H. Madoev

Genotype‐Phenotype Relations for the Parkinson's Disease Genes Parkin, PINK1, DJ1: MDSGene Systematic Review

I. König, K. Lohmann, L. Bertram, 2018, Movement disorders : official journal of the Movement Disorder Society.

Genotype‐phenotype relations for the Parkinson's disease genes SNCA, LRRK2, VPS35: MDSGene systematic review

I. König, K. Lohmann, C. Lill, 2018, Movement disorders : official journal of the Movement Disorder Society.

Genotype–Phenotype Relations for Isolated Dystonia Genes: MDSGene Systematic Review

I. König, K. Lohmann, C. Klein, 2021, Movement disorders : official journal of the Movement Disorder Society.

Motor protein binding and mitochondrial transport are altered by pathogenic TUBB4A variants

K. Lohmann, C. Sue, C. Klein, 2018, Human mutation.

Genotype–Phenotype Relations in Primary Familial Brain Calcification: Systematic MDSGene Review

K. Lohmann, C. Klein, M. Kasten, 2021, Movement disorders : official journal of the Movement Disorder Society.

Expanding Data Collection for the MDSGene Database: X‐linked Dystonia‐Parkinsonism as Use Case Example

N. Brüggemann, C. Klein, R. Rosales, 2020, Movement disorders : official journal of the Movement Disorder Society.

Genotype–Phenotype Relations for the Atypical Parkinsonism Genes:MDSGene Systematic Review

I. König, H. Huppertz, M. Stamelou, 2021, Movement disorders : official journal of the Movement Disorder Society.

Identification of genetic risk loci and causal insights associated with Parkinson's disease in African and African admixed populations: a genome-wide association study

Chelsea X Alvarado, D. Hernandez, M. Nalls, 2023, The Lancet Neurology.

Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2)

M. Nalls, A. Singleton, C. Blauwendraat, 2023, NPJ Parkinson's disease.

Monogenic portal of the global Parkinson's Genetics Program (GP2)

K. Lohmann, P. Heutink, E. Valente, 2021, Journal of the Neurological Sciences.