J. Bridgers

Systems-Based Analysis of the Sarcocystis neurona Genome Identifies Pathways That Contribute to a Heteroxenous Life Cycle

L. S. Swapna, J. Parkinson, Melissa A. Chiasson, 2015, mBio.

Diagnostic Utility of Exome Sequencing for Kidney Disease

Chunhua Weng, Krzysztof Kiryluk, Jai Radhakrishnan, 2019, The New England journal of medicine.

Loss of FBXO 11 function establishes a stem cell program in acute 1 myeloid leukemia through dysregulation of the mitochondrial protease 2 LONP 1 3

G. Morin, A. Karsan, J. Parker, 2022 .

Ultra-rare genetic variation in common epilepsies: a case-control sequencing study

Michael R. Johnson, I. Scheffer, H. Mefford, 2017, The Lancet Neurology.

A case-control collapsing analysis identifies epilepsy genes implicated in trio sequencing studies focused on de novo mutations

I. Scheffer, D. Goldstein, A. Allen, 2017, PLoS genetics.

The neoantigen landscape of the coding and noncoding cancer genome space.

E. Pleasance, A. Karsan, E. Titmuss, 2022, The Journal of molecular diagnostics : JMD.

An Exome Sequencing Study to Assess the Role of Rare Genetic Variation in Pulmonary Fibrosis

D. Goldstein, A. Allen, C. Malone, 2017, American journal of respiratory and critical care medicine.

BDNF Val66Met genotype and 6-month remission rates in late-life depression

W. Taylor, D. Steffens, D. Mcquoid, 2011, The Pharmacogenomics Journal.