C. Olds

Lissencephaly: Expanded imaging and clinical classification

Renzo Guerrini, William B Dobyns, A James Barkovich, 2017, American journal of medical genetics. Part A.

PIK3CA-associated developmental disorders exhibit distinct classes of mutations with variable expression and tissue distribution

Beth K. Martin, Martin, J. Shendure, 2016, JCI insight.

PIK3CA-associated developmental disorders exhibit distinct classes of mutations with variable expression and tissue distribution

J. Shendure, Martin Kircher, K. Devriendt, 2016, JCI insight.

Analysis of 17 genes detects mutations in 81% of 811 patients with lissencephaly

G. Carvill, D. Ledbetter, M. Ross, 2018, Genetics in Medicine.

Characterization of mutations of the phosphoinositide-3-kinase regulatory subunit, PIK3R2, in perisylvian polymicrogyria: a next generation sequencing study

Beth K. Martin, J. Shendure, K. Friend, 2015, The Lancet Neurology.

Update on the ACTG1‐associated Baraitser–Winter cerebrofrontofacial syndrome

A. Rump, W. Dobyns, J. Altmüller, 2016, American journal of medical genetics. Part A.

Mutations in CRADD Result in Reduced Caspase-2-Mediated Neuronal Apoptosis and Cause Megalencephaly with a Rare Lissencephaly Variant

E. Puffenberger, K. Strauss, K. Millen, 2016, American journal of human genetics.

Analysis of 17 genes detects mutations in 81% of 811 patients with lissencephaly

G. Carvill, D. Ledbetter, M. Ross, 2018, Genetics in Medicine.

Applying a modified metabarcoding approach for the sequencing of macrofungal specimens from fungarium collections

Andrew W. Wilson, Jessie W. Berta-Thompson, R. Levy, 2021, bioRxiv.