Ebba Lohmann

Complex relationship between Parkin mutations and Parkinson disease.

Jean-François Deleuze, Vincenzo Bonifati, Thomas Gasser, 2002, American journal of medical genetics.

How much phenotypic variation can be attributed to parkin genotype?

Alexandra Durr, Valérie Fraix, Vincenzo Bonifati, 2003, Annals of neurology.

Differentiating symptomatic Parkin mutations carriers from patients with idiopathic Parkinson's disease: contribution of automated segmentation neuroimaging method.

Ali Bilgin Arslan, Murat Emre, Ali Bayram, 2012, Parkinsonism & related disorders.

Mutational analysis of the PINK1 gene in early-onset parkinsonism in Europe and North Africa.

Stéphane Thobois, Yves Agid, Pablo Ibáñez, 2006, Brain : a journal of neurology.

Identification of PSEN1 and PSEN2 gene mutations and variants in Turkish dementia patients

Murat Emre, Hakan Gurvit, A. Singleton, 2012, Neurobiology of Aging.

A Multitracer Dopaminergic PET Study of Young-Onset Parkinsonian Patients With and Without Parkin Gene Mutations

Bruno Dubois, Stéphane Thobois, Emmanuel Broussolle, 2009, Journal of Nuclear Medicine.

Young-onset Parkinson disease with and without parkin gene mutations: a fluorodopa F 18 positron emission tomography study.

Nicolas Costes, Maria-Joao Ribeiro, Stéphane Thobois, 2003, Archives of neurology.

Genome-wide association study confirms BST1 and suggests a locus on 12q24 as the risk loci for Parkinson's disease in the European population.

Mohamad Saad, Alexandra Durr, Christophe Tzourio, 2011, Human molecular genetics.

A missense mutation in KCTD17 causes autosomal dominant myoclonus-dystonia.

Deborah Hughes, Christine Klein, Thomas Foltynie, 2015, American journal of human genetics.