Cheryl Halter

Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease

William C. Nichols, Nathan Pankratz, Dena Hernández et al. · The Lancet · 2005 · 454 citations

Life Sciences, Genetics, Molecular Genetics +14

Genomewide association study for susceptibility genes contributing to familial Parkinson disease

Nathan Pankratz, Jemma B. Wilk, Jeanne C. Latourelle et al. · Human Genetics · 2008 · 444 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Genome Screen to Identify Susceptibility Genes for Parkinson Disease in a Sample without parkin Mutations

Nathan Pankratz, William C. Nichols, Sean K. Uniacke et al. · The American Journal of Human Genetics · 2002 · 184 citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Significant Linkage of Parkinson Disease to Chromosome 2q36-37

Nathan Pankratz, William C. Nichols, Sean K. Uniacke et al. · The American Journal of Human Genetics · 2003 · 159 citations · Full text

Life Sciences, Genetics, Molecular Genetics +12

Presence of an APOE4 allele results in significantly earlier onset of Parkinson's disease and a higher risk with dementia

Nathan Pankratz, Lisa Byder, Cheryl Halter et al. · Movement Disorders · 2005 · 125 citations

Medicine, Genetics, Neurology +17