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1
Genetics in Parkinson disease: Mendelian versus non‐Mendelian inheritance
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Artigo
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Genetics in Parkinson disease: Mendelian versus non‐Mendelian inheritance

Hernandez, Dena G. ; Reed, Xylena ; Singleton, Andrew B.

Journal of neurochemistry, 2016-10, Vol.139 (S1), p.59-74 [Periódico revisado por pares]

England: Blackwell Publishing Ltd

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2
Exome Sequencing Reveals VCP Mutations as a Cause of Familial ALS
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Exome Sequencing Reveals VCP Mutations as a Cause of Familial ALS

Johnson, Janel O. ; Mandrioli, Jessica ; Benatar, Michael ; Abramzon, Yevgeniya ; Van Deerlin, Vivianna M. ; Trojanowski, John Q. ; Gibbs, J. Raphael ; Brunetti, Maura ; Gronka, Susan ; Wuu, Joanne ; Ding, Jinhui ; McCluskey, Leo ; Martinez-Lage, Maria ; Falcone, Dana ; Hernandez, Dena G. ; Arepalli, Sampath ; Chong, Sean ; Schymick, Jennifer C. ; Rothstein, Jeffrey ; Landi, Francesco ; Wang, Yong-Dong ; Calvo, Andrea ; Mora, Gabriele ; Sabatelli, Mario ; Monsurrò, Maria Rosaria ; Battistini, Stefania ; Salvi, Fabrizio ; Spataro, Rossella ; Sola, Patrizia ; Borghero, Giuseppe ; Galassi, Giuliana ; Scholz, Sonja W. ; Taylor, J. Paul ; Restagno, Gabriella ; Chiò, Adriano ; Traynor, Bryan J.

Neuron (Cambridge, Mass.), 2010-12, Vol.68 (5), p.857-864 [Periódico revisado por pares]

United States: Elsevier Inc

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3
Abundant quantitative trait loci exist for DNA methylation and gene expression in human brain
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Artigo
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Abundant quantitative trait loci exist for DNA methylation and gene expression in human brain

Gibbs, J Raphael ; van der Brug, Marcel P ; Hernandez, Dena G ; Traynor, Bryan J ; Nalls, Michael A ; Lai, Shiao-Lin ; Arepalli, Sampath ; Dillman, Allissa ; Rafferty, Ian P ; Troncoso, Juan ; Johnson, Robert ; Zielke, H Ronald ; Ferrucci, Luigi ; Longo, Dan L ; Cookson, Mark R ; Singleton, Andrew B Flint, Jonathan

PLoS genetics, 2010-05, Vol.6 (5), p.e1000952-e1000952 [Periódico revisado por pares]

United States: Public Library of Science

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4
Genome-wide meta-analysis for serum calcium identifies significantly associated SNPs near the calcium-sensing receptor (CASR) gene
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Artigo
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Genome-wide meta-analysis for serum calcium identifies significantly associated SNPs near the calcium-sensing receptor (CASR) gene

Kapur, Karen ; Johnson, Toby ; Beckmann, Noam D ; Sehmi, Joban ; Tanaka, Toshiko ; Kutalik, Zoltán ; Styrkarsdottir, Unnur ; Zhang, Weihua ; Marek, Diana ; Gudbjartsson, Daniel F ; Milaneschi, Yuri ; Holm, Hilma ; Diiorio, Angelo ; Waterworth, Dawn ; Li, Yun ; Singleton, Andrew B ; Bjornsdottir, Unnur S ; Sigurdsson, Gunnar ; Hernandez, Dena G ; Desilva, Ranil ; Elliott, Paul ; Eyjolfsson, Gudmundur I ; Guralnik, Jack M ; Scott, James ; Thorsteinsdottir, Unnur ; Bandinelli, Stefania ; Chambers, John ; Stefansson, Kari ; Waeber, Gérard ; Ferrucci, Luigi ; Kooner, Jaspal S ; Mooser, Vincent ; Vollenweider, Peter ; Beckmann, Jacques S ; Bochud, Murielle ; Bergmann, Sven Abecasis, Gonçalo R.

