Results
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61.
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Linkage and association analyses of type 2 diabetes/impaired glucose metabolism and adiponectin serum levels in Japanese Americans from Hawaii. [electronic resource] by
- Kovac, Ilija P
- Havlik, Richard J
- Foley, Daniel
- Peila, Rita
- Hernandez, Dena
- Wavrant-De Vrièze, Fabienne
- Singleton, Andrew
- Egan, Josephine
- Taub, Dennis
- Rodriguez, Beatriz
- Masaki, Kamal
- Curb, J David
- Fujimoto, Wilfred Y
- Wilson, Alexander F
Producer: 20070409
In:
Diabetes vol. 56
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62.
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Clinical and positron emission tomography of Parkinson's disease caused by LRRK2. [electronic resource] by
- Hernandez, Dena G
- Paisán-Ruíz, Coro
- McInerney-Leo, Aideen
- Jain, Shushant
- Meyer-Lindenberg, Andreas
- Evans, E Whitney
- Berman, Karen F
- Johnson, Janel
- Auburger, Georg
- Schäffer, Alejandro A
- Lopez, Grisel J
- Nussbaum, Robert L
- Singleton, Andrew B
Producer: 20050425
In:
Annals of neurology vol. 57
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63.
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Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study. [electronic resource] by
- Laaksovirta, Hannu
- Peuralinna, Terhi
- Schymick, Jennifer C
- Scholz, Sonja W
- Lai, Shaoi-Lin
- Myllykangas, Liisa
- Sulkava, Raimo
- Jansson, Lilja
- Hernandez, Dena G
- Gibbs, J Raphael
- Nalls, Michael A
- Heckerman, David
- Tienari, Pentti J
- Traynor, Bryan J
Producer: 20101018
In:
The Lancet. Neurology vol. 9
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64.
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Genome-wide assessment of Parkinson's disease in a Southern Spanish population. [electronic resource] by
- Bandrés-Ciga, Sara
- Price, Timothy Ryan
- Barrero, Francisco Javier
- Escamilla-Sevilla, Francisco
- Pelegrina, Javier
- Arepalli, Sampath
- Hernández, Dena
- Gutiérrez, Blanca
- Cervilla, Jorge
- Rivera, Margarita
- Rivera, Alberto
- Ding, Jing-Hui
- Vives, Francisco
- Nalls, Michael
- Singleton, Andrew
- Durán, Raquel
Producer: 20171017
In:
Neurobiology of aging vol. 45
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65.
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Human aging is characterized by focused changes in gene expression and deregulation of alternative splicing. [electronic resource] by
- Harries, Lorna W
- Hernandez, Dena
- Henley, William
- Wood, Andrew R
- Holly, Alice C
- Bradley-Smith, Rachel M
- Yaghootkar, Hanieh
- Dutta, Ambarish
- Murray, Anna
- Frayling, Timothy M
- Guralnik, Jack M
- Bandinelli, Stefania
- Singleton, Andrew
- Ferrucci, Luigi
- Melzer, David
Producer: 20120109
In:
Aging cell vol. 10
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66.
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Exome sequencing in an SCA14 family demonstrates its utility in diagnosing heterogeneous diseases. [electronic resource] by
- Sailer, Anna
- Scholz, Sonja W
- Gibbs, J Raphael
- Tucci, Arianna
- Johnson, Janel O
- Wood, Nicholas W
- Plagnol, Vincent
- Hummerich, Holger
- Ding, Jinhui
- Hernandez, Dena
- Hardy, John
- Federoff, Howard J
- Traynor, Bryan J
- Singleton, Andrew B
- Houlden, Henry
Producer: 20121004
In:
Neurology vol. 79
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67.
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DYT16, a novel young-onset dystonia-parkinsonism disorder: identification of a segregating mutation in the stress-response protein PRKRA. [electronic resource] by
- Camargos, Sarah
- Scholz, Sonja
- Simón-Sánchez, Javier
- Paisán-Ruiz, Coro
- Lewis, Patrick
- Hernandez, Dena
- Ding, Jinhui
- Gibbs, J Raphael
- Cookson, Mark R
- Bras, Jose
- Guerreiro, Rita
- Oliveira, Catarina Resende
- Lees, Andrew
- Hardy, John
- Cardoso, Francisco
- Singleton, Andrew B
Producer: 20080505
In:
The Lancet. Neurology vol. 7
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68.
