Genetics and genomics of Parkinson’s disease

av Lin, Michelle K, Farrer, Matthew J
Publicerad 2014

Dynamic control of the dopamine transporter in neurotransmission and homeostasis

av Bu, Mengfei, Farrer, Matthew J., Khoshbouei, Habibeh
I publikationen NPJ Parkinsons Dis (2021)

The genetics of Parkinson’s disease: progress and therapeutic implications

av Singleton, Andrew B., Farrer, Matthew J., Bonifati, Vincenzo
Publicerad 2013

Genetic association study of synphilin-1 in idiopathic Parkinson's disease

av Myhre, Ronny, Klungland, Helge, Farrer, Matthew J, Aasly, Jan O
Publicerad 2008

PSEN1 p.Met233Val in a Complex Neurodegenerative Movement and Neuropsychiatric Disorder

av Appel-Cresswell, Silke, Guella, Ilaria, Lehman, Anna, Foti, Dean, Farrer, Matthew J.
I publikationen J Mov Disord (2018)

Head injury, alpha-synuclein genetic variability and Parkinson’s disease

av Lee, Pei-Chen, Bordelon, Yvette, Bronstein, Jeff, Sinsheimer, Janet S., Farrer, Matthew, Ritz, Beate
I publikationen Eur J Neurol (2014)

Patient-Control Association Study of the LRRK2 Gene in South African Parkinson’s Disease Patients

av Bardien, Soraya, Blanckenberg, Janine, van der Merwe, Lize, Farrer, Matthew J., Ross, Owen A.
Publicerad 2013

LRRK2 parkinsonism in Tunisia and Norway: A comparative analysis of disease penetrance

av Hentati, Faycel, Trinh, Joanne, Thompson, Christina, Nosova, Ekaterina, Farrer, Matthew J., Aasly, Jan O.
Publicerad 2014

α-Synuclein Shares Physical and Functional Homology with 14-3-3 Proteins

av Ostrerova, Natalie, Petrucelli, Leonard, Farrer, Matthew, Mehta, Nitinkumar, Choi, Peter, Hardy, John, Wolozin, Benjamin
I publikationen J Neurosci (1999)

Chronic and Acute Manipulation of Cortical Glutamate Transmission Induces Structural and Synaptic Changes in Co-cultured Striatal Neurons

av Kuhlmann, Naila, Wagner Valladolid, Miriam, Quesada-Ramírez, Lucía, Farrer, Matthew J., Milnerwood, Austen J.
I publikationen Front Cell Neurosci (2021)

Clinical and Genetic Description of a Family With a High Prevalence of Autosomal Dominant Restless Legs Syndrome

av Young, Jessica E., Vilariño-Güell, Carles, Lin, Siong-Chi, Wszolek, Zbigniew K., Farrer, Matthew J.
Publicerad 2009

Reply to: SNCA Variants Are Associated With Increased Risk of Multiple System Atrophy

av Ross, Owen A., Vilariño-Güell, Carles, Wszolek, Zbigniew K., Farrer, Matthew J., Dickson, Dennis W.
I publikationen Ann Neurol (2010)

A Case of Parkinson's Disease with No Lewy Body Pathology due to a Homozygous Exon Deletion in Parkin

av Johansen, Krisztina Kunszt, Torp, Sverre Helge, Farrer, Matthew J., Gustavsson, Emil K., Aasly, Jan O.
I publikationen Case Rep Neurol Med (2018)

A Meta-Analysis of α-Synuclein Multiplication in Familial Parkinsonism

av Book, Adam, Guella, Ilaria, Candido, Tara, Brice, Alexis, Hattori, Nobutaka, Jeon, Beomseok, Farrer, Matthew J.
I publikationen Front Neurol (2018)

Elucidating the genetics and pathology of Perry syndrome

av Wider, Christian, Dachsel, Justus C., Farrer, Matthew J., Dickson, Dennis W., Tsuboi, Yoshio, Wszolek, Zbigniew K.
Publicerad 2009

A comparative study of Lrrk2 function in primary neuronal cultures

av Dächsel, Justus C., Behrouz, Bahareh, Yue, Mei, Beevers, Joel E., Melrose, Heather L., Farrer, Matthew J.
Publicerad 2010

Leucine-rich repeat kinase 2 (LRRK2) regulates α-synuclein clearance in microglia

av Maekawa, Tatsunori, Sasaoka, Toshikuni, Azuma, Sadahiro, Ichikawa, Takafumi, Melrose, Heather L., Farrer, Matthew J., Obata, Fumiya
I publikationen BMC Neurosci (2016)

Parkinsonism in GTP cyclohydrolase 1 mutation carriers

av Guella, Ilaria, Sherman, Holly E., Appel-Cresswell, Silke, Rajput, Alex, Rajput, Ali H., Farrer, Matthew J.
I publikationen Brain (2015)

Neuron-autonomous susceptibility to induced synuclein aggregation is exacerbated by endogenous Lrrk2 mutations and ameliorated by Lrrk2 genetic knock-out

av MacIsaac, Sarah, Quevedo Melo, Thaiany, Zhang, Yuting, Volta, Mattia, Farrer, Matthew J, Milnerwood, Austen J
I publikationen Brain Commun (2020)

Measuring dopaminergic function in the 6-OHDA-lesioned rat: a comparison of PET and microdialysis

av Walker, Matthew D, Dinelle, Katherine, Kornelsen, Rick, Lee, Anna, Farrer, Matthew J, Stoessl, A Jon, Sossi, Vesna
Publicerad 2013