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Material Type: Artigo
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Menopause accelerates biological agingLevine, Morgan E. ; Lu, Ake T. ; Chen, Brian H. ; Hernandez, Dena G. ; Singleton, Andrew B. ; Ferrucci, Luigi ; Bandinelli, Stefania ; Salfati, Elias ; Manson, JoAnn E. ; Quach, Austin ; Kusters, Cynthia D. J. ; Kuh, Diana ; Wong, Andrew ; Teschendorff, Andrew E. ; Widschwendter, Martin ; Ritz, Beate R. ; Absher, Devin ; Assimes, Themistocles L. ; Horvath, SteveProceedings of the National Academy of Sciences - PNAS, 2016-08, Vol.113 (33), p.9327-9332 [Periódico revisado por pares]United States: National Academy of SciencesTexto completo disponível |
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Material Type: Artigo
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DNA Methylation of Lipid-Related Genes Affects Blood Lipid LevelsPfeiffer, Liliane ; Wahl, Simone ; Pilling, Luke C ; Reischl, Eva ; Sandling, Johanna K ; Kunze, Sonja ; Holdt, Lesca M ; Kretschmer, Anja ; Schramm, Katharina ; Adamski, Jerzy ; Klopp, Norman ; Illig, Thomas ; Hedman, Åsa K ; Roden, Michael ; Hernandez, Dena G ; Singleton, Andrew B ; Thasler, Wolfgang E ; Grallert, Harald ; Gieger, Christian ; Herder, Christian ; Teupser, Daniel ; Meisinger, Christa ; Spector, Timothy D ; Kronenberg, Florian ; Prokisch, Holger ; Melzer, David ; Peters, Annette ; Deloukas, Panos ; Ferrucci, Luigi ; Waldenberger, MelanieCirculation. Cardiovascular genetics, 2015-04, Vol.8 (2), p.334-342 [Periódico revisado por pares]United States: American Heart Association, IncTexto completo disponível |
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Material Type: Artigo
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Mutations in GBA2 Cause Autosomal-Recessive Cerebellar Ataxia with SpasticityHammer, Monia B. ; Eleuch-Fayache, Ghada ; Schottlaender, Lucia V. ; Nehdi, Houda ; Gibbs, J. Raphael ; Arepalli, Sampath K. ; Chong, Sean B. ; Hernandez, Dena G. ; Sailer, Anna ; Liu, Guoxiang ; Mistry, Pramod K. ; Cai, Huaibin ; Shrader, Ginamarie ; Sassi, Celeste ; Bouhlal, Yosr ; Houlden, Henry ; Hentati, Fayçal ; Amouri, Rim ; Singleton, Andrew B.American journal of human genetics, 2013-02, Vol.92 (2), p.245-251 [Periódico revisado por pares]United States: Elsevier IncTexto completo disponível |
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Material Type: Artigo
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Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputationWood, Andrew R ; Perry, John R B ; Tanaka, Toshiko ; Hernandez, Dena G ; Zheng, Hou-Feng ; Melzer, David ; Gibbs, J Raphael ; Nalls, Michael A ; Weedon, Michael N ; Spector, Tim D ; Richards, J Brent ; Bandinelli, Stefania ; Ferrucci, Luigi ; Singleton, Andrew B ; Frayling, Timothy M Arking, Dan E.PloS one, 2013-05, Vol.8 (5), p.e64343-e64343 [Periódico revisado por pares]United States: Public Library of ScienceTexto completo disponível |
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Material Type: Artigo
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Parkinson's disease age at onset genome‐wide association study: Defining heritability, genetic loci, and α‐synuclein mechanismsBlauwendraat, Cornelis ; Heilbron, Karl ; Vallerga, Costanza L. ; Bandres‐Ciga, Sara ; von Coelln, Rainer ; Pihlstrøm, Lasse ; Simón‐Sánchez, Javier ; Schulte, Claudia ; Sharma, Manu ; Krohn, Lynne ; Siitonen, Ari ; Iwaki, Hirotaka ; Leonard, Hampton ; Noyce, Alastair J. ; Tan, Manuela ; Gibbs, J. Raphael ; Hernandez, Dena G. ; Scholz, Sonja W. ; Jankovic, Joseph ; Shulman, Lisa M. ; Lesage, Suzanne ; Corvol, Jean‐Christophe ; Brice, Alexis ; van Hilten, Jacobus J. ; Marinus, Johan ; Eerola‐Rautio, Johanna ; Tienari, Pentti ; Majamaa, Kari ; Toft, Mathias ; Grosset, Donald G. ; Gasser, Thomas ; Heutink, Peter ; Shulman, Joshua M. ; Wood, Nicolas ; Hardy, John ; Morris, Huw R. ; Hinds, David A. ; Gratten, Jacob ; Visscher, Peter M. ; Gan‐Or, Ziv ; Nalls, Mike A. ; Singleton, Andrew B.Movement disorders, 2019-06, Vol.34 (6), p.866-875 [Periódico revisado por pares]Chichester, UK: John Wiley & Sons, LtdTexto completo disponível |
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Material Type: Artigo
