Genetics in Parkinson disease: Mendelian versus non‐Mendelian inheritance
Hernandez, Dena G., Reed, Xylena, Singleton, Andrew B.
Published in Journal of neurochemistry (01.10.2016)
Published in Journal of neurochemistry (01.10.2016)
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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.
Published in Movement disorders (01.06.2019)
Published in Movement disorders (01.06.2019)
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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
Published in PLoS genetics (13.05.2010)
Published in PLoS genetics (13.05.2010)
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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
Published in Proceedings of the National Academy of Sciences - PNAS (16.08.2016)
Published in Proceedings of the National Academy of Sciences - PNAS (16.08.2016)
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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
Published in Lancet neurology (01.10.2010)
Published in Lancet neurology (01.10.2010)
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Genetic modifiers of risk and age at onset in GBA associated Parkinson's disease and Lewy body dementia
Blauwendraat, Cornelis, Reed, Xylena, Krohn, Lynne, Heilbron, Karl, Bandres-Ciga, Sara, Tan, Manuela, Gibbs, J Raphael, Hernandez, Dena G, Kumaran, Ravindran, Langston, Rebekah, Bonet-Ponce, Luis, Alcalay, Roy N, Hassin-Baer, Sharon, Greenbaum, Lior, Iwaki, Hirotaka, Leonard, Hampton L, Grenn, Francis P, Ruskey, Jennifer A, Sabir, Marya, Ahmed, Sarah, Makarious, Mary B, Pihlstrøm, Lasse, Toft, Mathias, van Hilten, Jacobus J, Marinus, Johan, Schulte, Claudia, Brockmann, Kathrin, Sharma, Manu, Siitonen, Ari, Majamaa, Kari, Eerola-Rautio, Johanna, Tienari, Pentti J, Pantelyat, Alexander, Hillis, Argye E, Dawson, Ted M, Rosenthal, Liana S, Albert, Marilyn S, Resnick, Susan M, Ferrucci, Luigi, Morris, Christopher M, Pletnikova, Olga, Troncoso, Juan, Grosset, Donald, Lesage, Suzanne, Corvol, Jean-Christophe, Brice, Alexis, Noyce, Alastair J, Masliah, Eliezer, Wood, Nick, Hardy, John, Shulman, Lisa M, Jankovic, Joseph, Shulman, Joshua M, Heutink, Peter, Gasser, Thomas, Cannon, Paul, Scholz, Sonja W, Morris, Huw, Cookson, Mark R, Nalls, Mike A, Gan-Or, Ziv, Singleton, Andrew B
Published in Brain (London, England : 1878) (01.01.2020)
Published in Brain (London, England : 1878) (01.01.2020)
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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
Published in Circulation (New York, N.Y.) (20.08.2019)
Published in Circulation (New York, N.Y.) (20.08.2019)
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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
Published in Human molecular genetics (01.11.2016)
Published in Human molecular genetics (01.11.2016)
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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.
Published in Neuron (Cambridge, Mass.) (20.10.2011)
Published in Neuron (Cambridge, Mass.) (20.10.2011)
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Journal Article
Blood Leukocyte DNA Methylation Predicts Risk of Future Myocardial Infarction and Coronary Heart Disease: A Longitudinal Study of 11 461 Participants From Population-Based Cohorts
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
Published in Circulation (New York, N.Y.) (20.08.2019)
Published in Circulation (New York, N.Y.) (20.08.2019)
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Distinct DNA methylation changes highly correlated with chronological age in the human brain
HERNANDEZ, Dena G, NALLS, Michael A, SINGLETON, Andrew B, RAPHAEL GIBBS, J, AREPALLI, Sampath, VAN DER BRUG, Marcel, CHONG, Sean, MOORE, Matthew, LONGO, Dan L, COOKSON, Mark R, TRAYNOR, Bryan J
Published in Human molecular genetics (15.03.2011)
Published in Human molecular genetics (15.03.2011)
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Journal Article
Accelerating Medicines Partnership: Parkinson's Disease. Genetic Resource
Iwaki, Hirotaka, Leonard, Hampton L., Makarious, Mary B., Bookman, Matt, Landin, Barry, Vismer, David, Casey, Bradford, Gibbs, J. Raphael, Hernandez, Dena G., Blauwendraat, Cornelis, Vitale, Daniel, Song, Yeajin, Kumar, Dinesh, Dalgard, Clifton L., Sadeghi, Mahdiar, Dong, Xianjun, Misquitta, Leonie, Scholz, Sonja W., Scherzer, Clemens R., Nalls, Mike A., Biswas, Shameek, Singleton, Andrew B.
