Canlyniadau Chwilio - Dena Hernandez
- Dangos 1 - 20 canlyniadau o 120
- Ewch i'r Dudalen Nesaf
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Race-specific alterations in DNA methylation among middle-aged African Americans and Whites with metabolic syndrome gan Kumaraswamy Naidu Chitrala, Dena Hernández, Michael A. Nalls, Nicolle A. Mode, Alan B. Zonderman, Ngozi Ezike, Michele K. Evans
Cyhoeddwyd 2019Artigo -
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Transcriptomic profiling of the human brain reveals that altered synaptic gene expression is associated with chronological aging gan Allissa Dillman, Elisa Majounie, Jinhui Ding, J. Raphael Gibbs, Dena Hernández, Sampath Arepalli, Bryan J. Traynor, Andrew Singleton, Dagmar Galter, Mark Cookson
Cyhoeddwyd 2017Artigo -
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Towards a gene expression biomarker set for human biological age gan Alice C. Holly, David Melzer, Luke C. Pilling, William Henley, Dena Hernandez, Andrew Singleton, Stefania Bandinelli, Jack M. Guralnik, Luigi Ferrucci, Lorna W. Harries
Cyhoeddwyd 2013Artigo -
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Advancing age is associated with gene expression changes resembling mTOR inhibition: Evidence from two human populations gan Lorna W. Harries, Alexander D. Fellows, Luke C. Pilling, Dena Hernandez, Andrew Singleton, Stefania Bandinelli, Jack M. Guralnik, Jonathan R. Powell, Luigi Ferrucci, David Melzer
Cyhoeddwyd 2012Artigo -
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Whole‐exome sequencing of the <scp>BDR</scp> cohort: evidence to support the role of the <i><scp>PILRA</scp></i> gene in Alzheimer's disease gan Tulsi Patel, Keeley J. Brookes, James Turton, Sraboni Chaudhury, Tamar Guetta-Baranés, Rita Guerreiro, José Brás, Dena Hernandez, Andy Singleton, Paul T. Francis, John Hardy, Kevin Morgan
Cyhoeddwyd 2017Artigo -
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Familial frontotemporal dementia with amyotrophic lateral sclerosis and a shared haplotype on chromosome 9p gan Justin Pearson, Nigel Williams, Elisa Majounie, Adrian J. Waite, J. Randall Stott, Victoria Newsway, Alex Murray, Dena Hernandez, Rita Guerreiro, Andrew Singleton, James Neal, Huw R. Morris
Cyhoeddwyd 2010Artigo -
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Splice Mutation in the Iron-Sulfur Cluster Scaffold Protein ISCU Causes Myopathy with Exercise Intolerance gan Fanny Mochel, Melanie A. Knight, Wing‐Hang Tong, Dena Hernández, Karen Ayyad, Tanja Taivassalo, Peter M. Andersen, Andrew Singleton, Tracey A. Rouault, Kenneth H. Fischbeck, Ronald G. Haller
Cyhoeddwyd 2008Artigo -
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Distinct DNA methylation changes highly correlated with chronological age in the human brain gan Dena Hernández, Michael A. Nalls, J. Raphael Gibbs, Sampath Arepalli, Marcel van der Brug, Sean Chong, Matthew Moore, Dan L. Longo, Mark Cookson, Bryan J. Traynor, Andrew Singleton
Cyhoeddwyd 2011Artigo -
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Penetrance of Parkinson's Disease in <i>LRRK2</i> p.G2019S Carriers Is Modified by a Polygenic Risk Score gan Hirotaka Iwaki, Cornelis Blauwendraat, Mary B. Makarious, Sara Bandrés‐Ciga, Hampton L. Leonard, J. Raphael Gibbs, Dena Hernández, Sonja W. Scholz, Faraz Faghri, Mike A. Nalls, Andrew Singleton
Cyhoeddwyd 2020Artigo -
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Genomic Variation in Seven Khoe-San Groups Reveals Adaptation and Complex African History gan Carina M. Schlebusch, Pontus Skoglund, Per Sjödin, Lucie M. Gattepaille, Dena Hernández, Flora Jay, Sen Li, Michael de Jongh, Andrew Singleton, Michaël G. B. Blum, Himla Soodyall, Mattias Jakobsson
Cyhoeddwyd 2012Artigo -
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Novel age-associated DNA methylation changes and epigenetic age acceleration in middle-aged African Americans and whites gan Salman M. Tajuddin, Dena Hernández, Brian H. Chen, Nicole Noren Hooten, Nicolle A. Mode, Mike A. Nalls, Andrew B. Singleton, Ngozi Ejiogu, Kumaraswamy Naidu Chitrala, Alan B. Zonderman, Michele K. Evans
Cyhoeddwyd 2019Artigo -
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Multimodal assessment of mitochondrial function in Parkinson's disease gan Thomas Payne, Toby Burgess, Stephen Bradley, Sarah Roscoe, Matilde Sassani, Mark Dunning, Dena Hernández, Sonja W. Scholz, Alisdair McNeill, Rosie Taylor, Li Su, Iain D. Wilkinson, Thomas M. Jenkins, Heather Mortiboys, Oliver Bandmann
Cyhoeddwyd 2023Artigo -
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Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study gan Hannu Laaksovirta, Terhi Peuralinna, Jennifer C. Schymick, Sonja W. Scholz, Shaoi-Lin Lai, Liisa Myllykangas, Raimo Sulkava, Lilja Jansson, Dena Hernández, J. Raphael Gibbs, Michael A. Nalls, David Heckerman, Pentti J. Tienari, Bryan J. Traynor
Cyhoeddwyd 2010Artigo -
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Exome sequencing reveals riboflavin transporter mutations as a cause of motor neuron disease gan Janel O. Johnson, J. Raphael Gibbs, André Mégarbané, J. Andoni Urtizberea, Dena Hernández, A. Reghan Foley, Sampath Arepalli, Amelie Pandraud, Javier Simón‐Sánchez, Peter T. Clayton, Mary M. Reilly, Francesco Muntoni, Yevgeniya Abramzon, Henry Houlden, Andrew Singleton
Cyhoeddwyd 2012Artigo -
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Human aging is characterized by focused changes in gene expression and deregulation of alternative splicing gan Lorna W. Harries, Dena Hernandez, William Henley, Andrew R. Wood, Alice C. Holly, Rachel Mary Bradley-Smith, Hanieh Yaghootkar, Ambarish Dutta, Anna Murray, Timothy M. Frayling, Jack M. Guralnik, Stefania Bandinelli, Andrew Singleton, Luigi Ferrucci, David Melzer
Cyhoeddwyd 2011Artigo
Offerynnau Chwilio:
Pynciau Perthynol
Biology
Genetics
Gene
Medicine
Genotype
Single-nucleotide polymorphism
Internal medicine
Disease
Genome-wide association study
Genetic association
Gene expression
Pathology
Population
Computational biology
Parkinson's disease
Environmental health
DNA methylation
Bioinformatics
Epigenetics
Locus (genetics)
Genome
Neuroscience
Mutation
Dementia
Endocrinology
Genetic variation
LRRK2
Linkage disequilibrium
Demography
Evolutionary biology