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Are you a UK Parkinson's researchers? You might be interested in this competition - parkinsons.org.uk/content/pictur… UKPDC

Cells transplanted into brains of people with Parkinson’s remained functional for more than a decade. j.mp/1rxNJ3Z via Dana Foundation🧠

GCH1 mutation is a novel risk factor of developing #Parkinsons disease. ucl.ac.uk/ukpdc/news-pub…

The PREDICT-PD Blog: Phenotypic variability of PINK1 expression: 12 Yea... predictpd.blogspot.com/2014/08/phenot…

Parkinson's disease: chameleons and mimics predictpd.blogspot.com/2014/09/parkin…

Paralysed man walks again after cell transplant bbc.in/1wgH4wp - UCL Queen Square Institute of Neurology research behind the operation

RT Parkinson's UK: We've launched Brain: the inside story a free resource for #Alevel biology braintheinsidestory.co.uk

Bioinformatician post @DMN_ION, UCL Institute of Neurology. Closes 4th December 2014. jobs.ac.uk/job/AJY201/bio…

What it's like to have Parkinson's for 15 minutes - tech - 19 November 2014 - New Scientist: newscientist.com/article/dn2658…

A new fellowship aims to grow the number of #Parkinsons specialists worldwide bit.ly/1pU8M2H

Biochemical Society webcast: Advances in Genetic Understanding of Parkinson's Disease, by Prof Nicholas Wood. goo.gl/yxXtK0

Our paper uses #geneontology find function LRRK2-interactors; drug clues peerj.com/articles/778/ lewislaboratory.com/Home_Page.php @DMN_ION #Parkinsons

How does the gene GB1A affect #Parkinsons? Researchers at The University of Sheffield investigate bit.ly/16YuW8g #findacure

UKPDC's Prof John Hardy presented the 2015 Pritzker Prize for Leadership in Parkinson's Research by Michael J. Fox. goo.gl/2f7r2T

John Hardy elected to EMBO membership @DMN_ION EMBOcomm tinyurl.com/nqkadxz

QSBB has a new website! Find out more about us! ucl.ac.uk/ion/department…

Prof Hardy awarded $3 million Breakthrough Prize for research into the genetic causes of neurodegenerative disease. goo.gl/BtY0xG

Online now! GWAS: Deletions at 22q11.2 in idiopathic #ParkinsonsDisease bit.ly/1q3y0Nd (open access)

New! Two groups identify PDE10A mutations that cause hyperkinetic movement disorders: bit.ly/23liJ8T & bit.ly/1RGA20c