Result Number | Material Type | Add to My Shelf Action | Record Details and Options |
---|---|---|---|
1 |
Material Type: Artigo
|
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 |
|
2 |
Material Type: Artigo
|
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 |
|
3 |
Material Type: Artigo
|
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 |
|
4 |
Material Type: Artigo
|
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]Switzerland: KargerTexto completo disponível |
|
5 |
Material Type: Artigo
|
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 |
|
6 |
Material Type: Artigo
|
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 |
|
7 |
Material Type: Artigo
|
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 |
|
8 |
Material Type: Artigo
|
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 |
|
9 |
Material Type: Artigo
|
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 |
|
10 |
Material Type: Artigo
|
MAPT expression and splicing is differentially regulated by brain region: relation to genotype and implication for tauopathiesTRABZUNI, Daniah ; WRAY, Selina ; AREPALLI, Sampath ; SINGLETON, Andrew B ; COOKSON, Mark R ; PITTMAN, Alan M ; DE SILVA, Rohan ; WEALE, Michael E ; HARDY, John ; RYTEN, Mina ; VANDROVCOVA, Jana ; RAMASAMY, Adaikalavan ; WALKER, Robert ; SMITH, Colin ; LUK, Connie ; RAPHAEL GIBBS, J ; DILLMAN, Allissa ; HERNANDEZ, Dena GHuman molecular genetics, 2012-09, Vol.21 (18), p.4094-4103 [Periódico revisado por pares]Oxford: Oxford University PressTexto completo disponível |