Jesse Hinckley

A novel mutation in PLP1 causes severe hereditary spastic paraplegia type 2.

L. Noetzli, P. Sanz, G. Brodsky, 2014, Gene.

Mutations in NBEAL2, encoding a BEACH protein, cause gray platelet syndrome

J. Parkinson, A. Weyrich, Jesse Hinckley, 2011, Nature Genetics.

Homozygosity mapping with SNP arrays confirms 3p21 as a recessive locus for gray platelet syndrome and narrows the interval significantly.

Jesse Hinckley, J. Di Paola, Gi-Yung Ryu, 2011, Blood.

Variable content of von Willebrand factor mutant monomer drives the phenotypic variability in a family with von Willebrand disease.

Junmei Chen, R. Montgomery, Jesse Hinckley, 2015, Blood.