Genomewide association study for susceptibility genes contributing to familial Parkinson disease
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Published in Human genetics (01.01.2009)
Published in Human genetics (01.01.2009)
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Mutation of FOXC1 and PITX2 induces cerebral small-vessel disease
French, Curtis R, Seshadri, Sudha, Destefano, Anita L, Fornage, Myriam, Arnold, Corey R, Gage, Philip J, Skarie, Jonathan M, Dobyns, William B, Millen, Kathleen J, Liu, Ting, Dietz, William, Kume, Tsutomu, Hofker, Marten, Emery, Derek J, Childs, Sarah J, Waskiewicz, Andrew J, Lehmann, Ordan J
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Six Novel Loci Associated with Circulating VEGF Levels Identified by a Meta-analysis of Genome-Wide Association Studies
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Published in PLoS genetics (24.02.2016)
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Copy number variation in familial Parkinson disease
Pankratz, Nathan, Dumitriu, Alexandra, Hetrick, Kurt N, Sun, Mei, Latourelle, Jeanne C, Wilk, Jemma B, Halter, Cheryl, Doheny, Kimberly F, Gusella, James F, Nichols, William C, Myers, Richard H, Foroud, Tatiana, DeStefano, Anita L
Published in PloS one (02.08.2011)
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Evidence for a Gene Influencing Blood Pressure on Chromosome 17: Genome Scan Linkage Results for Longitudinal Blood Pressure Phenotypes in Subjects From the Framingham Heart Study
Levy, Daniel, DeStefano, Anita L, Larson, Martin G, O’Donnell, Christopher J, Lifton, Richard P, Gavras, Haralambos, Cupples, L Adrienne, Myers, Richard H
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Published in Hypertension (Dallas, Tex. 1979) (01.10.2000)
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Conference Proceeding
Genetic correlates of brain aging on MRI and cognitive test measures: a genome-wide association and linkage analysis in the Framingham Study
Seshadri, Sudha, DeStefano, Anita L, Au, Rhoda, Massaro, Joseph M, Beiser, Alexa S, Kelly-Hayes, Margaret, Kase, Carlos S, D'Agostino, Sr, Ralph B, Decarli, Charles, Atwood, Larry D, Wolf, Philip A
Published in BMC medical genetics (19.09.2007)
Published in BMC medical genetics (19.09.2007)
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Meta-analysis of Parkinson's Disease: Identification of a novel locus, RIT2
Pankratz, Nathan, Beecham, Gary W., DeStefano, Anita L., Dawson, Ted M., Doheny, Kimberly F., Factor, Stewart A., Hamza, Taye H., Hung, Albert Y., Hyman, Bradley T., Ivinson, Adrian J., Krainc, Dmitri, Latourelle, Jeanne C., Clark, Lorraine N., Marder, Karen, Martin, Eden R., Mayeux, Richard, Ross, Owen A., Scherzer, Clemens R., Simon, David K., Tanner, Caroline, Vance, Jeffery M., Wszolek, Zbigniew K., Zabetian, Cyrus P., Myers, Richard H., Payami, Haydeh, Scott, William K., Foroud, Tatiana
Published in Annals of neurology (01.03.2012)
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Large‐scale sequencing studies expand the known genetic architecture of Alzheimer's disease
Xue, Diane, Bush, William S., Renton, Alan E., Marcora, Edoardo A., Bis, Joshua C., Kunkle, Brian W., Boerwinkle, Eric, DeStefano, Anita L., Farrer, Lindsay, Goate, Alison, Mayeux, Richard, Pericak‐Vance, Margaret, Schellenberg, Gerard, Seshadri, Sudha, Wijsman, Ellen, Haines, Jonathan L., Blue, Elizabeth E.
