Laurie J Ozelius

LRRK2 G2019S as a cause of Parkinson's disease in Ashkenazi Jews.

Christine Klein, Geetha Senthil, Michele Tagliati, 2006, The New England journal of medicine.

Mutations in the Na+/K+-ATPase α3 Gene ATP1A3 Are Associated with Rapid-Onset Dystonia Parkinsonism

William B Dobyns, Allison Brashear, S. Bressman, 2004, Neuron.

Phenotype‐ and genotype‐specific structural alterations in spasmodic dysphonia

Giovanni Battistella, Lazar Fleysher, Kristina Simonyan, 2017, Movement disorders : official journal of the Movement Disorder Society.

ATP1A3 mutations in infants: a new rapid‐onset dystonia–Parkinsonism phenotype characterized by motor delay and ataxia

Allison Brashear, J. Mink, L. Morrison, 2012, Developmental medicine and child neurology.

TorsinA in PC12 cells: Localization in the endoplasmic reticulum and response to stress

Vijaya Ramesh, X. Breakefield, P. Hanson, 2003, Journal of neuroscience research.

ε‐sarcoglycan mutations found in combination with other dystonia gene mutations

Christine Klein, Ruth H Walker, Norman Kock, 2002, Annals of neurology.

Novel mutations in ATP1A3 associated with catastrophic early life epilepsy, episodic prolonged apnea, and postnatal microcephaly

William B Dobyns, Allison Brashear, L. Ozelius, 2015, Epilepsia.

The phenotypic spectrum of rapid-onset dystonia-parkinsonism (RDP) and mutations in the ATP1A3 gene.

Alexander Münchau, Christine Klein, William B Dobyns, 2007, Brain : a journal of neurology.

Dystonia: clinical features, genetics, and treatment

Christine Klein, C. Klein, L. Ozelius, 2002, Current opinion in neurology.

Polygenic Risk of Spasmodic Dysphonia is Associated With Vulnerable Sensorimotor Connectivity

Giovanni Battistella, Kristina Simonyan, Mert R Sabuncu, 2018, Cerebral cortex.

Classification and genetics of dystonia

L. Ozelius, P. C. Aguiar, Laurie J Ozelius, 2002, The Lancet Neurology.