Estimation of genetic risk function with covariates in the presence of missing genotypes

Efficient estimation of nonparametric genetic risk function with censored data

(2015) Yuanjia Wang et al.   BIOMETRIKA

Identification of Genetic Factors that Modify Clinical Onset of Huntington’s Disease

(2015) Jong-Min Lee et al.   CELL

Age-specific penetrance ofLRRK2G2019S in the Michael J. Fox Ashkenazi Jewish LRRK2 Consortium

(2015) Karen Marder et al.   NEUROLOGY

Estimating time-varying effects for overdispersed recurrent events data with treatment switching

(2013) Q. Chen et al.   BIOMETRIKA

The current and projected economic burden of Parkinson's disease in the United States

(2013) Stacey L. Kowal et al.   MOVEMENT DISORDERS

Parkinson disease phenotype in Ashkenazi jews with and withoutLRRK2G2019S mutations

(2013) Roy N. Alcalay et al.   MOVEMENT DISORDERS

RAB7L1 Interacts with LRRK2 to Modify Intraneuronal Protein Sorting and Parkinson’s Disease Risk

(2013) David A. MacLeod et al.   NEURON

Kin-cohort analysis of LRRK2-G2019S penetrance in Parkinson's disease

(2011) Stefano Goldwurm et al.   MOVEMENT DISORDERS

Gender differences in the risk of familial parkinsonism: Beyond LRRK2?

(2011) R. Saunders-Pullman et al.   NEUROSCIENCE LETTERS

Statistical inference on the penetrances of rare genetic mutations based on a case-family design

(2010) H. Zhang et al.   BIOSTATISTICS

Statistical Methods for Analyzing Right-Censored Length-Biased Data under Cox Model

(2009) Jing Qin et al.   BIOMETRICS

Detecting gene–gene interactions that underlie human diseases

(2009) Heather J Cordell   NATURE REVIEWS GENETICS

Brain Morphology in Older African Americans, Caribbean Hispanics, and Whites From Northern Manhattan

(2008) Adam M. Brickman et al.   ARCHIVES OF NEUROLOGY

Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study

(2008) Daniel G Healy et al.   LANCET NEUROLOGY