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Exome sequencing reveals riboflavin transporter mutations as a cause of motor neuron disease. [electronic resource] by
- Johnson, Janel O
- Gibbs, J Raphael
- Megarbane, Andre
- Urtizberea, J Andoni
- Hernandez, Dena G
- Foley, A Reghan
- Arepalli, Sampath
- Pandraud, Amelie
- Simón-Sánchez, Javier
- Clayton, Peter
- Reilly, Mary M
- Muntoni, Francesco
- Abramzon, Yevgeniya
- Houlden, Henry
- Singleton, Andrew B
Producer: 20121205
In:
Brain : a journal of neurology vol. 135
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69.
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Genome-wide SNP assay reveals structural genomic variation, extended homozygosity and cell-line induced alterations in normal individuals. [electronic resource] by
- Simon-Sanchez, Javier
- Scholz, Sonja
- Fung, Hon-Chung
- Matarin, Mar
- Hernandez, Dena
- Gibbs, J Raphael
- Britton, Angela
- de Vrieze, Fabienne Wavrant
- Peckham, Elizabeth
- Gwinn-Hardy, Katrina
- Crawley, Anthony
- Keen, Judith C
- Nash, Josefina
- Borgaonkar, Digamber
- Hardy, John
- Singleton, Andrew
Producer: 20070403
In:
Human molecular genetics vol. 16
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70.
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Resolving the polymorphism-in-probe problem is critical for correct interpretation of expression QTL studies. [electronic resource] by
- Ramasamy, Adaikalavan
- Trabzuni, Daniah
- Gibbs, J Raphael
- Dillman, Allissa
- Hernandez, Dena G
- Arepalli, Sampath
- Walker, Robert
- Smith, Colin
- Ilori, Gigaloluwa Peter
- Shabalin, Andrey A
- Li, Yun
- Singleton, Andrew B
- Cookson, Mark R
- Hardy, John
- Ryten, Mina
- Weale, Michael E
Producer: 20130619
In:
Nucleic acids research vol. 41
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71.
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A candidate gene study of risk for dementia in older, postmenopausal women: Results from the Women's Health Initiative Memory Study. [electronic resource] by
- Driscoll, Ira
- Snively, Beverly M
- Espeland, Mark A
- Shumaker, Sally A
- Rapp, Stephen R
- Goveas, Joseph S
- Casanova, Ramon L
- Wactawski-Wende, Jean
- Manson, JoAnn E
- Rossom, Rebecca
- Brooks, Janet
- Hernandez, Dena G
- Singleton, Andrew B
- Resnick, Susan M
Producer: 20191220
In:
International journal of geriatric psychiatry vol. 34
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72.
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Identification and functional characterization of a novel R621C mutation in the synphilin-1 gene in Parkinson's disease. [electronic resource] by
- Marx, Frank P
- Holzmann, Carsten
- Strauss, Karsten M
- Li, Lei
- Eberhardt, Olaf
- Gerhardt, Ellen
- Cookson, Mark R
- Hernandez, Dena
- Farrer, Matt J
- Kachergus, Jennifer
- Engelender, Simone
- Ross, Christopher A
- Berger, Klaus
- Schöls, Ludger
- Schulz, Jörg B
- Riess, Olaf
- Krüger, Rejko
Producer: 20040130
In:
Human molecular genetics vol. 12
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73.
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Kinesin-associated protein 3 (KIFAP3) has no effect on survival in a population-based cohort of ALS patients. [electronic resource] by
- Traynor, Bryan J
- Nalls, Michael
- Lai, Shiao-Lin
- Gibbs, Raphael J
- Schymick, Jennifer C
- Arepalli, Sampath
- Hernandez, Dena
- van der Brug, Marcel P
- Johnson, Janel O
- Dillman, Allissa
- Cookson, Mark
- Moglia, Cristina
- Calvo, Andrea
- Restagno, Gabriella
- Mora, Gabriele
- Chiò, Adriano
Producer: 20100830
In:
Proceedings of the National Academy of Sciences of the United States of America vol. 107
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74.
