Barbara Jasinska-Myga

Role of sepiapterin reductase gene at the PARK3 locus in Parkinson's disease

Aldo Quattrone, Nobutaka Hattori, Anthony E. Lang, 2011, Neurobiology of Aging.

Creation of an Open-Access, Mutation-Defined Fibroblast Resource for Neurological Disease Research

Martin N. Rossor, Margaret Sutherland, Colin J. Mahoney, 2012, PloS one.

Novel A18T and pA29S substitutions in α-synuclein may be associated with sporadic Parkinson's disease.

Anna Potulska-Chromik, Piotr Janik, Dariusz Koziorowski, 2013, Parkinsonism & related disorders.

Identification of genetic variants associated with Huntington's disease progression: a genome-wide association study.

Enrico Amico, Philippe Allain, Mark Mühlau, 2017, The Lancet. Neurology.

Observing Huntington’s Disease: the European Huntington’s Disease Network’s REGISTRY

Alexander Münchau, Caroline Hallam, Andrea Ciarmiello, 2011, PLoS currents.

LINGO1 and LINGO2 variants are associated with essential tremor and Parkinson disease

Matthew J. Farrer, Owen A. Ross, Alexandra I. Soto-Ortolaza, 2010, neurogenetics.

Association of alpha-, beta-, and gamma-Synuclein with diffuse lewy body disease.

Christian Wider, Kenya Nishioka, Dennis W Dickson, 2010, Archives of neurology.