Jane Juusola

De novo mutations in PURA are associated with hypotonia and developmental delay

Wendy K. Chung, W. Chung, K. Retterer, 2015, Cold Spring Harbor molecular case studies.

De novo PHIP-predicted deleterious variants are associated with developmental delay, intellectual disability, obesity, and dysmorphic features

Wendy K. Chung, W. Chung, M. Bekheirnia, 2016, Cold Spring Harbor molecular case studies.

mRNA Profiling for Body Fluid Identification by Multiplex Quantitative RT‐PCR *

Jack Ballantyne, J. Ballantyne, J. Juusola, 2007, Journal of forensic sciences.

Mutations in SPATA5 Are Associated with Microcephaly, Intellectual Disability, Seizures, and Hearing Loss.

Katherine Mathews, Karin Panzer, Matthew Deardorff, 2015, American journal of human genetics.

An mRNA and DNA co-isolation method for forensic casework samples.

Jack Ballantyne, J. Ballantyne, J. Juusola, 2004, Analytical biochemistry.

Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling.

Michael J Parker, Katrina Tatton-Brown, Christian Gilissen, 2015, American journal of human genetics.

Multiplex mRNA profiling for the identification of body fluids.

Jack Ballantyne, J. Ballantyne, J. Juusola, 2005, Forensic science international.