The genetic architecture of Parkinson's disease von Blauwendraat, Cornelis, Nalls, Mike A, Singleton, Andrew B

Volltext

Genetics in Parkinson disease: Mendelian versus non‐Mendelian inheritance von Hernandez, Dena G., Reed, Xylena, Singleton, Andrew B.

Volltext

Genetics of Parkinson's disease: An introspection of its journey towards precision medicine von Bandres-Ciga, Sara, Diez-Fairen, Monica, Kim, Jonggeol Jeff, Singleton, Andrew B.

Volltext

The genetics and neuropathology of Parkinson’s disease von Houlden, Henry, Singleton, Andrew B.

Volltext

Reply to: ‘Letter to the Editor on “Sex Differences in Parkinson's Disease Phenotype and Caregiving Disparities”’ von Antar, Tarek, Iwaki, Hirotaka, Singleton, Andrew

Volltext

Genomewide Association Studies and Human Disease von Hardy, John, Singleton, Andrew

Volltext

The Evolution of Genetics: Alzheimer’s and Parkinson’s Diseases von Singleton, Andrew, Hardy, John

Volltext

The genetics of Parkinson's disease: Progress and therapeutic implications von Singleton, Andrew B., Farrer, Matthew J., Bonifati, Vincenzo

Volltext

Progress in the genetic analysis of Parkinson’s disease von Singleton, Andrew, Hardy, John

Volltext

A meta-analysis of genome-wide association studies identifies 17 new Parkinson's disease risk loci von Chang, Diana, Nalls, Mike A, Hallgrímsdóttir, Ingileif B, Hunkapiller, Julie, van der Brug, Marcel, Cai, Fang, Kerchner, Geoffrey A, Ayalon, Gai, Bingol, Baris, Sheng, Morgan, Hinds, David, Behrens, Timothy W, Singleton, Andrew B, Bhangale, Tushar R, Graham, Robert R

Volltext

Virus exposure and neurodegenerative disease risk across national biobanks von Levine, Kristin S., Leonard, Hampton L., Blauwendraat, Cornelis, Iwaki, Hirotaka, Johnson, Nicholas, Bandres-Ciga, Sara, Ferrucci, Luigi, Faghri, Faraz, Singleton, Andrew B., Nalls, Mike A.

Volltext

Abundant quantitative trait loci exist for DNA methylation and gene expression in human brain von 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

Volltext

Menopause accelerates biological aging von 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

Volltext

Parkinson's disease age at onset genome‐wide association study: Defining heritability, genetic loci, and α‐synuclein mechanisms von 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.

Volltext

Genetic variability in the regulation of gene expression in ten regions of the human brain von Ramasamy, Adaikalavan, Trabzuni, Daniah, Guelfi, Sebastian, Varghese, Vibin, Smith, Colin, Walker, Robert, De, Tisham, Coin, Lachlan, de Silva, Rohan, Cookson, Mark R, Singleton, Andrew B, Hardy, John, Ryten, Mina, Weale, Michael E

Volltext

Genome-wide CRISPRi/a screens in human neurons link lysosomal failure to ferroptosis von Tian, Ruilin, Abarientos, Anthony, Hong, Jason, Hashemi, Sayed Hadi, Yan, Rui, Dräger, Nina, Leng, Kun, Nalls, Mike A., Singleton, Andrew B., Xu, Ke, Faghri, Faraz, Kampmann, Martin

Volltext

A CRISPRi/a platform in human iPSC-derived microglia uncovers regulators of disease states von Dräger, Nina M., Sattler, Sydney M., Huang, Cindy Tzu-Ling, Teter, Olivia M., Leng, Kun, Hashemi, Sayed Hadi, Hong, Jason, Aviles, Giovanni, Clelland, Claire D., Zhan, Lihong, Udeochu, Joe C., Kodama, Lay, Singleton, Andrew B., Nalls, Mike A., Ichida, Justin, Ward, Michael E., Faghri, Faraz, Gan, Li, Kampmann, Martin

Volltext

The Discovery of LRRK2 Mutations as a Cause of Parkinson's Disease von Singleton, Andrew B., Gasser, Thomas

Volltext

Genome‐Wide Association Studies of Cognitive and Motor Progression in Parkinson's Disease von Tan, Manuela M.X., Lawton, Michael A., Jabbari, Edwin, Reynolds, Regina H., Iwaki, Hirotaka, Blauwendraat, Cornelis, Kanavou, Sofia, Pollard, Miriam I., Hubbard, Leon, Malek, Naveed, Grosset, Katherine A., Marrinan, Sarah L., Bajaj, Nin, Barker, Roger A., Burn, David J., Bresner, Catherine, Foltynie, Thomas, Wood, Nicholas W., Williams‐Gray, Caroline H., Hardy, John, Nalls, Michael A., Singleton, Andrew B., Williams, Nigel M., Ben‐Shlomo, Yoav, Hu, Michele T.M., Grosset, Donald G., Shoai, Maryam, Morris, Huw R.

Volltext

Super‐Clausius–Clapeyron scaling of rainfall in a model squall line von Singleton, Andrew, Toumi, Ralf

Volltext