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A candidate gene for autoimmune myasthenia gravis. [electronic resource] by
- Landouré, Guida
- Knight, Melanie A
- Stanescu, Horia
- Taye, Addis A
- Shi, Yijun
- Diallo, Oumarou
- Johnson, Janel O
- Hernandez, Dena
- Traynor, Bryan J
- Biesecker, Leslie G
- Elkahloun, Abdel
- Rinaldi, Carlo
- Vincent, Angela
- Willcox, Nick
- Kleta, Robert
- Fischbeck, Kenneth H
- Burnett, Barrington G
Producer: 20121024
In:
Neurology vol. 79
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75.
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Early-onset Parkinson's disease caused by a compound heterozygous DJ-1 mutation. [electronic resource] by
- Hague, Stephen
- Rogaeva, Ekaterina
- Hernandez, Dena
- Gulick, Cindy
- Singleton, Amanda
- Hanson, Melissa
- Johnson, Janel
- Weiser, Roberto
- Gallardo, Marisol
- Ravina, Bernard
- Gwinn-Hardy, Katrina
- Crawley, Anthony
- St George-Hyslop, Peter H
- Lang, Anthony E
- Heutink, Peter
- Bonifati, Vincenzo
- Hardy, John
- Singleton, Andrew
Producer: 20040105
In:
Annals of neurology vol. 54
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76.
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A duplication at chromosome 11q12.2-11q12.3 is associated with spinocerebellar ataxia type 20. [electronic resource] by
- Knight, Melanie A
- Hernandez, Dena
- Diede, Scott J
- Dauwerse, Hans G
- Rafferty, Ian
- van de Leemput, Joyce
- Forrest, Susan M
- Gardner, R J McKinlay
- Storey, Elsdon
- van Ommen, Gert-Jan B
- Tapscott, Stephen J
- Fischbeck, Kenneth H
- Singleton, Andrew B
Producer: 20090716
In:
Human molecular genetics vol. 17
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77.
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Allelic heterogeneity and more detailed analyses of known loci explain additional phenotypic variation and reveal complex patterns of association. [electronic resource] by
- Wood, Andrew R
- Hernandez, Dena G
- Nalls, Michael A
- Yaghootkar, Hanieh
- Gibbs, J Raphael
- Harries, Lorna W
- Chong, Sean
- Moore, Matthew
- Weedon, Michael N
- Guralnik, Jack M
- Bandinelli, Stefania
- Murray, Anna
- Ferrucci, Luigi
- Singleton, Andrew B
- Melzer, David
- Frayling, Timothy M
Producer: 20120123
In:
Human molecular genetics vol. 20
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78.
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Gene expression markers of age-related inflammation in two human cohorts. [electronic resource] by
- Pilling, Luke C
- Joehanes, Roby
- Melzer, David
- Harries, Lorna W
- Henley, William
- Dupuis, Josée
- Lin, Honghuang
- Mitchell, Marcus
- Hernandez, Dena
- Ying, Sai-Xia
- Lunetta, Kathryn L
- Benjamin, Emelia J
- Singleton, Andrew
- Levy, Daniel
- Munson, Peter
- Murabito, Joanne M
- Ferrucci, Luigi
Producer: 20160712
In:
Experimental gerontology vol. 70
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79.
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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. [electronic resource] by
- 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
Producer: 20131223
In:
PloS one vol. 8
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80.
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MAPT expression and splicing is differentially regulated by brain region: relation to genotype and implication for tauopathies. [electronic resource] by
- Trabzuni, Daniah
- Wray, Selina
- Vandrovcova, Jana
- Ramasamy, Adaikalavan
- Walker, Robert
- Smith, Colin
- Luk, Connie
- Gibbs, J Raphael
- Dillman, Allissa
- Hernandez, Dena G
- Arepalli, Sampath
- Singleton, Andrew B
- Cookson, Mark R
- Pittman, Alan M
- de Silva, Rohan
- Weale, Michael E
- Hardy, John
- Ryten, Mina
Producer: 20130117
In:
Human molecular genetics vol. 21
Availability: No items available.
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