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Refinado por: assunto: Genetics remover
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1
Genetics in Parkinson disease: Mendelian versus non‐Mendelian inheritance
Genetics in Parkinson disease: Mendelian versus non‐Mendelian inheritance
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Genetics in Parkinson disease: Mendelian versus non‐Mendelian inheritance

Hernandez, Dena G. ; Reed, Xylena ; Singleton, Andrew B.

Journal of neurochemistry, 2016-10, Vol.139 (S1), p.59-74 [Periódico revisado por pares]

England: Blackwell Publishing Ltd

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2
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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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
Mutations in GBA2 Cause Autosomal-Recessive Cerebellar Ataxia with Spasticity
Mutations in GBA2 Cause Autosomal-Recessive Cerebellar Ataxia with Spasticity
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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.

American journal of human genetics, 2013-02, Vol.92 (2), p.245-251 [Periódico revisado por pares]

United States: Elsevier Inc

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5
High-resolution inference of genetic relationships among Jewish populations
High-resolution inference of genetic relationships among Jewish populations
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High-resolution inference of genetic relationships among Jewish populations

Kopelman, Naama M ; Stone, Lewi ; Hernandez, Dena G ; Gefel, Dov ; Singleton, Andrew B ; Heyer, Evelyne ; Feldman, Marcus W ; Hillel, Jossi ; Rosenberg, Noah A

European journal of human genetics : EJHG, 2020-06, Vol.28 (6), p.804-814 [Periódico revisado por pares]

England: Nature Publishing Group

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6
Genome wide assessment of young onset Parkinson's disease from Finland
Genome wide assessment of young onset Parkinson's disease from Finland
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Genome wide assessment of young onset Parkinson's disease from Finland

Hernandez, Dena G ; Nalls, Michael A ; Ylikotila, Pauli ; Keller, Margaux ; Hardy, John A ; Majamaa, Kari ; Singleton, Andrew B Toft, Mathias

PloS one, 2012-07, Vol.7 (7), p.e41859-e41859 [Periódico revisado por pares]

United States: Public Library of Science

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7
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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8
Resolving the polymorphism-in-probe problem is critical for correct interpretation of expression QTL studies
Resolving the polymorphism-in-probe problem is critical for correct interpretation of expression QTL studies
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Resolving the polymorphism-in-probe problem is critical for correct interpretation of expression QTL studies

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

Nucleic acids research, 2013-04, Vol.41 (7), p.e88-e88 [Periódico revisado por pares]

England: Oxford University Press

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9
Genetic risk of Parkinson disease and progression
Genetic risk of Parkinson disease and progression
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Genetic risk of Parkinson disease and progression

Iwaki, Hirotaka ; Blauwendraat, Cornelis ; Leonard, Hampton L ; Liu, Ganqiang ; Maple-Grødem, Jodi ; Corvol, Jean-Christophe ; Pihlstrøm, Lasse ; van Nimwegen, Marlies ; Hutten, Samantha J ; Nguyen, Khanh-Dung H ; Rick, Jacqueline ; Eberly, Shirley ; Faghri, Faraz ; Auinger, Peggy ; Scott, Kirsten M ; Wijeyekoon, Ruwani ; van Deerlin, Vivianna M ; Hernandez, Dena G ; Day-Williams, Aaron G ; Brice, Alexis ; Alves, Guido ; Noyce, Alastair J ; Tysnes, Ole-Bjørn ; Evans, Jonathan R ; Breen, David P ; Estrada, Karol ; Wegel, Claire E ; Danjou, Fabrice ; Simon, David K ; Ravina, Bernard ; Toft, Mathias ; Heutink, Peter ; Bloem, Bastiaan R ; Weintraub, Daniel ; Barker, Roger A ; Williams-Gray, Caroline H ; van de Warrenburg, Bart P ; van Hilten, Jacobus J ; Scherzer, Clemens R ; Singleton, Andrew B ; Nalls, Mike A

Neurology. Genetics, 2024-03, Vol.5 [Periódico revisado por pares]

American Academy of Neurology

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10
Genome-wide meta-analysis for serum calcium identifies significantly associated SNPs near the calcium-sensing receptor (CASR) gene
Genome-wide meta-analysis for serum calcium identifies significantly associated SNPs near the calcium-sensing receptor (CASR) gene
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Genome-wide meta-analysis for serum calcium identifies significantly associated SNPs near the calcium-sensing receptor (CASR) gene

Kapur, Karen ; Johnson, Toby ; Beckmann, Noam D ; Sehmi, Joban ; Tanaka, Toshiko ; Kutalik, Zoltán ; Styrkarsdottir, Unnur ; Zhang, Weihua ; Marek, Diana ; Gudbjartsson, Daniel F ; Milaneschi, Yuri ; Holm, Hilma ; Diiorio, Angelo ; Waterworth, Dawn ; Li, Yun ; Singleton, Andrew B ; Bjornsdottir, Unnur S ; Sigurdsson, Gunnar ; Hernandez, Dena G ; Desilva, Ranil ; Elliott, Paul ; Eyjolfsson, Gudmundur I ; Guralnik, Jack M ; Scott, James ; Thorsteinsdottir, Unnur ; Bandinelli, Stefania ; Chambers, John ; Stefansson, Kari ; Waeber, Gérard ; Ferrucci, Luigi ; Kooner, Jaspal S ; Mooser, Vincent ; Vollenweider, Peter ; Beckmann, Jacques S ; Bochud, Murielle ; Bergmann, Sven Abecasis, Gonçalo R.

PLoS genetics, 2010-07, Vol.6 (7), p.e1001035-e1001035 [Periódico revisado por pares]

United States: Public Library of Science

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