Common variants in 22 loci are associated with QRS duration and cardiac ventricular conductionNona Sotoodehnia, L. Adrienne Cupples, Pim van der Harst et al.|Nature Genetics|2010Cited by 358
The LRRK2 I2012T, G2019S, and I2020T mutations are rare in Taiwanese patients with sporadic Parkinson's diseaseChin-Song Lu, Vincenzo Bonifati, Erik Simons et al.|Parkinsonism & Related Disorders|2005Cited by 79
Genetic Linkage Is Excluded for the D<sub>2</sub>-Dopamine Receptor &lambda;HD2Gl and Flanking Loci on Chromosome 11q22-q23 in Tourette SyndromeEric J. Devor, Ben A. Oostra, David K. Grandy et al.|Human Heredity|1990Cited by 41