Hasil Pencarian - Michael A Nalls

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  1. 1
    A large study reveals no association between APOE and Parkinson's disease

    A large study reveals no association between APOE and Parkinson's disease oleh Monica Federoff, Belen Jimenez-Rolando, Michael A. Nalls, Andrew B. Singleton

    Diterbitkan 2012-05-01
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  2. 2
    Genome wide assessment of young onset Parkinson's disease from Finland.

    Genome wide assessment of young onset Parkinson's disease from Finland. oleh Dena G Hernandez, Michael A Nalls, Pauli Ylikotila, Margaux Keller, John A Hardy, Kari Majamaa, Andrew B Singleton

    Diterbitkan 2012-01-01
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  3. 3
    Race-specific alterations in DNA methylation among middle-aged African Americans and Whites with metabolic syndrome

    Race-specific alterations in DNA methylation among middle-aged African Americans and Whites with metabolic syndrome oleh Kumaraswamy Naidu Chitrala, Dena G. Hernandez, Michael A. Nalls, Nicolle A. Mode, Alan B. Zonderman, Ngozi Ezike, Michele K. Evans

    Diterbitkan 2020-05-01
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  4. 4
    Genomic risk profiling of ischemic stroke: results of an international genome-wide association meta-analysis.

    Genomic risk profiling of ischemic stroke: results of an international genome-wide association meta-analysis. oleh James F Meschia, Andrew Singleton, Michael A Nalls, Stephen S Rich, Pankaj Sharma, Luigi Ferrucci, Mar Matarin, Dena G Hernandez, Kerra Pearce, Thomas G Brott, Robert D Brown, John Hardy, Bradford B Worrall

    Diterbitkan 2011-01-01
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  5. 5
    Measures of autozygosity in decline: globalization, urbanization, and its implications for medical genetics.

    Measures of autozygosity in decline: globalization, urbanization, and its implications for medical genetics. oleh Michael A Nalls, Javier Simon-Sanchez, J Raphael Gibbs, Coro Paisan-Ruiz, Jose Tomas Bras, Toshiko Tanaka, Mar Matarin, Sonja Scholz, Charles Weitz, Tamara B Harris, Luigi Ferrucci, John Hardy, Andrew B Singleton

    Diterbitkan 2009-03-01
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  6. 6
    Plasma 24-metabolite panel predicts preclinical transition to clinical stages of Alzheimer’s disease

    Plasma 24-metabolite panel predicts preclinical transition to clinical stages of Alzheimer’s disease oleh Massimo S Fiandaca, Xioagang eZhong, Amrita K Cheema, Michael H. Orquiza, Swathi eChidambaram, Ming T Tan, Carole Roan Gresenz, Kevin T FitzGerald, Michael A Nalls, Andrew B Singleton, Mark eMapstone, Howard J Federoff

    Diterbitkan 2015-11-01
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  7. 7
    Trans-ethnic meta-analysis identifies new loci associated with longitudinal blood pressure traits

    Trans-ethnic meta-analysis identifies new loci associated with longitudinal blood pressure traits oleh Mateus H. Gouveia, Amy R. Bentley, Hampton Leonard, Karlijn A. C. Meeks, Kenneth Ekoru, Guanjie Chen, Michael A. Nalls, Eleanor M. Simonsick, Eduardo Tarazona-Santos, Maria Fernanda Lima-Costa, Adebowale Adeyemo, Daniel Shriner, Charles N. Rotimi

    Diterbitkan 2021-02-01
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  8. 8
    Using genetic variation and environmental risk factor data to identify individuals at high risk for age-related macular degeneration.

    Using genetic variation and environmental risk factor data to identify individuals at high risk for age-related macular degeneration. oleh Kylee L Spencer, Lana M Olson, Nathalie Schnetz-Boutaud, Paul Gallins, Anita Agarwal, Alessandro Iannaccone, Stephen B Kritchevsky, Melissa Garcia, Michael A Nalls, Anne B Newman, William K Scott, Margaret A Pericak-Vance, Jonathan L Haines

    Diterbitkan 2011-03-01
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  9. 9
    Genetic variability in CLU and its association with Alzheimer's disease.

