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1
Exome Sequencing Reveals VCP Mutations as a Cause of Familial ALS
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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2
Menopause accelerates biological aging
Menopause accelerates biological aging
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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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3
DNA Methylation of Lipid-Related Genes Affects Blood Lipid Levels
DNA Methylation of Lipid-Related Genes Affects Blood Lipid Levels
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DNA Methylation of Lipid-Related Genes Affects Blood Lipid Levels

Pfeiffer, 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, Melanie

Circulation. Cardiovascular genetics, 2015-04, Vol.8 (2), p.334-342 [Periódico revisado por pares]

United States: American Heart Association, Inc

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4
Next-generation sequencing reveals substantial genetic contribution to dementia with Lewy bodies
Next-generation sequencing reveals substantial genetic contribution to dementia with Lewy bodies
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Next-generation sequencing reveals substantial genetic contribution to dementia with Lewy bodies

Geiger, Joshua T ; Ding, Jinhui ; Crain, Barbara ; Pletnikova, Olga ; Letson, Christopher ; Dawson, Ted M ; Rosenthal, Liana S ; Pantelyat, Alexander ; Gibbs, J. Raphael ; Albert, Marilyn S ; Hernandez, Dena G ; Hillis, Argye E ; Stone, David J ; Singleton, Andrew B ; Hardy, John A ; Troncoso, Juan C ; Scholz, Sonja W

Neurobiology of disease, 2016-10, Vol.94, p.55-62 [Periódico revisado por pares]

United States: Elsevier Inc

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5
Assessment of APOE in atypical parkinsonism syndromes
Assessment of APOE in atypical parkinsonism syndromes
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Assessment of APOE in atypical parkinsonism syndromes

Sabir, Marya S. ; Blauwendraat, Cornelis ; Ahmed, Sarah ; Serrano, Geidy E. ; Beach, Thomas G. ; Perkins, Matthew ; Rice, Ann C. ; Masliah, Eliezer ; Morris, Christopher M. ; Pihlstrom, Lasse ; Pantelyat, Alexander ; Resnick, Susan M. ; Cookson, Mark R. ; Hernandez, Dena G. ; Albert, Marilyn ; Dawson, Ted M. ; Rosenthal, Liana S. ; Houlden, Henry ; Pletnikova, Olga ; Troncoso, Juan ; Scholz, Sonja W.

Neurobiology of disease, 2019-07, Vol.127, p.142-146 [Periódico revisado por pares]

United States: Elsevier Inc

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6
Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation
Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation
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Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputation

Wood, 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 Science

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7
Parkinson's disease age at onset genome‐wide association study: Defining heritability, genetic loci, and α‐synuclein mechanisms
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
An exploratory analysis on gene-environment interactions for Parkinson disease
An exploratory analysis on gene-environment interactions for Parkinson disease
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An exploratory analysis on gene-environment interactions for Parkinson disease

Gao, Jianjun ; Nalls, Michael A ; Shi, Min ; Joubert, Bonnie R ; Hernandez, Dena G ; Huang, Xuemei ; Hollenbeck, Albert ; Singleton, Andrew B ; Chen, Honglei

Neurobiology of aging, 2012-10, Vol.33 (10), p.2528.e1-2528.e6 [Periódico revisado por pares]

United States: Elsevier Inc

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9
Analysis of repeated leukocyte DNA methylation assessments reveals persistent epigenetic alterations after an incident myocardial infarction
Analysis of repeated leukocyte DNA methylation assessments reveals persistent epigenetic alterations after an incident myocardial infarction
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Analysis of repeated leukocyte DNA methylation assessments reveals persistent epigenetic alterations after an incident myocardial infarction

Ward-Caviness, Cavin K ; Agha, Golareh ; Chen, Brian H ; Pfeiffer, Liliane ; Wilson, Rory ; Wolf, Petra ; Gieger, Christian ; Schwartz, Joel ; Vokonas, Pantel S ; Hou, Lifang ; Just, Allan C ; Bandinelli, Stefania ; Hernandez, Dena G ; Singleton, Andrew B ; Prokisch, Holger ; Meitinger, Thomas ; Kastenmüller, Gabi ; Ferrucci, Luigi ; Baccarelli, Andrea A ; Waldenberger, Melanie ; Peters, Annette

Clinical epigenetics, 2018-12, Vol.10 (1), p.161-161, Article 161 [Periódico revisado por pares]

Germany: BioMed Central Ltd

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10
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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