PLoS genetics, 2010-07, Vol.6 (7), p.e1001035-e1001035 [Periódico revisado por pares]

United States: Public Library of Science

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5
Menopause accelerates biological aging
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Artigo
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Menopause accelerates biological aging

Levine, 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, Steve

Proceedings of the National Academy of Sciences - PNAS, 2016-08, Vol.113 (33), p.9327-9332 [Periódico revisado por pares]

United States: National Academy of Sciences

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6
Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study
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Artigo
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Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study

Laaksovirta, 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, Dr

Lancet neurology, 2010-10, Vol.9 (10), p.978-985 [Periódico revisado por pares]

England: Elsevier Ltd

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7
Parkinson's disease age at onset genome‐wide association study: Defining heritability, genetic loci, and α‐synuclein mechanisms
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Parkinson's disease age at onset genome‐wide association study: Defining heritability, genetic loci, and α‐synuclein mechanisms

Blauwendraat, 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, Ltd

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8
A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD
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A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD

Renton, Alan E. ; Majounie, Elisa ; Waite, Adrian ; Simón-Sánchez, Javier ; Rollinson, Sara ; Gibbs, J. Raphael ; Schymick, Jennifer C. ; Laaksovirta, Hannu ; van Swieten, John C. ; Myllykangas, Liisa ; Kalimo, Hannu ; Paetau, Anders ; Abramzon, Yevgeniya ; Remes, Anne M. ; Kaganovich, Alice ; Scholz, Sonja W. ; Duckworth, Jamie ; Ding, Jinhui ; Harmer, Daniel W. ; Hernandez, Dena G. ; Johnson, Janel O. ; Mok, Kin ; Ryten, Mina ; Trabzuni, Danyah ; Guerreiro, Rita J. ; Orrell, Richard W. ; Neal, James ; Murray, Alex ; Pearson, Justin ; Jansen, Iris E. ; Sondervan, David ; Seelaar, Harro ; Blake, Derek ; Young, Kate ; Halliwell, Nicola ; Callister, Janis Bennion ; Toulson, Greg ; Richardson, Anna ; Gerhard, Alex ; Snowden, Julie ; Mann, David ; Neary, David ; Nalls, Michael A. ; Peuralinna, Terhi ; Jansson, Lilja ; Isoviita, Veli-Matti ; Kaivorinne, Anna-Lotta ; Hölttä-Vuori, Maarit ; Ikonen, Elina ; Sulkava, Raimo ; Benatar, Michael ; Wuu, Joanne ; Chiò, Adriano ; Restagno, Gabriella ; Borghero, Giuseppe ; Sabatelli, Mario ; Heckerman, David ; Rogaeva, Ekaterina ; Zinman, Lorne ; Rothstein, Jeffrey D. ; Sendtner, Michael ; Drepper, Carsten ; Eichler, Evan E. ; Alkan, Can ; Abdullaev, Ziedulla ; Pack, Svetlana D. ; Dutra, Amalia ; Pak, Evgenia ; Hardy, John ; Singleton, Andrew ; Williams, Nigel M. ; Heutink, Peter ; Pickering-Brown, Stuart ; Morris, Huw R. ; Tienari, Pentti J. ; Traynor, Bryan J.

Neuron (Cambridge, Mass.), 2011-10, Vol.72 (2), p.257-268 [Periódico revisado por pares]

United States: Elsevier Inc

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9
A whole-blood transcriptome meta-analysis identifies gene expression signatures of cigarette smoking
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A whole-blood transcriptome meta-analysis identifies gene expression signatures of cigarette smoking

Huan, 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, Daniel

Human molecular genetics, 2016-11, Vol.25 (21), p.4611-4623 [Periódico revisado por pares]

England: Oxford University Press

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10
Blood Leukocyte DNA Methylation Predicts Risk of Future Myocardial Infarction and Coronary Heart Disease
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Artigo
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Blood Leukocyte DNA Methylation Predicts Risk of Future Myocardial Infarction and Coronary Heart Disease

Agha, 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 A

Circulation (New York, N.Y.), 2019-08, Vol.140 (8), p.645 [Periódico revisado por pares]

United States

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