    Genetic variability in CLU and its association with Alzheimer's disease. oleh Rita J Guerreiro, John Beck, J Raphael Gibbs, Isabel Santana, Martin N Rossor, Jonathan M Schott, Michael A Nalls, Helena Ribeiro, Beatriz Santiago, Nick C Fox, Catarina Oliveira, John Collinge, Simon Mead, Andrew Singleton, John Hardy

    Diterbitkan 2010-03-01
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  10. 10
    Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation.

    Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based i... oleh Andrew R Wood, John R B Perry, Toshiko Tanaka, Dena G Hernandez, Hou-Feng Zheng, David Melzer, J Raphael Gibbs, Michael A Nalls, Michael N Weedon, Tim D Spector, J Brent Richards, Stefania Bandinelli, Luigi Ferrucci, Andrew B Singleton, Timothy M Frayling

    Diterbitkan 2013-01-01
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  11. 11
    NOTCH3 variants and risk of ischemic stroke.

    NOTCH3 variants and risk of ischemic stroke. oleh Owen A Ross, Alexandra I Soto-Ortolaza, Michael G Heckman, Christophe Verbeeck, Daniel J Serie, Sruti Rayaprolu, Stephen S Rich, Michael A Nalls, Andrew Singleton, Rita Guerreiro, Emma Kinsella, Zbigniew K Wszolek, Thomas G Brott, Robert D Brown, Bradford B Worrall, James F Meschia

    Diterbitkan 2013-01-01
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  12. 12
    Cooperative genome-wide analysis shows increased homozygosity in early onset Parkinson's disease.

    Cooperative genome-wide analysis shows increased homozygosity in early onset Parkinson's disease. oleh Javier Simón-Sánchez, Laura L Kilarski, Michael A Nalls, Maria Martinez, Claudia Schulte, Peter Holmans, International Parkinson's Disease Genomics Consortium, Wellcome Trust Case Control Consortium, Thomas Gasser, John Hardy, Andrew B Singleton, Nicholas W Wood, Alexis Brice, Peter Heutink, Nigel Williams, Huw R Morris

    Diterbitkan 2012-01-01
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  13. 13
    Abundant quantitative trait loci exist for DNA methylation and gene expression in human brain.

    Abundant quantitative trait loci exist for DNA methylation and gene expression in human brain. oleh J Raphael Gibbs, Marcel P van der Brug, Dena G Hernandez, Bryan J Traynor, Michael A Nalls, Shiao-Lin Lai, Sampath Arepalli, Allissa Dillman, Ian P Rafferty, Juan Troncoso, Robert Johnson, H Ronald Zielke, Luigi Ferrucci, Dan L Longo, Mark R Cookson, Andrew B Singleton

    Diterbitkan 2010-05-01
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  14. 14
    A network-based approach to prioritize results from genome-wide association studies.

    A network-based approach to prioritize results from genome-wide association studies. oleh Nirmala Akula, Ancha Baranova, Donald Seto, Jeffrey Solka, Michael A Nalls, Andrew Singleton, Luigi Ferrucci, Toshiko Tanaka, Stefania Bandinelli, Yoon Shin Cho, Young Jin Kim, Jong-Young Lee, Bok-Ghee Han, Bipolar Disorder Genome Study (BiGS) Consortium, Wellcome Trust Case-Control Consortium, Francis J McMahon

    Diterbitkan 2011-01-01
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  15. 15
    Influence of Coding Variability in APP-Aβ Metabolism Genes in Sporadic Alzheimer's Disease.

    Influence of Coding Variability in APP-Aβ Metabolism Genes in Sporadic Alzheimer's Disease. oleh Celeste Sassi, Perry G Ridge, Michael A Nalls, Raphael Gibbs, Jinhui Ding, Michelle K Lupton, Claire Troakes, Katie Lunnon, Safa Al-Sarraj, Kristelle S Brown, Christopher Medway, Jenny Lord, James Turton, ARUK Consortium, Kevin Morgan, John F Powell, John S Kauwe, Carlos Cruchaga, Jose Bras, Alison M Goate, Andrew B Singleton, Rita Guerreiro, John Hardy

    Diterbitkan 2016-01-01
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  16. 16
    A meta-analysis and genome-wide association study of platelet count and mean platelet volume in african americans.