Published in Movement disorders (01.08.2021)
Published in Movement disorders (01.08.2021)
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Journal Article
Race-specific alterations in DNA methylation among middle-aged African Americans and Whites with metabolic syndrome
Chitrala, Kumaraswamy Naidu, Hernandez, Dena G., Nalls, Michael A., Mode, Nicolle A., Zonderman, Alan B., Ezike, Ngozi, Evans, Michele K.
Published in Epigenetics (03.05.2020)
Published in Epigenetics (03.05.2020)
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APOE gene region methylation is associated with cognitive performance in middle-aged urban adults
Shen, Botong, Hernandez, Dena G., Chitrala, Kumaraswamy Naidu, Fanelli-Kuczmarski, Marie T., Noren Hooten, Nicole, Pacheco, Natasha L., Mode, Nicolle A., Zonderman, Alan B., Ezike, Ngozi, Evans, Michele K.
Published in Neurobiology of aging (01.08.2022)
Published in Neurobiology of aging (01.08.2022)
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MAPT expression and splicing is differentially regulated by brain region: relation to genotype and implication for tauopathies
TRABZUNI, 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 G
Published in Human molecular genetics (15.09.2012)
Published in Human molecular genetics (15.09.2012)
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Journal Article
Heterozygous PRKN mutations are common but do not increase the risk of Parkinson's disease
Zhu, William, Huang, Xiaoping, Yoon, Esther, Bandres-Ciga, Sara, Blauwendraat, Cornelis, Billingsley, Kimberly J, Cade, Joshua H, Wu, Beverly P, Williams, Victoria H, Schindler, Alice B, Brooks, Janet, Gibbs, J Raphael, Hernandez, Dena G, Ehrlich, Debra, Singleton, Andrew B, Narendra, Derek P
Published in Brain (London, England : 1878) (30.06.2022)
Published in Brain (London, England : 1878) (30.06.2022)
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Journal Article
Genomic Variation in Seven Khoe-San Groups Reveals Adaptation and Complex African History
Schlebusch, Carina M., Skoglund, Pontus, Sjödin, Per, Gattepaille, Lucie M., Hernandez, Dena, Jay, Flora, Li, Sen, De Jongh, Michael, Singleton, Andrew, Blum, Michael G. B., Soodyall, Himla, Jakobsson, Mattias
Published in Science (American Association for the Advancement of Science) (19.10.2012)
Published in Science (American Association for the Advancement of Science) (19.10.2012)
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Journal Article
Genome-wide association study reveals genetic risk underlying Parkinson's disease
Singleton, Andrew B, Gasser, Thomas, Simón-Sánchez, Javier, Schulte, Claudia, Bras, Jose M, Sharma, Manu, Gibbs, J Raphael, Berg, Daniela, Paisan-Ruiz, Coro, Lichtner, Peter, Scholz, Sonja W, Hernandez, Dena G, Krüger, Rejko, Federoff, Monica, Klein, Christine, Goate, Alison, Perlmutter, Joel, Bonin, Michael, Nalls, Michael A, Illig, Thomas, Gieger, Christian, Houlden, Henry, Steffens, Michael, Okun, Michael S, Racette, Brad A, Cookson, Mark R, Foote, Kelly D, Fernandez, Hubert H, Traynor, Bryan J, Schreiber, Stefan, Arepalli, Sampath, Zonozi, Ryan, Gwinn, Katrina, van der Brug, Marcel, Lopez, Grisel, Chanock, Stephen J, Schatzkin, Arthur, Park, Yikyung, Hollenbeck, Albert, Gao, Jianjun, Huang, Xuemei, Wood, Nick W, Lorenz, Delia, Deuschl, Günther, Chen, Honglei, Riess, Olaf, Hardy, John A
Published in Nature genetics (01.12.2009)
Published in Nature genetics (01.12.2009)
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Genetics of early onset Parkinson’s disease in Finland: exome sequencing and genome-wide association study
Siitonen, A, Nalls, M.A, Hernández, D, Gibbs, J.R, Ding, J, Ylikotila, P, Edsall, C, Singleton, A, Majamaa, K
Published in Neurobiology of aging (01.05.2017)
Published in Neurobiology of aging (01.05.2017)
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Journal Article
Mutations in GBA2 Cause Autosomal-Recessive Cerebellar Ataxia with Spasticity
Hammer, 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.
Published in American journal of human genetics (07.02.2013)
Published in American journal of human genetics (07.02.2013)
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