Published in Alzheimer's & dementia : diagnosis, assessment & disease monitoring (2021)
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Genomewide association study for onset age in Parkinson disease
Latourelle, Jeanne C, Pankratz, Nathan, Dumitriu, Alexandra, Wilk, Jemma B, Goldwurm, Stefano, Pezzoli, Gianni, Mariani, Claudio B, DeStefano, Anita L, Halter, Cheryl, Gusella, James F, Nichols, William C, Myers, Richard H, Foroud, Tatiana
Published in BMC medical genetics (22.09.2009)
Published in BMC medical genetics (22.09.2009)
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Network analysis of drug effect on triglyceride-associated DNA methylation
Lim, Elise, Xu, Hanfei, Wu, Peitao, Posner, Daniel, Wu, Jiayi, Peloso, Gina M, Pitsillides, Achilleas N, DeStefano, Anita L, Adrienne Cupples, L, Liu, Ching-Ti
Published in BMC proceedings (17.09.2018)
Published in BMC proceedings (17.09.2018)
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Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE Collaboration): a meta-analysis of genome-wide association studies
Traylor, Matthew, MSc, Farrall, Martin, FRCPath, Holliday, Elizabeth G, PhD, Sudlow, Cathie, FRCP, Hopewell, Jemma C, PhD, Cheng, Yu-Ching, PhD, Fornage, Myriam, PhD, Ikram, M Arfan, MD, Malik, Rainer, PhD, Bevan, Steve, PhD, Thorsteinsdottir, Unnur, PhD, Nalls, Mike A, PhD, Longstreth, WT, MD, Wiggins, Kerri L, MS, Yadav, Sunaina, MSc, Parati, Eugenio A, MD, DeStefano, Anita L, PhD, Worrall, Bradford B, MD, Kittner, Steven J, MD, Khan, Muhammad Saleem, MSc, Reiner, Alex P, MD, Helgadottir, Anna, MD, Achterberg, Sefanja, PhD, Fernandez-Cadenas, Israel, PhD, Abboud, Sherine, MD, Schmidt, Reinhold, MD, Walters, Matthew, MD, Chen, Wei-Min, PhD, Ringelstein, E Bernd, MD, O'Donnell, Martin, MD, Ho, Weang Kee, PhD, Pera, Joanna, MD, Lemmens, Robin, MD, Norrving, Bo, MD, Higgins, Peter, MRCP, Benn, Marianne, MD, Sale, Michele, PhD, Kuhlenbäumer, Gregor, MD, Doney, Alexander S F, PhD, Vicente, Astrid M, PhD, Delavaran, Hossein, MD, Algra, Ale, MD, Davies, Gail, PhD, Oliveira, Sofia A, PhD, Palmer, Colin N A, PhD, Deary, Ian, PhD, Schmidt, Helena, MD, Pandolfo, Massimo, MD, Montaner, Joan, MD, Carty, Cara, PhD, de Bakker, Paul I W, PhD, Kostulas, Konstantinos, MD, Ferro, Jose M, MD, van Zuydam, Natalie R, MSc, Valdimarsson, Einar, MD, Nordestgaard, Børge G, MD, Lindgren, Arne, MD, Thijs, Vincent, MD, Slowik, Agnieszka, MD, Saleheen, Danish, MD, Paré, Guillaume, MD, Berger, Klaus, MD, Thorleifsson, Gudmar, PhD, Hofman, Albert, MD, Mosley, Thomas H, PhD, Mitchell, Braxton D, PhD, Furie, Karen, MD, Clarke, Robert, FRCP, Levi, Christopher, MD, Seshadri, Sudha, MD, Gschwendtner, Andreas, MD, Boncoraglio, Giorgio B, MD, Sharma, Pankaj, PhD, Bis, Joshua C, PhD, Gretarsdottir, Solveig, PhD, Psaty, Bruce M, Rothwell, Peter M, FMedSci, Rosand, Jonathan, MD, Meschia, James F, MD, Stefansson, Kari, MD, Dichgans, Martin, MD, Markus, Hugh S, Dr
Published in Lancet neurology (01.11.2012)
Published in Lancet neurology (01.11.2012)
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BDNF genetic variants are associated with onset age of familial Parkinson disease: GenePD Study
Karamohamed, S, Latourelle, J C, Racette, B A, Perlmutter, J S, Wooten, G F, Lew, M, Klein, C, Shill, H, Golbe, L I, Mark, M H, Guttman, M, Nicholson, G, Wilk, J B, Saint-Hilaire, M, DeStefano, A L, Prakash, R, Tobin, S, Williamson, J, Suchowersky, O, Labell, N, Growdon, B N J, Singer, C, Watts, R, Goldwurm, S, Pezzoli, G, Baker, K B, Giroux, M L, Pramstaller, P P, Burn, D J, Chinnery, P, Sherman, S, Vieregge, P, Litvan, I, Gusella, J F, Myers, R H, Parsian, A
Published in Neurology (13.12.2005)
Published in Neurology (13.12.2005)
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Common Variants in the 5′ Region of the Leptin Gene Are Associated with Body Mass Index in Men from the National Heart, Lung, and Blood Institute Family Heart Study
Jiang, Y., Wilk, J.B., Borecki, I., Williamson, S., DeStefano, A.L., Xu, G., Liu, J., Ellison, R.C., Province, M., Myers, R.H.