    A meta-analysis and genome-wide association study of platelet count and mean platelet volume in african americans. oleh Rehan Qayyum, Beverly M Snively, Elad Ziv, Michael A Nalls, Yongmei Liu, Weihong Tang, Lisa R Yanek, Leslie Lange, Michele K Evans, Santhi Ganesh, Melissa A Austin, Guillaume Lettre, Diane M Becker, Alan B Zonderman, Andrew B Singleton, Tamara B Harris, Emile R Mohler, Benjamin A Logsdon, Charles Kooperberg, Aaron R Folsom, James G Wilson, Lewis C Becker, Alexander P Reiner

    Diterbitkan 2012-01-01
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  17. 17
    Reduced neutrophil count in people of African descent is due to a regulatory variant in the Duffy antigen receptor for chemokines gene.

    Reduced neutrophil count in people of African descent is due to a regulatory variant in the Duffy antigen receptor for chemokines gene. oleh David Reich, Michael A Nalls, W H Linda Kao, Ermeg L Akylbekova, Arti Tandon, Nick Patterson, James Mullikin, Wen-Chi Hsueh, Ching-Yu Cheng, Josef Coresh, Eric Boerwinkle, Man Li, Alicja Waliszewska, Julie Neubauer, Rongling Li, Tennille S Leak, Lynette Ekunwe, Joe C Files, Cheryl L Hardy, Joseph M Zmuda, Herman A Taylor, Elad Ziv, Tamara B Harris, James G Wilson

    Diterbitkan 2009-01-01
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  18. 18
    Fine-mapping, gene expression and splicing analysis of the disease associated LRRK2 locus.

    Fine-mapping, gene expression and splicing analysis of the disease associated LRRK2 locus. oleh Daniah Trabzuni, Mina Ryten, Warren Emmett, Adaikalavan Ramasamy, Karl J Lackner, Tanja Zeller, Robert Walker, Colin Smith, Patrick A Lewis, Adamantios Mamais, Rohan de Silva, Jana Vandrovcova, International Parkinson Disease Genomics Consortium (IPDGC), Dena Hernandez, Michael A Nalls, Manu Sharma, Sophie Garnier, Suzanne Lesage, Javier Simon-Sanchez, Thomas Gasser, Peter Heutink, Alexis Brice, Andrew Singleton, Huaibin Cai, Eric Schadt, Nicholas W Wood, Rina Bandopadhyay, Michael E Weale, John Hardy, Vincent Plagnol

    Diterbitkan 2013-01-01
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  19. 19
    Identification of nine novel loci associated with white blood cell subtypes in a Japanese population.

    Identification of nine novel loci associated with white blood cell subtypes in a Japanese population. oleh Yukinori Okada, Tomomitsu Hirota, Yoichiro Kamatani, Atsushi Takahashi, Hiroko Ohmiya, Natsuhiko Kumasaka, Koichiro Higasa, Yumi Yamaguchi-Kabata, Naoya Hosono, Michael A Nalls, Ming Huei Chen, Frank J A van Rooij, Albert V Smith, Toshiko Tanaka, David J Couper, Neil A Zakai, Luigi Ferrucci, Dan L Longo, Dena G Hernandez, Jacqueline C M Witteman, Tamara B Harris, Christopher J O'Donnell, Santhi K Ganesh, Koichi Matsuda, Tatsuhiko Tsunoda, Toshihiro Tanaka, Michiaki Kubo, Yusuke Nakamura, Mayumi Tamari, Kazuhiko Yamamoto, Naoyuki Kamatani

    Diterbitkan 2011-06-01
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  20. 20
    Genome-wide association studies of the PR interval in African Americans.

    Genome-wide association studies of the PR interval in African Americans. oleh J Gustav Smith, Jared W Magnani, Cameron Palmer, Yan A Meng, Elsayed Z Soliman, Solomon K Musani, Kathleen F Kerr, Renate B Schnabel, Steven A Lubitz, Nona Sotoodehnia, Susan Redline, Arne Pfeufer, Martina Müller, Daniel S Evans, Michael A Nalls, Yongmei Liu, Anne B Newman, Alan B Zonderman, Michele K Evans, Rajat Deo, Patrick T Ellinor, Dina N Paltoo, Christopher Newton-Cheh, Emelia J Benjamin, Reena Mehra, Alvaro Alonso, Susan R Heckbert, Ervin R Fox, Candidate-gene Association Resource (CARe) Consortium

    Diterbitkan 2011-02-01
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