P. C. Elhosary

Single-Neuron Sequencing Analysis of L1 Retrotransposition and Somatic Mutation in the Human Brain

C. Walsh, P. Park, E. Lee, 2012, Cell.

Single-Cell, Genome-wide Sequencing Identifies Clonal Somatic Copy-Number Variation in the Human Brain

Annapurna Poduri, Christopher A. Walsh, C. Walsh, 2014, Cell reports.

Integrated genome and transcriptome sequencing identifies a noncoding mutation in the genome replication factor DONSON as the cause of microcephaly-micromelia syndrome

Michael E. Coulter, C. Walsh, S. Wiemann, 2017, Genome research.

Single-cell, genome-wide sequencing identifies clonal somatic copy-number variation in the human brain.

Annapurna Poduri, Christopher A Walsh, C. Walsh, 2015, Cell reports.

Somatic Activation of AKT3 Causes Hemispheric Developmental Brain Malformations

Maria K. Lehtinen, C. Walsh, R. Beroukhim, 2012, Neuron.

Mutations in PYCR2, Encoding Pyrroline-5-Carboxylate Reductase 2, Cause Microcephaly and Hypomyelination.

Michael E. Coulter, A. Barkovich, J. Stoler, 2015, American journal of human genetics.

Candidate Gene Sequencing of LHX2, HESX1, and SOX2 in a Large Schizencephaly Cohort

C. Walsh, G. Shaw, A. Barkovich, 2010, American journal of medical genetics. Part A.