Field synopsis and systematic meta-analyses of genetic association studies in isolated dystonia

Ohlei O, Dobricic V, Lohmann K, Klein C, Lill CM, Bertram L.
Parkinsonism Relat Disord. 2018 Dec;57:50-57. doi: 10.1016/j.parkreldis.2018.07.018. Epub 2018 Jul 27.

A Klinefelter patient with an additional mitochondrial mutation: Implications for genotype-driven treatment and mitochondrial mutational load in different tissues and family members

Dulovic M, Schäffer E, Leypoldt F, Balck A, Schaake S, Hinrichs F, Kirchner H, Brüggemann N, Berg D, Lohmann K.
Parkinsonism Relat Disord. 2018 Sep;54:116-118. doi: 10.1016/j.parkreldis.2018.04.001. Epub 2018 Apr 3.

Environmental and Genetic Variables Influencing Mitochondrial Health and Parkinson’s Disease Penetrance

Alessandra Zanon, Peter P. Pramstaller, Andrew A. Hicks, and Irene Pichler corresponding author.
Parkinsons Dis. 2018; 2018: 8684906. Published online 2018 Mar 7. doi: 10.1155/2018/8684906

GCH1 mutations are common in Serbian patients with dystonia-parkinsonism: Challenging previously reported prevalence rates of DOPA-responsive dystonia

Dobričić V, Tomić A, Branković V, Kresojević N, Janković M, Westenberger A, Rašić VM, Klein C, Novaković I, Svetel M, Kostić VS.
Parkinsonism Relat Disord. 2017 Dec;45:81-84. doi: 10.1016/j.parkreldis.2017.09.017. Epub 2017 Sep 18.

Influence of L-dopa on subtle motor signs in heterozygous Parkin- and PINK1 mutation carriers.

Weissbach A, König IR, Hückelheim K, Pramstaller PP, Werner E, Brüggemann N, Tadic V, Lohmann K, Bäumer T, Münchau A, Kasten M, Klein C.
Parkinsonism Relat Disord. 2017 Jul 8. pii: S1353-8020(17)30236-5. doi: 10.1016/j.parkreldis.2017.07.003. [Epub ahead of print]

Evaluating the role of TMEM230 variants in Parkinson’s disease

Baumann H, Wolff S, Münchau A, Hagenah JM, Lohmann K, Klein C.
Parkinsonism Relat Disord. 2017 Feb;35:100-101. doi: 10.1016/j.parkreldis.2016.12.015. Epub 2016 Dec 20.