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SLC25A46 Mutations Associated with Autosomal Recessive Cerebellar Ataxia in North African FamiliesHammer, Monia B ; Ding, Jinhui ; Mochel, Fanny ; Eleuch-Fayache, Ghada ; Charles, Perrine ; Coutelier, Marie ; Gibbs, J Raphael ; Arepalli, Sampath K ; Chong, Sean B ; Hernandez, Dena G ; Majounie, Elisa ; Clipman, Steven ; Bouhlal, Yosr ; Nehdi, Houda ; Brice, Alexis ; Hentati, Faycal ; Stevanin, Giovanni ; Amouri, Rim ; Durr, Alexandra ; Singleton, Andrew BNeuro-degenerative diseases, 2017-01, Vol.17 (4-5), p.208-212 [Periódico revisado por pares]SwitzerlandTexto completo disponível |
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Material Type: Artigo
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Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association studyLaaksovirta, Hannu, MD ; Peuralinna, Terhi, MSc ; Schymick, Jennifer C, PhD ; Scholz, Sonja W, MD ; Lai, Shaoi-Lin, MD ; Myllykangas, Liisa, MD ; Sulkava, Raimo, MD ; Jansson, Lilja ; Hernandez, Dena G, MSc ; Gibbs, J Raphael, BS ; Nalls, Michael A, PhD ; Heckerman, David, MD ; Tienari, Pentti J, MD ; Traynor, Bryan J, DrLancet neurology, 2010-10, Vol.9 (10), p.978-985 [Periódico revisado por pares]England: Elsevier LtdTexto completo disponível |
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Material Type: Artigo
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A whole-blood transcriptome meta-analysis identifies gene expression signatures of cigarette smokingHuan, Tianxiao ; Joehanes, Roby ; Schurmann, Claudia ; Schramm, Katharina ; Pilling, Luke C ; Peters, Marjolein J ; Mägi, Reedik ; DeMeo, Dawn ; O'Connor, George T ; Ferrucci, Luigi ; Teumer, Alexander ; Homuth, Georg ; Biffar, Reiner ; Völker, Uwe ; Herder, Christian ; Waldenberger, Melanie ; Peters, Annette ; Zeilinger, Sonja ; Metspalu, Andres ; Hofman, Albert ; Uitterlinden, André G ; Hernandez, Dena G ; Singleton, Andrew B ; Bandinelli, Stefania ; Munson, Peter J ; Lin, Honghuang ; Benjamin, Emelia J ; Esko, Tõnu ; Grabe, Hans J ; Prokisch, Holger ; van Meurs, Joyce B J ; Melzer, David ; Levy, DanielHuman molecular genetics, 2016-11, Vol.25 (21), p.4611-4623 [Periódico revisado por pares]England: Oxford University PressTexto completo disponível |
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Material Type: Artigo
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Blood Leukocyte DNA Methylation Predicts Risk of Future Myocardial Infarction and Coronary Heart DiseaseAgha, Golareh ; Mendelson, Michael M ; Ward-Caviness, Cavin K ; Joehanes, Roby ; Huan, TianXiao ; Gondalia, Rahul ; Salfati, Elias ; Brody, Jennifer A ; Fiorito, Giovanni ; Bressler, Jan ; Chen, Brian H ; Ligthart, Symen ; Guarrera, Simonetta ; Colicino, Elena ; Just, Allan C ; Wahl, Simone ; Gieger, Christian ; Vandiver, Amy R ; Tanaka, Toshiko ; Hernandez, Dena G ; Pilling, Luke C ; Singleton, Andrew B ; Sacerdote, Carlotta ; Krogh, Vittorio ; Panico, Salvatore ; Tumino, Rosario ; Li, Yun ; Zhang, Guosheng ; Stewart, James D ; Floyd, James S ; Wiggins, Kerri L ; Rotter, Jerome I ; Multhaup, Michael ; Bakulski, Kelly ; Horvath, Steven ; Tsao, Philip S ; Absher, Devin M ; Vokonas, Pantel ; Hirschhorn, Joel ; Fallin, M Daniele ; Liu, Chunyu ; Bandinelli, Stefania ; Boerwinkle, Eric ; Dehghan, Abbas ; Schwartz, Joel D ; Psaty, Bruce M ; Feinberg, Andrew P ; Hou, Lifang ; Ferrucci, Luigi ; Sotoodehnia, Nona ; Matullo, Giuseppe ; Peters, Annette ; Fornage, Myriam ; Assimes, Themistocles L ; Whitsel, Eric A ; Levy, Daniel ; Baccarelli, Andrea ACirculation (New York, N.Y.), 2019-08, Vol.140 (8), p.645 [Periódico revisado por pares]United StatesTexto completo disponível |
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Material Type: Artigo
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Race-specific alterations in DNA methylation among middle-aged African Americans and Whites with metabolic syndromeChitrala, Kumaraswamy Naidu ; Hernandez, Dena G. ; Nalls, Michael A. ; Mode, Nicolle A. ; Zonderman, Alan B. ; Ezike, Ngozi ; Evans, Michele K.Epigenetics, 2020-05, Vol.15 (5), p.462-482 [Periódico revisado por pares]United States: Taylor & FrancisTexto completo disponível |