analysis of genetic correlation in dementia with Lewy bodies, Alzheimer’s and Parkinson’s diseases

    Genome-wide analysis of genetic correlation in dementia with Lewy bodies, Alzheimer’s and Parkinson’s diseases by Guerreiro, Rita, Escott-Price, Valentina, Darwent, Lee, Parkkinen, Laura, Ansorge, Olaf, Hernandez, Dena, Nalls, Michael A., Clark, Lorraine, Honig, Lawrence, Marder, Karen, Flier, Wiesje van der, Holstege, Henne, Louwersheimer, Eva, Lemstra, Afina, Scheltens, Philip, Barber, Imelda S., Braae, Anne, Brown, Kristelle, Morgan, Kevin

    Published 2016
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  18. 18
    Evaluating the role of pathogenic dementia variants in posterior cortical atrophy

    Evaluating the role of pathogenic dementia variants in posterior cortical atrophy by Carrasquillo, Minerva, Barber, Imelda S., Lincoln, Sarah J., Murray, Melissa E., Camsari, Gamze Balci, Khan, Qurat ul Ain, Nguyen, Thuy, Ma, Li, Bisceglio, Gina D., Crook, Julia E., Younkin, Steven G., Dickson, Dennis W., Boeve, Bradley F., Graff-Radford, Neill R., Morgan, Kevin, Ertekin-Taner, Nilüfer

    Published 2016
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  19. 19
    Investigating the genetic architecture of dementia with Lewy bodies: a two-stage genome-wide association study

    Investigating the genetic architecture of dementia with Lewy bodies: a two-stage genome-wide association study by Guerreiro, Rita, Ross, Owen A., Kun-Rodrigues, Celia, Hernandez, Dena, Orme, Tatiana, Eicher, John D., Shepherd, Claire, Parkkinen, Laura, Darwent, Lee, Heckman, Michael G., Scholz, Sonja W., Troncoso, Juan C., Pletnikova, Olga, Ansorge, Olaf, Clarimon, Jordi, Barber, Imelda S., Braae, Anne, Brown, Kristelle, Morgan, Kevin

    Published 2018
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  20. 20
    A rare loss-of-function variant of ADAM17 is associated with late-onset familial Alzheimer disease

    A rare loss-of-function variant of ADAM17 is associated with late-onset familial Alzheimer disease by Hartl, Daniela, May, Patrick, Gu, Wei, Mayhaus, Manuel, Pichler, Sabrina, Spaniol, Christian, Glaab, Enrico, Bobbili, Dheeraj Reddy, Antony, Paul, Koegelsberger, Sandra, Kurz, Alexander, Grimmer, Timo, Morgan, Kevin, Vardarajan, Badri N., Reitz, Christiane, Hardy, John, Bras, Jose, Guerreiro, Rita, Balling, Rudi, Schneider, Jochen G., Riemenschneider, Matthias

    Published 2018
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