Nathan Pankratz

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

Daniel Taliun, Daniel Harris, Michael D. Kessler et al. · Nature · 2021 · 2.2K citations · Full text

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 · 453 citations

Mendelian Disorder, Familial Parkinson, Genetic Disorder +7

Genomewide association study for susceptibility genes contributing to familial Parkinson disease

Nathan Pankratz, Jemma B. Wilk, Jeanne C. Latourelle et al. · Human Genetics · 2008 · 442 citations · Full text

Familial Parkinson Disease, Genomewide Association Study, Disease Susceptibility +10

Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program

Daniel Taliun, Daniel Harris, Michael D. Kessler et al. · 2019 · 422 citations · Full text

Engineering, Genetics, Genomics +21

Functional variants in the <i>LRRK2</i> gene confer shared effects on risk for Crohn’s disease and Parkinson’s disease

Ken Hui, Heriberto Fernandez-Hernandez, Jianzhong Hu et al. · Science Translational Medicine · 2018 · 397 citations · Full text