McNeill, Nathan

Whole exome sequencing in patients with white matter abnormalities

Vanderver, A., Simons, C., Helman, G., Crawford, J., Wolf, N. I., Bernard, G., Pizzino, A., Schmidt, J. L., Takanohashi, A., Miller, D., et al. (2016) · Annals of Neurology

Genomics and Rare DiseasesHereditary Neurological Disorders

Cited by 145

TIM, a targeted insertional mutagenesis method utilizing CRISPR/Cas9 in Chlamydomonas reinhardtii

Picariello, T., Hou, Y., Kubo, T., McNeill, N. A., Yanagisawa, H.-A., Oda, T., & Witman, G. B. (2020) · PLOS ONE

CRISPR and Genetic EngineeringPlant Genetic and Mutation Studies

Cited by 83