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Abundant quantitative trait loci exist for DNA methylation and gene expression in human brain
Abundant quantitative trait loci exist for DNA methylation and gene expression in human brain
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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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2
Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study
Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study
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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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3
A large study reveals no association between APOE and Parkinson's disease
A large study reveals no association between APOE and Parkinson's disease
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A large study reveals no association between APOE and Parkinson's disease

Federoff, Monica ; Jimenez-Rolando, Belen ; Nalls, Michael A ; Singleton, Andrew B

Neurobiology of disease, 2012-05, Vol.46 (2), p.389-392 [Periódico revisado por pares]

United States: Elsevier Inc

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4
Genetics of early onset Parkinson’s disease in Finland: exome sequencing and genome-wide association study
Genetics of early onset Parkinson’s disease in Finland: exome sequencing and genome-wide association study
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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

Neurobiology of aging, 2017-05, Vol.53, p.195.e7-195.e10 [Periódico revisado por pares]

United States: Elsevier Inc

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5
Race-specific alterations in DNA methylation among middle-aged African Americans and Whites with metabolic syndrome
Race-specific alterations in DNA methylation among middle-aged African Americans and Whites with metabolic syndrome
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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.

Epigenetics, 2020-05, Vol.15 (5), p.462-482 [Periódico revisado por pares]

United States: Taylor & Francis

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6
Variation in tau isoform expression in different brain regions and disease states
Variation in tau isoform expression in different brain regions and disease states
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Variation in tau isoform expression in different brain regions and disease states

Majounie, Elisa ; Cross, William ; Newsway, Victoria ; Dillman, Allissa ; Vandrovcova, Jana ; Morris, Christopher M ; Nalls, Michael A ; Ferrucci, Luigi ; Owen, Michael J ; O'Donovan, Michael C ; Cookson, Mark R ; Singleton, Andrew B ; de Silva, Rohan ; Morris, Huw R

Neurobiology of aging, 2013-07, Vol.34 (7), p.1922.e7-1922.e12 [Periódico revisado por pares]

United States: Elsevier Inc

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7
Measures of autozygosity in decline: globalization, urbanization, and its implications for medical genetics
Measures of autozygosity in decline: globalization, urbanization, and its implications for medical genetics
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Measures of autozygosity in decline: globalization, urbanization, and its implications for medical genetics

Nalls, Michael A ; Simon-Sanchez, Javier ; Gibbs, J Raphael ; Paisan-Ruiz, Coro ; Bras, Jose Tomas ; Tanaka, Toshiko ; Matarin, Mar ; Scholz, Sonja ; Weitz, Charles ; Harris, Tamara B ; Ferrucci, Luigi ; Hardy, John ; Singleton, Andrew B Visscher, Peter M.

PLoS genetics, 2009-03, Vol.5 (3), p.e1000415-e1000415 [Periódico revisado por pares]

United States: Public Library of Science

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8
Human Obesity Associated with an Intronic SNP in the Brain-Derived Neurotrophic Factor Locus
Human Obesity Associated with an Intronic SNP in the Brain-Derived Neurotrophic Factor Locus
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Human Obesity Associated with an Intronic SNP in the Brain-Derived Neurotrophic Factor Locus

Mou, Zongyang ; Hyde, Thomas M. ; Lipska, Barbara K. ; Martinowich, Keri ; Wei, Peter ; Ong, Chiew-Jen ; Hunter, Lindsay A. ; Palaguachi, Gladys I. ; Morgun, Eva ; Teng, Rujia ; Lai, Chen ; Condarco, Tania A. ; Demidowich, Andrew P. ; Krause, Amanda J. ; Marshall, Leslie J. ; Haack, Karin ; Voruganti, V. Saroja ; Cole, Shelley A. ; Butte, Nancy F. ; Comuzzie, Anthony G. ; Nalls, Michael A. ; Zonderman, Alan B. ; Singleton, Andrew B. ; Evans, Michele K. ; Martin, Bronwen ; Maudsley, Stuart ; Tsao, Jack W. ; Kleinman, Joel E. ; Yanovski, Jack A. ; Han, Joan C.

Cell reports (Cambridge), 2015-11, Vol.13 (6), p.1073-1080 [Periódico revisado por pares]

United States: Elsevier Inc

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9
Genome-wide association study reveals genetic risk underlying Parkinson's disease
Genome-wide association study reveals genetic risk underlying Parkinson's disease
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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

Nature genetics, 2009-12, Vol.41 (12), p.1308-1312 [Periódico revisado por pares]

New York, NY: Nature Publishing Group

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10
A genome-wide association study in multiple system atrophy
A genome-wide association study in multiple system atrophy
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A genome-wide association study in multiple system atrophy

Sailer, Anna ; Scholz, Sonja W ; Nalls, Michael A ; Schulte, Claudia ; Federoff, Monica ; Price, T Ryan ; Lees, Andrew ; Ross, Owen A ; Dickson, Dennis W ; Mok, Kin ; Mencacci, Niccolo E ; Schottlaender, Lucia ; Chelban, Viorica ; Ling, Helen ; OʼSullivan, Sean S ; Wood, Nicholas W ; Traynor, Bryan J ; Ferrucci, Luigi ; Federoff, Howard J ; Mhyre, Timothy R ; Morris, Huw R ; Deuschl, Günther ; Quinn, Niall ; Widner, Hakan ; Albanese, Alberto ; Infante, Jon ; Bhatia, Kailash P ; Poewe, Werner ; Oertel, Wolfgang ; Höglinger, Günter U ; Wüllner, Ullrich ; Goldwurm, Stefano ; Pellecchia, Maria Teresa ; Ferreira, Joaquim ; Tolosa, Eduardo ; Bloem, Bastiaan R ; Rascol, Olivier ; Meissner, Wassilios G ; Hardy, John A ; Revesz, Tamas ; Holton, Janice L ; Gasser, Thomas ; Wenning, Gregor K ; Singleton, Andrew B ; Houlden, Henry

Neurology, 2016-10, Vol.87 (15), p.1591-1598 [Periódico revisado por pares]

United States: American Academy of Neurology

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