Inmaculada Bernal-Bernal

The Genetic Architecture of Parkinson Disease in Spain: Characterizing Population‐Specific Risk, Differential Haplotype Structures, and Providing Etiologic Insight

Sonja W. Scholz, D. Hernandez, M. Nalls, 2019, Movement disorders : official journal of the Movement Disorder Society.

The genetic architecture of Parkinson disease in Spain: characterizing population-specific risk, differential haplotype structures, and providing etiologic insight

Sonja W. Scholz, D. Hernandez, M. Nalls, 2019, bioRxiv.

Analysis of c.801-2A>G mutation in the DNAJC6 gene in Parkinson's disease in southern Spain.

Inmaculada Bernal-Bernal, Marta Bonilla-Toribio, F. Carrillo, 2014, Parkinsonism & related disorders.

Regulatory sites for splicing in human basal ganglia are enriched for disease-relevant information

Sonja W. Scholz, Demis A. Kia, Miguel Ángel Martínez, 2020, Nature Communications.

Genetic factors influencing frontostriatal dysfunction and the development of dementia in Parkinson's disease

Inmaculada Bernal-Bernal, Marta Bonilla-Toribio, P. Gómez-Garre, 2017, PloS one.

GBA Variants Influence Motor and Non-Motor Features of Parkinson’s Disease

Inmaculada Bernal-Bernal, Marta Bonilla-Toribio, F. Carrillo, 2016, PloS one.

Lack of validation of variants associated with cervical dystonia risk: A GWAS replication study

Inmaculada Bernal-Bernal, Marta Bonilla-Toribio, F. Carrillo, 2014, Movement disorders : official journal of the Movement Disorder Society.

Identification of novel risk loci, causal insights, and heritable risk for Parkinson's disease: a meta-analysis of genome-wide association studies

Sonja W. Scholz, D. Hernandez, M. Nalls, 2019, The Lancet Neurology.

LRP10 in α-synucleinopathies

Sonja W. Scholz, D. Hernandez, M. Nalls, 2018, The Lancet Neurology.