Published in American journal of human genetics (01.08.2004)
Published in American journal of human genetics (01.08.2004)
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Evaluation of the Transdisciplinary Obesity Prevention Research Sciences Program
Hammons, Amber, PhD, Bowers, J., PhD, Teegarden, D., PhD, Destefano, L., PhD, Garcia, G., PhD, Koester, B., PhD, Parker, L., PhD, Childress, A., PhD, Fiese, B., PhD
Published in Journal of nutrition education and behavior (01.07.2016)
Published in Journal of nutrition education and behavior (01.07.2016)
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Heritability and a genome-wide linkage scan for arterial stiffness, wave reflection, and mean arterial pressure : The Framingham heart study
MITCHELL, Gary F, DESTEFANO, Anita L, LARSON, Martin G, BENJAMIN, Emelia J, CHEN, Ming-Huei, VASAN, Ramachandran S, VITA, Joseph A, LEVY, Daniel
Published in Circulation (New York, N.Y.) (12.07.2005)
Published in Circulation (New York, N.Y.) (12.07.2005)
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Cardiovascular health, genetic risk, and risk of dementia in the Framingham Heart Study
Peloso, Gina M, Beiser, Alexa S, Satizabal, Claudia L, Xanthakis, Vanessa, Vasan, Ramachandran S, Pase, Matthew P, Destefano, Anita L, Seshadri, Sudha
Published in Neurology (08.09.2020)
Published in Neurology (08.09.2020)
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Polygenic Overlap Between C-Reactive Protein, Plasma Lipids, and Alzheimer Disease
Desikan, Rahul S, Schork, Andrew J, Wang, Yunpeng, Thompson, Wesley K, Dehghan, Abbas, Ridker, Paul M, Chasman, Daniel I, McEvoy, Linda K, Holland, Dominic, Chen, Chi-Hua, Karow, David S, Brewer, James B, Hess, Christopher P, Williams, Julie, Sims, Rebecca, O'Donovan, Michael C, Choi, Seung Hoan, Bis, Joshua C, Ikram, M Arfan, Gudnason, Vilmundur, DeStefano, Anita L, van der Lee, Sven J, Psaty, Bruce M, van Duijn, Cornelia M, Launer, Lenore, Seshadri, Sudha, Pericak-Vance, Margaret A, Mayeux, Richard, Haines, Jonathan L, Farrer, Lindsay A, Hardy, John, Ulstein, Ingun Dina, Aarsland, Dag, Fladby, Tormod, White, Linda R, Sando, Sigrid B, Rongve, Arvid, Witoelar, Aree, Djurovic, Srdjan, Hyman, Bradley T, Snaedal, Jon, Steinberg, Stacy, Stefansson, Hreinn, Stefansson, Kari, Schellenberg, Gerard D, Andreassen, Ole A, Dale, Anders M
Published in Circulation (New York, N.Y.) (09.06.2015)
Published in Circulation (New York, N.Y.) (09.06.2015)
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Serum brain-derived neurotrophic factor and the risk for dementia: the Framingham Heart Study
Weinstein, Galit, Beiser, Alexa S, Choi, Seung Hoan, Preis, Sarah R, Chen, Tai C, Vorgas, Demetrios, Au, Rhoda, Pikula, Aleksandra, Wolf, Philip A, DeStefano, Anita L, Vasan, Ramachandran S, Seshadri, Sudha
Published in JAMA neurology (01.01.2014)
Published in JAMA neurology (01.01.2014)
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Exploiting family history in aggregation unit-based genetic association tests
Wang, Yanbing, Chen, Han, Peloso, Gina M, DeStefano, Anita L, Dupuis, Josée
Published in European journal of human genetics : EJHG (01.12.2022)
Published in European journal of human genetics : EJHG (01.12.2022)
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